0000000001314577

AUTHOR

Dalius Gudeika

showing 16 related works from this author

Structure–property relationship of isomeric diphenylethenyl-disubstituted dimethoxycarbazoles

2015

Isomeric 3,6-dimethoxy- and 2,7-dimethoxycarbazoles containing diphenylethenyl moieties were synthesized by condensation of the appropriate dimethoxycarbazoles with diphenylacetaldehyde. The solid-state structures and the molecular order of the compounds were proven by X-ray crystallography. Both compounds were found to be capable of glass formation with comparable glass transition temperatures (70–71 °C). They exhibited high thermal stabilities, with the 5% weight loss temperatures exceeding 375 °C. The isomer having diphenylethenyl groups at C-3 and C-6 positions and methoxy groups at C-2 and C-7 positions (3a) exhibited aggregation-induced emission (AIE), while its counterpart having dip…

Quenching (fluorescence)CarbazoleGeneral Chemical EngineeringGeneral ChemistryFluorescencechemistry.chemical_compoundCrystallographyDipolechemistryComputational chemistryDensity functional theoryGround stateGlass transitionDerivative (chemistry)RSC Advances
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A review of investigation on 4-substituted 1,8-naphthalimide derivatives

2020

DG acknowledges to the ERDF PostDoc project No. 1.1.1.2/VIAA/1/16/177. We are grateful to J. V. Grazulevičius for the valuable comments on the manuscript.

Materials scienceOrganic solar cell18-NaphthalimideMechanical EngineeringMetals and AlloysC-4 positionNanotechnology02 engineering and technologyElectroluminescence010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsOptoelectronic devices01 natural sciences0104 chemical sciencesElectronic Optical and Magnetic MaterialsElectron-donatingMechanics of MaterialsMaterials ChemistryOLED:NATURAL SCIENCES:Physics [Research Subject Categories]Electron-accepting0210 nano-technologyDiode
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4-(Diethylamino)salicylaldehyde-based twin compounds as NLO-active materials

2016

Abstract 4-(Diethylamino)salicylaldehyde-based twin compounds containing 1,3-indandione and 1,3-bisdicianovinylindane moieties were synthesized and their thermal, optical, photophysical, electrochemical, photoelectrical and nonlinear optical properties were studied. The synthesized compounds form glasses with the glass transition temperatures ranging from 79 to 103 °C. Photoluminescence spectra of the solutions of compounds exhibited red-shifts with the increase of the solvent polarity that was caused by the positive solvatochromic effect. The linear dependencies between the position of the photoluminescence maxima of compounds and the empirical parameter E T (30) of the different solvents …

PhotoluminescenceThin layers13-IndandioneProcess Chemistry and TechnologyGeneral Chemical EngineeringSolvatochromismAnalytical chemistry02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyElectrochemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundSalicylaldehydechemistryIonizationPhysical chemistry0210 nano-technologyGlass transitionDyes and Pigments
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Pyrenyl substituted 1,8-naphthalimide as a new material for weak efficiency-roll-off red OLEDs: a theoretical and experimental study

2018

Based on the theoretical calculations of excited states and semiconducting properties, a new 1,8-naphthalimide derivative having an electron-donating 1-pyrenyl group at the C-4 position was designed and synthesized. This derivative exhibited an excellent thermal stability and bipolar charge carrier transport ability. It was successfully utilized as a host in red phosphorescent organic light-emitting diodes showing an efficient energy transfer from the host to the phosphorescent emitter. The derivative may be a single material electroplex-forming host for PhOLEDs. The best fabricated red emitting device demonstrated maximum current, power, and external quantum efficiencies of 10.8 cd A−1, 7 …

Chemistrybusiness.industry02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundExcited stateMaterials ChemistryOLEDOptoelectronicsCharge carrierThermal stability0210 nano-technologybusinessPhosphorescenceDerivative (chemistry)DiodeCommon emitterNew Journal of Chemistry
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Derivatives of indandione and differently substituted triphenylamine with charge-transporting and NLO properties

