Functionalisation of fluorescent BODIPY dyes by nucleophilic substitution
The BODIPY chromophore can be easily modified by nucleophilic mono- or disubstitution of 3,5-dichloroBODIPY with O-, N-, S- and C-nucleophiles. Absorption and fluorescence spectral data of the new BODIPY derivatives are also reported.
Gespeichert in:
Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2006-01 (3), p.266-268 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 268 |
---|---|
container_issue | 3 |
container_start_page | 266 |
container_title | Chemical communications (Cambridge, England) |
container_volume | |
creator | Rohand, Taoufik Baruah, Mukulesh Qin, Wenwu Boens, Noël Dehaen, Wim |
description | The BODIPY chromophore can be easily modified by nucleophilic mono- or disubstitution of 3,5-dichloroBODIPY with O-, N-, S- and C-nucleophiles. Absorption and fluorescence spectral data of the new BODIPY derivatives are also reported. |
doi_str_mv | 10.1039/b512756d |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_67604216</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>67604216</sourcerecordid><originalsourceid>FETCH-LOGICAL-c367t-b6937e081d6ef2f1b078f60834de0e098f8f71dfe1bb3e0ecb2cc49dd9b26a003</originalsourceid><addsrcrecordid>eNpFkE9LAzEQxYMotlbBTyA5iZfVZLObP0dtrRYK9aCgp2WTTDCS7tbN5tBv7y4tOJd5DL95zDyErim5p4SpB13SXJTcnqApZbzIykJ-no66VJlgRTlBFzH-kKFoKc_RhHKmqMjVFK2WqTG9b5s6-FiPArcOu5DaDqKBpsdPm8Xq7QvbPUSs97hJJkC7-_bBGxyTjr3v07h3ic5cHSJcHfsMfSyf3-ev2Xrzspo_rjPDuOgzzRUTQCS1HFzuqCZCOk4kKywQIEo66QS1DqjWbJgYnRtTKGuVznlNCJuh24Pvrmt_E8S-2vrh0hDqBtoUKy44KfLhwxm6O4Cma2PswFW7zm_rbl9RUo2xVU-H2BYDenP0THoL9h885sT-AAudaKs</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>67604216</pqid></control><display><type>article</type><title>Functionalisation of fluorescent BODIPY dyes by nucleophilic substitution</title><source>Royal Society Of Chemistry Journals</source><source>Royal Society of Chemistry Journals Archive (1841-2007)</source><source>Alma/SFX Local Collection</source><creator>Rohand, Taoufik ; Baruah, Mukulesh ; Qin, Wenwu ; Boens, Noël ; Dehaen, Wim</creator><creatorcontrib>Rohand, Taoufik ; Baruah, Mukulesh ; Qin, Wenwu ; Boens, Noël ; Dehaen, Wim</creatorcontrib><description>The BODIPY chromophore can be easily modified by nucleophilic mono- or disubstitution of 3,5-dichloroBODIPY with O-, N-, S- and C-nucleophiles. Absorption and fluorescence spectral data of the new BODIPY derivatives are also reported.</description><identifier>ISSN: 1359-7345</identifier><identifier>EISSN: 1364-548X</identifier><identifier>DOI: 10.1039/b512756d</identifier><identifier>PMID: 16391729</identifier><language>eng</language><publisher>England</publisher><ispartof>Chemical communications (Cambridge, England), 2006-01 (3), p.266-268</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c367t-b6937e081d6ef2f1b078f60834de0e098f8f71dfe1bb3e0ecb2cc49dd9b26a003</citedby><cites>FETCH-LOGICAL-c367t-b6937e081d6ef2f1b078f60834de0e098f8f71dfe1bb3e0ecb2cc49dd9b26a003</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,2832,27929,27930</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16391729$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rohand, Taoufik</creatorcontrib><creatorcontrib>Baruah, Mukulesh</creatorcontrib><creatorcontrib>Qin, Wenwu</creatorcontrib><creatorcontrib>Boens, Noël</creatorcontrib><creatorcontrib>Dehaen, Wim</creatorcontrib><title>Functionalisation of fluorescent BODIPY dyes by nucleophilic substitution</title><title>Chemical communications (Cambridge, England)</title><addtitle>Chem Commun (Camb)</addtitle><description>The BODIPY chromophore can be easily modified by nucleophilic mono- or disubstitution of 3,5-dichloroBODIPY with O-, N-, S- and C-nucleophiles. Absorption and fluorescence spectral data of the new BODIPY derivatives are also reported.