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Highly Selective and Sensitive Dual Channel New Schiff base Chemosensor based on 5‐bromo‐2‐hydroxybenzaldehyde and its Co(II), Ni(II), Cu(II) and Zn(II) Complexes ‐ Synthesis, Spectral and Theoretical characterization and Pharmacological applications
A new Schiff base N,N’‐Bis(5‐Bromosalicylidine)‐1,8‐diaminonaphthalene (BBSDN) and its Co(II),Ni(II),Cu(II) and Zn(II) complexes were synthesized. All the compounds were characterized by various spectral studies (IR, UV, 1H NMR, 13C NMR and EI‐Mass) and DFT calculations. Conductance measurements, ma...
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Published in: | Vietnam journal of chemistry 2023-08, Vol.61 (4), p.429-444 |
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creator | Santhi, Sambamoorthy Renganathan, Rajalingam Amala, Subbiah Suganya, Gobalakrishnan Abinaya, Karikalan |
description | A new Schiff base N,N’‐Bis(5‐Bromosalicylidine)‐1,8‐diaminonaphthalene (BBSDN) and its Co(II),Ni(II),Cu(II) and Zn(II) complexes were synthesized. All the compounds were characterized by various spectral studies (IR, UV, 1H NMR, 13C NMR and EI‐Mass) and DFT calculations. Conductance measurements, magnetic study and metal estimation studies were performed for the complexes to establish the structure. Thermal studies were done to account for the coordination of water molecules. Redox property of the synthesized complexes was established by Cyclic Voltammetry studies. Synthesized compounds were screened against fungal and bacterial pathogens and in most of the cases the complexes were found to be more active than the Schiff base. MIC value for copper and zinc complexes against the fungal pathogen Candida albicans are determined as 25 ppm and 10 ppm respectively. Metal ion pertinency of the Schiff base was investigated by absorption and fluorescence methods and was found to be highly selective and sensitive for the detection of Cu(II) ion. Mode of interaction has been proved through 1H NMR titrations and the interaction is explained as due to CHEQ mechanism. Stability constant of the complex formed during the detection process was determined by Benesi‐Hildebrand plot. Detection limit was computed as 1.464×10‐6M. The chemosensor property of the Schiff base is applied in bioimaging studies on HeLa cell lines. |
doi_str_mv | 10.1002/vjch.202200150 |
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All the compounds were characterized by various spectral studies (IR, UV, 1H NMR, 13C NMR and EI‐Mass) and DFT calculations. Conductance measurements, magnetic study and metal estimation studies were performed for the complexes to establish the structure. Thermal studies were done to account for the coordination of water molecules. Redox property of the synthesized complexes was established by Cyclic Voltammetry studies. Synthesized compounds were screened against fungal and bacterial pathogens and in most of the cases the complexes were found to be more active than the Schiff base. MIC value for copper and zinc complexes against the fungal pathogen Candida albicans are determined as 25 ppm and 10 ppm respectively. Metal ion pertinency of the Schiff base was investigated by absorption and fluorescence methods and was found to be highly selective and sensitive for the detection of Cu(II) ion. Mode of interaction has been proved through 1H NMR titrations and the interaction is explained as due to CHEQ mechanism. Stability constant of the complex formed during the detection process was determined by Benesi‐Hildebrand plot. Detection limit was computed as 1.464×10‐6M. The chemosensor property of the Schiff base is applied in bioimaging studies on HeLa cell lines.</description><identifier>ISSN: 0866-7144</identifier><identifier>ISSN: 2572-8288</identifier><identifier>EISSN: 2572-8288</identifier><identifier>DOI: 10.1002/vjch.202200150</identifier><language>eng</language><publisher>Weinheim: WILEY‐VCH Verlag GmbH & Co. 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All the compounds were characterized by various spectral studies (IR, UV, 1H NMR, 13C NMR and EI‐Mass) and DFT calculations. Conductance measurements, magnetic study and metal estimation studies were performed for the complexes to establish the structure. Thermal studies were done to account for the coordination of water molecules. Redox property of the synthesized complexes was established by Cyclic Voltammetry studies. Synthesized compounds were screened against fungal and bacterial pathogens and in most of the cases the complexes were found to be more active than the Schiff base. MIC value for copper and zinc complexes against the fungal pathogen Candida albicans are determined as 25 ppm and 10 ppm respectively. Metal ion pertinency of the Schiff base was investigated by absorption and fluorescence methods and was found to be highly selective and sensitive for the detection of Cu(II) ion. Mode of interaction has been proved through 1H NMR titrations and the interaction is explained as due to CHEQ mechanism. Stability constant of the complex formed during the detection process was determined by Benesi‐Hildebrand plot. Detection limit was computed as 1.464×10‐6M. The chemosensor property of the Schiff base is applied in bioimaging studies on HeLa cell lines.