Metal-Π Complexes:: Metal Carbonyls: Structure and Bonding

CHAPTER 11
Metal-Π Complexes:
 Metal Carbonyls: Structure and Bonding
The bonding in coordination compounds is usually visualized as the donation of ligand electron pair
to the metal center only. However, there are some ligands which not only have filled atomic orbitals (donor
orbitals) but also have some empty orbitals (acceptor orbitals) of appropriate symmetry and energy to accept
electron density from a central metal atom or ion. This interaction is called π-backbonding or π-backdonation;
and is generally shown by CO, NO, PR3 and alkene-alkyne type ligands. Two of the most common examples
where π-backbonding occurs include Ni(CO)4 and Zeise's salt.
Furthermore, metal carbonyls are one of the most widely studied types of metal-π complexes, that
can simply be defined as the coordination compounds of transition metals with carbon monoxide as a ligand.
Metal carbonyls are very useful in synthetic organic chemistry and in homogeneous catalysis, like the process
of hydroformylation. In the Mond process, nickel carbonyl is used to produce pure nickel. In organometallic
chemistry, metal carbonyls act as precursors for the synthesis of many organometallic compounds. Metal
carbonyls are toxic by inhalation, skin contact, or ingestion, in part due to their ability to attach to the iron of
hemoglobin to give carboxyhemoglobin, which inhibits the binding of dioxygen. Metal carbonyls can be
classified on the basis of the number of metal centers; mononuclear carbonyls have only one metal atom or ion
such as Fe(CO)5, while polynuclear carbonyls contain more than one metal center like homonuclear Fe2(CO)9
and heteronuclear MnRe(CO)10. One more categorization basis of metal carbonyls is the bonding profile of
carbonyl ligand; non-bridging carbonyls and bridging carbonyls. Non-bridging carbonyls may or may not
contain metal-metal bonds. For instance, Ru(CO)5 and Mn2(CO)10 both have only terminal carbonyl groups
but Mn2(CO)10 has one metal-metal bond also. On the other hand, bridging metal carbonyls like Fe3(CO)12, in
addition to terminal CO groups, do have CO groups bridged to more than one metal center.
 General Methods of Preparation
1. By direct reaction: Some of the mononuclear carbonyls can be prepared by the direct reaction of carbon
monoxide with metal powder.
25°C
Ni + 4CO → Ni(CO)4
1 atm
200°C
Fe + 5CO → Fe(CO)5
200 atm
150°C
2Co + 8CO → Co2 (CO)8
35 atm
Copyright © Mandeep Dalal

CHAPTER 11 Metal-Π Complexes: 427
2. By reduction: One of the most widely used methods to synthesize metal carbonyls is the reduction of
corresponding metal salts in the presence of carbon monoxide.
AlCl3
CrCl3 + Al + 6CO → Cr(CO)6 + AlCl3
benzene
diglyme, 100°C
VCl3 + 4Na + 6CO → [(diglyme)2 Na][V(CO)6 ] + 3NaCl
high pressure
200°C
2CoI2 + 4Cu + 8CO → Co2 (CO)8 + 4CuI
200 atm
120 − 200°C
2CoCO3 + 2H2 + 8CO → Co2 (CO)8 + 2H2 O + 2CO2
250 − 300 atm
250°C
Re2 O7 + 17CO → Re2 (CO)10 + 7CO2
350 atm
In the last reaction, carbon monoxide is the reducing agent on its own.
3. From mononuclear carbonyls: Iron pentacarbonyl is sensitive to light and air and can be used to synthesize
Fe2(CO)9 by direct photolysis.
ℎ𝜈
2Fe(CO)5 → Fe2 (CO)9 + CO
Similarly
ℎ𝜈
2Os(CO)5 → Os2 (CO)9 + CO
ℎ𝜈
2Ru(CO)5 → Ru2 (CO)9 + CO
4. From iron pentacarbonyl: Carbon monoxide ligands in Fe(CO)5 are labile and therefore can be used to
synthesize other metal carbonyls.
110°C
MoCl6 + 3Fe(CO)5 → Mo(CO)6 + 3FeCl2 + 9CO
ether
110°C
WCl6 + 3Fe(CO)5 → W(CO)6 + 3FeCl2 + 9CO
ether
5. From metathesis reaction: Mixed-metal carbonyls can successfully be prepared via a metathesis reaction
route as:
KCo(CO)4 + [Ru(CO)3 Cl2 ]2 → 2RuCo2 (CO)11 + 4KCl
Buy the complete book with TOC navigation, Copyright © Mandeep Dalal
high resolution images and
no watermark.
428 A Textbook of Inorganic Chemistry – Volume I
 Structures of Metal Carbonyls

The structure of metal carbonyls can mainly be classified into three categories; first, as the
mononuclear systems that contain only one metal atom, the second one as binuclear systems that may or may
not contain bridging carbonyls, and the last one as the polynuclear systems which contain more than two metal
centers with all terminal, all bridging, or a mixture of two types of carbonyl groups.
1. Mononuclear metal carbonyls: The structure of mononuclear metal carbonyls is pretty simple and easy to
visualize. This is definitely due to the presence of only one metal center. The general examples of mononuclear
metal carbonyls include tetrahedral Ni(CO)4 and Pd(CO)4; the trigonal bipyramidal case of Fe(CO)5, Ru(CO)5
and Os(CO)5; and the octahedral geometries of V(CO)6, Cr(CO)6, Mo(CO)5 and W(CO)6.
Figure 1. The structures of some mononuclear metal carbonyls.
2. Binuclear metal carbonyls: The structure of the binuclear metal carbonyls comprises of two metal centers
and involve either metal-metal bonds or bridging CO groups or both. For example, the Co2(CO)8 is known to
exist in two isomers. The first one has a D3d symmetry with one metal-metal bond with zero bridging carbonyls;
the second one is of C2v symmetry and has two bridging CO ligands along with one metal-metal bond. The
structure of Fe2(CO)9 exist with D3h symmetry and contains three bridging CO ligands and six terminal CO
groups attached. Furthermore, M2CO10 (M = Mn, Tc, Re) exists with D4d symmetry with one metal-metal bond
and four CO ligands attached to each of the metal centers.
Figure 2. Continued on the next page…
no watermark.
Figure 2. The structures of some binuclear metal carbonyls.
3. Polynuclear metal carbonyls: The structures of the polynuclear metal carbonyls comprises of three or more
metal centers and involve all bridging, all terminal, or a mixture of two types of CO groups. For example, the
Ru3(CO)12 cluster has D3h symmetry, comprises of an equilateral triangle of Ru centers, each of which has two
axial and two equatorial CO ligands. Os3(CO)12 has the same structure, whereas Fe3(CO)12 is different, with
two bridging CO ligands, resulting in C2v symmetry. M4CO12 (M = Co, Rh) is consisted of a tetrahedral M4
core, but the molecular symmetry is C3v. Three carbonyl ligands are bridging ligands and nine are terminal.
However, Ir4(CO)12 has perfect Td symmetry with no bridging CO ligands groups. The Rh4 and Ir4 clusters are
more thermally robust than that of the Co4 compound, reflecting the usual trend in the strengths of metal-metal
bond for second and third-row metals vs those for the first row metals. Furthermore, [Re 4(CO)16]2− has D2h
symmetry with no bridging carbonyl. Furthermore, the structure of Os 4(CO)16, Os4(CO)15 and Os4(CO)14 are
somewhat more complex because of non-rigidity. The tetranuclear Os4(CO)16 is analogs to the cyclobutane
with a puckered structure. The X-ray diffraction analysis of Os4(CO)14 unveiled an irregular tetrahedral Os4
skeleton with four weakly semi-bridging CO groups and four different Os–Os bond lengths. The experimental
structure of Os4(CO)15 was determined to have a planar butterfly-like geometry consisting of two triangles
sharing an edge. The hexanuclear M6(CO)16 (M = Rh, Co) exists with an octahedral core with alternate faces
participating in the bridging; i.e. with four triply bridged and twelve terminal carbonyls.
no watermark.
no watermark.
Figure 3. The structures of some polynuclear metal carbonyls.
 Bonding in Metal Carbonyls

In order to rationalize the nature of the bonding between the metal center and the carbonyl ligand, we
must understand the bonding within the carbonyl ligand itself first. It is a quite well-known fact that the CO
group acts as a good sigma donor as well as a good π-acceptor ligand. Two popular approaches to study the
bonding in carbon monoxide, as well as metal carbonyls, are discussed below.
1. Valence bond theory: According to this model, the bonding within the CO molecule can be best shown as:
The carbon and oxygen atoms in CO are sp-hybridized with the following electronic configurations.
C (ground state) = 1s2, 2s2, 2px1, 2py1, 2pz0
C (hybridized state) = 1s2, (spx)2, (spx)1, 2py1, 2pz0
Similarly,
O (ground state) = 1s2, 2s2, 2px1, 2py1, 2pz2
O (hybridized state) = 1s2, (spx)2, (spx)1, 2py1, 2pz2
no watermark.
Now, the one half-filled spx-hybridized orbital of carbon atom overlap with half-filled spx-hybridized orbital
of the oxygen atom to form a σ bond, while spx-hybridized lone pairs on both atoms remain non-bonding in
nature. Moreover, two π bonds are formed as a result of the sidewise overlap; one between half-filled 2py
orbitals, and the second one as dative or coordinative interaction of fully filled 2pz orbital of oxygen with
empty 2pz orbital of carbon.
Figure 4. Bonding behavior in CO ligand according to the valence bond method.
Furthermore, the valence bond theory treats the bonding mode of the carbonyl with the metal center
in terms of hybridization and resonance phenomena. The central metal atom or ion provides the required
number of empty hybrid orbitals with proper orientation to accept the electron pair from surrounding ligands.
For instance, in Cr(CO)6 the chromium atom undergoes a d2sp3 hybridization to generate six empty hybrid
orbital of equivalent shapes and the same energy. When one of the carbonyl ligands approaches this metal ion
with its internuclear axis along x-axis, the filled hybrid lone pair of electron on carbon atom overlap with one
of the two empty hybrid orbitals orientated oppositely in x-direction. The metal-carbon multiple bonds is
explained in terms of various resonating structures which consequently reduces the bond strength of the
carbon-oxygen bond. It should also be noted that, though there are two hybrid lone pairs (one on carbon and
the other on the oxygen); the bonding of carbonyl group with metal takes place via a donation through carbon
end always. This can be explained in terms of the higher energy of hybrid lone pair carbon than oxygen.
no watermark.
Figure 5. The valence bond nature of σ and π overlap in metal carbonyls.
2. Molecular orbital theory: This is the best model to explain the bonding within the CO ligand as well as in
metal carbonyl complexes. There are total three molecular diagrams for carbonyl ligand which were proposed
from time to time. Though, all three molecular orbital (MO) diagrams are able to explain the nature of metal-
carbonyl π-bonding; the initial treatment was not so effective to explain the σ donation, the second one does
also suffer from some minor anomalies. The third molecular orbital diagram is most widely accepted in the
scientific community as it gives a logical explanation to what had been a mystery in metal carbonyl chemistry.
We will study these MO diagrams in the order they were proposed.
i) The first molecular orbital diagram of carbon monoxide assumes that the atomic orbitals of carbon and
oxygen interact with each other to create molecular orbitals. The electronic configurations of C and O are:
Carbon = 1s2, 2s2, 2p2
Oxygen = 1s2, 2s2, 2p4
The number of outer electrons in carbon and oxygen are four and six, respectively. Thus, a total of 10 electrons
are to be filled in the molecular orbitals of the carbon monoxide molecule. The higher energy of corresponding
atomic orbitals of carbon is due to its lower electronegativity, which makes the bonding and antibonding
molecular orbitals to receive different contributions from atomic orbitals of carbon and oxygen. The bonding
molecular orbitals will be rich in atomic orbitals of oxygen while antibonding molecular orbitals, that are closer
to carbon in energy, would be rich in atomic orbitals of carbon. The bonding molecular orbitals will have more
characteristics of atomic orbitals of Oxygen and antibonding Molecular orbitals would have more
no watermark.
characteristics of carbon. The electronic configuration of CO molecule will be σ2s², σ*2s², σ2pz², π2px², π2py²
which gives a bond order three i.e. triple bond between carbon and oxygen. The molecular orbital diagram and
expected bonding mode of the carbonyl ligand are given below.
Figure 6. The first generation molecular orbital diagram of carbonyl ligand.
The formation of molecular orbitals given above is actually an oversimplification of a ticklish

