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Charge‐Transfer Emission in Nonplanar Three‐Coordinate Organoboron Compounds for Fluorescent Sensing of Fluoride
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Third-order Nonlinear Optical Properties of Organoboron Compounds: Molecular Structures and Second Hyperpolarizabilities
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Die Borchemie leuchtet: optische Eigenschaften von Molekülen und Polymeren C.D.E. dankt EPSRC und Syngenta für Postgraduiertenstipendien und T.B.M. der University of Durham für Unterstützung sowie Prof. Dr. K. Tamao für einen Vorabdruck von Lit. 32.
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Boron Chemistry Lights the Way: Optical Properties of Molecular and Polymeric Systems C.D.E. thanks EPSRC for a postgraduate studentship and Syngenta for a postgraduate scholarship, and T.B.M. thanks the University of Durham for support and Prof. Dr. K. Tamao for a preprint of ref. 32.
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A theoretical investigation of intermolecular interaction of a phthalimide based “on–off” sensor with different halide ions: tuning its efficiency and electro-optical properties
inferred← citeshttps://doi.org/10.1007/s00214-009-0695-9openalex-snapshot
Theoretical design study on photophysical property of the B–N derivatives for OLED applications
inferred← citeshttps://doi.org/10.1007/s00604-019-3468-8openalex-snapshot
DNA-templated copper nanoclusters as a fluorescent probe for fluoride by using aluminum ions as a bridge
inferred← citeshttps://doi.org/10.1007/s10812-024-01738-4openalex-snapshot
Chromogenic Signaling Probes with Different "N, O" Donors for Fe3+ Sensing and Cell Imaging
inferred← citeshttps://doi.org/10.1007/s10895-011-0858-7openalex-snapshot
2-(4-Formylphenyl)phenanthroimidazole as a Colorimetric and Fluorometric Probe for Selective Fluoride Ion Sensing
inferred← citeshttps://doi.org/10.1007/s10895-013-1257-zopenalex-snapshot
A Schiff-Based Colorimetric Fluorescent Sensor with the Potential for Detection of Fluoride Ions
inferred← citeshttps://doi.org/10.1007/s11426-010-3190-1openalex-snapshot
A class of fascinating optoelectronic materials: Triarylboron compounds
inferred← citeshttps://doi.org/10.1007/s11426-011-4359-yopenalex-snapshot
A near-infrared phosphorescent probe for F− based on a cationic iridium(III) complex with triarylboron moieties
inferred← citeshttps://doi.org/10.1007/s11458-010-0105-9openalex-snapshot
A novel fluorescence enhancing F− probe based on intermolecular energy transfer
inferred← citeshttps://doi.org/10.1007/s12039-020-01762-9openalex-snapshot
trans-4-[4-(Dimethylamino)styryl]-1-methylpyridinium iodide@cyclopentanocucurbit[6]uril as a fluorescent probe for anion recognition
inferred← citeshttps://doi.org/10.1007/s40242-013-3129-0openalex-snapshot
Theoretical analysis on magnetic properties of conjugated organic molecules containing borepin
inferred← citeshttps://doi.org/10.1016/b978-0-08-097774-4.00140-6openalex-snapshot
Chemical Sensors: Main Group Compounds for Anion Detection
inferred← citeshttps://doi.org/10.1016/j.aca.2011.07.009openalex-snapshot
A carbohydrate modified fluoride ion sensor and its applications
inferred← citeshttps://doi.org/10.1016/j.bmcl.2007.01.099openalex-snapshot
4-N-Methyl-N′-(2-dihydroxyboryl-benzyl)amino benzonitrile and its boronate analogue sensing saccharides and fluoride ion
inferred← citeshttps://doi.org/10.1016/j.cclet.2016.06.007openalex-snapshot
Triarylborane π -electron systems with intramolecular charge-transfer transitions
inferred← citeshttps://doi.org/10.1016/j.ccr.2014.09.022openalex-snapshot
The role of 2,3-dihydro-1-H-1,3,2-diazaboroles in luminescent molecules
