0000000000048310

AUTHOR

Robert Francke

0000-0002-4998-1829

showing 7 related works from this author

Novel electrolytes for electrochemical double layer capacitors based on 1,1,1,3,3,3-hexafluoropropan-2-ol

2012

Abstract 1,1,1,3,3,3-Hexafluoropropan-2-ol (HFIP) was tested for its applicability as solvent in electrolytes for energy storage devices. A comprehensive characterization with respect to solubility, conductivity, as well as chemical and electrochemical stability was carried out with different conducting salts. Furthermore, different HFIP solutions containing standard supporting electrolytes and alkali metal fluorides, respectively, were applied in electrochemical double layer capacitor cells. Their behavior was studied with impedance spectroscopy and cyclic voltammetry at low scan rates and compared to the current benchmark electrolytes based on propylene carbonate (PC) and acetonitrile (AN…

chemistry.chemical_compoundchemistryGeneral Chemical EngineeringPropylene carbonateElectrodeInorganic chemistryElectrochemistryElectrolyteCyclic voltammetryGlassy carbonSolubilityElectrochemistryDielectric spectroscopyElectrochimica Acta
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Highly Fluorinated 2,2′-Biphenols and Related Compounds: Relationship between Substitution Pattern and Herbicidal Activity

2013

A broad range of halogenated 2,2'-biphenols was tested for applicability as crop protection agents. The activity of these compounds toward four typical pest plants was observed after application by spraying of diluted solutions. Despite their rather simple structure, it was found that the studied compounds reveal a surprisingly high herbicidal impact. To gain a better understanding of the structure-activity relationship, specific sites of the molecule were chemically modified and the core structures thus gradually changed. The influence of the substitution pattern on the herbicidal properties is discussed, and conclusions on the active site of the biphenol structure are drawn. It was observ…

HalogenationMolecular StructurebiologyHerbicidesChemistryFluorine CompoundsSubstitution (logic)Active siteGeneral ChemistryStructure-Activity Relationshipchemistry.chemical_compoundPhenolsHalogenbiology.proteinMoietyOrganic chemistryPhenolMoleculeGeneral Agricultural and Biological SciencesJournal of Agricultural and Food Chemistry
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Bis(2,2'-biphenoxy)borates for electrochemical double-layer capacitor electrolytes.

2010

Fluorine makes the difference! Bis(2,2'-biphenoxy)borates decorated with fluorine substituents have been synthesized and studied in supercapacitor test cells (see scheme). A clear trend towards higher electrochemical stability with the increase of the fluorine content has been observed. For a maximum performance, only two fluorine substituents per benzene moiety are required.

SupercapacitorChemistryOrganic ChemistryInorganic chemistrychemistry.chemical_elementGeneral ChemistryElectrolyteElectrochemistryCatalysischemistry.chemical_compoundFluorineMoietyPhenolsBenzeneBoronChemistry (Weinheim an der Bergstrasse, Germany)
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ChemInform Abstract: Synthesis of Highly Fluorinated 2,2′-Biphenols and 2,2′-Bisanisoles.

2011

The selective Ullmann-type reaction proceeds under solvent-free conditions and tolerates even a bromo substituent.

chemistry.chemical_compoundChemistrySubstituentGeneral MedicineMedicinal chemistryChemInform
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Cover Picture: Bis(2,2′‐biphenoxy)borates for Electrochemical Double‐Layer Capacitor Electrolytes (Chem. Eur. J. 11/2011)

2011

ChemistryOrganic ChemistryInorganic chemistryFluorinechemistry.chemical_elementCover (algebra)General ChemistryElectrolyteBoronElectrochemical double layer capacitorCatalysisEnergy storageChemistry – A European Journal
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Synthesis of Highly Fluorinated 2,2′-Biphenols and 2,2′-Bisanisoles

2010

Multiply fluorine-substituted iodo anisoles are efficiently coupled in an Ullmann-type reaction to provide the corresponding bisanisoles. The coupling is selective and even tolerates bromo moieties. Subsequent deprotection of hydroxy groups gives access to highly fluorinated biphenols.

Coupling (electronics)ChemistryOrganic ChemistryPhysical and Theoretical ChemistryBiochemistryCombinatorial chemistryOrganic Letters
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Azolylborates for Electrochemical Double Layer Capacitor Electrolytes

2017

Abstract Asymmetric tetraalkylammonium salts of azolylborates were synthesized and studied with respect to their suitability as supporting electrolytes in electrochemical double layer capacitors. In contrast to current conducting salts used in this device, azolylborates exhibit an excellent stability towards thermal load and moisture. In addition to good conductivity and stability towards cathodic reduction we found certain limitations when more positive potentials were applied.

Materials scienceSupporting electrolyteInorganic chemistryElectrolytePhysical and Theoretical ChemistryCyclic voltammetryElectrochemistryElectrochemical double layer capacitorZeitschrift für Physikalische Chemie
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