Copper(I) halide complexes of N-methylbenzothiazole-2-thione: Synthesis, structure, luminescence, antibacterial activity and interaction with DNA
The reactions of copper(I) halides, CuX (X=Cl, Br, I) with N-methylbenzothiazole-2-thione (mbtt), independent of the molar ration chosen (1:2 or 1:3), led to the formation of dinuclear complexes of the formula [CuX(mbtt)2]2, whereas the reactions of CuX and mbtt in the presence of two equivalents of...
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description | The reactions of copper(I) halides, CuX (X=Cl, Br, I) with N-methylbenzothiazole-2-thione (mbtt), independent of the molar ration chosen (1:2 or 1:3), led to the formation of dinuclear complexes of the formula [CuX(mbtt)2]2, whereas the reactions of CuX and mbtt in the presence of two equivalents of triphenylphosphine (PPh3) afforded mononuclear mixed-ligand complexes of the formula [CuX(PPh3)2(mbtt)]. The molecular structure of a representative compound from each of the two above types of complexes, namely [CuCl(mbtt)2]2 and [CuI(PPh3)2(mbtt)] have been established by single-crystal X-ray diffraction. The new complexes are strongly emissive both in the solid state and in solution. The complexes were also screened for antibacterial activity and their ability to interact with native calf thymus DNA (CT-DNA) in vitro. Both types of complexes showed significant activities against all the bacteria tested as compared to that of standard antibiotic ampicillin, however, the three mixed-ligand complexes including triphenylphosphane as ligand exhibited perceptibly stronger antibacterial activity than the three homoleptic ones possessing only the mbtt ligand. DNA electrophoretic mobility experiments showed that all complexes bind to CT-ds DNA resulting in high molecular weight complexes ending in DNA degradation.
N-methylbenzothiazole-2-thione as ligand in new dinuclear and mononuclear copper(I) halide complexes of composition [CuX(mbtt)2]2 and [CuX(mbtt)(PPh3)2] respectively, with remarkably high antimicrobial activity against several Gram-positive and Gram-negative microorganisms. [Display omitted]
► New copper(I) halide complexes containing N-methylbenzothiazole-2-thione as ligand. ► Intense room temperature luminescence both in the solid state and in solution. ► Remarcable antimicrobal activity against several microorganisms. |
doi_str_mv | 10.1016/j.jinorgbio.2013.01.001 |
format | Article |
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N-methylbenzothiazole-2-thione as ligand in new dinuclear and mononuclear copper(I) halide complexes of composition [CuX(mbtt)2]2 and [CuX(mbtt)(PPh3)2] respectively, with remarkably high antimicrobial activity against several Gram-positive and Gram-negative microorganisms. [Display omitted]
► New copper(I) halide complexes containing N-methylbenzothiazole-2-thione as ligand. ► Intense room temperature luminescence both in the solid state and in solution. ► Remarcable antimicrobal activity against several microorganisms.</description><identifier>ISSN: 0162-0134</identifier><identifier>EISSN: 1873-3344</identifier><identifier>DOI: 10.1016/j.jinorgbio.2013.01.001</identifier><identifier>PMID: 23376553</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Anti-Bacterial Agents - chemical synthesis ; Anti-Bacterial Agents - pharmacology ; Antimicrobial activity ; Benzothiazoles - chemistry ; Cations, Monovalent ; Cattle ; Coordination Complexes - chemical synthesis ; Coordination Complexes - pharmacology ; Copper - chemistry ; Copper(I) ; Crystal structures ; Crystallography, X-Ray ; DNA - chemistry ; DNA interaction ; Electrophoretic Mobility Shift Assay ; Gram-Negative Bacteria - drug effects ; Gram-Negative Bacteria - growth & development ; Gram-Positive Bacteria - drug effects ; Gram-Positive Bacteria - growth & development ; Halogens - chemistry ; Luminescence ; Microbial Sensitivity Tests ; Models, Chemical ; N-methylbenzothiazole-2-thione ; Organophosphorus Compounds - chemistry</subject><ispartof>Journal of inorganic biochemistry, 2013-04, Vol.121, p.121-128</ispartof><rights>2013 Elsevier Inc.</rights><rights>Copyright © 2013 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c404t-d95ba2897aa7941d84603b6a0734e505dfea7514daa31cdaf8dd1d1bda127ceb3</citedby><cites>FETCH-LOGICAL-c404t-d95ba2897aa7941d84603b6a0734e505dfea7514daa31cdaf8dd1d1bda127ceb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jinorgbio.2013.01.001$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23376553$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tsiaggali, M.A.</creatorcontrib><creatorcontrib>Andreadou, E.G.</creatorcontrib><creatorcontrib>Hatzidimitriou, A.G.</creatorcontrib><creatorcontrib>Pantazaki, A.A.</creatorcontrib><creatorcontrib>Aslanidis, P.</creatorcontrib><title>Copper(I) halide complexes of N-methylbenzothiazole-2-thione: Synthesis, structure, luminescence, antibacterial activity and interaction with DNA</title><title>Journal of inorganic biochemistry</title><addtitle>J Inorg Biochem</addtitle><description>The reactions of copper(I) halides, CuX (X=Cl, Br, I) with N-methylbenzothiazole-2-thione (mbtt), independent of the molar ration chosen (1:2 or 1:3), led to the formation of dinuclear complexes of the formula [CuX(mbtt)2]2, whereas the reactions of CuX and mbtt in the presence of two equivalents of triphenylphosphine (PPh3) afforded mononuclear mixed-ligand complexes of the formula [CuX(PPh3)2(mbtt)]. The molecular structure of a representative compound from each of the two above types of complexes, namely [CuCl(mbtt)2]2 and [CuI(PPh3)2(mbtt)] have been established by single-crystal X-ray diffraction. The new complexes are strongly emissive both in the solid state and in solution. The complexes were also screened for antibacterial activity and their ability to interact with native calf thymus DNA (CT-DNA) in vitro. Both types of complexes showed significant activities against all the bacteria tested as compared to that of standard antibiotic ampicillin, however, the three mixed-ligand complexes including triphenylphosphane as ligand exhibited perceptibly stronger antibacterial activity than the three homoleptic ones possessing only the mbtt ligand. DNA electrophoretic mobility experiments showed that all complexes bind to CT-ds DNA resulting in high molecular weight complexes ending in DNA degradation.
