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Arene complexes radical polymerization

Apart from titanocene initiators, iron arene complexes have also been applied for light-induced radical polymerization, namely of acrylates [202-204]. Iron arene complexes were originally developed for cationic polymerization because they release acid upon irradiation. However, light-induced reactions include the formation of alkyl radicals, which may be utilized for radical initiation. [Pg.181]

Applications of Crown Ethers.—Crown ethers have been found to form molecular complexes with bromine that can be used as reagents in bromination reactions, e.g. of alkenes. The crown-halogen interaction seems not to be encapsulation but rather to be the formation of a polymeric structure. The complexes of nitro-nium tetrafluoroborate (NO2BF4) with various crown ethers, for example the 1 1 complex with 18-crown-6, have been reported to be selective nitrating agents. A new rapid synthesis of alkylseleno- and alkyltelluro-arenes from arenediazon-ium tetrafluoroborates and dialkyl diselenides or ditellurides employs KOAc and 18-crown-6 as a phase-transfer catalyst a radical mechanism has been suggested. Fluorine-19 n.m.r. evidence has been presented to show that KF forms... [Pg.194]


See other pages where Arene complexes radical polymerization is mentioned: [Pg.462]    [Pg.344]    [Pg.182]    [Pg.193]    [Pg.1016]    [Pg.6]    [Pg.234]    [Pg.290]    [Pg.615]    [Pg.618]    [Pg.6]    [Pg.120]    [Pg.434]    [Pg.163]    [Pg.18]    [Pg.234]    [Pg.163]    [Pg.210]    [Pg.277]    [Pg.318]    [Pg.210]   
See also in sourсe #XX -- [ Pg.235 , Pg.236 , Pg.237 , Pg.238 , Pg.239 , Pg.240 , Pg.241 , Pg.242 ]




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