Supramolecular assembly of guanidinium benzilate and benzylammonium benzilate: structural and spectroscopic (FT-IR, UV–Vis and photoluminescence) analysesNivithaa Sankar, Nishanth Sudarsanan, Esther Jeyanthi Chellathurai, Nagaraja Karachalacherevu Seetharamai, and Karnan Chandran Department of Physics, Dr. M.G.R. Educational and Research Institute, Chennai, India
E-mail: c.karnan@yahoo.com Received: 8 February 2023 Accepted: 7 June 2023 Abstract: Guanidinium benzilate (GBA) and benzylammonium benzilate (BABA) have been prepared from guanidinium carbonate and benzylamine/benzilic acid (BA). GBA has inter-ionic, intraionic and intermolecular hydrogen bondings giving a three-dimensional supramolecular assembly. The carboxylate ion is present in the resonance form with C–O distances of 1.242 and 1.246 Å in GBA, whereas the C–O distances being 1.262 and 1.245 Å in BABA. In BABA, an inverted dimer with inter-ionic hydrogen bonding exist as a dimer with supramolecular assembly due to intermolecular hydrogen bonding between the ion pairs. So the counter cation decides the resonance form of the carboxylate ion, hydrogen-bonding network and the disposition of the phenyl rings in the benzilate and benzyl moiety. The IR, 1H NMR and 13C NMR spectral data have been interpreted using the crystal structure data and by the comparison between the two similar derivatives. Both the compounds show the formation of the ammonium benzilate or methylammonium benzilate moiety which decompose leaving no residue. Both the compounds exhibit the emission at 442 nm (blue) and 547.2 nm (green) on excitation at 257 nm. Chromaticity indicated excellent emission characteristics of both GBA and BABA which is necessary for OLED applications. Graphical abstract Keywords: Crystal structure; Guanidinium benzilate; Benzylammonium benzilate; NMR; Photoluminescence Full paper is available at www.springerlink.com. DOI: 10.1007/s11696-023-02936-8
Chemical Papers 77 (10) 6267–6284 (2023) |
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