0000000001302589

AUTHOR

Tomasz Marszalek

showing 10 related works from this author

Thermotropic properties and molecular packing of discotic tristriazolotriazines with rigid substituents.

2014

Tristriazolotriazines with a threefold dialkoxyaryl substitution have been prepared by Huisgen reaction of cyanuric chloride and the corresponding tetrazoles. Although these dyes show a negative or inverted solvatochromism of the UV/Vis absorption, their fluorescence is strongly positive solvatochromic. These discotic fluorophores are also emissive in their solid state and in their broad liquid-crystalline mesophase. The structural study indicates that the thermotropic properties and organization of these systems can be well tuned by the steric demand of the aryl groups. Depending on the substituents, the compounds showed either a pure crystalline phase or a highly complex helical superstru…

Steric effectsChemistryOrganic ChemistrySolvatochromismCyanuric chlorideMesophase02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesThermotropic crystalCatalysis0104 chemical sciences3. Good healthchemistry.chemical_compoundLiquid crystalPhase (matter)0210 nano-technologySuperstructure (condensed matter)Chemistry (Weinheim an der Bergstrasse, Germany)
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Tetrakis(oxadiazolylphenyl)pyrazines: New St. Andrew's Cross-Shaped Liquid Crystals.

2019

π-Conjugated molecules with the shape of St. Andrew's cross have been synthesized via fourfold Huisgen reaction. Four 2,5-diaryl-1,3,4-oxadiazol arms are attached to a central pyrazine nucleus. These fluorescent stars, when decorated with a rim of eight alkoxy side chains are discotic liquid crystals. Depending on the substitution pattern, the width of the liquid phase varies within a broad range of 25 °C to 250 °C. In their liquid crystalline phase, the molecules assemble in a typical hexagonal columnar supramolecular arrangement.

Materials sciencePyrazineDiscotic liquid crystalSupramolecular chemistry02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesAtomic and Molecular Physics and Optics0104 chemical scienceschemistry.chemical_compoundCrystallographychemistryLiquid crystalPhase (matter)Alkoxy groupSide chainMoleculePhysical and Theoretical Chemistry0210 nano-technologyChemphyschem : a European journal of chemical physics and physical chemistry
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Dicyanobenzothiadiazole Derivatives Possessing Switchable Dielectric Permittivities

2017

Benzothiadiazoles are important electron acceptors and are frequently employed as electron-deficient components of donor-acceptor polymers. We report the effect of nitrile functionalities on the reactivity, steric hindrance, optoelectronic properties, and dielectric permittivity in dicyanobenzothioadiazole (DCNBT). Dielectric spectroscopy in the bulk and in solution assisted by DFT-calculations revealed that these molecules can be engineered to engender maximum values of the dipole moment and of dielectric permittivity due to the strong electron-withdrawing effect of the nitrile groups. The self-assembly in the bulk was investigated by X-ray scattering performed on single crystals, fibers (…

chemistry.chemical_classificationMaterials scienceNitrileRelative permittivity02 engineering and technologyPolymerDielectric010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesDielectric spectroscopyDipolechemistry.chemical_compoundchemistryChemical physicsLiquid crystalPhase (matter)Organic chemistryGeneral Materials Science0210 nano-technologyACS Applied Materials & Interfaces
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CCDC 1533973: Experimental Crystal Structure Determination

2017

Related Article: Jakob Wudarczyk, George Papamokos, Tomasz Marszalek, Thomas Nevolianis, Dieter Schollmeyer, Wojciech Pisula, George Floudas, Martin Baumgarten, and Klaus Müllen|2017|ACS Applied Materials and Interfaces|9|20527|doi:10.1021/acsami.7b03060

Space GroupCrystallography47-bis(13-thiazol-5-yl)-213-benzothiadiazole-56-dicarbonitrileCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1826069: Experimental Crystal Structure Determination

2019

Related Article: Nico Röder, Tomasz Marszalek, Daniel Limbach, Wojciech Pisula, Heiner Detert|2019|ChemPhysChem|20|463|doi:10.1002/cphc.201800936

Space GroupCrystallographytetrakis{4-[5-(4-propoxyphenyl)-134-oxadiazol-2-yl]phenyl}pyrazine chloroform solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1533972: Experimental Crystal Structure Determination

2017

Related Article: Jakob Wudarczyk, George Papamokos, Tomasz Marszalek, Thomas Nevolianis, Dieter Schollmeyer, Wojciech Pisula, George Floudas, Martin Baumgarten, and Klaus Müllen|2017|ACS Applied Materials and Interfaces|9|20527|doi:10.1021/acsami.7b03060

Space GroupCrystallographyCrystal SystemCrystal Structure47-bis(13-thiazol-2-yl)-213-benzothiadiazole-56-dicarbonitrileCell ParametersExperimental 3D Coordinates
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CCDC 1533971: Experimental Crystal Structure Determination

2017

Related Article: Jakob Wudarczyk, George Papamokos, Tomasz Marszalek, Thomas Nevolianis, Dieter Schollmeyer, Wojciech Pisula, George Floudas, Martin Baumgarten, and Klaus Müllen|2017|ACS Applied Materials and Interfaces|9|20527|doi:10.1021/acsami.7b03060

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters47-bis(4-hexylthiophen-2-yl)-213-benzothiadiazole-56-dicarbonitrileExperimental 3D Coordinates
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CCDC 1533733: Experimental Crystal Structure Determination

2017

Related Article: Jakob Wudarczyk, George Papamokos, Tomasz Marszalek, Thomas Nevolianis, Dieter Schollmeyer, Wojciech Pisula, George Floudas, Martin Baumgarten, and Klaus Müllen|2017|ACS Applied Materials and Interfaces|9|20527|doi:10.1021/acsami.7b03060

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters47-bis(thiophen-2-yl)-213-benzothiadiazole-56-dicarbonitrileExperimental 3D Coordinates
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CCDC 1533970: Experimental Crystal Structure Determination

2017

Related Article: Jakob Wudarczyk, George Papamokos, Tomasz Marszalek, Thomas Nevolianis, Dieter Schollmeyer, Wojciech Pisula, George Floudas, Martin Baumgarten, and Klaus Müllen|2017|ACS Applied Materials and Interfaces|9|20527|doi:10.1021/acsami.7b03060

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters47-dibromo-213-benzothiadiazole-56-dicarbonitrileExperimental 3D Coordinates
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CCDC 1533734: Experimental Crystal Structure Determination

2017

Related Article: Jakob Wudarczyk, George Papamokos, Tomasz Marszalek, Thomas Nevolianis, Dieter Schollmeyer, Wojciech Pisula, George Floudas, Martin Baumgarten, and Klaus Müllen|2017|ACS Applied Materials and Interfaces|9|20527|doi:10.1021/acsami.7b03060

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters47-bis[(4-t-butylphenyl)ethynyl]-213-benzothiadiazole-56-dicarbonitrileExperimental 3D Coordinates
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