کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1321352 1499891 2014 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Hypoelectronic metallaboranes: Synthesis, structural characterization and electronic structures of metal-rich cobaltaboranes
ترجمه فارسی عنوان
متالورژی های هیپوالکترونیک: سنتز، مشخصات ساختاری و ساختارهای الکترونیکی کبالتبالان غنی از فلز
کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی معدنی
چکیده انگلیسی


• 6, 9, 11 and 12-vertex di-, tri-cobaltaborane clusters have been isolated.
• Structure of [(Cp*Co)2B7H6OMe] can be derived by DSD from a ttp core.
• The reactivity of [(Cp*Co)2B4H6] has been explored with Fe2(CO)9.

Reaction of [Cp∗CoCl]2 (Cp∗ = η5-C5Me5) with [LiBH4·THF] in toluene at −70 °C, followed by thermolysis with 2-mercaptobenzothiazole (C7H5NS2) in boiling toluene led to the isolation of a range of cobaltaborane clusters, [(Cp∗Co)2B7H6OMe], 1; [(Cp∗Co)3B8H7R], 2a, b (2a: R = H; 2b: R = Me); [(Cp∗Co)3B8H8S], 3 and [(Cp∗Co)2B4H4RR′], 4a–d (4a: R, R′ = H; 4b: R = Me, R′ = H; 4c: R = H, R′ = Me and 4d: R, R′ = Me). In parallel to the formation of compounds 1–4, the reaction also yielded known [(Cp∗Co)3B4H4] in good yield. Compound 1 may be considered as 9-vertex hypoelectronic cluster with C1 symmetry, where cobalt atoms occupy the degree 5 vertices. All the dicobaltaboranes 4a–d contains two μ3-H protons and found to be very reactive. As a result, one of them (4a) when reacted with Fe2(CO)9 and sulfur powder yielded, almost immediately, [(Cp∗Co)2B4H5SFe3(CO)9], 5 and [(Cp∗Co)2B3H3(μ-CO)Fe(CO)3], 6. All the new compounds have been characterized in solution by mass, 1H, 11B, 13C NMR spectroscopy and elemental analysis. The structural types were unequivocally established by X-ray crystallographic analysis of compounds 1–6. Density functional theory (DFT) calculations on the model compounds 1′ and 2′ (1′, and 2′ are the Cp analog of 1, and 2a respectively, Cp = C5H5) yield geometries in agreement with the structure determinations. The existence of large HOMO–LUMO gap of these molecules rationalizes the isocloso description for 2a. Bonding patterns in the structure have been analyzed on the grounds of DFT calculations.

Reaction of [Cp*CoCl]2, (Cp* = η5-C5Me5), with [LiBH4·thf] in toluene at −70 °C, followed by mild thermolysis with 2-mercaptobenzothiazole in boiling toluene yielded hypoelectronic metal rich cobaltaboranes, [(Cp*Co)2B7H6OMe], [(Cp*Co)3B8H7R] and closo-[(Cp*Co)3B8H8S]. Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Organometallic Chemistry - Volume 749, 1 January 2014, Pages 188–196
نویسندگان
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