4.7 Article

Structural, magnetic, and 1H NMR spectral study on lantern-type cis- and trans-diruthenium(II,III) complexes with two formamidinato and two acetato bridges

Journal

INORGANIC CHEMISTRY COMMUNICATIONS
Volume 33, Issue -, Pages 133-137

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.inoche.2013.04.001

Keywords

Diruthenium(II,III); Formamidinato and acetato bridges; Cis- and trans-(2:2) arrangements; Crystal structures; Magnetism; H-1 NMR

Funding

  1. Ministry of Education, Culture, Sports, Science and Technology [22550066, 22750052]
  2. MEXT-Supported Program for the Strategic Research Foundation at Private Universities
  3. Grants-in-Aid for Scientific Research [22750052, 22550066] Funding Source: KAKEN

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Lantern-type dinuclear complexes, cis-[Ru-2(4-Me-pf)(2)(O2CMe)(2)Cl] and trans-[Ru-2(2,6-Et-2-pf)(2)(O2CMe)(2)Cl] (4-Me-pf(-) = N,N'-bis(4-methylphenyl)formamidinate ion and 2,6-Et-2-pf(-) = N,N'-bis(2,6-diethylphenyl) formamidinate ion), were prepared and characterized. The dinuclear structures with cis- and trans-arrangements of the bridging ligands were confirmed by the X-ray crystal structures as well as H-1 NMR spectra (298 K) in CD2Cl2, where the proton signals were observed at widely spread positions delta = -80 to 25 ppm. Variable-temperature magnetic moments (2-300 K) showed the existence of three unpaired electrons in dinuclear units with large D values (65 cm(-1) for cis-Ru-2(II,III) and 90 cm(-1) for trans-Ru-2(II,III)). (c) 2013 Elsevier B.V. All rights reserved.

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