New Ni(II)-sulfonamide complexes: synthesis, structural characterization and antibacterial properties. X-ray diffraction of [Ni(sulfisoxazole)2(H2O)4].2H2O and [Ni(sulfapyridine)2]
The synthesis, structural characterization, voltammetric experiments and antibacterial activity of [Ni(sulfisoxazole)(2)(H(2)O)(4)].2H(2)O and [Ni(sulfapyridine)(2)] were studied and compared with similar previously reported copper complexes. [Ni(sulfisoxazole)(2)(H(2)O)(4)].2H(2)O crystallized in a...
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Veröffentlicht in: | Journal of inorganic biochemistry 2008-02, Vol.102 (2), p.285-292 |
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creator | Mondelli, Melina Bruné, Verónica Borthagaray, Graciela Ellena, Javier Nascimento, Otaciro R Leite, Clarice Q Batista, Alzir A Torre, María H |
description | The synthesis, structural characterization, voltammetric experiments and antibacterial activity of [Ni(sulfisoxazole)(2)(H(2)O)(4)].2H(2)O and [Ni(sulfapyridine)(2)] were studied and compared with similar previously reported copper complexes. [Ni(sulfisoxazole)(2)(H(2)O)(4)].2H(2)O crystallized in a monoclinic system, space group C2/c where the nickel ion was in a slightly distorted octahedral environment, coordinated with two sulfisoxazole molecules through the heterocyclic nitrogen and four water molecules. [Ni(sulfapyridine)(2)] crystallized in a orthorhombic crystal system, space group Pnab. The nickel ion was in a distorted octahedral environment, coordinated by two aryl amine N from two sulfonamides acting as monodentate ligands and four N atoms (two sulfonamidic N and two heterocyclic N) from two different sulfonamide molecules acting as bidentate ligands. Differential pulse voltammograms were recorded showing irreversible peaks at 1040 and 1070 mV, respectively, attributed to Ni(II)/Ni(III) process. [Ni(sulfisoxazole)(2)(H(2)O)(4)].2H(2)O and [Ni(sulfapyridine)(2)] presented different antibacterial behavior against Staphylococcus aureus and Escherichia coli from the similar copper complexes and they were inactive against Mycobacterium tuberculosis. |
doi_str_mv | 10.1016/j.jinorgbio.2007.09.001 |
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X-ray diffraction of [Ni(sulfisoxazole)2(H2O)4].2H2O and [Ni(sulfapyridine)2]</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Mondelli, Melina ; Bruné, Verónica ; Borthagaray, Graciela ; Ellena, Javier ; Nascimento, Otaciro R ; Leite, Clarice Q ; Batista, Alzir A ; Torre, María H</creator><creatorcontrib>Mondelli, Melina ; Bruné, Verónica ; Borthagaray, Graciela ; Ellena, Javier ; Nascimento, Otaciro R ; Leite, Clarice Q ; Batista, Alzir A ; Torre, María H</creatorcontrib><description>The synthesis, structural characterization, voltammetric experiments and antibacterial activity of [Ni(sulfisoxazole)(2)(H(2)O)(4)].2H(2)O and [Ni(sulfapyridine)(2)] were studied and compared with similar previously reported copper complexes. [Ni(sulfisoxazole)(2)(H(2)O)(4)].2H(2)O crystallized in a monoclinic system, space group C2/c where the nickel ion was in a slightly distorted octahedral environment, coordinated with two sulfisoxazole molecules through the heterocyclic nitrogen and four water molecules. [Ni(sulfapyridine)(2)] crystallized in a orthorhombic crystal system, space group Pnab. The nickel ion was in a distorted octahedral environment, coordinated by two aryl amine N from two sulfonamides acting as monodentate ligands and four N atoms (two sulfonamidic N and two heterocyclic N) from two different sulfonamide molecules acting as bidentate ligands. Differential pulse voltammograms were recorded showing irreversible peaks at 1040 and 1070 mV, respectively, attributed to Ni(II)/Ni(III) process. [Ni(sulfisoxazole)(2)(H(2)O)(4)].2H(2)O and [Ni(sulfapyridine)(2)] presented different antibacterial behavior against Staphylococcus aureus and Escherichia coli from the similar copper complexes and they were inactive against Mycobacterium tuberculosis.