inferred← citeshttps://doi.org/10.1016/j.chemphys.2008.10.050openalex-snapshot
Electron accepting abilities of arylborane derivatives: Effect of fluorine substituents
inferred← citeshttps://doi.org/10.1016/j.coelec.2017.02.007openalex-snapshot
Electrochemical properties and reactions of organoboron compounds
inferred← citeshttps://doi.org/10.1016/j.crci.2015.08.007openalex-snapshot
Photoinduced electron transfer in a triarylamine-organoboron-Ru(2,2′-bipyridine)32+ compound
inferred← citeshttps://doi.org/10.1016/j.dyepig.2012.11.016openalex-snapshot
A dual-channel probe for selective fluoride determination and application in live cell imaging
inferred← citeshttps://doi.org/10.1016/j.dyepig.2017.01.038openalex-snapshot
A two-photon fluorescent probe for imaging aqueous fluoride ions in living cells and tissues
inferred← citeshttps://doi.org/10.1016/j.dyepig.2018.05.053openalex-snapshot
Fluorescence turn-on detection of fluoride using HPQ-silyl ether reactive probes and its in vivo application
inferred← citeshttps://doi.org/10.1016/j.dyepig.2023.111233openalex-snapshot
Crystal packing and photoelectric property of bis(2-picolyl)amine-functionalized triarylborane and its complexes
inferred← citeshttps://doi.org/10.1016/j.electacta.2016.02.051openalex-snapshot
Electrochemical Properties and Reactions of Sulfur-Containing Organoboron Compounds
inferred← citeshttps://doi.org/10.1016/j.ica.2010.01.027openalex-snapshot
Synthesis, structures, photoluminescent and electroluminescent properties of boron complexes with anilido-imine ligands
inferred← citeshttps://doi.org/10.1016/j.ica.2017.01.011openalex-snapshot
Ruthenium(II) complexes of thiosemicarbazones: Synthesis, X-ray crystal structures, spectroscopy, electrochemistry, DFT studies and fluoride sensing properties
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2013.02.020openalex-snapshot
Lipophilic thioguanosine: An anion receptor for cesium fluoride
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2013.09.012openalex-snapshot
A colorimetric chemosensor for fluoride ions based on an indigo derivative
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2021.126748openalex-snapshot
A selectivity-enhanced ratiometric fluorescence imprinted sensor based on synergistic effect of covalent and non-covalent recognition units for ultrasensitive detection of ribavirin
inferred← citeshttps://doi.org/10.1016/j.jlumin.2011.06.027openalex-snapshot
Naphthalene-based fluorophores: Synthesis characterization, and photophysical properties
inferred← citeshttps://doi.org/10.1016/j.jlumin.2024.120692openalex-snapshot
Single-crystal-based excitation wavelength dependent fluorescence of an organometallic complex and applications in anti-counterfeiting and LED
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2009.01.031openalex-snapshot
Preparation of fluoride anion responsive poly(N-vinylcarbazole)-borane complexes
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2011.03.025openalex-snapshot
A DFT exploration of luminescent rhenium(I) tricarbonyl diimine complex with a triarylboron moiety and its F derivative
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2012.04.020openalex-snapshot
Turn-on colorimetric sensing of fluoride ions by a cationic triarylborane bearing benzothiazolium
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2012.12.012openalex-snapshot
Synthesis of novel colorimetric probe molecules and their application in anion recognition based on strong hydrogen bond
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2015.04.025openalex-snapshot
Photochemistry of hybrid organic–inorganic triarylborane-o-carboranes
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2022.122564openalex-snapshot
