Charge Ordering with Lattice Distortions in a Conductive MMX-Chain Complex, Pt2(d ta)4I (d ta = CH3CS2 -)

The charge-ordering states with lattice distortions of a halogen-bridged binuclear-metal mixed-valence complex (called MMX chain), Pt2(dta)4I (dta = CH3CS2 -), have been investigated by transport, magnetic, and optical measurements. This complex is a binuclear unit-assembled conductor containing met...

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Veröffentlicht in:Journal of the American Chemical Society 1999-11, Vol.121 (43), p.10068-10080
Hauptverfasser: Kitagawa, Hiroshi, Onodera, Noriaki, Sonoyama, Takuya, Yamamoto, Masahiro, Fukawa, Tadashi, Mitani, Tadaoki, Seto, Makoto, Maeda, Yutaka
Format: Artikel
Sprache:eng
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Zusammenfassung:The charge-ordering states with lattice distortions of a halogen-bridged binuclear-metal mixed-valence complex (called MMX chain), Pt2(dta)4I (dta = CH3CS2 -), have been investigated by transport, magnetic, and optical measurements. This complex is a binuclear unit-assembled conductor containing metal−metal bonds. It exhibits metallic conduction above room temperature, representing the first example of a metallic halogen-bridged one-dimensional transition-metal complex. Below 300 K it shows semiconducting behavior, which is considered to be of the Mott−Hubbard type due to electron correlation. The metal−semiconductor transition at 300 K (= T M - S) is derived from a valence transition of Pt from an averaged-valence state of 2.5+ to a trapped-valence state of 2+ and 3+. The charge-ordering modes are considered to be −IPt2+−Pt3+−IPt2+−Pt3+−IPt2+−Pt3+−IPt2+−Pt3+−I for the semiconducting phase below T M - S and −I−Pt2.5+−Pt2.5+−I−Pt2.5+−Pt2.5+−I−Pt2.5+−Pt2.5+−I−Pt2.5+−Pt2.5+−I− for the metallic phase above T M - S. 129I Mössbauer spectroscopic study is reported for a low-temperature insulating phase below 80 K. The low-temperature electronic structure is considered to be an alternate charge-ordering state with lattice distortions of IPt2+−Pt3+−I−Pt3+−Pt2+IPt2+−Pt3+−I−Pt3+−Pt2+I. The present binuclear platinum complex inherently possesses valence instability of the intermediate valence 2.5+. X-ray photoelectron spectroscopy and polarized reflection measurements are also reported.
ISSN:0002-7863
1520-5126
DOI:10.1021/ja9915910