2015

Abstract Derivatives containing electron-donaiting triphenylamino groups and electron-withdrawing indandione moieties were synthesized and their thermal, electrochemical, photoelectrical and nonlinear optical properties were studied. The synthesized compounds form glasses with the glass transition temperatures ranging from 69 to 118 °C. The ionization potentials of the solid samples of the synthesized materials were found to be in the range of 5.48–5.69 eV. Hole-drift mobilities estimated by xerographic time of flight technique in the amorphous layers of 2-({4-[(4-{[(2E)-1,3-dioxo-2,3-dihydro-1H-inden-2-ylidene]methyl}phenyl)(4-methoxyphenyl)amino]phenyl}methylidene)-2,3-dihydro-1H-indene-1…

Materials scienceProcess Chemistry and TechnologyGeneral Chemical EngineeringCharge (physics)ElectrochemistryTriphenylamineAmorphous solidchemistry.chemical_compoundchemistryElectric fieldIonizationPhysical chemistryOrganic chemistryIonization energyGlass transitionDyes and Pigments
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Effect of donor substituents on thermally activated delayed fluorescence of diphenylsulfone derivatives

2019

This research was funded by the European Social Fund according to the activity ‘Improvement of researchers’ qualification by implementing world-class R&D projects’ of Measure No. 09.3.3-LMT-K-712. DG acknowledges to the ERDF PostDoc project No. 1.1.1.2/VIAA/1/16/177;

TADFMaterials sciencePhotoluminescenceBiophysicsQuantum yield02 engineering and technologyDiphenylsulphone010402 general chemistryPhotochemistry01 natural sciencesBiochemistrychemistry.chemical_compoundBathochromic shift:NATURAL SCIENCES:Physics [Research Subject Categories]CarbazoleSolvatochromismGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsAtomic and Molecular Physics and Optics0104 chemical sciencesOLEDchemistryExcited stateDensity functional theoryEmitter0210 nano-technologyPhenoxazineJournal of Luminescence
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Donor and acceptor substituted triphenylamines exhibiting bipolar charge-transporting and NLO properties

2017

Donor-acceptor type triphenylamine-based malonodinitriles were synthesized and their thermal, optical, photophysical, electrochemical and nonlinear optical properties were studied. The synthesized compounds formed glasses with the glass transition temperatures ranging from 38 to 107 °C. The ionization potentials of the samples of the compounds established by cyclic voltammetry were found to be in the range of 5.50–5.57 eV, while those estimated by photoelectron emission spectrometry ranged from 5.36 to 5.74 eV. The electron affinity values of the compounds were found to be in the range of −3.41–−3.05 eV. The ambipolar charge-transporting properties were observed for the layers of triphenyla…

Materials scienceAmbipolarTriphenylamineGeneral Chemical EngineeringHyperpolarizability02 engineering and technology010402 general chemistryPhotochemistryTriphenylamine7. Clean energy01 natural scienceschemistry.chemical_compoundElectron affinityIonization:NATURAL SCIENCES:Physics [Research Subject Categories]Glass transition temperatureglass transition temperatureAmbipolar diffusionProcess Chemistry and TechnologyMalonodinitrile021001 nanoscience & nanotechnologyAcceptortriphenylamineambipolarSecond order hyperpolarizability0104 chemical scienceschemistrysecond order hyperpolarizabilityPhysical chemistrymalonodinitrileCyclic voltammetry0210 nano-technologyGlass transition
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Differently substituted benzonitriles for non-doped OLEDs

2020

DG acknowledges to the ERDF PostDoc grant No. 1.1.1.2/VIAA/1/16/177 . This research was funded by the European Regional Development Fund according to the supported activity ‘Research Projects Implemented by World-class Researcher Groups’ under Measure No. 01.2.2-LMT-K-718 .

