Enhanced chiral recognition by γ-cyclodextrin–cucurbit[6]uril-cowheeled [4]pseudorotaxanes

2018 ◽  
Vol 54 (21) ◽  
pp. 2643-2646 ◽  
Author(s):  
Ling Dai ◽  
Wanhua Wu ◽  
Wenting Liang ◽  
Wentong Chen ◽  
Xingke Yu ◽  
...  
Keyword(s):  
Chiral Recognition ◽  
Chiral Discrimination ◽  
Chiral Amines

γ-CD-CB[6]-cowheeled rotaxanes showed remarkably improved chiral discrimination towards chiral amines.

ChemInform Abstract: Chiral Discrimination of Fructo-Oligosaccharides Toward Amino Acid Derivatives by Induced-Fitting Chiral Recognition.

ChemInform ◽  
2010 ◽  
Vol 32 (32) ◽  
pp. no-no
Author(s):  
Motohiro Shizuma ◽  
Hiroshi Adachi ◽  
Mishio Kawamura ◽  
Yoshio Takai ◽  
Tokuji Takeda ◽  
...  
Keyword(s):  
Amino Acid ◽  
Chiral Recognition ◽  
Chiral Discrimination ◽  
Amino Acid Derivatives

Optical nanoprobes for chiral discrimination

The Analyst ◽  
2020 ◽  
Vol 145 (20) ◽  
pp. 6416-6434
Author(s):  
Arafeh Bigdeli ◽  
Forough Ghasemi ◽  
Nafiseh Fahimi-Kashani ◽  
Samira Abbasi-Moayed ◽  
Afsaneh Orouji ◽  
...  
Keyword(s):  
Chiral Recognition ◽  
Chiral Discrimination ◽  
Sensing Systems ◽  
Optical Nanoprobes ◽  
Luminescent Sensing

Chiral recognition can be achieved by exploiting chiral properties of nanoparticles within various colorimetric and luminescent sensing systems.

A novel electrochemical chiral sensor for 3,4-dihydroxyphenylalanine based on the combination of single-walled carbon nanotubes, sulfuric acid and square wave voltammetry

The Analyst ◽  
2014 ◽  
Vol 139 (9) ◽  
pp. 2243-2248 ◽  
Author(s):  
Lisha Chen ◽  
Fengxia Chang ◽  
Lingchen Meng ◽  
Meixian Li ◽  
Zhiwei Zhu
Keyword(s):  
Carbon Nanotubes ◽  
Sulfuric Acid ◽  
Chiral Recognition ◽  
Square Wave Voltammetry ◽  
Single Walled Carbon Nanotubes ◽  
Chiral Discrimination ◽  
Square Wave ◽  
Single Walled Carbon ◽  
Wave Voltammetry ◽  
Walled Carbon Nanotubes

The combination of SWV with chiral SWCNTs and H2SO4 shows chiral discrimination for 3,4-dihydroxyphenylalanine, and the three are indispensable for this chiral recognition.

C3-Symmetric Cage-like Receptors: Chiral Discrimination of α-Chiral Amines in a Confined Space

2010 ◽  
Vol 12 (19) ◽  
pp. 4228-4231 ◽  
Author(s):  
Sunderraman Sambasivan ◽  
Sung-Gon Kim ◽  
Sun Mi Choi ◽  
Young Min Rhee ◽  
Kyo Han Ahn
Keyword(s):  
Chiral Discrimination ◽  
Chiral Amines ◽  
Confined Space

scholarly journals Recognition and Sensing of Chiral Organic Molecules by Chiral Porphyrinoids: A Review

Chemosensors ◽  
2021 ◽  
Vol 9 (8) ◽  
pp. 204
Author(s):  
Gabriele Travagliante ◽  
Massimiliano Gaeta ◽  
Roberto Purrello ◽  
Alessandro D’Urso
Keyword(s):  
Scientific Community ◽  
Chiral Recognition ◽  
Organic Molecules ◽  
Chiral Discrimination ◽  
Spectroscopic Techniques ◽  
Chiral Molecules ◽  
Relevant Research ◽  
Non Covalent Interactions ◽  
Organic Guests ◽  
Covalent Interactions

Porphyrinoids are extremely attractive for their electronic, optical, and coordination properties as well as for their versatile substitution at meso/β-positions. All these features allow porphyrinoids to behave as chiroptical hosts for chiral recognition by means of non-covalent interactions towards chiral guests. Over the years, chiral discrimination of chiral molecules such as amino acids, alcohols, amines, hydroxy-carboxylic acids, etc. has aroused the interest of the scientific community. Hence, this review aims to report on the progress to date by illustrating some relevant research regarding the chiral recognition of a multitude of chiral organic guests through several chiral mono- and bis-porphyrins via different spectroscopic techniques.

