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Issue 21, 2013
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Supramolecular gels based on monopyrrolotetrathiafulvalene and its TCNQ charge-transfer complex

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Abstract

A novel series of monopyrrolotetrathiafulvalene (monopyrrolo-TTF)-based low molecular-mass organic gelators (LMOGs) were synthesized and characterized. Electrochemical investigations exhibited two reversible one-electron redox couples. The gelators could gelate some saturated hydrocarbons and alcohols. The FE-SEM images of xerogels revealed the characteristic gelation morphologies of microporous structures. The gelators reacted with tetracyano-p-quinodimethane (TCNQ) to form the charge-transfer (CT) complexes and the binary organogels, and the morphologies of binary gels changed to regular network and fiber in cyclohexane and n-hexane, respectively. XRD studies suggest that both the gelator and the CT complex maintain the lamellar molecular-packing mode in the organogel phase. The gel–sol transition of the organogel and the CT complex gel could be stimulated by fluorine and chlorine ions.

Graphical abstract: Supramolecular gels based on monopyrrolotetrathiafulvalene and its TCNQ charge-transfer complex

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Publication details

The article was received on 28 Feb 2013, accepted on 04 Apr 2013 and first published on 26 Apr 2013


Article type: Paper
DOI: 10.1039/C3SM50614B
Citation: Soft Matter, 2013,9, 5261-5269

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    Supramolecular gels based on monopyrrolotetrathiafulvalene and its TCNQ charge-transfer complex

    Y. Liu, N. Zheng, H. Li and B. Yin, Soft Matter, 2013, 9, 5261
    DOI: 10.1039/C3SM50614B

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