Search results for "photophysical properties"

showing 10 items of 14 documents

The Impact of a 1,2,3-Triazole Motif on the Photophysical Behavior of Non-K Tetrasubstituted Pyrene with a Substitution Pattern Providing the Long Ax…

2022

1,3,6,8-Tetrasubstituted pyrene derivatives with two types of substituents (4-(2,2-dimethylpropyloxy)pyridine, 1-decyl-1,2,3-triazole, 1-benzyl-1,2,3-triazole, and pyrazole), substituted in such a way that provides the long axial symmetry, are prepared and characterized in the present study. To the best of our knowledge, the pyrene derivative containing the same heteroaryl motif (triazole) but substituted by two various alkyls, straight decyl and benzyl-based side chains (C), is reported for the first time. For comparison, compounds with one kind of triazole motif and substituted pyridine or pyrazole groups were prepared (A and B). The photophysical properties of all molecules were evaluate…

triazole motifpyrene derivativestheoretical studysubstitution patternexperimental studyphotophysical propertiesMolecules
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Influence of Substituent and Benzoannulation on Photophysical Properties of 1-Benzoylmethyleneisoquinoline Difluoroborates

2015

A series of 1-benzoylmethyleneisoquinoline difluoroborates were synthesized, and their photophysical properties were determined. The effect of the substituent and benzoannulation on their properties was investigated to make a comparison with recently published results focused on related quinolines. The photophysical properties of isoquinoline derivatives differ from those of quinolines, and the most pronounced differences are found for the fluorescence quantum yields. Both experimental and theoretical approaches were used to explain the observed photophysical properties.

010405 organic chemistryOrganic ChemistrySubstituent010402 general chemistryPhotochemistry01 natural sciencesFluorescence0104 chemical scienceschemistry.chemical_compoundchemistryIsoquinolineta116photophysical propertiesJournal of Organic Chemistry
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The influence study of the number of substituted heteroaryls at the non-K region of pyrene structure on the photophysical properties based on the exa…

2022

The study of the photophysical properties (thermal - thermogravimetric analysis and optical - absorption, emission in the solution and in powder, quantum efficiency of emission and efficient fluorescence lifetime in the solution) with the focus on the influence of the number of substituted 1-decyl-1H-1,2,3-triazole groups at the non-K region of pyrene structure. To the best of our knowledge, the investigation of the impact of the number of heteroaryl groups at the non-K region of pyrene is reported for the first time. The obtained results for monosubstituted derivative (1) were compared to di- (2, 3) and tetra- (4) analogues previously reported by us in the literature. In addition, theoreti…

Experimental studyPyrene derivativeTriazole motifSubstitution patternPhotophysical propertiesJournal of Molecular Structure
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Ligand-Based Charge-Transfer Luminescence in Ionic Cyclometalated Iridium(III) Complexes Bearing a Pyrene-Functionalized Bipyridine Ligand: A Joint T…

2012

Two new heteroleptic iridium(III) complexes [Ir(ppy)(2)(pyr(2)bpy)][PF(6)] ([1a][PF(6)]) and [Ir(dfppy)(2)(pyr(2)bpy)][PF(6)] ([2a][PF(6)]), where Hppy = 2-phenylpyridine, Hdfppy = 2-(3,5-difluorophenyl)pyridine, and pyr(2)bpy = 5,5'-bis(pyren-1-yl)-2,2'-bipyridine, have been synthesized and fully characterized. The single-crystal structures of pyr(2)bpy and the complexes 4{[1a][PF(6)]}·2CH(2)Cl(2)·9H(2)O and [2a][PF(6)]·0.25CH(2)Cl(2)·H(2)O have been determined. The effect of the pyrene substituents on the electronic properties is investigated through a comprehensive photophysical and theoretical study on the two complexes in comparison to reference complexes without substituents on the an…

ELECTROLUMINESCENT DEVICESAbsorption spectroscopyEMITTING ELECTROCHEMICAL-CELLSchemistry.chemical_element02 engineering and technology010402 general chemistryPhotochemistry01 natural sciencesInorganic ChemistryBipyridinechemistry.chemical_compoundPyridineCRYSTAL-STRUCTURESIridiumPhysical and Theoretical ChemistryCHELATED RUTHENIUM(II) COMPLEXEXACT-EXCHANGEChemistryLigand021001 nanoscience & nanotechnologyTRANSITION-METAL-COMPLEXES0104 chemical sciences3. Good healthCrystallographyPHOTOPHYSICAL PROPERTIESQUANTUM YIELDSIntramolecular forcePyreneEXCITED-STATE PROPERTIESSENSITIZED SOLAR-CELLS0210 nano-technologyLuminescenceInorg. Chem.
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Iridium(III) Complexes with Phenyl-tetrazoles as Cyclometalating Ligands

