Infrared and structural investigations of the 3,5-diamino-1,2,4-dithiazolium salts
✍ Scribed by Giorgio Peyronel; Anna Pignedoli; Wanda Malavasi
- Publisher
- Elsevier Science
- Year
- 1982
- Tongue
- English
- Weight
- 273 KB
- Volume
- 38
- Category
- Article
- ISSN
- 1386-1425
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✦ Synopsis
The 3,5-diamino-1,2,4_dithiazolium salts DADTX [X = Cl dHrO), Br, I, ClO,, Nor, fSO,(H,O)] have been prepared and their i.r. spectra investigated in relation to that of dithiobiuret and to the molecular structure of the thiouret hydrohalides. In the DADTX salts the dithiobiuret v(NH& and 6(NHz) bands are observed at about the same frequencies as in the ligand, the v(NH) and S(NH) bands are absent and the v(CN) and v(CS) bands are shifted to higher and lower frequencies, respectively, in agreement with a shortening of the CN and an elongation of the CS bonds and a new v(SS) band is observed in the 430-410 cm-' region.
📜 SIMILAR VOLUMES
## Abstract Reaction of the 3,5‐diaryl‐1,2‐dithiolium salts 2 with the metal cyclopentadienides 4 and 9 leads to the formation of the tricyclic compounds 6 and 10 via a ring‐opened intermediate, which undergoes an intramolecular Diels‐Alder cyclization. Compounds 6 and 10 rearrange by treatment wit
## Abstract Reaction of the 1‐substituted‐3‐cyano‐isothioureas **6** with hydroxylamine gave mixtures of the 5‐amino‐3‐substituted‐amino‐1,2,4‐oxadiazoles **1** and the isomeric 3‐amino‐5‐substituted‐amino‐1,2,4‐oxadiazoles **8** in which **1** usually predominated. The structural assignment of the
## Abstract The 5‐amino‐3‐arylamino‐1,2,4‐oxadiazoles **2** are conveniently prepared by oxidative cyclization of the arylamidinoureas **10**. The process is also capable of producing a variety of the 5‐substituted‐amino analogs **32** when the appropriately substituted guanidine **31** is employed