Search
| Leader | 00000nz a2200037n 45 0 | ||
|---|---|---|---|
| 001 | WKP|Q87772574 (VIAF cluster) (Authority/Source Record) | ||
| 003 | WKP | ||
| 005 | 20241120235807.0 | ||
| 008 | 241120nneanz||abbn n and d | ||
| 035 | ‡a (WKP)Q87772574 | ||
| 024 | ‡a 0000-0002-2049-1324 ‡2 orcid | ||
| 035 | ‡a (OCoLC)Q87772574 | ||
| 100 | 0 | ‡a Cheng Yang ‡c researcher (ORCID 0000-0002-2049-1324) ‡9 en | |
| 670 | ‡a Author's A Supramolecular Strategy for Enhancing Photochirogenic Performance through Host/Guest Modification: Dicationic γ-Cyclodextrin-Mediated Photocyclodimerization of 2,6-Anthracenedicarboxylate | ||
| 670 | ‡a Author's An Ultimate Stereocontrol in Supramolecular Photochirogenesis: Photocyclodimerization of 2-Anthracenecarboxylate Mediated by Sulfur-Linked β-Cyclodextrin Dimers | ||
| 670 | ‡a Author's Effects of Temperature and Host Concentration on the Supramolecular Enantiodifferentiating [4 + 4] Photodimerization of 2-Anthracenecarboxylate through Triplet-Triplet Annihilation Catalyzed by Pt-Modified Cyclodextrins | ||
| 670 | ‡a Author's Efficient Triplet-Triplet Annihilation Upconversion with an Anti-Stokes Shift of 1.08 eV Achieved by Chemically Tuning Sensitizers | ||
| 670 | ‡a Author's Enantiodifferentiation in the Photoisomerization of (Z,Z)-1,3-Cyclooctadiene in the Cavity of γ-Cyclodextrin-Curcubit[6]uril-Wheeled [4]Rotaxanes with an Encapsulated Photosensitizer | ||
| 670 | ‡a Author's Enantioselective photoinduced cyclodimerization of a prochiral anthracene derivative adsorbed on helical metal nanostructures | ||
| 670 | ‡a Author's Fulleropillar[4]arene: The Synthesis and Complexation Properties | ||
| 670 | ‡a Author's pH-Controlled Chirality Inversion in Enantiodifferentiating Photocyclodimerization of 2-Antharacenecarboxylic Acid Mediated by γ-Cyclodextrin Derivatives | ||
| 670 | ‡a Author's Photocatalytic Supramolecular Enantiodifferentiating Dimerization of 2-Anthracenecarboxylic Acid through Triplet-Triplet Annihilation. | ||
| 670 | ‡a Author's Precise Manipulation of Temperature-Driven Chirality Switching of Molecular Universal Joints through Solvent Mixing | ||
| 670 | ‡a Author's Redox-Triggered Chirality Switching and Guest-Capture/Release with a Pillar[6]arene-Based Molecular Universal Joint | ||
| 670 | ‡a Author's Reversal of Regioselectivity during Photodimerization of 2-Anthracenecarboxylic Acid in a Water-Soluble Organic Cavitand | ||
| 670 | ‡a Author's Supramolecular enantiomeric and structural differentiation of amino acid derivatives with achiral pillar[5]arene homologs | ||
| 670 | ‡a Author's Supramolecular Photochirogenesis Driven by Higher-Order Complexation: Enantiodifferentiating Photocyclodimerization of 2-Anthracenecarboxylate to Slipped Cyclodimers via a 2:2 Complex with β-Cyclodextrin. | ||
| 670 | ‡a Author's Synergetic effects in the enantiodifferentiating photocyclodimerization of 2-anthracenecarboxylic acid mediated by β-cyclodextrin-pillar[5]arene-hybridized hosts | ||
| 670 | ‡a Author's Synthesis, enantioseparation and photophysical properties of planar-chiral pillar[5]arene derivatives bearing fluorophore fragments | ||
| 670 | ‡a Author's Temperature-Driven Planar Chirality Switching of a Pillar[5]arene-Based Molecular Universal Joint | ||
| 909 | ‡a (orcid) 0000000220491324 ‡9 1 | ||
| 919 | ‡a effectsoftemperatureandhostconcentrationonthesupramolecularenantiodifferentiatingphotodimerizationof2anthracenecarboxylatethroughtriplettripletannihilationcatalyzedbyptmodifiedcyclodextrins ‡A Effects of Temperature and Host Concentration on the Supramolecular Enantiodifferentiating [4 + 4] Photodimerization of 2-Anthracenecarboxylate through Triplet-Triplet Annihilation Catalyzed by Pt-Modified Cyclodextrins ‡9 1 | ||
| 919 | ‡a supramolecularstrategyforenhancingphotochirogenicperformancethroughhostguestmodificationdicationicγcyclodextrinmediatedphotocyclodimerizationof26anthracenedicarboxylate ‡A A Supramolecular Strategy for Enhancing Photochirogenic Performance through Host/Guest Modification: Dicationic γ-Cyclodextrin-Mediated Photocyclodimerization of 2,6-Anthracenedicarboxylate ‡9 1 | ||
