Radical cation of helical, cross-conjugated β-oligothiophene

Jerzy K. Zak; Makoto Miyasaka; Suchada Rajca; Mieczyslaw Lapkowski; Andrzej Rajca

doi:10.1021/ja910076n

Radical cation of helical, cross-conjugated β-oligothiophene

Jerzy K. Zak, Makoto Miyasaka, Suchada Rajca, Mieczyslaw Lapkowski, Andrzej Rajca

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

78 Scopus citations

Abstract

(Figure Presented) The radical cation of carbon-sulfur [7]helicene is configurationally stable in solution at room temperature. In contrast to the radical cations of α-oligothiophenes, which form diamagnetic π-dimers at low temperature, the radical cation of this helical, cross-conjugated β-oligothiophene shows a low propensity toward dimerization.

Original language	English (US)
Pages (from-to)	3246-3247
Number of pages	2
Journal	Journal of the American Chemical Society
Volume	132
Issue number	10
DOIs	https://doi.org/10.1021/ja910076n
State	Published - Mar 17 2010
Externally published	Yes

ASJC Scopus subject areas

Catalysis
Chemistry(all)
Biochemistry
Colloid and Surface Chemistry

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title = "Radical cation of helical, cross-conjugated β-oligothiophene",

abstract = "(Figure Presented) The radical cation of carbon-sulfur [7]helicene is configurationally stable in solution at room temperature. In contrast to the radical cations of α-oligothiophenes, which form diamagnetic π-dimers at low temperature, the radical cation of this helical, cross-conjugated β-oligothiophene shows a low propensity toward dimerization.",

author = "Zak, {Jerzy K.} and Makoto Miyasaka and Suchada Rajca and Mieczyslaw Lapkowski and Andrzej Rajca",

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T1 - Radical cation of helical, cross-conjugated β-oligothiophene

AU - Zak, Jerzy K.

AU - Miyasaka, Makoto

AU - Rajca, Suchada

AU - Lapkowski, Mieczyslaw

AU - Rajca, Andrzej

PY - 2010/3/17

Y1 - 2010/3/17

N2 - (Figure Presented) The radical cation of carbon-sulfur [7]helicene is configurationally stable in solution at room temperature. In contrast to the radical cations of α-oligothiophenes, which form diamagnetic π-dimers at low temperature, the radical cation of this helical, cross-conjugated β-oligothiophene shows a low propensity toward dimerization.

AB - (Figure Presented) The radical cation of carbon-sulfur [7]helicene is configurationally stable in solution at room temperature. In contrast to the radical cations of α-oligothiophenes, which form diamagnetic π-dimers at low temperature, the radical cation of this helical, cross-conjugated β-oligothiophene shows a low propensity toward dimerization.

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DO - 10.1021/ja910076n

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JO - Journal of the American Chemical Society

JF - Journal of the American Chemical Society

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Radical cation of helical, cross-conjugated β-oligothiophene

Abstract

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