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Computational Chemistry Comparison and Benchmark DataBase Release 22 (May 2022) Standard Reference Database 101 National Institute of Standards and Technology |
| You are here: Calculated > Geometry > Calculated geometry > One type of bond | |
QCISD/6-31G
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| 1.50 | 1.55 | 1.60 | 1.65 | 1.70 | 1.75 | 1.80 | 1.85 | 1.90 | 1.95 | 2.00 | 2.05 | 2.10 | ||||||||||||||||||||||||||||
| bond lengths (Å) | ||||||||||||||||||||||||||||||||||||||||
| Average bond length | Standard deviation |
|---|---|
| 1.813 | 0.114 |
| Species | Name | Bond Length (Å) | |
|---|---|---|---|
| Lowest value | HCS+ | Thioformyl cation | 1.549 |
| Highest value | SF5CF3 | Sulfur, pentafluoro(trifluoromethyl)- | 2.017 |
| Species | Name | Bond Length (Å) | Atom1 index | Atom2 index |
|---|---|---|---|---|
| CS- | carbon monosulfide anion | 1.780 | 1 | 2 |
| CS | carbon monosulfide | 1.625 | 1 | 2 |
| CS+ | carbon monosulfide cation | 1.572 | 1 | 2 |
| HCS- | Thioformyl anion | 1.820 | 1 | 3 |
| HCS+ | Thioformyl cation | 1.549 | 1 | 3 |
| H2CS- | thioformaldehyde anion | 1.816 | 1 | 2 |
| H2CS | Thioformaldehyde | 1.689 | 1 | 2 |
| H2CS+ | thioformaldehyde cation | 1.676 | 1 | 2 |
| H2CSH+ | Thioformaldehyde, protonated | 1.701 | 1 | 2 |
| CH3SH | Methanethiol | 1.912 | 1 | 2 |
| CH3SH+ | Methanethiol cation | 1.915 | 1 | 2 |
| CH3SH2+ | protonated methylsulfide | 1.941 | 1 | 2 |
| CS2- | Carbon disulfide anion | 1.731 | 1 | 2 |
| 1.731 | 1 | 3 | ||
| CS2 | Carbon disulfide | 1.621 | 1 | 2 |
| 1.621 | 1 | 3 | ||
| CS2+ | Carbon disulfide cation | 1.631 | 1 | 2 |
| 1.631 | 1 | 3 | ||
| OCS | Carbonyl sulfide | 1.643 | 1 | 3 |
| OCS+ | Carbonyl sulfide cation | 1.754 | 1 | 3 |
| SCN- | thiocyanide anion | 1.769 | 1 | 2 |
| SCN | thiocyanato radical | 1.745 | 1 | 2 |
| SCSe | Carbon sulfide selenide | 1.619 | 1 | 2 |
| HSCN | thiocyanic acid | 1.795 | 1 | 2 |
| HNCS | Isothiocyanic acid | 1.666 | 2 | 3 |
| CH2CS | Thioketene | 1.644 | 2 | 3 |
| CHSNH2 | thioformamide | 1.718 | 1 | 2 |
| NHCHSH | Methanimidothioic acid | 1.848 | 2 | 3 |
| C2H4S | Thiirane | 1.950 | 1 | 2 |
| 1.950 | 1 | 3 | ||
| CH2CHSH | Ethenethiol | 1.856 | 2 | 3 |
| CH3SSH | Hydrogen methyl disulfide | 1.911 | 1 | 2 |
| HSCH2SH | Methanedithiol | 1.903 | 1 | 2 |
| 1.903 | 1 | 3 | ||
| CH3CHS | Thioacetaldehyde | 1.695 | 1 | 3 |
| CH3CH2SH | ethanethiol | 1.921 | 2 | 3 |
| CH3SCH3 | Dimethyl sulfide | 1.903 | 1 | 2 |
| 1.903 | 1 | 3 | ||
| CH3SCH3+ | dimethyl sulfide cation | 1.906 | 1 | 2 |
| 1.906 | 1 | 3 | ||
| CS3-- | Carbonotrithioate | 1.822 | 1 | 2 |
| 1.822 | 1 | 3 | ||
| 1.822 | 1 | 4 | ||
| Cl2CS | Thiophosgene | 1.658 | 1 | 2 |
| CH3CSNH2 | Ethanethioamide | 1.733 | 1 | 2 |
| CH3SSCH3 | Disulfide, dimethyl | 1.911 | 1 | 3 |
| 1.911 | 2 | 4 | ||
| CH3CSCH3 | Thioacetone | 1.706 | 1 | 2 |
| C3H3NS | Thiazole | 1.848 | 1 | 2 |
| 1.824 | 1 | 3 | ||
| CH3SO2NH2 | methanesulfonamide | 1.880 | 1 | 2 |
| C2H6O2S | Dimethyl sulfone | 1.892 | 1 | 4 |
| 1.892 | 1 | 5 | ||
| CH2CHSCHCH2 | Divinyl sulfide | 1.857 | 1 | 2 |
| 1.857 | 1 | 3 | ||
| C4H6S | Thiophene, 2,5-dihydro- | 1.929 | 1 | 2 |
| 1.929 | 1 | 3 | ||
| CH3SSSCH3 | dimethyl trisulfide | 1.909 | 2 | 4 |
| 1.909 | 3 | 5 | ||
| C(CH3)3SH | 2-Propanethiol, 2-methyl- | 1.947 | 1 | 2 |
| C4H9SH | 1-Butanethiol | 1.923 | 1 | 2 |
| C2H4N2S2 | Ethanedithioamide | 1.745 | 1 | 3 |
| 1.745 | 2 | 4 | ||
| C3H6S3 | 1,3,5-Trithiane | 1.899 | 1 | 4 |
| 1.899 | 1 | 6 | ||
| 1.899 | 2 | 4 | ||
| 1.899 | 2 | 5 | ||
| 1.899 | 3 | 5 | ||
| 1.899 | 3 | 6 | ||
| C4H6OS | Vinyl sulfoxide | 1.898 | 1 | 3 |
| 1.898 | 1 | 4 | ||
| SF5CF3 | Sulfur, pentafluoro(trifluoromethyl)- | 2.017 | 1 | 2 |