about
Chirality and energy transfer amplified circularly polarized luminescence in composite nanohelix.Gelation induced supramolecular chirality: chirality transfer, amplification and application.Dynamic Evolution of Coaxial Nanotoruloid in the Self-Assembled Naphthyl-Containing l-Glutamide.Photopolymerization and formation of a stable purple Langmuir-Blodgett film based on the gemini-type amphiphilic diacetylene derivatives.Self-assembled ultralong chiral nanotubes and tuning of their chirality through the mixing of enantiomeric components.Self-assembly of L-glutamate based aromatic dendrons through the air/water interface: morphology, photodimerization and supramolecular chirality.Design and self-assembly of L-glutamate-based aromatic dendrons as ambidextrous gelators of water and organic solvents.Photon upconversion in supramolecular gel matrixes: spontaneous accumulation of light-harvesting donor-acceptor arrays in nanofibers and acquired air stability.A peptide dendron-based shrinkable metallo-hydrogel for charged species separation and stepwise release of drugs.Photon upconversion in organic nanoparticles and subsequent amplification by plasmonic silver nanowires.Amplification of Circularly Polarized Luminescence through Triplet-Triplet Annihilation-Based Photon Upconversion.Doublet-Triplet Energy Transfer-Dominated Photon Upconversion.All-or-none switching of photon upconversion in self-assembled organogel systems.Endowing Perovskite Nanocrystals with Circularly Polarized Luminescence.Self-assembly of π-conjugated gelators into emissive chiral nanotubes: emission enhancement and chiral detection.Self-Assembled Luminescent Quantum Dots To Generate Full-Color and White Circularly Polarized Light.Solvent-Regulated Self-Assembly of an Achiral Donor-Acceptor Complex in Confined Chiral Nanotubes: Chirality Transfer, Inversion and Amplification.Full-Color Tunable Circularly Polarized Luminescent Nanoassemblies of Achiral AIEgens in Confined Chiral Nanotubes.Light-triggered self-assembly of a cyanostilbene-conjugated glutamide from nanobelts to nanotoroids and inversion of circularly polarized luminescence.Structural Insights Into 9-Styrylanthracene-Based Luminophores: Geometry Control Versus Mechanofluorochromism and Sensing Properties.Aggregation-induced photon upconversion through control of the triplet energy landscapes of the solution and solid states.Advanced functional luminogens in the solid-state: general discussion.Photon upconverting liquids: matrix-free molecular upconversion systems functioning in air.Organogelation-controlled topochemical [2+2] cycloaddition and morphological changes: from nanofiber to peculiar coaxial hollow toruloid-like nanostructures.A metal ion triggered shrinkable supramolecular hydrogel and controlled release by an amphiphilic peptide dendron.Control over the emerging chirality in supramolecular gels and solutions by chiral microvortices in milliseconds.Circularly Polarized Luminescence from a Pyrene-Cyclodextrin Supra-DendronNanotrumpets and circularly polarized luminescent nanotwists hierarchically self-assembled from an achiral C3-symmetric esterProton triggered circularly polarized luminescence in orthogonal- and co-assemblies of chiral gelators with achiral perylene bisimideAmphiphilic Schiff Base Organogels: Metal-Ion-Mediated Chiral Twists and Chiral RecognitionInterfacial