</description><subject>bioimaging</subject><subject>chemosensor</subject><subject>coordination chemistry</subject><subject>Schiff base</subject><subject>transition metal complexes</subject><issn>0866-7144</issn><issn>2572-8288</issn><issn>2572-8288</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNqFUU1v1DAQDRVIrEqvnH0EqVkcO5uPIwqFXVQVpF1x4BJN7HHjyokjO_1IT_wEfmN_SZ0sgiMH68178954pImitwldJ5SyD3c3ol0zyhilyYaeRCu2yVlcsKJ4Ga1okWVxnqTp6-jM-xsaPEXGOU1WL062-ro1E9mjQTHqOyTQy8B6rxf26RYMqVroezTkCu_JXrRaKdKAx6BjZ33wWrcIktiebJ5-_W6c7WxAFl47SWcfpgb7RzASAz3-oUdPKvtut3t_Tq70EavbGZf2z34pK9sNBh_QkzCK7Kd-bNFrf072Q9jXheVm86FF63DUInDRggMxotOPMOqw0Gz4HsQOhDX2ejHBMJhQzH3_JnqlwHg8-4On0eHzxaHaxpffvuyqj5exYEVKYy5lQzHFtOSQC8VTWjaNUJBtZFAAMFW0ySRSJXNeiIKXVJUl8ECyLJf8NFofxwpnvXeo6sHpDtxUJ7Seb1jPN6z_3jAEymPgXhuc_uOuf3yttv-yz2M1p7Q</recordid><startdate>202308</startdate><enddate>202308</enddate><creator>Santhi, Sambamoorthy</creator><creator>Renganathan, Rajalingam</creator><creator>Amala, Subbiah</creator><creator>Suganya, Gobalakrishnan</creator><creator>Abinaya, Karikalan</creator><general>WILEY‐VCH Verlag GmbH & Co. KGaA</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>202308</creationdate><title>Highly Selective and Sensitive Dual Channel New Schiff base Chemosensor based on 5‐bromo‐2‐hydroxybenzaldehyde and its Co(II), Ni(II), Cu(II) and Zn(II) Complexes ‐ Synthesis, Spectral and Theoretical characterization and Pharmacological applications</title><author>Santhi, Sambamoorthy ; Renganathan, Rajalingam ; Amala, Subbiah ; Suganya, Gobalakrishnan ; Abinaya, Karikalan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2840-3ddb0e4e493a7cf3409bbcfa65d93aaae4f0b6de0fd738c8390f99a3738667d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>bioimaging</topic><topic>chemosensor</topic><topic>coordination chemistry</topic><topic>Schiff base</topic><topic>transition metal complexes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Santhi, Sambamoorthy</creatorcontrib><creatorcontrib>Renganathan, Rajalingam</creatorcontrib><creatorcontrib>Amala, Subbiah</creatorcontrib><creatorcontrib>Suganya, Gobalakrishnan</creatorcontrib><creatorcontrib>Abinaya, Karikalan</creatorcontrib><collection>CrossRef</collection><jtitle>Vietnam journal of chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Santhi, Sambamoorthy</au><au>Renganathan, Rajalingam</au><au>Amala, Subbiah</au><au>Suganya, Gobalakrishnan</au><au>Abinaya, Karikalan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Highly Selective and Sensitive Dual Channel New Schiff base Chemosensor based on 5‐bromo‐2‐hydroxybenzaldehyde and its Co(II), Ni(II), Cu(II) and Zn(II) Complexes ‐ Synthesis, Spectral and Theoretical characterization and Pharmacological applications</atitle><jtitle>Vietnam journal of chemistry</jtitle><date>2023-08</date><risdate>2023</risdate><volume>61</volume><issue>4</issue><spage>429</spage><epage>444</epage><pages>429-444</pages><issn>0866-7144</issn><issn>2572-8288</issn><eissn>2572-8288</eissn><abstract>A new Schiff base N,N’‐Bis(5‐Bromosalicylidine)‐1,8‐diaminonaphthalene (BBSDN) and its Co(II),Ni(II),Cu(II) and Zn(II) complexes were synthesized. All the compounds were characterized by various spectral studies (IR, UV, 1H NMR, 13C NMR and EI‐Mass) and DFT calculations. Conductance measurements, magnetic study and metal estimation studies were performed for the complexes to establish the structure. Thermal studies were done to account for the coordination of water molecules. Redox property of the synthesized complexes was established by Cyclic Voltammetry studies. Synthesized compounds were screened against fungal and bacterial pathogens and in most of the cases the complexes were found to be more active than the Schiff base. MIC value for copper and zinc complexes against the fungal pathogen Candida albicans are determined as 25 ppm and 10 ppm respectively. Metal ion pertinency of the Schiff base was investigated by absorption and fluorescence methods and was found to be highly selective and sensitive for the detection of Cu(II) ion. Mode of interaction has been proved through 1H NMR titrations and the interaction is explained as due to CHEQ mechanism. Stability constant of the complex formed during the detection process was determined by Benesi‐Hildebrand plot. Detection limit was computed as 1.464×10‐6M. The chemosensor property of the Schiff base is applied in bioimaging studies on HeLa cell lines.</abstract><cop>Weinheim</cop><pub>WILEY‐VCH Verlag GmbH & Co. KGaA</pub><doi>10.1002/vjch.202200150</doi><tpages>16</tpages><oa>free_for_read</oa></addata></record> |
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subjects | bioimaging chemosensor coordination chemistry Schiff base transition metal complexes |
title | Highly Selective and Sensitive Dual Channel New Schiff base Chemosensor based on 5‐bromo‐2‐hydroxybenzaldehyde and its Co(II), Ni(II), Cu(II) and Zn(II) Complexes ‐ Synthesis, Spectral and Theoretical characterization and Pharmacological applications |
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