Literature DB >> 12440923

Fluorescent sensors for the enantioselective recognition of mandelic acid: signal amplification by dendritic branching.

Ming-Hua Xu1, Jing Lin, Qiao-Sheng Hu, Lin Pu.   

Abstract

Novel chiral bisbinaphthyl compounds have been synthesized for the enantioselective fluorescent recognition of mandelic acid. By introducing dendritic branches to the chiral receptor unit, the fluorescence signals of the receptors are significantly amplified because of the light-harvesting effect of the dendritic structure. This has greatly increased the sensitivity of the sensors in the fluorescent recognition. Study of the three generation sensors demonstrates that the generation zero sensor is the best choice for the recognition of mandelic acid because of its greatly increased fluorescence signal over the core and its high enantioselectivity. This sensor is potentially useful for the high throughput screening of chiral catalysts for the asymmetric synthesis of alpha-hydroxycarboxylic acids.

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Year:  2002        PMID: 12440923     DOI: 10.1021/ja020989k

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  3 in total

1.  Enantioselective fluorescent recognition of amino alcohols by a chiral tetrahydroxyl 1,1'-binaphthyl compound.

Authors:  Qin Wang; Xi Chen; Lan Tao; Li Wang; Dan Xiao; Xiao-Qi Yu; Lin Pu
Journal:  J Org Chem       Date:  2007-01-05       Impact factor: 4.354

2.  Synthesis and spectroscopic investigation of a novel sensitive and selective fluorescent chemosensor for Ag+ based on a BINOL-glucose derivative.

Authors:  Yu Hu; Huayin Shen; Xiaohan Zhang; Yang Liu; Xiaoxia Sun
Journal:  RSC Adv       Date:  2018-06-26       Impact factor: 4.036

3.  Enantioselective fluorescent recognition of chiral acids by cyclohexane-1,2-diamine-based bisbinaphthyl molecules.

Authors:  Zi-Bo Li; Jing Lin; Michal Sabat; Marilise Hyacinth; Lin Pu
Journal:  J Org Chem       Date:  2007-05-27       Impact factor: 4.354

  3 in total

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