0000000001298805

AUTHOR

George Floudas

showing 31 related works from this author

Tapered Multiblock Star Copolymers: Synthesis, Selective Hydrogenation, and Properties

2020

Two series of well-defined multiblock four-arm tapered star copolymers with “arms” of the type poly(styrene)-block-poly(isoprene-grad-styrene), (SI/S)₄, were synthesized on a multigram scale with short reaction times. Targeted molecular weight (M) values ranged from 80 to 240 kg mol–¹ with polystyrene (PS) compositions of 40 and 60 wt %. Narrowly distributed (Đ = 1.04–1.12) copolymers were obtained regardless of M and without additional purification beyond precipitation. At sufficiently high M, members of the 40 wt % PS series possessed either a cylindrical or bicontinuous morphology, whereas the 60 wt % PS series yielded lamellae. The star copolymers outperformed their corresponding linear…

ToughnessMaterials sciencePolymers and PlasticsPrecipitation (chemistry)Organic ChemistryAnalytical chemistry02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyElastomer01 natural sciences0104 chemical sciencesStyreneInorganic Chemistrychemistry.chemical_compoundchemistryUltimate tensile strengthMaterials ChemistryCopolymerPolystyreneElongation0210 nano-technologyMacromolecules
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Tapered Multiblock Copolymers Based on Isoprene and 4-Methylstyrene: Influence of the Tapered Interface on the Self-Assembly and Thermomechanical Pro…

2019

The synthesis of tapered multiblock copolymers by statistical living anionic copolymerization of a mixture of isoprene (I) and 4-methylstyrene (4MS) in cyclohexane is based on vastly different reac...

Materials sciencePolymers and PlasticsCyclohexaneOrganic ChemistryMultiblock copolymer02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundchemistryChemical engineeringMaterials ChemistryCopolymer0210 nano-technologyIsopreneMacromolecules
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Tetrahydrofuran: More than a “Randomizer” in the Living Anionic Copolymerization of Styrene and Isoprene: Kinetics, Microstructures, Morphologies, an…

2020

The statistical anionic copolymerization of isoprene (I) and styrene (S) is commonly used to synthesize tapered block copolymers, enabling control of the phase behavior by adjusting the order–disor...

Materials sciencePolymers and PlasticsOrganic ChemistryKinetics02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyMicrostructure01 natural sciences0104 chemical sciencesStyreneInorganic Chemistrychemistry.chemical_compoundchemistryChemical engineeringPhase (matter)Materials ChemistryCopolymer0210 nano-technologyTetrahydrofuranIsopreneMacromolecules
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Orientation and Dynamics of ZnO Nanorod Liquid Crystals in Electric Fields.

2010

ZnO nanorod polymer hybrids (i.e., ZnO nanorods coated with a block copolymer with a short anchor block (dopamine) and a longer solubilizing block of polystyrene (PS)) form liquid crystalline (LC) phases if they are dispersed at high concentration e.g., in a PS oligomer matrix. Due to the high mobility of the low T(g)-matrix the nanorod polymer hybrids show a switching behavior under an applied AC electric field. Hence, the orientation of the nanorod mesogens can be changed from planar (parallel to the substrate) to homeotropic (perpendicular) in full analogy to the switching of low molecular liquid crystals in an electric field. Dielectric measurements show that such a switching is mainly …

Phase transitionMaterials sciencePolymers and PlasticsHomeotropic alignmentDielectricpolystyrenesemiconducting nanorodspressureliquid crystalsLiquid crystalElectric fieldnanostructuresPolymer chemistryMaterials Chemistryarraysnanoparticle polymer compositespolymerschemistry.chemical_classificationbehaviorbusiness.industryOrganic ChemistryPolymermatrixelectric fieldblock copolymersDipolechemistryOptoelectronicsNanorodphasesbusinesscharge-transportMacromolecular rapid communications
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Polymerized Ionic Liquids with Polythiophene Backbones: Self-Assembly, Thermal Properties, and Ion Conduction

2018

Single ion conductors, based on polymerized ionic liquids (PILs) with a polythiophene backbone bearing imidazolium salts with butyl, hexyl, octyl, and decyl side groups and six different counterani...

