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Reactions of Diaminonaphthalenes with a Cage-Opened C60 Derivative
Asian Journal of Organic Chemistry ( IF 2.7 ) Pub Date : 2024-04-02 , DOI: 10.1002/ajoc.202300634
Guanglin Huang 1 , Shumpei Sadai 1 , Yoshifumi Hashikawa 1 , Yasujiro Murata 2
Affiliation  

Cage-opened C60 derivatives with pyrazine and pyrimidine-fused naphthalene rings were synthesized by reactions with 1,2- and 1,8-diaminonaphthalenes, respectively. The perimidine-fused one provides a narrower HOMO–LUMO gap, achieving an intense NIR absorption tailing to ca. 850 nm.

中文翻译:

二氨基萘与开笼 C60 衍生物的反应

通过分别与1,2-和1,8-二氨基萘反应合成了具有吡嗪和嘧啶稠合萘环的开笼C 60衍生物。萘嵌间二氮杂苯融合提供了更窄的 HOMO-LUMO 能隙,实现了约 100% 的强烈近红外吸收拖尾。 850 纳米。
更新日期:2024-04-02
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