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双动力学门控信息棘轮自主驱动的碳二亚胺水合作用。

A Doubly Kinetically-Gated Information Ratchet Autonomously Driven by Carbodiimide Hydration.

机构信息

Department of Chemistry, University of Manchester, Oxford Road, Manchester M13 9PL, United Kingdom.

出版信息

J Am Chem Soc. 2021 Mar 24;143(11):4414-4420. doi: 10.1021/jacs.1c01172. Epub 2021 Mar 11.

Abstract

We report a rotaxane-based information ratchet in which the macrocycle distribution is pumped away from equilibrium using a carbodiimide fuel. A carboxylate group on the axle, nonequidistant between two macrocycle binding sites, efficiently catalyzes the hydration of a carbodiimide fuel to the corresponding urea waste, with >80% of the fuel molecules reacting through the machine-catalyzed pathway. The energy of the reaction is harnessed by kinetic differentiation of the mechanical states of the machine driving the macrocycle to the binding site distal to the catalyst. Steric hindrance between the macrocycle and the fuel slows the reaction of the carboxylate group (to form a barrier to macrocycle movement) in the proximal co-conformer, whereas hydrogen bonding between the macrocycle and the barrier accelerates hydrolysis of the activated ester proximal isomer. The two directionally biased processes reinforce each other's effect, resulting in a doubly kinetically gated ratchet that achieves 1:18 directionality, an exceptional degree of selectivity for a synthetic chemically fueled molecular motor.

摘要

我们报告了一种基于轮烷的信息棘轮,其中大环的分布通过使用碳二亚胺燃料从平衡中泵出。轴上的羧酸酯基团在两个大环结合位点之间不等距,可有效地催化碳二亚胺燃料的水合反应生成相应的脲废物,超过 80%的燃料分子通过机器催化途径反应。反应的能量通过机器的机械状态的动力学差异来利用,该机器将大环驱动到远离催化剂的结合位点。大环和燃料之间的空间位阻会减缓(形成大环运动的障碍)近共构物中羧酸酯基团的反应,而大环和障碍之间的氢键会加速活化酯近同构物的水解。这两个具有方向性的过程相互加强彼此的效果,导致双动力学门控棘轮实现了 1:18 的方向性,这是合成化学燃料分子马达的非凡选择性。

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