A new molecular metal based on Pd(dmit)2:: synthesis, structure and electrical properties of (C7H13NH)[Pd(dmit)2]2 (dmit2-=2-thioxo-1,3-dithiole-4,5-dithiolate)
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Naito, T
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Hokkaido Univ, Grad Sch Sci, Div Chem, Sapporo, Hokkaido 0600810, JapanHokkaido Univ, Grad Sch Sci, Div Chem, Sapporo, Hokkaido 0600810, Japan
Naito, T
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Inabe, T
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机构:Hokkaido Univ, Grad Sch Sci, Div Chem, Sapporo, Hokkaido 0600810, Japan
Inabe, T
Kobayashi, H
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机构:Hokkaido Univ, Grad Sch Sci, Div Chem, Sapporo, Hokkaido 0600810, Japan
Kobayashi, H
Kobayashi, A
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机构:Hokkaido Univ, Grad Sch Sci, Div Chem, Sapporo, Hokkaido 0600810, Japan
Kobayashi, A
机构:
[1] Hokkaido Univ, Grad Sch Sci, Div Chem, Sapporo, Hokkaido 0600810, Japan
[2] Inst Mol Sci, Okazaki, Aichi 4448585, Japan
[3] Univ Tokyo, Grad Sch Sci, Res Ctr Spectrochem, Bunkyo Ku, Tokyo 1130033, Japan
Air-oxidation of the acetone-acetic acid solution Of (C7H13NH)(2)[Pd(dmit)(2)] yielded black shiny platelets of (C7H13NH)[Pd(dmit)(2)](2). The crystal structure was characterized by a criss-cross columnar structure, which has been often observed in M(dmit)(2)-based (M = Ni, Pd) superconductors. Although the quinuclidinium cation (C7H13NH)(+) is found to be orientationally disordered on a 2-fold axis, the crystal exhibited metallic conductivity down to similar to 40 K. Under ambient pressure the room temperature conductivity is around 22 S cm(-1) and the resistivity gradually decreased with decreasing temperature down to 200 K, where it suddenly started to decrease more rapidly and kept decreasing down to similar to 40 K, where it started to increase steeply. At ea. 200 K the structural transition occurred, yet the crystal and molecular structures remained practically unaffected including the cation site disorder and the strong dimerization of the Pd(dmit)(2) molecules. The electrical behaviour under high pressure was rather unusual but could be compared with structurally related Pd(dmit)(2)-based superconductors.