Molecular Modeling Molecular Modeling

Molecular Modeling: Visualizations &

Predictions

• Numerical Methods

• Integral Method

• Semi-Empirical MO-SCF Methods

• Approximate MO Methods 

• Ab Initio Methods

HΨ = EΨH = Hamiltonian

H is an operator corresponding to the total energy of the system. Kinetic + potential energy

LCAO: linear combination of atomic orbitals

NDDO: neglect of diatomic differential overlap

The cost of calculations (cpu time required) increases rapidly as the basis set size is increased and as the amount of electron correlation increases.

Web MOhttp://butane.cabrillo.edu/

Username: your last namepassword: DVC id number

• Web MO: undergraduate molecular modeling college consortium

• Web-based, on-line accessible molecular modeling software, Graphic User Interface (GUI), free to DVC students, no cpu charges

• Uses MOPAC 7, GAMESS 2000, and GAUSSIAN

Web MOhttp://butane.cabrillo.edu/Username: your last name

password: DVC id#Output:

Dipole momentBond OrdersPartial ChargesVibrational ModesMolecular OrbitalsUltraviolet-Visible-Infrared GraphicsNMR Chemical Shifts

Molecular Orbital Theory(Review)

http://chemconnections.org/general/movies/html_swf/MolecularOrbitalTheory/MolecularOrbitalTheory.html

• Valence electrons are delocalized in Valence electrons are delocalized in molecular orbitals spread over the entire molecular orbitals spread over the entire molecule.molecule.

• First Principle: First Principle: The total # of molecular The total # of molecular orbitals equals the number of atomic orbitals equals the number of atomic orbitals contributed by the atoms that have orbitals contributed by the atoms that have combined.combined.

• Second Principle: Second Principle: The bonding molecular The bonding molecular orbitals are lower in energy than the orbitals are lower in energy than the parents orbitals and are more symmetrical parents orbitals and are more symmetrical (fewer nodes) than the antibonding orbitals (fewer nodes) than the antibonding orbitals which are higher in energy.which are higher in energy.

• Third Principle: Third Principle: The electrons of the The electrons of the molecule are assigned to orbitals of molecule are assigned to orbitals of successively higher energy according to successively higher energy according to the Pauli exclusion principle and Hundthe Pauli exclusion principle and Hund’’s s rule.rule.

Molecular Orbital TheoryMolecular Orbital Theory

Molecular Orbital TheoryMolecular Orbital Theory

1. # MO1. # MO’’s = # atomic orbitals s = # atomic orbitals used.used.2. Bonding MO is lower in 2. Bonding MO is lower in energy than atomic orbitals. energy than atomic orbitals. Antibonding MO is higher.Antibonding MO is higher.3. Electrons assigned to MO3. Electrons assigned to MO’’s s of higher and higher energy.of higher and higher energy.

Bond order = 1/2 [# e- in bonding MOs Bond order = 1/2 [# e- in bonding MOs - # e- in antibonding MOs]- # e- in antibonding MOs]

Analogy between Light Waves and Atomic Wave Functions

QUESTIONWhen comparing the M.O. theory of bonding to the Localized Electron model which of the following would be an incorrect claim?

A. For a molecule of H2; MO1 = 1s A + 1s B; MO2 = 1s A – 1s BB. The molecular orbitals (both bonding and antibonding) still have a maximum electron occupancy of two just as the localized orbitals.C. In H2, the bonding orbital (MO1) is lower in energy than the 1s orbital of hydrogen.D. Although not used in molecular bonding, the 1s orbital of hydrogen is present in H2.

Homo: Highest Occupied Molecular Orbital

Sigma Bond

Sigma Bond

Bond Length: C-C > C=C > CBond Length: C-C > C=C > CΞΞCC

Bond Energy: C-C < C=C < CBond Energy: C-C < C=C < CΞΞCC

Single bond: C-C Bond Order =1Single bond: C-C Bond Order =1

Pi Bond

and π Bonding inand π Bonding in CC22HH44

Double bond: C=C Bond Order =2Double bond: C=C Bond Order =2

Bond Length: C-C > C=C > CBond Length: C-C > C=C > CΞΞCC

Bond Energy: C-C < C=C < CBond Energy: C-C < C=C < CΞΞCC

Pi Bond

and π Bonding inand π Bonding in CC22HH22

Triple bond: CTriple bond: CΞΞC Bond Order =3C Bond Order =3

Bond Length: C-C > C=C > CBond Length: C-C > C=C > CΞΞCC

Bond Energy: C-C < C=C < CBond Energy: C-C < C=C < CΞΞCC

Consequences of Consequences of Multiple BondingMultiple Bonding

There is restricted rotation around C=C bond.There is restricted rotation around C=C bond.

Lumo: Lowest Unoccupied Molecular Orbital

Anti-bonding Orbital

QUESTIONConsider the two molecular orbitals of benzene that follow.

Which statement is correct?MO1 MO2

A. MO1 and MO2 are likely bonding orbitals.B. MO1 and MO2 are likely antibonding orbitals.C. MO1 is likely a bonding orbital and MO2 is likely an antibonding orbital.D. MO1 is likely an antibonding orbital and MO2 is likely a bonding orbital