| 919 | ‡a ultimatestereocontrolinsupramolecularphotochirogenesisphotocyclodimerizationof2anthracenecarboxylatemediatedbysulfurlinkedβcyclodextrindimers ‡A An Ultimate Stereocontrol in Supramolecular Photochirogenesis: Photocyclodimerization of 2-Anthracenecarboxylate Mediated by Sulfur-Linked β-Cyclodextrin Dimers ‡9 1 | ||
| 919 | ‡a temperaturedrivenplanarchiralityswitchingofapillararenebasedmolecularuniversaljoint ‡A Temperature-Driven Planar Chirality Switching of a Pillar[5]arene-Based Molecular Universal Joint ‡9 1 | ||
| 919 | ‡a synthesisenantioseparationandphotophysicalpropertiesofplanarchiralpillararenederivativesbearingfluorophorefragments ‡A Synthesis, enantioseparation and photophysical properties of planar-chiral pillar[5]arene derivatives bearing fluorophore fragments ‡9 1 | ||
| 919 | ‡a synergeticeffectsintheenantiodifferentiatingphotocyclodimerizationof2anthracenecarboxylicacidmediatedbyβcyclodextrinpillararenehybridizedhosts ‡A Synergetic effects in the enantiodifferentiating photocyclodimerization of 2-anthracenecarboxylic acid mediated by β-cyclodextrin-pillar[5]arene-hybridized hosts ‡9 1 | ||
| 919 | ‡a supramolecularphotochirogenesisdrivenbyhigherordercomplexationenantiodifferentiatingphotocyclodimerizationof2anthracenecarboxylatetoslippedcyclodimersviaa22complexwithβcyclodextrin ‡A Supramolecular Photochirogenesis Driven by Higher-Order Complexation: Enantiodifferentiating Photocyclodimerization of 2-Anthracenecarboxylate to Slipped Cyclodimers via a 2:2 Complex with β-Cyclodextrin. ‡9 1 | ||
| 919 | ‡a supramolecularenantiomericandstructuraldifferentiationofaminoacidderivativeswithachiralpillararenehomologs ‡A Supramolecular enantiomeric and structural differentiation of amino acid derivatives with achiral pillar[5]arene homologs ‡9 1 | ||
| 919 | ‡a reversalofregioselectivityduringphotodimerizationof2anthracenecarboxylicacidinawatersolubleorganiccavitand ‡A Reversal of Regioselectivity during Photodimerization of 2-Anthracenecarboxylic Acid in a Water-Soluble Organic Cavitand ‡9 1 | ||
| 919 | ‡a redoxtriggeredchiralityswitchingandguestcapturereleasewithapillararenebasedmolecularuniversaljoint ‡A Redox-Triggered Chirality Switching and Guest-Capture/Release with a Pillar[6]arene-Based Molecular Universal Joint ‡9 1 | ||
| 919 | ‡a precisemanipulationoftemperaturedrivenchiralityswitchingofmolecularuniversaljointsthroughsolventmixing ‡A Precise Manipulation of Temperature-Driven Chirality Switching of Molecular Universal Joints through Solvent Mixing ‡9 1 | ||
| 919 | ‡a photocatalyticsupramolecularenantiodifferentiatingdimerizationof2anthracenecarboxylicacidthroughtriplettripletannihilation ‡A Photocatalytic Supramolecular Enantiodifferentiating Dimerization of 2-Anthracenecarboxylic Acid through Triplet-Triplet Annihilation. ‡9 1 | ||
| 919 | ‡a phcontrolledchiralityinversioninenantiodifferentiatingphotocyclodimerizationof2antharacenecarboxylicacidmediatedbyγcyclodextrinderivatives ‡A pH-Controlled Chirality Inversion in Enantiodifferentiating Photocyclodimerization of 2-Antharacenecarboxylic Acid Mediated by γ-Cyclodextrin Derivatives ‡9 1 | ||
| 919 | ‡a fulleropillararenethesynthesisandcomplexationproperties ‡A Fulleropillar[4]arene: The Synthesis and Complexation Properties ‡9 1 | ||
| 919 | ‡a enantioselectivephotoinducedcyclodimerizationofaprochiralanthracenederivativeadsorbedonhelicalmetalnanostructures ‡A Enantioselective photoinduced cyclodimerization of a prochiral anthracene derivative adsorbed on helical metal nanostructures ‡9 1 | ||
| 919 | ‡a enantiodifferentiationinthephotoisomerizationofzz13cyclooctadieneinthecavityofγcyclodextrincurcubiturilwheeledrotaxaneswithanencapsulatedphotosensitizer ‡A Enantiodifferentiation in the Photoisomerization of (Z,Z)-1,3-Cyclooctadiene in the Cavity of γ-Cyclodextrin-Curcubit[6]uril-Wheeled [4]Rotaxanes with an Encapsulated Photosensitizer ‡9 1 | ||
| 919 | ‡a efficienttriplettripletannihilationupconversionwithanantistokesshiftof108evachievedbychemicallytuningsensitizers ‡A Efficient Triplet-Triplet Annihilation Upconversion with an Anti-Stokes Shift of 1.08 eV Achieved by Chemically Tuning Sensitizers ‡9 1 | ||
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| 997 | ‡a 0 0 lived 0 0 ‡9 1 |
