Activation of small molecules by U(III) cyclooctatetraene and pentalene complexes
被引:61
作者:
Summerscales, Owen T.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Sussex, Sch Life Sci, Dept Chem, Brighton BN1 9QG, E Sussex, EnglandUniv Sussex, Sch Life Sci, Dept Chem, Brighton BN1 9QG, E Sussex, England
Summerscales, Owen T.
[1
]
Cloke, F. Geoffrey N.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Sussex, Sch Life Sci, Dept Chem, Brighton BN1 9QG, E Sussex, EnglandUniv Sussex, Sch Life Sci, Dept Chem, Brighton BN1 9QG, E Sussex, England
Cloke, F. Geoffrey N.
[1
]
机构:
[1] Univ Sussex, Sch Life Sci, Dept Chem, Brighton BN1 9QG, E Sussex, England
来源:
ORGANOMETALLIC AND COORDINATION CHEMISTRY OF THE ACTINIDES
|
2008年
/
127卷
基金:
英国工程与自然科学研究理事会;
关键词:
activation;
cyclooctatetraene;
pentalene;
reduction chemistry;
small molecule;
uranium;
D O I:
10.1007/430_2007_078
中图分类号:
O61 [无机化学];
学科分类号:
070301 ;
081704 ;
摘要:
The low-valent complexes of uranium (i.e. those containing U(III) centres) are characterised as reactive, highly reducing species that can effect novel, and potentially useful, transformations of small molecules. In this chapter we review one particular class of these compounds - those supported by cyclooctatetraene and pentalene ligands - whose reduction chemistry has recently demonstrated novel and unexpected results, including the cyclooligomerisation of CO. The syntheses and structures of these compounds are presented, and their reactivity towards a variety of small molecules is examined and reviewed. The reactivity towards carbon monoxide is discussed in reference to the historical development of obtaining oxocarbons from CO.