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Combining Solid-state and Solution-based Techniques: Synthesis and Reactivity of ChalcogenidoplumbatesII or IV
Published on: December 29, 2016
An unusual Pd(III) oxidation state in the Pd-Cl chain complex with high thermal stability and electrical conductivity
Mohammad Rasel Mian1, Masanori Wakizaka1, Takefumi Yoshida1
1Department of Chemistry, Graduate School of Science, Tohoku University, 6-3 Aza-Aoba, Aramaki, Sendai 980-8578, Japan. masanori.wakizaka.a7@tohoku.ac.jp h-iguchi@tohoku.ac.jp yamasita.m@gmail.com.
Abstract:
The Pd(iii) oxidation state is unusual and unstable since it strongly tends to disproportionate. We synthesized the quasi-one-dimensional (1D) halogen-bridged Pd(iii)-Cl complex [Pd(dabdOH)2Cl]Cl2 (1-Cl; dabdOH = (2S,3S)-2,3-diaminobutane-1,4-diol) with multiple hydrogen bonds. From single-crystal X-ray diffraction, the bridging Cl- ions were located at the midpoint of the Pd-Cl-Pd moieties in the 1D chains, indicating that the Pd ions are in a Pd(iii) average valence (AV) state. Moreover, bright spots for the Pd(iii) dz2 orbitals in the upper Hubbard band above the Fermi level were observed every ∼5 Å using scanning tunnelling microscopy. These results clearly indicate that the Pd ions are in a Pd(iii) AV state in 1-Cl. In addition, 1-Cl has the highest thermal stability (470 K) among the Pd(iii) complexes reported and the highest electrical conductivity (0.6 S cm-1 at 300 K) among the 1D Pd-Cl chains reported so far.
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