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二氮杂环丁烷[2+2]光环加成反应中的大尺寸和长期光子能量存储

Large and long-term photon energy storage in diazetidines [2+2] photocycloaddition.

作者信息

Nguyen Han P Q, Mukherjee Anurag, Usuba Junichi, Wan Joshua, Han Grace G D

机构信息

Department of Chemistry, Brandeis University 415 South Street Waltham MA 02453 USA

出版信息

Chem Sci. 2024 Oct 22;15(45):18846-54. doi: 10.1039/d4sc05374e.

Abstract

We report a series of -functionalized phenylbenzoxazoles that offer remarkable energy storage, exceeding 300 J g, for the first time among intermolecular cycloaddition-based molecular solar thermal energy storage systems. The [2 + 2] photocycloaddition of phenylbenzoxazoles generates diazetidine cycloadducts that store energy for up to 23 years in the solid state and release energy upon triggered cycloreversion. The solid-state phase transition contributes to increasing overall energy storage densities, and the dearomative cycloaddition process is revealed to be critical for maximizing the intrinsic energy storage capacities. The solvent-assisted cycloreversion is also used to accelerate the energy release from the emerging molecular scaffold.

摘要

我们报道了一系列官能化的苯基苯并恶唑,在基于分子间环加成的分子太阳能热能存储系统中,首次实现了超过300 J/g的卓越储能性能。苯基苯并恶唑的[2 + 2]光环加成反应生成二氮杂环丁烷环加成产物,这些产物在固态下可储存能量长达23年,并在触发环反转时释放能量。固态相变有助于提高整体储能密度,且发现脱芳构化环加成过程对于最大化固有储能能力至关重要。溶剂辅助的环反转也被用于加速新兴分子支架的能量释放。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a818/11578219/ebc992899fe7/d4sc05374e-f1.jpg

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