## H2C=S, thioformaldehyde

 H3 \ C1 = S2 / H4
Tell me about the atomic charges, dipole moment, bond lengths, angles, bond orders,
molecular orbital energies, or total energy.
Tell me about the best Lewis structure.

## Atomic Charges and Dipole Moment

C1 charge=-0.122
S2 charge=-0.138
H3 charge= 0.130
H4 charge= 0.130
with a dipole moment of 1.77266 Debye

## Bond Lengths:

between C1 and S2: distance=1.630 ang___ between C1 and H3: distance=1.102 ang___
between C1 and H4: distance=1.102 ang___

## Bond Angles:

for H3-C1-S2: angle=121.7 deg___ for H4-C1-S2: angle=121.7 deg___

## Bond Orders (Mulliken):

between C1 and S2: order=1.909___ between C1 and H3: order=0.916___
between C1 and H4: order=0.923___

## Best Lewis Structure

The Lewis structure that is closest to your structure is determined. The hybridization of the atoms in this idealized Lewis structure is given in the table below.

### Hybridization in the Best Lewis Structure

1. A bonding orbital for C1-S2 with 1.9999 electrons
__has 41.04% C 1 character in a p-pi orbital ( 99.67% p 0.33% d)
__has 58.96% S 2 character in a p-pi orbital ( 99.32% p 0.68% d)

2. A bonding orbital for C1-S2 with 1.9987 electrons
__has 56.58% C 1 character in a sp1.65 hybrid
__has 43.42% S 2 character in a s0.83 p3 hybrid

3. A bonding orbital for C1-H3 with 1.9971 electrons
__has 60.06% C 1 character in a sp2.19 hybrid
__has 39.94% H 3 character in a s orbital

4. A bonding orbital for C1-H4 with 1.9971 electrons
__has 60.07% C 1 character in a sp2.19 hybrid
__has 39.93% H 4 character in a s orbital

11. A lone pair orbital for S2 with 1.9936 electrons

12. A lone pair orbital for S2 with 1.9367 electrons
__made from a p-pi orbital ( 99.98% p)

-With core pairs on: C 1 S 2 S 2 S 2 S 2 S 2 -

#### Donor Acceptor Interactions in the Best Lewis Structure

The localized orbitals in your best Lewis structure can interact strongly. A filled bonding or lone pair orbital can act as a donor and an empty or filled bonding, antibonding, or lone pair orbital can act as an acceptor. These interactions can strengthen and weaken bonds. For example, a lone pair donor->antibonding acceptor orbital interaction will weaken the bond associated with the antibonding orbital. Conversly, an interaction with a bonding pair as the acceptor will strengthen the bond. Strong electron delocalization in your best Lewis structure will also show up as donor-acceptor interactions.
Interactions greater than 20 kJ/mol for bonding and lone pair orbitals are listed below.

The interaction of the second lone pair donor orbital, 12, for S2 with the antibonding acceptor orbital, 66, for C1-H3 is 63.3 kJ/mol.

The interaction of the second lone pair donor orbital, 12, for S2 with the antibonding acceptor orbital, 67, for C1-H4 is 63.3 kJ/mol.

## Molecular Orbital Energies

The orbital energies are given in eV, where 1 eV=96.49 kJ/mol. Orbitals with very low energy are core 1s orbitals. More antibonding orbitals than you might expect are sometimes listed, because d orbitals are always included for heavy atoms and p orbitals are included for H atoms. Up spins are shown with a ^ and down spins are shown as v.

16 ----- 3.208

15 ----- 2.885

14 ----- 0.913

13 ----- -3.785

12 -^-v- -5.535

11 -^-v- -8.208

10 -^-v- -9.805

9 -^-v- -11.36

8 -^-v- -14.85

7 -^-v- -19.83

6 -^-v- -154.7

5 -^-v- -155.0

4 -^-v- -155.2

3 -^-v- -207.9

2 -^-v- -268.3

1 -^-v- -2387.

## Total Electronic Energy

The total electronic energy is a very large number, so by convention the units are given in atomic units, that is Hartrees (H). One Hartree is 2625.5 kJ/mol. The energy reference is for totally dissociated atoms. In other words, the reference state is a gas consisting of nuclei and electrons all at infinite distance from each other. The electronic energy includes all electric interactions and the kinetic energy of the electrons. This energy does not include translation, rotation, or vibration of the the molecule.

Total electronic energy = -437.5160707651 Hartrees