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The 59 checked references that resolve
resolves10.1007/s002400100192Evidence suggesting that high intake of fluoride provokes nephrolithiasis in tribal populations
resolves10.1021/am501546hHighly Selective Colorimetric/Fluorometric Dual-Channel Fluoride Ion Probe, and Its Capability of Differentiating Cancer Cells
resolves10.1021/ar040237qStructural and Molecular Recognition Studies with Acyclic Anion Receptors
resolves10.1021/cr400352mFluorescence and Colorimetric Chemosensors for Fluoride-Ion Detection
resolves10.1021/cr900401aFluoride Ion Complexation and Sensing Using Organoboron Compounds
resolves10.1039/C2CS35439JHighlights on contemporary recognition and sensing of fluoride anion in solution and in the solid state
resolves10.1021/ol0711873Chromogenic and Fluorescent Chemodosimeter for Detection of Fluoride in Aqueous Solution
resolves10.1021/ja409525jElectron-Deficient Triarylborane Block Copolymers: Synthesis by Controlled Free Radical Polymerization and Application in the Detection of Fluoride Ions
resolves10.1021/ja211944qPlanarized Triarylboranes: Stabilization by Structural Constraint and Their Plane-to-Bowl Conversion
resolves10.1039/c3cc43019gReceptor conformational change induces fluoride binding despite competitive water binding
resolves10.1002/ejoc.201700679Synthesis and Photophysical and Anion‐Sensing Properties of Triarylborane‐Substituted Cross‐Conjugated and Conjugated Thienothiophenes
resolves10.1002/chem.201502241Triarylboron‐Linked Conjugated Microporous Polymers: Sensing and Removal of Fluoride Ions
resolves10.1021/cr100026fAdvances in the Synthesis of Organoborane Polymers for Optical, Electronic, and Sensory Applications
resolves10.1021/cr900333nElectron-Precise Coordination Modes of Boron-Centered Ligands
resolves10.1021/jacs.6b02303Forming B–B Bonds by the Controlled Reduction of a Tetraaryl-diborane(6)
resolves10.1002/anie.201209706Azaborine Compounds for Organic Field‐Effect Transistors: Efficient Synthesis, Remarkable Stability, and BN Dipole Interactions
resolves10.1002/anie.201601305Polymer Acceptor Based on B←N Units with Enhanced Electron Mobility for Efficient All‐Polymer Solar Cells
resolves10.1021/jo502296zSynthesis, Characterization, Physical Properties, and OLED Application of Single BN-Fused Perylene Diimide
resolves10.1021/ja00898a014<b>New Heteroaromatic Compounds. XVIII.</b><sup>1</sup> <b>Boron-Containing Analogs of Benz[a]anthracene</b><sup>2</sup>
resolves10.1021/ja01462a037New Heteroaromatic Compounds. Part VIII. The Reactions of Some Borazarophenanthrenes<sup>1</sup> with Methyl- and Phenyllithium
resolves10.1021/jacs.5b01916Late-Stage Functionalization of 1,2-Dihydro-1,2-azaborines via Regioselective Iridium-Catalyzed C–H Borylation: The Development of a New N,N-Bidentate Ligand Scaffold
resolves10.1021/jacs.7b11062B–N Lewis Pair Functionalization of Anthracene: Structural Dynamics, Optoelectronic Properties, and O<sub>2</sub> Sensitization
resolves10.1002/chem.201605270Facile Access to Unprecedented Electron‐Precise Monohydrodiboranes(4), <i>cis</i>‐1,2‐Dihydrodiboranes(4), and a 1,1‐Dihydrodiborane(5)
resolves10.1021/ja208950cSynthesis of BN-Fused Polycyclic Aromatics via Tandem Intramolecular Electrophilic Arene Borylation
resolves10.1021/ic502784dRing Expansion Reactions of Pentaphenylborole with Dipolar Molecules as a Route to Seven-Membered Boron Heterocycles
resolves10.1021/acs.inorgchem.5b01040Reactions of Imines, Nitriles, and Isocyanides with Pentaphenylborole: Coordination, Ring Expansion, C–H Bond Activation, and Hydrogen Migration Reactions
resolves10.1039/c2sc20336gReaction of pentaarylboroles with carbon monoxide: an isolable organoboron carbonyl complex
resolves10.1021/om100334rDivergent Reactivity of Perfluoropentaphenylborole with Alkynes
resolves10.1039/C4CC04864DInvestigating the ring expansion reaction of pentaphenylborole and an azide
resolves10.1002/chem.201403101Antiaromaticity to Aromaticity: From Boroles to 1,2‐Azaborinines by Ring Expansion with Azides
resolves10.1039/c8cc01529eIntermolecular insertion reactions of azides into 9-borafluorenes to generate 9,10-B,N-phenanthrenes
resolves10.1039/b606759jNovel highly stable semiconductors based on phenanthrene for organic field-effect transistors
resolves10.1039/b504044bNovel thiophene-aryl co-oligomers for organic thin film transistors
resolves10.1021/ma061007pPoly(2,7-phenanthrylene)s and Poly(3,6-phenanthrylene)s as Polyphenylene and Poly(phenylenevinylene) Analogues
resolves10.1021/ol060433sTetraalkoxyphenanthrene: A New Precursor for Luminescent Conjugated Polymers
resolves10.1039/C1SC00500FBN-substituted diphenylacetylene: a basic model for conjugated π-systems containing the BN bond pair
resolves10.1039/c2sc20100cHeteroarene-fused boroles: what governs the antiaromaticity and Lewis acidity of the borole skeleton?
resolves10.1021/ja063302vLuminescent Triarylborane-Functionalized Polystyrene: Synthesis, Photophysical Characterization, and Anion-Binding Studies
resolves10.1021/ma201625uA Quinoliene-Containing Conjugated Polymer-Based Sensing Platform for Amino Acids
resolves10.1021/ja026689kDibenzoborole-Containing π-Electron Systems: Remarkable Fluorescence Change Based on the “On/Off” Control of the p<sub>π</sub>−π* Conjugation
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