Le Ho KH, Hijazi I, Rivier L, Gautier C, Jousselme B, De Miguel Rojas G, Nieto CR, Guldi DM, Heinrich B, Donnio B, Campidelli S (2013)
Publication Type: Journal article, Original article
Publication year: 2013
Original Authors: Ho K.-H.L., Hijazi I., Rivier L., Gautier C., Jousselme B., De Miguel Rojas G., Romero-Nieto C., Guldi D.M., Heinrich B., Donnio B., Campidelli S.
Publisher: Wiley-VCH Verlag
Book Volume: 19
Pages Range: 11374-11381
Journal Issue: 34
Herein the synthesis, characterization, and organization of a first-generation dendritic fulleropyrrolidine bearing two pending porphyrins are reported. Both the dendron and the fullerene derivatives were synthesized by Cu-catalyzed alkyne-azide cycloaddition (CuAAC). The electron-donor-acceptor conjugate possesses a shape that allows the formation of supramolecular complexes by encapsulation of C within the jaws of the two porphyrins of another molecule. The interactions between the two photoactive units (i.e., C and Zn-porphyrin) were confirmed by cyclic voltammetry as well as by steady-state and time-resolved spectroscopy. For example, a shift of about 85 mV was found for the first reduction of C in the electron-donor-acceptor conjugate compared with the parent molecules, which indicates that C is included in the jaws of the porphyrin. The fulleropyrrolidine compound exhibits a rich polymorphism, which was corroborated by AFM and SEM. In particular, it was found to form supramolecular fibrils when deposited on substrates. The morphology of the fibrils suggests that they are formed by several rows of fullerene-porphyrin complexes. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
APA:
Le Ho, K.-H., Hijazi, I., Rivier, L., Gautier, C., Jousselme, B., De Miguel Rojas, G.,... Campidelli, S. (2013). Host-guest complexation of [60]fullerenes and porphyrins enabled by "click chemistry". Chemistry - A European Journal, 19(34), 11374-11381. https://doi.org/10.1002/chem.201300793
MLA:
Le Ho, Khanh-Hy, et al. "Host-guest complexation of [60]fullerenes and porphyrins enabled by "click chemistry"." Chemistry - A European Journal 19.34 (2013): 11374-11381.
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