CCCBDB calculation results Page

Home
- All data for one species
- Geometry
  - Experimental
  - Calculated
  - Comparisons
  - Bad Calculations
    - Bad moment of inertia
  - Tutorials and Explanations
    - Angle formulas
- Vibrations
  - Experimental
    - Vibrational frequencies
  - Calculated
    - Frequencies
  - Scale factors
- Reactions
- Entropies
- Ions
  - List Ions
  - Energy
    - Calculated Ionization Energy
    - Compare Ionzation energy
  - Electron Affinity
    - Calculated Electron affinity
    - Compare Electron affinity
  - Proton Affinity
    - Calculated Proton affinity
    - Compare Proton affinity
  - Ionization changes point group
Experimental
Calculated
- Energy
  - Optimized
  - Reaction
    - Reaction Energy 0K
    - Reaction Energy 298K
  - Internal Rotation
  - Orbital
  - Nuclear repulsion energy
  - Correlation
    - Full vs Frozen core energies
    - Partial correlation energies
  - Ion
  - Excited State
  - Basis Set Extrapolation
    - BSE energy
    - BSE Bond lengths
- Geometry
  - Calculated geometry
    - AIM bond orders
    - One type of bond
  - Rotation
  - Point group
  - State symmetry
  - <r2>
    - Sorted by r2
  - Z-matrix
  - Bad Calculations
- Vibrations
  - Frequencies
    - Animated vibrations
    - Anharmonic
  - Zero point energy (ZPE)
  - Scale Factors
  - Bad Calculations
- Electrostatics
  - Charges
  - Dipole
  - Quadrupole
  - Polarizability
  - Spin
    - Spin density
- Entropy and Heat Capacity
- Reaction
  - Reaction Energy 0K
  - Reaction Energy 298K
  - Isodesmic reactions
  - Transition State
- Lookup by property
  - By frequency
Comparisons
- Geometry
- Vibrations
- Energy
  - Reaction
  - Single point vs optimized
  - DFT grid size on energy
  - Semiempirical enthalpy
  - Internal rotation
  - Similar molecules
- Entropy
- Electrostatics
- Ion
Resources
- Info on Results
  - Calculations Done
  - Basis functions used
  - I/O files
- Glossary
- Conversion Forms
- Links
  - NIST Links
  - External links
- Thermochemistry
- Tutorials
  - Vibrations
    - Why scale vibrations
    - Zero-point energies
  - Entropy
    - Methyl rotor entropy
    - Entropy and conformations
  - Energy
  - Electrostatics
    - Dipole parts by point group
    - Quadrupoles
  - Geometry
    - Angle formulas
  - Cost
    - Cost Comparison
    - Timings Comparison
- Bad Calculations
  - Geometry
  - Vibrations
  - Low excited states
  - Oddities
    - NaCN Is not linear
FAQ Help
- Units
  - Choose Units
  - Explanations
- Credits
- Just show me
  - Show me a calculated geometry
- Summary
- Using
- List
  - Recent molecules
    - Choose a few
  - Molecules
  - Geometry
  - Vibrations
    - Big anharmonicity
  - Energy
    - Enthalpy at 0 Kelvin
  - Similar molecules
  - Ions, Dipoles, etc.
- Index of CCCBDB
- Feedback
  - Error form
  - Wants

	hartrees
Energy at 0K	-194.509971
Energy at 298.15K	-194.517168
HF Energy	-193.937298
Nuclear repulsion energy	152.772366

Mode Number	Symmetry	Frequency (cm^-1)	Scaled Frequency (cm^-1)	IR Intensities (km mol^-1)
1	A	3264	3015	17.80
2	A	3250	3002	0.79
3	A	3217	2972	24.67
4	A	3155	2914	8.35
5	A	1607	1485	2.55
6	A	1578	1458	5.23
7	A	1548	1430	0.06
8	A	1506	1391	1.92
9	A	1231	1137	0.01
10	A	1162	1073	1.88
11	A	1131	1044	0.51
12	A	961	888	21.96
13	A	875	808	0.00
14	A	571	527	3.77
15	A	308	284	1.07
16	A	169	156	0.15
17	A	144	133	1.16
18	A	3264	3015	35.55
19	A	3249	3001	6.14
20	A	3217	2972	25.07
21	A	3153	2913	65.72
22	A	2185	2018	12.31
23	A	1589	1467	6.06
24	A	1577	1457	5.65
25	A	1506	1391	5.20
26	A	1393	1287	20.60
27	A	1169	1080	3.69
28	A	1129	1043	1.16
29	A	1018	941	9.48
30	A	757	700	17.33
31	A	603	557	11.36
32	A	235	217	0.78
33	A	154	142	0.73

