about
A remarkable effect of N,N-diethylamino functionality on the optoelectronic properties of a salicylimine-based probe for Al(3+).Simple bis-thiocarbono-hydrazones as sensitive, selective, colorimetric, and switch-on fluorescent chemosensors for fluoride anions.Controllable Photodynamic Therapy Implemented by Regulating Singlet Oxygen EfficiencyOrganic triplet sensitizer library derived from a single chromophore (BODIPY) with long-lived triplet excited state for triplet-triplet annihilation based upconversion.Photodynamic effect of light-harvesting, long-lived triplet excited state Ruthenium(II)-polyimine-coumarin complexes: DNA binding, photocleavage and anticancer studies.Chiral donor photoinduced-electron-transfer (d-PET) boronic acid chemosensors for the selective recognition of tartaric acids, disaccharides, and ginsenosides.Synthesis of novel bispyrene diamines and their application as ratiometric fluorescent probes for detection of DNA.The triplet excited state of Bodipy: formation, modulation and application.Accessing the Long-Lived Triplet Excited States in Transition-Metal Complexes: Molecular Design Rationales and Applications.An ICT-based strategy to a colorimetric and ratiometric fluorescence probe for hydrogen sulfide in living cells.Highly selective fluorescent OFF-ON thiol probes based on dyads of BODIPY and potent intramolecular electron sink 2,4-dinitrobenzenesulfonyl subunits.Effect of the electron donor/acceptor orientation on the fluorescence transduction efficiency of the d-PET effect of carbazole-based fluorescent boronic acid sensors.Diiodobodipy-styrylbodipy Dyads: Preparation and Study of the Intersystem Crossing and Fluorescence Resonance Energy Transfer.Long-lived emissive intra-ligand triplet excited states (3IL): next generation luminescent oxygen sensing scheme and a case study with red phosphorescent diimine Pt(II) bis(acetylide) complexes containing ethynylated naphthalimide or pyrene subunitsA highly selective OFF-ON red-emitting phosphorescent thiol probe with large stokes shift and long luminescent lifetime.Ethynylated triphenylamine monoboronic acid chemosensors: experimental and theoretical studies.Naked-eye recognition of Cu(II), Zn(II) and acetate ion by the first guanine-based difunctional chromoinophore.Rational design of d-PeT phenylethynylated-carbazole monoboronic acid fluorescent sensors for the selective detection of alpha-hydroxyl carboxylic acids and monosaccharides.Bodipy derivatives as organic triplet photosensitizers for aerobic photoorganocatalytic oxidative coupling of amines and photooxidation of dihydroxylnaphthalenes.Chiral binol-bisboronic acid as fluorescence sensor for sugar acids.Green light-excitable naphthalenediimide acetylide-containing cyclometalated Ir(III) complex with long-lived triplet excited states as triplet photosensitizers for triplet-triplet annihilation upconversion.An enantioselective fluorescent sensor for sugar acids.Intramolecular RET enhanced visible light-absorbing bodipy organic triplet photosensitizers and application in photooxidation and triplet-triplet annihilation upconversion.3,6-Disubstituted carbazole-based bisboronic acids with unusual fluorescence transduction as enantioselective fluorescent chemosensors for tartaric acid.Enhanced fluorescence and chiral discrimination for tartaric acid in a dual fluorophore boronic acid receptor.Red-light-absorbing diimine Pt(II) bisacetylide complexes showing near-IR phosphorescence and long-lived 3IL excited state of Bodipy for application in triplet-triplet annihilation upconversion.Chiral mono boronic acid as fluorescent enantioselective sensor for mono alpha-hydroxyl carboxylic acids.Bodipy-C60 triple hydrogen bonding assemblies as heavy atom-free triplet photosensitizers: preparation and study of the singlet/triplet energy transfer.Exploiting the reversible covalent bonding of boronic acids: recognition, sensing, and assembly.Triplet Excited State of BODIPY Accessed by Charge Recombination and Its Application in Triplet-Triplet Annihilation Upconversion.A Water-Stable Dual-Channel Luminescence Sensor for UO22+ Ions Based on an Anionic Terbium(III) Metal-Organic Framework.Rational Design of Emissive NIR-Absorbing Chromophores: Rh(III) Porphyrin-Aza-BODIPY Conjugates with Orthogonal Metal-Carbon Bonds.Radical-Enhanced Intersystem Crossing in New Bodipy Derivatives and Application for Efficient Triplet-Triplet Annihilation Upconversion.Highly Efficient Triplet Photosensitizers: A Systematic Approach to the Application of Ir(III) Complexes containing Extended Phenanthrolines.The unquenched triplet excited state of the fluorescent OFF/ON Bodipy-derived molecular probe based on photo-induced electron transfer.Iridium(III) Complexes Bearing Pyrene-Functionalized 1,10-Phenanthroline Ligands as Highly Efficient Sensitizers for Triplet-Triplet Annihilation Upconversion.Exploiting coumarin-6 as ancillary ligands in 1,10-phenanthroline Ir(iii) complexes: generating triplet photosensitisers with high upconversion capabilities.Novel ruthenium and iridium complexes of N-substituted carbazole as triplet photosensitisers.Enhanced Triplet-Triplet Energy Transfer and Upconversion Fluorescence through Host-Guest Complexation.Energy-funneling-based broadband visible-light-absorbing bodipy-C60 triads and tetrads as dual functional heavy-atom-free organic triplet photosensitizers for photocatalytic organic reactions.
