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Chitosan Catalyzed Novel Piperidinium Dicoumarol: Green Synthesis, X-ray Diffraction, Hirshfeld Surface and DFT Studies

The novel piperidinium dicoumarol has been synthesized by the reaction of 3-formylchromone, 4-hydroxycoumarin, and piperidine under chitosan catalyzed solvent-free green conditions. FT-IR and NMR spectroscopy established the structure of dicoumarol, which was further confirmed by a single X-ray diff...

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Autores principales: Asad, Mohammad, Arshad, Muhammad Nadeem, T.N., Mohammed Musthafa, Asiri, Abdullah M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9105048/
https://www.ncbi.nlm.nih.gov/pubmed/35567023
http://dx.doi.org/10.3390/polym14091854
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author Asad, Mohammad
Arshad, Muhammad Nadeem
T.N., Mohammed Musthafa
Asiri, Abdullah M.
author_facet Asad, Mohammad
Arshad, Muhammad Nadeem
T.N., Mohammed Musthafa
Asiri, Abdullah M.
author_sort Asad, Mohammad
collection PubMed
description The novel piperidinium dicoumarol has been synthesized by the reaction of 3-formylchromone, 4-hydroxycoumarin, and piperidine under chitosan catalyzed solvent-free green conditions. FT-IR and NMR spectroscopy established the structure of dicoumarol, which was further confirmed by a single X-ray diffraction study. The single diffraction study has revealed the hydrogen bonding interactions, which were further validated by Hirshfeld surface analysis. Geometry optimizations of dicoumarol have been performed at the DFT level of theory by the B3LYP acting along with Gaussian 16, revision B.01 to calculate the geometric and electronic structure parameters.
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spelling pubmed-91050482022-05-14 Chitosan Catalyzed Novel Piperidinium Dicoumarol: Green Synthesis, X-ray Diffraction, Hirshfeld Surface and DFT Studies Asad, Mohammad Arshad, Muhammad Nadeem T.N., Mohammed Musthafa Asiri, Abdullah M. Polymers (Basel) Article The novel piperidinium dicoumarol has been synthesized by the reaction of 3-formylchromone, 4-hydroxycoumarin, and piperidine under chitosan catalyzed solvent-free green conditions. FT-IR and NMR spectroscopy established the structure of dicoumarol, which was further confirmed by a single X-ray diffraction study. The single diffraction study has revealed the hydrogen bonding interactions, which were further validated by Hirshfeld surface analysis. Geometry optimizations of dicoumarol have been performed at the DFT level of theory by the B3LYP acting along with Gaussian 16, revision B.01 to calculate the geometric and electronic structure parameters. MDPI 2022-04-30 /pmc/articles/PMC9105048/ /pubmed/35567023 http://dx.doi.org/10.3390/polym14091854 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Asad, Mohammad
Arshad, Muhammad Nadeem
T.N., Mohammed Musthafa
Asiri, Abdullah M.
Chitosan Catalyzed Novel Piperidinium Dicoumarol: Green Synthesis, X-ray Diffraction, Hirshfeld Surface and DFT Studies
title Chitosan Catalyzed Novel Piperidinium Dicoumarol: Green Synthesis, X-ray Diffraction, Hirshfeld Surface and DFT Studies
title_full Chitosan Catalyzed Novel Piperidinium Dicoumarol: Green Synthesis, X-ray Diffraction, Hirshfeld Surface and DFT Studies
title_fullStr Chitosan Catalyzed Novel Piperidinium Dicoumarol: Green Synthesis, X-ray Diffraction, Hirshfeld Surface and DFT Studies
title_full_unstemmed Chitosan Catalyzed Novel Piperidinium Dicoumarol: Green Synthesis, X-ray Diffraction, Hirshfeld Surface and DFT Studies
title_short Chitosan Catalyzed Novel Piperidinium Dicoumarol: Green Synthesis, X-ray Diffraction, Hirshfeld Surface and DFT Studies
title_sort chitosan catalyzed novel piperidinium dicoumarol: green synthesis, x-ray diffraction, hirshfeld surface and dft studies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9105048/
https://www.ncbi.nlm.nih.gov/pubmed/35567023
http://dx.doi.org/10.3390/polym14091854
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