化学
单重态
亲核细胞
镓
分子
配体(生物化学)
群(周期表)
主组元素
计算化学
光化学
有机化学
催化作用
过渡金属
激发态
原子物理学
生物化学
物理
受体
作者
Bijoy Ghosh,Ashwini K. Phukan
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2022-09-05
卷期号:61 (37): 14606-14615
被引量:6
标识
DOI:10.1021/acs.inorgchem.2c01630
摘要
Computational investigations provide evidence toward the remarkable ability of strongly electron-donating ylidic functionalities in stabilizing singlet group 13 carbenoids with promising ligand properties. All of the proposed carbenoids are found to be considerably nucleophilic and possess significant singlet-triplet energy separation values. The calculated activation barriers and reaction free energies obtained for the cleavage of different enthalpically strong bonds by these carbenoids are found to be either comparable to or lower than those of the experimentally evaluated aluminum and gallium carbenoids, thereby indicating their potential in small-molecule activation.
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