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压力诱导偶氮苯的拓扑聚合得到有序范德华杂纳米带。

Ordered Van der Waals Hetero-nanoribbon from Pressure-Induced Topochemical Polymerization of Azobenzene.

机构信息

Center for High Pressure Science and Technology Advanced Research, Beijing 100193, People's Republic of China.

College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, People's Republic of China.

出版信息

J Am Chem Soc. 2023 Mar 29;145(12):6845-6852. doi: 10.1021/jacs.2c13753. Epub 2023 Mar 16.

Abstract

Pressure-induced topochemical polymerization of molecular crystals with various stackings is a promising way to synthesize materials with different co-existing sub-structures. Here, by compressing the azobenzene crystal containing two kinds of intermolecular stacking, we synthesized an ordered van der Waals carbon nanoribbon (CNR) heterostructure in one step. Azobenzene polymerizes via a [4 + 2] hetero-Diels-Alder (HDA) reaction of phenylazo-phenyl in layer A and a -polymerization reaction of phenyl in layer B at 18 GPa, as evidenced by in situ Raman and IR spectroscopies, X-ray diffraction, as well as gas chromatography-mass spectrometry and the solid-state nuclear magnetic resonance of the recovered products. The theoretical calculation shows that the obtained CNR heterostructure has a type II (staggered) band gap alignment. Our work highlights a high-pressure strategy to synthesize bulk CNR heterostructures.

摘要

压力诱导的具有各种堆积方式的分子晶体的拓扑化学聚合是合成具有不同共存亚结构的材料的一种很有前途的方法。在这里,通过压缩含有两种分子堆积的偶氮苯晶体,我们一步合成了有序的范德华碳纳米带(CNR)异质结构。偶氮苯通过层 A 中苯基偶氮-苯基的 [4+2] 杂-狄尔斯-阿尔德(HDA)反应和层 B 中苯基的 -聚合反应在 18GPa 下聚合,这可以通过原位拉曼和红外光谱、X 射线衍射以及气相色谱-质谱和回收产物的固态核磁共振来证明。理论计算表明,所得到的 CNR 异质结构具有 II 型(交错)能带隙排列。我们的工作强调了一种合成块状 CNR 异质结构的高压策略。

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