Synthesis, spectral (FT-IR, 1H, 13C) studies, and crystal structure of [(2,6-CO2)2C5H3NSnBu2(H2O)]2·CHCl3

Autor: Mamadou Sidibe, Florina Dumitru, Mouhamadou Birame Diop, Arie van der Lee, Cheikh Abdoul Khadir Diop, Mouhamadou Sembene Boye, Adrienne Ndiolene, Tidiane Diop
Rok vydání: 2021
Předmět:
Zdroj: Zeitschrift für Naturforschung B. 76:127-132
ISSN: 1865-7117
0932-0776
DOI: 10.1515/znb-2020-0195
Popis: Di-n-butyltin(IV) 2,6-pyridinedicarboxylate [(2,6-CO2)2C5H3NSnBu2(H2O)]2·CHCl3, has been synthesized and characterized by elemental analyses, infrared and NMR (1H and 13C) spectroscopy, and single-crystal X-ray diffraction. The title complex crystallizes in the triclinic space group P 1 ‾ $P‾{1}$ ; with a = 9.2330(4), b = 10.4790(5), c = 20.2489(8) Å, α = 89.439(4), β = 87.492(3), γ = 85.888(4)°, V = 1951.96(15) Å3, and Z = 2. In this complex, the 2,6-pyridinedicarboxylate groups are tetradentate, chelating, and bridging ligands for the tin(IV) atoms. NMR spectra showed that the ligands bind to the tin(IV) center in the anionic (COO−) form. In the asymmetric unit of the dimeric complex, the monomer is composed of an n-Bu2Sn unit bonded to one 2,6-pyridinedicarboxylate group through one nitrogen and two oxygen donor atoms. It is also coordinated by a water molecule. In the dimer formed by carboxylate bridging, a trans-heptacoordinated geometry around the tin(IV) atom is established. The chloroform molecule is connected to the dimer by C–H···O contacts. Compound exhibits extended O–H···O and C–H···O hydrogen bonding networks leading to a supramolecular layer topology.
Databáze: OpenAIRE
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