Photosensitized cationic polymerizations using dialkylphenacylsulfonium and dialkyl(4-hydroxyphenyl)sulfonium salt photoinitiators

1981 ◽  
Vol 14 (5) ◽  
pp. 1141-1147 ◽  
Author(s):  
J. V. Crivello ◽  
J. L. Lee
2021 ◽  
Author(s):  
Davy-Louis Versace ◽  
Louise Breloy ◽  
Yusuf Yagci ◽  
Ismail Yilmaz ◽  
Ozgur Yavuz

Phthalocyanines (Pcs) are interesting molecules offering a fascinating chemistry world which received tremendous interest in the last decade. Their certain features such as high thermal, chemical, and optical stability as...


Photochem ◽  
2021 ◽  
Vol 1 (2) ◽  
pp. 167-189
Author(s):  
Alexandre Mau ◽  
Guillaume Noirbent ◽  
Céline Dietlin ◽  
Bernadette Graff ◽  
Didier Gigmes ◽  
...  

In this work, eleven heteroleptic copper complexes were designed and studied as photoinitiators of polymerization in three-component photoinitiating systems in combination with an iodonium salt and an amine. Notably, ten of them exhibited panchromatic behavior and could be used for long wavelengths. Ferrocene-free copper complexes were capable of efficiently initiating both the radical and cationic polymerizations and exhibited similar performances to that of the benchmark G1 system. Formation of acrylate/epoxy IPNs was also successfully performed even upon irradiation at 455 nm or at 530 nm. Interestingly, all copper complexes containing the 1,1′-bis(diphenylphosphino)ferrocene ligand were not photoluminescent, evidencing that ferrocene could efficiently quench the photoluminescence properties of copper complexes. Besides, these ferrocene-based complexes were capable of efficiently initiating free radical polymerization processes. The ferrocene moiety introduced in the different copper complexes affected neither their panchromatic behaviors nor their abilities to initiate free radical polymerizations.


2021 ◽  
pp. 110525
Author(s):  
Shixiong Chen ◽  
Chun Cao ◽  
Xiaoming Shen ◽  
Yiwei Qiu ◽  
Cuifang Kuang ◽  
...  
Keyword(s):  

2014 ◽  
Vol 43 (9) ◽  
pp. 3424-3427
Author(s):  
D. E. Janzen ◽  
A. M. Kooyman

A trithiamacrocyclic ligand complex of Au(iii) undergoes a redox-mediated thermal reaction to form a chiral bicyclic sulfonium salt.


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