Recent development of three-coordinated boron-doped aromatics for optoelectronic applications
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2024.123412openalex-snapshot
C3-symmetric triarylboron building blocks: Synthesis, structures, and photophysical properties
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2019.112038openalex-snapshot
Furan/thiophene-based fluorescent hydrazones as fluoride and cyanide sensors
inferred← citeshttps://doi.org/10.1016/j.molstruc.2011.06.008openalex-snapshot
Two-photon excited fluorescence properties and anions recognition of a trivalent organoboron compound
inferred← citeshttps://doi.org/10.1016/j.polymer.2012.02.035openalex-snapshot
Triarylborane-functionalized polynorbornenes: Direct polymerization and signal amplification in fluoride sensing
inferred← citeshttps://doi.org/10.1016/j.saa.2013.04.010openalex-snapshot
Synthesis, characterization and density functional theory investigations of the electronic, photophysical and charge transfer properties of donor–bridge–acceptor triaminopyrazolo[1,5-a]pyrimidine dyes
inferred← citeshttps://doi.org/10.1016/j.saa.2015.06.028openalex-snapshot
Substituent effects on anion sensing of salicylidene Schiff base derivatives: Tuning sensitivity and selectivity
inferred← citeshttps://doi.org/10.1016/j.saa.2016.07.001openalex-snapshot
Design and synthesis of a new organic receptor and evaluation of colorimetric anion sensing ability in organo-aqueous medium
inferred← citeshttps://doi.org/10.1016/j.saa.2019.05.004openalex-snapshot
β-carboline-based turn-on fluorescence chemosensor for quantitative detection of fluoride at PPB level
inferred← citeshttps://doi.org/10.1016/j.snb.2008.03.006openalex-snapshot
A trivalent organoboron compound as one and two-photon fluorescent chemosensor for fluoride anion
inferred← citeshttps://doi.org/10.1016/j.snb.2010.06.005openalex-snapshot
A cationic triarylborane as water-tolerant fluorescent chemosensor for fluoride anions
inferred← citeshttps://doi.org/10.1016/j.snb.2012.09.049openalex-snapshot
Ratiometric fluorescence sensing of fluoride ions by triarylborane–phenanthroimidazole conjugates
inferred← citeshttps://doi.org/10.1016/j.snb.2014.01.058openalex-snapshot
A highly selective and real-time ratiometric fluorescent chemosensor for fluoride anion detection under either neutral or basic condition
inferred← citeshttps://doi.org/10.1016/j.snb.2014.03.054openalex-snapshot
“Reactive” probe for fluoride: “Turn-on” fluorescent sensing in aqueous solution and bioimaging in living cells
inferred← citeshttps://doi.org/10.1016/j.snb.2014.10.080openalex-snapshot
Synthesis and anion sensing properties of novel N,O-chelated perimidine–BF complex
inferred← citeshttps://doi.org/10.1016/j.snb.2015.08.087openalex-snapshot
AIE active pyridinium fused tetraphenylethene: Rapid and selective fluorescent “turn-on” sensor for fluoride ion in aqueous media
inferred← citeshttps://doi.org/10.1016/j.snb.2016.01.044openalex-snapshot
Dual binding site assisted chromogenic and fluorogenic discrimination of fluoride and cyanide by boryl functionalized BODIPY
inferred← citeshttps://doi.org/10.1016/j.snb.2017.09.072openalex-snapshot
Design for a small molecule based chemosensor containing boron and pyridine moieties to detect HF
inferred← citeshttps://doi.org/10.1016/j.snb.2017.11.091openalex-snapshot
Iodine is a common impurity in tetrabutylammonium fluoride
inferred← citeshttps://doi.org/10.1016/j.talanta.2017.08.101openalex-snapshot
Direct detection of fluoride ions in aquatic samples by surface-enhanced Raman scattering
inferred← citeshttps://doi.org/10.1016/j.tet.2008.10.002openalex-snapshot
Macrocyclic bis(amidonaphthol)s for anion sensing: tunable selectivity by ring size in proton transfer process