</description><identifier>ISSN: 0162-0134</identifier><identifier>DOI: 10.1016/j.jinorgbio.2007.09.001</identifier><identifier>PMID: 17976730</identifier><language>eng</language><publisher>United States</publisher><subject>Anti-Bacterial Agents - chemical synthesis ; Anti-Bacterial Agents - chemistry ; Anti-Bacterial Agents - pharmacology ; Bacteria - drug effects ; Crystallography, X-Ray ; Escherichia coli - drug effects ; Mycobacterium tuberculosis - drug effects ; Nickel - chemistry ; Organometallic Compounds - chemical synthesis ; Organometallic Compounds - chemistry ; Organometallic Compounds - pharmacology ; Staphylococcus aureus - drug effects ; Sulfapyridine - chemical synthesis ; Sulfapyridine - chemistry ; Sulfapyridine - pharmacology ; Sulfisoxazole - chemical synthesis ; Sulfisoxazole - chemistry ; Sulfisoxazole - pharmacology ; Sulfonamides - chemical synthesis ; Sulfonamides - chemistry ; Sulfonamides - pharmacology</subject><ispartof>Journal of inorganic biochemistry, 2008-02, Vol.102 (2), p.285-292</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c377t-d220003f1bf2b1d8815562ec6b31933779fe20b69dcd31ee1e5c78dda6139e243</citedby><cites>FETCH-LOGICAL-c377t-d220003f1bf2b1d8815562ec6b31933779fe20b69dcd31ee1e5c78dda6139e243</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17976730$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mondelli, Melina</creatorcontrib><creatorcontrib>Bruné, Verónica</creatorcontrib><creatorcontrib>Borthagaray, Graciela</creatorcontrib><creatorcontrib>Ellena, Javier</creatorcontrib><creatorcontrib>Nascimento, Otaciro R</creatorcontrib><creatorcontrib>Leite, Clarice Q</creatorcontrib><creatorcontrib>Batista, Alzir A</creatorcontrib><creatorcontrib>Torre, María H</creatorcontrib><title>New Ni(II)-sulfonamide complexes: synthesis, structural characterization and antibacterial properties. X-ray diffraction of [Ni(sulfisoxazole)2(H2O)4].2H2O and [Ni(sulfapyridine)2]</title><title>Journal of inorganic biochemistry</title><addtitle>J Inorg Biochem</addtitle><description>The synthesis, structural characterization, voltammetric experiments and antibacterial activity of [Ni(sulfisoxazole)(2)(H(2)O)(4)].2H(2)O and [Ni(sulfapyridine)(2)] were studied and compared with similar previously reported copper complexes. [Ni(sulfisoxazole)(2)(H(2)O)(4)].2H(2)O crystallized in a monoclinic system, space group C2/c where the nickel ion was in a slightly distorted octahedral environment, coordinated with two sulfisoxazole molecules through the heterocyclic nitrogen and four water molecules. [Ni(sulfapyridine)(2)] crystallized in a orthorhombic crystal system, space group Pnab. The nickel ion was in a distorted octahedral environment, coordinated by two aryl amine N from two sulfonamides acting as monodentate ligands and four N atoms (two sulfonamidic N and two heterocyclic N) from two different sulfonamide molecules acting as bidentate ligands. Differential pulse voltammograms were recorded showing irreversible peaks at 1040 and 1070 mV, respectively, attributed to Ni(II)/Ni(III) process. [Ni(sulfisoxazole)(2)(H(2)O)(4)].2H(2)O and [Ni(sulfapyridine)(2)] presented different antibacterial behavior against Staphylococcus aureus and Escherichia coli from the similar copper complexes and they were inactive against Mycobacterium tuberculosis.