Luminescent materials: locking π-conjugated and heterocyclic ligands with boron(III).
about
Aggregation-induced emission (AIE) of pyridyl-enamido-based organoboron luminophores.New AIE-active pyrimidine-based boronfluoride complexes with high solid-state emission and reversible mechanochromism luminescence behavior.Benzothiazole-pyrimidine-based BODIPY analogues: promising luminophores with fluorescence sensing and imaging ability and asymmetrization-induced solid-state emission.Push-pull dioxaborine as fluorescent molecular rotor: far-red fluorogenic probe for ligand-receptor interactions.Facile Arylation of Four-Coordinate Boron Halides by Borenium Cation Mediated Boro-desilylation and -destannylation.BOIMPY: Fluorescent Boron Complexes with Tunable and Environment-Responsive Light-Emitting Properties.Strongly Emissive and Photostable Four-Coordinate Organoboron N,C Chelates and Their Use in Fluorescence Microscopy.Detection of boronic acid derivatives in cells using a fluorescent sensor.Modeling excitation energy transfer in multi-BODIPY architectures.A Solution-Processable Donor-Acceptor Compound Containing Boron(III) Centers for Small-Molecule-Based High-Performance Ternary Electronic Memory Devices.Tuning of the colour and chemical stability of model boranils: a strong effect of structural modifications.One-pot synthesis of four-coordinate boron(III) complexes by the ligand-promoted organic group migration between boronic acids.Regioselective Amine-Borane Cyclization: Towards the Synthesis of 1,2-BN-3-Cyclohexene by Copper-Assisted Triazole/Gold Catalysis.A Diradical Approach towards BODIPY-Based Dyes with Intense Near-Infrared Absorption around λ=1100 nm.Highlights on the Road towards Highly Emitting Solid-State Luminophores: Two Classes of Thiazole-Based Organoboron Fluorophores with the AIEE/AIE Effect.Enhancing thermally activated delayed fluorescence characteristics by intramolecular B-N coordination in a phenylpyridine-containing donor-acceptor π-system.Aromatic metamorphosis: conversion of an aromatic skeleton into a different ring system.Sequential Reactions of Alkynes on an Iridium(III) Single Site.Two-photon absorption of BF2-carrying compounds: insights from theory and experiment.Modelling excitation energy transfer in covalently linked molecular dyads containing a BODIPY unit and a macrocycle.Synthesis, computational, and spectroscopic analysis of tunable highly fluorescent BN-1,2-azaborine derivatives containing the N-BOH moiety.Synthesis of carbazole-based BODIPY dimers showing red fluorescence in the solid state.An organoboron compound with a wide absorption spectrum for solar cell applications.Excitation energies, singlet-triplet energy gaps, spin-orbit matrix elements and heavy atom effects in BOIMPYs as possible photosensitizers for photodynamic therapy: a computational investigation.Boron complexes of aromatic ring fused iminopyrrolyl ligands: synthesis, structure, and luminescence properties.Air-Stable Spirofluorene-Containing Ladder-Type Bis(alkynyl)borane Compounds with Readily Tunable Full Color Emission Properties.A Modular Class of Fluorescent Difluoroboranes: Synthesis, Structure, Optical Properties, Theoretical Calculations and Applications for Biological Imaging.Carbazole-based BODIPYs with ethynyl substituents at the boron center: solid-state excimer fluorescence in the VIS/NIR region.Optical properties and mechanofluorochromism of new BODIPY dyes based on the pyridine-pyrimidine hybrid structure.Luminescent Di- and Trinuclear Boron Complexes Based on Aromatic Iminopyrrolyl Spacer Ligands: Synthesis, Characterization, and Application in OLEDs.Fluorescent benzene-centered mono-, bis- and tris-triazapentadiene-boron complexes.BOIMPYs: Rapid Access to a Family of Red-Emissive Fluorophores and NIR Dyes.New 3-(heteroaryl)-2-iminocoumarin-based borate complexes: synthesis, photophysical properties, and rational functionalization for biosensing/biolabeling applications.Dye-conjugated complementary lipophilic nucleosides as useful probes to study association processes by fluorescence resonance energy transfer.Pyridyl-1,2,4-triazole diphenyl boron complexes as efficient tuneable blue emitters.Dipyrrolylquinoxaline difluoroborates with intense red solid-state fluorescence.Boron(III)-Containing Donor-Acceptor Compound with Goldlike Reflective Behavior for Organic Resistive Memory Devices.Investigating the optical properties of BOIMPY dyes using ab initio tools.Synthesis of Boronate-Based Benzo[fg]tetracene and Benzo[hi]hexacene via Demethylative Direct Borylation.[Cr(ddpd)2](3+): A Molecular, Water-Soluble, Highly NIR-Emissive Ruby Analogue.