inferred← citeshttps://doi.org/10.1016/j.tet.2010.12.021openalex-snapshot
Colorimetric response of spiropyran derivative for anions in aqueous or organic media
inferred← citeshttps://doi.org/10.1016/j.tet.2011.03.047openalex-snapshot
The nature of 6,6′-bis(triphenylamine) substituted BINOL as chromophoric and fluorogenic hybrid chemosensor for selective fluoride detection
inferred← citeshttps://doi.org/10.1016/j.tet.2011.06.083openalex-snapshot
Double-coupling of dibromo arenes with aryltriolborates for synthesis of diaryl-substituted planar frameworks
inferred← citeshttps://doi.org/10.1016/j.tet.2014.06.114openalex-snapshot
Fluorescent sensor based on dimesitylborylthiophene derivative for probing fluoride and cyanide
inferred← citeshttps://doi.org/10.1016/j.tet.2015.10.081openalex-snapshot
Synthesis and photo-property of 2-cyano boron-dipyrromethene and the application for detecting fluoride ion
inferred← citeshttps://doi.org/10.1016/j.tet.2018.12.032openalex-snapshot
Impact of intramolecular H bond and n-π* interactions on photophysical and CO2 sensing properties of laterally appended D-π-A triarylboron compounds
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.09.026openalex-snapshot
Selective fluorescent PET sensing of fluoride (F−) using naphthalimide–thiourea and –urea conjugates
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.10.086openalex-snapshot
Unmodified fluorescein as a fluorescent chemosensor for fluoride ion detection
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.05.018openalex-snapshot
A BODIPY–indole conjugate as a colorimetric and fluorometric probe for selective fluoride anion detection
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.05.076openalex-snapshot
A highly emissive cruciform triarylborane as a ratiometric and solid state fluorescence sensor for fluoride ions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.11.099openalex-snapshot
Fluoride indicator that functions in mixed aqueous media: hydrogen bonding effects
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.02.112openalex-snapshot
A ratiometric fluorescent probe for fluoride ions with a tridentate receptor of boronic acid and imidazolium
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.06.094openalex-snapshot
New fluoro- and chromogenic chemosensors for the dual-channel detection of Hg2+ and F−
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.04.110openalex-snapshot
Stimuli-response fluorescence behaviors of dimesitylboron functionalized with tetraphenylethylene
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.07.017openalex-snapshot
Deboronation-induced ratiometric emission sensing of fluoride by 1,3,5-tris-(o-carboranyl-methyl)benzene
inferred← citeshttps://doi.org/10.1021/ac402592copenalex-snapshot
Self-Assembly of Graphene Oxide with a Silyl-Appended Spiropyran Dye for Rapid and Sensitive Colorimetric Detection of Fluoride Ions
inferred← citeshttps://doi.org/10.1021/ac500230popenalex-snapshot
Dual Binding Site Assisted Chromogenic and Fluorogenic Recognition and Discrimination of Fluoride and Cyanide by a Peripherally Borylated Metalloporphyrin: Overcoming Anion Interference in Organoboron Based Sensors
inferred← citeshttps://doi.org/10.1021/ac503177nopenalex-snapshot
Quaternary Ammonium Promoted Ultra Selective and Sensitive Fluorescence Detection of Fluoride Ion in Water and Living Cells
inferred← citeshttps://doi.org/10.1021/acs.accounts.4c00353openalex-snapshot
Modulating the Photophysical Properties of Twisted Donor–Acceptor–Donor π-Conjugated Molecules: Effect of Heteroatoms, Molecular Conformation, and Molecular Topology
inferred← citeshttps://doi.org/10.1021/acs.analchem.5b02237openalex-snapshot