Atom	x (Å)	y (Å)	z (Å)
C1	0.000	0.000	0.417
C2	0.000	1.304	0.414
C3	0.000	-1.304	0.414
C4	-0.877	2.156	-0.462
C5	0.877	-2.156	-0.462
H6	0.673	1.823	1.088
H7	-0.673	-1.823	1.088
H8	-1.518	2.800	0.142
H9	-0.275	2.803	-1.101
H10	-1.510	1.540	-1.096
H11	1.518	-2.800	0.142
H12	0.275	-2.803	-1.101
H13	1.510	-1.540	-1.096

	C1	C2	C3	C4	C5	H6	H7	H8	H9	H10	H11	H12	H13
C1		1.3039	1.3039	2.4878	2.4878	2.0563	2.0563	3.1967	3.1989	2.6340	3.1967	3.1989	2.6340
C2	1.3039		2.6077	1.5044	3.6752	1.0847	3.2690	2.1485	2.1489	2.1486	4.3840	4.3857	3.5561
C3	1.3039	2.6077		3.6752	1.5044	3.2690	1.0847	4.3840	4.3857	3.5561	2.1485	2.1489	2.1486
C4	2.4878	1.5044	3.6752		4.6551	2.2170	4.2752	1.0905	1.0905	1.0874	5.5372	5.1306	4.4450
C5	2.4878	3.6752	1.5044	4.6551		4.2752	2.2170	5.5372	5.1306	4.4450	1.0905	1.0905	1.0874
H6	2.0563	1.0847	3.2690	2.2170	4.2752		3.8875	2.5784	2.5783	3.1008	4.7942	5.1330	4.0960
H7	2.0563	3.2690	1.0847	4.2752	2.2170	3.8875		4.7942	5.1330	4.0960	2.5784	2.5783	3.1008
H8	3.1967	2.1485	4.3840	1.0905	5.5372	2.5784	4.7942		1.7572	1.7664	6.3698	6.0123	5.4343
H9	3.1989	2.1489	4.3857	1.0905	5.1306	2.5783	5.1330	1.7572		1.7666	6.0123	5.6321	4.6948
H10	2.6340	2.1486	3.5561	1.0874	4.4450	3.1008	4.0960	1.7664	1.7666		5.4343	4.6948	4.3132
H11	3.1967	4.3840	2.1485	5.5372	1.0905	4.7942	2.5784	6.3698	6.0123	5.4343		1.7572	1.7664
H12	3.1989	4.3857	2.1489	5.1306	1.0905	5.1330	2.5783	6.0123	5.6321	4.6948	1.7572		1.7666
H13	2.6340	3.5561	2.1486	4.4450	1.0874	4.0960	3.1008	5.4343	4.6948	4.3132	1.7664	1.7666

atom1	atom2	atom3	angle	atom1	atom2	atom3	angle
C1	C2	C4	124.567	C1	C2	H6	118.551
C1	C3	C5	124.567	C1	C3	H7	118.551
C2	C1	C3	179.801	C2	C4	H8	110.774
C2	C4	H9	110.803	C2	C4	H10	110.974
C3	C5	H11	110.774	C3	C5	H12	110.803
C3	C5	H13	110.974	C4	C2	H6	116.882
C5	C3	H7	116.882	H8	C4	H9	107.352
H8	C4	H10	108.401	H9	C4	H10	108.415
H11	C5	H12	107.352	H11	C5	H13	108.401
H12	C5	H13	108.415

All results from a given calculation for C₅H₈ (2,3-Pentadiene)

