Gas-Phase Reactivity of Ruthenium Carbonyl Cluster Anions

被引:21
|
作者
Henderson, Matthew A. [1 ]
Kwok, Samantha [1 ]
McIndoe, J. Scott [1 ]
机构
[1] Univ Victoria, Dept Chem, Victoria, BC V8W 3V6, Canada
基金
加拿大创新基金会; 加拿大自然科学与工程研究理事会;
关键词
IONIZATION MASS-SPECTROMETRY; C-H ACTIVATION; DEPENDENT ELECTROSPRAY-IONIZATION; METAL-CLUSTERS; CATALYTIC-HYDROGENATION; HOMOGENEOUS CATALYSIS; SHIFT REACTION; ION CHEMISTRY; TELL US; MECHANISM;
D O I
10.1016/j.jasms.2008.12.006
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Partially-ligated anionic ruthenium carbonyl clusters react with alkenes, arenes, and alkanes in the gas phase; the products undergo extensive C-H activation and lose dihydrogen and carbon monoxide under collision-induced dissociation conditions. Triethylsilane and phenylsilane are also reactive towards the unsaturated clusters, and oxygen was shown to rapidly break down the cluster core by oxidative cleavage of the metal-metal bonds. These qualitative gas-phase reactivity studies were conducted using an easily-installed and inexpensive modification of a commercial electrospray ionization mass spectrometer. Interpretation of the large amounts of data generated in these studies is made relatively straightforward by employing energy-dependent electrospray ionization mass spectrometry (EDESI-MS). (J Am Soc Mass Spectrom 2009, 20, 658-666) (C) 2009 Published by Elsevier Inc. on behalf of American Society for Mass Spectrometry
引用
收藏
页码:658 / 666
页数:9
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