“…This mechanism was also discussed for comparable maleimide dimerizations [43,66] as well as for dimerizations of dimethylmaleic anhydride [77].…”
Section: Photoinduced Dimerization Of Dmmi In Aqueous Solutionmentioning
confidence: 94%
“…In the present work, we employed the sodium salt of thioxanthone disulfonate. The sulfonate groups only act in terms of increasing the water solubility without affecting the spectral properties significantly [59,66].…”
Section: Theoretical Background and Strategy For The Present Workmentioning
“…This mechanism was also discussed for comparable maleimide dimerizations [43,66] as well as for dimerizations of dimethylmaleic anhydride [77].…”
Section: Photoinduced Dimerization Of Dmmi In Aqueous Solutionmentioning
confidence: 94%
“…In the present work, we employed the sodium salt of thioxanthone disulfonate. The sulfonate groups only act in terms of increasing the water solubility without affecting the spectral properties significantly [59,66].…”
Section: Theoretical Background and Strategy For The Present Workmentioning
“…On the other hand, when CBI and MDBZ which produce Lewis acids 18 upon UV irradiation were used as the catalysts, the reaction did not proceed at all. MDBZ contains a morpholino group that would be expected to interfere with cationic polymerization.…”
Section: Synthesis Of Phosphorus-containing 1-propenyl Ether Monomersmentioning
ABSTRACT:Polyfunctional 1-propenyl ether monomers (1a-c) were synthesized by the regioselective addition reaction of 1-propenyl glycidyl ether (PGE) with certain phosphonic dichlorides using quaternary onium salts as catalysts. The reaction of PGE with phenylphosphonic dichloride (PPDC) gave bis[1-(chloromethyl)-2-(propenyloxy)-ethyl]phenylphosphonate (1a) in 82% yield. Polycondensation of 1a with terephthalic acid (TPC) was also carried out using 1, 8-diazabicyclo[5.4.0]undecene-7 (DBU) as a base to afford the corresponding polymer containing 1-propenyl ether groups (2a). A multifunctional monomer (3a) containing both 1-propenyl ether groups as Vc and methacrylate groups as Vr was prepared by the reaction of 1a with methacrylic acid (MA) using DBU. Photoinitiated cationic polymerization of these 1-propenyl ether compounds proceeded rapidly using bis[4-(diphenylsulfonio)phenyl]sulfide bis(hexafluorophoshate) (DPSP), as a cationic photoinitiator without solvent upon UV irradiation.
“…It has been known for years [8,16] that (arene)(cyclopentadienyl)iron(II) complexes are strong UV absorbers with the spectra extending even to the visible range (i.e., typically more than 100 nm further towards longer wavelengths than iodonium salts). Therefore, photosensitization in a FP/iodonium salt system is plausible.…”
Section: Blends Of Ferrocenium and Iodonium Or Sulfonium Salts (Fp/iamentioning
confidence: 99%
“…It is known that a Brønsted acid is released during the photolysis of iodonium [6] and sulfonium [7] salts, whereas a Lewis acid is generated during the photolysis of ferrocenium salts [8]. Cationic polymerization of ECHC with five different types of photoinitiators capable of generating different acids was evaluated at various reaction temperatures using photo-DSC.…”
Abstract-Photoinitiated cationic polymerization is useful wherever the lack of oxygen inhibition, low shrinkage and formation of polymers with good adhesion properties are essential. Rates and conversions for cationic polymerizations of epoxycyclohexylmethyl-epoxycyclohexane carboxylate (ECHC) with various cationic photoinitiators and their blends were compared. Glass-transition temperatures of polymers were determined by dynamic mechanical analysis. When photopolymerizations of ECHC with initiator blends were compared with single-initiator systems, strong synergies leading to high polymerization rates and conversions were discovered for blends of diaryliodonium hexafluoroantimonate (IA) with tolylcumyliodonium tetrakis(pentafluorophenyl)borate (IB), and cumenecyclopentadienyliron(II) hexafluorophosphate with IA and IB. Mechanisms responsible for the discovered synergies are proposed.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.