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Design, synthesis, characterization and biological studies of copper(II) complexes with 2‐aminobenzimidazole derivatives as biomimetic agents
Four novel copper(II) complexes of 2‐aminobenzimidazole derivatives (obtained from the Knoevenagel condensation of acetylacetone (obtained from acetylacetone and halogen‐substituted benzaldehydes) and 2‐aminobenzimidazole) were synthesized. They were characterized using elemental analysis, molar con...
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Published in: | Applied organometallic chemistry 2017-04, Vol.31 (4), p.np-n/a |
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description | Four novel copper(II) complexes of 2‐aminobenzimidazole derivatives (obtained from the Knoevenagel condensation of acetylacetone (obtained from acetylacetone and halogen‐substituted benzaldehydes) and 2‐aminobenzimidazole) were synthesized. They were characterized using elemental analysis, molar conductance measurements, and fast atom bombardment mass, Fourier transform infrared, NMR, UV–visible and electron paramagnetic resonance spectroscopies. On the basis of the spectral studies, a distorted square planar geometry was assigned for all the complexes. The antibacterial screening of the ligands and their complexes revealed that all the complexes had higher activities than the free ligands. Superoxide dismutase and antioxidant activities of the copper complexes were also studied. The shifts in ΔEp, E1/2, Ipc and Ipa values were explored for the interaction of the complexes with calf thymus DNA using the electrochemical technique.
Antibacterial screening revealed that all the complexes showed higher activities than the free ligands. Superoxide dismutase and antioxidant activities of the copper complexes were also studied. The shift in ΔEp, E1/2, Ipc and Ipa values were explored for the interaction of the complexes with calf thymus DNA using the electrochemical technique. |
doi_str_mv | 10.1002/aoc.3585 |
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Antibacterial screening revealed that all the complexes showed higher activities than the free ligands. Superoxide dismutase and antioxidant activities of the copper complexes were also studied. The shift in ΔEp, E1/2, Ipc and Ipa values were explored for the interaction of the complexes with calf thymus DNA using the electrochemical technique.</description><identifier>ISSN: 0268-2605</identifier><identifier>EISSN: 1099-0739</identifier><identifier>DOI: 10.1002/aoc.3585</identifier><language>eng</language><publisher>Chichester: Wiley Subscription Services, Inc</publisher><subject>Acetylacetone ; Aminobenzimidazole ; Antiinfectives and antibacterials ; Antimicrobial ; antioxidant ; Antioxidants ; Biomimetics ; Chemistry ; complexes ; Condensation ; Coordination compounds ; Copper ; Copper compounds ; Deoxyribonucleic acid ; Derivatives ; Distortion ; DNA ; DNA binding ; Electron bombardment ; Electron paramagnetic resonance ; Fourier analysis ; Fourier transforms ; Infrared spectroscopy ; Ligands ; NMR ; Nuclear magnetic resonance ; Resistance ; Schiff base ; Superoxide dismutase ; Synthesis</subject><ispartof>Applied organometallic chemistry, 2017-04, Vol.31 (4), p.np-n/a</ispartof><rights>Copyright © 2016 John Wiley & Sons, Ltd.</rights><rights>Copyright © 2017 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3265-1eb3825bb3bd754aac443913ac27bd4b52bd519b69dff5c486716a75433505f53</citedby><cites>FETCH-LOGICAL-c3265-1eb3825bb3bd754aac443913ac27bd4b52bd519b69dff5c486716a75433505f53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Joseph, J.</creatorcontrib><creatorcontrib>Suman, A.</creatorcontrib><creatorcontrib>Balakrishnan, Nisha</creatorcontrib><title>Design, synthesis, characterization and biological studies of copper(II) complexes with 2‐aminobenzimidazole derivatives as biomimetic agents</title><title>Applied organometallic chemistry</title><description>Four novel copper(II) complexes of 2‐aminobenzimidazole derivatives (obtained from the Knoevenagel condensation of acetylacetone (obtained from acetylacetone and halogen‐substituted benzaldehydes) and 2‐aminobenzimidazole) were synthesized. They were characterized using elemental analysis, molar conductance measurements, and fast atom bombardment mass, Fourier transform infrared, NMR, UV–visible and electron paramagnetic resonance spectroscopies. On the basis of the spectral studies, a distorted square planar geometry was assigned for all the complexes. The antibacterial screening of the ligands and their complexes revealed that all the complexes had higher activities than the free ligands. Superoxide dismutase and antioxidant activities of the copper complexes were also studied. The shifts in ΔEp, E1/2, Ipc and Ipa values were explored for the interaction of the complexes with calf thymus DNA using the electrochemical technique.
