Diindenothienoacene–tetrathiafulvalene redox systems

Mikkel Andreas Christensen; Gabriel E. Rudebusch; Christian Richard Parker; Cecilie Lindholm Andersen; Anders Kadziola; Michael M. Haley; Ole Hammerich; Mogens Brøndsted Nielsen

doi:10.1039/c5ra09581f

Diindenothienoacene–tetrathiafulvalene redox systems

Mikkel Andreas Christensen, Gabriel E. Rudebusch, Christian Richard Parker, Cecilie Lindholm Andersen, Anders Kadziola, Michael M. Haley, Ole Hammerich, Mogens Brøndsted Nielsen

Kemisk Institut

12 Citationer (Scopus)

Abstract

Extended tetrathiafulvalenes with central diindenothienoacene cores were prepared and studied for their redox and spectroelectrochemical properties, which depended strongly on the orientation of the thiophene rings. The cations undergo remarkably strong associations, rendering them attractive as redox-controllable tectons in supramolecular chemistry, and in one case crystals were grown by electrocrystallization.

Originalsprog	Engelsk
Tidsskrift	RSC Advances
Vol/bind	2015
Udgave nummer	5
Sider (fra-til)	49748-49751
Antal sider	4
ISSN	2046-2069
DOI	https://doi.org/10.1039/c5ra09581f
Status	Udgivet - 2015

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10.1039/c5ra09581f

Citationsformater

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title = "Diindenothienoacene–tetrathiafulvalene redox systems",

abstract = "Extended tetrathiafulvalenes with central diindenothienoacene cores were prepared and studied for their redox and spectroelectrochemical properties, which depended strongly on the orientation of the thiophene rings. The cations undergo remarkably strong associations, rendering them attractive as redox-controllable tectons in supramolecular chemistry, and in one case crystals were grown by electrocrystallization.",

author = "Christensen, {Mikkel Andreas} and Rudebusch, {Gabriel E.} and Parker, {Christian Richard} and Andersen, {Cecilie Lindholm} and Anders Kadziola and Haley, {Michael M.} and Ole Hammerich and Nielsen, {Mogens Br{\o}ndsted}",

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doi = "10.1039/c5ra09581f",

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volume = "2015",

pages = "49748--49751",

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T1 - Diindenothienoacene–tetrathiafulvalene redox systems

AU - Christensen, Mikkel Andreas

AU - Rudebusch, Gabriel E.

AU - Parker, Christian Richard

AU - Andersen, Cecilie Lindholm

AU - Kadziola, Anders

AU - Haley, Michael M.

AU - Hammerich, Ole

AU - Nielsen, Mogens Brøndsted

PY - 2015

Y1 - 2015

N2 - Extended tetrathiafulvalenes with central diindenothienoacene cores were prepared and studied for their redox and spectroelectrochemical properties, which depended strongly on the orientation of the thiophene rings. The cations undergo remarkably strong associations, rendering them attractive as redox-controllable tectons in supramolecular chemistry, and in one case crystals were grown by electrocrystallization.

AB - Extended tetrathiafulvalenes with central diindenothienoacene cores were prepared and studied for their redox and spectroelectrochemical properties, which depended strongly on the orientation of the thiophene rings. The cations undergo remarkably strong associations, rendering them attractive as redox-controllable tectons in supramolecular chemistry, and in one case crystals were grown by electrocrystallization.

U2 - 10.1039/c5ra09581f

DO - 10.1039/c5ra09581f

M3 - Journal article

SN - 2046-2069

VL - 2015

SP - 49748

EP - 49751

JO - RSC Advances

JF - RSC Advances

IS - 5

ER -

Diindenothienoacene–tetrathiafulvalene redox systems

Abstract

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