using model chemistry: CID/6-31G*

States and conformations

	Computational Chemistry Comparison and Benchmark DataBase Release 22 (May 2022) Standard Reference Database 101 National Institute of Standards and Technology
	Home All data for one species Geometry Experimental Experimental Geometries Same bond/angle many molecules Internal Coordinates by type Bond angles Calculated Calculated geometry Rotational constant Moments of inertia Products of moments of inertia BSE Bond lengths Show me a calculated geometry Comparisons Bonds, angles Rotational Constants Products of moments of inertia Point group Bad Calculations Bad moment of inertia Tutorials and Explanations Angle formulas Vibrations Experimental Vibrational frequencies Calculated Frequencies Scale factors Reactions Entropies Ions List Ions Energy Calculated Ionization Energy Compare Ionzation energy Electron Affinity Calculated Electron affinity Compare Electron affinity Proton Affinity Calculated Proton affinity Compare Proton affinity Ionization changes point group Experimental One molecule all properties One property a few molecules Enthalpy of formation Entropy Integrated Heat Capacity Heat Capacity Rotational Constants Vibrational Frequencies Dipole moment Ionization Energy Polarizability Quadrupole Point Groups Geometry Experimental Geometries Internal Coordinates by type Bond angles Rotational Constants Point Groups Diatomic bond lengths Vibrations Vibrational frequencies Diatomic Triatomics Energy Atomization Energy Internal Rotation Electrostatics Dipole Quadrupole Polarizability Reference Data Reference states Spin Splittings Molecules with good enthalpy Enthalpy at 0 Kelvin Calculated Energy Optimized Energy Energy 298K Minimum conformation Hydrogen bonds H bond with counterpoise Reaction Reaction Energy 0K Reaction Energy 298K Internal Rotation Barriers to internal rotation Rotational barrier and dipole Rotational Barrier 2 molecules Orbital HOMO LUMO gap HOMO Orbital Energies Nuclear repulsion energy Correlation Full vs Frozen core energies Partial correlation energies Ion Calculated Ionization Energy Vertical ionization Energy Calculated Electron affinity Calculated Proton affinity Atom charge differences Excited State Singlet triplet gap Electronic state Transition state Basis Set Extrapolation BSE energy BSE Bond lengths Geometry Calculated geometry AIM bond orders One type of bond Rotation Rotational constant Products of moments of inertia Moments of inertia Inertial defects Second moments Point group State symmetry <r2> Sorted by r2 Z-matrix Bad Calculations Bad moment of inertia Bad Calculated Bond Lengths Bad point group Worst molecules Vibrations Frequencies Animated vibrations Anharmonic Zero point energy (ZPE) Scale Factors Scale factors Scale factor uncertainty Calculate a scale factor Why scale vibrations Set scaling factors Bad Calculations Bad Vib. HF vs MP2 Bad vib. Calc. vs exp. Big anharmonicity Electrostatics Charges Mulliken CHELP Aim ESP Dipole Dipole Dipole angle Dipole calculation types Quadrupole Polarizability Spin Spin density Entropy and Heat Capacity Entropy Reaction entropy Heat Capacity Reaction Reaction Energy 0K Reaction Energy 298K Isodesmic reactions Transition State Transition state Transition state frequencies Transition state geometries IRC Lookup by property By frequency Comparisons Geometry Bonds, angles Bond, angle, or dihedral DFT grid size on point group DFT grid on bond length Core correlation - bond length Same bond/angle many molecules Isoelectronic diatomics Isoelectronic triatomic angles Average bond lengths Rotation Rotational Constants Products of moments of inertia Point group Vibrations Vibrations 2 calculations Frequency differences One frequency Zero point energy Intensity Intensity for one mode Vibrational intensities Reduced mass comparison Anharmonic Triatomic Scale factors Energy Reaction Reaction Energy 0K Reaction Energy 298K Atomization 0K Atomization 298K Single point vs optimized DFT grid size on energy Semiempirical enthalpy Internal rotation Similar molecules Conformation Sets of isomers Sets of tautomers Isomers Entropy Entropy Heat capacity Entropy of several molecules Integrated heat capacity Reaction entropy Electrostatics Dipole Polarizability Several molecules Quadrupole Ion Compare Ionzation energy Koopman ionization energy Koopman IE for a few molecules Compare Electron affinity Compare Proton affinity Protonation Site Resources Info on Results Calculations Done Method and basis set List molecules One molecule Multiple conformers, states Multiple conformers, states Basis functions used I/O files Input/output files MOL file Z-matrix wfn files Glossary Conversion Forms B to I, I to B Angle formulas Integrated heat Capacity Calculating Enthalpy Links NIST Links NIST webbook bibliographic data CCCBDB Experimental data External links Basis Set Exchange Computational Chemistry List Thermochemistry in Gaussian Minnesota Database Collection Benchmark Energy and Geometry Point Groups Thermochemistry Thermochemistry Molecules with good enthalpy A → B + C Reference states Tutorials Vibrations Why scale vibrations Zero-point energies Entropy Methyl rotor entropy Entropy and conformations Energy Getting enthalpy of formation Vertical vs adiabatic IE Thermo from calculations Electrostatics Dipole parts by point group Quadrupoles Geometry Angle formulas Cost Cost Comparison Timings Comparison Bad Calculations Geometry Bad moment of inertia Bad Calculated Bond Lengths Bad point group Worst molecules Vibrations Bad vib. Calc. vs exp. Bad Vib. HF vs MP2 Bad scale factors Low excited states Oddities NaCN Is not linear FAQ Help Units Choose Units Energy Bond length Rotational Constant Moment of Inertia Dipole and Quadrupole Polarizability Explanations Hartree cm-1 Debye Credits Just show me Show me a calculated geometry Summary Using older interface Limit Basis sets Method options List Recent molecules Choose a few Molecules Number of atoms By heavy atoms Diatomics InChI Deuterated Dimers Geometry Point group Point group count Bonds types Isodesmic reactions Bad point group Multiple conformers, states Vibrations Big anharmonicity Energy Enthalpy at 0 Kelvin Similar molecules Similar Isomers Cis/trans Tautomers Multiple conformers, states Ions, Dipoles, etc. List Ions Ionization changes point group Dipole Quadrupole Polarizability Proton Affinities Index of CCCBDB Feedback Error form Wants
You are here: Calculated > Energy > Optimized > Energy

All results from a given calculation for C5H8 (2,3-Pentadiene)

using model chemistry: CID/6-31G*

States and conformations

All results from a given calculation for C₅H₈ (2,3-Pentadiene)