Bearing (mechanical)Materials sciencePolymers and PlasticsOrganic Chemistry02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyThermal conduction01 natural sciences0104 chemical sciencesIonlaw.inventionInorganic Chemistrychemistry.chemical_compoundChemical engineeringPolymerizationchemistrylawIonic liquidMaterials ChemistryPolythiopheneSelf-assembly0210 nano-technologyElectrical conductorMacromolecules
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Dipolar Relaxation in Functionalized Poly-p-phenylenes Bearing Ultrastrong Dipoles Perpendicular to the Backbone

2018

Local polymer dynamics are studied in polymers bearing dipoles rigidly attached to the backbone. The compounds are based on cyano-substituted dihydrobenzimidazoles bearing ultrastrong dipole moments (∼12 D per repeat unit) incorporated in a poly-p-phenylene backbone, giving rise to polymers with rigid dipoles perpendicular to the chain. They belong to type B polymers according to the Stockmayer classification. They are ideal model systems for studying rotational isomers in the gas phase and the self-assembly and local dynamics in the solid state. Gas phase calculations (DFT) provided the dipole moments, the energetic barriers, and the backbone conformation as a function of the dipole streng…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesBearing (mechanical)Materials sciencePolymers and PlasticsOrganic ChemistryIntermolecular forcePolymerMolecular physicslaw.inventionDielectric spectroscopyInorganic ChemistryDipolechemistrylawMoment (physics)Materials ChemistryPerpendicularPhysics::Atomic PhysicsRepeat unitMacromolecules
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Local and Subchain Relaxation of Polyisoprene in Multiblock Copolymers with a Tapered Interface

2020

We report on the local and (sub-) chain dynamics in a new class of tapered multiblock copolymers synthesized by the repeated statistical living anionic copolymerization of a mixture of isoprene and...

Materials sciencePolymers and PlasticsOrganic ChemistryRelaxation (NMR)Multiblock copolymer02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundchemistryChemical engineeringMaterials ChemistryCopolymer0210 nano-technologyIsopreneMacromolecules
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Hexasubstituted Benzenes with Ultrastrong Dipole Moments

2015

Hexasubstituted benzenes have been synthesized with the highest known dipole moments, as determined by dielectric spectroscopy and DFT methods. Based on the preparation of 4,5-diamino-3,6-dibromophthalonitrile, combined with a novel method to synthesize dihydrobenzimidazoles, these benzene derivatives have dipole moments in excess of 10 debye. Such dipole moments are desirable in ferroelectrics, nonlinear optics, and in organic photovoltaics. Structure determination was achieved through single-crystal X-ray crystallography, and the optical properties were determined by UV/Vis absorption and fluorescence spectroscopy.

Organic solar cellChemistryNonlinear optics02 engineering and technologyGeneral ChemistryElectrophilic aromatic substitution010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCatalysisFluorescence spectroscopy0104 chemical sciencesDielectric spectroscopyDipoleNuclear magnetic resonanceBenzene derivativesPhysical chemistry0210 nano-technologyAbsorption (electromagnetic radiation)Angewandte Chemie International Edition
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Capillary Imbibition, Crystallization, and Local Dynamics of Hyperbranched Poly(ethylene oxide) Confined to Nanoporous Alumina

2017

The crystallization and dynamics of hyperbranched poly(ethylene oxide) (hbPEO), obtained from the direct random copolymerization of EO and glycidol (PEO-co-PG), are studied both in bulk and within nanoporous alumina (AAO). Copolymerization decreases the degree of crystallinity and lowers the crystallization and melting temperatures as compared to linear PEO. The dynamics of capillary imbibition within AAO followed the t1/2 prediction but is slower than predicted by the classical Lucas–Washburn equation. The most prominent effect of confinement is the change in nucleation mechanism—from heterogeneous nucleation in bulk to homogeneous nucleation inside AAO. The homogeneous nucleation temperat…

Materials sciencePolymers and PlasticsEthylene oxideNanoporousOrganic ChemistryOxideNucleation02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceslaw.inventionInorganic ChemistryCrystallinitychemistry.chemical_compoundchemistryChemical engineeringlawPolymer chemistryMaterials ChemistryCopolymerImbibitionCrystallization0210 nano-technologyMacromolecules
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The Next 100 Years of Polymer Science

