N-H⋯S hydrogen bonding in 2-mercapto-5-methyl-1,3, 4-thiadiazole. Synthesis and crystal structures of mercapto functionalised 1,3,4-thiadiazoles

Frank Hipler, Manuela Winter, Roland A. Fischer

Research output: Contribution to journalArticlepeer-review

41 Scopus citations

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 languageEnglish
Pages (from-to)179-191
Number of pages13
JournalJournal of Molecular Structure
Volume658
Issue number3
DOIs
StatePublished - 15 Oct 2003
Externally publishedYes

Keywords

  • 1,3,4-Thiadiazole
  • DFT calculation
  • Hydrogen bonding
  • Single-crystal X-ray diffraction

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