On the public citation graph

C3-Symmetric Triarylboron Building Blocks: Synthesis, Structures, and Photophysical Properties

0 signed · 46 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/anie.200601286openalex-snapshot
Charge‐Transfer Emission in Nonplanar Three‐Coordinate Organoboron Compounds for Fluorescent Sensing of Fluoride
inferredcites →https://doi.org/10.1002/anie.201102390openalex-snapshot
A Triarylboron‐Based Fluorescent Thermometer: Sensitive Over a Wide Temperature Range
inferredcites →https://doi.org/10.1002/anie.201611344openalex-snapshot
Facile Synthesis of Polycyclic Pentalenes with Enhanced Hückel Antiaromaticity
inferredcites →https://doi.org/10.1002/chem.201201719openalex-snapshot
Thermodynamics and Conformations in the Formation of Excited States and Their Interconversions for Twisted Donor‐Substituted Tridurylboranes
inferredcites →https://doi.org/10.1002/chem.201405621openalex-snapshot
D–π–A Triarylboron Compounds with Tunable Push–Pull Character Achieved by Modification of Both the Donor and Acceptor Moieties
inferredcites →https://doi.org/10.1002/chem.201502268openalex-snapshot
Luminescent Quadrupolar Borazine Oligomers: Synthesis, Photophysics, and Two‐Photon Absorption Properties
inferredcites →https://doi.org/10.1002/ejic.201200069openalex-snapshot
2,2′‐Diborylazobenzenes with Double N–B Coordination: Control of Fluorescent Properties by Substituents and Redox Reactions
inferredcites →https://doi.org/10.1002/ejoc.201901151openalex-snapshot
An Azide‐Substituted Triarylborane: A Key Compound for the Facile Synthesis of Fluorescent Triarylboranes Bearing Triazole Moieties as Connectable π‐Conjugated System Linkages
inferredcites →https://doi.org/10.1016/j.cclet.2016.06.007openalex-snapshot
Triarylborane π -electron systems with intramolecular charge-transfer transitions
inferredcites →https://doi.org/10.1016/j.dyepig.2012.11.022openalex-snapshot
Fluorene/tridurylborane hybrids as solution-processible hosts for phosphorescent organic light-emitting diodes
inferredcites →https://doi.org/10.1016/j.tetlet.2013.03.080openalex-snapshot
Synthesis of tris(4-amino-2,6-dimethylphenyl)borane and facile extension of its π-conjugated system by utilizing the reactivity of the amino groups
inferredcites →https://doi.org/10.1021/acs.inorgchem.1c03578openalex-snapshot
Oligotriarylamine-Extended Organoboranes with Tunable Electron-Donating Strength by Changing the Number of Donor Units
inferredcites →https://doi.org/10.1021/acs.inorgchem.6b02847openalex-snapshot
Charge-Transfer Emitting Triarylborane π-Electron Systems
inferredcites →https://doi.org/10.1021/acs.inorgchem.9b03446openalex-snapshot
Effect of Branching on the Delayed Fluorescence and Phosphorescence of Simple Borylated Arylamines
inferredcites →https://doi.org/10.1021/acs.joc.1c02595openalex-snapshot
Synthesis and Characterization of Far-Red Emissive Boron-Based Triads Showing Large Stokes Shifts: Optical, TRANES, and Electrochemical Studies
inferredcites →https://doi.org/10.1021/acs.joc.5b00416openalex-snapshot
Charge Transfer Emission in Oligotriarylamine–Triarylborane Compounds
inferredcites →https://doi.org/10.1021/acs.orglett.3c02322openalex-snapshot
Chiral B–N AIEgens: Intense Blue Circularly Polarized Luminescence and Piezochromism
inferredcites →https://doi.org/10.1021/acsami.7b05615openalex-snapshot
Rigidity-Induced Delayed Fluorescence by Ortho Donor-Appended Triarylboron Compounds: Record-High Efficiency in Pure Blue Fluorescent Organic Light-Emitting Diodes
inferredcites →https://doi.org/10.1021/acscatal.1c04746openalex-snapshot
Triarylborane Catalyzed Carbene Transfer Reactions Using Diazo Precursors
inferredcites →https://doi.org/10.1021/ar900072uopenalex-snapshot
Impact of Donor−Acceptor Geometry and Metal Chelation on Photophysical Properties and Applications of Triarylboranes
inferredcites →https://doi.org/10.1021/ic400598xopenalex-snapshot
Porous and Robust Lanthanide Metal-Organoboron Frameworks as Water Tolerant Lewis Acid Catalysts
