Results 31 to 40 of about 1,028 (242)

A Practical Enantioselective Fluorescent Sensor for Mandelic Acid

open access: yes, 2016
A novel optically active bisbinaphthyl fluorescent sensor, (S,S)- or (R,R)-1, is designed for the recognition of chiral α-hydroxycarboxylic acids. A convenient method has been developed to synthesize this compound.
Qiao-Sheng Hu (1650490)   +3 more
core   +1 more source

Topological Materials and Related Applications

open access: yesAdvanced Electronic Materials, EarlyView.
This review covers topological materials—including topological insulators, quantum valley Hall and quantum spin Hall insulators, and topological Weyl and Dirac semimetals—as well as their most recent advancements in fields such as spintronics, electronics, photonics, thermoelectrics, and catalysis.
Carlo Grazianetti   +9 more
wiley   +1 more source

In Situ Generated 1:1 Zn(II)-Containing Polymer Complex Sensor for Highly Enantioselective Recognition of N‑Boc-Protected Alanine

open access: yes, 2016
A novel chiral (S)-BINAM-based fluorescence polymer sensor was designed and synthesized by the polymerization of 5,5′-((2,5-dioctyloxy-1,4-phenylene)­bis­(ethyne-2,1-diyl)­bis­(2-hydroxy-3-(piperidin-1-ylmethyl)­benzaldehyde (M-1) with (S)-2,2 ...
Yixiang Cheng (1424512)   +5 more
core   +1 more source

Enantioselective electrochemical sensors and biosensors: A mini-review

open access: yesElectrochemistry Communications, 2014
Abstract Review is based on 50 original papers, published mostly in last decade, and presents recent advances in design of electrochemical enantioselective sensors, which can be employed in potentiometric, amperometric and voltammetric measurements.
openaire   +1 more source

Electrochemical Sensor Based on Molecularly Imprinted Polyaniline for Enantioselective Detection of Tyrosine Enantiomers

open access: yesECS Sensors Plus
A novel electrochemical sensor based on molecularly imprinted polyaniline (MIP) was developed for the selective recognition and quantitative determination of tyrosine enantiomers, with a particular focus on D-tyrosine (D-Tyr) in the presence of L ...
Zahra Shanehsaz, Amir Abbas Rafati
doaj   +1 more source

A photo-stable fluorescent chiral thiourea probe for enantioselective discrimination of chiral guests

open access: yes, 2018
Herein, a chiral thiourea Schiff base derived from (1R,2R)-1,2-cyclohexanediamine and tetraphenylethylene (TPE) was applied as a highly effective chiral sensor for the enantioselective discrimination of various acids and aminesviaion-pair and hydrogen ...
Shengxin Chen   +3 more
core   +1 more source

Graphene-based hybrid for enantioselective sensing applications

open access: yes, 2021
Chirality is a major field of research of chemical biology and is essential in pharmacology. Accordingly, approaches for distinguishing between different chiral forms of a compound are of great interest.
Zor, Erhan   +5 more
core  

Highly Fluorinated Chiral Sensors for Enantioselective Fluorescent Recognition [PDF]

open access: yes, 2017
Various kinds of fluorinated organic sensors using 1, 1'-Bi-2-naphthol (BINOL) as the chiral core have been developed for the fluorescent recognition of chiral molecules. This study is potentially applicable for rapid enantiomeric excess determination and high throughput catalyst screening.
openaire   +1 more source

Furo-Fused BINOL Based Crown as a Fluorescent Chiral Sensor for Enantioselective Recognition of Phenylethylamine and Ethyl Ester of Valine

open access: yes, 2016
A furo-fused BINOL based chiral crown was developed as an enantioselective chiral sensor for phenylethylamine and ethyl ester of valine. Fusion of furan to BINOL has resulted in a highly stereo-discriminating backbone for the chiral crown developed. This
Evans C. Coutinho (554348)   +3 more
core   +1 more source

Enantioselective Recognition of Mandelic Acid by a 3,6-Dithiophen-2-yl-9H-carbazole-Based Chiral Fluorescent Bisboronic Acid Sensor

open access: yes, 2016
We have prepared chiral fluorescent bisboronic acid sensors with 3,6-dithiophen-2-yl-9H-carbazole as the fluorophore. The thiophene moiety was used to extend the π-conjugation framework of the fluorophore in order to red-shift the fluorescence emission ...
Tony D. James (1430470)   +3 more
core   +1 more source

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