Abstract

Three hydroxamic acid ligands (HL 1 = acetohydroxamic acid; HL 2 = benzohydroxamic acid; HL 3 = N–phenylbenzohydroxamic acid), have been used to synthesize series of mono- or dialkyltin(IV) complexes, which include (i) the carboxyl acid hybrid five-coordinated dialkyltin complexes (C 4H 9) 2SnL 1L 4 ( 1), [(CH 3) 2SnL 2L 5]·0.5C 6H 6 ( 2), (HL 4 = acetic acid; HL 5 = benzoic acid); (ii) the six-coordinated mono- n-butyltin complexes (C 4H 9)SnL 1·Cl 2·H 2O ( 3), (C 4H 9)SnL 2·Cl 2·H 2O ( 4), [(C 4H 9)SnL 3·Cl 2·H 2O]·H 2O ( 5), [(C 4H 9Sn) 2(L 3) 2·Cl 2·(OCH 3) 2] ( 6); and (iii) the alkali metal-mingled seven-coordinated mono- n-butyltin complexes [(C 4H 9Sn) 3L 2Na] +·Cl −·(CH 3CH 2) 2O ( 7), [(C 4H 9Sn) 3L 2K] +·Cl −·CH 2Cl 2 ( 8). All complexes were characterized by elemental analyses, IR, 1H, 13C, 119Sn NMR and X-ray single crystal diffraction. In these complexes, hydroxamic acids present bidentate coordination modes with the carbonyl O atom and the hydroxyl O atom binding to tin center. In complexes 1– 6, each tin atom is coordinated by one hydroxamic acid ligand. However, in complexes 7 and 8, tin atom is surrounded by three hydroxamic acid ligands, and all hydroxyl O atoms of the ligands also bind to the alkali metal center (Na or K). This kind of organotin(IV) framework containing one alkali metal is found for the first time. Furthermore, the supramolecular structures of 1, 3, 4 and 6 have been found to consist of 1D linear molecular chains formed by intermolecular N–H···X or C–H···X (X = O, N or Cl) hydrogen bonds. For complex 2, an interesting macrocyclic tetramer has been built by the intermolecular N–H···O hydrogen bonds. Fascinatingly, two unique symmetric dimeric structures are recognized in complexes 7 and 8, which is individually bridged by intermolecular N–H···Cl and N–H···O hydrogen bonds. In addition, for 8, the dimeric cycles have been further connected into a 1D supramolecular chain.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.