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具有增强太阳光谱匹配度的降冰片二烯-四环烷光开关

Norbornadiene-Quadricyclane Photoswitches with Enhanced Solar Spectrum Match.

作者信息

Aslam Adil S, Muhammad Lidiya M, Erbs Hillers-Bendtsen Andreas, Mikkelsen Kurt V, Moth-Poulsen Kasper

机构信息

Department of Chemistry and Chemical Engineering, Chalmers University of Technology, SE-41296, Gothenburg, Sweden.

Department of Chemistry, University of Copenhagen, Universitetsparken 5, 2100, Copenhagen, Denmark.

出版信息

Chemistry. 2024 Aug 19;30(46):e202401430. doi: 10.1002/chem.202401430. Epub 2024 Jul 26.

Abstract

Herein, we report monomeric and dimeric norbornadiene-quadricyclane molecular photoswitch systems intended for molecular solar thermal applications. A series of six new norbornadiene derivatives conjugated with benzothiadiazole as the acceptor unit and dithiafulvene as the donor unit were synthesized and fully characterized. The photoswitches were evaluated by experimentally and theoretically measuring optical absorption profiles and thermal conversion of quadricyclane to norbornadiene. Computational insight by density functional theory calculations at the M06-2X/def2-SVPD level of theory provided geometries, storage energies, UV-vis absorption spectra, and HOMO-LUMO levels that are used to describe the function of the molecular systems. The studied molecules exhibit absorption onset ranging from 416 nm to 595 nm due to a systemic change in their donor-acceptor character. This approach was advantageous due to the introduction of benzothiadiazole and the dimeric nature of molecular structures. The best-performing system has a half-life of 3 days with quantum yields over 50 %.

摘要

在此,我们报道了用于分子太阳能热应用的单体和二聚降冰片二烯-四环烷分子光开关系统。合成了一系列六种新的降冰片二烯衍生物,它们以苯并噻二唑作为受体单元,二硫富烯作为供体单元,并对其进行了全面表征。通过实验和理论测量四环烷向降冰片二烯的光吸收曲线和热转化,对光开关进行了评估。在M06-2X/def2-SVPD理论水平上通过密度泛函理论计算获得的计算见解提供了用于描述分子系统功能的几何结构、储能、紫外可见吸收光谱以及最高占据分子轨道-最低未占据分子轨道能级。由于供体-受体特性的系统性变化,所研究的分子表现出416 nm至595 nm的吸收起始波长范围。由于引入了苯并噻二唑以及分子结构的二聚性质,这种方法具有优势。性能最佳的系统半衰期为3天,量子产率超过50%。

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