Abstract
The synthesis and crystal structures of three mercapto functionalised 1,3,4-thiadiazoles and the crystal structure of 2-mercapto-5-methyl-1,3,4-thiadiazole are described. In the solid state, 2-mercapto-5-methyl-1,3,4-thiadiazole 1 forms a thioamide tautomer as shown by FRIR and Raman spectroscopy as well as X-ray crystallography and as theoretically predicted. The molecules are connected to form chains via N-H⋯S hydrogen bonds with N⋯S = 328.3 pm. Bis(2-methyl-1,3,4-thiadiazolyl)-5,5′-disulfide 2, the disulfide of 1, as well as 2-(tert-butyldithio)-5-methyl-1,3,4-thiadiazole 3 and 2,5-bis(tert-butyldithio)-1,3,4-thiadiazole 4 have been synthesised and characterised by vibrational spectroscopy and X-ray diffraction.
| Original language | English |
|---|---|
| Pages (from-to) | 179-191 |
| Number of pages | 13 |
| Journal | Journal of Molecular Structure |
| Volume | 658 |
| Issue number | 3 |
| DOIs | |
| State | Published - 15 Oct 2003 |
| Externally published | Yes |
Keywords
- 1,3,4-Thiadiazole
- DFT calculation
- Hydrogen bonding
- Single-crystal X-ray diffraction
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