problem. This statement is made on the basis of two facts. The first one is that when one electron removed
from CO to form CO+, the bond order actually increases, which is actually the opposite of what is expected if
the electron is lost from the highest occupied molecular orbital (HOMO) of bonding nature. Its bond order
should be decreased from the removal of an electron from π2px² or π2py², which suggests that the HOMO of
carbon monoxide should be of antibonding nature rather bonding. The second anomaly also arises from the
MO diagram of CO ligand which clearly shows that in order to donate electron density from π-bonding
molecular orbital, the carbonyl ligand must approach the metal center with its carbon-oxygen internuclear axis
perpendicular to x, y or z-axis assigned to the central atom. This explains how the empty π*2px and π*2py could
be used to accept electron density from filled d-orbitals of central metal atom or ion. However, in actual
practice, the carbonyl ligand binds to the metal center in linear fashion via carbon end only.
no watermark.
Figure 7. The expected nature of σ and π overlap in metal carbonyls from the first MO of CO.
ii) The second molecular orbital diagram of carbon monoxide was suggested by Coulson which assumes that
the first molecular orbital diagram of CO is not correct. According to Coulson, 2s and 2px atomic orbitals of
both carbon and oxygen undergo hybridization before they create molecular orbitals. The carbon and oxygen
atoms in carbon monoxide are sp-hybridized with the following electronic configurations.
C (hybridized state) = 1s2, (spx)2, (spx)1, 2py1, 2pz0
O (hybridized state) = 1s2, (spx)2, (spx)1, 2py1, 2pz2
The total number of valence electrons in carbon and oxygen are four and six, respectively; and thus, ten
electrons are to be filled in the molecular orbitals of CO molecule. The half-filled spx hybrid orbitals of carbon
and oxygen interact to form σ and σ * molecular orbitals; while the fully-filled spx hybrid lone pair orbitals of
carbon and oxygen remain non-bonding. Moreover, doubly degenerate sets of π-bonding and π-antibonding
molecular orbitals are also formed due to the sidewise overlap of 2py orbitals and 2pz orbitals.
Figure 8. The nature of σ and π in carbonyl ligand.
The bonding molecular orbitals will be rich in atomic orbitals of oxygen while antibonding molecular orbitals,
that are closer to carbon in energy, would be rich in atomic orbitals of carbon. The bonding molecular orbitals
no watermark.
will have more characteristics of atomic orbitals of oxygen and antibonding molecular orbitals would have
more characteristics of carbon. The molecular orbital diagram carbon monoxide proposed by Coulson is given
below.
Figure 9. The second molecular orbital diagram of carbonyl ligand.
The MO diagram shown above is very useful in explaining the bonding between the metal center and
carbonyl ligand. This diagram eliminates the possibility of sigma donation through bonding molecular orbital
and perpendicular orientation CO ligand as the HOMO is now non-bonding hybrid lone pair rather π-bonding.
This also explains why the carbonyl group prefers to bond via carbon end in a linear manner. This also explains
how the lowest unoccupied molecular orbital (LUMO) π*2pz and π*2py could be used to accept electron density
from filled d-orbitals of central metal atom or ion. Moreover, the reduced CO stretching frequency of metal
coordinated carbonyl can be attributed to the reduced bond order due to the transfer of d-electron density from
metal to π* orbital carbonyl ligand. However, the increase in bond order when one electron is removed from
no watermark.
CO to form CO+ is still a mystery because the electron is lost from the highest occupied molecular orbital
(HOMO) of nonbonding bonding nature, and the bond order should have remained the same.
Figure 10. The nature of σ and π overlap in metal carbonyls.
iii) This molecular orbital diagram of carbon monoxide is most widely accepted to rationalize its σ-donor and
π-acceptor strength. The total number of valence electrons in carbon and oxygen are four and six, respectively;
and thus, ten electrons are to be filled in the molecular orbitals of CO molecule. A total of four singly
degenerate σ- molecular orbitals and two doubly degenerate sets of π- molecular orbitals are formed. One
doubly degenerate set of π molecular orbitals will be bonding while the other one will be antibonding in nature.
The nature of σ molecular orbitals is more complex as three out of four are of bonding character. Initially, the
σ5 was thought to be of antibonding to justify the higher bond order of CO+. However, the σ5 is slightly bonding
in nature because there is some mixing with the p atomic orbitals of the right symmetry. Out of four σ-
molecular orbitals, only σ6 possesses the antibonding character, while σ5 goes with expected bonding
characteristics. The σ5 is essentially non-bonding and almost centered on the oxygen atom. Moreover, doubly
degenerate sets of π-bonding and π-antibonding molecular orbitals are also formed due to the sidewise overlap
of 2py orbitals and 2pz orbitals. The π-bonding molecular orbitals set will be rich in atomic orbitals of oxygen
while antibonding molecular orbitals, that are closer to carbon in energy, will be rich in atomic orbitals of
carbon atom.
However, the problem that why does the bond order increases when an electron is removed from CO
still persists. Because we are removing the electron from a bonding molecular orbital, its bond order must be
decreased. The possible explanation for the shortening of the bond after ionization is that the ionization induces
a shift of the electron-polarization in CO ligand. In other words, the ionization occurs as the loss of an electron
from a σ-HOMO orbital which is mostly carbon-centered; and since the HOMO-σ orbital is only slightly
bonding in nature, the loss of bonding character is quite small and could easily be compensated by the
advantage in covalent character; i.e. the formation of a positive partial charge on the carbon atom increases the
strength of the covalence of the bond and thus decreases the bond length. This enhanced covalent character
can also be visualized in terms of better interaction of two atomic orbitals if their energies are comparable. In
carbon monoxide molecule the atomic orbitals of oxygen lie energetically a lot below then the atomic orbitals
of carbon; But when the CO is oxidized to CO+, the partial positive charge on carbon shifts the atomic orbitals
of carbon down in energy, and thereby makes the energies closer to the related atomic orbitals of oxygen,
which leads to a stronger interaction when bonds are made.
no watermark.
Figure 11. Third molecular orbital diagram of carbonyl ligand.
The MO diagram shown above is very useful in explaining the bonding between the metal center and
carbonyl ligand. The carbonyl ligand uses its HOMO for sigma donation while simultaneously accepts electron
density from filled metal d-orbital to its π* LUMO.
Figure 12. The nature of σ and π overlap in metal carbonyls using third MO diagram of CO.
no watermark.
 Vibrational Spectra of Metal Carbonyls for Bonding and Structure

Elucidation
Vibrational spectroscopy is one of the most important methods used for the characterization of metal
carbonyls. This technique provides very useful information not only about the structural prototype of different
metal carbonyl compositions but also rationalizes the nature of bonding in them. Now, it is quite a well-known
fact that the C–O vibration for free carbonyl group (CO gas) is typically denoted as ν CO, and absorbs at 2143
cm−1. However, this C–O absorption shifts downward (sometimes upward) to cover a very wide range of
wavenumber as the carbonyl ligand gets attached to a metal center. This is obviously due to the fact that the
energies of the νCO band for the metal carbonyls directly correlate with the strength of the carbon-oxygen bond,
and are inversely correlated with the strength of the π-backbonding between the metal and the carbon. In other
words, the molecular orbital diagram of carbonyl group suggests that the highest occupied molecular orbital,
used for σ-donation is weakly bonding; but the lowest unoccupied molecular orbital, used for accepting d-
electron density from metal center is strongly antibonding; therefore, the σ-donation does not affect the CO
bond order very much but the acceptance of electron density in π * orbital decreases the bond order and
consequently the bond strength in a significant way. This effect reduces the force constant of C–O bond, while
the magnitude of force constant for M–C will be increased by this backbonding. As a result, the enhancement
of backbonding shifts the metal-carbon and carbon-oxygen stretching to higher and lower values, respectively.
The main features about the bonding and structure of metal carbonyls which can be obtained from the
vibrational spectra of metal carbonyls are discussed below:
 1. π-Basicity of the Metal Centre
The π-basicity of the metal center (and thus the C–O stretching frequency) depends upon a lot of
factors like the nature and magnitude of the charge on metal center, and the π-accepting tendency of ligands
attached other than the carbonyl. A negative charge on the metal center, or ligands with greater σ-donation and
weaker π-accepter strength, are expected to decrease the CO stretching frequency; while an accumulation of
positive charge on metal center, or ligands with weaker σ-donation stronger π-accepter strength are bound to
increase the CO stretching frequency. For example, in the isoelectronic series of Ti⟶Fe, the hexacarbonyls
show decreasing π-backbonding as one increases (makes more positive) the charge on the metal.
Compound [Ti(CO)6]2− [V(CO)6]1− [Cr(CO)6] [Mn(CO)6]1+ [Fe(CO)6]2+
νCO (cm−1) 1748 1859 2000 2095 2204
Compound [Hf(CO)6]2− [Ta(CO)6]1− [W(CO)6] [Re(CO)6]1+ [Os(CO)6]2+
νCO (cm−1) 1757 1850 1977 2085 2190
Hence, π-basic ligands increase π-electron density at the metal, and improved backbonding reduces νCO.

