کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1339132 979694 2008 12 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Metal complexes derived from hydrazoneoxime ligands: IV. Molecular and supramolecular structures of some nickel(II) complexes derived from diacetylmonoxime S-benzyldithiocarbazonate
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی معدنی
پیش نمایش صفحه اول مقاله
Metal complexes derived from hydrazoneoxime ligands: IV. Molecular and supramolecular structures of some nickel(II) complexes derived from diacetylmonoxime S-benzyldithiocarbazonate
چکیده انگلیسی

Four new nickel(II) complexes, [{Ni(L)}2], [NiL · HPyr], [NiL · HIm] and [Ni(HL)2] · H2O, derived from diacetylmonoxime-S-benzyldithiocarbazonate (H2L) have been synthesized and characterized by elemental analyses, field desorption and electrospray ionization mass spectra, UV–Vis, infrared absorption spectra, as well as 1H NMR spectra. X-ray molecular structures showed that the Ni(II) in both [NiL · HPyr] and [NiL · HIm] are in a distorted square planar environment and is coordinated to the dianionic NNS tridentate hydrazoneoxime ligand via deprotonated oximate nitrogen, hydrazone imine nitrogen, and thiolate sulphur. The fourth coordination sites are occupied, respectively, by the pyrazole and imidazole nitrogens. The oximate O1 of [NiL · HPyr] is involved in intramolecular hydrogen bond with the pyrazole NH proton as well as intermolecular hydrogen bond pyrazole C6H proton, forming a helical chain propagating along the b-axis. The structure is stabilized by a set of π⋯π and CH⋯π interactions. The molecular units in [NiL · HIm] are linked together by hydrogen bond formation between the oximate oxygen and imidazole NH proton, giving rise to an infinite zigzag chain extended along the a-axis. The chains are interconnected by π⋯π and CH⋯O interactions. In [Ni(HL)2] · H2O, the Ni(II) is in a distorted octahedral environment. The two mononegative hydrazoneoxime ligands are coordinated in the meridional configuration where the two thiol sulphur atoms and the two oxime nitrogen atoms are cis to each other, while the imine nitrogen atoms are trans. The oxime proton O2H is involved in a reciprocal bifurcated hydrogen bond formation with both N2 and S3 of the adjacent molecule giving rise to hydrogen bonded dimer. This dimeric structure is further stabilized by a pair of reciprocal CH⋯O interactions. A one dimensional chain of alternating dimeric unit and water molecule propagating along the c-axis is formed via hydrogen bond formation between the oxime O1 oxygen and the bridged water molecule proton.

Four new nickel(II) complexes, [{Ni(L)}2], [NiL · HPyr], [NiL · HIm] and [Ni(HL)2] · H2O, derived from diacetylmonoxime-S-benzyldithiocarbazonate (H2L) have been synthesized and characterized. The molecular and supramolecular structures of [NiL · HPyr], [NiL · HIm] and [Ni(HL)2] · H2O, were determined by single crystal x-ray analysis.Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Polyhedron - Volume 27, Issue 15, 17 October 2008, Pages 3215–3226
نویسندگان
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