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A New Method of Synthesis of Polythiols Schiff Base with Sulphur and Azomethine Donors and their Characterizations by Willgeordt Kindller


Article Information

Title: A New Method of Synthesis of Polythiols Schiff Base with Sulphur and Azomethine Donors and their Characterizations by Willgeordt Kindller

Authors: Ambreen Shah, Mehtab Mirrani, G. Zuhra Memon

Journal: Pakistan Journal of Scientific and Industrial Research (Series A: Physical Sciences)

HEC Recognition History
Category From To
Y 2023-07-01 2024-09-30
Y 2022-07-01 2023-06-30
Y 2021-07-01 2022-06-30
Y 2020-07-01 2021-06-30
Y 1900-01-01 2005-06-30

Publisher: Pakistan Council of Scientific and Industrial Research

Country: Pakistan

Year: 2023

Volume: 66

Issue: 1

Language: en

Keywords: polythiolssynthesisWillgerodt Kindler (WK) reactionFT-IRTG/DTAenthalpy

Categories

Abstract

Some new polythiols were derived from aromatic aldehyde (2-hydroxy benzaldehyde) and different diamines (semicarbazide, 4-phenyl, 3-thiosemicarbazide, 4-4'-oxydianiline and N, N'- dimethyl p-phenylenediamine), in the presence of elemental sulphur.The process of condensation is carried out by the Willgerodt Kindler (WK) reaction of azomethine donor or derivatives with elemental sulphur in the presence of a strong base as a catalyst. The polythiols (polythioamides) were characterized by different techniques like elemental micro analysis, FTIR, UV- Vis spectroscopies, thermal analysis and viscosity measurement. The FT-IR showed the main band around 1235-1265/cm-1 because of the formation of thiol groups in respected polythiols to vC=S vibrations. The polythiols indicated improved thermal solidity up to 600 °C. These polythiols were soluable in highly polar organic solvents due to their complex structures. The intrinsic visco-metrical data of these polythiols reached about 0.393-0.5201 dL/g in THF.


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