1. A New Method of Synthesis of Polythiols Schiff Base with Sulphur and Azomethine Donors and their Characterizations by Willgeordt Kindlier.
- Author
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Shah, Ambreen, Mirrani, Mehtab, and Memon, G. Zuhra
- Subjects
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SULFUR , *POLAR solvents , *SULFHYDRYL group , *PHENYLENEDIAMINES , *ELEMENTAL analysis , *DIAMINES , *THERMAL analysis - Abstract
Some new polythiols were derived from aromatie aldehyde (2-hydroxy benzaldehyde) and different diamines (semiearbazide, 4-phenyl, 3-thiosemiearbazide, 4-4'-oxydianiline and N, N'- dimethyl p-phenylenediamine), in the presenee of elemental sulphur. The proeess of eondensation is earried out by the Willgerodt Kindler (WK) reaetion of azomethine donor or derivatives with elemental sulphur in the presenee of a strong base as a eatalyst. The polythiols (polythioamides) were eharaeterized by different teehniques like elemental miero analysis, FTIR, UV-Vis speetroseopies, thermal analysis and viseosity measurement. The FT-IR showed the main band around 1235-1265/em-1 beeause of the formation of thiol groups in respeeted polythiols to vC=S vibrations. The polythiols indieated improved thermal solidity up to 600 °C. These polythiols were soluable in highly polar organie solvents due to their eomplex struetures. The intrinsie viseo-metrieal data of these polythiols reaehed about 0.393-0.5201 dL/g in THF. [ABSTRACT FROM AUTHOR]
- Published
- 2023