2014

Ir(II) cationic complexes with cyclometalating tetrazolate ligands were prepared for the first time, following a two-step strategy based on (i) a silver-assisted cyclometalation reaction of a tetrazole derivative with IrCl3 affording a bis-cyclometalated solvato-complex P ([Ir(ptrz)(2)(CH3CN)(2)](+), Hptrz = 2-methyl-5-phenyl-2H-tetrazole); (ii) a substitution reaction with five neutral ancillary ligands to get [Ir(ptrz)(2)L](+), with L = 2,2'-bypiridine (1), 4,4'-di-tert-butyl-2,2'-bipyridine (2), 1,10-phenanthroline (3), and 2-(1-phenyl-1H-1,2,3-triazol-4-yl)pyridine (4), and [Ir(ptrz)(2)L-2](+), with L = tertbutyl isocyanide (5). X-ray crystal structures of P, 2, and 3 were solved. Elect…

Substitution reactionIr(III) complexePhenanthrolineIsocyanidechemistry.chemical_elementphenyl tetrazolesPhotochemistryMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundBipyridinechemistryPyridineEMITTING ELECTROCHEMICAL-CELLS; TRANSITION-METAL-COMPLEXES; IR(III) COMPLEXES; ELECTROLUMINESCENT DEVICES; ANCILLARY LIGAND; SOLID-STATE; PHOTOPHYSICAL PROPERTIES; POLYPYRIDINE COMPLEXES; BLUE PHOSPHORESCENCE; ISOCYANIDE COMPLEXESTetrazoleIridiumPhysical and Theoretical ChemistryAcetonitrile
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Origin of the large spectral shift in electroluminescence in a blue light emitting cationic iridium(III) complex

2007

A new, but archetypal compound [ Ir( ppy- F-2) (2)Me(4)phen] PF6, where ppy- F2 is 2-(2',4'- fluorophenyl) pyridine and Me(4)phen is 3,4,7,8- tetramethyl- 1,10- phenanthroline, was synthesized and used to prepare a solid-state light-emitting electrochemical cell (LEEC). This complex emits blue light with a maximum at 476 nm when photoexcited in a thin film, with a photoluminescence quantum yield of 52%. It yields an efficient single-component solid-state electroluminescence device with a current efficiency reaching 5.5 cd A(-1) and a maximum power efficiency of 5.8 Lm Watt(-1). However, the electroluminescence spectrum is shifted with respect to the photoluminescence spectrum by 80 nm resul…

education.field_of_studyFunctional Response TheoryPhotoluminescenceExcitation-EnergiesTransition-Metal-ComplexesChemistryPopulationQuantum yieldSolid-StateGeneral ChemistryExcited-State PropertiesElectroluminescencePhotochemistryOptical SpectroscopyExcited stateMaterials ChemistryLight emissionEmission spectrumElectrochemical-CellsTriplet stateeducationRoom-TemperatureSingle-LayerPhotophysical Properties
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Multinuclear Cytotoxic Metallodrugs: Physicochemical Characterization and Biological Properties of Novel Heteronuclear Gold-Titanium Complexes

2011

An unprecedented series of titanocene-gold bi- and trimetallic complexes of the general formula [[(η(5)-C(5)H(5))(μ-η(5):κ(1)-C(5)H(4)(CH(2))(n)PPh(2))TiCl(2)](m)AuCl(x)](q+) (n = 0, 2, or 4; m = 1, x = 1, q = 0 or m = 2, x = 0, q = 1) have been prepared and characterized spectroscopically. The luminescence spectroscopy and photophysics of one of the compounds, [[(η(5)-C(5)H(5))(μ-η(5):κ(1)-C(5)H(4)PPh(2))TiCl(2)](2)Au]PF(6), have been investigated in 2MeTHF solution and in the solid state at 77 and 298 K. Evidence for interfragment interactions based on the comparison of electronic band positions and emission lifetimes, namely, triplet energy transfer (ET) from the Au- to the Ti-containing…

