Cultural advice

The Australian National University acknowledges, celebrates and pays our respects to the Ngunnawal and Ngambri people of the Canberra region and to all First Nations Australians on whose traditional lands we meet and work, and whose cultures are among the oldest continuing cultures in human history.

Aboriginal and Torres Strait Islander peoples are advised that ANU Library collections may include images, names, voices, and other representations of deceased persons.

Material in the collection may contain terms, language or views that reflect the period in which the item was created and may be considered inappropriate today.

Substituent Effects on Photoinitiation Ability of Monoaminoanthraquinone-Based Photoinitiating Systems for Free Radical Photopolymerization under LEDs

Loading...
Thumbnail Image

Date

Authors

Zhang, Jing
Lalevee, Jacques
Hill, Nicholas
Kiehl, Jonathan
Zhu, Di
Cox, Nicholas
Langley, Julien
Stenzel, Martina H
Coote, Michelle
Xiao, Pu

Journal Title

Journal ISSN

Volume Title

Publisher

Wiley

Abstract

Three monoamino‐substituted anthraquinone derivatives (AAQs), that is, 1‐aminoanthraquinone (AAQ), 1‐(methylamino)anthraquinone (MAAQ), and 1‐(benzamido)anthraquinone (BAAQ), incorporated with various additives [e.g., triethanolamine (TEAOH) and phenacyl bromide (PhC(═O)CH2Br)] are investigated for their roles as photoinitiating systems of free radical photopolymerization of (meth)acrylate monomers upon the exposure to UV to green LEDs. The AAQs‐based photoinitiating systems, AAQ/TEAOH/PhC(═O)CH2Br and BAAQ/TEAOH/PhC(═O)CH2Br photoinitiators exhibit the highest efficiency for the free radical photopolymerization of DPGDA under the irradiation of blue LED and UV LED, respectively, which is consistent with the extent of overlap between their absorption spectra and the emission spectra of the LEDs. AAQ/TEAOH/PhC(═O)CH2Br photoinitiator can also initiate the free radical photopolymerization of different (meth)acrylate monomers, with an efficiency dependent on the chemical structures of these monomers.

Description

Citation

Source

Macromolecular Rapid Communications

Book Title

Entity type

Access Statement

License Rights

Restricted until

2099-12-31