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多倍Sonogashira偶联反应:一种获得具有可调光物理性质的四炔基蒽的新颖便捷方法。

Multi-fold Sonogashira coupling: a new and convenient approach to obtain tetraalkynyl anthracenes with tunable photophysical properties.

作者信息

Islam Khadimul, Narjinari Himani, Bisarya Akshara, Kumar Akshai

机构信息

Department of Chemistry, Indian Institute of Technology Guwahati, Guwahati - 781039, Assam, India.

Centre for Nanotechnology, Indian Institute of Technology Guwahati, Guwahati - 781039, Assam, India.

出版信息

Org Biomol Chem. 2021 Nov 18;19(44):9692-9704. doi: 10.1039/d1ob01861b.

Abstract

For the first time, a direct single-step one-pot route to access nine new symmetric tetraalkynylated anthracenes Pd(CHCN)Cl/cataCXium®A catalyzed tetra-fold Sonogashira coupling is reported. Five of these tetraalkynylated anthracenes have been crystallographically characterized, with two of them exhibiting multiple interactions that significantly shorten the inter-planar distances in the solid-state structure. The rich photophysical properties exhibited by these molecules hold immense promise for future applications in sensors and optoelectronic devices. Two of the considered tetraalkynylated anthracenes comprising a D-π-A-π-D motif demonstrate solvatochromism and halochromism, with one of them showing a low bandgap of 1.79 eV. The remaining compounds demonstrate bandgaps in the range of 1.79-2.04 eV.

摘要

首次报道了一种直接的单步一锅法合成九种新型对称四炔基化蒽的方法,该反应由Pd(CHCN)Cl/cataCXium®A催化进行四重Sonogashira偶联。其中五种四炔基化蒽已通过晶体学表征,其中两种表现出多种相互作用,显著缩短了固态结构中的平面间距。这些分子所展现出的丰富光物理性质在传感器和光电器件的未来应用中具有巨大潜力。所研究的两种包含D-π-A-π-D结构单元的四炔基化蒽表现出溶剂致变色和酸致变色,其中一种的带隙低至1.79 eV。其余化合物的带隙在1.79 - 2.04 eV范围内。

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