N-methylbenzothiazole-2-thione as ligand in new dinuclear and mononuclear copper(I) halide complexes of composition [CuX(mbtt)2]2 and [CuX(mbtt)(PPh3)2] respectively, with remarkably high antimicrobial activity against several Gram-positive and Gram-negative microorganisms. [Display omitted]
► New copper(I) halide complexes containing N-methylbenzothiazole-2-thione as ligand. ► Intense room temperature luminescence both in the solid state and in solution. ► Remarcable antimicrobal activity against several microorganisms.</description><subject>Animals</subject><subject>Anti-Bacterial Agents - chemical synthesis</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Antimicrobial activity</subject><subject>Benzothiazoles - chemistry</subject><subject>Cations, Monovalent</subject><subject>Cattle</subject><subject>Coordination Complexes - chemical synthesis</subject><subject>Coordination Complexes - pharmacology</subject><subject>Copper - chemistry</subject><subject>Copper(I)</subject><subject>Crystal structures</subject><subject>Crystallography, X-Ray</subject><subject>DNA - chemistry</subject><subject>DNA interaction</subject><subject>Electrophoretic Mobility Shift Assay</subject><subject>Gram-Negative Bacteria - drug effects</subject><subject>Gram-Negative Bacteria - growth & development</subject><subject>Gram-Positive Bacteria - drug effects</subject><subject>Gram-Positive Bacteria - growth & development</subject><subject>Halogens - chemistry</subject><subject>Luminescence</subject><subject>Microbial Sensitivity Tests</subject><subject>Models, Chemical</subject><subject>N-methylbenzothiazole-2-thione</subject><subject>Organophosphorus Compounds - chemistry</subject><issn>0162-0134</issn><issn>1873-3344</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc9u1DAQxi1ERZfCK4CPRWqCHTtxlttqy59KVTkAZ8uxJ8SrxA62U7p9C94Yr7bttaeZ-fybGWs-hN5TUlJCm4-7cmedD78768uKUFYSWhJCX6AVbQUrGOP8JVplsiryKz9Fr2PcEULqmotX6LRiTDR1zVbo39bPM4Tzqw94UKM1gLWf5hHuIGLf45tigjTsxw7cvU-DVfd-hKIqcuodfMI_9i4NEG28wDGFRaclwAUel8k6iBqczpVyyXZKJwhWjTgn9tamfZYNti6rB8U7_NemAV_ebN6gk16NEd4-xDP068vnn9tvxfX3r1fbzXWhOeGpMOu6U1W7FkqJNaem5Q1hXaOIYBxqUpselKgpN0oxqo3qW2OooZ1RtBIaOnaGzo9z5-D_LBCTnGz-8jgqB36JkuYhjK8r1j6PMtqQumEtz6g4ojr4GAP0cg52UmEvKZEH6-ROPlknD9ZJQmW2Lne-e1iydBOYp75HrzKwOQKQr3JrIcio7eHExgbQSRpvn13yH_vDsZA</recordid><startdate>201304</startdate><enddate>201304</enddate><creator>Tsiaggali, M.A.</creator><creator>Andreadou, E.G.</creator><creator>Hatzidimitriou, A.G.</creator><creator>Pantazaki, A.A.</creator><creator>Aslanidis, P.</creator><general>Elsevier Inc</general><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><scope>7QL</scope><scope>7T7</scope><scope>7TM</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>201304</creationdate><title>Copper(I) halide complexes of N-methylbenzothiazole-2-thione: Synthesis, structure, luminescence, antibacterial activity and interaction with DNA</title><author>Tsiaggali, M.A. ; Andreadou, E.G. ; Hatzidimitriou, A.G. ; Pantazaki, A.A. ; Aslanidis, P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c404t-d95ba2897aa7941d84603b6a0734e505dfea7514daa31cdaf8dd1d1bda127ceb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animals</topic><topic>Anti-Bacterial Agents - chemical synthesis</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Antimicrobial activity</topic><topic>Benzothiazoles - chemistry</topic><topic>Cations, Monovalent</topic><topic>Cattle</topic><topic>Coordination Complexes - chemical synthesis</topic><topic>Coordination Complexes - pharmacology</topic><topic>Copper - chemistry</topic><topic>Copper(I)</topic><topic>Crystal structures</topic><topic>Crystallography, X-Ray</topic><topic>DNA - chemistry</topic><topic>DNA interaction</topic><topic>Electrophoretic Mobility Shift Assay</topic><topic>Gram-Negative Bacteria - drug effects</topic><topic>Gram-Negative Bacteria - growth & development</topic><topic>Gram-Positive Bacteria - drug effects</topic><topic>Gram-Positive Bacteria - growth & development</topic><topic>Halogens - chemistry</topic><topic>Luminescence</topic><topic>Microbial Sensitivity Tests</topic><topic>Models, Chemical</topic><topic>N-methylbenzothiazole-2-thione</topic><topic>Organophosphorus Compounds - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tsiaggali, M.A.