TY - JOUR
T1 - Charge-density-wave to Mott-Hubbard phase transition in quasi-one-dimensional bromo-bridged Pd compounds
AU - Takaishi, Shinya
AU - Takamura, Mitsuhito
AU - Kajiwara, Takashi
AU - Miyasaka, Hitoshi
AU - Yamashita, Masahiro
AU - Iwata, Muneaki
AU - Matsuzaki, Hiroyuki
AU - Okamoto, Hiroshi
AU - Tanaka, Hisaaki
AU - Kuroda, Shin Ichi
AU - Nishikawa, Hiroyuki
AU - Oshio, Hiroki
AU - Kato, Kenichi
AU - Takata, Masaki
PY - 2008/9/10
Y1 - 2008/9/10
N2 - A -PdIIIBr-PdIII- Mott-Hubbard state was observed in a quasi-one-dimensional bromo-bridged Pd compound [Pd(Bn)2Br](C 5-Y)2·H2O (en = ethylenediamine, C 5-Y = dipentylsulfosuccinate) for the first time. The phase transition between Mott-Hubbard and charge-density-wave states occurred at 206 ± 2 K and was confirmed by using X-ray, ESR, Raman and electronic spectroscopies, electrical resistivity, and heat capacity. From X-ray powder diffraction patterns and Raman spectra of a series of Pd-Br compounds, [Pd(en)2Br](Cn-Y)2·H2O (n = 4, 5, 6, 7, 8, 9, and 12), chemical pressure from the alkyl chains of the counterions caused the phase transition.
AB - A -PdIIIBr-PdIII- Mott-Hubbard state was observed in a quasi-one-dimensional bromo-bridged Pd compound [Pd(Bn)2Br](C 5-Y)2·H2O (en = ethylenediamine, C 5-Y = dipentylsulfosuccinate) for the first time. The phase transition between Mott-Hubbard and charge-density-wave states occurred at 206 ± 2 K and was confirmed by using X-ray, ESR, Raman and electronic spectroscopies, electrical resistivity, and heat capacity. From X-ray powder diffraction patterns and Raman spectra of a series of Pd-Br compounds, [Pd(en)2Br](Cn-Y)2·H2O (n = 4, 5, 6, 7, 8, 9, and 12), chemical pressure from the alkyl chains of the counterions caused the phase transition.
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U2 - 10.1021/ja8032026
DO - 10.1021/ja8032026
M3 - Article
AN - SCOPUS:51749095044
SN - 0002-7863
VL - 130
SP - 12080
EP - 12084
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 36
ER -