Supramolecular hydrogen bonding interactions of novel 1,3,5-benzenetricarbonyl trisubstituted alkyl for anion sensor applications

Herein we report the first example of benzene-1,3,5-tricarboxamide bearing hydrophobic aminododecane side chains (1) which spontaneously forms supramolecular network by a hydrogen bonding interaction. The compound 1 was synthesized by Schotten-Baumann reaction of 1,3,5-benzenetricarbonyl trichloride...

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Main Authors: Matmin, Juan, Yuliati, Leny, Shamsuddin, Mustaffa, Lintang, Hendrik Oktendy
Format: Article
Published: Trans Tech Publication 2014
Subjects:
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author Matmin, Juan
Yuliati, Leny
Shamsuddin, Mustaffa
Lintang, Hendrik Oktendy
author_facet Matmin, Juan
Yuliati, Leny
Shamsuddin, Mustaffa
Lintang, Hendrik Oktendy
author_sort Matmin, Juan
collection ePrints
description Herein we report the first example of benzene-1,3,5-tricarboxamide bearing hydrophobic aminododecane side chains (1) which spontaneously forms supramolecular network by a hydrogen bonding interaction. The compound 1 was synthesized by Schotten-Baumann reaction of 1,3,5-benzenetricarbonyl trichloride and 1-aminododecane in the presence of N,N-diisopropylethylamine. Nuclear Magnetic Resonance (NMR), Mass Spectrometry (MS), and Fourier Transform Infrared (FTIR) spectroscopies have proved the successful synthesis of 1 in 93% as white powder solid. The supramolecular organization was successfully utilized for sensing of nitrate anions by deformation of the hydrogen bonding to form inactive nitroso groups.
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spelling utm.eprints-627322017-06-05T03:05:59Z http://eprints.utm.my/62732/ Supramolecular hydrogen bonding interactions of novel 1,3,5-benzenetricarbonyl trisubstituted alkyl for anion sensor applications Matmin, Juan Yuliati, Leny Shamsuddin, Mustaffa Lintang, Hendrik Oktendy Q Science Herein we report the first example of benzene-1,3,5-tricarboxamide bearing hydrophobic aminododecane side chains (1) which spontaneously forms supramolecular network by a hydrogen bonding interaction. The compound 1 was synthesized by Schotten-Baumann reaction of 1,3,5-benzenetricarbonyl trichloride and 1-aminododecane in the presence of N,N-diisopropylethylamine. Nuclear Magnetic Resonance (NMR), Mass Spectrometry (MS), and Fourier Transform Infrared (FTIR) spectroscopies have proved the successful synthesis of 1 in 93% as white powder solid. The supramolecular organization was successfully utilized for sensing of nitrate anions by deformation of the hydrogen bonding to form inactive nitroso groups. Trans Tech Publication 2014 Article PeerReviewed Matmin, Juan and Yuliati, Leny and Shamsuddin, Mustaffa and Lintang, Hendrik Oktendy (2014) Supramolecular hydrogen bonding interactions of novel 1,3,5-benzenetricarbonyl trisubstituted alkyl for anion sensor applications. Advanced Materials Research, 925 . pp. 228-232. ISSN 1022-6680 http://dx.doi.org/10.4028/www.scientific.net/AMR.925.228 DOI:10.4028/www.scientific.net/AMR.925.228
spellingShingle Q Science
Matmin, Juan
Yuliati, Leny
Shamsuddin, Mustaffa
Lintang, Hendrik Oktendy
Supramolecular hydrogen bonding interactions of novel 1,3,5-benzenetricarbonyl trisubstituted alkyl for anion sensor applications
title Supramolecular hydrogen bonding interactions of novel 1,3,5-benzenetricarbonyl trisubstituted alkyl for anion sensor applications
title_full Supramolecular hydrogen bonding interactions of novel 1,3,5-benzenetricarbonyl trisubstituted alkyl for anion sensor applications
title_fullStr Supramolecular hydrogen bonding interactions of novel 1,3,5-benzenetricarbonyl trisubstituted alkyl for anion sensor applications
title_full_unstemmed Supramolecular hydrogen bonding interactions of novel 1,3,5-benzenetricarbonyl trisubstituted alkyl for anion sensor applications
title_short Supramolecular hydrogen bonding interactions of novel 1,3,5-benzenetricarbonyl trisubstituted alkyl for anion sensor applications
title_sort supramolecular hydrogen bonding interactions of novel 1 3 5 benzenetricarbonyl trisubstituted alkyl for anion sensor applications
topic Q Science
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