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The Synthesis of [Sn10(Si(SiMe3)3)4]2- Using a Metastable Sn(I) Halide Solution Synthesized via a Co-condensation Technique
Published on: November 28, 2016
Tetra-chloridobis(dibenzyl sulfoxide-κO)tin(IV)
Thy Chun Keng1, Kong Mun Lo, Seik Weng Ng
1Department of Chemistry, University of Malaya, 50603 Kuala Lumpur, Malaysia.
This study details the crystal structure of a tin(IV) compound, [SnCl(4)(C(14)H(14)OS)(2)]. The tin atom exhibits a cis-SnCl(4)O(2) octahedral geometry with specific chlorine-sulfur interactions influencing bond lengths.
Area of Science:
- Inorganic Chemistry
- Crystallography
- Coordination Chemistry
Background:
- Tin(IV) compounds are versatile in coordination chemistry.
- Understanding the structural nuances of organotin complexes is crucial for their application.
- The specific ligand C(14)H(14)OS presents unique coordination possibilities.
Purpose of the Study:
- To elucidate the precise three-dimensional structure of the title compound, [SnCl(4)(C(14)H(14)OS)(2)].
- To investigate the coordination geometry around the central tin(IV) atom.
- To analyze the interactions between the tin-bound chlorine atoms and the sulfur atoms of the ligands.
Main Methods:
- Single-crystal X-ray diffraction was employed to determine the molecular structure.
- The crystal structure was solved and refined to high accuracy.
- Bond lengths, bond angles, and intermolecular interactions were analyzed.
Main Results:
- The tin(IV) atom is six-coordinate with a cis-SnCl(4)O(2) octahedral geometry.
- Two of the four chlorine atoms exhibit close proximity to adjacent sulfur atoms (Cl⋯S distances of 3.320(1) and 3.376(1) Å).
- The Sn-Cl bonds associated with these interacting chlorine atoms are significantly longer than the other two Sn-Cl bonds.
Conclusions:
- The crystal structure reveals a distinct coordination environment for the tin(IV) center.
- The observed chlorine-sulfur interactions play a role in modulating the Sn-Cl bond characteristics.
- This structural insight contributes to the understanding of bonding and reactivity in tin(IV) complexes.
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