کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1326521 977435 2007 12 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Mono and dinuclear rhodium, iridium and ruthenium complexes containing chelating 2,2′-bipyrimidine ligands: Synthesis, molecular structure, electrochemistry and catalytic properties
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی معدنی
پیش نمایش صفحه اول مقاله
Mono and dinuclear rhodium, iridium and ruthenium complexes containing chelating 2,2′-bipyrimidine ligands: Synthesis, molecular structure, electrochemistry and catalytic properties
چکیده انگلیسی

The mononuclear cations [(η5-C5Me5)RhCl(bpym)]+ (1), [(η5-C5Me5)IrCl(bpym)]+ (2), [(η6-p-PriC6H4Me)RuCl(bpym)]+ (3) and [(η6-C6Me6)RuCl(bpym)]+ (4) as well as the dinuclear dications [{(η5-C5Me5)RhCl}2(bpym)]2+ (5), [{(η5-C5Me5)IrCl}2(bpym)]2+ (6), [{(η6-p-PriC6H4Me)RuCl}2(bpym)]2+ (7) and [{(η6-C6Me6)RuCl}2(bpym)]2+ (8) have been synthesised from 2,2′-bipyrimidine (bpym) and the corresponding chloro complexes [(η5-C5Me5)RhCl2]2, [(η5-C5Me5)IrCl2]2, [(η6-PriC6H4Me)RuCl2]2 and [(η6-C6Me6)RuCl2]2, respectively. The X-ray crystal structure analyses of [3][PF6], [5][PF6]2, [6][CF3SO3]2 and [7][PF6]2 reveal a typical piano-stool geometry around the metal centres; in the dinuclear complexes the chloro ligands attached to the two metal centres are found to be, with respect to each other, cis oriented for 5 and 6 but trans for 7. The electrochemical behaviour of 1–8 has been studied by voltammetric methods. In addition, the catalytic potential of 1–8 for transfer hydrogenation reactions in aqueous solution has been evaluated: All complexes catalyse the reaction of acetophenone with formic acid to give phenylethanol and carbon dioxide. For both the mononuclear and dinuclear series the best results were obtained (50 °C, pH 4) with rhodium complexes, giving turnover frequencies of 10.5 h−1 for 1 and 19 h−1 for 5.

A series of mono and dinuclear organometallic cations have been synthesised from 2,2′-bipyrimidine (bpym) and the corresponding chloro complexes [(η5-C5Me5)MCl2]2, (M = Rh, Ir), and [(η6-arene)RuCl2]2 (arene = PriC6H4Me, C6Me6). On the basis of a structural and electrochemical characterisation, the catalytic potential of these complexes for transfer hydrogenation reactions has been studied. All complexes catalyse the reaction of acetophenone with formic acid to give phenylethanol and carbon dioxide. The best results were obtained (50 °C, pH 4) for both the mono and dinuclear series with rhodium complexes, giving turnover frequencies of 10.5 h−1 and 19 h−1, respectively.Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Organometallic Chemistry - Volume 692, Issue 17, 1 August 2007, Pages 3664–3675
نویسندگان
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