 2. Toleman Electronic Parameter

The electron-donating or withdrawing ability of a ligand is calculated in terms of the Tolman
electronic parameter (TEP), named after the inventor, Chadwick A. Tolman. It is determined by measuring the
frequency of the A1 vibrational mode of the carbonyl group in complex, Ni(CO)3L by infrared spectroscopy,
where L is the ligand being studied. Ni(CO)3L was chosen as the model compound because such complexes
can easily be synthesized from Ni(CO)4.
The CO band is pretty much unique and is rarely affected by other bands in the analyte's IR spectra. Moreover,
owing to the small size of carbonyl ligand, steric factors do not muddle the analysis. The coordination of CO
to a metal typically decreases νCO value from 2143 cm−1 (free CO). This can be rationalized by π-backbonding,
resulting from the sidewise overlap of metal orbitals of π-symmetry with the empty anti-bonding π* orbitals
on CO ligand. This increases the strength of the metal-carbon bond, but also weakens the C−O bond. If some
other ligand enhances the π-electrons-density on the metal, the CO bond strength decreases and so the νCO
value. On the other hand, if other ligands present compete with CO for π-backbonding, νCO increases. TEPs
for selected phosphines are given below.
L P(t-bu)3 P(Me)3 P(Ph)3 P(OEt)3 PCl3 PF3
νCO (cm−1) 2056.1 2064.1 2068.9 2076.3 2097.0 2110.8
The Tolman electronic parameter has been widely used to characterize the electronic properties of phosphine
based ligands.
 3. Structural Prototype of Metal Carbonyls
The symmetry behavior of different metal carbonyls can be used to determine the number of infrared
active vibrational modes, which in turn enable us to comment on structural prototypes. In other words, it is
well known from the group theory that only those vibrational modes will be observed which transform as the
electric-dipole moment operator; therefore, the number of observable infrared transitions for a particular
geometry can be predicted theoretically. These predictions are then matched with the experimentally observed
infrared spectra to shortlist the various possible structural prototypes. For instance, consider the case of five-
coordinated homoleptic metal carbonyl complexes. The two possible geometries are square-pyramidal and
trigonal bipyramidal.
no watermark.
Square pyramidal
Trigonal bipyramidal
Figure 13. Two possible geometries of Iron pentacarbonyl i.e. Fe(CO)5 complex.
For trigonal bipyramidal geometry, a reducible representation based on five C–O bonds is:
D3h E 2C3 3C2 σh 2S3 3σd Irreducible components
Γπ 5 2 1 3 0 3 2A1´ + A2´´ + E´
Out of four irreducible representations, A2´´ transforms as z-component while E´ transforms with x- and y-
components of the dipole moment. Now, owing to two doubly degenerate vibrational modes (E´), only two
peaks are expected in the experimental infrared spectrum. However, in the Raman infrared spectrum, three
peaks are expected as only 2A1´ and E´ irreducible components transform alongside the polarizability tensors.
For square pyramidal geometry, a reducible representation based on five C–O bonds is:
C4v E 2C4 C2 2σv 2σd Irreducible components
Γπ 5 2 1 3 3 2A1 + B1 + E
Out of four irreducible representations, 2A1 transforms as z-component while E transforms with x- and y-
components of the dipole moment. Now, owing to two doubly degenerate vibrational modes (E), only three
peaks are expected in the experimental infrared spectrum. However, in the Raman infrared spectrum, four
peaks are expected as all of the irreducible components transform alongside the polarizability tensors.
Similarly, the CO ligands of octahedral complexes, e.g. Cr(CO)6, transform as A1g, Eg, and T1u, but
only the T1u mode (anti-symmetric stretch of the apical carbonyl ligands) is infrared-active; and therefore, only
a single carbonyl stretching is observed in the IR-spectra of the octahedral metal hexacarbonyls. Spectra for
complexes of lower symmetry are more complex. For example, the IR spectrum of Fe2(CO)9 displays CO
bands at 2082, 2019, 1829 cm−1. The number of observable infrared-active vibrational modes for some metal
carbonyls are listed in the following below.
no watermark.
Table 1. The number of IR-active vibrational modes of several prototypical metal carbonyl complexes.
No. of carbonyls Structural prototype (No. of IR-peaks) Structural prototype (No. of IR-peaks)
Three
(1)
(2)
(3) (3)
(2) (3)
Four
(1) (4)
Table 1. Continued on the next page…
no watermark.
(3)
(4)
(3)
Five
(2)
(3)
Six
(1)
It is worthy to note that these rules apply to metal carbonyls in solution or the gas phase.
no watermark.
 4. Differentiation of Terminal and Bridging Carbonyl Groups

The mode of attachment of the carbonyl group to the metal center can also be determined by observed
CO stretching frequencies. Terminal carbonyls absorb at the higher wavenumber in comparison to the bridging
ones, which is obviously due to the fact that the extant of backbonding increases with the number of metal
centers. Three main modes of attachment of the carbonyl group with the metal center are:
Terminal µ2-bridging
µ3-bridging
The νCO follows the order: Terminal CO > µ2-bridging > µ3-bridging. The IR-range absorption for various
types of carbonyls groups is listed below.
Table 2. The CO stretching frequencies in different metal carbonyl complexes.
Bonding mode of CO νCO (cm−1)
Free CO 2143
Free CO+ 2184
Terminal CO 2120 - 1850
Symmetric µ2-CO 1860 - 1750
Symmetric µ3-CO 1730 - 1600
For instance, consider the rhodium carbonyl complexes:
Compound µ1-CO, νCO (cm−1) µ2-CO, νCO (cm−1) µ3-CO, νCO (cm−1)
Rh2(CO)8 2060, 2084 1846, 1862
Rh4(CO)12 2044, 2070, 2074 1886
Rh6(CO)16 2045, 2075 1819
There is also a semi-bridging mode that lies in between bridging and terminal bonding profile and is usually
labeled as asymmetric bridging carbonyls.
no watermark.
 5. Calculation of CO Bond Order

Owing to the well-known fact that the highest occupied molecular orbital (HOMO) set in carbonyl
ligand is of antibonding nature, a close correlation between the magnitude of backbonding and carbon-oxygen
bond order can easily be established. The vibrational frequency of a bond depends upon the strength of the
bond (which is measured by its force constant), and is given as:
(1)
1 𝑘
𝜈𝐶𝑂 (𝑐𝑚−1 ) = √
2𝜋𝑐 µ
Where k is the force constant and µ is the reduced mass. The physical significance of k is implied in the fact
that it is proportional to the strength of the bond involved. Therefore, any factor that increases the electron
density on CO group will decrease its bond order and its force constant; and the vice-versa is also true. In other
words, the decrease in νCO indicates a decrease in CO bond order while the increase in carbonyl stretching is
associated with increasing CO bond order. For instance, the infrared absorption of free CO occurs at 2143 cm−1
while the metal coordinated CO absorbs generally in the range of 2120-1800 cm−1. This clearly establishes the
fact that metal to ligand back donation does occur which in turn reduces its bond order. Hence, the
accumulation of positive charge or the deficiency of electron density will impart a larger CO bond order than
neutral or ionic carbonyl complexes. Consider the following trend in isoelectronic-isostructural carbonyls.
Compound [Ni(CO)4] [Co(CO)4]1− [Fe(CO)4]2−
νCO (cm−1) 2046 1890 1730
M–C Bond order 1.33 1.89 2.16
C–O Bond order 2.64 2.14 1.85
M–C + C–O Bond order 3.97 4.03 4.01
A similar trend is observed in the case of mixed carbonyls i.e. metal carbonyls having some other
ligands alongside CO group. If the other ligand is electron-withdrawing in nature, it would attract the electron
density from the metal center, which in turn would oppose the metal-carbonyl back bonding, yielding
somewhat higher carbon-oxygen bond order and higher carbonyl stretching frequency. On the other hand, If
the other ligand is electron-donating in nature, it would donate the electron density to the metal center, which
in turn would support the metal-carbonyl back bonding, yielding somewhat lower carbon-oxygen bond order
and lower carbonyl stretching frequency.
Compound [Ni(CO)4] [Ni(PF3)(CO)3] [Ni(PMe3)(CO)3]
νCO (cm−1) 2046 1990 1980
Hence, the bond order of CO in [Ni(PMe3)(CO)3] is definitely lower than in [Ni(PF3)(CO)3] because PMe3 is
a weaker π-acceptor than PF3 ligand.
no watermark.
 6. Study of Reaction Kinetics in Metal Carbonyls

Infrared spectroscopy is a very useful tool in the determination of reaction kinetics of metal carbonyl
complexes. From Beer’s Lambert Law, we know that the absorbance (A) is related to concentration (c) and
path length (l) of the sample as:
1 (1)
𝐴 = 𝜀𝑐𝑙 = 𝑙𝑜𝑔
𝑇
Where ε is the molar extinction coefficient and T is the transmittance of the solution. Therefore, the rate of
disappearance or appearance of a characteristic infrared absorption band can be used to estimate the rate of
change of concentration for the corresponding reactant or product. In other words, the rate of intensity decrease
in IR peaks of reactant, or the rate of intensity increase in IR peaks of product metal carbonyl is proportional
to the rate of change of concentration; which in turn enable us to record various kinetic parameters from
reaction order to activation energy or rate constants.
 Important Reactions of Metal Carbonyls

Metal carbonyls are important precursors for the synthesis of a mixed carbonyl or some important
organometallic complexes. Some of the main reactions shown by metal carbonyls are discussed below.
 1. Ligand Displacement Reactions
The displacement or substitution of CO ligands can be induced photochemically or thermally by some
other donor ligands. The ligand-domain is quite wide and comprises of cyanide (CN−), phosphines, nitrogen
donors, and ethers also. Olefins are very effective ligands that can afford synthetically useful derivatives. The
displacement reaction in 18-electron complexes usually follows a dissociative pathway, via a 16-electron
intermediate complex. The ligand-displacement-rate in 18-electron complexes is catalyzed by catalytic
amounts of oxidants through the electron-transfer phenomena. The displacement in 17-electron complexes
proceeds via an associative route with a 19-electron intermediate complex. It is worthy to note that the
replacement by bidentate ligands like o-phenanthroline(o-phen) and o-phenylene-bis(dimethyl arsine) (diars)
occurs in the multiple of two for carbonyl groups. For example:
Ni(CO)4 + o − phen → Ni(CO)2 (o − phen) + 2CO
Ni(CO)4 + 4CNR → Ni(CNR)4 + 4CO
Ni(CO)4 + 4PF3 → Ni(PF3 )4 + 4CO
Mo(CO)6 + 3Py → Mo(CO)3 (Py3 ) + 3CO
Fe(CO)5 + 2CNR → Fe(CO)3 (CNR)2 + 2CO
Mn2 (CO)10 + 2PR 3 → 2Mn(CO)4 (PR 3 ) + 2CO

The displacement reactions in metal carbonyls also point toward the differences in the bonding nature
of the attached ligands. For instance, radiochemical tracer studies for Mn(CO)5Br have unveiled that only four
carbonyl groups undergo exchange with 14CO.
Mn(CO)5 Br + 4 14CO → Mn( 14CO)4 (CO)(Br) + 4CO
In the structure of Mn(CO)5Br, four carbonyl groups undergoing exchange phenomena are present in the same
plane; which means that the CO group trans to bromido is bound more firmly because the Br group is not
competition for π-backbonding. On the other hand, four in-plane CO groups compete with each other all of
them are good acceptors, causing a labilization of each other.
(a) (b)
Figure 14. The structures of (a) Mn(CO)5Br and (b) Mn(CO)3(Py)3.
Furthermore, the reaction of Mn(CO)6 with py always results in the formation of a facial isomer of
Mn(CO)3(py)3 i.e. all the three carbonyl groups are located trans to the py ligands. This is obviously due to the
fact that the extent of π-donation to the three CO groups is maximum in facial configuration, owing to the
difference in the ability of CO and py for π-backbonding. When entering ligands are very good π-acceptors,
all the carbonyl groups may be displaced, just in Ni(CO)4 where PF3 ligands lead to the formation of Ni(PF3)4.
 2. Formation of Carbonylate Anions
It is quite a well-known fact that many carbonylate anions like [Fe(CO)4]2−, [Co(CO)4]−, [Mn(CO)5]−
and [V(CO)6]− follow the effective atomic number (EAN) rule. These ions are generally synthesized either by
the reaction of metal carbonyl with a strong reducing agent or by the reaction with strong bases.
Cr(CO)6 + 2Na → Na2 [Cr(CO)5 ] + Co
Mn2 (CO)10 + 2Na → 2Na[Mn(CO)5 ]
Co2 (CO)8 + 2Na → 2Na[Co(CO)4 ]
Fe(CO)5 + 3NaOH → Na[HFe(CO)4 ] + Na2 CO3 + H2 O
Fe2 (CO)9 + 4OH − → [Fe2 (CO)8 ]2− + CO2−

