کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1308426 1499192 2013 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Bis(isothiocyanato)iron(II) complexes with bithiazole ligands: Structure and magnetic studies
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی معدنی
پیش نمایش صفحه اول مقاله
Bis(isothiocyanato)iron(II) complexes with bithiazole ligands: Structure and magnetic studies
چکیده انگلیسی

Two new mononuclear iron(II) complexes, [Fe(4bt)2(NCS)2] (1) and [Fe(dm4bt)2(NCS)2] (2), were prepared from the treatment of FeCl2·4H2O and KSCN salts with 4,4′-bithiazole (4bt) and 2,2′-dimethyl-4,4′-bithiazole (dm4bt), respectively and their structures and magnetisms were studied. Crystal structure determination revealed similar distorted octahedral [FeN6] moiety for both high spin iron(II) complexes. Fe–N distances are seen in 1 and 2 to be in the range of 2.085(8)–2.173(3) for Fe–NNCS and 2.178(3)–2.279(7) Å for Fe–Nbt which is consistent with the assigned iron spin and oxidation states. Temperature dependent χmT showed that the complexes are magnetically resembled and behave as S = 2 systems with some zero-field splitting. Complexes 1 and 2 were also studied in solution by means of 1H NMR and UV–Vis spectroscopy techniques.

This article is a detail study on isothiocyanato iron complexes with bithiazole ligands, 4bt = 4,4′-bithiazole and dm4bt = 2,2′-dimethyl-4,4′-bithiazole, with formula [Fe(N–N)2(NCS)2], (N–N = 4bt and dm4bt). Both complexes were fully characterized by means of IR, NMR, UV spectroscopy and single-crystal structure. Furthermore Magnetism study was performed and the correlations between structure and magnetism were discussed.Figure optionsDownload as PowerPoint slideHighlights
► Two new isothiocyanato iron(II) complexes were prepared.
► Their crystal structure was determined.
► Both complexes behave as S = 2 systems, magnetically.
► Correlation between structure and magnetic properties was discussed.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Inorganica Chimica Acta - Volume 395, 30 January 2013, Pages 58–66
نویسندگان
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