Free Radical Telomerization 1974
DOI: 10.1016/b978-0-12-663650-5.50006-7
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Reactivity in Free Radical Telomerization

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Cited by 13 publications
(12 citation statements)
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“…Thus, telomerization of Tris(hydroxymethyl)acrylamidomethane in a presence of this hydrophobic thiol molecule as telogen was performed in a THF/methanol mixture at 65°C under an argon atmosphere, using a,a 0 -azobis isobutyronitrile (AIBN) as radical initiator. The AIBN concentration in the reaction mixture was roughly ten times lower than the thiol molecule (called telogen) [17].…”
Section: Detergent Synthesismentioning
confidence: 96%
“…Thus, telomerization of Tris(hydroxymethyl)acrylamidomethane in a presence of this hydrophobic thiol molecule as telogen was performed in a THF/methanol mixture at 65°C under an argon atmosphere, using a,a 0 -azobis isobutyronitrile (AIBN) as radical initiator. The AIBN concentration in the reaction mixture was roughly ten times lower than the thiol molecule (called telogen) [17].…”
Section: Detergent Synthesismentioning
confidence: 96%
“…This coupling is not possible at present for NMR, but is common practice for mass spectrometry. For just this reason we were prompted to explore the use of mass spectrometry coupled with high resolution gas chromatography (GC-MS) in the analysis of an oligomeric mixture for the study of some aspects of the polymerization mechanism Our method of investigation is not completely new: the use of quenchers for studying the structure and fate of primary radicals is reported in the literature (4), as is the study of product distribution in oligomerization (5,6). We took advantage of very efficient separation methods (capillary GC columns) and directed our research to the study of the chain transfer reaction and to the presence of chain-end effects.…”
Section: Dipartimentomentioning
confidence: 99%
“…The birth and development of radical polymerization dates back to the first half of this century and was due to the efforts of a great number of scientists who proposed a consistent explanation for most of the experimental facts known at that Our method of investigation is not completely new: the use of quenchers for studying the structure and fate of primary radicals is reported in the literature (4), as is the study of product distribution in oligomerization (5,6). We took advantage of very efficient separation methods (capillary GC columns) and directed our research to the study of the chain transfer reaction and to the presence of chain-end effects.…”
mentioning
confidence: 99%
“…Tri-and tetrahaloalkanes were extensively studied as telogens in redox telomerization [22][23][24]52 (very few examples of dichlorinated, 54 -56 monobrominated, 57,58 and monochlorinated 53 active telogens were reported). Among them, polychloroalkanes were the most frequently used.…”
Section: Introductionmentioning
confidence: 99%
“…Among them, and as an extension of redox telomerization of an alkene with a (poly)haloalkane, [22][23][24] leading to low molecular weight products-generally monoadducts-with a high selectivity, several authors [25][26][27][28][29][30][31][32][33][34][35][36][37][38][39][40][41][42][43] developed transition metal catalyzed systems to control radical polymerization of various monomers.…”
Section: Introductionmentioning
confidence: 99%