Push‐pull substituted polythiophenes: towards charge confinement in molecular quantum wells

Frederic Demanze; Abderrahim Yassar; Francis Garnier

doi:10.1002/adma.19950071107

Push‐pull substituted polythiophenes: towards charge confinement in molecular quantum wells

Frederic Demanze
, Abderrahim Yassar
, Francis Garnier

Laboratoire Materiaux Moleculaires
Centre national de la recherche scientifique

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

38 Citations (Scopus)

Abstract

Poly(bithiophene) dervatives unsymmetrically substituted with strong electron‐donating groups and strong electron‐withdrawing groups (e.g. see Fig.) have been synthesized. The substituents induce electronic push–pull effects along the conjugated chain which could be exploited in the design of organic‐based multiple quantum well structures (Figure Presented.) .

Original language	English
Pages (from-to)	907-910
Number of pages	4
Journal	Advanced Materials
Volume	7
Issue number	11
DOIs	https://doi.org/10.1002/adma.19950071107
Publication status	Published - 1 Jan 1995

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@article{2f6c41a728824ab097411e43c3d50e69,

title = "Push‐pull substituted polythiophenes: towards charge confinement in molecular quantum wells",

abstract = "Poly(bithiophene) dervatives unsymmetrically substituted with strong electron‐donating groups and strong electron‐withdrawing groups (e.g. see Fig.) have been synthesized. The substituents induce electronic push{\textendash}pull effects along the conjugated chain which could be exploited in the design of organic‐based multiple quantum well structures (Figure Presented.) .",

author = "Frederic Demanze and Abderrahim Yassar and Francis Garnier",

year = "1995",

month = jan,

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doi = "10.1002/adma.19950071107",

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T1 - Push‐pull substituted polythiophenes

T2 - towards charge confinement in molecular quantum wells

AU - Demanze, Frederic

AU - Yassar, Abderrahim

AU - Garnier, Francis

PY - 1995/1/1

Y1 - 1995/1/1

N2 - Poly(bithiophene) dervatives unsymmetrically substituted with strong electron‐donating groups and strong electron‐withdrawing groups (e.g. see Fig.) have been synthesized. The substituents induce electronic push–pull effects along the conjugated chain which could be exploited in the design of organic‐based multiple quantum well structures (Figure Presented.) .

AB - Poly(bithiophene) dervatives unsymmetrically substituted with strong electron‐donating groups and strong electron‐withdrawing groups (e.g. see Fig.) have been synthesized. The substituents induce electronic push–pull effects along the conjugated chain which could be exploited in the design of organic‐based multiple quantum well structures (Figure Presented.) .

U2 - 10.1002/adma.19950071107

DO - 10.1002/adma.19950071107

M3 - Article

AN - SCOPUS:0029405434

SN - 0935-9648

VL - 7

SP - 907

EP - 910

JO - Advanced Materials

JF - Advanced Materials

IS - 11

ER -

Push‐pull substituted polythiophenes: towards charge confinement in molecular quantum wells

Abstract

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