Anderson, David G. and Davidson, R. Stephen and Elvery, J.J. (1996) Thioxanthones: Their fate when used as photoinitiators. Polymer, 37 (12). pp. 2477-2484. ISSN 0032-3861. (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided)
It has been shown that when thioxanthones are used in conjunction with an amine synergist they initiate the polymerization of lauryl acrylate. Gel permeation chromatography (g.p.c.) showed that the polymer which is formed contains thioxanthone residues. It is suggested that the thioxanthyl ketyl radical acts as a chain terminator, with reactions occurring at the 2-, 4-, 5-, 7-, and 9-positions. Reactions at positions other than 9- can lead to incorporation of thioxanthone residues. When the aromatic amine synergist, ethyl p-dimethylaminobenzoate, is used the aromatic amine is also incorporated into the polymer. (C) 1996 Elsevier Science Ltd.
|Uncontrolled keywords:||lauryl acrylate; thioxanthones; photoinitiators|
|Divisions:||Faculties > Science Technology and Medical Studies > School of Physical Sciences|
|Depositing User:||M.A. Ziai|
|Date Deposited:||17 May 2009 08:51|
|Last Modified:||16 May 2014 09:17|
|Resource URI:||https://kar.kent.ac.uk/id/eprint/18787 (The current URI for this page, for reference purposes)|