Cargando…
Synthesis, intermolecular interactions and biological activities of two new organic–inorganic hybrids C(6)H(10)N(2),2Br and C(6)H(10)N(2),2Cl·H(2)O
A slow evaporation method has permitted the crystallization of two novel crystals of (2-aminomethyl)pyridindiumdihalide C(6)H(10)N(2),2Br (1) and C(6)H(10)N(2),2Cl·H(2)O (2). The structures of the prepared compounds (1) and (2) were elucidated by single-crystal X-ray diffraction which revealed that...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9049630/ https://www.ncbi.nlm.nih.gov/pubmed/35497437 http://dx.doi.org/10.1039/c9ra09294c |
_version_ | 1784696182137683968 |
---|---|
author | Hamdi, Intissar Bkhairia, Intidhar Roodt, Andreas Roisnel, Thierry Nasri, Moncef Naïli, Houcine |
author_facet | Hamdi, Intissar Bkhairia, Intidhar Roodt, Andreas Roisnel, Thierry Nasri, Moncef Naïli, Houcine |
author_sort | Hamdi, Intissar |
collection | PubMed |
description | A slow evaporation method has permitted the crystallization of two novel crystals of (2-aminomethyl)pyridindiumdihalide C(6)H(10)N(2),2Br (1) and C(6)H(10)N(2),2Cl·H(2)O (2). The structures of the prepared compounds (1) and (2) were elucidated by single-crystal X-ray diffraction which revealed that they crystallize, respectively, with triclinic and monoclinic symmetries. Their crystal packing was stabilized by non-covalent interactions, including N–H⋯Br, C–H⋯Br, N–H⋯Cl, O–H⋯Cl and N–H⋯O hydrogen bonds. 3-D Hirshfeld surface analysis followed by 2-D fingerprint schemes gives insights into the intermolecular interactions in the crystalline structure. Furthermore, the FT-IR spectroscopy of these two compounds was carried out. The synthesized products were also screened for in vitro antioxidant and antimicrobial activities, which reveals their favourable antioxidant activities against 1,1-diphenyl-2-picrylhydrazyl (DPPH) as well as the discolouration of β-carotene. |
format | Online Article Text |
id | pubmed-9049630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90496302022-04-29 Synthesis, intermolecular interactions and biological activities of two new organic–inorganic hybrids C(6)H(10)N(2),2Br and C(6)H(10)N(2),2Cl·H(2)O Hamdi, Intissar Bkhairia, Intidhar Roodt, Andreas Roisnel, Thierry Nasri, Moncef Naïli, Houcine RSC Adv Chemistry A slow evaporation method has permitted the crystallization of two novel crystals of (2-aminomethyl)pyridindiumdihalide C(6)H(10)N(2),2Br (1) and C(6)H(10)N(2),2Cl·H(2)O (2). The structures of the prepared compounds (1) and (2) were elucidated by single-crystal X-ray diffraction which revealed that they crystallize, respectively, with triclinic and monoclinic symmetries. Their crystal packing was stabilized by non-covalent interactions, including N–H⋯Br, C–H⋯Br, N–H⋯Cl, O–H⋯Cl and N–H⋯O hydrogen bonds. 3-D Hirshfeld surface analysis followed by 2-D fingerprint schemes gives insights into the intermolecular interactions in the crystalline structure. Furthermore, the FT-IR spectroscopy of these two compounds was carried out. The synthesized products were also screened for in vitro antioxidant and antimicrobial activities, which reveals their favourable antioxidant activities against 1,1-diphenyl-2-picrylhydrazyl (DPPH) as well as the discolouration of β-carotene. The Royal Society of Chemistry 2020-02-04 /pmc/articles/PMC9049630/ /pubmed/35497437 http://dx.doi.org/10.1039/c9ra09294c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Hamdi, Intissar Bkhairia, Intidhar Roodt, Andreas Roisnel, Thierry Nasri, Moncef Naïli, Houcine Synthesis, intermolecular interactions and biological activities of two new organic–inorganic hybrids C(6)H(10)N(2),2Br and C(6)H(10)N(2),2Cl·H(2)O |
title | Synthesis, intermolecular interactions and biological activities of two new organic–inorganic hybrids C(6)H(10)N(2),2Br and C(6)H(10)N(2),2Cl·H(2)O |
title_full | Synthesis, intermolecular interactions and biological activities of two new organic–inorganic hybrids C(6)H(10)N(2),2Br and C(6)H(10)N(2),2Cl·H(2)O |
title_fullStr | Synthesis, intermolecular interactions and biological activities of two new organic–inorganic hybrids C(6)H(10)N(2),2Br and C(6)H(10)N(2),2Cl·H(2)O |
title_full_unstemmed | Synthesis, intermolecular interactions and biological activities of two new organic–inorganic hybrids C(6)H(10)N(2),2Br and C(6)H(10)N(2),2Cl·H(2)O |
title_short | Synthesis, intermolecular interactions and biological activities of two new organic–inorganic hybrids C(6)H(10)N(2),2Br and C(6)H(10)N(2),2Cl·H(2)O |
title_sort | synthesis, intermolecular interactions and biological activities of two new organic–inorganic hybrids c(6)h(10)n(2),2br and c(6)h(10)n(2),2cl·h(2)o |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9049630/ https://www.ncbi.nlm.nih.gov/pubmed/35497437 http://dx.doi.org/10.1039/c9ra09294c |
work_keys_str_mv | AT hamdiintissar synthesisintermolecularinteractionsandbiologicalactivitiesoftwoneworganicinorganichybridsc6h10n22brandc6h10n22clh2o AT bkhairiaintidhar synthesisintermolecularinteractionsandbiologicalactivitiesoftwoneworganicinorganichybridsc6h10n22brandc6h10n22clh2o AT roodtandreas synthesisintermolecularinteractionsandbiologicalactivitiesoftwoneworganicinorganichybridsc6h10n22brandc6h10n22clh2o AT roisnelthierry synthesisintermolecularinteractionsandbiologicalactivitiesoftwoneworganicinorganichybridsc6h10n22brandc6h10n22clh2o AT nasrimoncef synthesisintermolecularinteractionsandbiologicalactivitiesoftwoneworganicinorganichybridsc6h10n22brandc6h10n22clh2o AT nailihoucine synthesisintermolecularinteractionsandbiologicalactivitiesoftwoneworganicinorganichybridsc6h10n22brandc6h10n22clh2o |