Search results for "Chromis"

showing 10 items of 172 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
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Induction of Hsp70 by the Herbicide Oxyfluorfen (Goal) in the Egyptian Nile Fish, Oreochromis niloticus

1999

This paper deals with the expression of the biomarker hsp70 in the liver and kidney of the freshwater fish Oreochromis niloticus following exposure to the herbicide oxyfluorfen (Goal). Fishes were exposed to three concentrations, the 96-h LC50 (3 mg/L), the 96-h (1/2)LC50 (1.5 mg/L), and the 96-h (1/4)LC50 (0.75 mg/L) of oxyfluorfen for 6, 15, and 24 days, respectively, and samples were taken at three different time periods for each concentration. The livers responded to the herbicide by an induction of the expression of both the constitutive (hsp75; Mr 75 kDa) and the inducible (hsp73; Mr 73 kDa) hsp70 proteins. In kidney, the herbicide induced a time-dependent increase in the expression o…

food.ingredientHealth Toxicology and MutagenesisBiologyKidneyToxicologyAnimal sciencefoodHalogenated Diphenyl EthersAnimalsEcotoxicologyHSP70 Heat-Shock ProteinsIncubationEcologyPhenyl EthersTilapiaGeneral MedicinePesticidebiology.organism_classificationPollutionHsp70OreochromisLiverToxicityFreshwater fishEgyptElectrophoresis Polyacrylamide GelTilapiaArchives of Environmental Contamination and Toxicology
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Preparation and Thermochromic Switching between Phosphorescence and Thermally Activated Delayed Fluorescence of Mononuclear Copper(I) Complexes

2020

Instructive, inexpensive, and environmentally friendly laboratory syntheses of two highly luminescent copper(I) complexes CuI(PPh3)2(pyR) (pyR = pyridine, 4-cyanopyridine) are described for second-year/upper-division undergraduate inorganic chemistry students. Both complexes exhibit bright thermally activated delayed fluorescence (TADF) at ambient temperature and phosphorescence at low temperature. The laboratory experiments familiarize the students with mechanochemical syntheses, cluster and complex formation, ligand substituent effects, and the fascinating phenomenon of luminescence thermochromism.

chemistry.chemical_classificationThermochromismchemistry.chemical_elementGeneral ChemistryPhotochemistryCopperFluorescenceFluorescence spectroscopyEducationCoordination complexchemistry.chemical_compoundchemistryPyridinePhosphorescenceLuminescenceJournal of Chemical Education
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Probing the Folding of Peptide–Polymer Conjugates Using the π-Dimerization of Viologen End-Groups

2020

The synthesis of a foldable viologen-functionalized peptide–polymer conjugate is presented. The ABA-type triblock conjugate with a PEG polymer was capped with a FHFHF pentapeptide sequence and further modified with a viologen building block at both chain ends. The pH-responsive peptide domains fold into an intermediate structure inducing close proximity of the viologen units, which upon a reduction step form π-dimers of the radical cation. Overall the intramolecular folding and intermolecular self-assembly process leads to the formation of supramolecular nanorods. Mixing of viologen-peptide–polymer conjugates with unfunctionalized conjugates leads to crosslinking of the nanorods and hydroge…

chemistry.chemical_classificationstimuli-responsive polymerspeptide conjugation010405 organic chemistrySupramolecular chemistrytechnology industry and agricultureViologenPolymersupramolecular materials010402 general chemistry01 natural sciencesPentapeptide repeat0104 chemical scienceslcsh:ChemistrychemistryRadical ionlcsh:QD1-999Intramolecular forcePolymer chemistrySelf-healing hydrogelsmedicineelectrochromismhydrogelmedicine.drugConjugateOrganic Materials
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The Two‐Step Spin Conversion in a Supramolecular Triple Helicate Dinuclear Iron(II) Complex Studied by Mössbauer Spectroscopy

2006

The triple helicate dinuclear iron(II) complex, [Fe-2(L)(3)](ClO4)(4)center dot 2H(2)O (1), previously reported by Tuna et al. (Chem. Eur. J. 2004, 10, 5737), was prepared and characterised by detailed SQUID and Fe-57 Mbssbauer measurements. Compound 1 exhibits a thermochromic two-step spin conversion at T-SC((1)) ca. 240 K and T-SC((2)) ca. 120 K, but does not switch its spin state further below 20 K as proven by Mossbauer spectroscopy. The sharp variation of the susceptibility below 20 K is due to zero-field splitting of the remaining iron(II) high-spin species. Applied field Fe-57 Mossbauer spectroscopy experiments at 4.2 K indicate that the gradual thermal spin conversion from [HS-HS] p…

