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Langmuir. 2014 Oct 21;30(41):12429-37. doi: 10.1021/la503459y. Epub 2014 Oct 8.

Conducting nanofibers and organogels derived from the self-assembly of tetrathiafulvalene-appended dipeptides.

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1
WestCHEM, Department of Pure & Applied Chemistry, University of Strathclyde , Glasgow G1 1XL, United Kingdom.

Abstract

We demonstrate the nonaqueous self-assembly of a low-molecular-mass organic gelator based on an electroactive p-type tetrathiafulvalene (TTF)-dipeptide bioconjugate. We show that a TTF moiety appended with diphenylalanine amide derivative (TTF-FF-NH2) self-assembles into one-dimensional nanofibers that further lead to the formation of self-supporting organogels in chloroform and ethyl acetate. Upon doping of the gels with electron acceptors (TCNQ/iodine vapor), stable two-component charge transfer gels are produced in chloroform and ethyl acetate. These gels are characterized by various spectroscopy (UV-vis-NIR, FTIR, and CD), microscopy (AFM and TEM), rheology, and cyclic voltammetry techniques. Furthermore, conductivity measurements performed on TTF-FF-NH2 xerogel nanofiber networks formed between gold electrodes on a glass surface indicate that these nanofibers show a remarkable enhancement in the conductivity after doping with TCNQ.

PMID:
25259412
DOI:
10.1021/la503459y
[Indexed for MEDLINE]
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