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Controllable branching degree for hyperbranched polymers: cocyclotrimerization of mono-and bifunctional terminal acctylenes

机译:超支化聚合物的可控制支化度:单官能和双官能末端丙烯的共环三聚

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摘要

A set of well-defined, completely soluble polyphenyl derivatives (Samples 1 approx 6 refer to cocyclotrimerization of 1, 8-nonadiyne with 1-octyne (1) or phenylacetylene (2 approx 6) with initial mol ratio of bifunctional to monofunctional moiety equals to 0.8, 1.0, 1.5, 2.0, and 3.0 respectively) has been synthesized with high yield via cocyclotrimerization technique using niobium chlride (V) as catalyst and characterized by IR, ~1H and ~(13)C NMR, DSC, UV, etc.
机译:一组定义明确,完全可溶的聚苯基衍生物(样品1约6表示1、8-壬二炔与1-辛炔(1)或苯乙炔(2约6)的共环三聚,双官能团与单官能团的初始摩尔比等于分别使用氯化铌(V)作为催化剂通过共环三聚技术高收率合成了0.8、1.0、1.5、2.0和3.0),并通过IR,〜1H和〜(13)C NMR,DSC,UV等进行了表征。

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