ThermochromismSpin statesChemistryStereochemistryTwo stepSupramolecular chemistrylaw.inventionInorganic ChemistrySQUIDCrystallographySpin crossoverlawMössbauer spectroscopySpin (physics)European Journal of Inorganic Chemistry
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Generalized synthesis of periodic surfactant/inorganic composite materials

1994

THE recent synthesis of silica-based mesoporous materials1,2 by the cooperative assembly of periodic inorganic and surfactant-based structures has attracted great interest because it extends the range of molecular-sieve materials into the very-large-pore regime. If the synthetic approach can be generalized to transition-metal oxide mesostructures, the resulting nanocomposite materials might find applications in electrochromic or solid-electrolyte devices3,4, as high-surface-area redox catalysts5 and as substrates for biochemical separations. We have proposed recently6 that the matching of charge density at the surfactant/inorganic interfaces governs the assembly process; such co-organizatio…

chemistry.chemical_classificationchemistry.chemical_compoundMultidisciplinaryNanocompositePulmonary surfactantchemistryElectrochromismOxideCationic polymerizationCounterionComposite materialMesoporous materialElectrostaticsNature
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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
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Density Functional Theory Study of the Trans-Trans-Cis (TTC)→Trans-Trans-Trans (TTT) Isomerization of a Photochromic Spiropyran Merocyanine

2008

Density Functional Theory (DFT) calculations have been performed on the TTC→TTT isomerization reaction of the open forms of the 1',3'-dihydro-8-bromo-6-nitro- 1',3',3'-trimethylspiro[2H-1-benzopyran-2,2'-(2H)indole (8-Br-6-nitro-BIPS) system. The calculations were carried out in vacuo and in methylene chloride solution at different temperatures. Results are compared with the available experimental values of free energy difference and activation energy in solution.

Models MolecularIndolesVacuumSpiropyran; photochromism; DFT calculation; solvent influence on activation energy; merocyanine.merocyaninesolvent influence on activation energyPharmaceutical ScienceDFT calculationPyrimidinonesPhotochemistryArticleAnalytical Chemistrylcsh:QD241-441Photochromismchemistry.chemical_compoundlcsh:Organic chemistryDrug DiscoveryBenzopyransMerocyaninePhysical and Theoretical ChemistryMethyleneFluorescent DyesIndole testSpiropyranMethylene ChlorideOrganic ChemistryStereoisomerismModels TheoreticalNitro CompoundsphotochromismSolutionschemistrymerocyanine.Chemistry (miscellaneous)ThermodynamicsMolecular MedicineDensity functional theorySpiropyranIsomerizationCis–trans isomerismMolecules
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SWEET IONIC LIQUIDS BASED MATERIALS FOR ENVIRONMENTAL APPLICATIONS

Settore CHIM/06 - Chimica OrganicaIonic Liquids Sustainable Chemistry Ionic Liquid Gels Desulfurisation Energy storage Thermochromism Polymeric film
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N,N′-Disubstituted Indigos as Readily Available Red-Light Photoswitches with Tunable Thermal Half-Lives

2017

Some rare indigo derivatives have been known for a long time to be photochromic upon irradiation with red light, which should be advantageous for many applications. However, the absence of strategies to tune their thermal half-lives by modular molecular design as well as the lack of proper synthetic methods to prepare a variety of such molecules from the parent indigo dye have so far precluded their use. In this work, several synthetic protocols for N-functionalization have been developed, and a variety of N-alkyl and N-aryl indigo derivatives have been prepared. By installation of electron-withdrawing substituents on the N-aryl moieties, the thermal stability of the Z-isomers could be enha…

010405 organic chemistryChemistryIndigos photoswitchesIndigo dyeGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciencesBiochemistryCatalysisIndigo0104 chemical sciencesPhotochromismchemistry.chemical_compoundColloid and Surface ChemistryThermal[CHIM]Chemical SciencesMoleculeOrganic chemistryThermal stabilityIrradiationAbsorption (electromagnetic radiation)Journal of the American Chemical Society
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