Electron mobilityTADFMaterials scienceGeneral Chemical EngineeringAnalytical chemistryCarbazolePhenothiazine02 engineering and technologyElectroluminescence010402 general chemistry7. Clean energy01 natural scienceschemistry.chemical_compoundOLED:NATURAL SCIENCES:Physics [Research Subject Categories]PhenoxazineCarbazoleProcess Chemistry and TechnologyDimethylacridine021001 nanoscience & nanotechnology3. Good health0104 chemical sciencesThermogravimetryBenzonitrilechemistrySublimation (phase transition)Ionization energy0210 nano-technologyBipolar charge transportDyes and Pigments
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Diphenylsulfone-based hosts for electroluminescent devices: Effect of donor substituents

2020

DG acknowledges to the ERDF PostDoc project No. 1.1.1.2/VIAA/1/16/177. This work was supported by the project of scientific co-operation program between Latvia, Lithuania and Taiwan ?Polymeric Emitters with Controllable Thermally Activated Delayed Fluorescence for Solution-processable OLEDs? (grant No. S-LLT-19-4). Support of the Lithuanian Academy of Sciences is gratefully acknowledged; Institute of Solid State Physics, University of Latvia as the Center of Excellence has received funding from the European Union’s Horizon 2020 Framework Programme H2020-WIDESPREAD-01-2016-2017-TeamingPhase2 under grant agreement No. 739508, project CAMART²

TADFMaterials sciencePhotoluminescenceGeneral Chemical EngineeringCarbazoleQuantum yield02 engineering and technologyElectroluminescence010402 general chemistry01 natural scienceschemistry.chemical_compoundOLED:NATURAL SCIENCES:Physics [Research Subject Categories]TrifluoromethylCarbazoleProcess Chemistry and TechnologyHost021001 nanoscience & nanotechnologyDiphenylsulfone0104 chemical sciencesCrystallographyOLEDchemistryQuantum efficiency0210 nano-technologyGlass transitionDyes and Pigments
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Synthesis and properties of vinyl-functionalized phenanthroimidazole-based self-polymerizable monomers

2018

Vinyl-functionalized phenanthroimidazole-based monomers were synthesized and their thermal, optical, photophysical, and electrochemical properties were investigated. The monomers exhibited high the...

Materials science02 engineering and technologyGeneral ChemistryActivation energy010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsElectrochemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundMonomerchemistryPolymer chemistryGeneral Materials Science0210 nano-technologyMolecular Crystals and Liquid Crystals
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Flexible diphenylsulfone versus rigid dibenzothiophene-dioxide as acceptor moieties in donor-acceptor-donor TADF emitters for highly efficient OLEDs

2020

DG acknowledges funding from the ERDF PostDoc project No. 1.1.1.2/VIAA/1/16/177 . This research is/was funded by the European Regional Development Fund according to the supported activity ‘ Research Projects Implemented by World-class Researcher Groups ’ under Measure No. 01.2.2-LMT-K-718 . Ministry of Science and Technology (MOST), Taiwan , Grant No. MOST 106-2923-E-155-002-MY3 . This work was also supported by the Ministry of Education and Science of Ukraine (projects no. 0117U003908 and 0118U003862 ), and by the Olle Engkvist Byggmästare foundation (contract No. 189-0223 ). The quantum-chemical calculations were performed with computational resources provided by the High Performance Comp…

Electron mobilityPhotoluminescenceMaterials science02 engineering and technology010402 general chemistryPhotochemistry7. Clean energy01 natural sciencesBiomaterialsMaterials ChemistryOLED:NATURAL SCIENCES:Physics [Research Subject Categories]MoleculeMoietySinglet stateDibenzothiophene dioxideElectrical and Electronic Engineeringdi-tert-butyldimethyldihydroacridineGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsDiphenylsulfoneAcceptor0104 chemical sciencesElectronic Optical and Magnetic MaterialsThermally activated delayed fluorescencQuantum efficiency0210 nano-technologyBipolar charge transportOrganic Electronics
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Methoxycarbazolyl-disubstituted dibenzofuranes as holes- and electrons-transporting hosts for phosphorescent and TADF-based OLEDs

2020

This research was funded by European Social Fund (Project No 09.3.3-LMT-K-712-02-0105). DG acknowledges to the ERDF PostDoc grant No. 1.1.1.2/VIAA/1/16/177.