Cell and in Vivo Imaging of Fluoride Ion with Highly Selective Bioluminescent Probes
inferred← citeshttps://doi.org/10.1021/acs.analchem.5b02578openalex-snapshot
Visualizing Fluoride Ion in Mitochondria and Lysosome of Living Cells and in Living Mice with Positively Charged Ratiometric Probes
inferred← citeshttps://doi.org/10.1021/acs.analchem.6b04421openalex-snapshot
Boric-Acid-Functional Lanthanide Metal–Organic Frameworks for Selective Ratiometric Fluorescence Detection of Fluoride Ions
inferred← citeshttps://doi.org/10.1021/acs.cgd.4c00878openalex-snapshot
Crystalline o-Carborane Derivatives as a Fluorescence Turning-On Probe for Acid Environments
inferred← citeshttps://doi.org/10.1021/acs.chemrev.3c00202openalex-snapshot
LNL-Carbazole Pincer Ligand: More than the Sum of Its Parts
inferred← citeshttps://doi.org/10.1021/acs.chemrev.7b00425openalex-snapshot
Long-Lived Emissive Probes for Time-Resolved Photoluminescence Bioimaging and Biosensing
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.0c00348openalex-snapshot
Backbone Boron-Functionalized Imidazoles/Imidazolium Salts: Synthesis, Structure, Metalation Studies, and Fluoride Sensing Properties
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.0c03196openalex-snapshot
Millisecond Time-scale Photoluminescence of B–N-doped Tetrathienonaphthalene with Borane/Amine Substituents
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.1c03578openalex-snapshot
Oligotriarylamine-Extended Organoboranes with Tunable Electron-Donating Strength by Changing the Number of Donor Units
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.6b02847openalex-snapshot
Charge-Transfer Emitting Triarylborane π-Electron Systems
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.8b01830openalex-snapshot
Supramolecular Pt(II) and Ru(II) Trigonal Prismatic Cages Constructed with a Tris(pyridyl)borane Donor
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.9b03159openalex-snapshot
Donor–Acceptor-Appended Triarylboron Lewis Acids: Ratiometric or Time-Resolved Turn-On Fluorescence Response toward Fluoride Binding
inferred← citeshttps://doi.org/10.1021/acs.joc.5b00416openalex-snapshot
Charge Transfer Emission in Oligotriarylamine–Triarylborane Compounds
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01015openalex-snapshot
Donor−π–Acceptor Type Unsymmetrical Triarylborane-Based Fluorophores: Synthesis, Fluorescence Properties, and Photostability
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02942openalex-snapshot
Pyrazinoindole-Based Lewis-Acid/Base Assembly: Intriguing Intramolecular Charge-Transfer Switching through the Dual-Sensing of Fluoride and Acid
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00836openalex-snapshot
Charge-Separated Mixed Valency in an Unsymmetrical Acceptor–Donor–Donor Triad Based on Diarylboryl and Triarylamine Units
inferred← citeshttps://doi.org/10.1021/acs.jpcc.4c05319openalex-snapshot
Thermally Activated Delayed Fluorescence of Dibenzophenazine-Cored Phenazaborines in Solid State: Anion Modulation of Photophysics
inferred← citeshttps://doi.org/10.1021/acs.jpclett.1c02668openalex-snapshot
A Multiple Excited-State Engineering of Boron-Functionalized Diazapentacene Via a Tuning of the Molecular Orbital Coupling
inferred← citeshttps://doi.org/10.1021/acs.langmuir.5b01513openalex-snapshot
Design of Fe3O4@SiO2@Carbon Quantum Dot Based Nanostructure for Fluorescence Sensing, Magnetic Separation, and Live Cell Imaging of Fluoride Ion
inferred← citeshttps://doi.org/10.1021/acs.organomet.1c00115openalex-snapshot
Enhancing Charge Transfer in (BIMCA)Pt(II) Alkynyls through the Use of Substituted Boranes
inferred← citeshttps://doi.org/10.1021/acs.organomet.6b00574openalex-snapshot
