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All results from a given calculation for C3 (carbon trimer)

using model chemistry: CID/6-311+G(3df,2p)

19 10 17 12 22

States and conformations

State Conformation minimum conformation conformer description state description
1 1 yes D*H 1Σg
1 2 no C2V 1A1

Conformer 1 (D*H)

Jump to S1C2
Energy calculated at CID/6-311+G(3df,2p)
 hartrees
Energy at 0K-113.752131
Energy at 298.15K 
HF Energy-113.388075
Nuclear repulsion energy37.201731
The energy at 298.15K was derived from the energy at 0K and an integrated heat capacity that used the calculated vibrational frequencies.
Vibrational Frequencies calculated at CID/6-311+G(3df,2p)
Mode Number Symmetry Frequency
(cm-1)
Scaled Frequency
(cm-1)
IR Intensities
(km mol-1)
Raman Act
4/u)
Dep P Dep U
1 Σg 1295 1196 0.00      
2 Σu 2231 2061 1117.64      
3 Πu 90 84 12.29      
3 Πu 90 84 12.29      

Unscaled Zero Point Vibrational Energy (zpe) 1853.1 cm-1
Scaled (by 0.924) Zero Point Vibrational Energy (zpe) 1712.3 cm-1
See section III.C.1 List or set vibrational scaling factors to change the scale factors used here.
See section III.C.2 Calculate a vibrational scaling factor for a given set of molecules to determine the least squares best scaling factor.
Rotational Constants (cm-1) from geometry optimized at CID/6-311+G(3df,2p)
B
0.42857

See section I.F.4 to change rotational constant units
Geometric Data calculated at CID/6-311+G(3df,2p)

Point Group is D∞h

Cartesians (Å)
Atom x (Å) y (Å) z (Å)
C1 0.000 0.000 0.000
C2 0.000 0.000 1.280
C3 0.000 0.000 -1.280

Atom - Atom Distances (Å)
  C1 C2 C3
C11.28021.2802
C21.28022.5604
C31.28022.5604

picture of carbon trimer state 1 conformation 1
More geometry information
Calculated Bond Angles
atom1 atom2 atom3 angle atom1 atom2 atom3 angle
C2 C1 C3 180.000
Electronic energy levels
Charges, Dipole, Quadrupole and Polarizability

Conformer 2 (C2V)

Jump to S1C1
Energy calculated at CID/6-311+G(3df,2p)
 hartrees
Energy at 0K-113.752131
Energy at 298.15K 
HF Energy-113.388075
Nuclear repulsion energy37.201649
The energy at 298.15K was derived from the energy at 0K and an integrated heat capacity that used the calculated vibrational frequencies.
Vibrational Frequencies calculated at CID/6-311+G(3df,2p)
Mode Number Symmetry Frequency
(cm-1)
Scaled Frequency
(cm-1)
IR Intensities
(km mol-1)
Raman Act
4/u)
Dep P Dep U
1 A1 1295 1196 0.00      
2 A1 91 84 12.29      
3 B2 2231 2061 1117.63      

Unscaled Zero Point Vibrational Energy (zpe) 1807.9 cm-1
Scaled (by 0.924) Zero Point Vibrational Energy (zpe) 1670.5 cm-1
See section III.C.1 List or set vibrational scaling factors to change the scale factors used here.
See section III.C.2 Calculate a vibrational scaling factor for a given set of molecules to determine the least squares best scaling factor.
Rotational Constants (cm-1) from geometry optimized at CID/6-311+G(3df,2p)
B
0.42857

See section I.F.4 to change rotational constant units
Geometric Data calculated at CID/6-311+G(3df,2p)

Point Group is C2v

Cartesians (Å)
Atom x (Å) y (Å) z (Å)
C1 0.000 0.000 -0.000
C2 0.000 1.280 0.000
C3 0.000 -1.280 0.000

Atom - Atom Distances (Å)
  C1 C2 C3
C11.28021.2802
C21.28022.5604
C31.28022.5604

picture of carbon trimer state 1 conformation 2
More geometry information
Calculated Bond Angles
atom1 atom2 atom3 angle atom1 atom2 atom3 angle
C2 C1 C3 179.978
Electronic energy levels
Charges, Dipole, Quadrupole and Polarizability