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Pronounced electrochemical amphotericity of a fused donor-acceptor compound: A planar merge of TTF with a TCNQ-Ttype bithienoquinoxaline

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Pronounced electrochemical amphotericity of a fused donor-acceptor compound: A planar merge of TTF with a TCNQ-Ttype bithienoquinoxaline. / Guégano, X.; Kanibolotsky, A.L.; Blum, C. et al.
In: Chemistry - A European Journal, Vol. 15, No. 1, 2009, p. 63-66.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Guégano, X, Kanibolotsky, AL, Blum, C, Mertens, SFL, Liu, S-X, Neels, A, Hagemann, H, Skabara, PJ, Leutwyler, S, Wandlowski, T, Hauser, A & Decurtins, S 2009, 'Pronounced electrochemical amphotericity of a fused donor-acceptor compound: A planar merge of TTF with a TCNQ-Ttype bithienoquinoxaline', Chemistry - A European Journal, vol. 15, no. 1, pp. 63-66. https://doi.org/10.1002/chem.200802011

APA

Guégano, X., Kanibolotsky, A. L., Blum, C., Mertens, S. F. L., Liu, S-X., Neels, A., Hagemann, H., Skabara, P. J., Leutwyler, S., Wandlowski, T., Hauser, A., & Decurtins, S. (2009). Pronounced electrochemical amphotericity of a fused donor-acceptor compound: A planar merge of TTF with a TCNQ-Ttype bithienoquinoxaline. Chemistry - A European Journal, 15(1), 63-66. https://doi.org/10.1002/chem.200802011

Vancouver

Guégano X, Kanibolotsky AL, Blum C, Mertens SFL, Liu S-X, Neels A et al. Pronounced electrochemical amphotericity of a fused donor-acceptor compound: A planar merge of TTF with a TCNQ-Ttype bithienoquinoxaline. Chemistry - A European Journal. 2009;15(1):63-66. doi: 10.1002/chem.200802011

Author

Guégano, X. ; Kanibolotsky, A.L. ; Blum, C. et al. / Pronounced electrochemical amphotericity of a fused donor-acceptor compound : A planar merge of TTF with a TCNQ-Ttype bithienoquinoxaline. In: Chemistry - A European Journal. 2009 ; Vol. 15, No. 1. pp. 63-66.

Bibtex

@article{8d9c836363f54de98c528c42f1203c88,
title = "Pronounced electrochemical amphotericity of a fused donor-acceptor compound: A planar merge of TTF with a TCNQ-Ttype bithienoquinoxaline",
abstract = "Narrowing the gap: A compactly fused π‐conjugated molecule combines a high‐lying HOMO with a low‐lying LUMO (Eox−Ered=0.52 eV) and a fairly low‐lying LUMO+1 on the bridging unit, giving rise to strong optical charge‐transfer transitions. A facile electron transfer has been observed by EPR and NMR spectroscopies. ",
keywords = "Charge transfer, Donor-acceptor systems, HOMO-LUMO gap, Redox chemistry, Tetrathiafulvalenes, Electronic structure, Ion exchange, Mass transfer, Organic polymers, Solid solutions, Acceptor moieties, Acceptor properties, CT transitions, Electron donors, EPR signals, IR stretching, Large amplitudes, RAMAN spectrum, Solid states, Synthetic routes, Tetrathiafulvalene (TTF) derivatives, Electron spin resonance spectroscopy",
author = "X. Gu{\'e}gano and A.L. Kanibolotsky and C. Blum and S.F.L. Mertens and S.-X. Liu and A. Neels and H. Hagemann and P.J. Skabara and S. Leutwyler and T. Wandlowski and A. Hauser and S. Decurtins",
year = "2009",
doi = "10.1002/chem.200802011",
language = "English",
volume = "15",
pages = "63--66",
journal = "Chemistry - A European Journal",
issn = "0947-6539",
publisher = "Wiley-VCH Verlag",
number = "1",

}

RIS

TY - JOUR

T1 - Pronounced electrochemical amphotericity of a fused donor-acceptor compound

T2 - A planar merge of TTF with a TCNQ-Ttype bithienoquinoxaline

AU - Guégano, X.

AU - Kanibolotsky, A.L.

AU - Blum, C.

AU - Mertens, S.F.L.

AU - Liu, S.-X.

AU - Neels, A.

AU - Hagemann, H.

AU - Skabara, P.J.

AU - Leutwyler, S.

AU - Wandlowski, T.

AU - Hauser, A.

AU - Decurtins, S.

PY - 2009

Y1 - 2009

N2 - Narrowing the gap: A compactly fused π‐conjugated molecule combines a high‐lying HOMO with a low‐lying LUMO (Eox−Ered=0.52 eV) and a fairly low‐lying LUMO+1 on the bridging unit, giving rise to strong optical charge‐transfer transitions. A facile electron transfer has been observed by EPR and NMR spectroscopies.

AB - Narrowing the gap: A compactly fused π‐conjugated molecule combines a high‐lying HOMO with a low‐lying LUMO (Eox−Ered=0.52 eV) and a fairly low‐lying LUMO+1 on the bridging unit, giving rise to strong optical charge‐transfer transitions. A facile electron transfer has been observed by EPR and NMR spectroscopies.

KW - Charge transfer

KW - Donor-acceptor systems

KW - HOMO-LUMO gap

KW - Redox chemistry

KW - Tetrathiafulvalenes

KW - Electronic structure

KW - Ion exchange

KW - Mass transfer

KW - Organic polymers

KW - Solid solutions

KW - Acceptor moieties

KW - Acceptor properties

KW - CT transitions

KW - Electron donors

KW - EPR signals

KW - IR stretching

KW - Large amplitudes

KW - RAMAN spectrum

KW - Solid states

KW - Synthetic routes

KW - Tetrathiafulvalene (TTF) derivatives

KW - Electron spin resonance spectroscopy

U2 - 10.1002/chem.200802011

DO - 10.1002/chem.200802011

M3 - Journal article

VL - 15

SP - 63

EP - 66

JO - Chemistry - A European Journal

JF - Chemistry - A European Journal

SN - 0947-6539

IS - 1

ER -