P2860
Q30872095-2AEC6988-FF17-441B-84CD-C116A716FAF5Q31052382-4775E465-F437-4A53-B6C4-64EF0FE27988Q31135877-28196C98-55FE-45D1-8D47-B16F6B7E94F8Q33647602-EAFEA18F-C71A-4A0D-A11B-7E85CBC3FE6BQ36761426-BF927953-DD46-476E-96AA-88E2F376B777Q38809997-858E8935-0929-4790-A210-FFEC96CC360AQ38838532-D0AEC08E-AF9A-4928-B1D1-50D8942671D9Q38869760-AAC62DBD-BBFF-4B54-BE24-475CC09DC125Q38961363-01BC72EE-B02E-4917-86CC-05EB021EB3AAQ38984246-4EA656A4-733F-4367-94EA-92D257DA351AQ40254213-E07AF943-E028-4AB3-BAAB-EADB5071E26CQ42274158-3149D8AB-653F-49EB-B76C-82D5D4AB72C6Q45040481-E273343A-A3DB-429D-8D0A-1117E95685B6Q46605843-B8C62DC0-05CC-44C3-ADBB-F2C13860F28CQ47755923-5A0260C7-B6A5-43BA-9AC1-75FA9D940CE4Q47903470-430C2995-9971-4FF5-AB7A-4A9DE1F41CDAQ48046740-648A3DE7-1276-4C2D-A362-C8C4C0F745C5Q48235601-ACED63A8-08FC-4262-93FD-2F42543E64CDQ48263284-85DF0429-8986-4241-8EB1-F95B8B842FBFQ49332265-13AE3922-7EB0-47F5-9F35-4644EE33C985Q49687111-D823DC7E-67D7-4306-87DC-DB7427647399Q50079236-E0D79430-1F9E-4A68-906F-031BAAD9D5F0Q50095424-AD8D6EBD-822F-4402-BDDE-C83426A24B30Q50107727-57053D45-08F5-4E14-AB3F-8BEE1A131BD5Q50196717-DE609CFC-C00E-413D-AC8B-74422B0F4CBCQ50197412-F47F7D9A-49FD-4421-90D0-C0EEA487CA72Q50198751-5E077E93-28BA-4980-8D4D-A234BEDF8C18Q50200512-BCABE103-D977-44BA-A74C-D64F52DD5279Q50201954-9C5A3BA5-C0B7-4B74-A126-4FDDE2AE73F8Q50214184-78A2BD7C-2671-4C5B-BA67-4B4ED8D42AC8Q50214781-14BFBA55-0421-453A-BD26-EDCA7069FA4FQ50228505-174AC33C-5BDD-4B14-8ABA-46002F3580C1Q50247683-3395BDA8-50A2-42F2-8ABE-154D31CD23C9Q50250819-29DB795A-6FFB-4B7E-9A1F-04E61D222D44Q50426354-8BD0BCDE-0DA7-49DC-B286-FF212625CE95Q50441031-7382EFDB-6672-4F73-8BBF-075ADE2409A4Q50669992-A96F21D8-3D5D-4B13-9D26-6CBBA6295AD5Q50738633-49FA0F53-F62E-4DB4-B3C8-CCA1529D7CD9Q50795559-A7E28FF6-0410-463A-9EA5-310641A87ED0Q50946694-A7D31F1E-EBD1-4300-9A7F-57E149AB99DA
P2860
Luminescent materials: locking π-conjugated and heterocyclic ligands with boron(III).
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Luminescent materials: locking π-conjugated and heterocyclic ligands with boron(III).
@en
type
label
Luminescent materials: locking π-conjugated and heterocyclic ligands with boron(III).
@en
prefLabel
Luminescent materials: locking π-conjugated and heterocyclic ligands with boron(III).
@en
P356
P1476
Luminescent materials: locking π-conjugated and heterocyclic ligands with boron(III)
@en
P2093
Julien Massue
Raymond Ziessel
P304
P356
10.1002/ANIE.201305554
P407
P577
2014-01-31T00:00:00Z