电泳剂
化学
催化作用
键离解能
配体(生物化学)
亲电加成
复分解
计算化学
轨道能级差
异构化
离解(化学)
组合化学
药物化学
有机化学
光化学
分子
生物化学
受体
聚合
聚合物
作者
José Luis García Martínez,Bartosz Trzaskowski
标识
DOI:10.1002/cphc.202200580
摘要
The dissociative mechanism of initiation for a series of Hoveyda-Grubbs type metathesis catalysts modified at the para and meta positions in the isopropoxybenzylidene ligand is investigated by means of DFT calculations. The electron donating/withdrawing capacity of the ligand was screened through the incorporation of various substituents such as halogens, nitro, alkoxides, ketones, esters, amines, and amides. Variations in structural parameters, energy barriers for the Ru-O bond dissociation, and Ru-O bond strength were examined as a function of the Hammett constant. It was found that electronic properties of the catalysts such as chemical potential, hardness, and electrophilicity correlate linearly with the dissociative energy barriers. These findings enable a systematic rationalization and prediction of rate of precatalyst initiation through the calculation of only the HOMO-LUMO gap of catalysts, as the faster the initiation, the more electrophilic the catalyst.
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