Synthesis of Dibenzothiazolyldibenzo‐18‐Crown‐6 and its Applications in Colorimetric Recognition of Palladium and as Antimicrobial Agent

Dibenzothiazolyldibenzo‐18‐crown‐6‐ether was designed and synthesized by formylation of dibenzo‐18‐crown‐6‐ether followed by condensation with 2‐aminothiophenol. A simple and rapid UV‐Visible spectrophotometric method is developed for detection of trace of palladium ions. Furthermore it was assessed...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of heterocyclic chemistry 2017-01, Vol.54 (1), p.161-164
Hauptverfasser: Jagadale, S. D., Sawant, A. D., Deshmukh, M. B.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 164
container_issue 1
container_start_page 161
container_title Journal of heterocyclic chemistry
container_volume 54
creator Jagadale, S. D.
Sawant, A. D.
Deshmukh, M. B.
description Dibenzothiazolyldibenzo‐18‐crown‐6‐ether was designed and synthesized by formylation of dibenzo‐18‐crown‐6‐ether followed by condensation with 2‐aminothiophenol. A simple and rapid UV‐Visible spectrophotometric method is developed for detection of trace of palladium ions. Furthermore it was assessed for antimicrobial activity against bacterial strains Staphylococcus aureus (Gram+ve), Escherichia coli (Gram−ve) as well as fungal strains Aspergillus niger and Candida albicans respectively.
doi_str_mv 10.1002/jhet.2561
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1872819072</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1872819072</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3301-e3e301fd23c2d975c9c862f37b6680118703336e7c6e0d71c237586407739db33</originalsourceid><addsrcrecordid>eNp1kc1KAzEUhYMoWKsL3yDgRhfT5qeTzCxLrVYpKFrB3ZBmMjYlTeokpbQrn0B8Rp_ETOtKcJPD5X7ncm8OAOcYdTBCpDufqdAhKcMHoIXzHk1SnNND0Io9kuCUvB6DE-_nscSU8xb4fN7YMFNee-gqeK2nym5dmGmxdWZjyn39_fGFs_gMare2URkUtoQ6eNhfLo2WImhnPdQWDpxxtV6oUGsJn5R0b1Y3zWb4ozBGlHq12LlFNNugF1rWbqqFgf03ZcMpOKqE8ersV9vg5WY4GYyS8cPt3aA_TiSlCCeKqihVSagkZc5TmcuMkYryKWMZwjjjiFLKFJdMoZJjSShPM9ZDnNO8nFLaBpf7ucvava-UD8VCe6nigla5lS_iBJLhHHES0Ys_6Nytahu3ixRDrJfmFEfqak_Fc7yvVVUs4z-IelNgVDTJFE0yRZNMZLt7dq2N2vwPFvej4WTn-AEBcJOb</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1860645931</pqid></control><display><type>article</type><title>Synthesis of Dibenzothiazolyldibenzo‐18‐Crown‐6 and its Applications in Colorimetric Recognition of Palladium and as Antimicrobial Agent</title><source>Wiley Online Library Journals Frontfile Complete</source><creator>Jagadale, S. D. ; Sawant, A. D. ; Deshmukh, M. B.</creator><creatorcontrib>Jagadale, S. D. ; Sawant, A. D. ; Deshmukh, M. B.</creatorcontrib><description>Dibenzothiazolyldibenzo‐18‐crown‐6‐ether was designed and synthesized by formylation of dibenzo‐18‐crown‐6‐ether followed by condensation with 2‐aminothiophenol. A simple and rapid UV‐Visible spectrophotometric method is developed for detection of trace of palladium ions. Furthermore it was assessed for antimicrobial activity against bacterial strains Staphylococcus aureus (Gram+ve), Escherichia coli (Gram−ve) as well as fungal strains Aspergillus niger and Candida albicans respectively.</description><identifier>ISSN: 0022-152X</identifier><identifier>EISSN: 1943-5193</identifier><identifier>DOI: 10.1002/jhet.2561</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc</publisher><subject>Antimicrobial agents ; Aspergillus niger ; Candida albicans ; Escherichia coli ; Staphylococcus aureus</subject><ispartof>Journal of heterocyclic chemistry, 2017-01, Vol.54 (1), p.161-164</ispartof><rights>2015 HeteroCorporation</rights><rights>2017 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3301-e3e301fd23c2d975c9c862f37b6680118703336e7c6e0d71c237586407739db33</citedby><cites>FETCH-LOGICAL-c3301-e3e301fd23c2d975c9c862f37b6680118703336e7c6e0d71c237586407739db33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjhet.2561$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjhet.2561$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids></links><search><creatorcontrib>Jagadale, S. D.</creatorcontrib><creatorcontrib>Sawant, A. D.</creatorcontrib><creatorcontrib>Deshmukh, M. B.</creatorcontrib><title>Synthesis of Dibenzothiazolyldibenzo‐18‐Crown‐6 and its Applications in Colorimetric Recognition of Palladium and as Antimicrobial Agent</title><title>Journal of heterocyclic chemistry</title><description>Dibenzothiazolyldibenzo‐18‐crown‐6‐ether was designed and synthesized by formylation of dibenzo‐18‐crown‐6‐ether followed by condensation with 2‐aminothiophenol. A simple and rapid UV‐Visible spectrophotometric method is developed for detection of trace of palladium ions. Furthermore it was assessed for antimicrobial activity against bacterial strains Staphylococcus aureus (Gram+ve), Escherichia coli (Gram−ve) as well as fungal strains Aspergillus niger and Candida albicans respectively.