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ChemInform Abstract: Conversion of Uncharged Methyl Complexes of Ruthenium(II) Into a Cationic Acyl Complex: a Mechanistic Study.

K. Michelle McCooey, E. Jane Probitts, Roger J. Mawby

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Abstract

Abstract Spectroscopic studies of the reactions of (I) with the isonitrile (II) reveal that the end‐product (V), isolated as its tetraphenylborate salt, is formed via the two isomers (III) and (IV), which can be isolated using certain conditions.

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What this paper is about

Abstract Spectroscopic studies of the reactions of (I) with the isonitrile (II) reveal that the end‐product (V), isolated as its tetraphenylborate salt, is formed via the two isomers (III) and (IV), which can be isolated using certain conditions.

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Available abstract

Abstract Spectroscopic studies of the reactions of (I) with the isonitrile (II) reveal that the end‐product (V), isolated as its tetraphenylborate salt, is formed via the two isomers (III) and (IV), which can be isolated using certain conditions.

Key concepts: Chemistry, Tetraphenylborate, Cationic polymerization, Ruthenium, Sodium tetraphenylborate, Salt (chemistry), Medicinal chemistry, Organic chemistry

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ChemInform Abstract: Conversion of Uncharged Methyl Complexes of Ruthenium(II) Into a Cationic Acyl Complex: a Mechanistic Study. — Research Paper | ScholarLens