Synthesis, spectroscopic, and structural characterization of new functionalized gem-bisphosphonate complexes of tin(IV) chloride
Abstract
Bisphosphonates of the types X(P(O)(OEt)2)2 (X = CH2=C (1a), CNCH2CH (1b) and PhCH2NCH2CH (1c)) react with SnCl4 in anhydrous dichloromethane to produce the new tin(IV) adducts [SnCl4(1a)] (2a), [SnCl4(1b)] (2b) and [SnCl4(1c)] (2c) in 72-80% yields. These complexes were characterized using IR, multinuclear (1H, 13C, 31P, 119Sn) NMR spectroscopy, elemental analysis, and in one case by single crystal X-ray diffraction. The NMR data show that the bisphosphonate ligands are coordinated to the tin center in a bidentate fashion forming cis octahedral tin complexes. Furthermore, the X-ray structure of complex 2b reveals that the bisphosphonate ligand is coordinated in a bidentate manner to the metal center in a distorted octahedral arrangement with Sn-O-P bond angles in the range 135.95(16)–137.99(18)°. The P=O and Sn-O bond lengths of 1.495(3)-1.497(3) and 2.134(3)-2.146(2) Å, respectively are in the order expected for phosphonate tin(IV) complexes. The results are discussed and compared with closely related analogues.
Citation
Yahyaoui , M , Sanhoury , M A , Carpenter-Warren , C L , Slawin , A M Z , Woollins , J D , Touil , S & Samarat , A 2018 , ' Synthesis, spectroscopic, and structural characterization of new functionalized gem -bisphosphonate complexes of tin(IV) chloride ' , Chemical Data Collections , vol. In press . https://doi.org/10.1016/j.cdc.2018.11.009
Publication
Chemical Data Collections
Status
Peer reviewed
Type
Journal article
Rights
© 2018 Published by Elsevier B.V. This work has been made available online in accordance with the publisher’s policies. This is the author created accepted version manuscript following peer review and as such may differ slightly from the final published version. The final published version of this work is available at https://doi.org/10.1016/j.cdc.2018.11.009
Description
The authors are grateful to the Tunisian Ministry of High Education and Scientific Research and Technology for financial support of this researchCollections
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