π-Back-Bonding Interaction Depending on the Bridging Chain Lengths of Chelated N-Heterocyclic Carbene Platinum Units in Heterometallic Trinuclear Complexes Affecting Their Electrochemical Property

Author:

Maeda Yuri1,Hashimoto Hideki23,Kinoshita Isamu13,Nishioka Takanori1

Affiliation:

1. Department of Chemistry, Graduate School of Science, Osaka City University, Sumiyoshi-ku, Osaka 558-8585, Japan

2. Department of Physics, Graduate School of Science, Osaka City University, Sumiyoshi-ku, Osaka 558-8585, Japan

3. The OCU Advanced Research Institute for Natural Science and Technology (OCARINA), Osaka City University, Sumiyoshi-ku, Osaka 558-8585, Japan

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Physical and Theoretical Chemistry

Reference55 articles.

1. Atkins, P.; Overton, T.; Rourke, J.; Weller, M.; Armstrong, F.Shriver & Atkins Inorganic Chemistry,4thed.Oxford University Press:Oxford, U.K., 2006; pp557–558.

2. Cotton, F. A.; Wilkinson, G.; Murillo, C. A.; Bochmann, M.Advanced Inorganic Chemistry,6thed.John Wiley & Sons Inc.:New York, 1999; pp534–535.

3. Oxosulfido Complexes of Platinum — (Ph 3 P) 2 Pt(S 2 O) and (Ph 3 P) 4 Pt 2 (μ‐S)(μ‐SO) — Their Formation and Properties

4. Oxygen Atom Transfer Reactions from Dioxygen to Phosphines via a Bridging Sulfur Dioxide in a Trinuclear Cluster Complex of Rhenium, [(Ph3P)2N][Re3(μ3-S)(μ-S)2(μ-SO2)Cl6(PMe2Ph)3]

5. Rearrangement of Molybdocene Tetraoxotetrasulfide Cp2MoS4O4 to Give [(Cp2MoS2H)2](HSO4)2:  A Novel Proton-Stabilized Molybdocene Disulfide Dimer

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