TY - GEN
T1 - Boroxyl-based radical initiators and polymerization
AU - Chung, T. C.
AU - Hong, H.
PY - 2003
Y1 - 2003
N2 - This paper discusses a new family of living free radical initiators, alkylperoxy-dialkylborane (C-O-O-BR2), which show living polymerization of acrylate and methacrylate monomers at ambient temperature. The C-O-O-BR2 species can be prepared by in situ selective mono-oxidation of an asymmetrical trialkylborane (-C-BR2) with a control amount of oxygen. Apparently, in the presence of polar monomers the C-O-O-BR2 engages spontaneously hemolytic cleavage to form active alkoxyl radical (C-O*) and "stable" boroxyl radical (*O-BR2), due to the delocalization of the free radical with the empty p-orbital of boron. The alkoxyl radical is active in initiating the polymerization of vinyl monomers. On the other hand, the stable borinate radical may form a reversible bond with the propagating radical site to prevent undesirable termination reactions. The living polymerization was characterized by predictable polymer molecular weight, narrow molecular weight distribution, and the formation of telechelic polymers and block copolymers by sequential monomer addition.
AB - This paper discusses a new family of living free radical initiators, alkylperoxy-dialkylborane (C-O-O-BR2), which show living polymerization of acrylate and methacrylate monomers at ambient temperature. The C-O-O-BR2 species can be prepared by in situ selective mono-oxidation of an asymmetrical trialkylborane (-C-BR2) with a control amount of oxygen. Apparently, in the presence of polar monomers the C-O-O-BR2 engages spontaneously hemolytic cleavage to form active alkoxyl radical (C-O*) and "stable" boroxyl radical (*O-BR2), due to the delocalization of the free radical with the empty p-orbital of boron. The alkoxyl radical is active in initiating the polymerization of vinyl monomers. On the other hand, the stable borinate radical may form a reversible bond with the propagating radical site to prevent undesirable termination reactions. The living polymerization was characterized by predictable polymer molecular weight, narrow molecular weight distribution, and the formation of telechelic polymers and block copolymers by sequential monomer addition.
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U2 - 10.1021/bk-2003-0854.ch034
DO - 10.1021/bk-2003-0854.ch034
M3 - Conference contribution
AN - SCOPUS:27744548482
SN - 9780841238541
T3 - ACS Symposium Series
SP - 481
EP - 495
BT - Advances in Controlled/Living Radical Polymerization
PB - American Chemical Society
ER -