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Triazole-Bridged Zinc Dinuclear Complexes: Mechanochemical Synthesis, Crystal Structure, and Biological Activity
[Image: see text] Two zinc (Zn) complexes, [Zn(2)(DAT)(2)Cl(4)] (I) and [Zn(2)(DAT)(2)(NO(3))(4)] (II), were prepared by grinding 3,5-diamino-1,2,4-triazole (C(2)H(5)N(5), DAT) with Zn precursors such as ZnCl(2) and Zn(NO(3))(2), respectively. This solid-state reaction gives the corresponding Zn com...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9670724/ https://www.ncbi.nlm.nih.gov/pubmed/36406524 http://dx.doi.org/10.1021/acsomega.2c03715 |
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author | Park, Hee Sun Sun, Ruijing Lee, Eun Joo Kim, Jungho Hur, Nam Hwi |
author_facet | Park, Hee Sun Sun, Ruijing Lee, Eun Joo Kim, Jungho Hur, Nam Hwi |
author_sort | Park, Hee Sun |
collection | PubMed |
description | [Image: see text] Two zinc (Zn) complexes, [Zn(2)(DAT)(2)Cl(4)] (I) and [Zn(2)(DAT)(2)(NO(3))(4)] (II), were prepared by grinding 3,5-diamino-1,2,4-triazole (C(2)H(5)N(5), DAT) with Zn precursors such as ZnCl(2) and Zn(NO(3))(2), respectively. This solid-state reaction gives the corresponding Zn complex as the sole product in over 99% yield. This mechanochemical method promotes the selective formation of Zn complexes different from those obtained using the conventional solution-based route. The crystal structures of the two complexes were analyzed by single-crystal X-ray diffraction. Complex (I) crystallizes in the monoclinic space group P2(1)/c, whereas complex (II) crystallizes in the triclinic space group P(1̅). Each complex is characterized by the presence of a characteristic DAT-bridged dimer with one DAT ligand per Zn atom, and the DAT ligand provides a bridge between the two Zn metals. All Zn centers of (I) and (II) adopted a slightly distorted tetrahedral geometry. Both complexes contain a hexanuclear Zn(2)N(4) ring, but their ring structures are different. Complex (I) possesses a boat geometry, while complex (II) has a nearly planar structure. The Zn-bound chlorides of complex (I) form intermolecular N–H···Cl hydrogen bonds that link neighboring molecules. In complex (II), the O atoms in the nitrate groups are hydrogen-bonded to the DAT ligand via O···H–N linkages. Both complexes exhibit blue emissions in the solid state at ambient temperature. They were evaluated as anticancer agents in HeLa, NCCIT, and MCF-7 cancer cell lines, exhibiting promising anticancer activities. |
format | Online Article Text |
id | pubmed-9670724 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-96707242022-11-18 Triazole-Bridged Zinc Dinuclear Complexes: Mechanochemical Synthesis, Crystal Structure, and Biological Activity Park, Hee Sun Sun, Ruijing Lee, Eun Joo Kim, Jungho Hur, Nam Hwi ACS Omega [Image: see text] Two zinc (Zn) complexes, [Zn(2)(DAT)(2)Cl(4)] (I) and [Zn(2)(DAT)(2)(NO(3))(4)] (II), were prepared by grinding 3,5-diamino-1,2,4-triazole (C(2)H(5)N(5), DAT) with Zn precursors such as ZnCl(2) and Zn(NO(3))(2), respectively. This solid-state reaction gives the corresponding Zn complex as the sole product in over 99% yield. This mechanochemical method promotes the selective formation of Zn complexes different from those obtained using the conventional solution-based route. The crystal structures of the two complexes were analyzed by single-crystal X-ray diffraction. Complex (I) crystallizes in the monoclinic space group P2(1)/c, whereas complex (II) crystallizes in the triclinic space group P(1̅). Each complex is characterized by the presence of a characteristic DAT-bridged dimer with one DAT ligand per Zn atom, and the DAT ligand provides a bridge between the two Zn metals. All Zn centers of (I) and (II) adopted a slightly distorted tetrahedral geometry. Both complexes contain a hexanuclear Zn(2)N(4) ring, but their ring structures are different. Complex (I) possesses a boat geometry, while complex (II) has a nearly planar structure. The Zn-bound chlorides of complex (I) form intermolecular N–H···Cl hydrogen bonds that link neighboring molecules. In complex (II), the O atoms in the nitrate groups are hydrogen-bonded to the DAT ligand via O···H–N linkages. Both complexes exhibit blue emissions in the solid state at ambient temperature. They were evaluated as anticancer agents in HeLa, NCCIT, and MCF-7 cancer cell lines, exhibiting promising anticancer activities. American Chemical Society 2022-11-04 /pmc/articles/PMC9670724/ /pubmed/36406524 http://dx.doi.org/10.1021/acsomega.2c03715 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Park, Hee Sun Sun, Ruijing Lee, Eun Joo Kim, Jungho Hur, Nam Hwi Triazole-Bridged Zinc Dinuclear Complexes: Mechanochemical Synthesis, Crystal Structure, and Biological Activity |
title | Triazole-Bridged Zinc Dinuclear Complexes: Mechanochemical
Synthesis, Crystal Structure, and Biological Activity |
title_full | Triazole-Bridged Zinc Dinuclear Complexes: Mechanochemical
Synthesis, Crystal Structure, and Biological Activity |
title_fullStr | Triazole-Bridged Zinc Dinuclear Complexes: Mechanochemical
Synthesis, Crystal Structure, and Biological Activity |
title_full_unstemmed | Triazole-Bridged Zinc Dinuclear Complexes: Mechanochemical
Synthesis, Crystal Structure, and Biological Activity |
title_short | Triazole-Bridged Zinc Dinuclear Complexes: Mechanochemical
Synthesis, Crystal Structure, and Biological Activity |
title_sort | triazole-bridged zinc dinuclear complexes: mechanochemical
synthesis, crystal structure, and biological activity |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9670724/ https://www.ncbi.nlm.nih.gov/pubmed/36406524 http://dx.doi.org/10.1021/acsomega.2c03715 |
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