Antibacterial screening revealed that all the complexes showed higher activities than the free ligands. Superoxide dismutase and antioxidant activities of the copper complexes were also studied. The shift in ΔEp, E1/2, Ipc and Ipa values were explored for the interaction of the complexes with calf thymus DNA using the electrochemical technique.</description><subject>Acetylacetone</subject><subject>Aminobenzimidazole</subject><subject>Antiinfectives and antibacterials</subject><subject>Antimicrobial</subject><subject>antioxidant</subject><subject>Antioxidants</subject><subject>Biomimetics</subject><subject>Chemistry</subject><subject>complexes</subject><subject>Condensation</subject><subject>Coordination compounds</subject><subject>Copper</subject><subject>Copper compounds</subject><subject>Deoxyribonucleic acid</subject><subject>Derivatives</subject><subject>Distortion</subject><subject>DNA</subject><subject>DNA binding</subject><subject>Electron bombardment</subject><subject>Electron paramagnetic resonance</subject><subject>Fourier analysis</subject><subject>Fourier transforms</subject><subject>Infrared spectroscopy</subject><subject>Ligands</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Resistance</subject><subject>Schiff base</subject><subject>Superoxide dismutase</subject><subject>Synthesis</subject><issn>0268-2605</issn><issn>1099-0739</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp1kd1KHDEYhkNR6KqFXkKgJwqO5mcyMzmUrT8Lgif2OHzJZHYjM8k0mdXuHnkH9hp7JWa1UCh49L18PDy88CL0lZIzSgg7h2DOuGjEJzSjRMqC1FzuoRlhVVOwiojP6CClB0KIrGg5Qy_fbXJLf4rTxk-rnNMpNiuIYCYb3RYmFzwG32LtQh-WzkCP07RunU04dNiEcbTxeLE4yXEYe_sr_5_ctMLsz_NvGJwP2vqtG1wL29Bb3GbrY7Y-Zg7Szjq4wU7OYFhaP6UjtN9Bn-yXv_cQ_bi6vJ_fFLd314v5xW1hOKtEQa3mDRNac93WogQwZckl5WBYrdtSC6ZbQaWuZNt1wpRNVdMKMsm5IKIT_BAdv3vHGH6ubZrU4JKxfQ_ehnVStJHZR0tCM_rtP_QhrKPP7RSVjJSM1JT-E5oYUoq2U2N0A8SNokTtllF5GbVbJqPFO_rkerv5kFMXd_M3_hV5mpH6</recordid><startdate>201704</startdate><enddate>201704</enddate><creator>Joseph, J.</creator><creator>Suman, A.</creator><creator>Balakrishnan, Nisha</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>201704</creationdate><title>Design, synthesis, characterization and biological studies of copper(II) complexes with 2‐aminobenzimidazole derivatives as biomimetic agents</title><author>Joseph, J. ; Suman, A. ; Balakrishnan, Nisha</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3265-1eb3825bb3bd754aac443913ac27bd4b52bd519b69dff5c486716a75433505f53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Acetylacetone</topic><topic>Aminobenzimidazole</topic><topic>Antiinfectives and antibacterials</topic><topic>Antimicrobial</topic><topic>antioxidant</topic><topic>Antioxidants</topic><topic>Biomimetics</topic><topic>Chemistry</topic><topic>complexes</topic><topic>Condensation</topic><topic>Coordination compounds</topic><topic>Copper</topic><topic>Copper compounds</topic><topic>Deoxyribonucleic acid</topic><topic>Derivatives</topic><topic>Distortion</topic><topic>DNA</topic><topic>DNA binding</topic><topic>Electron bombardment</topic><topic>Electron paramagnetic resonance</topic><topic>Fourier analysis</topic><topic>Fourier transforms</topic><topic>Infrared spectroscopy</topic><topic>Ligands</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Resistance</topic><topic>Schiff base</topic><topic>Superoxide dismutase</topic><topic>Synthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Joseph, J.</creatorcontrib><creatorcontrib>Suman, A.</creatorcontrib><creatorcontrib>Balakrishnan, Nisha</creatorcontrib><collection>CrossRef</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Applied organometallic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Joseph, J.</au><au>Suman, A.</au><au>Balakrishnan, Nisha</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Design, synthesis, characterization and biological studies of copper(II) complexes with 2‐aminobenzimidazole derivatives as biomimetic agents</atitle><jtitle>Applied organometallic chemistry</jtitle><date>2017-04</date><risdate>2017</risdate><volume>31</volume><issue>4</issue><spage>np</spage><epage>n/a</epage><pages>np-n/a</pages><issn>0268-2605</issn><eissn>1099-0739</eissn><abstract>Four novel copper(II) complexes of 2‐aminobenzimidazole derivatives (obtained from the Knoevenagel condensation of acetylacetone (obtained from acetylacetone and halogen‐substituted benzaldehydes) and 2‐aminobenzimidazole) were synthesized. They were characterized using elemental analysis, molar conductance measurements, and fast atom bombardment mass, Fourier transform infrared, NMR, UV–visible and electron paramagnetic resonance spectroscopies. On the basis of the spectral studies, a distorted square planar geometry was assigned for all the complexes. The antibacterial screening of the ligands and their complexes revealed that all the complexes had higher activities than the free ligands. Superoxide dismutase and antioxidant activities of the copper complexes were also studied. The shifts in ΔEp, E1/2, Ipc and Ipa values were explored for the interaction of the complexes with calf thymus DNA using the electrochemical technique.
Antibacterial screening revealed that all the complexes showed higher activities than the free ligands. Superoxide dismutase and antioxidant activities of the copper complexes were also studied. The shift in ΔEp, E1/2, Ipc and Ipa values were explored for the interaction of the complexes with calf thymus DNA using the electrochemical technique.</abstract><cop>Chichester</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/aoc.3585</doi><tpages>9</tpages></addata></record> |
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subjects | Acetylacetone Aminobenzimidazole Antiinfectives and antibacterials Antimicrobial antioxidant Antioxidants Biomimetics Chemistry complexes Condensation Coordination compounds Copper Copper compounds Deoxyribonucleic acid Derivatives Distortion DNA DNA binding Electron bombardment Electron paramagnetic resonance Fourier analysis Fourier transforms Infrared spectroscopy Ligands NMR Nuclear magnetic resonance Resistance Schiff base Superoxide dismutase Synthesis |
title | Design, synthesis, characterization and biological studies of copper(II) complexes with 2‐aminobenzimidazole derivatives as biomimetic agents |
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