2020

International audience; The year 2020 marks the 100th anniversary of the first article on poly merization, published by Hermann Staudinger. It is Staudinger who realized that polymers consist of long chains of covalently linked building blocks. Polymers have had a tremendous impact on the society ever since this initial publication. People live in a world that is almost impossible to imagine without synthetic polymers. But what does the future hold for polymer science? In this article, the editors and advisory board of Macromolecular Chemistry and Physics reflect on this question.

chemistry.chemical_classificationPolymers and PlasticsPolymer scienceChemistryOrganic Chemistry02 engineering and technologyPolymer010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciences[CHIM.POLY]Chemical Sciences/PolymersPolymerizationPolymer chemistryMaterials ChemistryPhysical and Theoretical Chemistry0210 nano-technology
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Structure Formation of Polymeric Building Blocks: Complex Polymer Architectures

2013

This chapter describes macromolecules with a complex structure, their defined aggregation in solution, their adsorption to surfaces, and their possible aggregation on surfaces. The term “complex structure” implies that the macromolecules show different, distinct structural elements or building blocks on a supra-atomic length scale. Key to understanding the complex structure of macromolecules, their aggregation, and adsorption to surfaces are intra- and intermolecular interactions such as van der Waals, electrostatic, π–π interactions, and hydrogen bonds.

chemistry.chemical_classificationMaterials scienceHydrogen bondIntermolecular forcePolymerPolyelectrolytesymbols.namesakeAdsorptionchemistryChemical physicssymbolsSelf-assemblyvan der Waals forceMacromolecule
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Building Bridges by Blending: Morphology and Mechanical Properties of Binary Tapered Diblock/Multiblock Copolymer Blends

2021

Materials scienceMorphology (linguistics)Polymers and PlasticsOrganic ChemistryMultiblock copolymerBinary numberCondensed Matter Physics540MiscibilityChemical engineeringPolymer chemistryMaterials ChemistryGradient copolymersPolymer blendPhysical and Theoretical Chemistry
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Hexasubstituierte Benzolderivate mit ultrastarken Dipolmomenten

2016

Materials science02 engineering and technologyGeneral Medicine010402 general chemistry021001 nanoscience & nanotechnology0210 nano-technology01 natural sciences0104 chemical sciencesAngewandte Chemie
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Tapered Multiblock Copolymers Based on Farnesene and Styrene: Impact of Biobased Polydiene Architectures on Material Properties

2020

The reactivity of the biobased monomer β-farnesene in the statistical anionic copolymerization with styrene and the effect of the bottlebrush-like polyfarnesene structure on the phase separation be...

Materials sciencePolymers and PlasticsFarneseneOrganic ChemistryMultiblock copolymer02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesStyreneInorganic Chemistrychemistry.chemical_compoundMonomerchemistryChemical engineeringMaterials ChemistryCopolymerReactivity (chemistry)0210 nano-technologyMaterial propertiesMacromolecules
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Towards bio-based tapered block copolymers: the behaviour of myrcene in the statistical anionic copolymerisation

2019

To explore the potential of myrcene (Myr) as a bio-based monoterpene comonomer for styrenic copolymers and to establish its general applicability for the carbanionic copolymerisation, several statistical copolymerisations of myrcene and common monomers like isoprene (I), styrene (S) and 4-methylstyrene (4MS) were carried out in cyclohexane and monitored by in situ1H NMR spectroscopy. Real-time NMR kinetic studies permitted the determination of the reactivity ratios and the composition profile for each monomer combination. While the copolymerisation of Myr/I yielded a gradient copolymer and reactivity ratios of moderate disparity (rMyr = 4.4; rI = 0.23), the statistical copolymerisation of M…

Polymers and PlasticsComonomerOrganic ChemistrymyrBioengineering02 engineering and technologyNuclear magnetic resonance spectroscopy010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesBiochemistry0104 chemical sciencesStyrenechemistry.chemical_compoundMonomerchemistryPolymer chemistryCopolymerReactivity (chemistry)0210 nano-technologyGlass transitionPolymer Chemistry
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Isoprene/Styrene Tapered Multiblock Copolymers with up to Ten Blocks: Synthesis, Phase Behavior, Order, and Mechanical Properties

2018

The living anionic copolymerization of isoprene and styrene in cyclohexane affords tapered block copolymers due to the highly disparate reactivity ratios of rI = 12.8 and rS = 0.051. Repeated addit...

