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    3 Assumptions and Approximations

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    Jack Ryder
    The document outlines three key approximations used to simplify solving the Schrodinger equation for molecules: 1) The Born-Oppenheimer approximation, which treats nuclear and electronic motion independently. 2) The independent electron/orbital approximation, which considers electrons moving in an average potential and allows separating the electronic Hamiltonian. 3) The linear combination of atomic orbitals (LCAO) approximation, which constructs molecular orbitals from linear combinations of atomic orbitals centered on individual atoms.

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    3 Assumptions and Approximations

    Uploaded by

    Jack Ryder
    47 views5 pages
    The document outlines three key approximations used to simplify solving the Schrodinger equation for molecules: 1) The Born-Oppenheimer approximation, which treats nuclear and electronic motion independently. 2) The independent electron/orbital approximation, which considers electrons moving in an average potential and allows separating the electronic Hamiltonian. 3) The linear combination of atomic orbitals (LCAO) approximation, which constructs molecular orbitals from linear combinations of atomic orbitals centered on individual atoms.

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    The document outlines three key approximations used to simplify solving the Schrodinger equation for molecules: 1) The Born-Oppenheimer approximation, which treats nuclear and electronic motion independently. 2) The independent electron/orbital approximation, which considers electrons moving in an average potential and allows separating the electronic Hamiltonian. 3) The linear combination of atomic orbitals (LCAO) approximation, which constructs molecular orbitals from linear combinations of atomic orbitals centered on individual atoms.

    Copyright:

    © All Rights Reserved
    Download as PDF, TXT or read online from Scribd
    Download as pdf or txt
    47 views5 pages

    3 Assumptions and Approximations

    Uploaded by

    Jack Ryder
    The document outlines three key approximations used to simplify solving the Schrodinger equation for molecules: 1) The Born-Oppenheimer approximation, which treats nuclear and electronic motion independently. 2) The independent electron/orbital approximation, which considers electrons moving in an average potential and allows separating the electronic Hamiltonian. 3) The linear combination of atomic orbitals (LCAO) approximation, which constructs molecular orbitals from linear combinations of atomic orbitals centered on individual atoms.

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    At a glance
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    The key takeaways are the Born-Oppenheimer approximation, orbital approximation, and LCAO approximation which are used to simplify the molecular Schrödinger equation and allow it to be solved.

    The Born-Oppenheimer approximation treats the nuclear and electronic motions independently, allowing the molecular Schrödinger equation to be separated into electronic and nuclear parts.

    The orbital approximation considers each electron to move independently in an average potential, allowing the electronic Hamiltonian to be separated into one-electron parts corresponding to each electron.

    3 The Way Forward - Assumptions and Approximations

    Simplification 1

    The electrons move much faster than the nuclei (since they are much lighter) - we will therefore treat
    the nuclear and electronic motion entirely independently.

    ….. this is the Born-Oppenheimer approximation.

    The approach is:

    ¾ Freeze the molecule with a fixed internuclear separation ( RAB , hereafter called R ); then carry
    out calculations to obtain the total energy, U, and wavefunctions for that R value.
    ¾ Repeat for different values of R , to obtain the complete potential energy function , U(R).

    This gives results of the following form:

    E U(R) - the potential energy function

    Re R

    "Potential well" due to electronic


    bonding - with well-defined equilibrium
    internuclear separation, Re .
    Ee

    The total energy of the free ("unfrozen") bound-molecule is then given by:

    Etotal = Ee + Evrt

    Electronic energy (incl. Vibrational, rotational and


    total energy of electrons in translational energy of the
    molecular environment molecules
    and internuclear repulsion)

    To actually determine the electronic energy we still have to solve a Schrödinger equation, but this
    first approximation means that it is now a much simpler equation.

    3.1
    For a particular value of R (the internuclear separation), the equation is:

    ĤeΨe (r1 , r2 ) = U(R) Ψe (r1 , r2 )


    or
    ĤeΨe (r1 , r2 ) = Ee Ψe (r1 , r2 ) at R = Re

    where:
    Ĥe is the electronic Hamiltonian, i.e. the full Hamiltonian, Ĥ , but without the
    nuclear KE terms.
    Ψe (r1 , r2 ) is the electronic wavefunction for the molecule
    (which is a function of the vectorial positions of the two electrons)

    Unfortunately, the Schrödinger equation is still impossible to solve  e2 


    because the interelectronic repulsion term (opposite) depends upon V12 =  
     4πε 0 r12 
    the positions of both electrons (since r12 = | r1 – r2 | ).

    Simplification 2

    ….. is known as the independent electron model or orbital approximation .

    Consider each electron to move in some sort of "average potential" which incorporates the
    interactions with the two nuclei and an "averaged interaction" with the other electron.

