催化作用
表面改性
配体(生物化学)
联轴节(管道)
组合化学
化学
材料科学
有机化学
生物化学
受体
物理化学
冶金
作者
Nathaniel G. Larson,Jacob P. Norman,Sharon R. Neufeldt
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2024-04-23
卷期号:14 (9): 7127-7135
被引量:6
标识
DOI:10.1021/acscatal.4c00646
摘要
We describe a detailed investigation into why bulky ligands-those that enable catalysis at "12e -" Pd0-tend to promote overfunctionalization during Pd-catalyzed cross-couplings of dihalogenated substrates. After one cross-coupling event takes place, PdL initially remains coordinated to the π system of the nascent product. Selectivity for mono- vs. difunctionalization arises from the relative rates of π-decomplexation versus a second oxidative addition. Under the Suzuki coupling conditions in this work, direct dissociation of 12e - PdL from the π-complex cannot outcompete oxidative addition. Instead, Pd must be displaced from the π-complex as 14e - PdL(L') by a second incoming ligand L'. The incoming ligand is another molecule of dichloroarene if the reaction conditions do not include π-coordinating solvents or additives. More overfunctionalization tends to result when increased ligand or substrate sterics raises the energy of the bimolecular transition state for separating 14e - PdL(L') from the mono-cross-coupled product. This work has practical implications for optimizing selectivity in cross-couplings involving multiple halogens. For example, we demonstrate that small coordinating additives like DMSO can largely suppress overfunctionalization and that precatalyst structure can also impact selectivity.
科研通智能强力驱动
Strongly Powered by AbleSci AI