期刊
CHEMICAL COMMUNICATIONS
卷 58, 期 37, 页码 5578-5581出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d2cc01137a
关键词
-
资金
- MCIN [PID2019-104778GB-I00, PID2020115100GB-I00, CEX2019-000919-M]
- Generalitat Valenciana [SEJI/2020/034, PROMETEO/2021/054]
- Fondazione CARIPLO [2019-2090]
- European Research Council [814804]
- Juan de la Cierva program [RYC2019-027940-I]
- Ramon y Cajal program [IJC2018-036514-I]
- Ministero dell'Istruzione, dell'Universitae della Ricerca
- ITQ
- European Research Council (ERC) [814804] Funding Source: European Research Council (ERC)
Allylic alcohol epoxidation and dehydrogenation reactivity exhibit distinct behavior when VO(acac)(2) is used in solution or anchored in a metal-organic framework (MOF). The chemical mechanism is dependent on the electronic profile of alkene substituents when the vanadyl complex is used in the homogeneous phase. However, the confinement effects of MOF channels enable control over the chemoselectivity towards the dehydrogenation product.
Allylic alcohol epoxidation and dehydrogenation reactivity is distinguished when VO(acac)(2) is used in solution or anchored in a metal-organic framework (MOF). The chemical mechanism depends on the electronic profile of alkene substituents when the vanadyl complex is used in the homogenous phase. However, confinement effects imparted by MOF channels allow gaining control of the chemoselectivity toward the dehydrogenation product.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据