Materials sciencePolymers and PlasticsCyclohexaneOrganic ChemistryMultiblock copolymerSynthesis Phase02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesStyreneInorganic Chemistrychemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryCopolymerOrder (group theory)Reactivity (chemistry)0210 nano-technologyIsopreneMacromolecules
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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 1421613: Experimental Crystal Structure Determination

2016

Related Article: Jakob Wudarczyk, George Papamokos, Vasilis Margaritis, Dieter Schollmeyer, Felix Hinkel, Martin Baumgarten, George Floudas, Klaus Müllen|2016|Angew.Chem.,Int.Ed.|55|3220|doi:10.1002/anie.201508249

Space GroupCrystallographyCrystal SystemCrystal Structure45-Diamino-36-dibromophthalonitrileCell ParametersExperimental 3D Coordinates
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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 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 1421614: Experimental Crystal Structure Determination

2016

Related Article: Jakob Wudarczyk, George Papamokos, Vasilis Margaritis, Dieter Schollmeyer, Felix Hinkel, Martin Baumgarten, George Floudas, Klaus Müllen|2016|Angew.Chem.,Int.Ed.|55|3220|doi:10.1002/anie.201508249

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters56-Diaminobenzene-1234-tetracarbonitrile NN-dimethylformamide solvateExperimental 3D Coordinates
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CCDC 1421615: Experimental Crystal Structure Determination

2016

Related Article: Jakob Wudarczyk, George Papamokos, Vasilis Margaritis, Dieter Schollmeyer, Felix Hinkel, Martin Baumgarten, George Floudas, Klaus Müllen|2016|Angew.Chem.,Int.Ed.|55|3220|doi:10.1002/anie.201508249

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters56-Diaminobenzene-1234-tetracarbonitrile tetrahydrofuran solvateExperimental 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 1421617: Experimental Crystal Structure Determination

2016

Related Article: Jakob Wudarczyk, George Papamokos, Vasilis Margaritis, Dieter Schollmeyer, Felix Hinkel, Martin Baumgarten, George Floudas, Klaus Müllen|2016|Angew.Chem.,Int.Ed.|55|3220|doi:10.1002/anie.201508249

22-Dimethyl-23-dihydro-1H-benzimidazole-4567-tetracarbonitrile tetrahydrofuran solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 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 1814647: Experimental Crystal Structure Determination

2018

Related Article: George Papamokos, Jakob Wudarczyk, Robert Graf, Dieter Schollmeyer, Martin Baumgarten, Klaus Müllen, George Floudas|2018|Macromolecules|51|3330|doi:10.1021/acs.macromol.8b00215

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters47-dibromo-22-diheptyl-13-dimethyl-23-dihydro-1H-benzimidazole-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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CCDC 1814646: Experimental Crystal Structure Determination

2018

Related Article: George Papamokos, Jakob Wudarczyk, Robert Graf, Dieter Schollmeyer, Martin Baumgarten, Klaus Müllen, George Floudas|2018|Macromolecules|51|3330|doi:10.1021/acs.macromol.8b00215

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters47-dibromo-22-diheptyl-23-dihydro-1H-benzimidazole-56-dicarbonitrileExperimental 3D Coordinates
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CCDC 1421616: Experimental Crystal Structure Determination

2016

Related Article: Jakob Wudarczyk, George Papamokos, Vasilis Margaritis, Dieter Schollmeyer, Felix Hinkel, Martin Baumgarten, George Floudas, Klaus Müllen|2016|Angew.Chem.,Int.Ed.|55|3220|doi:10.1002/anie.201508249

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates47-Dibromo-22-dimethyl-23-dihydro-1H-benzimidazole-56-dicarbonitrile
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CCDC 1814648: Experimental Crystal Structure Determination

2018

Related Article: George Papamokos, Jakob Wudarczyk, Robert Graf, Dieter Schollmeyer, Martin Baumgarten, Klaus Müllen, George Floudas|2018|Macromolecules|51|3330|doi:10.1021/acs.macromol.8b00215

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters47-bis(4-chlorophenyl)-22-diheptyl-13-dimethyl-23-dihydro-1H-benzimidazole-56-dicarbonitrileExperimental 3D Coordinates
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