Metal ions Organometallic chemistry Transition

Keywords. Electrospray ionization, Ion-molecule chemistry, Transition-metal coordination compounds, Organometallic catalysis... 

Soft metal ions are not restricted to complexation by heteroatom donors. Their electron-rich nature and large, uncontracted orbitals allow some very interesting complexation behaviour with n-aciA ligands at the boundary between supramolecular and organometallic chemistry. A large range of transition metals... 

Over the past several years, the area of gas-phase transition metal ion chemistry has been gaining increasing attention from the scientific community [1-16]. Its appeal is manifold first, it has broad implications to a spectrum of other areas such as atmospheric chemistry, corrosion chemistry, solution organometallic chemistry, and surface chemistry secondly, an arsenal of gas phase techniques are available to study the thermochemistry, kinetics, and mechanisms of these "unusual" species in the absence of such complications as solvent and ligand... 

Michael J. Clarke is the program director for inorganic, bioinorganic and organometallic, chemistry at NSF and holds a permanent position as a professor of chemistry at Boston College. His research focus is on how unusual transition metal ions interact with biological systems. He has... 

Applications of electrospray mass spectrometry (ESMS) to the study of reactions mediated by transition-metal complexes are reviewed. ESMS has become increasingly popular as an analytical tool in inorganic and organometallic chemistry, in particular with regard to the identification of short-lived intermediates of catalytic cycles. Going one step further, the coupling of electrospray ionization to ion-molecule techniques in the gas phase yields detailed information about single reaction steps of catalytic cycles. This method allows the study of transient intermediates that have previously not been within reach of condensed-phase techniques on both a qualitative and quantitative level. 

Some attempts which I had made in 1946 to obtain PtPh2 or [PtPhJ from the reaction of phenylmagnesium bromide with [ PtCl2(C2H4)2 2] in ether had yielded biphenyl as the only pure solid product, and this served to confirm in my mind the belief that transition metals had no normal organometallic chemistry. I decided then to concentrate on the platinum(II)-olefin complexes. The first question was whether the olefin-metal bond used the d electrons normally involved in the oxidation of platinum(II) to platinum(IV) (valence d electrons) to bind the olefin, as required by such structures as (I), or whether, as was then generally believed, they were olefin coordination compounds formed independently of the presence of d electrons, even by Main Group element ions. 

Chromium Organometallic Chemistry Coordination Organometallic Chemistry Principles Magnetism of Transition Metal Ions Metal Ion Toxicity Nutritional Aspects of Metals Trace Elements Oxidation Catalysis by Transition Metal Complexes. 

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