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用于低催化剂负载量的外向二环戊二烯的前沿开环易位聚合反应

Frontal Ring-Opening Metathesis Polymerization of Exo-Dicyclopentadiene for Low Catalyst Loadings.

作者信息

Robertson Ian D, Pruitt Emmy L, Moore Jeffrey S

机构信息

Department of Chemistry and the ‡Beckman Institute for Advanced Science and Technology, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, United States.

Department of Chemistry and the Beckman Institute for Advanced Science and Technology, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, United States.

出版信息

ACS Macro Lett. 2016 May 17;5(5):593-596. doi: 10.1021/acsmacrolett.6b00227. Epub 2016 Apr 25.

Abstract

Polydicyclopentadiene (PDCPD) is a polymer of growing importance in industrial applications. Frontal ring-opening metathesis polymerization (FROMP) offers a means to rapidly cure PDCPD with minimal input energy owing to a propagating reaction wave sustained by the exothermic polymerization. Previous examples of FROMP have required the use of relatively high concentrations of costly ruthenium catalyst, negating many of the benefits of FROMP synthesis. In this contribution, we demonstrate that by using the highly reactive exo-dicyclopentadiene isomer for FROMP the concentration of catalyst is reduced over 3-fold, while maintaining a high frontal velocity. Reducing the amount of ruthenium required for FROMP makes this technique attractive for the production of large PDCPD structural components.

摘要

聚双环戊二烯(PDCPD)在工业应用中是一种日益重要的聚合物。由于放热聚合反应维持的传播反应波,前开环易位聚合(FROMP)提供了一种以最小输入能量快速固化PDCPD的方法。FROMP的先前例子需要使用相对高浓度的昂贵钌催化剂,这抵消了FROMP合成的许多优点。在本论文中,我们证明通过将高反应活性的外向双环戊二烯异构体用于FROMP,催化剂浓度降低了3倍以上,同时保持了较高的前沿速度。减少FROMP所需的钌量使得该技术对于大型PDCPD结构部件的生产具有吸引力。

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