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	-337.680019
Energy at 298.15K	-337.688533
Nuclear repulsion energy	250.543521

Mode Number	Symmetry	Frequency (cm^-1)	Scaled Frequency (cm^-1)	IR Intensities (km mol^-1)
1	A	3118	3101	0.09
2	A	3118	3101	0.43
3	A	3040	3023	35.72
4	A	3037	3020	1.19
5	A	2942	2925	72.54
6	A	2937	2921	14.50
7	A	1540	1531	15.34
8	A	1526	1518	2.72
9	A	1523	1515	20.65
10	A	1506	1498	22.75
11	A	1429	1421	5.10
12	A	1416	1408	5.96
13	A	1304	1297	111.76
14	A	1229	1222	1.41
15	A	1177	1171	1.60
16	A	1142	1136	5.36
17	A	1100	1094	6.47
18	A	1031	1025	210.22
19	A	1008	1003	0.39
20	A	853	849	75.10
21	A	723	719	14.83
22	A	631	628	10.37
23	A	532	529	9.44
24	A	511	508	2.26
25	A	375	373	5.13
26	A	353	351	4.08
27	A	195	194	15.91
28	A	149	149	0.00
29	A	101	100	0.68
30	A	61	61	0.20

Atom	x (Å)	y (Å)	z (Å)
O1	1.411	1.166	0.039
O2	1.412	-1.165	0.037
H3	-1.490	1.353	1.151
H4	-2.229	1.342	-0.494
H5	-0.607	2.088	-0.234
C6	-1.284	1.282	0.066
H7	-1.495	-1.350	1.151
H8	-0.604	-2.088	-0.227
H9	-2.226	-1.347	-0.497
C10	-1.284	-1.282	0.067
N11	0.835	0.000	-0.029
N12	-0.624	-0.000	-0.293

	O1	O2	H3	H4	H5	C6	H7	H8	H9	C10	N11	N12
O1		2.3312	3.1122	3.6827	2.2351	2.6975	4.0014	3.8359	4.4527	3.6410	1.3021	2.3684
O2	2.3312		4.0006	4.4528	3.8383	3.6413	3.1187	2.2324	3.6816	2.6988	1.3021	2.3687
H3	3.1122	4.0006		1.8032	1.7994	1.1070	2.7032	3.8109	3.2476	2.8572	2.9375	2.1602
H4	3.6827	4.4528	1.8032		1.8038	1.0997	3.2394	3.8049	2.6890	2.8453	3.3771	2.1023
H5	2.2351	3.8383	1.7994	1.8038		1.0944	3.8113	4.1753	3.8059	3.4505	2.5455	2.0889
C6	2.6975	3.6413	1.1070	1.0997	1.0944		2.8549	3.4499	2.8484	2.5642	2.4784	1.4861
H7	4.0014	3.1187	2.7032	3.2394	3.8113	2.8549		1.7995	1.8032	1.1070	2.9402	2.1601
H8	3.8359	2.2324	3.8109	3.8049	4.1753	3.4499	1.7995		1.8038	1.0944	2.5430	2.0884
H9	4.4527	3.6816	3.2476	2.6890	3.8059	2.8484	1.8032	1.8038		1.0997	3.3767	2.1028
C10	3.6410	2.6988	2.8572	2.8453	3.4505	2.5642	1.1070	1.0944	1.0997		2.4786	1.4862
N11	1.3021	1.3021	2.9375	3.3771	2.5455	2.4784	2.9402	2.5430	3.3767	2.4786		1.4823
N12	2.3684	2.3687	2.1602	2.1023	2.0889	1.4861	2.1601	2.0884	2.1028	1.4862	1.4823

atom1	atom2	atom3	angle	atom1	atom2	atom3	angle
O1	N11	O2	127.060	O1	N11	N12	116.403
O2	N11	N12	116.425	H3	C6	H4	109.599
H3	C6	H5	109.647	H3	C6	N12	111.998
H4	C6	H5	110.597	H4	C6	N12	107.851
H5	C6	N12	107.115	C6	N12	C10	119.242
C6	N12	N11	113.216	H7	C10	H8	109.661
H7	C10	H9	109.604	H7	C10	N12	111.990
H8	C10	H9	110.598	H8	C10	N12	107.073
H9	C10	N12	107.881	C10	N12	N11	113.229

All results from a given calculation for C₂H₆N₂O₂ (Dimethylnitroamine)

using model chemistry: BLYP/3-21G

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

Number	Element	Mulliken
1	O	-0.272
2	O	-0.272
3	H	0.191
4	H	0.205
5	H	0.237
6	C	-0.382
7	H	0.191
8	H	0.237
9	H	0.205
10	C	-0.383
11	N	0.353
12	N	-0.311

	x	y	z	Total
	-3.860	-0.000	0.400	3.880
CHELPG
AIM
ESP

<r²>	157.957
(<r²>)^1/2	12.568

All results from a given calculation for C2H6N2O2 (Dimethylnitroamine)

using model chemistry: BLYP/3-21G

States and conformations

All results from a given calculation for C₂H₆N₂O₂ (Dimethylnitroamine)