2016
Schiff pentadentate ligands based on an [ON2O2] core displaying structural isomerism and their coordination to dibutyltin moieties. Jovana Pérez-Pérez, José G. Alvarado-Rodríguez*, Noemí Andrade-López, Julián Cruz Borbolla, Diego Martínez-Otero, José Manuel Vásquez-Pérez. Inorg. Chem. Commun. 70 (2016) 75-78. http://dx.doi.org/10.1016/j.inoche.2016.05.015
Abstract
Two tin compounds [Sn(nBu)2(Ln)], where L1double bond; length as m-dash{O(C6H4-2-Ndouble bond; length as m-dashC(H)C6H4-2?-O)2}2 ? and L2double bond; length as m-dash{O(C6H4-2-C(H)double bond; length as m-dashNC6H4-2?-O)2}2 ? enclosing five electron donors in an [ON2O2] core, were synthesized and structurally characterized by infrared and NMR spectroscopy and by single crystal X-ray crystallographic studies at room temperature. The hepta-coordinate geometry around the Sn centers is achieved through the bonding of two monodentate n-butyl groups and the coordination of the pentadentate Ln ligands, where the [ON2O2] core is forming a pentagonal base. The two types of oxygen atoms displayed different bonding situations around the Sn atom. DFT calculations with Gaussian 09 using PBEPBE/6-31G**/SDD level were carried out for both compounds. The topological analysis indicated that bond critical points are present along the Snsingle bondOether direction.
Mild Oxidation of C?C Bonds of Benzoiridacycles
Structural Studies by NMR and X-Ray Crystallography of N-(p-Toluenesulfonyl)-Amino Acids
Study on the intramolecular transannular chalcogentin interactions in dithiastannecine compounds.