区域选择性
分子内力
炔烃
多米诺骨牌
化学
配体(生物化学)
催化作用
组合化学
级联反应
纳米技术
材料科学
立体化学
有机化学
生物化学
受体
作者
Wenlong Yang,Radha Bam,Vincent J. Catalano,Wesley A. Chalifoux
标识
DOI:10.1002/ange.201808043
摘要
Abstract The properties of nanographenes can be tuned by changing their shapes, therefore the development of new methods suitable for the synthesis of various nanographenes is highly desirable. Described herein is an intramolecular InCl 3 /AgNTf 2 ‐catalyzed regioselective domino benzannulation reaction of buta‐1,3‐diynes to build irregular nanographenes. Different nanographene compounds were easily obtained in moderate to high yields through careful design of the precursor compounds. This new domino reaction was successfully applied to a fourfold alkyne benzannulation of dimethoxy‐1,1′‐binaphthalene derivatives to arrive at novel chiral butterfly ligand precursors. The regioselectivity of the benzannulation reaction was unambiguously confirmed by X‐ray crystallography. Moreover, this new method enables us to synthesize different nanographene isomers and study their optical properties as a function of shape.
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