Synthesis by Stille cross-coupling procedure and electrochemical characterization of branched polymers based on substituted 1,3,5-triarylbenzenes

Krzysztof R. Idzik; Rainer Beckert; Eric Tauscher; Przemyslaw Ledwon; Sylwia Golba; Mieczyslaw Lapkowski; Peter Rapta; Lothar Dunsche; Jaroslaw Frydel

doi:10.4028/www.scientific.net/MSF.663-665.876

Synthesis by Stille cross-coupling procedure and electrochemical characterization of branched polymers based on substituted 1,3,5-triarylbenzenes

Krzysztof R. Idzik
, Rainer Beckert
, Eric Tauscher
, Przemyslaw Ledwon
, Sylwia Golba
, Mieczyslaw Lapkowski
, Peter Rapta
, Lothar Dunsche
, Jaroslaw Frydel

Department of Physical Chemistry and Technology of Polymers (RCH/RCH4)

Friedrich Schiller University Jena
Silesian University of Technology
Polish Academy of Sciences
Leibniz Institute for Solid State and Materials Research Dresden
Slovak University of Technology in Bratislava
Technische Universität Darmstadt

Research output: Chapter in Book/Report/Conference proceeding › Conference contribution › peer-review

3 Citations (Scopus)

Abstract

A series of various substituted 1,3,5-triarylbenzenes, 2,4,6-triaryl-1- phenoles, 1,3,5-triaryl-1-methoxybenzenes and 2,4,6-triaryl-1,3,5- trimethoxybenzenes were synthesized by a Stille cross-coupling procedure. Their structures were confirmed by ¹H NMR, ¹³C NMR, and elemental analysis. Containing thienyl, furyl and EDOT groups polymers obtained in the process of electropolymerization could be carefully considered as a building material in a wide range of organic-electronic devices. We compare properties of monomers and related polymers depending on aryls moieties and their influence of hydroxyl and methoxyl groups attached to the central benzene core.

Original language	English
Title of host publication	Optoelectronic Materials
Editors	Yuan Ming Huang
Publisher	Trans Tech Publications Ltd.
Pages	876-879
Number of pages	4
ISBN (Print)	0878492119, 9780878492114
DOIs	https://doi.org/10.4028/www.scientific.net/MSF.663-665.876
Publication status	Published - 2011

Publication series

Name	Materials Science Forum
Volume	663-665
ISSN (Print)	0255-5476
ISSN (Electronic)	1662-9752

Keywords

Cyclic voltammetry
Electrochemical polymerization
Hyperbranched polymers
Stille coupling procedure

ASJC Scopus subject areas

General Materials Science
Condensed Matter Physics
Mechanics of Materials
Mechanical Engineering

Access to Document

10.4028/www.scientific.net/MSF.663-665.876

Cite this

Idzik, K. R., Beckert, R., Tauscher, E., Ledwon, P., Golba, S., Lapkowski, M., Rapta, P., Dunsche, L., & Frydel, J. (2011). Synthesis by Stille cross-coupling procedure and electrochemical characterization of branched polymers based on substituted 1,3,5-triarylbenzenes. In Y. M. Huang (Ed.), Optoelectronic Materials (pp. 876-879). (Materials Science Forum; Vol. 663-665). Trans Tech Publications Ltd.. https://doi.org/10.4028/www.scientific.net/MSF.663-665.876

@inproceedings{e190f8d6bb4a40178d10458b20bf96c6,

title = "Synthesis by Stille cross-coupling procedure and electrochemical characterization of branched polymers based on substituted 1,3,5-triarylbenzenes",

abstract = "A series of various substituted 1,3,5-triarylbenzenes, 2,4,6-triaryl-1- phenoles, 1,3,5-triaryl-1-methoxybenzenes and 2,4,6-triaryl-1,3,5- trimethoxybenzenes were synthesized by a Stille cross-coupling procedure. Their structures were confirmed by 1H NMR, 13C NMR, and elemental analysis. Containing thienyl, furyl and EDOT groups polymers obtained in the process of electropolymerization could be carefully considered as a building material in a wide range of organic-electronic devices. We compare properties of monomers and related polymers depending on aryls moieties and their influence of hydroxyl and methoxyl groups attached to the central benzene core.",

keywords = "Cyclic voltammetry, Electrochemical polymerization, Hyperbranched polymers, Stille coupling procedure",

author = "Idzik, \{Krzysztof R.\} and Rainer Beckert and Eric Tauscher and Przemyslaw Ledwon and Sylwia Golba and Mieczyslaw Lapkowski and Peter Rapta and Lothar Dunsche and Jaroslaw Frydel",

