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Hydrogen-Bonded Organic–Inorganic Hybrid Based on Hexachloroplatinate and Nitrogen Heterocyclic Cations: Their Synthesis, Characterization, Crystal Structures, and Antitumor Activities In Vitro
Three new crystal structures containing [PtCl(6)](2−), pyridinium and benzimidazole groups have been prepared: [PtCl(6)]·(H-bzm)(2)·2(H(2)O) (1), [PtCl(6)]·(H-bipy)(2)·2(H(2)O) (2), [PtCl(6)]·(H-dimethyl-bipy)(2)·2(H(2)O) (3) [H-bzm: benzimidazole cation, H-bipy: 2,2′-bipyridine cation, H-dimethyl-b...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099602/ https://www.ncbi.nlm.nih.gov/pubmed/29890688 http://dx.doi.org/10.3390/molecules23061397 |
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author | Zhao, Jin Chen, Fuming Han, Yutong Chen, Huaqing Luo, Zhidong Tian, Hao Zhao, Yi Ma, Aiqing Zhu, Longguan |
author_facet | Zhao, Jin Chen, Fuming Han, Yutong Chen, Huaqing Luo, Zhidong Tian, Hao Zhao, Yi Ma, Aiqing Zhu, Longguan |
author_sort | Zhao, Jin |
collection | PubMed |
description | Three new crystal structures containing [PtCl(6)](2−), pyridinium and benzimidazole groups have been prepared: [PtCl(6)]·(H-bzm)(2)·2(H(2)O) (1), [PtCl(6)]·(H-bipy)(2)·2(H(2)O) (2), [PtCl(6)]·(H-dimethyl-bipy)(2)·2(H(2)O) (3) [H-bzm: benzimidazole cation, H-bipy: 2,2′-bipyridine cation, H-dimethyl-bipy: 4,4′-bimethyl-2,2′-bipyridine cation]. All compounds have been fully characterized by elemental analyses, single-crystal X-ray analyses, IR spectra, TG analyses, and fluorescence studies. Single-crystal X-ray diffraction analysis suggests that the primary synthon contains (+)N–H···Cl(−), including ionic bonding and hydrogen bonding interactions. The dimensions are enhanced further by secondary O–H ∙∙Cl and N–H ∙∙O hydrogen bonding interactions between donor and acceptor atoms located at the periphery of these synthons. Moreover, coulombic attractions between the ions play an important role in reinforcing the structures of these complexes. In addition, antitumor activity against human lung adenocarcinoma cell line (A549) and human nasopharyngeal carcinoma cell line (CNE-2) was performed. These complexes all showed inhibition to the two cell lines, while complex 3 exhibited higher efficiency than complexes 1–2. |
format | Online Article Text |
id | pubmed-6099602 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-60996022018-11-13 Hydrogen-Bonded Organic–Inorganic Hybrid Based on Hexachloroplatinate and Nitrogen Heterocyclic Cations: Their Synthesis, Characterization, Crystal Structures, and Antitumor Activities In Vitro Zhao, Jin Chen, Fuming Han, Yutong Chen, Huaqing Luo, Zhidong Tian, Hao Zhao, Yi Ma, Aiqing Zhu, Longguan Molecules Article Three new crystal structures containing [PtCl(6)](2−), pyridinium and benzimidazole groups have been prepared: [PtCl(6)]·(H-bzm)(2)·2(H(2)O) (1), [PtCl(6)]·(H-bipy)(2)·2(H(2)O) (2), [PtCl(6)]·(H-dimethyl-bipy)(2)·2(H(2)O) (3) [H-bzm: benzimidazole cation, H-bipy: 2,2′-bipyridine cation, H-dimethyl-bipy: 4,4′-bimethyl-2,2′-bipyridine cation]. All compounds have been fully characterized by elemental analyses, single-crystal X-ray analyses, IR spectra, TG analyses, and fluorescence studies. Single-crystal X-ray diffraction analysis suggests that the primary synthon contains (+)N–H···Cl(−), including ionic bonding and hydrogen bonding interactions. The dimensions are enhanced further by secondary O–H ∙∙Cl and N–H ∙∙O hydrogen bonding interactions between donor and acceptor atoms located at the periphery of these synthons. Moreover, coulombic attractions between the ions play an important role in reinforcing the structures of these complexes. In addition, antitumor activity against human lung adenocarcinoma cell line (A549) and human nasopharyngeal carcinoma cell line (CNE-2) was performed. These complexes all showed inhibition to the two cell lines, while complex 3 exhibited higher efficiency than complexes 1–2. MDPI 2018-06-08 /pmc/articles/PMC6099602/ /pubmed/29890688 http://dx.doi.org/10.3390/molecules23061397 Text en © 2018 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Zhao, Jin Chen, Fuming Han, Yutong Chen, Huaqing Luo, Zhidong Tian, Hao Zhao, Yi Ma, Aiqing Zhu, Longguan Hydrogen-Bonded Organic–Inorganic Hybrid Based on Hexachloroplatinate and Nitrogen Heterocyclic Cations: Their Synthesis, Characterization, Crystal Structures, and Antitumor Activities In Vitro |
title | Hydrogen-Bonded Organic–Inorganic Hybrid Based on Hexachloroplatinate and Nitrogen Heterocyclic Cations: Their Synthesis, Characterization, Crystal Structures, and Antitumor Activities In Vitro |
title_full | Hydrogen-Bonded Organic–Inorganic Hybrid Based on Hexachloroplatinate and Nitrogen Heterocyclic Cations: Their Synthesis, Characterization, Crystal Structures, and Antitumor Activities In Vitro |
title_fullStr | Hydrogen-Bonded Organic–Inorganic Hybrid Based on Hexachloroplatinate and Nitrogen Heterocyclic Cations: Their Synthesis, Characterization, Crystal Structures, and Antitumor Activities In Vitro |
title_full_unstemmed | Hydrogen-Bonded Organic–Inorganic Hybrid Based on Hexachloroplatinate and Nitrogen Heterocyclic Cations: Their Synthesis, Characterization, Crystal Structures, and Antitumor Activities In Vitro |
title_short | Hydrogen-Bonded Organic–Inorganic Hybrid Based on Hexachloroplatinate and Nitrogen Heterocyclic Cations: Their Synthesis, Characterization, Crystal Structures, and Antitumor Activities In Vitro |
title_sort | hydrogen-bonded organic–inorganic hybrid based on hexachloroplatinate and nitrogen heterocyclic cations: their synthesis, characterization, crystal structures, and antitumor activities in vitro |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099602/ https://www.ncbi.nlm.nih.gov/pubmed/29890688 http://dx.doi.org/10.3390/molecules23061397 |
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