6533b7cffe1ef96bd1259b56

RESEARCH PRODUCT

Reactivity of di-tert-butyldimethoxystannane with carbon dioxide and methanol: X-ray structure of the resulting complex

Stéphane ChambreyDanielle Ballivet-tkatchenkoLaurent PlasseraudRomain BurgatPhilippe Richard

subject

Steric effectsInorganic chemistry[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistryPhotochemistry01 natural sciencesBiochemistryStannaneCatalysisInorganic Chemistrychemistry.chemical_compounddimethyl carbonateMaterials ChemistryReactivity (chemistry)Physical and Theoretical ChemistryComputingMilieux_MISCELLANEOUSmethanolcatalysis010405 organic chemistryOrganic Chemistrycarbon dioxide[ CHIM.INOR ] Chemical Sciences/Inorganic chemistry0104 chemical sciencesCatalytic cyclechemistrystannanekineticstrinuclearCarbon dioxideMethanolDimethyl carbonateorganotin

description

Abstract The synthesis of dimethyl carbonate from carbon dioxide and methanol was studied with ditert-butyldimethoxystannane under pressure at temperatures ⩽423 K. The formation of dimethyl carbonate is accompanied by transformation of the stannane into a trinuclear complex, the structure of which has been determined by single-crystal X-ray diffraction technique. The relevance of this specie in the catalytic cycle is demonstrated by conducting recycling runs. A preliminary kinetic study underlines the steric influence of the tert-butyl ancillary ligands in the stabilisation of intermediates, by comparison with the n-butyl homologue.

10.1016/j.jorganchem.2005.11.013https://hal.archives-ouvertes.fr/hal-00469855