Pushing a bistable [2]rotaxane out of equilibrium and isolation of the metastable-state co-conformation.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-10-29 DOI:10.1039/d4ob01419g
Mathias S Neumann, Sofie K Jensen, Rikke Frederiksen, Sissel S Andersen, Kasper M Beck, Jan O Jeppesen
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引用次数: 0

Abstract

Incorporating a steric barrier between the two stations in a bistable [2]rotaxane based on monopyrrolotetrathiafulvalene and cyclobis(paraquat-p-phenylene) allows the high-energy metastable-state co-conformation to be physically isolated following a single redox cycle, thus making it possible to store energy (4.4 J L-1) and to follow its interconversion back to the ground-state co-conformation.

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将双稳态 [2]rotaxane 推离平衡状态并分离出蜕变态共构象。
在基于单吡咯四硫杂戊烯和环双(百草枯-对苯二酚)的双稳态[2]轮烷中,在两个位点之间加入一个立体屏障,可使高能量的蜕变态共构象在单次氧化还原循环后被物理隔离,从而有可能储存能量(4.4 J L-1),并跟踪其相互转换回到基态共构象。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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