about
The influence of pentafluorophenyl groups on the nonlinear optical (NLO) performance of high generation dendrons and dendrimers.Functional hyperbranched polymers with advanced optical, electrical and magnetic properties.New hyperbranched conjugated polymers containing hexaphenylbenzene and oxadiazole units: convenient synthesis and efficient deep blue emitters for PLEDs application.From nitro- to sulfonyl-based chromophores: improvement of the comprehensive performance of nonlinear optical dendrimers.Dendrimers with large nonlinear optical performance by introducing isolation chromophore, utilizing the Ar/ArF self-assembly effect, and modifying the topological structure.Using two simple methods of Ar-Ar(F) self-assembly and isolation chromophores to further improve the comprehensive performance of NLO dendrimers.A Highly Efficient and Photostable Photosensitizer with Near-Infrared Aggregation-Induced Emission for Image-Guided Photodynamic Anticancer Therapy.Precise Two-Photon Photodynamic Therapy using an Efficient Photosensitizer with Aggregation-Induced Emission Characteristics.Smart activatable and traceable dual-prodrug for image-guided combination photodynamic and chemo-therapy.Highly efficient photosensitizers with aggregation-induced emission characteristics obtained through precise molecular design.Morphology and Structure Engineering in Nanofiber Reactor: Tubular Hierarchical Integrated Networks Composed of Dual Phase Octahedral CoMn2 O4 /Carbon Nanofibers for Water Oxidation.Nanocrystallization: A Unique Approach to Yield Bright Organic Nanocrystals for Biological Applications.Far Red/Near-Infrared AIE Dots for Image-Guided Photodynamic Cancer Cell Ablation.A biosensor based on self-clickable AIEgen: a signal amplification strategy for ultrasensitive immunoassays.A Porphyrin-Based Conjugated Polymer for Highly Efficient In Vitro and In Vivo Photothermal Therapy.A series of hyperbranched polytriazoles containing perfluoroaromatic rings from AB2-type monomers: convenient syntheses by click chemistry under copper(I) catalysis and enhanced optical nonlinearity.Metal-Organic-Framework-Assisted In Vivo Bacterial Metabolic Labeling and Precise Antibacterial Therapy.Multicolor monitoring of cellular organelles by single wavelength excitation to visualize the mitophagy process.Novel Functional Conjugative Hyperbranched Polymers with Aggregation-Induced Emission: Synthesis Through One-Pot “A2+B4” Polymerization and Application as Explosive Chemsensors and PLEDsSynthesis of conjugated polymers bearing pendant bipyridine ruthenium complexesAnomalously steep dips of earthquakes in the 2011 Tohoku-Oki source region and possible explanationsVisualizing Photodynamic Therapy in Transgenic Zebrafish Using Organic Nanoparticles with Aggregation-Induced EmissionHigh-generation second-order nonlinear optical (NLO) dendrimers: convenient synthesis by click chemistry and the increasing trend of NLO effectsNew hyperbranched polytriazoles containing isolation chromophore moieties derived from AB4 monomers through click chemistry under copper(I) catalysis: improved optical transparency and enhanced NLO effectsDendronlike main-chain nonlinear optical (NLO) polyurethanes constructed from "H"-type chromophores: synthesis and NLO propertiesHigh-generation second-order nonlinear optical (NLO) Dendrimers that contain isolation chromophores: convenient synthesis by using click chemistry and their increased NLO effectsTwo types of nonlinear optical polyurethanes containing the same isolation groups: syntheses, optical properties, and influence of binding modeFurther enhancement of the second-order nonlinear optical (NLO) coefficient and the stability of NLO polymers