Search results for "solvatochromism"

showing 10 items of 31 documents

The influence of sigma and pi acceptors on two-photon absorption and solvatochromism of dipolar and quadrupolar unsaturated organic compounds.

2003

Two-photon absorption cross sections delta and solvatochromic properties were determined for a series of quadrupolar and dipolar compounds by using femtosecond excitation in the spectral range between 710 and 960 nm. The compounds investigated were distyrylbenzenes and polyenes bearing appropriate pi or sigma acceptors. The delta values for the centrosymmetric compounds trans, trans- 1,4-bis[2-(2',5'-dihexyloxy)phenylethenyl]-2,3,5,6-tetrafluorobenzene (6), trans, trans-1,4-bis[2-(4'-dibutylamino)phenylethenyl]- 2,3,5,6-tetrafluorobenzene (2), trans, trans-1,4-bis[2-(4'dimethylamino)phenylbutadienyl]- 2,3,5,6-tetrafluorobenzene (7), trans,-trans-1,4-bis[2-(4'-dimethylamino)phenylethenyl]2,5…

CrystallographyDipoleChemistryExcited stateIntramolecular forceSolvatochromismHyperpolarizabilityPhysical and Theoretical ChemistryChromophorePhotochemistryTwo-photon absorptionFluorescenceAtomic and Molecular Physics and OpticsChemphyschem : a European journal of chemical physics and physical chemistry
researchProduct

Diaryldistyrylpyrazines: Solvatochromic and Acidochromic Fluorophores

2013

Diaryldimethylpyrazines are the starting materials for the synthesis of C2-symmetric donor- or acceptor-substituted distyrylpyrazines. The optical properties of these cruciform-shaped dyes are dominated by the distyrylpyrazine units; the photophysics is controlled by the styryl substitution, the diaryl substituents on the central pyrazine only having a small effect. Protonation occurs on the pyrazine and/or lateral amines or azines, thereby altering the absorption and emission properties. Hypso- and bathochromism as well as fluorescence quenching depend on the nature of the terminal substituent. This, and a significant positive solvatochromism of the fluorescence, allow optical sensing of t…

chemistry.chemical_compoundchemistryPyrazinePolarity (physics)Optical sensingOrganic ChemistrySolvatochromismSubstituentProtonationPhysical and Theoretical ChemistryAbsorption (chemistry)PhotochemistryFluorescenceEuropean Journal of Organic Chemistry
researchProduct

Quantitation of hydrophobicity in micellar liquid chromatography

1999

Abstract Micellar liquid chromatography (MLC) is shown to be a promising technique for measuring the hydrophobicity of solutes. The presence of micelles has a profound effect on the chromatographic characteristics of reversed-phase columns. The linear relationships between the logarithm, log k , of the retention factor and such diverse properties as the number of carbon atoms in homologous series, octanol–water partition coefficients and solvatochromic parameters, which are observed in conventional reversed-phase liquid chromatography (RPLC), are not usually valid in MLC. For series of compounds exhibiting a wide range of hydrophobicity, k itself is linearly related to these properties. The…

ChromatographySolvatochromismAnalytical chemistryReversed-phase chromatographyMicelleMicellar electrokinetic chromatographyAnalytical ChemistryPartition coefficientHydrophobic effectHomologous serieschemistry.chemical_compoundchemistryMicellar liquid chromatographySpectroscopyTrAC Trends in Analytical Chemistry
researchProduct

Polarity study of ionic liquids with the solvatochromic dye Nile Red: a QSPR approach using in silico VolSurf+ descriptors

2016

The in silico VolSurfþ descriptors, accounting for both cationic and anionic structural features of ionic liquids (ILs) were used to develop a Partial Least Squares (PLS) model able to establish a Quantitative Structure Property Relationship (QSPR) correlation with their solvatochromic dye Nile Red polarity. The PLS model allowed prediction of ENR values for 116 ILs providing an in silico ILs polarity database.

Quantitative structure–activity relationship010405 organic chemistryPolarity (physics)In silicoOrganic ChemistrySolvatochromismNile redIonic Liquids Polarity Nile Red QSPRSettore CHIM/06 - Chimica Organica010402 general chemistry01 natural sciencesBiochemistry0104 chemical sciencesQuantitative Structure Property Relationshipchemistry.chemical_compoundchemistryComputational chemistryDrug DiscoveryIonic liquidPartial least squares regressionOrganic chemistryTetrahedron
researchProduct

Elongated push–pull diphenylpolyenes for nonlinear optics: molecular engineering of quadratic and cubic optical nonlinearities via tuning of intramol…

1999

Abstract Push–pull polyenes are of particular interest for nonlinear optics (NLO) as well as model compounds for long-distance intramolecular charge transfer (ICT). In order to tune the ICT phenomenon and control the linear and nonlinear optical properties, we have synthesized and investigated several series of soluble push–pull diphenylpolyenes of increasing length and having various donor (D) and acceptor (A) end groups. Their linear and NLO properties have been studied by performing electro-optical absorption measurements (EOAM) and third-harmonic generation (THG) experiments in solution. Each push–pull molecule exhibits an intense ICT absorption band in the visible characterized by an i…

