Gelation-induced visible supramolecular chiral recognition by fluorescent metal complexes of quinolinol-glutamide

Three metal complexes consisting of Li(+), Zn(2+), and Al(3+) and quinolinol-functionalized L-glutamides (HQLG), (abbreviated as LiHQLG, Zn(HQLG)2, and Al(HQLG)3) were found to form fluorescent metallogels in several organic solvents. In solution, these chiral complexes showed neither any CD signal...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1992. - 29(2013), 18 vom: 07. Mai, Seite 5435-42
1. Verfasser: Miao, Wangen (VerfasserIn)
Weitere Verfasser: Zhang, Li, Wang, Xiufeng, Qin, Long, Liu, Minghua
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2013
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Gels Hydroxyquinolines Macromolecular Substances Organometallic Compounds Glutamine 0RH81L854J Lithium 9FN79X2M3F mehr... Aluminum CPD4NFA903 Zinc J41CSQ7QDS
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100 1 |a Miao, Wangen  |e verfasserin  |4 aut 
245 1 0 |a Gelation-induced visible supramolecular chiral recognition by fluorescent metal complexes of quinolinol-glutamide 
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520 |a Three metal complexes consisting of Li(+), Zn(2+), and Al(3+) and quinolinol-functionalized L-glutamides (HQLG), (abbreviated as LiHQLG, Zn(HQLG)2, and Al(HQLG)3) were found to form fluorescent metallogels in several organic solvents. In solution, these chiral complexes showed neither any CD signal in the chromophore region nor chiral recognition of the chiral species. However, upon gel formation, the supramolecular chirality emerged because of the self-assembled nanostructures, which provided an opportunity for the chiral recognition of enantiomeric ligands. The metallogels showed different fluorescence changes when they met with enantiomeric (R,R)- or (S,S)-1,2-diaminocyclohexane. Among them, the Al(HQLG)3 metallogels did not show any change whereas the LiHQLG gels exhibited the same decrease in fluorescence. Interestingly, the Zn(HQLG)2 gels showed obviously different fluorescent color with respect to (R,R)- and (S,S)-1,2-diaminocyclohexane, thus providing visible chiral recognition via the naked eye. Such different recognition ability was discussed on the basis of the assembled chiral nanostructures and the primary molecular structures of the metal complexes. It was shown that both of them played important roles in chiral recognition 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
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650 7 |a Hydroxyquinolines  |2 NLM 
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650 7 |a Organometallic Compounds  |2 NLM 
650 7 |a Glutamine  |2 NLM 
650 7 |a 0RH81L854J  |2 NLM 
650 7 |a Lithium  |2 NLM 
650 7 |a 9FN79X2M3F  |2 NLM 
650 7 |a Aluminum  |2 NLM 
650 7 |a CPD4NFA903  |2 NLM 
650 7 |a Zinc  |2 NLM 
650 7 |a J41CSQ7QDS  |2 NLM 
700 1 |a Zhang, Li  |e verfasserin  |4 aut 
700 1 |a Wang, Xiufeng  |e verfasserin  |4 aut 
700 1 |a Qin, Long  |e verfasserin  |4 aut 
700 1 |a Liu, Minghua  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Langmuir : the ACS journal of surfaces and colloids  |d 1992  |g 29(2013), 18 vom: 07. Mai, Seite 5435-42  |w (DE-627)NLM098181009  |x 1520-5827  |7 nnns 
773 1 8 |g volume:29  |g year:2013  |g number:18  |g day:07  |g month:05  |g pages:5435-42 
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