Triarylborane-Supported Polyferrocenyl Systems: Impact of the Linking Unit on Electronic and Electrochemical Properties
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b02604openalex-snapshot
Ru-Catalyzed Benzannulation Leads to Luminescent Boron-Containing Polycyclic Aromatic Hydrocarbons
inferred← citeshttps://doi.org/10.1021/acsomega.7b01379openalex-snapshot
Mopping up the Oil, Metal, and Fluoride Ions from Water
inferred← citeshttps://doi.org/10.1021/acsomega.7b01631openalex-snapshot
Anion Sensing with a Blue Fluorescent Triarylboron-Functionalized Bisbenzimidazole and Its Bisbenzimidazolium Salt
inferred← citeshttps://doi.org/10.1021/acsomega.8b03042openalex-snapshot
Forster Resonance Energy-Transfer-Based Ratiometric Fluorescent Indicator for Quantifying Fluoride Ion in Water and Toothpaste
inferred← citeshttps://doi.org/10.1021/ar8001816openalex-snapshot
Fluoride Ion Recognition by Chelating and Cationic Boranes
inferred← citeshttps://doi.org/10.1021/ar900072uopenalex-snapshot
Impact of Donor−Acceptor Geometry and Metal Chelation on Photophysical Properties and Applications of Triarylboranes
inferred← citeshttps://doi.org/10.1021/cm901987topenalex-snapshot
Optically pH and H2O2 Dual Responsive Composite Colloids through the Directed Assembly of Organic Dyes on Responsive Microgels
inferred← citeshttps://doi.org/10.1021/cr900401aopenalex-snapshot
Fluoride Ion Complexation and Sensing Using Organoboron Compounds
inferred← citeshttps://doi.org/10.1021/ic1004159openalex-snapshot
Extending π-Conjugation of Triarylborons with a 2,2-Bpy Core: Impact of Donor−Acceptor Geometry on Luminescence, Anion Sensing, and Metal Ion Binding
inferred← citeshttps://doi.org/10.1021/ic1021966openalex-snapshot
Tuning and Switching MLCT Phosphorescence of [Ru(bpy)3]2+ Complexes with Triarylboranes and Anions
inferred← citeshttps://doi.org/10.1021/ic202521zopenalex-snapshot
Triarylboron-Functionalized Cu(II) Carboxylate Paddlewheel Complexes
inferred← citeshttps://doi.org/10.1021/ic402441wopenalex-snapshot
Going beyond Red with a Tri- and Tetracoordinate Boron Conjugate: Intriguing Near-IR Optical Properties and Applications in Anion Sensing
inferred← citeshttps://doi.org/10.1021/ic501286mopenalex-snapshot
Heteroleptic Cyclometalated Iridium(III) Complexes Supported by Triarylborylpicolinate Ligand: Ratiometric Turn-On Phosphorescence Response upon Fluoride Binding
inferred← citeshttps://doi.org/10.1021/ic501335eopenalex-snapshot
Selective Sensitization of Eu(III) and Tb(III) Emission with Triarylboron-Functionalized Dipicolinic Acids
inferred← citeshttps://doi.org/10.1021/ic800500copenalex-snapshot
Highly Selective Phosphorescent Chemosensor for Fluoride Based on an Iridium(III) Complex Containing Arylborane Units
inferred← citeshttps://doi.org/10.1021/ic9000335openalex-snapshot
Conjugated Triarylboryl Donor−Acceptor Systems Supported by 2,2′-Bipyridine: Metal Chelation Impact on Intraligand Charger Transfer Emission, Electron Accepting Ability, and “Turn-on” Fluoride Sensing
inferred← citeshttps://doi.org/10.1021/ic9007069openalex-snapshot
Impact of Constitutional Isomers of (BMes2)phenylpyridine on Structure, Stability, Phosphorescence, and Lewis Acidity of Mononuclear and Dinuclear Pt(II) Complexes
inferred← citeshttps://doi.org/10.1021/ic900803aopenalex-snapshot
Synthesis and Characterization of Luminescent Rhenium(I) Tricarbonyl Diimine Complexes with a Triarylboron Moiety and the Study of Their Fluoride Ion-Binding Properties
inferred← citeshttps://doi.org/10.1021/ic901673uopenalex-snapshot
Evaluation of Electronics, Electrostatics and Hydrogen Bond Cooperativity in the Binding of Cyanide and Fluoride by Lewis Acidic Ferrocenylboranes
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