    The electronic Hamiltonian can then be separated into two parts:

    Ĥe = Ĥ1 + Ĥ2
    where:
    Ĥ1 is dependent only upon the properties of electron (1) and upon R .
    Ĥ2 is dependent only upon the properties of electron (2) and upon R .

    This is a major step forward since we can now (see explanation and caveat in box overleaf) look for
    solutions of the form:

    Ψe (r1 , r2 ) = ψa(1). ψb(2)

    Molecular orbital "a" - Molecular orbital "b" -


    containing electron 1 containing electron 2

    where
    Ĥ1 ψa = εa ψa and εa is the energy of orbital "a"
    Ĥ2 ψb = εb ψb and εb is the energy of orbital "b"

    3.2
    and the total electronic energy (at the equilibrium bond length) is given by:

    Ee = εa + εb

    i.e. by the sum of the energies of the individual occupied molecular orbitals.

    Consequences of the Orbital Approximation

    ĤeΨe = (Ĥ1 + Ĥ2 )( ψa(1).ψb(2) )

    = Ĥ1 ( ψa(1).ψb(2) ) + Ĥ2 ( ψa(1).ψb(2) )

    = ( Ĥ1ψa(1) ).ψb(2) + ( Ĥ2ψb(2) ).ψa(1)

    ( since Ĥ1 acts only upon the wavefunction for electron 1, i.e. on ψa(1), etc.)

    ⇒ ĤeΨe = εa ψa(1) ψb(2) + εb ψb(2) ψa(1)

    = (εa + εb ) ψa(1) ψb(2)

    i.e ĤeΨe = Ee Ψe where Ee = εa + εb

    In actual fact a wavefunction of the form Ψe (r1 , r2 ) = ψa(1). ψb(2) is unacceptable since:
    - it permits the two electrons to be distinguished
    - the wavefunction is not antisymmetric upon exchange of the two electons

    The wavefunction can however be modified to meet these criteria


    Ψe (r1 , r2 ) = ψa(1). ψb(2) – ψa(2). ψb(1)
    without compromising the additional simplicity afforded by the orbital approximation.

    Simplification 3

    So all we now need to do is to solve the one-electron Schrödinger equation:

    Ĥ1 ψa = εa ψa [1]

    Effective one-electron One-electron wavefunction,


    Hamiltonian a molecular orbital .

    3.3
    The solutions are the molecular orbital wavefunctions, {ψa }, and molecular orbital energies, {εa }.

    To actually do this we make one final approximation which

    ….. is the linear combination of atomic orbitals (LCAO) approximation .

    This supposes that we can construct molecular orbitals from linear superpositions of atomic orbitals
    centred on individual atoms.

    i.e. ψ = ∑i (ciφ i )

    Molecular orbital An atomic orbital

    Summation Mixing coefficient

    ….. this is an idea with which you should already be partly familiar. In its simplest form a molecular
    orbital may be constructed from a summation of one orbital on one atom, with a second orbital on a
    different atom.

    Example : Hydrogen ( H2 )

    Each hydrogen atom has a single valence orbital, this being the 1s orbital. Two molecular orbitals
    may be formed by the constructive and destructive overlap of these two atomic orbitals.

    1s ± 1s Diagram showing the superposition of


    A B the two 1s atomic orbitals

    φ1s,A φ1s,B

    1s σ A B Bonding molecular orbital


    ( 1σg ) ψ + = c +φ1s , A + c +φ1s , B = c + (φ1s , A + φ1s , B )

    or

    1s σ∗ A B Antibonding molecular orbital


    ( 1σu ) ψ − = c −φ1s , A − c −φ1s , B = c − (φ1s , A − φ1s , B )

    3.4
    This interaction of atomic orbitals, which gives rise to the molecular orbitals, may also be
    represented in the form of an orbital (electron) energy diagram which shows the relative energies of
    the orbitals. In the specific case of hydrogen each of the isolated atoms has one electron in its 1s
    orbital and when the atoms combine to form H2 the two electrons may be accommodated (with
    opposite spins) in the bonding molecular orbital, as illustrated below.

    1σu

    Electron
    Energy 1sA 1sB

    1σg

    H H2 H

    ( Atom A ) (Molecule) ( Atom B )

    Note that in this instance two atomic orbitals give rise to two molecular orbitals - we shall see later
    that this is a general characteristic, i.e. linear combinations of n atomic orbitals give rise to n
    molecular orbitals.

    However this pictorial approach fails to answer some important questions


    1. what are the values of the mixing coefficients ?
    2. what are the exact energies of the molecular orbitals ?

    Important : Change of Notation


    …. from hereon, we will switch to using numerical labels for the atomic orbitals and their
    associated coefficients, e.g.
    ψ = c1φ1 + c 2φ 2
    where φi simply represents a specific atomic orbital on a specific atom (i).

    3.5

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