共 192 条
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
相关论文