0000000000606320

AUTHOR

Meik Blanke

showing 11 related works from this author

Mesogens with Aggregation-Induced Emission Formed by Hydrogen Bonding

2019

In this contribution, we report a supramolecular approach toward mesogens showing aggregation-induced emission (AIE). AIE-active aromatic thioethers, acting as hydrogen-bond donors, were combined with alkoxystilbazoles as hydrogen-bond acceptors. Upon self-assembly, hydrogen-bonded complexes with monotropic liquid crystalline behavior were obtained. In addition, it was found that the introduction of a chiral citronellyl side chain leads to drastic bathochromic shift of the emission, which was not observed for linear alkyl chains. The mesomorphic behavior, as well as the photophysical properties as a solid and in the mesophase of the liquid crystalline assemblies, were studied in detail.

Materials scienceHydrogen bondGeneral Chemical EngineeringChemieBiomedical EngineeringSupramolecular chemistryGeneral Materials ScienceSettore CHIM/07 - Fondamenti Chimici Delle TecnologieAggregation-induced emissionPhotochemistryAggregation-Induced-Emission Hydrogen Bonding Liquid Crystals Supramolecular Chemistry Computational ChemistryACS Materials Letters
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Naturally occurring polyphenols as building blocks for supramolecular liquid crystals – substitution pattern dominates mesomorphism

2021

A modular supramolecular approach towards hydrogen-bonded liquid crystalline assemblies based on naturally occurring polyphenols is reported. The combination of experimental observations, crystallographic studies and semi-empirical analyses of the assemblies provides insight into the structure–property relationships of these materials. Here a direct correlation of the number of donor OH-groups as well as their orientation with the mesomorphic behavior is reported. We discovered that the number and orientation of the OH-groups have a stronger influence on the mesomorphic behavior of the supramolecular assemblies than the connectivity (e.g. stilbenoid or chalconoid) of the hydrogen bond donor…

ChemistryHydrogen bondLiquid crystallineProcess Chemistry and TechnologyChemieBiomedical EngineeringSupramolecular chemistryEnergy Engineering and Power Technology02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesIndustrial and Manufacturing Engineering0104 chemical sciencesCrystallographyChemistry (miscellaneous)Liquid crystalSupramolecular Chemistry Liquid Crystals Crystal Engineering Hydrogen BondingMaterials ChemistryChemical Engineering (miscellaneous)Settore CHIM/07 - Fondamenti Chimici Delle Tecnologie0210 nano-technologyMolecular Systems Design & Engineering
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Alkyloxy modified pyrene fluorophores with tunable photophysical and crystalline properties

2019

Novel alkyloxy modified 2,7-di-tert-butyl-4,5,9,10-tetra(arylethynyl)pyrenes were prepared through a straightforward Sonogashira coupling approach. Optical properties such as quantum yields and absorption/emission spectra of the fluorophores were investigated by UV/Vis and fluorescence measurements. Aggregation induced excimer formation of the chromophores in polar solvents and in the solid state was proved by the presence of a characteristic bathochromically shifted emission band and a decrease of the emission capability. These results strongly indicate the unexpected observation that the excimer formation of adjacent pyrene rings is not prevented by the introduction of bulky tert-butyl su…

ChemistryChemieSonogashira coupling02 engineering and technologyGeneral ChemistryChromophore010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistryExcimer01 natural sciencesFluorescenceCatalysis0104 chemical sciencesLiquid crystals Luminophore pyrene crystal packingchemistry.chemical_compoundMaterials ChemistryMoleculePyreneEmission spectrumSettore CHIM/07 - Fondamenti Chimici Delle TecnologieAbsorption (chemistry)0210 nano-technology
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Photo-switching and -cyclisation of hydrogen bonded liquid crystals based on resveratrol

2020

A series of hydrogen-bonded liquid crystals based on resveratrol and resveratrone is reported and investigated with respect to their photo-switchability (at 405 nm) and photo-cyclisation (at 300 nm).

