A Series of Polyamide Receptor Based PET Fluorescent Sensor Molecules:  Positively Cooperative Hg2+ Ion Binding with High Sensitivity

A series of PET fluorescent sensor molecules were designed and synthesized based on BODIPY fluorophore and polyamide receptors. Comparison of the photophysical properties of these sensor molecules, equipped with di-, tri-, and tetraamide receptor, provided a deep insight into the polyamide−Hg2+ inte...

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Published inOrganic letters Vol. 8; no. 17; pp. 3721 - 3724
Main Authors Wang, Jiaobing, Qian, Xuhong
Format Journal Article
LanguageEnglish
Published WASHINGTON American Chemical Society 17.08.2006
Amer Chemical Soc
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ISSN1523-7060
1523-7052
DOI10.1021/ol061297u

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Abstract A series of PET fluorescent sensor molecules were designed and synthesized based on BODIPY fluorophore and polyamide receptors. Comparison of the photophysical properties of these sensor molecules, equipped with di-, tri-, and tetraamide receptor, provided a deep insight into the polyamide−Hg2+ interactions, and an unusual positively cooperative tetraamide−Hg2+ complexation was disclosed. In addition, sensor S3 displayed several favorable sensing properties.
AbstractList A series of PET fluorescent sensor molecules were designed and synthesized based on BODIPY fluorophore and polyamide receptors. Comparison of the photophysical properties of these sensor molecules, equipped with di-, tri-, and tetraamide receptor, provided a deep insight into the polyamide-Hg2+ interactions, and an unusual positively cooperative tetraamide-Hg2+ complexation was disclosed. In addition, sensor S3 displayed several favorable sensing properties.
[structure: see text] A series of PET fluorescent sensor molecules were designed and synthesized based on BODIPY fluorophore and polyamide receptors. Comparison of the photophysical properties of these sensor molecules, equipped with di-, tri-, and tetraamide receptor, provided a deep insight into the polyamide-Hg2+ interactions, and an unusual positively cooperative tetraamide-Hg2+ complexation was disclosed. In addition, sensor S3 displayed several favorable sensing properties.
A series of PET fluorescent sensor molecules were designed and synthesized based on BODIPY fluorophore and polyamide receptors. Comparison of the photophysical properties of these sensor molecules, equipped with di-, tri-, and tetraamide receptor, provided a deep insight into the polyamide−Hg2+ interactions, and an unusual positively cooperative tetraamide−Hg2+ complexation was disclosed. In addition, sensor S3 displayed several favorable sensing properties.
[structure: see text] A series of PET fluorescent sensor molecules were designed and synthesized based on BODIPY fluorophore and polyamide receptors. Comparison of the photophysical properties of these sensor molecules, equipped with di-, tri-, and tetraamide receptor, provided a deep insight into the polyamide-Hg2+ interactions, and an unusual positively cooperative tetraamide-Hg2+ complexation was disclosed. In addition, sensor S3 displayed several favorable sensing properties.[structure: see text] A series of PET fluorescent sensor molecules were designed and synthesized based on BODIPY fluorophore and polyamide receptors. Comparison of the photophysical properties of these sensor molecules, equipped with di-, tri-, and tetraamide receptor, provided a deep insight into the polyamide-Hg2+ interactions, and an unusual positively cooperative tetraamide-Hg2+ complexation was disclosed. In addition, sensor S3 displayed several favorable sensing properties.
Author Wang, Jiaobing
Qian, Xuhong
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Cites_doi 10.1021/ja045798r
10.1021/ja037604y
10.1021/ja037944j
10.1039/b511319a
10.1002/tox.10116
10.1002/anie.200454172
10.1021/ja0517724
10.1021/ja0557987
10.1021/jo052642g
10.1002/anie.200500583
10.1021/ic034388l
10.1021/ja0290779
10.1021/ja0545766
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DESIGN
DYES
SELECTIVITY
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References CASEY, KG (WOS:A1988R007000023) 1988; 92
Ros-Lis, JV (WOS:000230521800030) 2005; 44
Gabe, Y (WOS:000220192000064) 2004; 126
Nolan, EM (WOS:000186722200030) 2003; 125
Guo, XF (WOS:000189279700007) 2004; 126
Zhang, ZC (WOS:000225026200017) 2004; 66
Coronado, E (WOS:000231637100062) 2005; 127
Descalzo, AB (WOS:000181755800009) 2003; 125
Tchounwou, PB (WOS:000183481600001) 2003; 18
Wang, JB (WOS:000237654000037) 2006; 71
Su, CY (WOS:000185219500037) 2003; 42
Kollmannsberger, M (WOS:000077543700004) 1998; 102
Miller, JR (WOS:A1996UE41100027) 1996; 86
Rurack, K (WOS:000085294700034) 2000; 122
VALEUR B (WOS:000239655500026.17) 2002
Caballero, A (WOS:000233535400003) 2005; 127
Wang, JB (WOS:000234096700026) 2006
Ono, A (WOS:000223603600009) 2004; 43
Dickerson, TJ (WOS:000225808200064) 2004; 126
Yoon, S (WOS:000233445900019) 2005; 127
HAUGLAND RP (WOS:000239655500026.8) 2002
References_xml – volume: 126
  start-page: 16582
  year: 2004
  ident: WOS:000225808200064
  article-title: A precipitator for the detection of thiophilic metals in aqua
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja045798r
– volume: 126
  start-page: 2272
  year: 2004
  ident: WOS:000189279700007
  article-title: A highly selective and sensitive fluorescent chemosensor for Hg2+ in neutral buffer aqueous solution