Models MolecularSpectrometry Mass Electrospray IonizationLuminescenceMagnetic Resonance SpectroscopyTransfer Excited-StatesCell SurvivalStereochemistryAntineoplastic AgentsCharge-TransferUnsaturated-HydrocarbonsCrystallography X-RayElectronic-StructuresInorganic ChemistryStructure-Activity Relationshipchemistry.chemical_compoundCell Line TumorOrganometallic CompoundsHumansPhysical and Theoretical ChemistrySpectroscopyGroup 2 organometallic chemistryTitaniumArene-Ruthenium ComplexesX-rayTitanocene dichlorideNuclear magnetic resonance spectroscopyChromophoreTitanocene DichlorideCrystallographychemistryHeteronuclear moleculeAnticancer AgentsSpectrophotometry UltravioletGoldLuminescenceGold(Iii) CompoundsPhotophysical Properties
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Synthesis, structure and photophysical properties of a highly luminescent terpyridine-diphenylacetylene hybrid fluorophore and its metal complexes

2015

A new fluorescent terpyridyl-diphenylacetylene hybrid fluorophore 4′-[4-{(4-methoxyphenyl)ethynyl}phenyl]-2,2′:6′,2′′-terpyridine, L, was synthesized via Sonogashira cross-coupling of 4′-(4-bromophenyl)-2,2′:6′,2′′-terpyridine and 4-ethynylanisole in the presence of Pd(PPh3)4/CuI as a catalyst. The solid state structure of L shows a trans arrangement of pyridine nitrogen atoms along the interannular bond in the terpyridine domain. Five transition metal complexes of L, {[FeL2](CF3SO3)2 (1), [ZnL2](ClO4)2 (2), [CdL2](ClO4)2 (3), [RuL2](PF6)2 (4), and PtMe3IL (5)}, have also been synthesized and characterized by spectroscopic methods and single crystal X-ray analysis. The X-ray crystal structu…

fluorophorecrystal structuresfluoroforitterpyridiinivalofysikaaliset ominaisuudetmetal complexessynteesiterpyridinevalmistusmetallikompleksitphotophysical propertieskiderakenteet
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Supramolecular Construction of Cyanide-Bridged Re I Diimine Multichromophores

2019

The reactions of labile [Re(diimine)(CO)3(H2O)]+ precursors (diimine = 2,2′-bipyridine, bpy; 1,10-phenanthroline, phen) with dicyanoargentate anion produce the dirhenium cyanide-bridged compounds [{Re(diimine)(CO)3}2CN)]+ (1 and 2). Substitution of the axial carbonyl ligands in 2 for triphenylphosphine gives the derivative [{Re(phen)(CO)2(PPh3)}2CN]+ (3), while the employment of a neutral metalloligand [Au(PPh3)(CN)] affords heterobimetallic complex [{Re(phen)(CO)3}NCAu(PPh3)]+ (4). Furthermore, the utilization of [Au(CN)2]−, [Pt(CN)4]2–, and [Fe(CN)6]4–/3– cyanometallates leads to the higher nuclearity aggregates [{Re(diimine)(CO)3NC}xM]m+ (M = Au, x = 2, 5 and 6; Pt, x = 4, 7 and 8; Fe, x…

CARBONYL-COMPLEXESSPECTROSCOPIC PROPERTIESCyanideSupramolecular chemistryEXCITED-STATECrystal structure010402 general chemistry01 natural sciencesInorganic Chemistrychemistry.chemical_compoundCRYSTAL-STRUCTUREPhysical and Theoretical ChemistryTriphenylphosphineta116MULTIPLE EMISSIONSDiimineDENSITY-FUNCTIONAL METHODS010405 organic chemistryLUMINESCENT RE(I)0104 chemical sciencesRHENIUM(I) TRICARBONYL COMPLEXESCrystallographychemistryExcited statePHOTOPHYSICAL PROPERTIESPhosphorescenceCOORDINATION POLYMERSDerivative (chemistry)INORGANIC CHEMISTRY
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The photophysics of distorted nanographenes: Ultra-slow relaxation dynamics, memory effects, and delayed fluorescence

2023

The controlled deformation and engineering of the sp2 carbon network in atomically-precise nanographenes, and their substantially larger size as compared to typical optical dyes, opens new opportunities for the modulation of optical and electronic properties, but the peculiar photophysics of these systems is still poorly understood. Here, through a detailed comparative study of two well-defined distorted nanographenes, we show that they can exhibit interesting photophysical features, such as triplet-triplet annihilation delayed fluorescence, ultra-slow excited state dynamics, and excitation-wavelength memory effects on the nanosecond and sub-nanosecond relaxation cascades. Some of these beh…

Atomically-precise distorted nanographenesExcitation memory-effectsSettore FIS/01 - Fisica SperimentaleGeneral Materials ScienceGeneral ChemistrySlow dynamical structural relaxationDelayed fluorescencePhotophysical properties
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