Burke Laboratory, Department of Chemistry, Dartmouth College, Hanover, New Hampshire 03755, USA.
School of Chemistry, University of Birmingham, Birmingham B15 2TT, U.K.
J Am Chem Soc. 2023 Jul 5;145(26):14169-14183. doi: 10.1021/jacs.2c12665. Epub 2023 Jun 21.
All chemists are familiar with the idea that, at equilibrium steady state, the relative concentrations of species present in a system are predicted by the corresponding equilibrium constants, which are related to the free energy differences between the system components. There is also no net flux between species, no matter how complicated the reaction network. Achieving and harnessing non-equilibrium steady states, by coupling a reaction network to a second spontaneous chemical process, has been the subject of work in several disciplines, including the operation of molecular motors, the assembly of supramolecular materials, and strategies in enantioselective catalysis. We juxtapose these linked fields to highlight their common features and challenges as well as some common misconceptions that may be serving to stymie progress.
所有化学家都熟悉这样一种观点,即在平衡稳态下,系统中存在的物质的相对浓度可以通过相应的平衡常数来预测,而平衡常数与系统成分之间的自由能差有关。无论反应网络多么复杂,物质之间也没有净通量。通过将反应网络与第二个自发化学过程耦合来实现和利用非平衡稳态,一直是几个学科的研究课题,包括分子马达的操作、超分子材料的组装以及对映选择性催化中的策略。我们将这些相关领域并列,以突出它们的共同特征和挑战,以及一些可能阻碍进展的常见误解。