DipoleChemistryAbsorption bandComputational chemistryIntramolecular forceSolvatochromismGeneral Physics and AstronomyNonlinear opticsPhysical and Theoretical ChemistryAbsorption (electromagnetic radiation)Molecular physicsAcceptorExcitationChemical Physics
researchProduct

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)
researchProduct

Synthesis and structural characterization of new transition metal complexes of a highly luminescent amino-terpyridine ligand

2020

Abstract The synthesis, NMR and UV–Vis spectroscopy measurements and X-ray diffraction analysis of four new metal complexes of the amino terpyridine ligand 4′-[4-(4-aminophenyl)phenyl]-2,2′:6′,2″-terpyridine L, namely [FeL2](ClO4)2 (1), [ZnL2](ClO4)2 (2), [CdL2](ClO4)2 (3) and [PtMe3IL] (4), are reported. The X-ray crystal structures of complexes 1–3 are 1:2 metal:ligand structures with tridentate ligands decorated around the octahedral metal centers. In complex 4, with L in a bidentate coordination mode, the Pt(IV) coordinated methyl and iodine groups form a fac-arrangement. The 1H NMR spectrum of 4 shows three 195Pt-1H resonances for the methyl groups incorporating the fac-arrangement, wh…

Denticity010405 organic chemistryLigandSolvatochromismCrystal structure010402 general chemistry01 natural sciences3. Good health0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryTransition metalPyridineMaterials ChemistryProton NMRPhysical and Theoretical ChemistryTerpyridinePolyhedron
researchProduct

Tristriazolotriazines with π-Conjugated Segments: Star-Shaped Fluorophors and Discotic Liquid Crystals

2012

C3-symmetrical tristriazolotriazines substituted with phenylene rings carrying lateral flexible alkoxy side chains were prepared via condensation/ring transformation of cyanuric chloride and tetrazoles. These star-shaped, planar compounds can form broad thermotropic mesophases. Due to the extensive π-conjugation, these compounds are highly emissive and the octupolar donor-acceptor electronic structure results in non-linear optical properties like solvatochromism. Brønstedt acids provoke halochromism of the absorption and of the fluorescence.

chemistry.chemical_compoundMaterials sciencechemistryPhenyleneDiscotic liquid crystalCyanuric chlorideSolvatochromismHalochromismSide chainColumnar phasePhotochemistryThermotropic crystalAdvances in Science and Technology
researchProduct

Combined Theoretical and Experimental Study of the Photophysics of Asulam

2013

The photophysics of the neutral molecular form of the herbicide asulam has been described in a joint experimental and theoretical, at the CASPT2 level, study. The unique π → π* aromatic electronic transition (f, ca. 0.5) shows a weak red-shift as the polarity of the solvent is increased, whereas the fluorescence band undergoes larger red-shifts. Solvatochromic data point to higher dipole moment in the excited state than in the ground state (μ(g)μ(e)). The observed increase in pKa in the excited state (pKa* - pKa, ca. 3) is consistent with the results of the Kamlet-Abboud-Taft and Catalán et al. multiparametric approaches. Fluorescence quantum yield varies with the solvent, higher in water (…

LightEstat excitatAnalytical chemistryQuantum yieldElectrons1-PropanolFluorescenceMolecular electronic transitionWater PollutantsPhysical and Theoretical ChemistryPhotolysisAqueous solutionHerbicidesChemistryMethanolSolvatochromismWaterHydrogen-Ion ConcentrationFluorescenceFluorescènciaKineticsExcited stateSolventsQuantum TheoryThermodynamicsCarbamatesGround statePhosphorescenceFisicoquímica
researchProduct

Synthesis, Thermal, and Optical Properties of Tris(5‐aryl‐1,3,4‐oxadiazol‐2‐yl)‐1,3,5‐triazines, New Star‐Shaped Fluorescent Discotic Liquid Crystals

2019

Abstract The synthesis of tris(aryloxadiazolyl)triazines (TOTs), C 3‐symmetrical star‐shaped mesogenes with a 1,3,5‐triazine center, 5‐phenyl‐1,3,4‐oxadiazole arms, and various peripheral alkoxy side chains is reported. Threefold Huisgen reaction on a central triazine tricarboxylic acid and suitable aryltetrazoles yields the title compounds. Selected analogues with a benzene center are included in this study and allow for an evaluation of the impact of the central unit on the physical properties. Thermal (differential scanning calorimetry, DSC; polarization optical microscopy, POM), optical (UV/Vis, fluorescence), electric (time of flight, TOF), and structural (single crystal; wide‐angle X‐…

540 Chemistry and allied sciencessolvatochromism010402 general chemistry01 natural sciencesCatalysischemistry.chemical_compoundliquid crystalsDifferential scanning calorimetryLiquid crystalSide chainTriazineheterocyclesFull Paper010405 organic chemistryDiscotic liquid crystalOrganic ChemistrySolvatochromismLiquid Crystals | Hot PaperGeneral ChemistryFull PapersX-ray scattering0104 chemical sciencesCrystallographychemistry540 ChemieAlkoxy groupfluorescenceSingle crystalChemistry – A European Journal
researchProduct