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Hyper-branched triphenylamine Schiff base preparation and complexation
International Conference on Polymerization Catalysis, Flexible Polymer and Nanotechnology
September 06-07, 2018 Dubai, UAE

Ideisan I Abu-Abdoun

University of Sharjah, UAE

Scientific Tracks Abstracts: J Nanomater Mol Nanotechnol

Abstract:

A triphenylamine hyper-branched Schiff base was prepared in a good yield and molecular weight using Schiff reaction between mono- and tri-formyl derivatives of Triphenylamine (TPA) and selected aromatic and aliphatic diamine compounds to give amine-imine multi-anchored product. Triphenylamine as electron donor and hole transport group was devised and synthesized and complexation of the multifunctional products isolated with metals such as Cu2+, Ni2+, Pt2+, Ni2+ was carried out. The structural properties of the isolated products can be verified by Fourier Transform IR (FT-IR) spectroscopy and other techniques. Chemical oxidation of the product of the condensation reactions gives a stable cation radical which can be used in polymerization of epoxide and vinyl monomers and as a powerful one electron oxidizing reagent in organic reactions, at room temperature.

Biography :

Ideisan I. Abu-Abdoun is Professor of Chemistry at the Department of Chemistry, University of Sharjah, United Arab Emirates. He holds his Ph.D. degree from the University of Liverpool, Liverpool, United Kingdom in polymer Chemistry (1982). Prior to join the University of Sharjah, he worked at different universities including King Fahd University of Petroleum and Minerals (KFUPM), Dhahran, Saudi Arabia; Aal-Albayat University, Jordan; Bowling green State University (BGSU), USA; and Liverpool University (UK).

E-mail: abuabdoun@sharjah.ac.ae