P50
Q30811066-2F73906C-49F3-432B-B16A-7AD90424A9D2Q31089532-985D5C9E-38CA-4C95-9D80-7B448D215A53Q33914878-EAD9FCB7-FC31-4AA6-BACC-03567AB5374FQ33970277-CF309FAE-DF84-401C-B24D-9F9B2C25AD32Q36409416-72DEAB37-EBAF-40E3-AC3E-B14E2AC7F775Q38335012-DD1B2F3E-A21D-49C2-BD53-469CCD2D3154Q38353486-9274D7F1-1883-420D-931C-BF3BC9B14B1AQ38606837-233D8010-C56B-456D-BD5B-2B4CD30496FCQ38652775-B9B5EEA6-8B60-4462-9251-145F6057340BQ39403507-A549EC9C-0214-408E-A43B-7D583D3008F4Q39559557-C69AA51E-5FD7-4EF2-9828-C66A1DEBAF33Q39889847-A2877785-92B6-41F7-B084-7030D86DE1B9Q40873940-FD994607-599B-4A2B-A0F6-6D56CD73DC15Q42909704-F3F65EC6-6542-476C-89EE-4FF14191ABFFQ43054987-DC330DC0-6529-40A5-B295-ECC184109916Q43060773-4CF7B861-BDE8-4F21-96D6-5D7A81F9F62CQ43147576-19179302-5E26-4E3F-AE42-B8DFBF8023C6Q43248802-D5F87B99-7D18-4DBA-B797-012E8AEE5163Q43772292-94E36707-87D5-4914-B96A-8C99CB1F9A79Q44955101-A3EDF002-FEC1-44E6-8C3D-1C66B27EB756Q45109426-C5811970-9D8E-46C9-8C77-28B6AAEA9577Q45177651-0CD9D5AD-C8CD-4B10-8466-B928584358EEQ45337409-C4ED1199-F275-46A4-8BE1-287FFB62E539Q46163465-439F275C-9FD4-4610-BC1A-A96B87ECF05AQ46408619-B4E85B8F-91D5-4AAD-A90F-72D687F18289Q46474103-A909C1B9-2567-4DB2-8BC9-8115DB7A430AQ46571935-6652F8EE-63EF-43FC-AC3C-90EDF5E442AEQ47155440-DD5D804F-ACFF-47AE-8340-FF53CCA4BF16Q47562366-4292FC96-15E0-4AF7-B0F8-0012385DC0ABQ47722902-71E4244D-D717-43B5-9926-7D7A645C6311Q48062738-D66DDA5E-FA58-487D-9359-A41B61161F06Q48115441-C0F5B848-EE3B-4255-80D4-3498C1E3F13BQ48121219-CDBA3F76-4616-4847-A0FF-B3FC19787119Q48176960-F1A2FCD7-F004-46DA-9D0F-27CF7689267DQ48255232-F51F1251-6469-433D-9019-A4DDB9C68537Q48288524-0AEE4FFB-300F-4610-BA8F-D0DEE4324D46Q50065592-F802CD58-4146-4E6E-B26A-AB96D18E2276Q50074260-6AD5F19C-BED2-462C-B99A-128564AD5EA7Q50216485-9DA9BED5-5F90-4C62-85B8-C5431771A691Q50227438-93415692-A85C-40AC-BFE6-927806B802B9
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Jianzhang Zhao
@ast
Jianzhang Zhao
@en
Jianzhang Zhao
@es
Jianzhang Zhao
@nl
Jianzhang Zhao
@sl
type
label
Jianzhang Zhao
@ast
Jianzhang Zhao
@en
Jianzhang Zhao
@es
Jianzhang Zhao
@nl
Jianzhang Zhao
@sl
prefLabel
Jianzhang Zhao
@ast
Jianzhang Zhao
@en
Jianzhang Zhao
@es
Jianzhang Zhao
@nl
Jianzhang Zhao
@sl
P106
P1153
15761416900
P31
P496
0000-0002-5405-6398