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通过交替开环易位聚合制备的可降解聚缩醛/缩酮

Degradable Polyacetals/Ketals from Alternating Ring-Opening Metathesis Polymerization.

作者信息

Elling Benjamin R, Su Jessica K, Xia Yan

机构信息

Department of Chemistry, Stanford University, Stanford, California 94305, United States.

出版信息

ACS Macro Lett. 2020 Feb 18;9(2):180-184. doi: 10.1021/acsmacrolett.9b00936. Epub 2020 Jan 17.

Abstract

We report the synthesis of degradable polyacetals and polyketals with controlled molecular weights and low dispersities using alternating ring-opening metathesis polymerization (AROMP) of 1,1-disubstituted cyclopropenes and dioxepins. Under optimized conditions, high degrees of alternation and controlled polymerization were achieved between nonpropagating cyclopropenes and low-strain dioxepins. The high degrees of alternation allowed the resulting polymers to fully degrade into small molecules under acidic conditions at variable rates depending on the acetal/ketal structures. This synthetic strategy illustrates the use of AROMP to incorporate functionalities into both the polymer backbone as well as the side chains.

摘要

我们报道了使用1,1-二取代环丙烯和二氧六环的交替开环易位聚合(AROMP)合成具有可控分子量和低分散度的可降解聚缩醛和聚缩酮。在优化条件下,非增长性环丙烯和低应变二氧六环之间实现了高度的交替和可控聚合。高度的交替使得所得聚合物在酸性条件下能够根据缩醛/缩酮结构以不同速率完全降解为小分子。这种合成策略展示了利用AROMP将官能团引入聚合物主链和侧链的方法。

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