Organometallics · 2016 · 28 citations · 48 references
Natural SciencesChemistryComputational ChemistryInorganic ChemistryOrganic ChemistryAlkyne ComplexesCoordination ChemistryHeterocycle SynthesisHeterocyclic ChemistryMetal-ligand BondingTransition Metal ComplexesAlkyne Cycloaddition ReactionsBridged Alkyne Complexes
Described in this work are the preparation and characterization of an extensive family of Co III (cyclam)-oligoynyl compounds (cyclam = 1,4,8,11-tetraazacyclotetradecane) and elucidation of their electronic structures through DFT calculations. Monomeric Co compounds bearing one oligoynyl, namely, [Co(cyclam)(C 2 n R)Cl] + with n = 1–3, and two butadiynyls [Co(cyclam)(C 4 H) 2 ] + were prepared from the reactions between [Co(cyclam)Cl 2 ]Cl, Et 3 N or Et 2 NH, and the corresponding alkynes. The oligoyndiyl-bridged (μ - C 2 m ) dimers of Co III (cyclam)Cl with m = 2 and 3 were prepared via the same process by varying alkyne stoichiometry, while those with m = 4 and 6 were prepared using the Glaser coupling reaction. The complexes were prepared in moderate yield (with the exception of m = 6) under mild conditions without requiring an anaerobic or anhydrous environment and are generally stable toward ambient atmosphere. Voltammetric analysis of the dimeric complexes revealed a weak Co–Co interaction through the bridge, which is attenuated by the length of the oligoyne. The orbital origin of the Co–Co interaction is rationalized through DFT analysis.
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George M. Sheldrick · Acta Crystallographica Section A Foundations of Crystallography · 2007 · 87.4K citations · Full text