Loading…
A laser flash photolysis study of di-, tri- and tetrafluorinated phenylnitrenes; implications for photoaffinity labeling
Several fluorinated aryl azides (2,6 and 2,4-difluorophenyl azide, 2,4,6-triflurorophenyl azide, and methyl 4-azido-2,3,5,6-tetrafluorobenzoate) were studied by laser flash photolysis techniques. In each case, the azides from singlet nitrenes which can be intercepted with pyridine to form ylides. Th...
Saved in:
Published in: | Bioconjugate chemistry 1993-03, Vol.4 (2), p.178-183 |
---|---|
Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-a269t-a0456d116755db1b9cc73f34311cf71ae07d02efac89e3b952b11a07abc119f23 |
---|---|
cites | |
container_end_page | 183 |
container_issue | 2 |
container_start_page | 178 |
container_title | Bioconjugate chemistry |
container_volume | 4 |
creator | Schnapp, Karlyn A Platz, Matthew S |
description | Several fluorinated aryl azides (2,6 and 2,4-difluorophenyl azide, 2,4,6-triflurorophenyl azide, and methyl 4-azido-2,3,5,6-tetrafluorobenzoate) were studied by laser flash photolysis techniques. In each case, the azides from singlet nitrenes which can be intercepted with pyridine to form ylides. This allowed determination of the rate constant for ring expansion of the singlet nitrene to the dehydroazepine and measurement of the absolute rate constants for reaction of the singlet nitrenes with typical quenchers. |
doi_str_mv | 10.1021/bc00020a011 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_76309866</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>76309866</sourcerecordid><originalsourceid>FETCH-LOGICAL-a269t-a0456d116755db1b9cc73f34311cf71ae07d02efac89e3b952b11a07abc119f23</originalsourceid><addsrcrecordid>eNptkM1rFTEUxYMota2uXAtZ6UKn5mY-MkNXpViVPrC0FdyFO5nEpuYlzyQDnf_elHkUF67OhfO758Ah5A2wE2AcPo2KMcYZMoBn5BBazqqmB_683KypK-gZf0mOUrov2AA9PyAHohd117JD8nBGHSYdqSlyR3d3IQe3JJtoyvO00GDoZKuPNEdbUfQTzTpHNG4O0XrMeiov2i_O2xy11-mU2u3OWYXZBp-oCXHNRGNsYZbSNmpn_a9X5IVBl_TrvR6THxefb8-_VpvvX76dn20q5N2QK2RN200AnWjbaYRxUErUpm5qAGUEoGZiYlwbVP2g63Fo-QiATOCoAAbD62Pybs3dxfBn1inLrU1KO4dehzlJ0dVs6LuugB9WUMWQUtRG7qLdYlwkMPm4s_xn50K_3cfO41ZPT-x-2OJXq29T1g9PNsbfshO1aOXt1Y28Epvry5-bRj7mvV95VEnehzn6Msp_m_8CGlWVng</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>76309866</pqid></control><display><type>article</type><title>A laser flash photolysis study of di-, tri- and tetrafluorinated phenylnitrenes; implications for photoaffinity labeling</title><source>ACS CRKN Legacy Archives</source><creator>Schnapp, Karlyn A ; Platz, Matthew S</creator><creatorcontrib>Schnapp, Karlyn A ; Platz, Matthew S</creatorcontrib><description>Several fluorinated aryl azides (2,6 and 2,4-difluorophenyl azide, 2,4,6-triflurorophenyl azide, and methyl 4-azido-2,3,5,6-tetrafluorobenzoate) were studied by laser flash photolysis techniques. In each case, the azides from singlet nitrenes which can be intercepted with pyridine to form ylides. This allowed determination of the rate constant for ring expansion of the singlet nitrene to the dehydroazepine and measurement of the absolute rate constants for reaction of the singlet nitrenes with typical quenchers.</description><identifier>ISSN: 1043-1802</identifier><identifier>EISSN: 1520-4812</identifier><identifier>DOI: 10.1021/bc00020a011</identifier><identifier>PMID: 7873650</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Affinity Labels - chemistry ; Azides - chemistry ; Fluorine - chemistry ; Lasers ; Photolysis ; Spectrum Analysis</subject><ispartof>Bioconjugate chemistry, 1993-03, Vol.4 (2), p.178-183</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a269t-a0456d116755db1b9cc73f34311cf71ae07d02efac89e3b952b11a07abc119f23</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/bc00020a011$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/bc00020a011$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,27041,27901,27902,56741,56791</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7873650$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schnapp, Karlyn A</creatorcontrib><creatorcontrib>Platz, Matthew S</creatorcontrib><title>A laser flash photolysis study of di-, tri- and tetrafluorinated phenylnitrenes; implications for photoaffinity labeling</title><title>Bioconjugate chemistry</title><addtitle>Bioconjugate Chem</addtitle><description>Several fluorinated aryl azides (2,6 and 2,4-difluorophenyl azide, 2,4,6-triflurorophenyl azide, and methyl 4-azido-2,3,5,6-tetrafluorobenzoate) were studied by laser flash photolysis techniques. In each case, the azides from singlet nitrenes which can be intercepted with pyridine to form ylides. This allowed determination of the rate constant for ring expansion of the singlet nitrene to the dehydroazepine and measurement of the absolute rate constants for reaction of the singlet nitrenes with typical quenchers.