about
Non-covalent calixarene-amino acid complexes formed by MALDI-MS.Chiral exciton coupling of merocyanine dyes within a well defined hydrogen-bonded assembly.Inherently chiral calixarenes: synthesis, optical resolution, chiral recognition and asymmetric catalysis.Intelligent chiral sensing based on supramolecular and interfacial concepts.How was the proton transfer process in bis-3, 6-(2- benzoxazolyl)-pyrocatechol, single or double proton transfer?Recognition of amino acids by functionalized calixarenes.Rapid determination of enantiomeric excess: a focus on optical approaches.Surveying macrocyclic chemistry: from flexible crown ethers to rigid cyclophanes.Design of Selenium-Based Chiral Chemical Probes for Simultaneous Enantio- and Chemosensing of Chiral Carboxylic Acids with Remote Stereogenic Centers by NMR Spectroscopy.Chirality- and sequence-selective successive self-sorting via specific homo- and complementary-duplex formations.A coumarin-based fluorescent probe as a central nervous system disease biomarker.The entrapment of chiral guests with gated baskets: can a kinetic discrimination of enantiomers be governed through gating?Multi-temporal self-organizations in 1,3-O,O'-bis(dodecyl)calix[4]arene.Absorption, fluorescence, and cd spectroscopic study of chiral recognition by a binaphthyl-derived chromogenic calixcrown host.Noncovalent chirality sensing ensembles for the detection and reaction monitoring of amino acids, peptides, proteins, and aromatic drugs.Organometallic calixarenes: syceelike tetrarhenium(I) cavitands with tunable size, color, functionality, and coin-slot complexation.A Chiral Recognition System Orchestrated by Self-Assembly: Molecular Chirality, Self-Assembly Morphology, and Fluorescence Response.Copper(ii)-benzimidazole complexes as efficient fluorescent probes for l-cysteine in water.Chiral Discrimination through 1 H NMR and Luminescence Spectroscopy: Dynamic Processes and Solid Strip for Chiral Recognition.Toward Fluorescence-Based High-Throughput Screening for Enantiomeric Excess in Amines and Amino Acid Derivatives.Determination of enantiomeric excess in amine derivatives with molecular self-assemblies.A chiral ionic polymer for direct visual enantioselective recognition of α-amino acid anions.Induced helical chirality of perylenebisimide aggregates allows for enantiopurity determination and differentiation of α-hydroxy carboxylates by using circular dichroism.Enantioselective analysis of melagatran via an LSPR biosensor integrated with a microfluidic chip.Application of L-proline derivatives as chiral shift reagents for enantiomeric recognition of carboxylic acids.Synthesis and conformational studies of chiral macrocyclic [1.1.1]metacyclophanes containing benzofuran rings.Excited-state intramolecular proton transfer and charge transfer in 2-(2'-hydroxyphenyl)benzimidazole crystals studied by polymorphs-selected electronic spectroscopy.Enantioselective synthesis of helical polydiacetylene by application of linearly polarized light and magnetic field.Solid-phase extraction with metal-organic frameworks for the analysis of chiral compounds.A colorimetric and fluorescent chemosensor for the detection of an explosive—2,4,6-trinitrophenol (TNP)Novel chiral recognition beyond the limitation due to the law of mass action: highly enantioselective chiral sensing based on non-linear response in phase transition eventsIn SituArrangement of Supramolecules Throughout Direct Separation of Carbuterol Enantiomers in RP-HPLC System with Helical Additives in Mobile PhaseEnantioselective recognition of an inherently chiral calix[4]arene crown-6 carboxylic acid cone conformer towards chiral aminoalcoholsChiral discrimination using piezoelectric and optical gas sensorsDynamic Processes in Prochiral Solvating Agents (pro-CSAs) Studied by NMR SpectroscopyLangmuir monolayers of a cholesterol-armed cyclen complex that can control enantioselectivity of amino acid recognition by surface pressure
P2860
Q30846413-84B76663-866F-402C-8838-003F78B17761Q33942917-95AC070A-295F-4797-828D-94FFE5F826BCQ34578126-F827A835-DD7C-445D-8034-DDB623DAADD8Q35593865-88B0BD47-2871-41D4-A8E3-A64408997ADAQ36882037-37C65F75-795F-40CD-9113-EDAD138332F6Q37842159-0B13F6E5-3876-429A-BBDF-A44E2D8AFC38Q37926513-DB19640A-8434-4DF0-B935-23C7398E3F1BQ39277880-2368563F-8985-4212-BA7F-AA4F46252D14Q39394546-6126BADF-908A-4A1A-8DAD-2BA549B79D70Q42203566-D1A37802-3EB8-4746-B9F8-54500B9166BEQ42267503-43F5C499-84FF-4C5D-97E6-3A1344FE305EQ43728425-21A60C01-471D-48D8-AEC9-860D914AE07DQ44115285-1B5759D5-FB03-4B55-BAF4-EA83847C2F0CQ44760789-603C0C0F-E4C8-431C-BA83-378A4A55DAACQ46442397-0FD0725C-5CEA-4DE9-991C-434347E475D5Q47391057-C79F5ED0-0601-4B54-BAC2-5D4ED04C648BQ47874406-B2646FFA-3EAD-4758-A517-75C013A6FA72Q47926090-82ED49FD-6E3C-4A9A-BF6E-0A65EEA0D5CBQ48050734-3AE83FEA-1456-4B33-B3C7-8BF61B137287Q50226428-5FA8E960-2336-443A-808D-DB66BF23043AQ50278700-4CFD191A-4870-4DA5-B44C-FD2AAE962416Q50483354-151C4AFC-51F5-41EC-9793-1B9E7162DB99Q51065308-B906F8D2-D99A-4DDB-B3D6-BE8DC105777DQ51538439-A9D4E686-B07B-486A-9E0F-D91357D81B8FQ51581250-EE7943F5-036C-43A8-BA73-8625161CDB39Q51830333-5ACB62A6-052F-4DC8-9A7E-C3D4123CFCE3Q53133940-E3D53623-F857-4C34-A5F3-4441E8CA83F8Q53437019-2184D225-F9DC-4682-92CC-A59803E55C21Q53657477-797B2686-7C3F-4680-A56F-7C878E923FFDQ57363772-D4C67506-09BE-4A74-9FB8-2432FE9A24B5Q57363781-81A2EF68-361A-4052-9166-FA5F52CFAB37Q58278681-E889F061-A9E0-4C5F-BE59-626DA1BD99BEQ58322733-4556B48E-F2A2-43A7-9F68-E62E7D5AF4E4Q58981310-8B169513-9D48-4D16-B437-2B70E4C5FB6EQ59264464-643E72CD-84A1-4D3B-AC1D-2742386826A2Q59264746-068F3C65-1F04-4B53-AB1B-37E8E36CA1D5
P2860
description
article publié dans la revue scientifique Nature
@fr
scientific article published in Nature
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в Nature в серпні 1996
@uk
name
Colorimetric chiral recognition by a molecular sensor
@en
Colorimetric chiral recognition by a molecular sensor
@nl
type
label
Colorimetric chiral recognition by a molecular sensor
@en
Colorimetric chiral recognition by a molecular sensor
@nl
prefLabel
Colorimetric chiral recognition by a molecular sensor
@en
Colorimetric chiral recognition by a molecular sensor
@nl
P2093
P356
P1433
P1476
Colorimetric chiral recognition by a molecular sensor
@en
P2093
Masao Kubo
Shin'ya Maeda
Sumio Tokita
P2888
P304
P356
10.1038/382522A0
P407
P577
1996-08-01T00:00:00Z
P6179
1032593308