4.4 Article

Synthesis of green organogelators with a sulfide linkage via solvent-free Michael addition: soft templates for the preparation of size-controlled gold nanoparticles

Journal

TETRAHEDRON LETTERS
Volume 54, Issue 7, Pages 651-656

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2012.11.145

Keywords

Thioether organogelators; Solvent-free Michael addition; Soft template; Gold nanoparticles

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Green organogelators with a sulfide linkage and free amino groups were synthesized via phase transfer catalysis using a N-benzylcinchonidinium bromide catalyst. Their self-assemblies in various common solvents were examined. These compounds exhibit high gelation ability especially in aromatic and highly polar solvents with a low critical gelation of 0.1 wt %. The organogels were analyzed by H-1 nuclear magnetic resonance (H-1 NMR) and Fourier transfer-infrared spectroscopies (FT-IR), and their phase transition temperatures were determined by differential scanning calorimetry. The homogeneity of the gel networks was examined by field emission scanning electron microscopy and transmission electron microscopy (TEM). A lamellar structure was also confirmed by X-ray diffraction analysis. The organogels were employed as soft-templates for the in situ generation of stable gold nanoparticles dispersed in the gel matrix, and the resulting GNP dispersions were studied by H-1 NMR and UV-vis absorption. Transmission electron microscopy showed that GNPs assemble into a thin membrane-like structure. (c) 2012 Elsevier Ltd. All rights reserved.

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