Abstract
AbstractIn this paper, we presented four novel visible light photoinitiating systems, which employed nitro‐stilbenzene derivatives as photoinitiators. Visible light photopolymerization of these systems was studied completely. The results showed that the chemical structures of the photoinitiators, photoinduced electron transfer approach, solvent polarity, and monomers played significant effects on the visible light photopolymerization. The electrochemistry of nitro‐stilbenzene was dramatically influenced by the linking benzophenone moiety. The cyclic voltammograms of four photoinitiators were determined and discussed. We further estimated the thermodriving force for electron transfer between nitro‐stilbenzene and benzophenone. Thermal stabilities of new photoinitators were determined by the analysis of differential scanning calorimetry (DSC) and thermogravimetry (TG) in this paper. Copyright © 2009 John Wiley & Sons, Ltd.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
