Supramolecular assemblies of organotin(iv)–diphosphoryl adducts: insights from X-rays and DFT. Issue 119 (20th November 2015)

• Record Type: Journal Article
• Authors: Gholivand, Khodayar; Gholami, Akram; Schenk, Kurt J.; Esrafili, Mehdi D.; Farshadfar, Kaveh
• Is Part Of: RSC advances. Volume 5:Issue 119(2015)
• Page Start: 98610
• Page End: 98617
• Publication Date: 2015-11-20
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c5ra15645a
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : The influence of tin-bonded substituents on the organization of the crystal structures and also coordination interactions were discussed using geometrical parameters, Hirshfeld analysis and theoretical calculations. Abstract : Mono-, di- and tri-phenyltin(iv ) adducts containing a neutral diphosphoryl ligand, Ph2 P(O)OC6 H4 OP(O)Ph2, were synthesized and characterized. These 2 : 1 adducts of two trans-organotin(iv ) moieties and the bridging ligand all crystallize around a centre of inversion. The influence of tin-substituents on the building up of multidimensional architectures, as well as, strength of the Sn–O interactions are discussed in terms of geometrical parameters, Hirshfeld surface analysis and theoretical calculations. The CH⋯Cl interactions make a substantial contribution to directing 1D self-assembly of the tin adducts. Replacement of Cl atoms with Ph groups on tin(iv ) in these complexes has increased the probability of CH⋯π and H⋯H interactions and weakens the Sn–O bonds. QTAIM and NBO analyses reveal that the Sn–O interactions are principally electrostatic in nature (donor–acceptor like) with only a small amount of covalence increasing from the tri- to the mono-phenyltin adduct.