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Oxalate complexes of the (n6-p-cymene)ruthenium(II) fragment: m-oxalato-k2O1,O2:k2O1,O2-bis[n6-p-cymene)(triphenylphosphine-P)ruthenium(II)] bis(tetrafluoroborate) and (6-p-cymene)(oxalato-2O,O')(pyridine-3,5-dicarboxylic acid-kN)ruthenium(II)
Lookup NU author(s)
Dr Sophie Dale
Dr Mark Elsegood
Author(s)
Dale, S, Elsegood, M
Publication type
Article
Journal
Acta Crystallographica C
Year
2006
Volume
62
Issue
4
Pages
m166-m170
ISSN (print)
0108-2701
ISSN (electronic)
1600-5759
Full text is available for this publication:
Full text file 1
The crystal structure of dimeric -oxalato-bis[(6-p-cymene)(triphenylphosphine)ruthenium(II)] bis(tetrafluoroborate), [Ru2(C2O4)(C10H14)2(C18H15P)2](BF4)2, has the cation lying on an inversion centre. The complex demonstrates the trans bond-weakening influence, with the longest Ru-C(6-p-cymene) bonds in the complex lying trans to the phosphine group. The related mononuclear species (6-p-cymene)(oxalato)(pyridine-3,5-dicarboxylic acid)ruthenium(II), [Ru(C2O4)(C10H14)(C7H5NO4)], crystallizes as hydrogen-bonded tapes linked through O-HO hydrogen bonds.
Publisher
International Union of Crystallography / Wiley-Blackwell Munksgaard
URL
http://dx.doi.org/10.1107/S0108270106007487
DOI
10.1107/S0108270106007487
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