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A series of industrially relevant fluoroalkenes react with a monomeric AlI complex. These reactions break strong sp2 and sp3 C?F bonds, and result in the formation of a diverse array of organoaluminium compounds. Mechanistic studies show that two mechanisms are likely in operation: 1) direct oxidative addition of the C?F bond to AlI occurs with retention of alkene stereochemistry, and 2) stepwise formation and decomposition of a metallocyclopropane intermediate occurs with inversion of alkene stereochemistry. As part of this mechanistic analysis, we have isolated the first aluminium metallocyclopropane complex from oxidative addition of an alkene to AlI. Remarkably this reaction is reversible and reductive elimination of the alkene occurs at higher temperature reforming AlI. Furthermore, in selected cases the organoaluminium products are susceptible toward β‐fluoride elimination to yield a double C?F activation pathway.  相似文献   
2.
A simple, one-pot procedure is reported for the selective defluoroalkylation of trifluoromethyl alkene derivatives with aldehydes and ketones. The reaction sequence allows construction of a new C−C bond in a highly selective manner from a single sp3 C−F bond of a CF3 group in the presence of sp2 C−F bonds. The scope incorporates industrially relevant fluorocarbons including HFO-1234yf and HFO-1234ze. No catalyst, additives or transition metals are required, rather the methodology relies on a recently developed boron reagent. Remarkably, the boron site of this reagent plays a dual role in the reaction sequence, being nucleophilic at boron in the C−F cleavage step (SN2’) but electrophilic at boron en route to the carbon–carbon bond-forming step (SE2’). The duplicitous behaviour is underpinned by a hydrogen atom migration from boron to the carbon atom of a carbene ligand.  相似文献   
3.
氢氟烯烃(HFOs)是重要的精细化工中间体, 气相氟化合成HFOs具有可连续生产、 避免对反应釜的严重腐蚀等优点, 简化生产工艺已成为国内外生产氟化工产物的重要方法. 本文简要介绍了合成HFOs的常见催化反应类型以及反应机制, 并按照主催化剂成分分类概述气相氟化合成所用的催化剂, 介绍了各类催化剂的传统制备方法(如沉淀法等)和新的制备方法(如自组装法、 溶液燃烧合成法、 硬模板法、 静电纺丝法等), 以及催化性能, 提出了该催化剂的未来发展方向.  相似文献   
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