3 + 2H2 O
no watermark.
 3. Formation of Carbonylate Cations

Carbonylate cations are not as common as carbonylate anions and can be synthesized either by the
protonation of metal carbonyl in strong acids or, by the reaction with carbon monoxide and some Lewis acids.
Fe(CO)5 + HCl + BCl3 → [HFe(CO)5 ]+ [BCl4 ]−
[Mn(CO)5 Cl] + CO + AlCl3 → [Mn(CO)6 ]+ [AlCl4 ]−
The use of strong acids succeeded in preparing gold carbonyl cations such as [Au(CO)2]+, which is used as a
catalyst for the carbonylation of olefins. The cationic platinum carbonyl complex [Pt(CO)4]+ can be prepared
by working in so-called super acids such as antimony pentafluoride.
 4. Synthesis of Metal Carbonyl Hydrides
Carbonyl hydrides are generally synthesized either by the acidification of the solutions containing
the corresponding carbonylate anion, or by the reactions of metal carbonyls with hydrogen. For instance:
Co2 (CO)8 + H2 → 2[HCo(CO)4 )]
Mn2 (CO)10 + H2 → 2[HMn(CO)5 )]
[Co(CO)4 ]− + H + (aq) → [HCo(CO)4 ]
Na[HFe(CO)4 ] + H + (aq) → [H2 Fe(CO)4 ] + Na+ (aq)
Some of the metal carbonyl hydrides can be prepared by direct reaction of the metal with CO and H 2. For
example:
150°C
2Co + 8CO + H2 → 2[HCo(CO)4 )]
50 atm
 5. Synthesis of Metal Carbonyl Halides or Metal Halides

The metal carbonyl complexes are relatively unreactive toward many electrophiles; however, most
metal carbonyls do undergo halogenation. For example, Fe(CO)5 forms ferrous carbonyl halides. In some
reactions, metal-metal bonds are also broken by halogens. On the basis of the electron-counting scheme used,
this can be considered as oxidation of the metal center.
Fe(CO)5 + X 2 → [Fe(CO)4 𝑋2 ] + 𝐶𝑂
Mn2 (CO)10 + Cl2 → 2[Mn(CO)5 Cl]
Furthermore, some metal carbonyls also get decomposed into metal halides when treated with halogens as:
Ni(CO)4 + Br2 →NiBr2 + 4CO
Co2 (CO)8 + 2X2 → 2CoX2 + 8CO
no watermark.
 6. Formation of Metal Carbonyl Nitrosyls or Metal Nitrosyls

The metal carbonyl complexes react with nitrosyl ligand to form either metal carbonyl nitrosyls or
metal nitrosyl complexes. For example:
Fe(CO)5 + 2NO → [Fe(CO)2 (NO)2 ] + 3CO
Co2 (CO)8 + 2NO → 2[Co(CO)3 NO] + 2CO
Fe3 (CO)12 + 6NO → 3[Fe(CO)2 (NO)2 ] + 6CO
Ni(CO)4 + 4NO → [Ni(NO)(NO)2 ] + 4CO + N2 O
The displacement of carbonyl by the nitrosyl cation may be achieved using [NO][BF4] i.e nitrosyl
tetrafluoroborate. On applying to the hexacarbonyls of tungsten and molybdenum, the NO binds to the metal.
Some indirect methods involve the use of NO group from some other species, usually accompanied by
oxidation and reduction processes. For instance, the brown ring test in which the nitric oxide ligand is actually
supplied by the nitrate ion.
 7. Disproportionation Reactions
Many metal carbonyls show disproportionation reactions when exposed to some other coordinating
ligands. For instance, Fe(CO)5 reacts with amines to produce hexaaminoiron(II) tetracarbonylferrate(−II); or
Co2(CO)8 reacts with amine to form Hexaamminecobalt(II) bis-tetracarbonylcobaltate(−I) as:
2Fe(CO)5 + 6NH3 → [Fe(NH3 )6 ]2+ [Fe(CO)4 ]2− + 6CO
Co2 (CO)8 + 6NH3 → [Co(NH3 )6 ][Co(CO)4 ]2
The driving force for the above two reactions can be understood in terms of the ease of formation of the
carbonylate ions and the favorable coordination number for iron(II) involved. The disproportionation in both
cases generates a positive metal center and a metal center with a negative oxidation state. The carbonyl ligand,
being a soft base, prefers to bind to the softer acids, i.e., metal center with negative charge; on the other hand,
the ligands with nitrogen as donor site are hard Lewis bases, and therefore, prefer to bind to the harder acid
i.e. metal center with more positive charge on it.
A variety of carbonylate complexes can be synthesized via these disproportionation reactions which
makes this type quite important as far as the practical applications are concerned. For example, the [Ni2(CO)6]2−
anion and [Co(CNR)5][Co(CO)4] can be synthesized by the following reactions.:
3Ni(CO)4 + 3phen → [Ni(phen)3 ][Ni2 (CO)6 ] + 6CO
Co2 (CO)8 + 5RNC→ [Co(CNR)5 ][Co(CO)4 ] + 4CO
It is also worthy to note that the range of coordinating agents that will cause disproportionation is rather wide.
no watermark.
 Preparation, Bonding, Structure and Important Reactions of Transition

Metal Nitrosyl, Dinitrogen and Dioxygen Complexes
Besides carbon monoxide, there are many other important ligands which form π-complexes with
transition metal center; some of them are NO, N2 and O2 molecules. The methods of preparations, nature of
bonding, structure and their important reactions are discussed in detail below.
 1. Metal Nitrosyl Complexes
Metal nitrosyls are the complexes that contain nitric oxide (NO) bonded to a metal center (usually
transition element). There are various kinds of nitrosyl complexes known so far, which vary in respect of
coligand, structure and nature of bonding. Metal complexes having nitrosyl ligands only are labeled as isoleptic
nitrosyls. They are very rare, one of the special members of this class is Cr(NO)4. On one hand, polycarbonyl
complexes are very much common, even trinitrosyl complexes are rare on the other.
Preparation: i) Metal nitrosyl complexes can be prepared via many routes, but direct formation from nitric
oxide gas is much more common. For example:
Co2 (CO)8 + 2NO → 2[Co(CO)3 NO] + 2CO
Ni(Ph3 P)2 (CO)2 + 2NO → Ni(Ph3 P)2 (NO)2 + 2CO
Cr(CO)6 + 4NO → Cr(NO)4 + 6CO
[(η5 ‐ C5 H5 )Fe(CO)2 ]2 + 2NO → [(η5 ‐ C5 H5 )Fe(CO)(NO)]2 + 2CO
ii) From nitrosonium salts:
[Ir(CO)(PPh3 )2 Cl] + (NO)BF4 → [Ir(CO)(NO)(PPh3 )2 Cl]BF4
iii) From nitrosyl halides:
Et 4 N[HB(3,5‐ Me2 ‐ pz)3 Mo(CO)3 ] + ClNO

→ [HB(3,5‐ Me2 ‐ pz)3 Mo(CO)2 (NO)] + CO + [Et 4 N]Cl
iv) From N-nitrosamides:
HMn(CO)5 + p‐ tolylSO2 N(Me)(NO) → Mn(CO)4 (NO) + CO + p‐ tolylSO2 NHMe
v) From nitrite salts:
Na[Co(CO)4 ] + Na(NO2 ) + 2HOAc → [Co(CO)3 (NO)] + CO + 2NaOAc + H2 O
vi) From nitronium (NO2+) salts:
(η5 ‐ C5 H5 )Re(CO)3 + [NO2 ]PF6 → [(η5 ‐ C5 H5 )Re(CO)2 (NO)]PF6 + CO2

Bonding: Most of the metal nitrosyl complexes can be viewed as derivatives of the nitrosyl cation (NO+) or
anion (NO−). The nitrosyl cation (with a bond order of 3) is isoelectronic with carbon monoxide, thus the
bonding between a nitrosyl ligand and a metal follows the same principles as the bonding in carbonyl
complexes. However, the bond order of neutral nitrosyl and anion are 2.5 and 2, respectively; and therefore,
in order to rationalize the nature of the bonding between metal center and the nitrosyl ligand, we must
understand molecular orbital diagram for the nitrosyl ligand first.
Figure 15. The molecular orbital diagram of nitric oxide (NO).
After looking at the molecular orbital diagram for NO, one can immediately recognize the difference
from the carbonyl ligand that there is one extra electron in the π*-orbital. This suggests that NO ligand can be
one, two or three electron donors, depending upon the type of orbital used in bonding. If the electron present
in π*-orbital resides on NO, i.e., not transferred to the metal center, nitrosyl ligand would behave as a two-
no watermark.
electron donor, and the nature of metal complex should be paramagnetic. There are some nitrosyl complexes
of iron and cobalt such as [Fe(NO)2(CO)2] and [Co(NO)(CO)3], which were thought to be derived from neutral
NO ligand but these compounds are diamagnetic in nature; and therefore do not contain unpaired electrons.
This suggests that the nitrosyl ligand is not neutral in these complexes. This assumption is also supported by
the fact that the displacement of a previously attached ligand by any other neutral ligand in metal carbonyl
nitrosyl complexes is always accompanied by the release of CO group. Moreover, there are also many
complexes like [Cr(NO)(CN)5]3− and [Mn(NO)(CN)5]2−, which are actually paramagnetic and were also
thought to be having neutral nitrosyl ligand. However, in the later years, it was found that the unpaired electron
of the nitrosyl group is actually transferred to the metal center making NO as NO+ ligand. Thus, we can say
that the coordination of neutral nitrosyl is highly unlikely.
Figure 16. The nature of σ and π overlap in metal nitrosyl complexes.
i) Complexes containing NO+: Nitric oxide molecule can easily release the odd electron from its antibonding
molecular orbital to form a stable nitrosonium ion (NO+). This also very obvious from the comparison of
infrared absorption wavenumbers of free NO (1880 cm−1) with the nitrosonium salts (2200 – 2300 cm−1); and
can be explained in terms of increased bond order from 2.5 to 3, and consequently the force constant value.
Actually, most of the metal nitrosyls exist with nitrosyl ligand as three electron donor. For instance, the
effective atomic numbers (EAN) for [Mn(CO)(NO)3] and [Fe(NO)2(CO)2] complexes are 36 for each, which
is possible only if the NO ligand act as NO+ i.e. three electron donor.
In the initial step, the π* electron of the NO transfers to the metal center, reducing M to M− and itself forming
NO+ ion. Then NO+ donates a lone pair of electron via N just like the carbon in metal carbonyls. However, the
total number of electrons donated by NO, in this case, would be three while carbonyl can donate only two. The
back donation of electron charge from filled d-orbital of metal to π*-orbital of NO would result in a
considerable decrease in the nitrogen-oxygen bond order. The infrared absorption peak of NO+ in metal
nitrosonium complexes lies in the range of 1900−1600 cm−1 which is far less than what has been observed in
nitrosonium ionic salts. Moreover, the magnitude of decrease in carbonyl stretching frequency is less than the
magnitude of decrease in nitrosonium stretching frequency as we go from their corresponding free unit to
metal-coordinated unit. This, therefore, confirms the better π-acceptor strength of NO+ ligand; which is further
increased by an accumulation of negative charge on nitrosonium complexes.
no watermark.
ii) Complexes containing NO−: Nitric oxide molecule can also accept an electron from the metal center to its
antibonding molecular orbital forming a NO− ion. The metal center in this process would get oxidized from
Mn+ to M(n+1)+ ion. Then the NO− ion donates a lone pair of electron via N just like the carbon in metal
carbonyls. However, the total number of electrons donated by NO, in this case, would be one while the carbonyl
can donate only two. The infrared absorption wavenumbers of NO− in metal nitrosyl complexes are found in
the range of 1100−1200 cm−1 (much lower than NO), which can be explained in terms of complete transfer of
one electron from d-π orbital of metal center to antibonding molecular orbital on nitrosyl ligand. For example,
during the formation of [Co(CN)5(NO)]3− and [Co(NH3)5(NO)]2+ complexes (passing NO through amine and
cyanide salts of Co2+), the Co(II) gets converted into low spin Co(III) with t2g6 configuration. Both of these
complexes, in respect of charge and magnetic moment, resemble [Co(CN)5Br]3− and [Co(NH3)5Cl]2+,
respectively.
In nitrosyl complexes, the M−N−O unit is generally linear, or no more than 15° from linear.
However, in some complexes, especially where back-bonding is not that much important, the M−N−O angle
can largely deviate from 180°. The linear and bent NO ligands can be differentiated using infrared
spectroscopy. The linear M−N−O groups absorb in the range 1650–1900 cm−1 (close to metal coordinated
NO+); whereas the bent nitrosyls absorb in the range 1525–1690 cm−1 (close to metal coordinated NO−). The
difference of vibrational frequencies reflects the difference in N−O bond orders for linear (triple bond) and
bent NO (double bond). The bent NO ligand is sometimes described as the anion, NO −. Prototypes for such
compounds are the organic nitroso compounds, such as nitrosobenzene. A complex with a bent NO ligand is
trans-[Co(en)2(NO)Cl]+. The adoption of linear vs bent bonding can be analyzed with the Enemark-Feltham
notation. In their framework, the factor that determines the bent vs linear NO ligands is the sum of electrons
of π-symmetry.
Complexes with "π-electrons" in excess of 6 tend to have bent NO ligands. Thus, [Co(en)2(NO)Cl]+, with seven
electrons of π-symmetry (six in t2g orbitals and one on NO), adopts a bent NO ligand, whereas
[Fe(CN)5(NO)]3−, with six electrons of pi-symmetry, adopts a linear nitrosyl. In a further illustration, the
M−N−O d-electron count of the [Cr(CN)5NO]3− anion is shown. In this example, the cyanide ligands are
"innocent", i.e., they have a charge of −1 each, −5 total. To balance the fragment's overall charge, the charge
on Cr−N−O is thus +2 (−3 = −5 + 2). Using the neutral electron counting scheme, Cr has 6 d-electrons and
NO has one odd electron for a total of 7. Two electrons are subtracted to take into account that fragment's
overall charge of +2, to give 5. Written in the Enemark-Feltham notation, the d-electron count in Cr−N−O unit
is five. The results are the same if the nitrosyl ligand were considered NO+ or NO−.
no watermark.
Structure: The structure of metal nitrosyls can mainly be classified into three categories; first as the metal-
complex systems that contain NO as a terminal ligand only, the second one as having only bridging nitrosyl
group, and the third one with nitrosyl groups with the terminal as well as bridging profile.
i) Metal complexes with terminal nitrosyl: The NO group as a monodentate ligand in metal complexes acts
either as a 12-electron unit (when NO− forms a single bond with the metal center and M−N−O unit is linear),
or as a 10-electron unit (when NO+ forms a multiple bonds with the metal center and M−N−O unit is bent).
Figure 17. Metal complexes with terminal nitrosyls.
ii) Metal complexes with bridging nitrosyl: In some of the metal nitrosyl complexes, all NO groups are present
in bridging mode. One of the common examples is given below.
iii) Metal complexes with the terminal as well as bridging nitrosyl: In some of the metal nitrosyl complexes,
NO groups are present in the terminal as well as in bridging mode. Some of the common examples are:
no watermark.
Reactions: i) The nucleophilic attack:
[Fe(CN)5 NO]2− + 2OH − ⇌ [Fe(CN)5 (NO2 )]4− + H2 O
[Fe(CN)5 NO]2− + 2NH3 ⇌ [Fe(CN)5 (NH3 )]3− + N2 + H3 O+
ii) Reduction of metal nitrosyls:
[Fe(CN)5 NO]2− + e ⇌ [Fe(CN)5 NO)]3−
[Ru(NH3 )5 NO]3+ + e ⇌ [Ru(NH3 )5 NO]2+
iii) Reactions of nitrosyls with electrophiles:
2[Co(en)2 NO]2+ + 2CH3 CN + O2 ⇌ 2[Co(CH3 CN)(en)2 (NO2 )]2+
2[Ir(PPh3 )(NO)2 ]+ + O2 ⇌ 2[Ir(PPh3 )(NO2 )(NO)]
iv) Formation of carbon-nitrogen bonds:
[Co(CH3 )2 (PMe3 )2 (NO)] → [Co(CH3 )(PMe3 )2 (CH3 NO)]
2[(C5 H5 )Mo(CO)2 (NO)] + 3PPh3

