Synthesis and properties of selenium containing TTM-TTP conductors

M. Ashizawa; H. Nii; T. Kawamoto; T. Mori; Y. Misaki; K. Tanaka; K. Takimiya; T. Otsubo

doi:10.1016/S0379-6779(02)00814-7

Synthesis and properties of selenium containing TTM-TTP conductors

M. Ashizawa, H. Nii, T. Kawamoto, T. Mori, Y. Misaki, K. Tanaka, K. Takimiya, T. Otsubo

SCI - Chemistry

Research output: Contribution to journal › Article › peer-review

8 Citations (Scopus)

Abstract

Selenium substitution of the outer 1,3-dithiole rings of TTM-TTP and TMET-TTP has been performed. The selenium analogues of TTM-TTP give the phases isostractural to (TTM-TTP)(I₃)_5/3. The selenium substitution of the single outer ring does not suppress the 25 K transition, whereas the substitution of both outer rings affords a practically metallic phase.

Original language	English
Pages (from-to)	627-628
Number of pages	2
Journal	Synthetic Metals
Volume	135-136
DOIs	https://doi.org/10.1016/S0379-6779(02)00814-7
Publication status	Published - 2003 Apr 4

Keywords

Coupling reactions
Organic conductors based on radical cation and/or anion salts

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10.1016/S0379-6779(02)00814-7

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abstract = "Selenium substitution of the outer 1,3-dithiole rings of TTM-TTP and TMET-TTP has been performed. The selenium analogues of TTM-TTP give the phases isostractural to (TTM-TTP)(I3)5/3. The selenium substitution of the single outer ring does not suppress the 25 K transition, whereas the substitution of both outer rings affords a practically metallic phase.",

keywords = "Coupling reactions, Organic conductors based on radical cation and/or anion salts",

author = "M. Ashizawa and H. Nii and T. Kawamoto and T. Mori and Y. Misaki and K. Tanaka and K. Takimiya and T. Otsubo",

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T1 - Synthesis and properties of selenium containing TTM-TTP conductors

AU - Ashizawa, M.

AU - Nii, H.

AU - Kawamoto, T.

AU - Mori, T.

AU - Misaki, Y.

AU - Tanaka, K.

AU - Takimiya, K.

AU - Otsubo, T.

PY - 2003/4/4

Y1 - 2003/4/4

N2 - Selenium substitution of the outer 1,3-dithiole rings of TTM-TTP and TMET-TTP has been performed. The selenium analogues of TTM-TTP give the phases isostractural to (TTM-TTP)(I3)5/3. The selenium substitution of the single outer ring does not suppress the 25 K transition, whereas the substitution of both outer rings affords a practically metallic phase.

AB - Selenium substitution of the outer 1,3-dithiole rings of TTM-TTP and TMET-TTP has been performed. The selenium analogues of TTM-TTP give the phases isostractural to (TTM-TTP)(I3)5/3. The selenium substitution of the single outer ring does not suppress the 25 K transition, whereas the substitution of both outer rings affords a practically metallic phase.

KW - Coupling reactions

KW - Organic conductors based on radical cation and/or anion salts

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U2 - 10.1016/S0379-6779(02)00814-7

DO - 10.1016/S0379-6779(02)00814-7

M3 - Article

AN - SCOPUS:2142731462

SN - 0379-6779

VL - 135-136

SP - 627

EP - 628

JO - Synthetic Metals

JF - Synthetic Metals

ER -

Synthesis and properties of selenium containing TTM-TTP conductors

Abstract

Keywords

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