Abstract
Contact and support
Need help, have a question, or want to contact the ResearchHub team?
© 2026 ResearchHub. Built for responsible scholarly connection.
Zhiwu Wei, Wenliang Li, Sifan Tu, Xiaohong Zhao, Yu Hu, Zhongyi Yuan
Abstract
Authors
Institutions
Provenance
crossref
Confidence 100%
No local reference links have been materialized yet.
No local citing links have been materialized yet.
Rational design of organic NIR-II fluorophores for advanced photothermal and photodynamic therapy
10.1016/j.ccr.2026.217643 · 2026
Molecular engineering of NIR-II fluorophores for improved biomedical detection
10.1002/anie.202007040 · 2021
The latest developments of near-infrared fluorescent probes from NIR-I to NIR-II for bioimaging
10.1007/s44211-025-00735-7 · 2025
Activatable molecular probes with clinical promise for NIR-II fluorescent imaging
10.1002/smll.202411787 · 2025
Near-infrared electron acceptors with cyano-substituted 2-(3-oxo-2, 3-dihydroinden-1-ylidene)malononitrile end-groups for organic solar cells
10.1021/acsenergylett.3c00664 · 2023
Silicon-rhodamine-enabled identification for near-infrared light controlled proximity labeling in vitro and in vivo
10.1038/s41467-025-63496-x · 2025
Dual-mode narrowband organic photodetectors for self-aligned imaging in NIR-I and NIR-II
10.1038/s41467-025-62394-6 · 2025
Interface-engineered organic near-infrared photodetector for imaging applications
10.1021/acsami.3c03708 · 2023
Bright aggregation-induced-emission dots for targeted synergetic NIR-II fluorescence and NIR-I photoacoustic imaging of orthotopic brain tumors
openalex
Confidence 95%
datacite
Confidence 0%
10.1002/adma.201800766 · 2018
Integrated perovskite/bulk-heterojunction organic solar cells
10.1002/adma.201805843 · 2020
Unimolecular micellization strategy for achieving NIR-II excited fluorophores with enhanced brightness in aqueous media
10.1002/anie.202514722 · 2026
Noncovalently fused-ring electron acceptors with near-infrared absorption for high-performance organic solar cells
10.1038/s41467-019-11001-6 · 2019
Construction and optimization of organic fluorophores in NIR-II fluorescence imaging
10.1039/d5cs00063g · 2025
Phthalocyanines as contrast agents for photothermal therapy
10.1016/j.ccr.2020.213548 · 2021
Chiral boron dipyrromethene dye with acid-responsive near-infrared emission and chiral optical behavior
10.1002/cplu.202500237 · 2025
Naphthofluorescein-based organic nanoparticles with superior stability for near-infrared photothermal therapy
10.1039/d2nr02284b · 2022
Aza-BODIPY-based fluorescent and colorimetric sensors and probes
10.2174/1570179419666220216123033 · 2023
Tuning the properties of azadipyrromethene-based near-infrared dyes using intramolecular BO chelation and peripheral substitutions
10.1021/acs.inorgchem.1c01597 · 2021
Azadipyrromethenes: From traditional dye chemistry to leading edge applications
10.1039/c6cs00200e · 2016
A zinc(II) complex of di(naphthylethynyl) azadipyrromethene with low synthetic complexity leads to OPV with high industrial accessibility
10.1039/c9ta08654d · 2019
Stable twisted conformation aza-bodipy NIR-II fluorescent nanoparticles with ultra-large stokes shift for imaging-guided phototherapy
10.1039/d1tb02066h · 2022
Azadipyrromethene-based Zn (II) complexes as nonplanar conjugated electron acceptors for organic photovoltaics
10.1002/adma.201400647 · 2014
Synthesis, structure, and properties of near-infrared [b]phenanthrene-fused BF2 azadipyrromethenes
10.1002/asia.201700876 · 2017
Near-IR absorbing J-aggregate of an amphiphilic BF2-azadipyrromethene dye by kinetic cooperative self-assembly
10.1002/anie.201701788 · 2017
O-chelated azadipyrromethenes as near-IR probes
10.1021/ol8018506 · 2008
Design of stable diradicals based on group 13 dyes of N2O2-bis(phenolate) aza-dipyrromethene and aza-BODIPY
10.1021/acs.inorgchem.5c03026 · 2025
Self-assembly of metallo-supramolecular amphiphiles based on azadipyrromethenes: Consecutive pathways to nanodiscs and nanosheets
