Fluorescent properties and resonance energy transfer of 3,4-bis(2,4-difluorophenyl)-maleimideElectronic supplementary information (ESI) available. CCDC XXXXXX. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c2ob25981h
A fluorescent compound 3,4-bis(2,4-difluorophenyl)-maleimide 1 from the 3,4-diaryl-substituted maleimides was synthesized and determined to have a Stokes shift of 140 nm ( λ abs 341 nm, λ em 481 nm), a high fluorescent quantum yield ( Φ fl 0.61) and an extinction coefficient (340) of 48 400 M −1 cm...
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creator | Nacheva, Katya P Maza, William A Myers, David Z Fronczek, Frank R Larsen, Randy W Manetsch, Roman |
description | A fluorescent compound 3,4-bis(2,4-difluorophenyl)-maleimide
1
from the 3,4-diaryl-substituted maleimides was synthesized and determined to have a Stokes shift of 140 nm (
λ
abs
341 nm,
λ
em
481 nm), a high fluorescent quantum yield (
Φ
fl
0.61) and an extinction coefficient
(340)
of 48 400 M
−1
cm
−1
in dichloromethane. For the first time we demonstrated the successful implementation of a 3,4-diaryl-substituted maleimide molecule as a donor component in FRET experiments.
A fluorescent compound 3,4-bis(2,4-difluorophenyl)-maleimide
1
from the 3,4-diaryl-substituted maleimide was synthesized and determined to have a Stokes shift of 140 nm (
λ
abs
341 nm,
λ
em
481 nm), a high fluorescent quantum yield (
Φ
fl
0.61) and an extinction coefficient
(340)
of 48 400 M
−1
cm
−1
in dichloromethane. |
doi_str_mv | 10.1039/c2ob25981h |
format | Article |
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1
from the 3,4-diaryl-substituted maleimides was synthesized and determined to have a Stokes shift of 140 nm (
λ
abs
341 nm,
λ
em
481 nm), a high fluorescent quantum yield (
Φ
fl
0.61) and an extinction coefficient
(340)
of 48 400 M
−1
cm
−1
in dichloromethane. For the first time we demonstrated the successful implementation of a 3,4-diaryl-substituted maleimide molecule as a donor component in FRET experiments.
A fluorescent compound 3,4-bis(2,4-difluorophenyl)-maleimide
1
from the 3,4-diaryl-substituted maleimide was synthesized and determined to have a Stokes shift of 140 nm (
λ
abs
341 nm,
λ
em
481 nm), a high fluorescent quantum yield (
Φ
fl
0.61) and an extinction coefficient
(340)
of 48 400 M
−1
cm
−1
in dichloromethane.</description><identifier>ISSN: 1477-0520</identifier><identifier>EISSN: 1477-0539</identifier><identifier>DOI: 10.1039/c2ob25981h</identifier><language>eng</language><creationdate>2012-09</creationdate><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Nacheva, Katya P</creatorcontrib><creatorcontrib>Maza, William A</creatorcontrib><creatorcontrib>Myers, David Z</creatorcontrib><creatorcontrib>Fronczek, Frank R</creatorcontrib><creatorcontrib>Larsen, Randy W</creatorcontrib><creatorcontrib>Manetsch, Roman</creatorcontrib><title>Fluorescent properties and resonance energy transfer of 3,4-bis(2,4-difluorophenyl)-maleimideElectronic supplementary information (ESI) available. CCDC XXXXXX. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c2ob25981h</title><description>A fluorescent compound 3,4-bis(2,4-difluorophenyl)-maleimide
1
from the 3,4-diaryl-substituted maleimides was synthesized and determined to have a Stokes shift of 140 nm (
λ
abs
341 nm,
λ
em
481 nm), a high fluorescent quantum yield (
Φ
fl
0.61) and an extinction coefficient
(340)
of 48 400 M
−1
cm
−1
in dichloromethane. For the first time we demonstrated the successful implementation of a 3,4-diaryl-substituted maleimide molecule as a donor component in FRET experiments.
