Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/82990
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Type: Journal article
Title: Syntheses and structural studies of several group 8 metal complexes derived from 1,3-butadiyne
Author: Bruce, M.
Cole, M.
Costuas, K.
Ellis, B.
Kramarczuk, K.
Lapinte, C.
Nicholson, B.
Perkins, G.
Skelton, B.
White, A.
Zaitseva, N.
Citation: Zeitschrift fur Anorganische und Allgemeine Chemie, 2013; 639(12-13):2216-2223
Publisher: Wiley-V C H Verlag GMBH
Issue Date: 2013
ISSN: 0044-2313
1521-3749
Statement of
Responsibility: 
Michael I. Bruce, Marcus L. Cole, Karine Costuas, Benjamin G. Ellis, Kathy A. Kramarczuk, Claude Lapinte, Brian K. Nicholson, Gary J. Perkins, Brian W. Skelton, Allan H. White and Natasha N. Zaitseva
Abstract: As part of an extensive investigation into the chemistry of complexes containing metal-ligand centers linked by chains of C(sp) atoms, the preparation, characterization, and single-crystal X-ray diffraction molecular structure determinations of four complexes {MLn}-C≡CC≡C-{M′L′m} [MLn = Ru(dppe)Cp*, M′L′m = Fe(dppp)Cp* (1), Ru(dppe)Cp* (2), MLn = M′L′m = Os(PPh3)2Cp (3)], and {Cp*(dppe)Ru}C≡CC≡C{trans-RuCl(dppe)2} (4), in which the alternating C(sp)–C(sp) bonds have values between 1.375 and 1.40 Å (single) and between 1.20 and 1.259 Å (triple), respectively, are described. In addition, a structure determination of Ru3(μ-H){μ3-C2C≡C[Ru(PPh3)2Cp]}(CO)9 (5) shows that the C2 fragment attached to the HRu3 cluster shows the expected lengthening [to 1.311(7) Å] and bending at the two carbon atoms [to 152.6(6) and 157.6(5)°] (resulting from back-bonding from the Ru3 cluster into the C≡C π* orbitals) compared with the essentially linear Ru–CC– moiety [C≡C 1.222(6) Å, angles at C of 178.0(5), 172.3(6)°],
Keywords: Diynyl; Structural analyses; Ruthenium; Osmium
Rights: © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
RMID: 0020134648
DOI: 10.1002/zaac.201300282
Appears in Collections:Chemistry and Physics publications

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