Abstract
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Jing-Jing Dai, Hui-Ling Chen, Guo-Ying Chen, Lei Xu, Huan Zhu, Feng-Qing Yang
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10.1016/j.microc.2024.110207 · doi-reference
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10.1016/j.microc.2026.117671 · doi-reference
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10.1016/j.biomaterials.2010.01.087 · doi-reference
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10.1016/j.talanta.2025.128309 · doi-reference
Cobalt-doped ZIF-8 nanozyme with bifunctional catalytic activity for integrated monitoring and remediation of sulfadiazine contaminants
10.1016/j.isci.2025.113678 · doi-reference
Tailoring Chirality and Optimizing Enantioselective Recognition in Strategic Defect Engineering of Chiral Metal–Organic Frameworks
10.1021/acs.analchem.4c06114 · doi-reference
Inducing nucleation of MOF-74(Ni) with sepiolite for construction of hierarchically porous composites to synergistically enhance CO2 adsorption and desorption performance
10.1016/j.seppur.2025.136006 · doi-reference
Integrated Chiral Recognition and Enantiomeric Separation of Histidine by Metal–Organic Frameworks Engineered with Chiral Linkers
10.1021/acs.analchem.5c07182 · doi-reference
Enhanced Enantioselective Sensing of 1,1′-Bi-2-naphthol and Mandelic Acid by Proportional Fluorescence Sensor 3DOM Zn-MOF-74- L -Trp with Hierarchical Macro–Micropore Structure
10.1021/acs.inorgchem.4c04464 · doi-reference
Biphasic Enantioselective Fluorescent Recognition of Amino Acids by a Fluorophilic Probe
10.1002/chem.201900880 · doi-reference
Defect-engineered chiral metal-organic frameworks
10.1007/s00604-024-06534-7 · doi-reference
Indirect Construction of Chiral Metal–Organic Frameworks for Enantioselective Luminescence Sensing
10.1021/acs.accounts.4c00795 · doi-reference
Amino-ligand-coordinated versatile chiral MOF-based enzyme trap for enantioselective recognition and catalysis
10.1016/j.cej.2025.164745 · doi-reference
Oxidase-like MOF-818 Nanozyme with High Specificity for Catalysis of Catechol Oxidation
10.1021/jacs.0c07273 · doi-reference
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10.1016/j.bios.2024.116593 · doi-reference
Chitosan-wrapped MOF-808 surface for amplifying electrochemical chiral recognition signal
10.1007/s00604-025-07206-w · doi-reference
A Novel Chiral Molecularly Imprinted Electrochemical Sensor Based on β-CD Functionalized Graphene Quantum Dots for Enantioselective Detection of D-Carnitine
10.3390/foods14091648 · doi-reference
Enantioselective recognition-driven antibacterial activity by a multifunctional MOF-based chiral nanozyme
10.1016/j.cej.2026.177227 · doi-reference
Electrochemiluminescent enantiorecognition in a defective chiral metal organic framework
10.1016/j.electacta.2025.147726 · doi-reference
On-Line Three-DimensionalHigh-Performance LiquidChromatographic System for the Comprehensive and Enantio/StereoselectiveDetermination of All Proteinogenic Amino Acids in Human Plasma andUrine
10.1021/acs.analchem.6c03014 · doi-reference
Rigid urea-based structures drive analysis of chiral amino acids
10.1016/j.cclet.2025.112039 · doi-reference
Green and controlled synthesis of copper-based tryptophan flower-like chiral metal-organic framework for enantioselective recognition and volatile organic compound separation
10.1016/j.chroma.2025.466020 · doi-reference
A Surface Mediated Supramolecular Chiral Phenomenon for Recognition of l- and d-Cysteine
10.3390/nano8121027 · doi-reference
A novel achiral fluorescent nanoprobe for the chiral recognition of cysteine enantiomers
10.1016/j.snb.2023.134262 · doi-reference
Nano-molecular dual-dimensional collaborative sensor for chiral amino acid discrimination and mechanism insights
10.1016/j.bios.2025.118093 · doi-reference
A highly selective ratiometric fluorescent probe for cysteine detection
10.1016/j.molstruc.2025.142031 · doi-reference
Manganese-doped iron coordination polymer nanoparticles with enhanced peroxidase-like activity for colorimetric detection of antioxidants
10.1039/d1an01953h · doi-reference
Novel potential and current type chiral amino acids biosensor based on L/D-handed double helix carbon nanotubes@polypyrrole@Au nanoparticles@L/D-cysteine
10.1016/j.snb.2019.126667 · doi-reference
Fluorescence and colorimetric dual-mode sensor based on red-emitting chiral carbon dots for discrimination of serine enantiomers and basic amino acids
10.1016/j.snb.2026.139559 · doi-reference
Exploring the frontiers of emerging amino acid sensors: a review
10.1016/j.jiec.2025.01.015 · doi-reference
Chirality in Chemistry
10.1126/science.935852 · doi-reference
Chiral recognition and determination of enantiomeric excess by mass spectrometry: a review
10.1016/j.aca.2017.03.021 · doi-reference
Carbon dots as fluorescent probes for “off–on” detection of Cu2+ and l-cysteine in aqueous solution
10.1016/j.bios.2013.07.042 · doi-reference