</description><subject>Antimicrobial agents</subject><subject>Aspergillus niger</subject><subject>Candida albicans</subject><subject>Escherichia coli</subject><subject>Staphylococcus aureus</subject><issn>0022-152X</issn><issn>1943-5193</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp1kc1KAzEUhYMoWKsL3yDgRhfT5qeTzCxLrVYpKFrB3ZBmMjYlTeokpbQrn0B8Rp_ETOtKcJPD5X7ncm8OAOcYdTBCpDufqdAhKcMHoIXzHk1SnNND0Io9kuCUvB6DE-_nscSU8xb4fN7YMFNee-gqeK2nym5dmGmxdWZjyn39_fGFs_gMare2URkUtoQ6eNhfLo2WImhnPdQWDpxxtV6oUGsJn5R0b1Y3zWb4ozBGlHq12LlFNNugF1rWbqqFgf03ZcMpOKqE8ersV9vg5WY4GYyS8cPt3aA_TiSlCCeKqihVSagkZc5TmcuMkYryKWMZwjjjiFLKFJdMoZJjSShPM9ZDnNO8nFLaBpf7ucvava-UD8VCe6nigla5lS_iBJLhHHES0Ys_6Nytahu3ixRDrJfmFEfqak_Fc7yvVVUs4z-IelNgVDTJFE0yRZNMZLt7dq2N2vwPFvej4WTn-AEBcJOb</recordid><startdate>201701</startdate><enddate>201701</enddate><creator>Jagadale, S. D.</creator><creator>Sawant, A. D.</creator><creator>Deshmukh, M. B.</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>C1K</scope></search><sort><creationdate>201701</creationdate><title>Synthesis of Dibenzothiazolyldibenzo‐18‐Crown‐6 and its Applications in Colorimetric Recognition of Palladium and as Antimicrobial Agent</title><author>Jagadale, S. D. ; Sawant, A. D. ; Deshmukh, M. B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3301-e3e301fd23c2d975c9c862f37b6680118703336e7c6e0d71c237586407739db33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Antimicrobial agents</topic><topic>Aspergillus niger</topic><topic>Candida albicans</topic><topic>Escherichia coli</topic><topic>Staphylococcus aureus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jagadale, S. D.</creatorcontrib><creatorcontrib>Sawant, A. D.</creatorcontrib><creatorcontrib>Deshmukh, M. B.</creatorcontrib><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Journal of heterocyclic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jagadale, S. D.</au><au>Sawant, A. D.</au><au>Deshmukh, M. B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of Dibenzothiazolyldibenzo‐18‐Crown‐6 and its Applications in Colorimetric Recognition of Palladium and as Antimicrobial Agent</atitle><jtitle>Journal of heterocyclic chemistry</jtitle><date>2017-01</date><risdate>2017</risdate><volume>54</volume><issue>1</issue><spage>161</spage><epage>164</epage><pages>161-164</pages><issn>0022-152X</issn><eissn>1943-5193</eissn><abstract>Dibenzothiazolyldibenzo‐18‐crown‐6‐ether was designed and synthesized by formylation of dibenzo‐18‐crown‐6‐ether followed by condensation with 2‐aminothiophenol. A simple and rapid UV‐Visible spectrophotometric method is developed for detection of trace of palladium ions. Furthermore it was assessed for antimicrobial activity against bacterial strains Staphylococcus aureus (Gram+ve), Escherichia coli (Gram−ve) as well as fungal strains Aspergillus niger and Candida albicans respectively.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/jhet.2561</doi><tpages>4</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0022-152X
ispartof Journal of heterocyclic chemistry, 2017-01, Vol.54 (1), p.161-164
issn 0022-152X
1943-5193
language eng
recordid cdi_proquest_miscellaneous_1872819072
source Wiley Online Library Journals Frontfile Complete
subjects Antimicrobial agents
Aspergillus niger
Candida albicans
Escherichia coli
Staphylococcus aureus
title Synthesis of Dibenzothiazolyldibenzo‐18‐Crown‐6 and its Applications in Colorimetric Recognition of Palladium and as Antimicrobial Agent
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-17T12%3A57%3A26IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthesis%20of%20Dibenzothiazolyldibenzo%E2%80%9018%E2%80%90Crown%E2%80%906%20and%20its%20Applications%20in%20Colorimetric%20Recognition%20of%20Palladium%20and%20as%20Antimicrobial%20Agent&rft.jtitle=Journal%20of%20heterocyclic%20chemistry&rft.au=Jagadale,%20S.%20D.&rft.date=2017-01&rft.volume=54&rft.issue=1&rft.spage=161&rft.epage=164&rft.pages=161-164&rft.issn=0022-152X&rft.eissn=1943-5193&rft_id=info:doi/10.1002/jhet.2561&rft_dat=%3Cproquest_cross%3E1872819072%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1860645931&rft_id=info:pmid/&rfr_iscdi=true