→ [(C5 H5 )Mo(PPh3 )(CO)(NO)] + CO
+ [(C5 H5 )Mo(CO)(PPh3 )(NCO)] + PH3 PO
 2. Metal Dinitrogen Complexes

Metal dinitrogen complexes are the coordination compounds that contain the dinitrogen ligand (N2)
attached to a metal center. The first complex of dinitrogen, [Ru(NH3)5(N2)]2+ was reported by Allen and Senoff
in 1965, which is consisted of a 16e-[Ru(NH3)5]2+ center attached to one end of N2. The interest in such
complexes arises because N2 comprises the majority of the atmosphere and there are many useful compounds
containing nitrogen atoms.
Preparation: i) Metal dinitrogen complexes can be prepared via many routes, but direct formation from
dinitrogen is very common. For example:
[CoH2 (PPh3 )3 ] + N2 → [Co(PPh3 )3 (N2 )] + H2
[RuH4 (PPh3 )3 ] + N2 → [RuH2 (PPh3 )3 (N2 )] + H2
[CoH3 (PPh3 )3 ] + N2 → [CoH(PPh3 )3 (N2 )] + H2
[FeH4 (PEtPh2 )3 ] + N2 → [FeH2 (PEtPh2 )3 (N2 )] + H2
ii) From compounds containing chains of nitrogen atoms:
[Ru(NH3 )5 L]n+ + N3− → [Ru(NH3 )5 (𝑁2 )]2+ + L
no watermark.
𝑡𝑟𝑎𝑛𝑠– [Ir(Cl)(CO)(PR 3 )2 ] + RCON3 + EtOH

→ 𝑡𝑟𝑎𝑛𝑠– [Ir(Cl)(N2 )(PR 3 )2 ] + RCONHCO2 Et
𝑡𝑟𝑎𝑛𝑠– [Rh(Cl)(CO)(PR 3 )2 ] + RCON3 + EtOH

→ 𝑡𝑟𝑎𝑛𝑠– [Rh(Cl)(N2 )(PR 3 )2 ] + RCONHCO2 Et
[OsH4 (PR 3 )3 ] + CH3 C6 H4 SO2 N3 → [OsH2 (N2 )(PR 3 )3 ]
iii) Preparations in which two nitrogen atoms are combined to give a dinitrogen group:
[Fe(CN)5 NO]2− + N2 H4 → [Fe(CN)5 (N2 )]2−
RuCl3 + Zn + NH3 → [Ru(NH3 )6 ]Cl2 + [Ru(NH3 )(N2 )]Cl2
[Os(NH3 )5 (CO)]2+ + HNO2 → 𝑐𝑖𝑠– [Os(NH3 )4 (N2 )(CO)]2+ + 2H2 O
[Ru(NH3 )6 ]3+ + NO + OH − → [Ru(NH3 )5 (N2 )]2+ + 2H2 O
Bonding: In order to rationalize the nature of the bonding between the metal center and the N2, we must
understand the bonding within the dinitrogen ligand first. The molecular orbital diagram for N2 is given below.
Figure 20. The molecular orbital diagram of dinitrogen molecule.
no watermark.
Though the N2 molecule is isoelectronic with CO and NO+, it does not form a large number of metal complexes
like the two. This is obviously due to the fact that it is a poor ligand and cannot act as a strong π-acceptor due
to the lack of polarity. In other words, N2 ligand is neither a good σ-donor nor good π-acceptor as there is no
polarity in N−O bond. The different bridging modes of dinitrogen ligand are given below.
Figure 21. Bonding modes of N2 ligand in metal-dinitrogen complexes.
The most common binding mode of dinitrogen ligand with transition metal center is end-on i.e. just
like in the case of isocyanides, carbon monoxide and nitric oxide. These observations are also supported by
the theoretical treatment of some dinitrogen complexes which indicated that end-on bonding is more beneficial
than side on as far as the stability of the complex is concerned. The end-on bonding involves the donation of
the lone pair of N2 to the empty metal orbital and, the back-donation from filled metal d-orbital to the empty
π* orbitals of N2 ligand. In contrast, the side-on bonding comprises of electron donation from the π and σ
bonding molecular orbital of the dinitrogen to the empty orbitals of the metal and the back-donation of electron
density from filled orbitals of the metal to the π* molecular orbital of the N2 ligand. Though the side-on bonding
mode is quite common in metal-acetylenes and metal-olefin complexes, there are very few reports of side-on
bonded dinitrogen complexes. Consider the example of [Ru(NH3)5(N2)]2+ complex, Ru−N bond length in
Ru−N−N unit is shorter than Ru−N bond length in Ru−NH3 unit. This shows that there is some extent of
backbonding from filled d-orbital the metal center to the empty π* molecular orbital of dinitrogen. This is also
very obvious from the vibrational Raman stretching frequency of free N2 (2331 cm−1) and infrared active
stretching frequency of metal coordinated ligand (2105 cm−1) in [Ru(NH3)5(N2)]Cl2 complex. However, it is
also worthy to note that metal-carbon bond in carbonyl complexes is stronger than the metal-nitrogen bond in
dinitrogen complexes, which shows that CO is definitely a stronger σ-donor a better π-acceptor as highest
occupied molecular orbital (HOMO) is predominantly concentrated on carbon due to high polarity.
no watermark.
Structure: The structures of metal-dinitrogen complexes can mainly be classified into two categories; metal-
complex that contains N2 as an end-on ligand and with N2 group as a side-on ligand.
i) Metal complexes with end-on dinitrogen: As a ligand, N2 usually binds to metals as an end-on ligand, as
illustrated by Allen and Senoff's complex. Such complexes are usually analogous to related CO derivatives.
Figure 22. Metal-dinitrogen complexes with end-on N2 ligand.
ii) Metal complexes with side-on dinitrogen: In some of the metal-dinitrogen complexes, the N−N vector is
perpendicular to the M−M vector. Some of the most common examples are given below.
Figure 23. Metal-dinitrogen complexes with side-on N2 ligand.
no watermark.
Reactions: i) The displacement of dinitrogen ligand by some other groups:
𝑡𝑟𝑎𝑛𝑠– [Mo(N2 )2 (dppe)2 ] + 2C2 H4 → 𝑡𝑟𝑎𝑛𝑠– [Mo(C2 H4 )2 (dppe)2 ] + 2N2
𝑡𝑟𝑎𝑛𝑠– [Mo(N2 )2 (dppe)2 ] + 2RNC → 𝑡𝑟𝑎𝑛𝑠– [Mo(RNC)2 (dppe)2 ] + 2N2
𝑡𝑟𝑎𝑛𝑠– [Mo(N2 )2 (dppe)2 ] + 2CO → 𝑡𝑟𝑎𝑛𝑠– [Mo(CO)2 (dppe)2 ] + 2N2
ii) Reactions of Ligating N2 with Lewis Acids:
[ReCl(N2 )(PMe2 Ph)4 ] + [Mo(Cl4 )(THF)2 ]

CH2 Cl2 , MeOH
→ [(PMe2 Ph)4 ClReN2 MoCl4 (OMe)]
[ReCl(N2 )(PMe2 Ph)4 ] + [MoCl4 (PPh3 )2 ] → [MoCl4 {(N2 )ReCl(PMe2 Ph)4 }2 ]
iii) Formation of metal-hydrazido complxes from ligating N2:
𝑡𝑟𝑎𝑛𝑠– [Mo(N2 )2 (dppe)2 ] + 2HCl → [MoCl(NNH2 )(dppe)2 ]Cl + N2
THF
𝑡𝑟𝑎𝑛𝑠– [W(N2 )2 (dppe)2 ] + 2HBF4 → [WF(NNH2 )(dppe)2 ][BF4 ]
+ BF3 . THF + N2
iv) Formation of carbon-nitrogen bonds:
[W(N2 )2 (dppe)2 ] + RCOCl + HCl → [WCl(N2 HCOR)(dppe)2 ]Cl
[Mo(N2 )(RCN)(dppe)2 ] + PhCOCl → [MoCl(NNCOPh)(dppe)2 ]
[Mo(N2 )2 (dppe)2 ] + RCOCl + HCl → [MoCl(N2 HCOR)(dppe)2 ]Cl
 3. Metal Dioxygen Complexes

