Carbon oxygenate transformations by actinide compounds and catalysts

被引:95
作者
Arnold, Polly L. [1 ]
Turner, Zoe R. [2 ]
机构
[1] Univ Edinburgh, EaStCHEM Sch Chem, Kings Bldg, Edinburgh EH9 3FJ, Midlothian, Scotland
[2] Univ Oxford, Chem Res Lab, 12 Mansfield Rd, Oxford OX1 3TA, England
基金
英国工程与自然科学研究理事会;
关键词
RING-OPENING POLYMERIZATION; BOND DISRUPTION ENTHALPIES; F-ELEMENT THERMOCHEMISTRY; SMALL-MOLECULE ACTIVATION; MONOXIDE ACTIVATION; STRUCTURAL-CHARACTERIZATION; ELECTRON-TRANSFER; INSERTION CHEMISTRY; CO2; INSERTION; U-III;
D O I
10.1038/s41570-016-0002
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Carbon oxygenates represent an increasingly important class of feedstock in the development of a sustainable chemical economy. Their catalytic transformation into value-added chemicals is a crucial target, because it would reduce our ties to fossil fuels and non-renewable resources. In this Review, we discuss the unique reactivity offered by actinide metal complexes with respect to s-, p- and d-block metals resulting from the chemical properties particular to these metals. This reactivity is governed by large ionic radii, high coordination numbers, kinetic lability, the involvement of f orbitals in bonding, and single-electron redox processes or sigma-bond metathesis, which are distinct from the oxidative addition and reductive elimination pathways commonly seen for catalysts derived from d-block metals. We conclude with a discussion of the current progress in the use of these complexes towards catalytic transformations of oxygenated hydrocarbons.
引用
收藏
页数:16
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