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja037604y
– volume: 86
  start-page: 373
  year: 1996
  ident: WOS:A1996UE41100027
  article-title: Dispersal of mercury-contaminated sediments by geomorphic processes, Sixmile Canyon, Nevada, USA: Implications to site characterization and remediation of fluvial environments
  publication-title: WATER AIR AND SOIL POLLUTION
– volume: 126
  start-page: 3357
  year: 2004
  ident: WOS:000220192000064
  article-title: Highly sensitive fluorescence probes for nitric oxide based on boron dipyrromethene chromophore-rational design of potentially useful bioimaging fluorescence probe
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja037944j
– start-page: 109
  year: 2006
  ident: WOS:000234096700026
  article-title: Two regioisomeric and exclusively selective Hg(II) sensor molecules composed of a naphthalimide fluorophore and an o-phenylenediamine derived triamide receptor
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/b511319a
– volume: 18
  start-page: 149
  year: 2003
  ident: WOS:000183481600001
  article-title: Environmental exposure to mercury and its toxicopathologic implications for public health
  publication-title: ENVIRONMENTAL TOXICOLOGY
  doi: 10.1002/tox.10116
– volume: 43
  start-page: 4300
  year: 2004
  ident: WOS:000223603600009
  article-title: Highly selective oligonucleotide-based sensor for mercury(II) in aqueous solutions
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.200454172
– volume: 66
  start-page: 2279
  year: 2004
  ident: WOS:000225026200017
  article-title: Fluorescent imaging of acute mercuric chloride exposure on cultured human kidney tubular epithelial cells
  publication-title: KIDNEY INTERNATIONAL
– volume: 127
  start-page: 12351
  year: 2005
  ident: WOS:000231637100062
  article-title: Reversible colorimetric probes for mercury sensing
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja0517724
– volume: 127
  start-page: 16030
  year: 2005
  ident: WOS:000233445900019
  article-title: Screening mercury levels in fish with a selective fluorescent chemosensor
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja0557987
– volume: 122
  start-page: 968
  year: 2000
  ident: WOS:000085294700034
  article-title: A selective and sensitive fluoroionophore for Hg(II), Ag(I), and Cu(II) with virtually decoupled fluorophore and receptor units
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
– volume: 71
  start-page: 4308
  year: 2006
  ident: WOS:000237654000037
  article-title: Detecting Hg2+ ions with an ICT fluorescent sensor molecule: Remarkable emission spectra shift and unique selectivity
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/jo052642g
– year: 2002
  ident: WOS:000239655500026.8
  publication-title: HDB FLUORESCENT PROB
– volume: 125
  start-page: 14270
  year: 2003
  ident: WOS:000186722200030
  article-title: A "Turn-On" fluorescent sensor for the selective detection of mercuric ion in aqueous media
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
– volume: 44
  start-page: 4405
  year: 2005
  ident: WOS:000230521800030
  article-title: A regenerative chemodosimeter based on metal-induced dye formation for the highly selective and sensitive optical determination of Hg2+ ions
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.200500583
– volume: 42
  start-page: 5685
  year: 2003
  ident: WOS:000185219500037
  article-title: Formation of dinuclear, macrocyclic, and chain structures from Hgl(2) and a semirigid benzimidazole-based bridging ligand: An example of ring-opening supramolecular isomerism
  publication-title: INORGANIC CHEMISTRY
  doi: 10.1021/ic034388l
– year: 2002
  ident: WOS:000239655500026.17
  publication-title: MOL FLUORESCENCE PRI
– volume: 125
  start-page: 3418
  year: 2003
  ident: WOS:000181755800009
  article-title: Coupling selectivity with sensitivity in an integrated chemosensor framework: Design of a Hg2+-responsive probe, operating above 500 nm
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja0290779
– volume: 102
  start-page: 10211
  year: 1998
  ident: WOS:000077543700004
  article-title: Ultrafast charge transfer in amino-substituted boron dipyrromethene dyes and its inhibition by cation complexation: A new design concept for highly sensitive fluorescent probes
  publication-title: JOURNAL OF PHYSICAL CHEMISTRY A
– volume: 92
  start-page: 6590
  year: 1988
  ident: WOS:A1988R007000023
  article-title: EFFECT OF SOLVENT POLARITY ON NONRADIATIVE PROCESSES IN XANTHENE DYES - RHODAMINE-B IN NORMAL ALCOHOLS
  publication-title: JOURNAL OF PHYSICAL CHEMISTRY
– volume: 127
  start-page: 15666
  year: 2005
  ident: WOS:000233535400003
  article-title: Highly selective chromogenic and redox or fluorescent sensors of Hg2+ in aqueous environment based on 1,4-disubstituted azines
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja0545766
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Snippet A series of PET fluorescent sensor molecules were designed and synthesized based on BODIPY fluorophore and polyamide receptors. Comparison of the photophysical...
[structure: see text] A series of PET fluorescent sensor molecules were designed and synthesized based on BODIPY fluorophore and polyamide receptors....
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Chemistry, Organic
Physical Sciences
Science & Technology
Title A Series of Polyamide Receptor Based PET Fluorescent Sensor Molecules:  Positively Cooperative Hg2+ Ion Binding with High Sensitivity
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