Metal dioxygen complexes are the coordination compounds which contain O2 ligand attached to a
metal center. The principal driving force behind the analysis of these compounds are oxygen-carrying proteins
such as myoglobin, hemoglobin, hemocyanin, and hemerythrin. Many transition metals form complexes with
O2, and many of these complexes form reversibly. The binding of O2 is the first step in many important
phenomena, such as cellular corrosion, respiration and in industrial chemistry. The first synthetic oxygen
complex was demonstrated in 1938 with Co2+ complex reversibly bound O2. Most of the organometallic metal-
dioxygen complexes are synthesized by the reaction of gaseous molecular oxygen with complexes (having d7,
d8, or dl0 electronic configuration) solution.
Preparation: i) Formation of a mononuclear dioxygen adduct with or without displacement of ligands
[IrCl(CO)(PPh3 )2 ] + O2 ⇌ [IrCl(CO)(PPh3 )2 O2 )]
[Co(DMG)2 ] + O2 + Pyridine → [Co(DMG)2 (O2 )(Pyridine)]
no watermark.
ii) Formation of a dimer or a binuclear dioxygen adduct:
2[Rh(PPh3 )2 𝐶𝑙] + 2O2 → [Rh(PPh3 )2 (O2 )Cl]2
2[Co(histidine)2 ] + O2 → [Co2 (histidine)4 (O2 )]
iii) Oxidation of ligands with the oxidized ligand remaining coordinated:
[Ru(PPh3 )2 (CO)2 (SO2 )] + O2 → [Ru(PPh3 )2 (CO)2 (SO4 )]
iv) Displacement of free oxidized ligand:
[Pt(PPh3 )4 ] + 2O2 → [Pt(PPh3 )2 (O2 )] + 2Ph3 PO
Bonding: The nature of bonding in metal-dioxygen complexes is usually evaluated by single-crystal X-ray
crystallography, focusing both on the overall geometry as well as the O–O distances, which reveals the bond
order of the O2 ligand. However, in order to rationalize the initial idea of the metal-ligand bonding, we must
understand the bonding within the dioxygen ligand first. The molecular orbital diagram for O2 is given below.
Figure 24. The molecular orbital diagram of the dioxygen molecule.
no watermark.
The experimental results show that the bent structure of the dioxygen unit in oxyhemoglobin is actually
diamagnetic in nature; which suggests that π*2px and π*2py orbitals are not completely degenerate in the
complex as they are in free dioxygen. A linear M−O−O structure would result in a degenerate set of π*2px and
π*2py orbitals with a triplet state. In addition to the σ-bonding, there are two types of interactions between the
d-orbitals of the metal and the π* orbitals of the dioxygen. One is through an overlap of the 3dxz of the metal
with the π* orbitals perpendicular to the Fe−O−O plane; while the other is through the overlap of the 3d orbital
of the metal with the πy* orbital in the Fe−O−O plane. The different bridging modes of dinitrogen ligand are
given below.
Figure 25. Bonding modes of O2 ligand in metal-dioxygen complexes.
The O2 ligand binds to a single metal center either end-on (η1-) or in a side-on (η2-) manner. Dioxygen
adducts derived from Co2+ and Fe2+ complexes of porphyrin (and related anionic macrocyclic ligands) exhibit
this bonding mode. The hemoglobin and myoglobin are two famous examples, and many other synthetic
analogs have been reported which behave in a similar manner. Binding of O2 is usually described as proceeding
by electron transfer from the metal(II) center to give superoxide (O−2) complexes of metal(III) centers. The η2-
bonding is the most common motif seen in the coordination chemistry of dioxygen. Since O2 has a triplet
ground state and Vaska's complex is a singlet, the reaction is slower than when singlet oxygen is used.
Complexes containing η2-O2 ligands are fairly common, but most are generated using hydrogen peroxide, not
O2. The O2 can bind to one metal of a bimetallic unit via the same modes discussed above for mononuclear
complexes. A well-known example in nature is hemerythrin, which features a diiron carboxylate that binds O2
at one Fe center. The dinuclear complexes can also cooperate in the binding, although the initial attack of O2
probably occurs at a single metal. These binding modes include μ2-η2, η2-, μ2-η1, η1-, and μ2-η1, η2-. Depending
on the degree of electron-transfer from the dimetal unit, these O2 ligands can again be described as peroxo or
superoxo. In nature, such dinuclear dioxygen complexes often feature copper.
no watermark.
Structure: The structures of metal-dioxygen complexes can mainly be classified into two categories; the first
one as the metal-complex that contains dioxygen (O2) ligand attached to one metal center and the second one
with O2 group connected to two or more metal centers. A brief discussion on both of the categories is given
below with suitable examples.
i) Mononuclear metal-dioxygen complexes: As a ligand, O2 can bind to a single metal-center either as an end-
on ligand or as a side-on ligand. The structures of some representative metal-dioxygen complexes of such type
are given below.
Figure 26. Mononuclear metal-O2 complexes.
ii) Binuclear metal-dioxygen complexes: In binuclear metal-dioxygen complexes, the O2 molecule can bind
either to one or both metals center as an end-on/end-on, end-on/side-on and side-on/side-on ligand. The
structures of some representative metal-dioxygen complexes of such type are given below.
Figure 27. Metal-dioxygen complexes with side-on O2 ligand.
no watermark.
Reactions: i) The displacement of molecular oxygen by some other ligand:
[Ni(O2 )(𝑡– BuNC)2 ] + 4t– BuNC ⇌ [Ni(𝑡– BuNC)4 ] + 2t– BuNCO
[Ni(O2 )(𝑡– BuNC)2 ] + 4PPh3 ⇌ [Ni(𝑡– BuNC)2 (PPh3 )2 ] + 2Ph3 PO
[Pt(PPh3 )2 (O2 )] + 3PPh3 ⇌ [Pt(PPh3 )3 ] + 2Ph3 PO
ii) The formation of complexes of oxidized substrates:
[Ir(PPh3 )2 (CO)Cl(O2 )] + SO2 → [Ir(PPh3 )2 (CO)Cl(SO4 )]
[Pt(PPh3 )2 (O2 )] + SO2 → [Pt(PPh3 )2 (SO2 )]
[Pd(PPh3 )2 (O2 )] + NO2 → [Pd(PPh3 )2 (NO3 )2 ]
 Tertiary Phosphine as Ligand

The compound phosphine (PH3) is extremely important in coordination chemistry due to its large
number of derivatives which can be used as L-type ligands (2 electron donor neutral ligands) for many metal
complexes. These phosphine based ligands are the compounds with the formula PRnH3−n, and are often
classified according to the value of n; the values 1, 2, 3 correspond to primary, secondary and tertiary
phosphines, respectively. For instance, the most popular phosphine ligand used is organometallic chemistry is
triphenylphosphine, which is obviously a tertiary phosphine. All of these phosphine ligands adopt pyramidal
structures that are quite favorable for the metal center to be approached. Unlike most metal ammine complexes,
metal phosphine complexes tend to be lipophilic, showing very good solubility in organic solvents. They also
are compatible with metals in multiple oxidation states. Therefore, owing to these two features, metal
phosphine complexes are quite useful in homogeneous catalysis.
 General Methods of Preparation and Reactivity
The first phosphine complexes were cis- and trans-[PtCl2(PEt3)2], reported by Cahours and Gal in
1870. Being a L-type ligand, the phosphines do not change the overall charge of the metal complex. These
complexes may simply be prepared by the addition of phosphines to a coordinatively unsaturated metal
precursor, or by ligand displacement of another L-type complex, such as a solvent molecule acting as a ligand.
However, it should also be noted that the replacement of X-type ligand (1-electron donor neutral ligand) can
also yield such complexes.
[PdCl2 ]𝑛 + 2𝑛PPh3 → n[PdCl2 (PPh3 )2 ]
[Cr(CO)6 ] + PPh3 → [Cr(CO)5 (PPh3 )] + CO
K 4 [Ni(CN)4 ] + 4PPh3 → [Ni(PPh3 )4 ] + 4KCN

As far as the reactivity is concerned, the nature of phosphine ligands is a spectator rather than the
actor. Coordinated phosphines generally do not participate in chemical reactions, except their dissociation from
the metal center. However, in some high-temperature hydroformylation processes, the scission of
phosphorus−carbon bonds is also observed. The thermal stability of phosphine ligands is enhanced when they
are incorporated into pincer complexes. Some complexes dissociate in solutions to yield a product with a lower
coordination number.
[Rh(PPh3 )3 Cl] → [Rh(PPh3 )2 Cl] + PPh3
[Pt(PPh3 )3 ] + MeI → [Pt(I)(Me)(PPh3 )2 ] + PPh3
 Structure and Bonding in of Tertiary Phosphine Complexes

