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Preparation and Reactivity of Bimetallic (pincer)Ir Complexes
Organometallics ( IF 2.8 ) Pub Date : 2020-09-15 , DOI: 10.1021/acs.organomet.0c00403
Jonathan M. Goldberg 1 , Louise M. Guard 1 , Gene W. Wong 1 , Daniel F. Brayton 1 , Werner Kaminsky 1 , Karen I. Goldberg 1 , D. Michael Heinekey 1
Affiliation  

A new pincer ligand framework based on the commonly used “POCOP” (POCOP = κ3-C6H3-1,3-(OPR2)2, R = tBu, iPr) motif is reported, in which two POCOP units are tethered using an anthracene linker to support bimetallic complexes. Metalation using Ir precursors affords products dictated by steric factors. A comparison of the reactivity of RPOCOP-supported Ir(I) carbonyl monomeric and dimeric species with alkyl halides is explored. For R = tBu, the complexes are unreactive, but for R = iPr, both types of complexes react with alkyl halides to form Ir(III) products.

中文翻译:

双金属(pin)Ir配合物的制备和反应性

根据常用的“POCOP”(POCOP =κ阿新钳形配体框架3 -C 6 ħ 3 -1,3-(OPR 22,R =卜,PR)基序被报告,其中两个POCOP使用蒽接头将单元束缚以支持双金属配合物。使用Ir前驱物进行金属化可得到由空间因素决定的产物。探索了R POCOP负载的Ir(I)羰基单体和二聚体物种与烷基卤的反应性的比较。对于R = t Bu,络合物是不反应的,但是对于R = i Pr,两种类型的络合物都与卤代烷反应形成Ir(III)产物。
更新日期:2020-09-28
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