</description><subject>Affinity Labels - chemistry</subject><subject>Azides - chemistry</subject><subject>Fluorine - chemistry</subject><subject>Lasers</subject><subject>Photolysis</subject><subject>Spectrum Analysis</subject><issn>1043-1802</issn><issn>1520-4812</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><recordid>eNptkM1rFTEUxYMota2uXAtZ6UKn5mY-MkNXpViVPrC0FdyFO5nEpuYlzyQDnf_elHkUF67OhfO758Ah5A2wE2AcPo2KMcYZMoBn5BBazqqmB_683KypK-gZf0mOUrov2AA9PyAHohd117JD8nBGHSYdqSlyR3d3IQe3JJtoyvO00GDoZKuPNEdbUfQTzTpHNG4O0XrMeiov2i_O2xy11-mU2u3OWYXZBp-oCXHNRGNsYZbSNmpn_a9X5IVBl_TrvR6THxefb8-_VpvvX76dn20q5N2QK2RN200AnWjbaYRxUErUpm5qAGUEoGZiYlwbVP2g63Fo-QiATOCoAAbD62Pybs3dxfBn1inLrU1KO4dehzlJ0dVs6LuugB9WUMWQUtRG7qLdYlwkMPm4s_xn50K_3cfO41ZPT-x-2OJXq29T1g9PNsbfshO1aOXt1Y28Epvry5-bRj7mvV95VEnehzn6Msp_m_8CGlWVng</recordid><startdate>19930301</startdate><enddate>19930301</enddate><creator>Schnapp, Karlyn A</creator><creator>Platz, Matthew S</creator><general>American Chemical Society</general><scope>BSCLL</scope><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></search><sort><creationdate>19930301</creationdate><title>A laser flash photolysis study of di-, tri- and tetrafluorinated phenylnitrenes; implications for photoaffinity labeling</title><author>Schnapp, Karlyn A ; Platz, Matthew S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a269t-a0456d116755db1b9cc73f34311cf71ae07d02efac89e3b952b11a07abc119f23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Affinity Labels - chemistry</topic><topic>Azides - chemistry</topic><topic>Fluorine - chemistry</topic><topic>Lasers</topic><topic>Photolysis</topic><topic>Spectrum Analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schnapp, Karlyn A</creatorcontrib><creatorcontrib>Platz, Matthew S</creatorcontrib><collection>Istex</collection><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><jtitle>Bioconjugate chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schnapp, Karlyn A</au><au>Platz, Matthew S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A laser flash photolysis study of di-, tri- and tetrafluorinated phenylnitrenes; implications for photoaffinity labeling</atitle><jtitle>Bioconjugate chemistry</jtitle><addtitle>Bioconjugate Chem</addtitle><date>1993-03-01</date><risdate>1993</risdate><volume>4</volume><issue>2</issue><spage>178</spage><epage>183</epage><pages>178-183</pages><issn>1043-1802</issn><eissn>1520-4812</eissn><abstract>Several fluorinated aryl azides (2,6 and 2,4-difluorophenyl azide, 2,4,6-triflurorophenyl azide, and methyl 4-azido-2,3,5,6-tetrafluorobenzoate) were studied by laser flash photolysis techniques. In each case, the azides from singlet nitrenes which can be intercepted with pyridine to form ylides. This allowed determination of the rate constant for ring expansion of the singlet nitrene to the dehydroazepine and measurement of the absolute rate constants for reaction of the singlet nitrenes with typical quenchers.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>7873650</pmid><doi>10.1021/bc00020a011</doi><tpages>6</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1043-1802 |
ispartof | Bioconjugate chemistry, 1993-03, Vol.4 (2), p.178-183 |
issn | 1043-1802 1520-4812 |
language | eng |
recordid | cdi_proquest_miscellaneous_76309866 |
source | ACS CRKN Legacy Archives |
subjects | Affinity Labels - chemistry Azides - chemistry Fluorine - chemistry Lasers Photolysis Spectrum Analysis |
title | A laser flash photolysis study of di-, tri- and tetrafluorinated phenylnitrenes; implications for photoaffinity labeling |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-23T23%3A12%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=A%20laser%20flash%20photolysis%20study%20of%20di-,%20tri-%20and%20tetrafluorinated%20phenylnitrenes;%20implications%20for%20photoaffinity%20labeling&rft.jtitle=Bioconjugate%20chemistry&rft.au=Schnapp,%20Karlyn%20A&rft.date=1993-03-01&rft.volume=4&rft.issue=2&rft.spage=178&rft.epage=183&rft.pages=178-183&rft.issn=1043-1802&rft.eissn=1520-4812&rft_id=info:doi/10.1021/bc00020a011&rft_dat=%3Cproquest_cross%3E76309866%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-a269t-a0456d116755db1b9cc73f34311cf71ae07d02efac89e3b952b11a07abc119f23%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=76309866&rft_id=info:pmid/7873650&rfr_iscdi=true |