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Computational Chemistry Comparison and Benchmark DataBase Release 22 (May 2022) Standard Reference Database 101 National Institute of Standards and Technology |
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| Species | Name | Experimental Angle | Calculated Angle | Difference |
|---|---|---|---|---|
| C3H7NO | dimethylformamide | 117.0 | 112.5 | 4.5 |
| C3H7NO | dimethylformamide | 110.1 | 108.0 | 2.1 |
| HCN | Hydrogen cyanide | 180.0 | 180.0 | 0.0 |
| CHONH2 | formamide | 112.7 | 112.2 | 0.5 |
| CH2NOH | formaldoxime | 121.8 | 122.7 | -0.9 |
| CH2NOH | formaldoxime | 115.6 | 117.8 | -2.3 |
| N(CH3)3 | Trimethylamine | 111.7 | 112.8 | -1.1 |
| N(CH3)3 | Trimethylamine | 110.1 | 109.4 | 0.7 |
| CH3NO2 | Methane, nitro- | 107.2 | 106.8 | 0.4 |
| C4H5N | Pyrrole | 121.5 | 121.5 | -0.0 |
| CH3NHCH3 | Dimethylamine | 109.7 | 109.5 | 0.2 |
| CH3NHCH3 | Dimethylamine | 108.2 | 109.0 | -0.8 |
| CH3NHCH3 | Dimethylamine | 113.8 | 113.7 | 0.1 |
| C2H5N | Aziridine | 118.3 | 118.4 | -0.1 |
| C2H5N | Aziridine | 114.3 | 114.6 | -0.3 |
| C3H4N2 | 1H-Pyrazole | 119.3 | 120.4 | -1.1 |
| C3H4N2 | 1H-Pyrazole | 121.4 | 122.2 | -0.8 |
| C3H3NO | Oxazole | 127.9 | 130.2 | -2.3 |
| C3H3NO | Oxazole | 121.9 | 122.5 | -0.6 |
| C4H4N2 | Pyridazine | 111.7 | 115.9 | -4.2 |
| C4H4N2 | 1,3-Diazine | 117.9 | 117.0 | 0.9 |
| C4H4N2 | Pyrazine | 117.9 | 117.7 | 0.2 |
| CH3NC | methyl isocyanide | 109.6 | 109.6 | 0.0 |
| CH3NO | nitrosomethane | 111.1 | 110.0 | 1.1 |
| CH3NO | nitrosomethane | 107.3 | 107.3 | -0.0 |
| CH2NH | Methanimine | 123.4 | 125.3 | -1.9 |
| CH2NH | Methanimine | 119.7 | 119.2 | 0.5 |
| C2H6N2O2 | Dimethylnitroamine | 101.9 | 110.3 | -8.4 |
HF/3-21G* for aHCN
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| -10 | -8 | -6 | -4 | -2 | 0 | 2 | 4 | 6 | 8 | 10 | 12 | 14 | ||||||||||||||||||||||||||||
| Angle difference calc. - exp. (degrees) | ||||||||||||||||||||||||||||||||||||||||
| Species | Name | Difference (degrees) | |
|---|---|---|---|
| Most negative difference | C2H6N2O2 | Dimethylnitroamine | -8.4 |
| Most positive difference | C3H7NO | dimethylformamide | 4.5 |