Polymerizations of Monomers Involving Aromatization.

Various radical polymerizations of glycerol-based monomers

Various radical polymerizations of glycerol-based monomers -Review-

This review aims at making the state of the art of the radical polymerizations of glycerol-based monomers, especially (meth)acrylate and vinylic/allylic derivatives. Acrylate and methacrylate derivatives bearing numerous secondary groups like ester, cyclocarbonate, acetal and urethane were involved in free radical polymerization and radical controlled polymerizations as well as in the photopoly...

Ultra-precise insertion of functional monomers in chain-growth polymerizations

Chain-growth polymerizations are popular methods because they allow synthesis of highmolecular weight polymers in high yields and in short times. However, copolymers prepared by such processes generally exhibit uncontrolled monomer sequences. The controlled radical copolymerization of styrene with N-substituted maleimides is an interesting exception allowing preparation of controlled primary st...

Use of N‐methyliminodiacetic acid boronate esters in suzuki‐miyaura cross‐coupling polymerizations of triarylamine and fluorene monomers

Polytriarylamine copolymers can be prepared by Suzuki-Miyaura cross-coupling reactions of bis N-methyliminodiacetic acid (MIDA) boronate ester substituted arylamines with dibromo arenes. The roles of solvent composition, temperature, reaction time, and co-monomer structure were examined and (co)polymers prepared containing 9, 9-dioctylfluorene (F8), 4-sec-butyl or 4-octylphenyl diphenyl amine (...

Multiple Olefin Metathesis Polymerizations (MOMP)

Olefin metathesis polymerization, in particularly ring-opening metathesis polymerization (ROMP), has been a popular topic of modern research. Two other types are acyclic diene metathesis polymerization (ADMET) and cyclopolymerization of diynes. To date, there has been no report on a metathesis polymerization utilizing more than one metathesis process. Herein, the concept of multiple olefin meta...