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Impact of Electronic Coupling, Symmetry, and Planarization on One- and Two-Photon Properties of Triarylamines with One, Two, or Three Diarylboryl Acceptors

https://doi.org/10.1021/jp211878u
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inferred← citeshttps://doi.org/10.1039/c9qm00627copenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c9tc04309hopenalex-snapshot
B–N coordinated triaryl pyrazole: effect of dimerization, and optical and NLO properties
inferred← citeshttps://doi.org/10.1039/c9tc05938eopenalex-snapshot
Bis(hexamethylazatriangulene)sulfone: a high-stability deep blue-violet fluorophore with 100% quantum yield and CIE y < 0.07
inferred← citeshttps://doi.org/10.1039/d0cp01726dopenalex-snapshot
Excitation/detection energy controlled anisotropy dynamics in asymmetrically cyano substituted tri-podal molecules
inferred← citeshttps://doi.org/10.1039/d0dt01024copenalex-snapshot
Synthesis of π-extended B ← N coordinated phenanthroimidazole dimers and their linear and nonlinear optical properties
inferred← citeshttps://doi.org/10.1039/d0tc05241hopenalex-snapshot
Deep-blue fluorophores with imidazoacridine acceptors: enhancing photostability and two-photon fluorescence using structural constraint
inferred← citeshttps://doi.org/10.1039/d0tc05702aopenalex-snapshot
Facile access to multi-state redox-active, push–pull naphthalenediimides: panchromatic radical anions and supramolecular networks
inferred← citeshttps://doi.org/10.1039/d1cp03346hopenalex-snapshot
Two-photon absorption properties of multipolar triarylamino/tosylamido 1,1,4,4-tetracyanobutadienes
inferred← citeshttps://doi.org/10.1039/d1sc02409dopenalex-snapshot
One- and two-electron reduction of triarylborane-based helical donor–acceptor compounds
inferred← citeshttps://doi.org/10.1039/d2cp05189copenalex-snapshot
Unveiling the molecular structure and two-photon absorption properties relationship of branched oligofluorenes
inferred← citeshttps://doi.org/10.1039/d3cp03125jopenalex-snapshot
Molecular torsion controls the excited state relaxation pathways of multibranched tetraphenylpyrazines: effect of substitution of morpholine vs. phenoxazine
inferred← citeshttps://doi.org/10.1039/d3tc00877kopenalex-snapshot
Centripetal triazine chromophores: towards efficient two-photon absorbers and highly emissive polyimide films
inferred← citeshttps://doi.org/10.1039/d4cp02227kopenalex-snapshot
Synthesis, photophysics and two-photon absorption of imidazole-centred tripodal chromophores
inferred← citeshttps://doi.org/10.1039/d5cp00589bopenalex-snapshot
The role of branching in the ultrafast dynamics and two-photon absorption of two pyrimidine push–pull molecules
inferred← citeshttps://doi.org/10.1063/1.4926998openalex-snapshot
Solvent-dependent intramolecular charge transfer delocalization/localization in multibranched push-pull chromophores
inferred← citeshttps://doi.org/10.1063/5.0227780openalex-snapshot
A review of non-linear optical (NLO) activity of organic compounds
inferred← citeshttps://doi.org/10.11606/t.76.2017.tde-26012017-090852openalex-snapshot
Não linearidades de segunda e terceira ordem de sistemas moleculares ramificados
inferred← citeshttps://doi.org/10.11606/t.76.2022.tde-18082022-090321openalex-snapshot
Determinando os efeitos de absorção de dois fótons e suas relações com a estrutura molecular de derivados de polifluorenos, purinas e imidazopiridinas
inferred← citeshttps://doi.org/10.1246/cl.200290openalex-snapshot
Dimesitylboron Endcapped S,N-Heteroacenes: Syntheses, Photophysical and Fluoride-binding Properties
inferred← citeshttps://doi.org/10.1351/pac196511030371openalex-snapshot
The exciton model in molecular spectroscopy
inferred← citeshttps://doi.org/10.1364/laop.2012.lt2a.21openalex-snapshot
Effect of Electron Withdrawing Substituents on the two-photon absorption Properties of a Novel Class of Push-Pull Triarylamine Compounds
inferred← citeshttps://doi.org/10.3390/ma10030223openalex-snapshot
Lighting the Way to See Inside Two-Photon Absorption Materials: Structure–Property Relationship and Biological Imaging
inferred← citeshttps://doi.org/10.3998/ark.5550190.0014.106openalex-snapshot
Stabilization of pi-conjugated organoboron scaffolds by structural constraint
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