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 in | Organic letters Vol. 8; no. 17; pp. 3721 - 3724 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
WASHINGTON
American Chemical Society
17.08.2006
Amer Chemical Soc |
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ISSN | 1523-7060 1523-7052 |
DOI | 10.1021/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. |
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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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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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Title | A Series of Polyamide Receptor Based PET Fluorescent Sensor Molecules: Positively Cooperative Hg2+ Ion Binding with High Sensitivity |
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