that contain isolation chromophore moieties by using the "suitable isolation group" concept and the Ar/Ar(F) self-assembly effectThe utilization of isolation chromophore in an "A3 +B2 " type second-order nonlinear optical hyperbranched polymerPoly(9,9'-diheylfluorene carbazole) functionalized with reduced graphene oxide: convenient synthesis using nitrogen-based nucleophiles and potential applications in optical limitingDual-Responsive Metabolic Precursor and Light-Up AIEgen for Cancer Cell Bio-orthogonal Labeling and Precise AblationBright Aggregation-Induced-Emission Dots for Targeted Synergetic NIR-II Fluorescence and NIR-I Photoacoustic Imaging of Orthotopic Brain TumorsA Light-Up Probe with Aggregation-Induced Emission for Real-Time Bio-orthogonal Tumor Labeling and Image-Guided Photodynamic TherapyHybrid Nanospheres to Overcome Hypoxia and Intrinsic Oxidative Resistance for Enhanced Photodynamic TherapyA Cross-linked Conjugated Polymer Photosensitizer Enables Efficient Sunlight-Induced PhotooxidationSpecific Near-Infrared Probe for Ultrafast Imaging of Lysosomal β-Galactosidase in Ovarian Cancer CellsVisualize Embryogenesis and Cell Fate Using Fluorescent Probes with Aggregation-Induced EmissionPolymerization-Enhanced Two-Photon Photosensitization for Precise Photodynamic TherapyEngineered Cell-Assisted Photoactive Nanoparticle Delivery for Image-Guided Synergistic Photodynamic/Photothermal Therapy of CancerCancer-Cell-Activated Photodynamic Therapy Assisted by Cu(II)-Based Metal-Organic Framework
P50
Q34106482-AE25821A-6979-4049-A4C8-7BE0B28B4A22Q38244540-0E7938FF-75F9-4132-9D9E-3DD9ECC834CEQ42999675-15652073-C9A3-4310-90F3-0DCB8288F41BQ44101905-37031E96-68CD-43C1-851F-5F87D36FA7D3Q44614830-E7C961F9-F81A-4CDB-8CE6-DEF3B972A886Q45777253-975CE664-60EC-401A-8A23-D560631ABE25Q46341432-220448DF-D687-439B-AC41-5B068E4EEDA0Q46359253-A9D9D482-CFC8-4EE8-B6A0-72387C511490Q47775389-A3C8A2DC-86A1-471F-AC5F-18FBAA214230Q47903423-9E98F034-4171-4F67-9D91-34FDDF63EBBAQ48028571-55B386B7-7320-40A6-AE10-3513E8512052Q48946636-B979F82A-BAEB-4083-BBDF-66215429AFC8Q50232788-AB38F915-9534-4AC7-889E-DC614F9D488BQ50652629-0DCE23E6-F3CB-43A2-86E5-76601937B60EQ51152911-10588E57-C4CA-423F-959F-559D584E6F7FQ51537647-A729A394-58B4-4E29-B724-A06DF7E4D51CQ52674667-903E52C5-6284-4833-BDB1-BF7AF436939DQ55071931-54218C3E-6A6C-48EC-88C6-193D2C1D1F74Q57343419-07B6AEF2-F41A-45E2-ACC5-46EBF6068B8EQ57756408-B4D0943E-7AF8-44CD-8E9E-FDCFD54E3708Q57869573-d3c9e8b7-4805-2bc8-7581-49465f50945dQ58582328-526400E5-56EA-449B-B4A5-27AE8F2056ADQ83166492-7D6C8DA2-E2EB-4797-AFDD-AEA6B64CADCBQ83507134-B932DE4A-77E8-472E-B194-C51439B4B94FQ83960968-F8B3652B-2B30-4828-8C78-0FA6CF881296Q84615901-FC0B2D99-AFB3-4C6C-8C6C-51CF027F6C2AQ84732094-5A8A1F18-5942-494A-986B-2988AFC13241Q86485372-F51BBE0D-A17F-4193-81DC-1820A74C43FBQ86860842-4A196936-171C-4000-8301-BBDEAFB16ADDQ87371728-CF805AE5-D9B6-4340-8122-AEDCE1F01445Q88511211-45F637AB-E3C4-434F-B729-7B5E1E760FE4Q88879421-0E9EEF25-1ACA-4DF6-9534-E61E4F8E8F8AQ89360197-4339F0B2-F336-4957-BD0A-19E856596770Q89546285-60FF6EAA-5E3D-4121-AF3A-3299204169B4Q90483588-1D99F97A-AFDE-4409-B2D3-C7A8BB4577CFQ90652747-E35DB9B3-4FAC-4076-AB4B-341BCE5953AFQ91106247-A044332F-F415-4703-95A3-E882F3D8D4B1Q91576719-43E85A9D-2CF0-4624-957F-595F76C5AD7EQ92643505-D4E76999-BD88-495C-9509-8D85E24FDA0CQ92719437-E3C4439A-71F2-4FC8-9661-DE5165B29808
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Wenbo Wu
@ast
Wenbo Wu
@en
Wenbo Wu
@es
Wenbo Wu
@nl
Wenbo Wu
@sl
type
label
Wenbo Wu
@ast
Wenbo Wu
@en
Wenbo Wu
@es
Wenbo Wu
@nl
Wenbo Wu
@sl
prefLabel
Wenbo Wu
@ast
Wenbo Wu
@en
Wenbo Wu
@es
Wenbo Wu
@nl
Wenbo Wu
@sl
P1053
G-2731-2013
P106
P1153
8438112000
P31
P3829
P496
0000-0002-6794-217X