The metal-phosphine complexes are not considered as the organometallic compounds because of the
lack of metal-carbon bonds. However, many good inorganic textbooks discuss them in their organometallic
section due to their excellent bonding similarities with the carbonyl ligand. For instance, phosphines can act
as very good σ-donors as well as respectable π acceptors just like CO ligand. The σ-donation occurs via a
hybrid lone pair on phosphorus and the π-acceptance in orbitals that are a mixture of empty d-orbital on
phosphorus and σ* of the phosphorus-carbon bond. For a long time in coordination chemistry, the pure empty
d-orbitals of phosphorus were thought to be used for the acceptance of π-electron density; and this theory was
also affirmed by the fact that as the R groups attached to phosphorus become more electronegative, phosphine
becomes stronger π-acceptor and vice-versa. The concept of mixing of σ* of the phosphorus-carbon bond into
empty d-orbitals of phosphorus was developed later on.
Figure 28. The π-acceptor orbitals of phosphines in metal-phosphine complexes.
no watermark.
Therefore, the nature of R groups in tertiary phosphines governs the relative donor-acceptor strength
of the corresponding ligand. For instance, PMe3 acts as a stronger σ donor than PF3 due to the large electron-
donating effect of the three methyl groups. However, it is a relatively weaker π-acceptor in comparison to PF3,
which easily be explained in terms of a larger electron-withdrawing effect of 3 fluorines. Hence, the σ-donor
and π-acceptor strength of tertiary phosphines can be fine-tuned just by changing the R groups.
 Steric and Electronic Properties
The most valuable thing about tertiary phosphines as ligands is that their steric and electronic
properties can easily be manipulated just by changes in one or more of the three organic substituents. This
fine-tuning of the electronic and steric profile of phosphine ligands is of great importance in the manipulation
of catalytic properties transition metals. The ligand cone angle and Tolman electronic parameter are used to
categorize various phosphines on the basis of their steric and electronic behavior, respectively. However, these
parameters are not just limited to phosphines but have been extended to other ligand types also.
1. Ligand cone angle: The ligand cone angle is a measure of the size of a ligand. It is defined as the solid
angle formed with the metal at the vertex and the other atoms at the perimeter of the cone. Tertiary phosphine
ligands are commonly classified using this parameter, but the method can be applied to any ligand. The term
cone angle was introduced by the American chemist, Chadwick A. Tolman. Originally applied to phosphines
(called Tolman cone angle), the cone angles were originally determined by taking measurements from accurate
physical models of them. The concept of the cone angle is most easily visualized with symmetrical ligands,
e.g. PR3. Nevertheless, this approach has been refined to include less symmetrical ligands of the type PRR′R″
as well as diphosphines by using equation (1).
2 𝜃𝑖 (1)
𝜃= ∑
3 2
𝑖
Where θi/2 are the half of individual angles made by R, R′ and R″ on M−P bond. In the case of diphosphines,
the θi/2 of the backbone is estimated as half of the bite angle of chelate, taking a bite angle of 90°, 85° and 74°,
for propylene, ethylene and diphosphines with methylene backbones, respectively.
Figure 29. The ligand cone angle in metal-phosphine complexes.
no watermark.
The ligand-cone-angle method accepts empirical bond data and considers the perimeter as the
maximum possible circumscription of a substituent which spins freely. The concept of solid-angle derives the
bond length and the perimeter from the empirical crystal structure profile obtained from X-ray diffraction of
solid sample. Each system has its own advantages. The exact cone angle (θ) can be found if the geometry of a
ligand is known from either crystallography or computational studies. Unlike the Tolman route, no
assumptions regarding the geometry are made. The cone-angle-concept is practically important in
homogeneous catalysis due to the affected reactivity of the metal center from the ligand size. In a famous
example, the selectivity of hydroformylation catalysts is strongly affected by the size of the coligands attached.
Now though phosphines are monovalent, some are large enough to fill more than half of the coordination
sphere around the metal center. The values of the cone angles of selected ligands are given below.
Table 3. The cone angle values of selected ligands.
Ligand Cone angle Ligand Cone angle
PH3 87° P(Me)(PPh)2 136°
PF3 104° P(CF3)3 137°
P(OMe)3 107° P(O-o-C6H4CH3)3 141°
P(OEt)3 109° PPh3 145°
PMe3 118° P(cyclo-C6H11)3 170°
PCl3 124° P(t-C4H9)3 182°
P(Me)3Ph 127° P(C6F5)3 184°
PBr3 131° P(o-C6H4CH3)3 194°
PEt3 132° P(mesityl)3 212°
The presence of bulky ligands (ligands with large cone angles) is found to enhance the rate of dissociation;
which can be explained in terms of increased steric repulsion due to crowding around the metal center.
2. Tolman electronic parameter: The Tolman electronic parameter (TEP) is named after its inventor,
Chadwick A. Tolman, and is a measure of the electron-donating or withdrawing strength of a ligand. It is
determined by measuring the frequency of the A1 vibrational mode of carbonyl stretching frequency of
Ni(CO)3L complex by infrared spectroscopy, where L is the ligand being studied. The Ni(CO) 3L is chosen as
the model compound because such complexes can easily be prepared from Ni(CO)4. Moreover, the carbonyl
band is quite distinctive, and is rarely obscured by other bands in the observed infrared spectrum; and being a
small ligand, steric factors are unable to complicate the analysis.
no watermark.
Figure 30. The A1 stretch of Ni(CO)3L used to determine the TEP in metal-phosphine complexes.
Upon coordination to a metal, ν(CO) typically decreases from 2143 cm−1 of free CO. This can be
explained by π backbonding i.e. the metal is able to form a π-bond with the carbonyl ligand by donating
electrons through its d-orbitals into the empty antibonding π* orbitals on CO. This increases the strength of
metal–carbon bond, but also weakens the bond between carbon and oxygen. Moreover, the C−O bond is further
weakened if other ligands present increase the π-electrons-density on the metal center, and νCO decreases.
However, if other ligands compete with CO for π backbonding, νCO would increase. Tolman analyzed a series
of seventy ligands in reference to P(t-Bu)3, because three t-butyl groups make it as the strongest donor ligand.
Consequently, the A1 absorption band of carbonyl ligands in Ni(CO)3[P(t-Bu)3] complex appears at the lowest
wavenumber (2056.1 cm–1), which is obviously due to the largest magnitude of back-bonding among all
phosphines. Based on these observations, Tolman proposed a parameter χi to show the effect of individual
substituents (R, R′, R″) on this band as accorded by equation (2):
3 (2)
−1 −1
𝜈𝐶𝑂 = 2056.1 cm + ∑ 𝜒𝑖 cm
𝑖=1
Now the calculation of the value of χi for each individual substituent in symmetrical phosphines can be done
just by putting their observed spectral band. Let's say, we want to calculate the Tolman electronic parameter
for PCl3. The infrared absorption of A1 symmetry for Ni(CO)3(PF3) is observed at 2097.0 cm–1. On putting this
value for νCO in the equation (2), we get:
3 (3)
−1 −1
2097.0 cm = 2056.1 cm + ∑ 𝜒𝑖 cm−1
𝑖=1
2097.0 cm−1 = 2056.1 cm−1 + 3 × 𝜒𝑖 (Cl) cm−1 (4)
𝜒𝑖 = 14.8 cm−1 (5)
The values of χ for different substituents are listed in ‘Table 4’; which in turn can easily be used to calculate
the theoretical position of A1 absorption band in case of tertiary phosphine ligands in which R, R′, and R″ are
not the same anymore.
no watermark.
Table 4. Substituent χ Factors for Phosphine and Related Ligands.
Substituent χi (cm–1) Substituent χi (cm–1)
–tBu 0.0 –OEt 6.8
–Cyclohexyl 0.1 –OMe 7.7
–iPr 1.0 –H 8.3
–Et 1.8 –OPh 9.7
–Me 2.6 –C6H5 11.2
–Ph 4.3 –Cl 14.8
–p-C6H4F 5.0 –F 18.2
–m-C6H4F 6.0 –CF3 19.6
The Tolman electronic parameter (TEP) and the ligand cone angle are used to characterize the electronic and
steric profile of phosphines, which are very popular ligands for catalysts.
no watermark.
 Problems
Q 1. Give the principal routes to synthesize metal carbonyl complexes.
Q 2. Discuss the nature of bonding for transition metal complexes in the framework of the molecular orbital
theory.
Q 3. Draw and discuss the structure of Fe3(CO)12 and Ir4(CO)16.
Q 4. Write a short note on the structure of osmium-carbonyl complexes with special emphasis on Os4(CO)14,
Os4(CO)15 and Os4(CO)16.
Q 5. How many metal-metal bonds and terminal carbonyls are present in Rh6(CO)16?
Q 6. How would you distinguish between square-pyramidal and trigonal bipyramidal geometries of Fe(CO)5
using their vibration spectra?
Q 7. Discuss the effect of backbonding on the carbonyl stretching frequency in hexacarbonyl complexes of the
first transition series.
Q 8. How would you calculate the reaction rate for metal carbonyls using infrared spectroscopy?
Q 9. Discuss the points of difference between linear and bent mode of bonding for nitrosyl ligand.
Q 10. Explain the structure and bonding of metal-dioxygen complexes in detail.
Q 11. How does the end-on bonding mode differ from side-on bonding mode in dinitrogen complexes of
transition metals?
Q 12. Give important reactions of coordinated ligands with reference to N2, O2 and NO complexes.
Q 13. Why is tertiary phosphine so important in organometallic chemistry?
Q 14. What kind of orbitals do the tertiary phosphine use for backbonding? Explain in detail.
Q 15. Define the ligand cone angle and the Tolman electronic parameter.

 Bibliography
[1] J. E. House, Inorganic Chemistry, Academic Press, California, USA, 2008.
[2] B. R. Puri, L. R. Sharma, K. C. Kalia, Principals of Inorganic Chemistry, Milestone Publishers, Delhi,
India, 2012.
[3] J. E. Huheey, E. A. Keiter, R. L. Keiter, Inorganic Chemistry: Principals of Structure and Reactivity,
HarperCollins College Publishers, New York, USA, 1993.
[4] B. Xu, Q. S. Li, Y. Xie, R. B. King, H. F. Schaefer, Homoleptic Tetranuclear Osmium Carbonyls: From
the Rhombus via the Butterfly to the Tetrahedron, Dalton Trans., 2008, 1366.
[5] T. T. Shi, Q. S. Li, Y. Xie, R. B. King, H. F. Schaefer, Neutral Homoleptic Tetranuclear Iron Carbonyls:
Why Haven’t They Been Synthesized as Stable Molecules?, New J. Chem., 34, 2010, 208.
[6] V. J. Johnston, F. W. B. Einstein, R. K. Pomeroy, Structures of the New Binary Metal Carbonyl OS4(CO)15
and (η5-C5Me5)(OC)IrOs3(CO)11). Clusters with Three-Center-Two-Electron Metal-Metal Bonds?, J. Am.
Chem. Soc., 109, 1987, 7220.
[7] P. S. Braterman, Reactions of Coordinated Ligands: Volume 2, Plenum Press, New York, USA, 1989.
[8] L. L. Ingraham, D. L. Meyer, Biochemistry of Dioxygen, Plenum Press, New York, USA, 1985.
[9] M. Merce, R. H. Crabtree, R. L. Richar, A µ-Dinitrogen Complex with a Long N-N Bond. X-Ray Crystal
Structure of [(PMe2Ph)4CReN2MoC14(OMe)], J.C.S. Chem. Comm., 1973, 808.
[10] P. L. Holland, Metal-Dioxygen and Metal-Dinitrogen Complexes: Where Are the Electrons?, Dalton
Trans., 39, 2010, 5415.
[11] A. D. Allen, R. O. Harris, B. R. Loescher, J. R. Stevens, R. N. Whiteley, Dinitrogen Complexes of the
Transition Metals, Chemical Reviews, 73, 1973, 11.
[12] J. S. Valentine, The Dioxygen Ligand in Mononuclear Group VIII Transition Metal Complexes, Chemical
Reviews, 73, 1973, 235.
[13] G. O. Spessard, G. L. Miessler, Organometallic Chemistry, Oxford University Press, New York, USA,
2010.
[14] N. N. Greenwood, A. Earnshaw, Chemistry of the Elements, Butterworth-Heinemann, Oxford, Britain,
1998.
[15] B. W. Pfennig, Principles of Inorganic Chemistry, John Wiley & Sons, New Jersey, USA, 2015.

LEGAL NOTICE
This document is an excerpt from the book entitled “A
Textbook of Inorganic Chemistry – Volume 1 by
Mandeep Dalal”, and is the intellectual property of the
Author/Publisher. The content of this document is
protected by international copyright law and is valid
only for the personal preview of the user who has
originally downloaded it from the publisher’s website
(www.dalalinstitute.com). Any act of copying (including
plagiarizing its language) or sharing this document will
result in severe civil and criminal prosecution to the
maximum extent possible under law.
This is a low resolution version only for preview purpose. If you

want to read the full book, please consider buying.
Buy the complete book with TOC navigation, high resolution

images and no watermark.
D DALAL
INSTITUTE
Home Classes Books Videos Location Contact Us About Us °' Followus: O O O G O
Home
CLASSES BOOKS VIDEOS
NET-JRF, llT-GATE, M.Sc Entrance & Publications Video Lectures

llT-JAM
Are you interested in books (Print and Ebook) Want video lectures in chemistry for CSIR UGC
Want to study chemistry for CSIR UGC - NET published by Dalal Institute? - NET JRF. llT-GATE. M.Sc Entrance, llT-JAM,
JRF, llT-GATE, M.Sc Entrance, llT-JAM, UPSC, READ MORE UPSC, ISRO, II Sc, TIFR, DRDO, BARC, JEST, GRE,
ISRO, II Sc, TIFR, DRDO, BARC, JEST, GRE, Ph.D Ph.D Entrance or any other competitive
Entrance or any other competitive examination where chemistry is a paper?
examination where chemistry is a paper? READ MORE
READ MORE
Home: https://www.dalalinstitute.com/
Classes: https://www.dalalinstitute.com/classes/
Books: https://www.dalalinstitute.com/books/
Videos: https://www.dalalinstitute.com/videos/
Location: https://www.dalalinstitute.com/location/
Contact Us: https://www.dalalinstitute.com/contact-us/
About Us: https://www.dalalinstitute.com/about-us/
Postgraduate Level Classes Undergraduate Level Classes

