Cationic polymerization of cyclohexene oxide initiated by a ternary system consisting of free radical photoinitiator, diphenyl acetylene and triphenylsulphonium salt

1996 ◽  
Vol 37 (6) ◽  
pp. 723-728 ◽  
Author(s):  
Ash Okan ◽  
I. Ersin Serhath ◽  
Yusuf Yağci
2015 ◽  
Vol 48 (6) ◽  
pp. 1658-1663 ◽  
Author(s):  
Mustafa Ciftci ◽  
Senem Kork ◽  
Guangjuan Xu ◽  
Michael R. Buchmeiser ◽  
Yusuf Yagci

e-Polymers ◽  
2001 ◽  
Vol 1 (1) ◽  
Author(s):  
Fatma Bayramoglu ◽  
Aysen Onen ◽  
Yusuf Yagci

AbstractAllylthiophenium salts with various substituents at the allylic moiety were synthesized, characterized and shown to be efficient coinitiators in radicallly promoted cationic photopolymerization of cyclohexene oxide. The relative efficiencies of these salts in combination with benzoin and benzophenone as free radical sources in the photopolymerizations are compared. Both additionfragmentation and electron transfer mechanisms are proposed and their relative merits discussed.


Molecules ◽  
2021 ◽  
Vol 26 (11) ◽  
pp. 3192
Author(s):  
Nicolas Giacoletto ◽  
Frédéric Dumur

Over the past several decades, photopolymerization has become an active research field, and the ongoing efforts to develop new photoinitiating systems are supported by the different applications in which this polymerization technique is involved—including dentistry, 3D and 4D printing, adhesives, and laser writing. In the search for new structures, bis-chalcones that combine two chalcones’ moieties within a unique structure were determined as being promising photosensitizers to initiate both the free-radical polymerization of acrylates and the cationic polymerization of epoxides. In this review, an overview of the different bis-chalcones reported to date is provided. Parallel to the mechanistic investigations aiming at elucidating the polymerization mechanisms, bis-chalcones-based photoinitiating systems were used for different applications, which are detailed in this review.


1994 ◽  
Vol 27 (14) ◽  
pp. 3683-3693 ◽  
Author(s):  
Yubai Bi ◽  
Douglas C. Neckers

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