inferredcites →https://doi.org/10.1021/ic501801fopenalex-snapshot
Synthesis of Two Triarylboron-Functionalized Metal–Organic Frameworks: In Situ Decarboxylic Reaction, Structure, Photoluminescence, and Gas Adsorption Properties
inferredcites →https://doi.org/10.1021/ja015957wopenalex-snapshot
Colorimetric Fluoride Ion Sensing by Boron-Containing π-Electron Systems
inferredcites →https://doi.org/10.1021/ja0435135openalex-snapshot
Bimetallic Anilido-Aldimine Zinc Complexes for Epoxide/CO2 Copolymerization
inferredcites →https://doi.org/10.1021/jacs.7b10578openalex-snapshot
One-Shot Multiple Borylation toward BN-Doped Nanographenes
inferredcites →https://doi.org/10.1021/ol006660qopenalex-snapshot
Tridurylboranes Extended by Three Arylethynyl Groups as a New Family of Boron-Based π-Electron Systems
inferredcites →https://doi.org/10.1021/ol048771lopenalex-snapshot
Highly Efficient Stereoconservative Amidation and Deamidation of α-Amino Acids
inferredcites →https://doi.org/10.1021/ol101612zopenalex-snapshot
Synthesis and Fluorescence Properties of a Pyridomethene−BF2 Complex
inferredcites →https://doi.org/10.1021/om701237topenalex-snapshot
A BODIPY−Borane Dyad for the Selective Complexation of Cyanide Ion
inferredcites →https://doi.org/10.1039/c2cc17663gopenalex-snapshot
The equilibria and conversions between three excited states: the LE state and two charge transfer states, in twisted pyrene-substituted tridurylboranes
inferredcites →https://doi.org/10.1039/c2dt30118kopenalex-snapshot
Aryl(hydro)boranes: versatile building blocks for boron-doped π-electron materials
inferredcites →https://doi.org/10.1039/c2jm14920fopenalex-snapshot
Highly water-soluble neutral near-infrared emissive BODIPY polymeric dyes
inferredcites →https://doi.org/10.1039/c3cc43383hopenalex-snapshot
A 4 + 4 strategy for synthesis of zeolitic metal–organic frameworks: an indium-MOF with SOD topology as a light-harvesting antenna
inferredcites →https://doi.org/10.1039/c5tc00670hopenalex-snapshot
[3+3] Imine and β-ketoenamine tethered fluorescent covalent-organic frameworks for CO 2 uptake and nitroaromatic sensing
inferredcites →https://doi.org/10.1039/c5tc02406dopenalex-snapshot
Stimuli and shape responsive ‘boron-containing’ luminescent organic materials
inferredcites →https://doi.org/10.1039/c6sc04245gopenalex-snapshot
Recent developments in and perspectives on three-coordinate boron materials: a bright future
inferredcites →https://doi.org/10.1039/c6tc01353hopenalex-snapshot
Boosting reverse intersystem crossing by increasing donors in triarylboron/phenoxazine hybrids: TADF emitters for high-performance solution-processed OLEDs
inferredcites →https://doi.org/10.1039/c7cc06045aopenalex-snapshot
A water-soluble two-photon ratiometric triarylboron probe with nucleolar targeting by preferential RNA binding
inferredcites →https://doi.org/10.1039/c9cs00769eopenalex-snapshot
Halogenated triarylboranes: synthesis, properties and applications in catalysis
inferredcites →https://doi.org/10.1039/d1mh00696gopenalex-snapshot
Applications of triarylborane materials in cell imaging and sensing of bio-relevant molecules such as DNA, RNA, and proteins
inferredcites →https://doi.org/10.1063/1.1798975openalex-snapshot
One- and two-photon absorption of three-coordinate compounds with different centers (B,Al,N) and a 2,2′-dipyridylnitrogen functional group
inferredcites →https://doi.org/10.1107/s0021889899011486openalex-snapshot
DIAMOND – Visual Crystal Structure Information System
inferredcites →https://doi.org/10.1107/s0108767313094026openalex-snapshot
OLEX2– a complete package for molecular crystallography
inferredcites →https://doi.org/10.1107/s2053229614024218openalex-snapshot
Crystal structure refinement with SHELXL
inferredcites →https://doi.org/10.1107/s2053273314026370openalex-snapshot
SHELXT – Integrated space-group and crystal-structure determination
inferredcites →https://doi.org/10.3390/molecules22091522openalex-snapshot
Triarylborane-Based Materials for OLED Applications
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.