Intramolecular versus intermolecular electronic interactions between [5,6]-open and [6,6]-closed C60 adducts with exTTF

Takano Y, Schubert C, Mizorogi N, Feng L, Iwano A, Katayama M, Angeles Herranz M, Guldi DM, Martin N, Nagase S, Akasaka T (2013)

Publication Type: Journal article, Original article

Publication year: 2013

Journal

Chemical Science Royal Society of Chemistry

Original Authors: Takano Y., Schubert C., Mizorogi N., Feng L., Iwano A., Katayama M., Herranz M.A., Guldi D.M., Martin N., Nagase S., Akasaka T.

Publisher: Royal Society of Chemistry

Book Volume: 4

Pages Range: 3166-3171

Journal Issue: 8

DOI: 10.1039/c3sc00004d

Abstract

Intramolecular and intermolecular electronic interactions are important concepts for fabricating fullerene-based nanostructures such as bulk heterojunction (BHJ) solar cells and supramolecular assemblies. To ascertain differences of the molecular interactions depending on the electronic characteristics of the fullerene adducts, we have synthesized and investigated the [5,6]-open and [6,6]-closed adducts of C, which are covalently linked to π-extended tetrathiafulvalene (exTTF) by a flexible σ-bond chain. The two adducts were synthesized by means of cycloaddition reactions and were characterized using spectroscopic methods such as MALDI-TOF mass spectrometry and NMR spectroscopy. Electronic properties of the [5,6]-open and [6,6]-closed adducts were investigated in the ground and excited states using steady-state absorption spectroscopy, cyclic and differential pulse voltammetry (CV and DPV), fluorescence spectroscopy, and femtosecond time-resolved absorption spectroscopy. DFT calculations of the two adducts predict that the flexible bridge between C and exTTF enables a closer proximity than the interlayer distance of graphite (3.35 Å), which dictates considerable π-π interactions. In comparing the [5,6]- and [6,6]-adducts, it is noteworthy to mention that the [6,6]-adduct revealed longer lifetimes of the photochemically formed radical ion pair states than that of the [5,6]-adduct, which is in contrast to results of recent investigations related to the photodynamics of [5,6]- and [6,6]-adducts of C. Titration experiments using references, namely [5,6]- and [6,6]-PCBM, inferred that the [6,6]-adduct gives rise to stronger electronic interactions with exTTF than the [5,6]-adduct. Comprehensive understanding of the different molecular properties, which the [5,6]- and [6,6]-adducts exhibit, provides valuable information regarding the morphology and/or the electronic properties of C-based nanocomposites, such as C-based BHJ solar cells or supramolecular assemblies. © 2013 The Royal Society of Chemistry.

Authors with CRIS profile

Christina Schubert
Dirk Michael Guldi Lehrstuhl für Physikalische Chemie I

Involved external institutions

Kyoto University / 京都大学 Kyōto daigaku JP Japan (JP) University of Tsukuba / 筑波大学 JP Japan (JP) Universidad Complutense de Madrid (UCM) ES Spain (ES)

How to cite

APA:

Takano, Y., Schubert, C., Mizorogi, N., Feng, L., Iwano, A., Katayama, M.,... Akasaka, T. (2013). Intramolecular versus intermolecular electronic interactions between [5,6]-open and [6,6]-closed C60 adducts with exTTF. Chemical Science, 4(8), 3166-3171. https://doi.org/10.1039/c3sc00004d

MLA:

Takano, Yuta, et al. "Intramolecular versus intermolecular electronic interactions between [5,6]-open and [6,6]-closed C60 adducts with exTTF." Chemical Science 4.8 (2013): 3166-3171.

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