</description><issn>1359-7345</issn><issn>1364-548X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNpFkE9LAzEQxYMotlbBTyA5iZfVZLObP0dtrRYK9aCgp2WTTDCS7tbN5tBv7y4tOJd5DL95zDyErim5p4SpB13SXJTcnqApZbzIykJ-no66VJlgRTlBFzH-kKFoKc_RhHKmqMjVFK2WqTG9b5s6-FiPArcOu5DaDqKBpsdPm8Xq7QvbPUSs97hJJkC7-_bBGxyTjr3v07h3ic5cHSJcHfsMfSyf3-ev2Xrzspo_rjPDuOgzzRUTQCS1HFzuqCZCOk4kKywQIEo66QS1DqjWbJgYnRtTKGuVznlNCJuh24Pvrmt_E8S-2vrh0hDqBtoUKy44KfLhwxm6O4Cma2PswFW7zm_rbl9RUo2xVU-H2BYDenP0THoL9h885sT-AAudaKs</recordid><startdate>20060121</startdate><enddate>20060121</enddate><creator>Rohand, Taoufik</creator><creator>Baruah, Mukulesh</creator><creator>Qin, Wenwu</creator><creator>Boens, Noël</creator><creator>Dehaen, Wim</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20060121</creationdate><title>Functionalisation of fluorescent BODIPY dyes by nucleophilic substitution</title><author>Rohand, Taoufik ; Baruah, Mukulesh ; Qin, Wenwu ; Boens, Noël ; Dehaen, Wim</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c367t-b6937e081d6ef2f1b078f60834de0e098f8f71dfe1bb3e0ecb2cc49dd9b26a003</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rohand, Taoufik</creatorcontrib><creatorcontrib>Baruah, Mukulesh</creatorcontrib><creatorcontrib>Qin, Wenwu</creatorcontrib><creatorcontrib>Boens, Noël</creatorcontrib><creatorcontrib>Dehaen, Wim</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Chemical communications (Cambridge, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rohand, Taoufik</au><au>Baruah, Mukulesh</au><au>Qin, Wenwu</au><au>Boens, Noël</au><au>Dehaen, Wim</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Functionalisation of fluorescent BODIPY dyes by nucleophilic substitution</atitle><jtitle>Chemical communications (Cambridge, England)</jtitle><addtitle>Chem Commun (Camb)</addtitle><date>2006-01-21</date><risdate>2006</risdate><issue>3</issue><spage>266</spage><epage>268</epage><pages>266-268</pages><issn>1359-7345</issn><eissn>1364-548X</eissn><abstract>The BODIPY chromophore can be easily modified by nucleophilic mono- or disubstitution of 3,5-dichloroBODIPY with O-, N-, S- and C-nucleophiles. Absorption and fluorescence spectral data of the new BODIPY derivatives are also reported.</abstract><cop>England</cop><pmid>16391729</pmid><doi>10.1039/b512756d</doi><tpages>3</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1359-7345 |
ispartof | Chemical communications (Cambridge, England), 2006-01 (3), p.266-268 |
issn | 1359-7345 1364-548X |
language | eng |
recordid | cdi_proquest_miscellaneous_67604216 |
source | Royal Society Of Chemistry Journals; Royal Society of Chemistry Journals Archive (1841-2007); Alma/SFX Local Collection |
title | Functionalisation of fluorescent BODIPY dyes by nucleophilic substitution |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-13T10%3A16%3A11IST&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=Functionalisation%20of%20fluorescent%20BODIPY%20dyes%20by%20nucleophilic%20substitution&rft.jtitle=Chemical%20communications%20(Cambridge,%20England)&rft.au=Rohand,%20Taoufik&rft.date=2006-01-21&rft.issue=3&rft.spage=266&rft.epage=268&rft.pages=266-268&rft.issn=1359-7345&rft.eissn=1364-548X&rft_id=info:doi/10.1039/b512756d&rft_dat=%3Cproquest_cross%3E67604216%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=67604216&rft_id=info:pmid/16391729&rfr_iscdi=true |