10.1002/chem.202403855 · 2025
A near-infrared azadipyrromethene dye: Photophysical properties under different acidity conditions
10.1016/j.inoche.2020.107942 · 2020
Functionalized BF2 chelated azadipyrromethene dyes
10.1016/j.tet.2008.01.117 · 2008
Al(III) and Ga(III) bisphenolate azadipyrromethene-based ″N2O2″ complexes as efficient NIR-fluorophores
10.1021/acs.inorgchem.2c03918 · 2023
Wazagay: An innovative aza-BODIPY-derived near-infrared fluorescent probe for enhanced tumor imaging
10.1021/acs.jmedchem.4c01435 · 2024
An amphiphilic near-infrared Mn,O-chelated metallo-azadipyrromethene dye: Synthesis, acid-responsive properties, and aggregation pathway control
10.1016/j.dyepig.2023.111573 · 2023
Synthesis, photophysical and redox properties of highly stable radicals of Ni(II) bis(2-aminophenyl)-azadipyrromethene
10.1021/acs.inorgchem.5c00662 · 2025
Synthesis and property study of phthalocyanine tetraimides as solution processable electron acceptors
10.1016/j.dyepig.2019.107980 · 2020
Silicon naphthalocyanine tetraimides: Cathode interlayer materials for highly efficient organic solar cells
10.1002/anie.202106364 · 2021
Solution-processable silicon naphthalocyanine tetraimides as near infrared electron acceptors in organic solar cells
10.1016/j.dyepig.2021.109846 · 2022
Metalloporphyrin/Phthalocyanine Catalysts for Electrocatalytic Nitrogen Fixation
10.1002/advs.202509323 · 2025
A2B2 Type Porphyrins with meso-Donor Groups: Synthesis, X-ray Structures, DFT Studies, and Photocatalytic Application Using Sunlight
10.1016/j.dyepig.2022.110861 · 2023
Ni, Cu, Zn, Pd, Ag, and Cd Tetraphenylporphyrin Ab Initio Thermochemistry: Enthalpy of Formation of ZnTPP Revisited
10.1021/acs.inorgchem.4c00662 · 2024
Metal Phthalocyanine Organic Thin-Film Transistors: Changes in Electrical Performance and Stability in Response to Temperature and Environment
10.1039/c9ra03648b · 2019
Julolidine-Functionalized Amphiphilic Aza-BODIPY Dyes: Synthesis, Near-Infrared-II Emission, and pH-Response
10.1002/ejoc.70488 · doi-reference
Direct Synthesis of an Unprecedented Stable Radical of Nickel(II) 3,5-Bis(dimedonyl)azadiisoindomethene with Strong and Narrow Near-Infrared Absorption at λ = 1000 nm
10.1021/acs.inorgchem.7b01140 · doi-reference
Development of a Class of Easily Scalable, Electron-Deficient, Core-Extended Benzo-Fused Azadipyrromethene Derivatives (“MB-DIPY”)
10.1021/acs.joc.9b02074 · doi-reference
Probing Electronic Communication and Excited-State Dynamics in the Unprecedented Ferrocene-Containing Zinc MB-DIPY
10.1021/acsomega.0c03764 · doi-reference
Radical Complexes of Nickel(II)/Copper(II) and Redox Noninnocent MB-DIPY Ligands: Unusual Stability and Strong Near-Infrared Absorption at λmax = 1300 nm
10.1002/chem.202201181 · doi-reference
Radical and Redox Forms of Pyridyl Appended MB-DIPYs
10.1002/asia.202500694 · doi-reference
Metal Phthalocyanine Organic Thin-Film Transistors: Changes in Electrical Performance and Stability in Response to Temperature and Environment
10.1039/c9ra03648b · doi-reference
Ni, Cu, Zn, Pd, Ag, and Cd Tetraphenylporphyrin Ab Initio Thermochemistry: Enthalpy of Formation of ZnTPP Revisited
10.1021/acs.inorgchem.4c00662 · doi-reference
A2B2 Type Porphyrins with meso-Donor Groups: Synthesis, X-ray Structures, DFT Studies, and Photocatalytic Application Using Sunlight
10.1016/j.dyepig.2022.110861 · doi-reference
Metalloporphyrin/Phthalocyanine Catalysts for Electrocatalytic Nitrogen Fixation
10.1002/advs.202509323 · doi-reference
Solution-processable silicon naphthalocyanine tetraimides as near infrared electron acceptors in organic solar cells
10.1016/j.dyepig.2021.109846 · doi-reference
Silicon naphthalocyanine tetraimides: Cathode interlayer materials for highly efficient organic solar cells
10.1002/anie.202106364 · doi-reference
Synthesis and property study of phthalocyanine tetraimides as solution processable electron acceptors