assembly of a series of trigonal Schiff base amphiphiles in organized molecular filmsSelf-Assembled Organic Nanotubes through Instant Gelation and Universal Capacity for Guest Molecule EncapsulationSelf-Assembling Nanotubes Consisting of Rigid Cyclic γ-PeptidesHierarchical self-assembly of amphiphilic peptide dendrons: evolution of diverse chiral nanostructures through hydrogel formation over a wide pH range.Hierarchical co-assembly of chiral lipid nanotubes with an azobenzene derivative: optical and chiroptical switchingIsomeric effect in the self-assembly of pyridine-containing L-glutamic lipid: substituent position controlled morphology and supramolecular chiralityLangmuir−Blodgett Films and Chiroptical Switch of an Azobenzene-Containing Dendron Regulated by the in Situ Host−Guest Reaction at the Air/Water Interface†Multiresponsive Chiroptical Switch of an Azobenzene-Containing Lipid: Solvent, Temperature, and Photoregulated Supramolecular ChiralityRegulation of the Chiral Twist and Supramolecular Chirality in Co-Assemblies of Amphiphilic L-Glutamic Acid with BipyridinesTowards a universal organogelator: A general mixing approach to fabricate various organic compounds into organogels
P50
Q33786403-75CDB6F2-2C9A-4066-B653-DA571A10A488Q38224220-48258BA9-2E97-4E81-B396-16095BDFD8B8Q39396848-89FB14D5-5C4C-43CB-A99D-B12B9FFC7C3DQ43007857-3EB9BB8B-0DE7-4BA9-A5A7-F6ED4310948AQ43045548-76206B5D-F4AD-4DF3-A9DD-FFFF9C64A5BAQ43091115-9400E5AA-9CB1-45FD-91AC-DA797A81616EQ43202329-A06A64FE-27EB-4B09-9C55-0EF6501AB192Q46785275-1EDC15F7-7185-47C1-8541-4675C4FE7049Q46833048-CE6C3BCE-FB08-469C-8732-AF55C327CAD5Q47229662-A1A46B89-68C7-4E1B-84F3-A98981880CE0Q47949394-F3CD2248-F485-4362-B51A-AA8C314EC56EQ48048800-2A1C2732-1F47-4AAA-8F19-682D4606ECE8Q48919907-DD23CEC9-D58E-43C7-A56D-E6B6AE1F21C1Q49834084-F782636C-CFE7-4CC7-9C22-09FF5BD1021EQ50226044-6C727387-33F1-4B67-AAF4-73869B91827CQ50516105-2C4CD737-68CE-4B8F-9603-F784780FF8CCQ50947727-9B118294-F00F-4540-B698-99F558011399Q50958652-68A49B85-3A25-44F6-9496-60DB5B3ADF34Q52645465-7E6B5876-2C4A-49E4-BCEC-FAAA6EC1EC7BQ53466698-FE1E7098-CF76-4C0E-BFC9-FBF8B0BE03ADQ53503105-1ED2165D-D176-4FD1-9C5A-1D1C6250E296Q54356158-97940BAC-3E2C-497C-B84F-580DA6954DEAQ54456337-67528687-23E8-4614-8DDF-992C39D5BB6DQ54765843-12708D4D-2F1E-4803-8F5D-686842860CDDQ54767538-F7F4C095-3C79-47D1-9A0B-3382B1F3051CQ55414724-02F730A8-6673-4468-A101-B53B6AE9598DQ60481293-0BC3AAFF-A434-4B3B-96C9-5434685E47A0Q60481302-43D81227-C6C3-475E-A4B2-1C781478ACF1Q60481305-ADE9DEBE-E287-43FB-AFA1-8C994DB37D2CQ60481427-6556CAD3-0401-4A15-9420-9B05FD978A07Q60481443-902F86E9-4220-4F8C-AFEA-232D1220B970Q60481455-8DE72598-B1C1-4CB2-9287-02CED791C7E4Q60481457-89C83C95-DFF9-4364-AEE4-EA690C4C5089Q60481469-AD765431-53A3-4E28-97E1-2E7D2AA2656DQ60481471-95C13F5E-E578-4188-9656-7980798710FDQ60481477-461EBB2F-8276-4532-B522-3289ADECA0A3Q60481479-E973B7DF-5C25-4A55-9FC2-A461C10DAD65Q60481485-572C3FE6-3EFA-4A0F-B2C1-3D052D49BC87Q60481486-089C32D8-5B66-4D7A-B62E-F2B7D3503AF9Q60481497-61870D2C-E46B-4D01-94EF-DF9BF7CC2097
P50
description
researcher ORCID: 0000-0002-5971-7546
@en
name
Pengfei Duan
@ast
Pengfei Duan
@en
Pengfei Duan
@es
Pengfei Duan
@nl
type
label
Pengfei Duan
@ast
Pengfei Duan
@en
Pengfei Duan
@es
Pengfei Duan
@nl
prefLabel
Pengfei Duan
@ast
Pengfei Duan
@en
Pengfei Duan
@es
Pengfei Duan
@nl
P106
P31
P496
0000-0002-5971-7546