</description><subject>Anti-Bacterial Agents - chemical synthesis</subject><subject>Anti-Bacterial Agents - chemistry</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Bacteria - drug effects</subject><subject>Crystallography, X-Ray</subject><subject>Escherichia coli - drug effects</subject><subject>Mycobacterium tuberculosis - drug effects</subject><subject>Nickel - chemistry</subject><subject>Organometallic Compounds - chemical synthesis</subject><subject>Organometallic Compounds - chemistry</subject><subject>Organometallic Compounds - pharmacology</subject><subject>Staphylococcus aureus - drug effects</subject><subject>Sulfapyridine - chemical synthesis</subject><subject>Sulfapyridine - chemistry</subject><subject>Sulfapyridine - pharmacology</subject><subject>Sulfisoxazole - chemical synthesis</subject><subject>Sulfisoxazole - chemistry</subject><subject>Sulfisoxazole - pharmacology</subject><subject>Sulfonamides - chemical synthesis</subject><subject>Sulfonamides - chemistry</subject><subject>Sulfonamides - pharmacology</subject><issn>0162-0134</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkd1q3DAQhXWR0Py0r5DoqmShdvWztta5C6FtFkJy00KhBCFLo0SLbbmSTLN5rj5g5e42vRgGRt-Zw-ggdE5JSQmtP27KjRt8eGydLxkhoiRNSQg9QMf5lRWE8uUROolxQwipqqV4g46oaEQtODlGv-_gF75zF-v1oohTZ_2gemcAa9-PHTxDvMRxO6QniC5-wDGFSacpqA7rJxWUThDci0rOD1gNJldy7W6akTH4EUJyEEv8vQhqi42zdlbNvLf4RzaeTV30z-rFd7BgFzfsfrF8KFnuf1f-Y9S4Dc64ITMPb9GhVV2Ed_t-ir59_vT1-qa4vf-yvr66LTQXIhWG5e8g3NLWspaa1YpWVc1A1y2nDc9IY4GRtm6MNpwCUKi0WBmjasobYEt-it7v9uZLfk4Qk-xd1NB1agA_RSkIow0VNINiB-rgYwxg5Rhcr8JWUiLnkORGvoYk55AkaWQOKSvP9hZT24P5r9snxP8AmVGVvg</recordid><startdate>200802</startdate><enddate>200802</enddate><creator>Mondelli, Melina</creator><creator>Bruné, Verónica</creator><creator>Borthagaray, Graciela</creator><creator>Ellena, Javier</creator><creator>Nascimento, Otaciro R</creator><creator>Leite, Clarice Q</creator><creator>Batista, Alzir A</creator><creator>Torre, María H</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>200802</creationdate><title>New Ni(II)-sulfonamide complexes: synthesis, structural characterization and antibacterial properties. X-ray diffraction of [Ni(sulfisoxazole)2(H2O)4].2H2O and [Ni(sulfapyridine)2]</title><author>Mondelli, Melina ; Bruné, Verónica ; Borthagaray, Graciela ; Ellena, Javier ; Nascimento, Otaciro R ; Leite, Clarice Q ; Batista, Alzir A ; Torre, María H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c377t-d220003f1bf2b1d8815562ec6b31933779fe20b69dcd31ee1e5c78dda6139e243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Anti-Bacterial Agents - chemical synthesis</topic><topic>Anti-Bacterial Agents - chemistry</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Bacteria - drug effects</topic><topic>Crystallography, X-Ray</topic><topic>Escherichia coli - drug effects</topic><topic>Mycobacterium tuberculosis - drug effects</topic><topic>Nickel - chemistry</topic><topic>Organometallic Compounds - chemical synthesis</topic><topic>Organometallic Compounds - chemistry</topic><topic>Organometallic Compounds - pharmacology</topic><topic>Staphylococcus aureus - drug effects</topic><topic>Sulfapyridine - chemical synthesis</topic><topic>Sulfapyridine - chemistry</topic><topic>Sulfapyridine - pharmacology</topic><topic>Sulfisoxazole - chemical synthesis</topic><topic>Sulfisoxazole - chemistry</topic><topic>Sulfisoxazole - pharmacology</topic><topic>Sulfonamides - chemical synthesis</topic><topic>Sulfonamides - chemistry</topic><topic>Sulfonamides - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mondelli, Melina</creatorcontrib><creatorcontrib>Bruné, Verónica</creatorcontrib><creatorcontrib>Borthagaray, Graciela</creatorcontrib><creatorcontrib>Ellena, Javier</creatorcontrib><creatorcontrib>Nascimento, Otaciro R</creatorcontrib><creatorcontrib>Leite, Clarice Q</creatorcontrib><creatorcontrib>Batista, Alzir A</creatorcontrib><creatorcontrib>Torre, María H</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of inorganic biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mondelli, Melina</au><au>Bruné, Verónica</au><au>Borthagaray, Graciela</au><au>Ellena, Javier</au><au>Nascimento, Otaciro R</au><au>Leite, Clarice Q</au><au>Batista, Alzir A</au><au>Torre, María H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>New Ni(II)-sulfonamide complexes: synthesis, structural characterization and antibacterial properties. X-ray diffraction of [Ni(sulfisoxazole)2(H2O)4].2H2O and [Ni(sulfapyridine)2]</atitle><jtitle>Journal of inorganic biochemistry</jtitle><addtitle>J Inorg Biochem</addtitle><date>2008-02</date><risdate>2008</risdate><volume>102</volume><issue>2</issue><spage>285</spage><epage>292</epage><pages>285-292</pages><issn>0162-0134</issn><abstract>The synthesis, structural characterization, voltammetric experiments and antibacterial activity of [Ni(sulfisoxazole)(2)(H(2)O)(4)].2H(2)O and [Ni(sulfapyridine)(2)] were studied and compared with similar previously reported copper complexes. [Ni(sulfisoxazole)(2)(H(2)O)(4)].2H(2)O crystallized in a monoclinic system, space group C2/c where the nickel ion was in a slightly distorted octahedral environment, coordinated with two sulfisoxazole molecules through the heterocyclic nitrogen and four water molecules. [Ni(sulfapyridine)(2)] crystallized in a orthorhombic crystal system, space group Pnab. The nickel ion was in a distorted octahedral environment, coordinated by two aryl amine N from two sulfonamides acting as monodentate ligands and four N atoms (two sulfonamidic N and two heterocyclic N) from two different sulfonamide molecules acting as bidentate ligands. Differential pulse voltammograms were recorded showing irreversible peaks at 1040 and 1070 mV, respectively, attributed to Ni(II)/Ni(III) process. [Ni(sulfisoxazole)(2)(H(2)O)(4)].2H(2)O and [Ni(sulfapyridine)(2)] presented different antibacterial behavior against Staphylococcus aureus and Escherichia coli from the similar copper complexes and they were inactive against Mycobacterium tuberculosis.</abstract><cop>United States</cop><pmid>17976730</pmid><doi>10.1016/j.jinorgbio.2007.09.001</doi><tpages>8</tpages></addata></record> |
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subjects | Anti-Bacterial Agents - chemical synthesis Anti-Bacterial Agents - chemistry Anti-Bacterial Agents - pharmacology Bacteria - drug effects Crystallography, X-Ray Escherichia coli - drug effects Mycobacterium tuberculosis - drug effects Nickel - chemistry Organometallic Compounds - chemical synthesis Organometallic Compounds - chemistry Organometallic Compounds - pharmacology Staphylococcus aureus - drug effects Sulfapyridine - chemical synthesis Sulfapyridine - chemistry Sulfapyridine - pharmacology Sulfisoxazole - chemical synthesis Sulfisoxazole - chemistry Sulfisoxazole - pharmacology Sulfonamides - chemical synthesis Sulfonamides - chemistry Sulfonamides - pharmacology |
title | New Ni(II)-sulfonamide complexes: synthesis, structural characterization and antibacterial properties. X-ray diffraction of [Ni(sulfisoxazole)2(H2O)4].2H2O and [Ni(sulfapyridine)2] |
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