Publication | Open Access
A novel method for the synthesis of alkoxyamine initiators for nitroxide-mediated radical polymerization using Mn(OAc)3 as electron-transfer reagent
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Citations
14
References
2004
Year
Radical PolymerizationFavorable MnEngineeringAlkoxyamine InitiatorsOrganic ChemistryChemistryPolymersChemical EngineeringMacromolecular EngineeringPolymer ChemistryRadical (Chemistry)CatalysisSynthesis MethodPolymer SciencePolymerization KineticsNitroxide-mediated Radical PolymerizationPolymer ReactionSynthetic ChemistryPolymer SynthesisElectron-transfer ReagentAbstract O
Abstract O -substituted hydroxylamines which are known to initiate and promote nitroxide-mediated radical polymerization were synthesized in high yield by a novel and facile synthetic approach. Using the favorable Mn(OAc)3 as electron transfer agent in the in situ generation of benzylic radicals and their trapping by nitroxide radicals provides a new powerful and more economic way to the desired alkoxyamine initiators for this controlled, living radical polymerization. TEMPO, TIPNO and the protected tris-hydroxy derivative of TIPNO were used to synthesize the appropriate alkoxyamines. Keywords: NMRP INITIATORSMN(OAC) 3ALKOXYAMINESNITROXIDE RADICALS
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