Abstraction of the pyS ligand from [Re2Ru2(μ4-S) (μ-C5H4N)(μ-pyS)(CO)13] by [Ru3(CO)12]. Crystal structure of [Re2Ru2(μ-H)(μ4-S)(μ-C5H4N)(CO)14]
Author:
Publisher
Elsevier BV
Subject
Materials Chemistry,Inorganic Chemistry,Physical and Theoretical Chemistry
Reference11 articles.
1. Synthesis and structures of two isomers of [Re3Ru(S)(C5H4N)(C5H4NS)2(CO)11] which differ in the distribution of pyridine-2-thionato ligands between doubly- and triply-bridging positions
2. Mixed tetranuclear rhenium–ruthenium compounds formed by carbon–sulphur bond cleavage in reactions of [Re2(pyS)2(CO)6](pyS = pyridine-2-thionate) with [Ru3(CO)12]. Crystal structures of [ReRu3(µ4-S)(µ-C5H4N)(CO)14] and [Re2Ru2(µ-S)(µ-C5H4N)(µ-pyS)(CO)13]
3. Suppression of cluster unsaturation by formation of extensive but long-range metal-metal bonding: crystal structures of [Ru3H(pyS)(CO)9] and [{Ru3H(pyS)(CO)7}3], where pyS is the pyridine-2-thiolato ligand
4. Penta- and hexa-nuclear ruthenium µ-2-pyridyl complexes
5. Redetermination of the crystal structure of dimanganese decacarbonyl and determination of the crystal structure of dirhenium decacarbonyl. Revised values for the manganese-manganese and rhenium-rhenium bond lengths in dimanganese decacarbonyl and dirhenium decacarbonyl
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