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Templated mesoporous carbons designed around the pyridine functionality have been made using the cyclotrimerization of a variety of diethynylpyridines. The substitution pattern of the ethynyl moieties about the pyridine ring system was found to have a significant impact on the structure and properties of the final product. A model is proposed that focuses on the self-assembly of the diethynylpyridine monomer on the silica surface and the order and orientation of the ethynyl moieties within this monolayer.
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Shin et al. (2007) studied this question.
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