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endo-Selective (3+2) cycloaddition polymerizations of nitrone monomers with olefins utilising high pressure conditions

机译:利用高压条件对内酯单体与烯烃进行内选(3 + 2)环加成聚合

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摘要

A high pressure mediated (3+2) cycloaddition polymerization strategy has been employed to afford linear poly(isoxazolidine) architectures. Under these high pressure conditions this cycloaddition process was found to afford primarily endoheterocycles which when translated to the polymerization should ultimately affect the tacticity and resultant properties of the polymer. The stereoselectivity occurred as a result of a lower volume of activation for the endo-transition state and the application of a 'type-I' regime (HOMODipole-LUMODipolarophile) cycloaddition process that features secondary orbital interactions within the extended molecular orbitals. A variety of linker segments were employed in an attempt to affect the physical properties of the polymeric cycloadducts such as T-g and solubility in order to tailor these materials for use in coating applications. (C) 2007 Elsevier Ltd. All rights reserved.
机译:高压介导的(3 + 2)环加成聚合策略已用于提供线性聚(异恶唑烷)结构。在这些高压条件下,发现该环加成过程主要提供内杂环,当其转化为聚合反应时,其最终将影响聚合物的立构规整度和所得性质。立体选择性的发生是由于对内过渡态的活化作用量降低和应用“ I型”(HOMODipole-LUMODipolarophile)环加成过程所致,该过程具有扩展分子轨道内的次级轨道相互作用。为了尝试影响聚合环加合物的物理性质,例如T-g和溶解度,采用了多种连接体链段,以使这些材料适合用于涂料应用。 (C)2007 Elsevier Ltd.保留所有权利。

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