Effect of Tartaric Acid on the Electrochemical Behavior of K3[Fe(CN)6] on the Electrodes Coated with Cyclodextrin Modified Multi-Walled Carbon Nanotubes

2013 ◽  
Vol 781-784 ◽  
pp. 346-351
Author(s):  
Hai Tao Wang ◽  
Shi Zhao Kang ◽  
Qiu Ling Yang ◽  
Jin Mu
Keyword(s):  
Carbon Nanotubes ◽  
Tartaric Acid ◽  
Electrochemical Behavior ◽  
Chiral Recognition ◽  
Electrochemical Reaction ◽  
Chiral Discrimination ◽  
Molecular Chirality ◽  
Control Step ◽  
Multi Walled Carbon Nanotubes ◽  
Walled Carbon Nanotubes

The effect of tartaric acid on the electrochemical behavior of K3[Fe(CN)6] was investigated on bare ITO electrodes, electrodes coated with multi-walled carbon nanotubes possessing carboxyl groups (MWNT-COOHs), and electrodes coated with cyclodextrin modified multi-walled carbon nanotubes (MWNT-CDs), respectively. It is found that the molecular chirality of tartaric acid can hardly influence the electrochemical behavior of K3[Fe(CN)6] on bare ITO electrodes. When the electrodes coated with MWNT-COOHs are used, the effect of the molecular chirality becomes distinguish. In the case of the electrodes coated with MWNT-CDs, the enhanced chiral discrimination between D-tartaric acid (D-TA) and L-tartaric acid (L-TA) can be observed. The control step in the electrochemical reaction of K3[Fe(CN)6] on the electrodes coated with MWNT-CDs is deduced to be different when D-TA or L-TA is introduced into the solution, respectively. Therefore, the enhanced chiral discrimination on the electrodes coated with MWNT-CDs is probably due to the change of the control step in the electrochemical reaction of K3[Fe(CN)6] caused by the chiral recognition of cyclodextrin moieties to D-TA and L-TA.

On the applicability of functional-group symmetry-adapted perturbation theory and other partitioning models for chiral recognition – the case of popular drug molecules interacting with chiral phases

2019 ◽  
Vol 21 (40) ◽  
pp. 22491-22510
Author(s):  
Michał Chojecki ◽  
Dorota Rutkowska-Zbik ◽  
Tatiana Korona
Keyword(s):  
Perturbation Theory ◽  
Interaction Energy ◽  
Chiral Recognition ◽  
Functional Group ◽  
Chiral Discrimination ◽  
Group Symmetry ◽  
Intermolecular Interaction Energy ◽  
Drug Molecules ◽  
Chiral Phases ◽  
Interacting Quantum Atoms

The F-SAPT partitioning of the intermolecular interaction energy, supported with the Interacting-Quantum-Atoms analysis, is a powerful tool for studies of the origin of chiral discrimination within diastereoisomeric complexes of the RR and RS types.

Highly sensitive chiral recognition of amino propanol in serum with R-mandelic acid-linked calix[4]arene modified graphene

2015 ◽  
Vol 3 (6) ◽  
pp. 1325-1329 ◽  
Author(s):  
Xiaowei Mao ◽  
Haiyang Zhao ◽  
Li Luo ◽  
Demei Tian ◽  
Haibing Li
Keyword(s):  
Mandelic Acid ◽  
Chiral Recognition ◽  
Chiral Discrimination ◽  
Highly Sensitive ◽  
Modified Graphene

An efficient chiral discrimination system for amino propanol enantiomers was reported based on R-mandelic acid calix[4]arene (FC4D) clicked graphene.

Colorimetric chiral discrimination of lysine enantiomers and configurable logic gate operation based on fluorescein-functionalized polydiacetylene vesicles

2020 ◽  
Vol 12 (5) ◽  
pp. 673-678 ◽  
Author(s):  
Guang Yang ◽  
Jie Ji ◽  
Siyu Zhang ◽  
Guangyao Li ◽  
Bin Li
Keyword(s):  
Chiral Recognition ◽  
Logic Gate ◽  
Chiral Discrimination ◽  
Gate Operation ◽  
Naked Eye ◽  
Sensitive Sensor ◽  
Colorimetric Visualization

This study describes a sensitive sensor for based on fluorescein-functionalized diacetylene (F-DA) chromatic conjugated vesicle which allows colorimetric visualization for the chiral recognition of lysine by the naked-eye.

Chiral Discrimination through 1 H NMR and Luminescence Spectroscopy: Dynamic Processes and Solid Strip for Chiral Recognition

2017 ◽  
Vol 23 (72) ◽  
pp. 18303-18313 ◽  
Author(s):  
Monalisa Gangopadhyay ◽  
Arunava Maity ◽  
Ananta Dey ◽  
P. R. Rajamohanan ◽  
Sapna Ravindranathan ◽  
...  
Keyword(s):  
Chiral Recognition ◽  
Chiral Discrimination ◽  
Luminescence Spectroscopy ◽  
Dynamic Processes ◽  
H Nmr
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