Small Molecule Activation by Intermolecular Zr(IV)-Phosphine Frustrated Lewis Pairs

被引：71

作者：

Metters, Owen J. ^{[1
]}

Forrest, Sebastian J. K. ^{[1
]}

Sparkes, Hazel A. ^{[1
]}

Manners, Ian ^{[1
]}

Wass, Duncan F. ^{[1
]}

机构：

[1] Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England

来源：

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | 2016年 / 138卷 / 06期

基金：

英国工程与自然科学研究理事会;

关键词：

ZIRCONOCENE-PHOSPHINOARYLOXIDE COMPLEXES; CARBON-DIOXIDE; CATALYTIC DEHYDROGENATION; DIHYDROGEN ACTIVATION; ADDUCT FORMATION; AMINE-BORANES; CHEMISTRY; P/B; HYDROGENATION; CLEAVAGE;

D O I：

10.1021/jacs.5b12536

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

We report intermolecular transition metal frustrated Lewis pairs (FLPs) based on zirconocene aryloxide and phosphine moieties that exhibit a broad range of small molecule activation chemistry that has previously been the preserve of only intramolecular pairs. Reactions with D-2, CO2, THF, and PhCCH are reported. By contrast with previous intramolecular examples, these systems allow facile access to a variety of steric and electronic characteristics at the Lewis acidic and Lewis basic components, with the three-step syntheses of 10 new intermolecular transition metal FLPs being reported. Systematic variation to the phosphine Lewis base is used to unravel steric considerations, with the surprising conclusion that phosphines with relatively small Tolman steric parameters not only give highly reactive FLPs but are often seen to have the highest selectivity for the desired product. DOSY NMR spectroscopic studies on these systems reveal for the first time the nature of the Lewis acid/Lewis base interactions in transition metal FLPs of this type.

引用

页码：1994 / 2003

页数：10

共 54 条

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