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化学燃料驱动的自主溶胶-凝胶-溶胶-凝胶-溶胶转变。

Chemically Fueled Autonomous Sol→Gel→Sol→Gel→Sol Transitions.

机构信息

Université de Strasbourg, CNRS, UMR7140, 4 Rue Blaise Pascal, 67081, Strasbourg, France.

Institute of Advanced Materials (INAM) and Departament de Química Inorgànica i Orgànica, Universitat Jaume I, Avda Sos Baynat s/n, 12006, Castelló, Spain.

出版信息

Angew Chem Int Ed Engl. 2023 Jun 5;62(23):e202301529. doi: 10.1002/anie.202301529. Epub 2023 Apr 26.

Abstract

Complex non-equilibrium phase behaviors are a hallmark of natural self-assembling systems. Here we show how intricate phase transitions can be achieved through a chemically fueled reaction cycle to yield autonomous sol→gel→sol→gel→sol transitions. A relay of chemical transformations based on thiazinane metathesis leads to two consecutive transient gelations in a closed system. Within seconds of fuel addition to deactivated thiazinane monomers, an imine-based hydrogel forms that consists of fibrillar microspheres. This gel quickly loses its mechanical strength and forms a solution, from which a second aldehyde-based gel nucleates and remains stable for over one day. Overall, our reaction cycle gives rise to two consecutive re-entrant phase transitions without any experimental intervention.

摘要

复杂的非平衡相行为是自然自组装系统的标志。在这里,我们展示了如何通过化学燃料反应循环来实现复杂的相转变,从而产生自主的溶胶-凝胶-溶胶-凝胶-溶胶转变。基于噻嗪烷复分解的化学转化接力导致在封闭系统中发生两次连续的瞬态凝胶化。在向失活的噻嗪烷单体中添加燃料后的几秒钟内,形成基于亚胺的水凝胶,其由纤维状微球组成。该凝胶很快失去机械强度并形成溶液,其中第二个醛基凝胶成核并稳定超过一天。总的来说,我们的反应循环无需任何实验干预即可引发两个连续的重入相变。

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