</creatorcontrib><creatorcontrib>Andreadou, E.G.</creatorcontrib><creatorcontrib>Hatzidimitriou, A.G.</creatorcontrib><creatorcontrib>Pantazaki, A.A.</creatorcontrib><creatorcontrib>Aslanidis, P.</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><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Journal of inorganic biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tsiaggali, M.A.</au><au>Andreadou, E.G.</au><au>Hatzidimitriou, A.G.</au><au>Pantazaki, A.A.</au><au>Aslanidis, P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Copper(I) halide complexes of N-methylbenzothiazole-2-thione: Synthesis, structure, luminescence, antibacterial activity and interaction with DNA</atitle><jtitle>Journal of inorganic biochemistry</jtitle><addtitle>J Inorg Biochem</addtitle><date>2013-04</date><risdate>2013</risdate><volume>121</volume><spage>121</spage><epage>128</epage><pages>121-128</pages><issn>0162-0134</issn><eissn>1873-3344</eissn><abstract>The reactions of copper(I) halides, CuX (X=Cl, Br, I) with N-methylbenzothiazole-2-thione (mbtt), independent of the molar ration chosen (1:2 or 1:3), led to the formation of dinuclear complexes of the formula [CuX(mbtt)2]2, whereas the reactions of CuX and mbtt in the presence of two equivalents of triphenylphosphine (PPh3) afforded mononuclear mixed-ligand complexes of the formula [CuX(PPh3)2(mbtt)]. The molecular structure of a representative compound from each of the two above types of complexes, namely [CuCl(mbtt)2]2 and [CuI(PPh3)2(mbtt)] have been established by single-crystal X-ray diffraction. The new complexes are strongly emissive both in the solid state and in solution. The complexes were also screened for antibacterial activity and their ability to interact with native calf thymus DNA (CT-DNA) in vitro. Both types of complexes showed significant activities against all the bacteria tested as compared to that of standard antibiotic ampicillin, however, the three mixed-ligand complexes including triphenylphosphane as ligand exhibited perceptibly stronger antibacterial activity than the three homoleptic ones possessing only the mbtt ligand. DNA electrophoretic mobility experiments showed that all complexes bind to CT-ds DNA resulting in high molecular weight complexes ending in DNA degradation.
N-methylbenzothiazole-2-thione as ligand in new dinuclear and mononuclear copper(I) halide complexes of composition [CuX(mbtt)2]2 and [CuX(mbtt)(PPh3)2] respectively, with remarkably high antimicrobial activity against several Gram-positive and Gram-negative microorganisms. [Display omitted]
► New copper(I) halide complexes containing N-methylbenzothiazole-2-thione as ligand. ► Intense room temperature luminescence both in the solid state and in solution. ► Remarcable antimicrobal activity against several microorganisms.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>23376553</pmid><doi>10.1016/j.jinorgbio.2013.01.001</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Anti-Bacterial Agents - chemical synthesis Anti-Bacterial Agents - pharmacology Antimicrobial activity Benzothiazoles - chemistry Cations, Monovalent Cattle Coordination Complexes - chemical synthesis Coordination Complexes - pharmacology Copper - chemistry Copper(I) Crystal structures Crystallography, X-Ray DNA - chemistry DNA interaction Electrophoretic Mobility Shift Assay Gram-Negative Bacteria - drug effects Gram-Negative Bacteria - growth & development Gram-Positive Bacteria - drug effects Gram-Positive Bacteria - growth & development Halogens - chemistry Luminescence Microbial Sensitivity Tests Models, Chemical N-methylbenzothiazole-2-thione Organophosphorus Compounds - chemistry |
title | Copper(I) halide complexes of N-methylbenzothiazole-2-thione: Synthesis, structure, luminescence, antibacterial activity and interaction with DNA |
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