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布朗斯特酸催化的聚酯动态共价网络中的交换反应

Brønsted-Acid-Catalyzed Exchange in Polyester Dynamic Covalent Networks.

作者信息

Self Jeffrey L, Dolinski Neil D, Zayas Manuel S, Read de Alaniz Javier, Bates Christopher M

出版信息

ACS Macro Lett. 2018 Jul 17;7(7):817-821. doi: 10.1021/acsmacrolett.8b00370. Epub 2018 Jun 22.

Abstract

The effect of catalyst strength on polyester-alcohol dynamic covalent exchange was systematically studied using Brønsted acids and a low- poly(4-methylcaprolactone) vitrimer formulation. Relaxation times, activation energies, and Arrhenius prefactors are correlated with p. Strong protic acids induce facile network relaxation at 25 °C on the order of 10-10 s, significantly faster than Lewis acid alternatives that function only above 100 °C. Activation energies span 49-67 kJ/mol and increase as p decreases. The opposite trend is observed with the Arrhenius prefactor. We anticipate that the quantitative understanding of Brønsted acid effects disclosed herein will be of utility in future studies that exploit acid-catalyzed dynamic covalent bond exchange.

摘要

使用布朗斯特酸和低聚(4-甲基己内酯)玻璃态高聚物配方,系统研究了催化剂强度对聚酯-醇动态共价交换的影响。弛豫时间、活化能和阿累尼乌斯前因子与p相关。强质子酸在25℃时能诱导网络快速弛豫,弛豫时间约为10⁻¹⁰秒,比仅在100℃以上起作用的路易斯酸替代品快得多。活化能范围为49-67kJ/mol,并随着p的降低而增加。阿累尼乌斯前因子呈现相反的趋势。我们预计,本文所揭示的对布朗斯特酸效应的定量理解将有助于未来利用酸催化动态共价键交换的研究。

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