Poly-1,4-diketones obtained by the Stetter reaction: a new route to conducting heterocyclic polymers

K.L. Pouwer; T.R. Vries; E.E. Havinga; E.W. Meijer; H. Wynberg

Poly-1,4-diketones obtained by the Stetter reaction: a new route to conducting heterocyclic polymers

K.L. Pouwer
, T.R. Vries
, E.E. Havinga
, E.W. Meijer
, H. Wynberg

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

31 Citations (Scopus)

213 Downloads (Pure)

Abstract

Polymers with p-phenylene-2,5-pyrrole or p-phenylene-2,5-thiophene repeat units were prepd. by reaction of terephthalaldehyde and the bis-Mannich base of 1,4-diacetylbenzene (Stetter reaction), followed by heterocyclic ring closure with ammonia or Lawesson's reagent, resp. The polymers exhibited elec. cond. ?0.1 S.cm-1 upon doping with I or AsF5. [on SciFinder (R)]

Original language	English
Pages (from-to)	1432-1433
Journal	Journal of the Chemical Society, Chemical Communications
Issue number	21
Publication status	Published - 1988

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title = "Poly-1,4-diketones obtained by the Stetter reaction: a new route to conducting heterocyclic polymers",

abstract = "Polymers with p-phenylene-2,5-pyrrole or p-phenylene-2,5-thiophene repeat units were prepd. by reaction of terephthalaldehyde and the bis-Mannich base of 1,4-diacetylbenzene (Stetter reaction), followed by heterocyclic ring closure with ammonia or Lawesson's reagent, resp. The polymers exhibited elec. cond. ?0.1 S.cm-1 upon doping with I or AsF5. [on SciFinder (R)]",

author = "K.L. Pouwer and T.R. Vries and E.E. Havinga and E.W. Meijer and H. Wynberg",

year = "1988",

language = "English",

pages = "1432--1433",

journal = "Journal of the Chemical Society, Chemical Communications",

issn = "0022-4936",

publisher = "Chemical Society",

number = "21",

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TY - JOUR

T1 - Poly-1,4-diketones obtained by the Stetter reaction: a new route to conducting heterocyclic polymers

AU - Pouwer, K.L.

AU - Vries, T.R.

AU - Havinga, E.E.

AU - Meijer, E.W.

AU - Wynberg, H.

PY - 1988

Y1 - 1988

N2 - Polymers with p-phenylene-2,5-pyrrole or p-phenylene-2,5-thiophene repeat units were prepd. by reaction of terephthalaldehyde and the bis-Mannich base of 1,4-diacetylbenzene (Stetter reaction), followed by heterocyclic ring closure with ammonia or Lawesson's reagent, resp. The polymers exhibited elec. cond. ?0.1 S.cm-1 upon doping with I or AsF5. [on SciFinder (R)]

AB - Polymers with p-phenylene-2,5-pyrrole or p-phenylene-2,5-thiophene repeat units were prepd. by reaction of terephthalaldehyde and the bis-Mannich base of 1,4-diacetylbenzene (Stetter reaction), followed by heterocyclic ring closure with ammonia or Lawesson's reagent, resp. The polymers exhibited elec. cond. ?0.1 S.cm-1 upon doping with I or AsF5. [on SciFinder (R)]

M3 - Article

SN - 0022-4936

SP - 1432

EP - 1433

JO - Journal of the Chemical Society, Chemical Communications

JF - Journal of the Chemical Society, Chemical Communications

IS - 21

ER -

Poly-1,4-diketones obtained by the Stetter reaction: a new route to conducting heterocyclic polymers

Abstract

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