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(Isocyanide)ruthenate Analogues of Tetracarbonylferrate

Identifieur interne : 001497 ( Istex/Curation ); précédent : 001496; suivant : 001498

(Isocyanide)ruthenate Analogues of Tetracarbonylferrate

Auteurs : Joseph A. Corella Ii [États-Unis] ; Robert L. Thompson [États-Unis] ; N. John Cooper [États-Unis]

Source :

RBID : ISTEX:5B2A596A43FE94B5156514EA9F4BAA6B73D360BD

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Abstract

The potassium–naphthalene reduction of dichloro(tetraisocyanide)ruthenium complexes 1 affords the (tetraisocyanide)ruthenate dianions 2, which can be trapped with electrophiles and partially characterized by IR spectroscopy. Thus 2 reacts with Ph3SnCl by oxidative addition to give 3 (trans isomers). But 2 also reacts analogous to [Fe(CO)4]2−, with Si‐ and C‐electrophiles. R = tBu, 2,6‐Me2C6H3.

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DOI: 10.1002/anie.199200831

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ISTEX:5B2A596A43FE94B5156514EA9F4BAA6B73D360BD

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<div type="abstract">The potassium–naphthalene reduction of dichloro(tetraisocyanide)ruthenium complexes 1 affords the (tetraisocyanide)ruthenate dianions 2, which can be trapped with electrophiles and partially characterized by IR spectroscopy. Thus 2 reacts with Ph3SnCl by oxidative addition to give 3 (trans isomers). But 2 also reacts analogous to [Fe(CO)4]2−, with Si‐ and C‐electrophiles. R = tBu, 2,6‐Me2C6H3.</div>
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