year = "2011",

doi = "10.4028/www.scientific.net/MSF.663-665.876",

language = "English",

isbn = "0878492119",

series = "Materials Science Forum",

publisher = "Trans Tech Publications Ltd.",

pages = "876--879",

editor = "Huang, \{Yuan Ming\}",

booktitle = "Optoelectronic Materials",

address = "Switzerland",

}

Idzik, KR, Beckert, R, Tauscher, E, Ledwon, P, Golba, S, Lapkowski, M, Rapta, P, Dunsche, L & Frydel, J 2011, Synthesis by Stille cross-coupling procedure and electrochemical characterization of branched polymers based on substituted 1,3,5-triarylbenzenes. in YM Huang (ed.), Optoelectronic Materials. Materials Science Forum, vol. 663-665, Trans Tech Publications Ltd., pp. 876-879. https://doi.org/10.4028/www.scientific.net/MSF.663-665.876

Synthesis by Stille cross-coupling procedure and electrochemical characterization of branched polymers based on substituted 1,3,5-triarylbenzenes. / Idzik, Krzysztof R.; Beckert, Rainer; Tauscher, Eric et al.
Optoelectronic Materials. ed. / Yuan Ming Huang. Trans Tech Publications Ltd., 2011. p. 876-879 (Materials Science Forum; Vol. 663-665).

Research output: Chapter in Book/Report/Conference proceeding › Conference contribution › peer-review

TY - GEN

T1 - Synthesis by Stille cross-coupling procedure and electrochemical characterization of branched polymers based on substituted 1,3,5-triarylbenzenes

AU - Idzik, Krzysztof R.

AU - Beckert, Rainer

AU - Tauscher, Eric

AU - Ledwon, Przemyslaw

AU - Golba, Sylwia

AU - Lapkowski, Mieczyslaw

AU - Rapta, Peter

AU - Dunsche, Lothar

AU - Frydel, Jaroslaw

PY - 2011

Y1 - 2011

N2 - A series of various substituted 1,3,5-triarylbenzenes, 2,4,6-triaryl-1- phenoles, 1,3,5-triaryl-1-methoxybenzenes and 2,4,6-triaryl-1,3,5- trimethoxybenzenes were synthesized by a Stille cross-coupling procedure. Their structures were confirmed by 1H NMR, 13C NMR, and elemental analysis. Containing thienyl, furyl and EDOT groups polymers obtained in the process of electropolymerization could be carefully considered as a building material in a wide range of organic-electronic devices. We compare properties of monomers and related polymers depending on aryls moieties and their influence of hydroxyl and methoxyl groups attached to the central benzene core.

AB - A series of various substituted 1,3,5-triarylbenzenes, 2,4,6-triaryl-1- phenoles, 1,3,5-triaryl-1-methoxybenzenes and 2,4,6-triaryl-1,3,5- trimethoxybenzenes were synthesized by a Stille cross-coupling procedure. Their structures were confirmed by 1H NMR, 13C NMR, and elemental analysis. Containing thienyl, furyl and EDOT groups polymers obtained in the process of electropolymerization could be carefully considered as a building material in a wide range of organic-electronic devices. We compare properties of monomers and related polymers depending on aryls moieties and their influence of hydroxyl and methoxyl groups attached to the central benzene core.

KW - Cyclic voltammetry

KW - Electrochemical polymerization

KW - Hyperbranched polymers

KW - Stille coupling procedure

UR - https://www.scopus.com/pages/publications/78649976871

U2 - 10.4028/www.scientific.net/MSF.663-665.876

DO - 10.4028/www.scientific.net/MSF.663-665.876

M3 - Conference contribution

AN - SCOPUS:78649976871

SN - 0878492119

SN - 9780878492114

T3 - Materials Science Forum

SP - 876

EP - 879

BT - Optoelectronic Materials

A2 - Huang, Yuan Ming

PB - Trans Tech Publications Ltd.

ER -

Idzik KR, Beckert R, Tauscher E, Ledwon P, Golba S, Lapkowski M et al. Synthesis by Stille cross-coupling procedure and electrochemical characterization of branched polymers based on substituted 1,3,5-triarylbenzenes. In Huang YM, editor, Optoelectronic Materials. Trans Tech Publications Ltd. 2011. p. 876-879. (Materials Science Forum). doi: 10.4028/www.scientific.net/MSF.663-665.876

Synthesis by Stille cross-coupling procedure and electrochemical characterization of branched polymers based on substituted 1,3,5-triarylbenzenes

Abstract

Publication series

Keywords

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this