(NET-JRF & IIT-GATE) (M.Sc Entrance & IIT-JAM)
Admission Admission
Regular Program Distance Learning Regular Program Distance Learning
Test Series Result Test Series Result
A Textbook of Inorganic Chemistry – Volume 1
“A Textbook of Inorganic Chemistry – Volume 1 by Mandeep Dalal” is now available globally; including India,
America and most of the European continent. Please ask at your local bookshop or get it online here.
-------- READ
Share this article/info with MORE
your classmates and friends
Join the revolution by becoming a part of our community and get all of the member benefits
like downloading any PDF document for your personal preview.
Sign Up
join the revolution by becoming a part of our community and get all of the member benefits like downloading any PDF document for your personal preview.
Sign Up
Copyright© 2019 Dalal Institute

Table of Contents
CHAPTER 1 ..................................................................................................................................... 11
Stereochemistry and Bonding in Main Group Compounds: ........................................................ 11
 VSEPR Theory ................................................................................................................................ 11
 dπ–pπ Bonds .................................................................................................................................... 23
 Bent Rule and Energetic of Hybridization....................................................................................... 28
 Problems .......................................................................................................................................... 42
 Bibliography .................................................................................................................................... 43
CHAPTER 2 ..................................................................................................................................... 44
Metal-Ligand Equilibria in Solution:................................................................................................. 44
 Stepwise and Overall Formation Constants and Their Interactions ................................................ 44
 Trends in Stepwise Constants .......................................................................................................... 46
 Factors Affecting Stability of Metal Complexes with Reference to the Nature of Metal Ion and
Ligand .............................................................................................................................................. 49
 Chelate Effect and Its Thermodynamic Origin................................................................................ 56
 Determination of Binary Formation Constants by pH-metry and Spectrophotometry .................... 63
 Problems .......................................................................................................................................... 68
 Bibliography .................................................................................................................................... 69
CHAPTER 3 ..................................................................................................................................... 70
Reaction Mechanism of Transition Metal Complexes – I: ............................................................ 70
 Inert and Labile Complexes............................................................................................................. 70
 Mechanisms for Ligand Replacement Reactions ............................................................................ 77
 Formation of Complexes from Aquo Ions ....................................................................................... 82
 Ligand Displacement Reactions in Octahedral Complexes- Acid Hydrolysis, Base Hydrolysis .... 86
 Racemization of Tris Chelate Complexes ....................................................................................... 89
 Electrophilic Attack on Ligands ...................................................................................................... 92
 Problems .......................................................................................................................................... 94
 Bibliography .................................................................................................................................... 95
CHAPTER 4 ..................................................................................................................................... 96
Reaction Mechanism of Transition Metal Complexes – II:...................................................... 96
 Mechanism of Ligand Displacement Reactions in Square Planar Complexes ................................ 96
 The Trans Effect .............................................................................................................................. 98
 Theories of Trans Effect ................................................................................................................ 103
 Mechanism of Electron Transfer Reactions – Types; Outer Sphere Electron Transfer Mechanism and
Inner Sphere Electron Transfer Mechanism .................................................................................. 106
 Electron Exchange ......................................................................................................................... 117
 Problems ........................................................................................................................................ 121
 Bibliography .................................................................................................................................. 122
CHAPTER 5 ................................................................................................................................... 123

Isopoly and Heteropoly Acids and Salts: ........................................................................................ 123
 Isopoly and Heteropoly Acids and Salts of Mo and W: Structures of Isopoly and Heteropoly
Anions ............................................................................................................................................123
 Problems ........................................................................................................................................ 152
 Bibliography .................................................................................................................................. 153
CHAPTER 6 ................................................................................................................................... 154

Crystal Structures: ............................................................................................................................... 154
 Structures of Some Binary and Ternary Compounds Such as Fluorite, Antifluorite, Rutile, Antirutile,
Crystobalite, Layer Lattices - CdI2, BiI3; ReO3, Mn2O3, Corundum, Pervoskite, Ilmenite and
Calcite.............................................................................................................................................154
 Problems ........................................................................................................................................ 178

 Bibliography .................................................................................................................................. 179
CHAPTER 7 ................................................................................................................................... 180

Metal-Ligand Bonding: ....................................................................................................................... 180
 Limitation of Crystal Field Theory ................................................................................................ 180
 Molecular Orbital Theory – Octahedral, Tetrahedral or Square Planar Complexes...................... 184
 π-Bonding and Molecular Orbital Theory ..................................................................................... 198
 Problems ........................................................................................................................................ 212
 Bibliography .................................................................................................................................. 213
CHAPTER 8 ................................................................................................................................... 214
Electronic Spectra of Transition Metal Complexes: .................................................................... 214
 Spectroscopic Ground States ......................................................................................................... 214
 Correlation and Spin-Orbit Coupling in Free Ions for 1st Series of Transition Metals ................. 243
 Orgel and Tanabe-Sugano Diagrams for Transition Metal Complexes (d1 – d9 States) ................ 248
 Calculation of Dq, B and β Parameters ......................................................................................... 280
 Effect of Distortion on the d-Orbital Energy Levels ..................................................................... 300
 Structural Evidence from Electronic Spectrum ............................................................................. 307
 Jahn-Tellar Effect .......................................................................................................................... 312
 Spectrochemical and Nephelauxetic Series ................................................................................... 324
 Charge Transfer Spectra ................................................................................................................ 328
 Electronic Spectra of Molecular Addition Compounds................................................................. 336
 Problems ........................................................................................................................................ 340
 Bibliography .................................................................................................................................. 341
CHAPTER 9 ................................................................................................................................... 342

Magnetic Properties of Transition Metal Complexes: ................................................................. 342
 Elementary Theory of Magneto-Chemistry ................................................................................... 342
 Guoy’s Method for Determination of Magnetic Susceptibility ..................................................... 351
 Calculation of Magnetic Moments ................................................................................................ 354
 Magnetic Properties of Free Ions ................................................................................................... 359
 Orbital Contribution: Effect of Ligand-Field ................................................................................ 362
 Application of Magneto-Chemistry in Structure Determination ................................................... 370
 Magnetic Exchange Coupling and Spin State Cross Over ............................................................ 375
 Problems ........................................................................................................................................ 384
 Bibliography .................................................................................................................................. 385
CHAPTER 10 ................................................................................................................................. 386

Metal Clusters: ...................................................................................................................................... 386
 Structure and Bonding in Higher Boranes ..................................................................................... 386
 Wade’s Rules ................................................................................................................................. 401
 Carboranes ..................................................................................................................................... 407
 Metal Carbonyl Clusters- Low Nuclearity Carbonyl Clusters....................................................... 412
 Total Electron Count (TEC) .......................................................................................................... 417
 Problems ........................................................................................................................................ 424
 Bibliography .................................................................................................................................. 425
CHAPTER 11 ................................................................................................................................. 426

Metal-Π Complexes: ............................................................................................................................ 426
 Metal Carbonyls: Structure and Bonding ...................................................................................... 426
 Vibrational Spectra of Metal Carbonyls for Bonding and Structure Elucidation .......................... 439
 Important Reactions of Metal Carbonyls....................................................................................... 446
 Preparation, Bonding, Structure and Important Reactions of Transition Metal Nitrosyl, Dinitrogen
and Dioxygen Complexes.............................................................................................................. 450
 Tertiary Phosphine as Ligand ........................................................................................................ 463
 Problems ........................................................................................................................................ 469
 Bibliography .................................................................................................................................. 470
INDEX ............................................................................................................................................. 471

Metal-Π Complexes:: Metal Carbonyls: Structure and Bonding

Uploaded by

Copyright:

Available Formats

Metal-Π Complexes:: Metal Carbonyls: Structure and Bonding

Uploaded by

Document Information

Original Title

Copyright

Available Formats

Share this document

Share or Embed Document

Sharing Options

Did you find this document useful?

Is this content inappropriate?

Copyright:

Available Formats

Metal-Π Complexes:: Metal Carbonyls: Structure and Bonding

Uploaded by

Copyright:

Available Formats

CHAPTER 11

Copyright © Mandeep Dalal

KCo(CO)4 + [Ru(CO)3 Cl2 ]2 → 2RuCo2 (CO)11 + 4KCl

 Structures of Metal Carbonyls

Figure 1. The structures of some mononuclear metal carbonyls.

Figure 2. Continued on the next page…

Figure 2. The structures of some binuclear metal carbonyls.

Figure 3. Continued on the next page…

Figure 3. Continued on the next page…

Figure 3. The structures of some polynuclear metal carbonyls.

 Bonding in Metal Carbonyls

C (ground state) = 1s2, 2s2, 2px1, 2py1, 2pz0

C (hybridized state) = 1s2, (spx)2, (spx)1, 2py1, 2pz0

O (ground state) = 1s2, 2s2, 2px1, 2py1, 2pz2

O (hybridized state) = 1s2, (spx)2, (spx)1, 2py1, 2pz2

Figure 4. Bonding behavior in CO ligand according to the valence bond method.

Figure 5. The valence bond nature of σ and π overlap in metal carbonyls.

Carbon = 1s2, 2s2, 2p2

Oxygen = 1s2, 2s2, 2p4

Figure 6. The first generation molecular orbital diagram of carbonyl ligand.

The formation of molecular orbitals given above is actually an oversimplification of a ticklish

C (hybridized state) = 1s2, (spx)2, (spx)1, 2py1, 2pz0

O (hybridized state) = 1s2, (spx)2, (spx)1, 2py1, 2pz2

Figure 8. The nature of σ and π in carbonyl ligand.

Figure 9. The second molecular orbital diagram of carbonyl ligand.

Figure 10. The nature of σ and π overlap in metal carbonyls.

Figure 11. Third molecular orbital diagram of carbonyl ligand.

 Vibrational Spectra of Metal Carbonyls for Bonding and Structure

Compound [Ti(CO)6]2− [V(CO)6]1− [Cr(CO)6] [Mn(CO)6]1+ [Fe(CO)6]2+

νCO (cm−1) 1748 1859 2000 2095 2204

Compound [Hf(CO)6]2− [Ta(CO)6]1− [W(CO)6] [Re(CO)6]1+ [Os(CO)6]2+

νCO (cm−1) 1757 1850 1977 2085 2190

Copyright © Mandeep Dalal

 2. Toleman Electronic Parameter

L P(t-bu)3 P(Me)3 P(Ph)3 P(OEt)3 PCl3 PF3

νCO (cm−1) 2056.1 2064.1 2068.9 2076.3 2097.0 2110.8

D3h E 2C3 3C2 σh 2S3 3σd Irreducible components

C4v E 2C4 C2 2σv 2σd Irreducible components

Table 1. Continued on the next page…

 4. Differentiation of Terminal and Bridging Carbonyl Groups

Table 2. The CO stretching frequencies in different metal carbonyl complexes.

Bonding mode of CO νCO (cm−1)

Free CO+ 2184

Terminal CO 2120 - 1850

Symmetric µ2-CO 1860 - 1750

Symmetric µ3-CO 1730 - 1600

For instance, consider the rhodium carbonyl complexes:

Rh2(CO)8 2060, 2084 1846, 1862

Rh4(CO)12 2044, 2070, 2074 1886

Rh6(CO)16 2045, 2075 1819

 5. Calculation of CO Bond Order

Compound [Ni(CO)4] [Co(CO)4]1− [Fe(CO)4]2−

νCO (cm−1) 2046 1890 1730

M–C Bond order 1.33 1.89 2.16

C–O Bond order 2.64 2.14 1.85

M–C + C–O Bond order 3.97 4.03 4.01

Compound [Ni(CO)4] [Ni(PF3)(CO)3] [Ni(PMe3)(CO)3]

νCO (cm−1) 2046 1990 1980

 6. Study of Reaction Kinetics in Metal Carbonyls