Materials scienceHydrogenMetals and AlloysChemiechemistry.chemical_elementGeneral ChemistryResveratrolPhotochemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundchemistryLiquid crystalMaterials ChemistryCeramics and CompositesSettore CHIM/07 - Fondamenti Chimici Delle TecnologiePhotoswitching Liquid Crystals Hydrogen Bonding Packing Analysis
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CCDC 1939466: Experimental Crystal Structure Determination

2020

Related Article: Meik Blanke, Jan Balszuweit, Marco Saccone, Christoph Wölper, David Doblas Jiménez, Markus Mezger, Jens Voskuhl, Michael Giese|2020|Chem.Commun.|56|1105|doi:10.1039/C9CC07721A

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinatestris(4-{2-[4-(octyloxy)phenyl]ethenyl}pyridine) 5-[2-(4-hydroxyphenyl)ethenyl]benzene-13-diol
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CCDC 1895646: Experimental Crystal Structure Determination

2019

Related Article: Andreas Kapf, Hassan Eslahi, Meik Blanke, Marco Saccone, Michael Giese, Marcel Albrecht|2019|New J.Chem.|43|6361|doi:10.1039/C9NJ00652D

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates27-di-t-butyl-45910-tetrakis{[4-(decyloxy)phenyl]ethynyl}pyrene
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CCDC 1939467: Experimental Crystal Structure Determination

2020

Related Article: Meik Blanke, Jan Balszuweit, Marco Saccone, Christoph Wölper, David Doblas Jiménez, Markus Mezger, Jens Voskuhl, Michael Giese|2020|Chem.Commun.|56|1105|doi:10.1039/C9CC07721A

Space GroupCrystallographybis(4-{2-[4-(octyloxy)phenyl]ethenyl}pyridine) 4-(68-dihydroxynaphthalen-2-yl)but-3-en-2-oneCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1942435: Experimental Crystal Structure Determination

2021

Related Article: Jan Balszuweit, Meik Blanke, Marco Saccone, Markus Mezger, Constantin G. Daniliuc, Christoph Wölper, Michael Giese, Jens Voskuhl|2021|MSDE|6|390|doi:10.1039/D0ME00171F

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters4-[2-(35-dihydroxyphenyl)ethenyl]benzene-12-diol tris(4-{2-[4-(octyloxy)phenyl]ethenyl}pyridine)Experimental 3D Coordinates
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CCDC 1895645: Experimental Crystal Structure Determination

2019

Related Article: Andreas Kapf, Hassan Eslahi, Meik Blanke, Marco Saccone, Michael Giese, Marcel Albrecht|2019|New J.Chem.|43|6361|doi:10.1039/C9NJ00652D

Space GroupCrystallography45910-tetrakis[(4-butoxyphenyl)ethynyl]-27-di-t-butylpyreneCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1945777: Experimental Crystal Structure Determination

2021

Related Article: Jan Balszuweit, Meik Blanke, Marco Saccone, Markus Mezger, Constantin G. Daniliuc, Christoph Wölper, Michael Giese, Jens Voskuhl|2021|MSDE|6|390|doi:10.1039/D0ME00171F

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters4-[2-(35-dihydroxyphenyl)ethenyl]benzene-12-diol tris(4-{[4-(octyloxy)phenyl]diazenyl}pyridine)Experimental 3D Coordinates
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CCDC 1938656: Experimental Crystal Structure Determination

2021

Related Article: Marco Saccone, Meik Blanke, Constantin G. Daniliuc, Heikki Rekola, Jacqueline Stelzer, Arri Priimagi, Jens Voskuhl, Michael Giese|2019|ACS Materials Lett.|1|589|doi:10.1021/acsmaterialslett.9b00371

46-bis[(3-hydroxyphenyl)sulfanyl]benzene-13-dicarbonitrile bis(4-{2-[4-(octyloxy)phenyl]ethenyl}pyridine)Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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