One-pot synthesis of poly(thioarylene)s: Predominant sulphide bond formation through oxidative and electrophilic reaction

Kimihisa Yamamoto; Mitsutoshi Jikei; Yasuhiro Murakami; Hiroyuki Nishide; Eishun Tsuchida

doi:10.1039/C39910000596

One-pot synthesis of poly(thioarylene)s: Predominant sulphide bond formation through oxidative and electrophilic reaction

Kimihisa Yamamoto, Mitsutoshi Jikei, Yasuhiro Murakami, Hiroyuki Nishide, Eishun Tsuchida^*

^*Corresponding author for this work

Waseda Research Institute for Science and Engineering

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

17 Citations (Scopus)

Abstract

Poly(thioarylene)s are conveniently prepared in high yield at room temperature and atmospheric pressure through oxidative and electrophilic reaction of disulphur dichloride (S₂Cl₂) and aromatic compounds.

Original language	English
Pages (from-to)	596-597
Number of pages	2
Journal	Journal of the Chemical Society, Chemical Communications
Issue number	8
DOIs	https://doi.org/10.1039/C39910000596
Publication status	Published - 1991

ASJC Scopus subject areas

Molecular Medicine

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title = "One-pot synthesis of poly(thioarylene)s: Predominant sulphide bond formation through oxidative and electrophilic reaction",

abstract = "Poly(thioarylene)s are conveniently prepared in high yield at room temperature and atmospheric pressure through oxidative and electrophilic reaction of disulphur dichloride (S2Cl2) and aromatic compounds.",

author = "Kimihisa Yamamoto and Mitsutoshi Jikei and Yasuhiro Murakami and Hiroyuki Nishide and Eishun Tsuchida",

year = "1991",

doi = "10.1039/C39910000596",

language = "English",

pages = "596--597",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

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T1 - One-pot synthesis of poly(thioarylene)s

T2 - Predominant sulphide bond formation through oxidative and electrophilic reaction

AU - Yamamoto, Kimihisa

AU - Jikei, Mitsutoshi

AU - Murakami, Yasuhiro

AU - Nishide, Hiroyuki

AU - Tsuchida, Eishun

PY - 1991

Y1 - 1991

N2 - Poly(thioarylene)s are conveniently prepared in high yield at room temperature and atmospheric pressure through oxidative and electrophilic reaction of disulphur dichloride (S2Cl2) and aromatic compounds.

AB - Poly(thioarylene)s are conveniently prepared in high yield at room temperature and atmospheric pressure through oxidative and electrophilic reaction of disulphur dichloride (S2Cl2) and aromatic compounds.

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DO - 10.1039/C39910000596

M3 - Article

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SP - 596

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JO - Chemical Communications

JF - Chemical Communications

IS - 8

ER -

One-pot synthesis of poly(thioarylene)s: Predominant sulphide bond formation through oxidative and electrophilic reaction

Abstract

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