Progress in Fluorescent Chemosensors for Chiral Enantiomer Recognition Based on 2,2’-Naphthol Derivatives

杨丽,; 徐括喜,; 王晨娟,; 王超杰,

doi:10.6023/cjoc201306015

Cited by 3 publications

(2 citation statements)

References 17 publications

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“…In this context, macrocycles and supramolecular oligomers/polymers which operate through supramolecular interactions have been reported . Another frequent structural motif encountered in enantioselective fluorescent sensors is the binaphthol system . Several BINOL-derived compounds have been reported, and in some cases, the dendrimeric shape is used for signal amplification or even a derivative containing terpyridine (BINOL-terpyridine) or bis-BINOL connected by a monoamine can be found …”

Section: Introductionmentioning

confidence: 99%

Synthesis of Amino Acid-Derived 1,2,3-Triazoles: Development of a Nontrivial Fluorescent Sensor in Solution for the Enantioselective Sensing of a Carbohydrate and Bovine Serum Albumin Interaction

et al. 2018

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A series of amino acid-derived 1,2,3-triazoles presenting the amino acid and the aromatic moieties connected by a triazole-4-carboxylate spacer is discussed in this work. These compounds were achieved in good yields by organocatalytic enamine-azide [3 + 2] cycloadditions. One of the molecules obtained, bearing a 7-chloroquinoline moiety, was photoactive in the UV-violet region and was successfully employed as a probe for substrate-specific enantiomeric sensing using d-(-)-arabinose and l-(+)-arabinose. The potential application as a fluorescent probe to detect protein in phosphate buffer solution was also explored using as model bovine serum albumin (BSA). The studied compounds presented both suppression and association behavior in the presence of BSA. In addition, theoretical calculations were performed at levels ωB97XD/cc-pVDZ and PBE1PBE/6-311+G(d,p) together with the polarizable continuum model to understand the interaction of the molecules with the enantiomers.

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Section: Introductionmentioning

confidence: 99%

Synthesis of Amino Acid-Derived 1,2,3-Triazoles: Development of a Nontrivial Fluorescent Sensor in Solution for the Enantioselective Sensing of a Carbohydrate and Bovine Serum Albumin Interaction

et al. 2018

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“…[4,5] As a result of their simplicity and sensitivity, fluorescence sensors have played a significant role in sensing biologically important species in vitro and in vivo. [6][7][8][9][10][11][12][13] In recent years the development of fluorescence sensors based on boronic acids for recognitions of different saccharides has attracted considerable attention owing to their unique ability to effect in aqueous media. [1,[14][15][16] Phenylboronic acid has been reported to rapidly and reversibly interact with 1,2-diols and 1,3-diols to form cyclic esters in aqueous media, [17,18] which means the saccharides that comprise at least two diols groups can interact with boronic acids groups.…”

Section: Introductionmentioning

confidence: 99%

A BINOL Based Fluorescence Sensor for Distinction of D‐Glucose

Hou

et al. 2014

Chin. J. Chem.

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A saccharide fluorescent receptor based on 1,1'-binaphthol was developed. The boronic acids groups are directly attached to the 3,3'-positions of BINOL which acted as probes to saccharides. The methyl protected receptor R1 showed better response to D-fructose compared to other saccharides in the fluorescence quenching experiment. To improve the selectivity of D-glucose, the triethylene glycol protected receptor R2 was developed. Receptor R2 has a better water-solubility than R1 that can be applied in completely aqueous environment. With receptor R2, D-glucose has a different response to other saccharides that can be useful for the distinction of D-glucose.

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A Novel Highly Selective "Turn‐On" Fluorescence Sensor for Silver Ions Based on Schiff Base

et al. 2014

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A novel optical chemical sensor L was designed and synthesized for the determination of silver ions. The sensor L was derived from 1‐naphthaldehyde and 3,4,5‐tris(hexadecyloxy)benzohydrazide. The sensor L shows high sensitivity and selectivity for Ag+ detection in comparison to other metal cations (Mg2+, Ca2+, Al3+, Cr3+, Fe3+, Co2+, Ni2+, Cu2+, Zn2+, Cd2+, Hg2+, Pb2+) and has no significant response to other common metal cations. Upon addition of Ag+, the fluorescent emission of the sensor L was enhanced dramatically but other metal cations had no same response. The detection limit for Ag+ was 1.2×10−7 mol/L. Therefore, the sensor L is useful for Ag+ detection with some advantages including sensitivity, selectivity, simplicity and low‐cost.

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Progress in Fluorescent Chemosensors for Chiral Enantiomer Recognition Based on 2,2’-Naphthol Derivatives

Cited by 3 publications

References 17 publications

Synthesis of Amino Acid-Derived 1,2,3-Triazoles: Development of a Nontrivial Fluorescent Sensor in Solution for the Enantioselective Sensing of a Carbohydrate and Bovine Serum Albumin Interaction

Synthesis of Amino Acid-Derived 1,2,3-Triazoles: Development of a Nontrivial Fluorescent Sensor in Solution for the Enantioselective Sensing of a Carbohydrate and Bovine Serum Albumin Interaction

A BINOL Based Fluorescence Sensor for Distinction of D‐Glucose

A Novel Highly Selective "Turn‐On" Fluorescence Sensor for Silver Ions Based on Schiff Base

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