کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1326468 977432 2009 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Mn(II) azamacrocyclic bromide complexes with different nuclearities
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی معدنی
پیش نمایش صفحه اول مقاله
Mn(II) azamacrocyclic bromide complexes with different nuclearities
چکیده انگلیسی

The coordination behaviour of a series of pyridyl azamacrocyclic ligands, some of them containing cyanomethyl and cyanoethyl pendant-arms, towards Mn(II) ion was studied. All the complexes were characterized by microanalysis, LSI mass spectrometry, IR, UV–Vis spectroscopy and magnetic measurements. Crystal structures of [MnL1][MnBr4] (1), [MnL3][MnBr4] · 2CH3CN (3), [Mn2L5Br4] · 2CH3CN (5) and [Mn2L6Br4] (6) complexes have been determined. The X-ray studies show the presence of an ionic mixed octahedral–tetrahedral complex for 1 and 2, with the manganese ion of the cation complex, endomacrocyclicly coordinated by the six nitrogen donor atoms from the macrocyclic backbone in a distorted octahedral geometry. Instead, the complexes 5 and 6 are dinuclear, and both manganese ions are coordinated by one pyridinic and two amine nitrogen atoms from the macrocyclic backbone and two bromide ions, being the geometry around the metal better described as distorted square pyramidal. In all cases, the nitrile pendant-arms do not show coordination to the metal ion.

The coordination behaviour of a series of pyridyl azamacrocyclic ligands, some of them containing cyanomethyl and cyanoethyl pendant-arms, towards Mn(II) ion was studied. All the complexes were characterized by microanalysis, LSI mass spectrometry, IR, UV–Vis spectroscopy and magnetic measurements. Crystal structures of [MnL1][MnBr4] (1), [MnL3][MnBr4] · 2CH3CN (3), [Mn2L5Br4] · 2CH3CN (5) and [Mn2L6Br4] (6) complexes have been determined. The X-ray studies show the presence of an ionic mixed octahedral–tetrahedral complex for 1 and 3, with the manganese ion of the cation complex, endomacrocyclicly coordinated by the six nitrogen donor atoms from the macrocyclic backbone in a distorted octahedral geometry. Instead, the complexes 5 and 6 are dinuclear, and both manganese ions are coordinated by one pyridinic and two amine nitrogen atoms from the macrocyclic backbone and two bromide ions, being the geometry around the metal better described as distorted square pyramidal. In all cases, the nitrile pendant-arms do not show coordination to the metal ion.Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Organometallic Chemistry - Volume 694, Issue 14, 15 June 2009, Pages 2185–2190
نویسندگان
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