Determining the Attenuation Factor in Molecular Wires Featuring Covalent and Noncovalent Tectons

Vela S, Bauroth S, Atienza C, Molina-Ontoria A, Guldi DM, Martin N (2016)

Publication Type: Journal article

Publication year: 2016

Journal

Angewandte Chemie International Edition Wiley

Book Volume: 55

Pages Range: 15076-15080

Journal Issue: 48

DOI: 10.1002/anie.201608973

Abstract

Hybrid covalent/supramolecular porphyrin–fullerene structures were synthesized as highly efficient molecular wires with a remarkably low attenuation factor (β=0.07±0.01 Å−1). Hydrogen-bonding interactions and p-phenylene oligomers of different lengths are responsible for efficient electron transfer in the molecular wires.

Authors with CRIS profile

Stefan Bauroth Lehrstuhl für Physikalische Chemie I Dirk Michael Guldi Lehrstuhl für Physikalische Chemie I

Involved external institutions

Universidad Complutense de Madrid (UCM) ES Spain (ES) IMDEA-Nanociencia ES Spain (ES)

How to cite

APA:

Vela, S., Bauroth, S., Atienza, C., Molina-Ontoria, A., Guldi, D.M., & Martin, N. (2016). Determining the Attenuation Factor in Molecular Wires Featuring Covalent and Noncovalent Tectons. Angewandte Chemie International Edition, 55(48), 15076-15080. https://doi.org/10.1002/anie.201608973

MLA:

Vela, Sonia, et al. "Determining the Attenuation Factor in Molecular Wires Featuring Covalent and Noncovalent Tectons." Angewandte Chemie International Edition 55.48 (2016): 15076-15080.

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