chemistry of some 2,4,6-triphenylpyridine derivatives. by Pai-Lin Nie

Cover of: chemistry of some 2,4,6-triphenylpyridine derivatives. | Pai-Lin Nie

Published by University of East Anglia in Norwich .

Written in English

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Thesis (Ph.D.) - University of East Anglia, School of Chemical Sciences, 1977.

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Open LibraryOL13845739M

Download chemistry of some 2,4,6-triphenylpyridine derivatives.

A series of novel 2,4,6-triphenylpyridine derivatives containing 1,8-naphthalimide groups have been prepared in good yields using Suzuki couplings reactions.

The relationship of the photoluminescence property of the compounds was systematically investigated via a thermogravimetric analyzer, UV-vis, fluorescence and electrochemical by: 3. CHEMISTRY» Acids & Bases S - 2,4,6-TRIPHENYLPYRIDINE EMAIL THIS PAGE TO A FRIEND.

To Email: From Email: Message: S 2,4,6-TRIPHENYLPYRIDINE Aldrich CPR. CAS Number Linear Formula C 23 H 17 N. Molecular Weight MDL number. Use of the information, documents and data from the ECHA website is subject to the terms and conditions of this Legal Notice, and subject to other binding limitations provided for under applicable law, the information, documents and data made available on the ECHA website may be reproduced, distributed and/or used, totally or in part, for non-commercial purposes provided that ECHA is.

The Chemistry of some 2, 4, 6 - Triphenylpyridine Derivatives. Author: Nie, P. ISNI: Awarding Body: University of East Anglia Current Institution: University of East Anglia Date of Award: Availability of Full Text: Access from EThOS. A novel ‐type triamine was synthesized for the first time and employed to prepare a series of amine‐ and anhydride‐terminated triphenylpyridine‐containing hyperbranched polyimides under microwave irradiation.

The structure of the triamine monomer and polymers were verified by FTIR and 1 H NMR spectroscopy. The predominantly amorphous polyimides were soluble in m‐cresol, NMP, DMSO Cited by: Due to their -stacking ability, some pyridines are used in supramolecular chemistry Previously, 2,4,6-triarylpyridines have been prepared by the condensation of 1,5-diketones with formamide-formic acid 9, reaction of (aroylmethylene).

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