10.1016/j.dyepig.2019.107980 · doi-reference
Synthesis, photophysical and redox properties of highly stable radicals of Ni(II) bis(2-aminophenyl)-azadipyrromethene
10.1021/acs.inorgchem.5c00662 · doi-reference
An amphiphilic near-infrared Mn,O-chelated metallo-azadipyrromethene dye: Synthesis, acid-responsive properties, and aggregation pathway control
10.1016/j.dyepig.2023.111573 · doi-reference
Wazagay: An innovative aza-BODIPY-derived near-infrared fluorescent probe for enhanced tumor imaging
10.1021/acs.jmedchem.4c01435 · doi-reference
Al(III) and Ga(III) bisphenolate azadipyrromethene-based ″N2O2″ complexes as efficient NIR-fluorophores
10.1021/acs.inorgchem.2c03918 · doi-reference
Functionalized BF2 chelated azadipyrromethene dyes
10.1016/j.tet.2008.01.117 · doi-reference
A near-infrared azadipyrromethene dye: Photophysical properties under different acidity conditions
10.1016/j.inoche.2020.107942 · doi-reference
Self-assembly of metallo-supramolecular amphiphiles based on azadipyrromethenes: Consecutive pathways to nanodiscs and nanosheets
10.1002/chem.202403855 · doi-reference
Design of stable diradicals based on group 13 dyes of N2O2-bis(phenolate) aza-dipyrromethene and aza-BODIPY
10.1021/acs.inorgchem.5c03026 · doi-reference
O-chelated azadipyrromethenes as near-IR probes
10.1021/ol8018506 · doi-reference
Near-IR absorbing J-aggregate of an amphiphilic BF2-azadipyrromethene dye by kinetic cooperative self-assembly
10.1002/anie.201701788 · doi-reference
Synthesis, structure, and properties of near-infrared [b]phenanthrene-fused BF2 azadipyrromethenes
10.1002/asia.201700876 · doi-reference
Azadipyrromethene-based Zn (II) complexes as nonplanar conjugated electron acceptors for organic photovoltaics
10.1002/adma.201400647 · doi-reference
Stable twisted conformation aza-bodipy NIR-II fluorescent nanoparticles with ultra-large stokes shift for imaging-guided phototherapy
10.1039/d1tb02066h · doi-reference
A zinc(II) complex of di(naphthylethynyl) azadipyrromethene with low synthetic complexity leads to OPV with high industrial accessibility
10.1039/c9ta08654d · doi-reference
Azadipyrromethenes: From traditional dye chemistry to leading edge applications
10.1039/c6cs00200e · doi-reference
Tuning the properties of azadipyrromethene-based near-infrared dyes using intramolecular BO chelation and peripheral substitutions
10.1021/acs.inorgchem.1c01597 · doi-reference
Aza-BODIPY-based fluorescent and colorimetric sensors and probes
10.2174/1570179419666220216123033 · doi-reference
Naphthofluorescein-based organic nanoparticles with superior stability for near-infrared photothermal therapy
10.1039/d2nr02284b · doi-reference
Chiral boron dipyrromethene dye with acid-responsive near-infrared emission and chiral optical behavior
10.1002/cplu.202500237 · doi-reference
Phthalocyanines as contrast agents for photothermal therapy
10.1016/j.ccr.2020.213548 · doi-reference
Construction and optimization of organic fluorophores in NIR-II fluorescence imaging
10.1039/d5cs00063g · doi-reference
Noncovalently fused-ring electron acceptors with near-infrared absorption for high-performance organic solar cells
10.1038/s41467-019-11001-6 · doi-reference
Unimolecular micellization strategy for achieving NIR-II excited fluorophores with enhanced brightness in aqueous media
10.1002/anie.202514722 · doi-reference
Integrated perovskite/bulk-heterojunction organic solar cells
10.1002/adma.201805843 · doi-reference
Bright aggregation-induced-emission dots for targeted synergetic NIR-II fluorescence and NIR-I photoacoustic imaging of orthotopic brain tumors
10.1002/adma.201800766 · doi-reference
Interface-engineered organic near-infrared photodetector for imaging applications
10.1021/acsami.3c03708 · doi-reference
Dual-mode narrowband organic photodetectors for self-aligned imaging in NIR-I and NIR-II
10.1038/s41467-025-62394-6 · doi-reference