Materials scienceMethoxycabazoleProcess Chemistry and TechnologyGeneral Chemical EngineeringHost02 engineering and technologyElectroluminescence010402 general chemistry021001 nanoscience & nanotechnologyElectrochemistryPhotochemistry01 natural sciences0104 chemical sciences3. Good healthOLEDOLED:NATURAL SCIENCES:Physics [Research Subject Categories]MoietyThermal stabilityQuantum efficiencyDibenzofuran0210 nano-technologyPhosphorescenceDiodeDyes and Pigments
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Multifunctional derivatives of dimethoxy-substituted triphenylamine containing different acceptor moieties

2020

This project has received funding from the Research Council of Lithuania (LMTLT), Agreement No. [S-LZ-19-2]. This research was funded by the Région Centre, the Tunisian ministry of research, University of Monastir and the French ministry of Higher Education and Research. J. Bouclé would like to thank the Sigma-Lim LabEx environment for financial supports, and the PLATINOM facility at XLIM laboratory regarding device fabrication and characterizations. DG acknowledges the Lithuanian Academy of Sciences for the financial support.

Materials scienceKerr effectGeneral Chemical EngineeringGeneral Physics and AstronomyTwo photon absorption effect02 engineering and technology010402 general chemistryPhotochemistryTriphenylamine7. Clean energy01 natural sciencesTwo-photon absorptionRhodanine-3-acetic acidAcetic acidchemistry.chemical_compoundCyanoacrylic acidDimethoxy-substituted triphenylamineKerr effect:NATURAL SCIENCES:Physics [Research Subject Categories]General Materials Science[SPI.NANO]Engineering Sciences [physics]/Micro and nanotechnologies/MicroelectronicsComputingMilieux_MISCELLANEOUSGeneral Environmental Science[PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics]Energy conversion efficiencyGeneral Engineering021001 nanoscience & nanotechnologyAcceptor3. Good health0104 chemical sciencesDye-sensitized solar cellchemistry[PHYS.COND.CM-MS]Physics [physics]/Condensed Matter [cond-mat]/Materials Science [cond-mat.mtrl-sci]General Earth and Planetary SciencesDye-sensitized solar cell0210 nano-technologyGlass transition
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CCDC 1830576: Experimental Crystal Structure Determination

2018

Related Article: Oleksandr Bezvikonnyi, Dalius Gudeika, Dmytro Volyniuk, Juozas V. Grazulevicius, Gintautas Bagdziunas|2018|New J.Chem.|42|12492|doi:10.1039/C8NJ01866A

Space GroupCrystallography2-(2-ethylhexyl)-6-(pyren-1-yl)-1H-benzo[de]isoquinoline-13(2H)-dione tetrahydrofuran solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1042467: Experimental Crystal Structure Determination

2015

Related Article: Audrius Bucinskas, Gintautas Bagdziunas, Ausra Tomkeviciene, Dmytro Volynyuk, Nataliya Kostiv, Dalius Gudeika, Vygintas Jankauskas, Martins Rutkis, Juozas V. Grazulevicius|2015|RSC Advances|5|49577|doi:10.1039/C5RA09161F

Space GroupCrystallographyCrystal SystemCrystal Structure36-bis(22-Diphenylvinyl)-9-(2-ethylhexyl)-27-dimethoxy-9H-carbazoleCell ParametersExperimental 3D Coordinates
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CCDC 1042468: Experimental Crystal Structure Determination

2015

Related Article: Audrius Bucinskas, Gintautas Bagdziunas, Ausra Tomkeviciene, Dmytro Volynyuk, Nataliya Kostiv, Dalius Gudeika, Vygintas Jankauskas, Martins Rutkis, Juozas V. Grazulevicius|2015|RSC Advances|5|49577|doi:10.1039/C5RA09161F

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates27-bis(22-Diphenylvinyl)-9-(2-ethylhexyl)-36-dimethoxy-9H-carbazole methanol solvate
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