Issue 2, 2016

Novel naphthalimide–amine based photoinitiators operating under violet and blue LEDs and usable for various polymerization reactions and synthesis of hydrogels

Abstract

A series of naphthalimide derivatives containing tertiary amine groups (DNNDs) have been prepared. Some of these derivatives (e.g. DNND3, DNND4 and DNND5) exhibit interesting shifted absorption so that they can be utilized as versatile photoinitiators upon exposure to various violet and blue LEDs (385, 405, 455 and 470 nm). They are particularly efficient for the cationic photopolymerization of an epoxide and the free radical photopolymerization of an acrylate. The thiol–ene photopolymerization, as well as the synthesis of interpenetrating polymer networks (of epoxide/acrylate blend) IPNs, is feasible. Remarkably, the production of hydrogels can also be easily achieved using a DNND derivative after inclusion in a cyclodextrin cavity. The photochemical mechanisms have been comprehensively investigated by steady state photolysis, Electron Spin Resonance (ESR), fluorescence, electrochemistry and laser flash photolysis and discussed in detail.

Graphical abstract: Novel naphthalimide–amine based photoinitiators operating under violet and blue LEDs and usable for various polymerization reactions and synthesis of hydrogels

Supplementary files

Article information

Article type
Paper
Submitted
07 Oct 2015
Accepted
30 Oct 2015
First published
02 Nov 2015

Polym. Chem., 2016,7, 418-429

Author version available

Novel naphthalimide–amine based photoinitiators operating under violet and blue LEDs and usable for various polymerization reactions and synthesis of hydrogels

N. Zivic, J. Zhang, D. Bardelang, F. Dumur, P. Xiao, T. Jet, D. Versace, C. Dietlin, F. Morlet-Savary, B. Graff, J. P. Fouassier, D. Gigmes and J. Lalevée, Polym. Chem., 2016, 7, 418 DOI: 10.1039/C5PY01617G

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements