کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1327593 | 977490 | 2006 | 10 صفحه PDF | دانلود رایگان |
The 2-picolylcyclopentadienyl derivatives of rhodium(I) and iridium(I) of formula [M{η5-C5H4(2-CH2C5H4N)}(η4-C8H12)] (3) (M = Rh) and (4) (M = Ir) are obtained in good yields by reacting 2-picolylcyclopentadienyllithium (7) with [RhCl(η4-C8H12)]2 and [IrCl(η4-C8H12)]2, respectively. The corresponding dicarbonyl derivatives, [M{η5-C5H4(2-CH2C5H4N)}(CO)2] (5) (M = Rh) and 6 (M = Ir), are obtained in good yields by reacting 2-picolylcyclopentadienylthallium(I) (8) with [RhCl(CO)2]2 and [IrCl(C5H5N)(CO)2], respectively. 5 has already been reported in the literature. The new complexes were characterized by elemental analysis, mass spectrometry, 1H NMR, FT-IR, and UV–Vis (210–330 nm) spectroscopy. The UV–Vis spectra indicate the existence of some electronic interaction between the 2-picolinic chromophore and the cyclopentadienyl-metal moiety. The study of the electrochemical behaviour of 3–6 by cyclic voltammetry (CV) allows the interpretation of the electrode processes and gives information about the location of the redox sites. Moreover, various synthetic strategies were tested in order to try to coordinate the complexes 3–6 to a ruthenium(II) centre, but most of them failed. Instead, the hetero-bimetallic complex bis(2,2′-bipyridine)[(η5-2-picolylcyclopentadienyl)(η4-cycloocta-1,5-diene)rhodium(I)]chlororuthenium(II)-(hexafluorophosphate) (13), was obtained, although in poor yields (10%), by reacting the nitrosyl complex [RuCl(bipy)2(NO)][PF6]214 (bipy = 2,2′-bipyridine) first with potassium azide and then with the rhodium(I) complex 3. The analogous complex bis(2,2′-bipyridine)(2-picoline)chlororuthenium(II)-(hexafluorophosphate) (15), that carries a ruthenium-bonded 2-picoline molecule instead of 3, has prepared in the same way. 13 and 15 were characterized by elemental analysis, mass spectrometry, and 1H NMR.
Four 2-picolylcyclopentadienyl derivatives of rhodium(I) and iridium(I) were prepared (L2 = 1,5-COD; L = CO), and characterized by elemental analysis, MS, 1H NMR, UV–Vis spectroscopy, FT-IR, and cyclic voltammetry, and used for assembling hetero-bimetallic complexes.Figure optionsDownload as PowerPoint slide
Journal: Journal of Organometallic Chemistry - Volume 691, Issue 7, 15 March 2006, Pages 1425–1434