Abstract:The length of weak dative bonds in donor functionalized organo aluminum alkoxides [R 2 AlϪOϪR'ϪY] 2 (Y ϭ NR 2 , OR, SR) show a temperature dependence in the solid state that is distinctively different from the common effect of libration. This observation is interpreted as being caused by thermal excitation. The
The X-ray structure analysis of the alkylaluminum and -indium compounds derived from methyl thiosalicylate, Me 2 Al(SC 6 H 4 -2-CO 2 Me) and [Me 2 In(µ-SC 6 H 4 -2-CO 2 Me)] 2 , revealed that the intermolecular S···C(π) interaction between the Al-S thiolate units and the ester π-surface can effectively compete with the hypercoordinate sulfur-metal dative bond. The former compound exists as the noncovalently bonded
The structures of [(iPr 3 P) 2 Cu(μ-SSiMe 3 )(InMe 3 )] and [(iPr 3 P) 2 -Cu(μ-SeSiMe 3 )(InMe 3 )] were determined by single-crystal X-ray diffraction. Both complexes are Lewis acid-base adducts of the InMe 3 acceptor and the chalcogen donor atom linking a Me 3 Si group and a (iPr 3 P) 2 Cu moiety. They are very
[a]4727 unstable under atmospheric conditions and decompose at ambient temperatures. Results of DFT calculations for these complexes and the related hypothetical [(Me 3 P) 2 Cu(μ-SSi-Me 3 )(InMe 3 )] compound show that the unusual planar coordination of the chalcogen atoms is due to steric crowding.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.