A fluorescent compound 3,4-bis(2,4-difluorophenyl)-maleimide
1
from the 3,4-diaryl-substituted maleimide was synthesized and determined to have a Stokes shift of 140 nm (
λ
abs
341 nm,
λ
em
481 nm), a high fluorescent quantum yield (
Φ
fl
0.61) and an extinction coefficient
(340)
of 48 400 M
−1
cm
−1
in dichloromethane.</description><issn>1477-0520</issn><issn>1477-0539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFUE1Lw0AQXUTB-nHxLoy3FkzNR2uN17TBnjzowVuZJpNmZbO7zG6F_Hpdq9iDoHN5w7zHe48R4iKJx0mc5TdVatbpNL9L2gMxSCazWRRPs_zwZ0_jY3Hi3GscJ_nsdjIQ76XaGiZXkfZg2VhiL8kB6hrC2WjUFQFp4k0PnlG7hhhMA9n1JFpLN0wD1rL5dDG2Jd2rUdShItnJmhaKKs9Gywrc1lpFXYhB7kHqxnCHXhoNw8XTcgT4hlLhWtEYimJewMtuxlAahiDYFaq4dx6VMhtG2wbTGj0GLyiWJQSd8W0oR_vQrxBwRDB_XN7D7zediaMGlaPzbzwVl-XiuXiI2FUry7ILbVd7efY_f_UXv7J1k30AHbaIQA</recordid><startdate>20120912</startdate><enddate>20120912</enddate><creator>Nacheva, Katya P</creator><creator>Maza, William A</creator><creator>Myers, David Z</creator><creator>Fronczek, Frank R</creator><creator>Larsen, Randy W</creator><creator>Manetsch, Roman</creator><scope/></search><sort><creationdate>20120912</creationdate><title>Fluorescent properties and resonance energy transfer of 3,4-bis(2,4-difluorophenyl)-maleimideElectronic supplementary information (ESI) available. CCDC XXXXXX. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c2ob25981h</title><author>Nacheva, Katya P ; Maza, William A ; Myers, David Z ; Fronczek, Frank R ; Larsen, Randy W ; Manetsch, Roman</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_c2ob25981h3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nacheva, Katya P</creatorcontrib><creatorcontrib>Maza, William A</creatorcontrib><creatorcontrib>Myers, David Z</creatorcontrib><creatorcontrib>Fronczek, Frank R</creatorcontrib><creatorcontrib>Larsen, Randy W</creatorcontrib><creatorcontrib>Manetsch, Roman</creatorcontrib></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nacheva, Katya P</au><au>Maza, William A</au><au>Myers, David Z</au><au>Fronczek, Frank R</au><au>Larsen, Randy W</au><au>Manetsch, Roman</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fluorescent properties and resonance energy transfer of 3,4-bis(2,4-difluorophenyl)-maleimideElectronic supplementary information (ESI) available. CCDC XXXXXX. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c2ob25981h</atitle><date>2012-09-12</date><risdate>2012</risdate><volume>1</volume><issue>38</issue><spage>784</spage><epage>7846</epage><pages>784-7846</pages><issn>1477-0520</issn><eissn>1477-0539</eissn><abstract>A fluorescent compound 3,4-bis(2,4-difluorophenyl)-maleimide
1
from the 3,4-diaryl-substituted maleimides was synthesized and determined to have a Stokes shift of 140 nm (
λ
abs
341 nm,
λ
em
481 nm), a high fluorescent quantum yield (
Φ
fl
0.61) and an extinction coefficient
(340)
of 48 400 M
−1
cm
−1
in dichloromethane. For the first time we demonstrated the successful implementation of a 3,4-diaryl-substituted maleimide molecule as a donor component in FRET experiments.
A fluorescent compound 3,4-bis(2,4-difluorophenyl)-maleimide
1
from the 3,4-diaryl-substituted maleimide was synthesized and determined to have a Stokes shift of 140 nm (
λ
abs
341 nm,
λ
em
481 nm), a high fluorescent quantum yield (
Φ
fl
0.61) and an extinction coefficient
(340)
of 48 400 M
−1
cm
−1
in dichloromethane.</abstract><doi>10.1039/c2ob25981h</doi><tpages>7</tpages></addata></record> |
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source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
title | Fluorescent properties and resonance energy transfer of 3,4-bis(2,4-difluorophenyl)-maleimideElectronic supplementary information (ESI) available. CCDC XXXXXX. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c2ob25981h |
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