化学
互变异构体
吲哚试验
闪光灯(摄影)
异氰
立体化学
光化学
组合化学
艺术
视觉艺术
作者
Joseph A. Zurakowski,Lucie Taylor,Marcus W. Drover
出处
期刊:Organometallics
[American Chemical Society]
日期:2025-01-24
卷期号:44 (6): 713-715
标识
DOI:10.1021/acs.organomet.4c00505
摘要
Treatment of a tucked-in iron(II) diphosphine complex with 2,6-dimethylphenylisonitrile (CN–Xyl) results in cyclization to afford a pair of iron(II) indole tautomers. This reaction outcome contrasts with that of a structurally analogous acyclic iron(II)-methyl complex, which shows no reaction with CN–Xyl. The structure and onward reactivity of these Fe-bound N -heterocycles are assessed experimentally and computationally.
科研通智能强力驱动
Strongly Powered by AbleSci AI