Gas-phase reactivity of ruthenium carbonyl cluster anions
Author(s) -
Matthew A. Henderson,
Samantha Kwok,
J. Scott McIndoe
Publication year - 2008
Publication title -
journal of the american society for mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.961
H-Index - 127
eISSN - 1879-1123
pISSN - 1044-0305
DOI - 10.1016/j.jasms.2008.12.006
Subject(s) - chemistry , ruthenium , mass spectrometry , electrospray ionization , reactivity (psychology) , phenylsilane , dissociation (chemistry) , metal carbonyl , carbon monoxide , cluster chemistry , photochemistry , cluster (spacecraft) , chemical ionization , metal , ionization , organic chemistry , catalysis , ion , chromatography , alternative medicine , pathology , medicine , computer science , programming language
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).
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