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
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页数:16
相关论文
共 192 条
[1]   Reductive coupling of carbon monoxide by U(III) complexes-a computational study [J].
Aitken, Georgina ;
Hazari, Nilay ;
Frey, Alistair S. P. ;
Cloke, F. Geoffrey N. ;
Summerscales, O. ;
Green, Jennifer C. .
DALTON TRANSACTIONS, 2011, 40 (42) :11080-11088
[2]   Organoactinides promote the Tishchenko reaction: The myth of inactive actinide-alkoxo complexes [J].
Andrea, Tamer ;
Barnea, Eyal ;
Eisen, Moris S. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (08) :2454-2455
[3]   Synthesis and reactivity of a terminal uranium(IV) sulfide supported by siloxide ligands [J].
Andrez, Julie ;
Pecaut, Jacques ;
Scopelliti, Rosario ;
Kefalidis, Christos E. ;
Maron, Laurent ;
Rosenzweig, Michael W. ;
Meyer, Karsten ;
Mazzanti, Marinella .
CHEMICAL SCIENCE, 2016, 7 (09) :5846-5856
[4]   Electrocatalytic CO2 Conversion to Oxalate by a Copper Complex [J].
Angamuthu, Raja ;
Byers, Philip ;
Lutz, Martin ;
Spek, Anthony L. ;
Bouwman, Elisabeth .
SCIENCE, 2010, 327 (5963) :313-315
[5]  
Arnold P. L., 2016, 1487672 CCDC, DOI [10.5517/ccdc.csd.cc11y1f0, DOI 10.5517/CCDC.CSD.CC11Y1F0]
[6]   C3-symmetric lanthanide tris(alkoxide) complexes formed by preferential complexation and their stereoselective polymerization of rac-lactide [J].
Arnold, Polly L. ;
Buffet, Jean-Charles ;
Blaudeck, Robert P. ;
Sujecki, Slawomir ;
Blake, Alexander J. ;
Wilson, Claire .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2008, 47 (32) :6033-6036
[7]   Subtle Interactions and Electron Transfer between UIII, NpIII, or PuIII and Uranyl Mediated by the Oxo Group [J].
Arnold, Polly L. ;
Dutkiewicz, Michal S. ;
Zegke, Markus ;
Walter, Olaf ;
Apostolidis, Christos ;
Hollis, Emmalina ;
Pecharman, Anne-Frederique ;
Magnani, Nicola ;
Griveau, Jean-Christophe ;
Colineau, Eric ;
Caciuffo, Roberto ;
Zhang, Xiaobin ;
Schreckenbach, Georg ;
Love, Jason B. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2016, 55 (41) :12797-12801
[8]   Carbon monoxide and carbon dioxide insertion chemistry of f-block N-heterocyclic carbene complexes [J].
Arnold, Polly L. ;
Turner, Zoee R. ;
Germeroth, Anne I. ;
Casely, Ian J. ;
Nichol, Gary S. ;
Bellabarba, Ronan ;
Tooze, Robert P. .
DALTON TRANSACTIONS, 2013, 42 (05) :1333-1337
[9]   Uranium-mediated activation of small molecules [J].
Arnold, Polly L. .
CHEMICAL COMMUNICATIONS, 2011, 47 (32) :9005-9010
[10]   Carbon monoxide coupling and functionalisation at a simple uranium coordination complex [J].
Arnold, Polly L. ;
Turner, Zoe R. ;
Bellabarba, Ronan M. ;
Tooze, Robert P. .
CHEMICAL SCIENCE, 2011, 2 (01) :77-79