Freie Universität Berlin, Institut für Chemie und Biochemie, Fabeckstr. 34-36, 14195 Berlin, Germany.
Dalton Trans. 2010 Nov 7;39(41):9745-59. doi: 10.1039/c0dt00097c. Epub 2010 Aug 12.
The coordination chemistry of alkenes is among the fundamentals of organometallic chemistry. However, despite the beneficial effects of fluorination to organic molecules, their fluorinated counterparts are rarely found in transition-metal complexes and most examples are limited to simple monoalkenes like tetrafluoroethene. The paucity of fluorodiene complexes is contrasted by their structural diversity. Seemingly similar dienes containing conjugated, isolated or cumulated double bonds exhibit largely different ligand properties. While the most prominent group, the conjugated fluorodienes, is very flexible in hapticity, their analogues bearing isolated double bonds behave more like monoalkenes. Fluorinated cumulenes in contrast are thermally labile, their chemistry is dominated by the stabilising effect of metal coordination. This review outlines the synthesis, structure and reactivity of transition-metal complexes derived from fluorinated dienes.
烯烃的配位化学是有机金属化学的基础之一。然而,尽管氟化对有机分子有有益的影响,但它们的氟化对应物在过渡金属配合物中很少见,大多数例子仅限于简单的单烯烃,如四氟乙烯。氟二烯配合物的缺乏与它们的结构多样性形成对比。看似相似的二烯含有共轭、孤立或累积双键,表现出很大不同的配体性质。虽然最突出的共轭氟二烯在触感上非常灵活,但它们含有孤立双键的类似物的行为更像单烯烃。相比之下,氟化累积物在热上不稳定,其化学性质主要受金属配位的稳定作用支配。本综述概述了源自氟化二烯的过渡金属配合物的合成、结构和反应性。