Search results for "COMPOUND"

showing 10 items of 35174 documents

Hyaluronan Graft Copolymers Bearing Fatty-Acid Residues as Self-Assembling Nanoparticles for Olanzapine Delivery

2019

In order to evaluate the potential of a technology platform based on hyaluronan copolymers grafted with propargylated ferulate fluorophores (HA-FA-Pg) in the development of drug delivery systems, the propargyl groups of HA-FA-Pg derivatives were employed with oleic acid (OA) or stearic acid (SA) residues across a biocompatible hexa(ethylene glycol) (HEG) spacer. The designed materials (i.e., HA-FA-HEG-OA or HA-FA-HEG-SA) showed clear-cut aggregation features in an aqueous environment, as confirmed by dynamic light scattering (DLS) and transmission electron microscopy (TEM), generating nanoaggregate systems. In fact, HA-FA-HEG-OA and HA-FA-HEG-SA derivatives showed the property to create sel…

olanzapinePharmaceutical Science02 engineering and technologyself-assembling nanocarrier010402 general chemistry01 natural sciencesArticlechemistry.chemical_compounddrug delivery systemsDynamic light scatteringhyaluronic acidCopolymerSide chainSolubilityDrug delivery systems; Ferulic acid; Hyaluronic acid; Olanzapine; Oleic acid; Self-assembling nanocarriers; Stearic acidSelf-assembling nanocarriersstearic acid021001 nanoscience & nanotechnology0104 chemical sciencesOleic acidchemistryChemical engineeringoleic acidDrug deliveryStearic acid0210 nano-technologyEthylene glycolferulic acid
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Increasing Yield and Antioxidative Performance of Litchi Pericarp Procyanidins in Baked Food by Ultrasound-Assisted Extraction Coupled with Enzymatic…

2018

Extraction with organic solvents is a traditional method to isolate bioactive compounds, which is energy-wasting and time-consuming. Therefore, enzyme and ultrasound treatments were combined to assist the extraction of oligomeric procyanidins from litchi pericarp (LPOPC), as an innovative approach to replace conventional extraction methods. Under optimum conditions (enzyme concentration 0.12 mg/mL, ultrasonic power 300 W, ultrasonic time 80 min, and liquid/solid ratio 10 mL/g), the yield of LPOPC could be improved up to 13.5%. HPLC analysis indicated that the oligomeric procyanidins (OPC) content of LPOPC from proposed extraction was up to 89.6%, mainly including (&minus

oligomeric procyanidinsPharmaceutical Sciencelitchi pericarpChemical FractionationHigh-performance liquid chromatographyPeroxideAntioxidantsArticleAnalytical Chemistrylcsh:QD241-441Lipid peroxidationchemistry.chemical_compound0404 agricultural biotechnologylcsh:Organic chemistryLitchiDrug DiscoveryRSM (Response Surface Methodology)Physical and Theoretical ChemistryChromatography High Pressure LiquidAnalysis of VarianceChromatographyMolecular StructurePlant ExtractsOrganic ChemistryExtraction (chemistry)04 agricultural and veterinary sciences040401 food sciencebaked foodMonomerProanthocyanidinchemistryUltrasonic WavesChemistry (miscellaneous)Yield (chemistry)Molecular MedicineHPLCProcyanidin A1Molecules
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The role of SAXS and molecular simulations in 3D structure elucidation of a DNA aptamer against lung cancer

2021

Aptamers are short, single-stranded DNA or RNA oligonucleotide molecules that function as synthetic analogs of antibodies and bind to a target molecule with high specificity. Aptamer affinity entirely depends on its tertiary structure and charge distribution. Therefore, length and structure optimization are essential for increasing aptamer specificity and affinity. Here, we present a general optimization procedure for finding the most populated atomistic structures of DNA aptamers. Based on the existed aptamer LC-18 for lung adenocarcinoma, a new truncated LC-18 (LC-18t) aptamer LC-18t was developed. A three-dimensional (3D) shape of LC-18t was reported based on small-angle X-ray scattering…

oligonucleotideMolecular modelAptamer610RM1-950chemistry.chemical_compoundDrug DiscoveryA-DNAddc:610Binding siteOligonucleotideaptamerSAXSspatial structurelung adenocarcinomamolecular dynamicsProtein tertiary structurefragment molecular orbitalchemistrysmall-angle X-ray scatteringBiophysicsMolecular MedicineOriginal Articletertiary structureTherapeutics. Pharmacologymolecular simulationsDNAFragment molecular orbital
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Solvatochromic behaviour of new donor–acceptor oligothiophenes

2021

Oligothiophene derivatives play a central role in the formulation of materials used in devices in the field of organic electronics. In this work, we report the results of the study of UV-vis absorption and fluorescence spectra, in several solvents, of a series of oligothiophenes recently synthesized in our laboratory. The studied oligothiophenes present different structures due to several factors: the donor– acceptor (D–A) or acceptor–donor–acceptor (A–D–A) architecture, the number of thiophene rings in the backbone (ranging from three to eight), the number and position of solubilizing octyl chains in the backbone, and the type of acceptor moieties (from Knoevenagel condensation either with…

oligothiophenessolvatochromism02 engineering and technology010402 general chemistryElectrochemistryPhotochemistry01 natural sciencesCatalysischemistry.chemical_compoundMaterials ChemistryThiopheneOrganic electronicsanodic dimerizationSolvatochromismSettore CHIM/06 - Chimica OrganicaGeneral Chemistry021001 nanoscience & nanotechnologyAcceptor0104 chemical scienceschemistryoligothiophenes; solvatochromism; anodic dimerizationKnoevenagel condensationAbsorption (chemistry)0210 nano-technologyDonor acceptorOligothiophenes fluorescence donor-acceptor systemsNew Journal of Chemistry
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Optical Absorption of Excimer Laser‐Induced Dichlorine Monoxide in Silica Glass and Excitation of Singlet Oxygen Luminescence by Energy Transfer from…

2021

An optical absorption (OA) band of interstitial dichlorine monoxide molecules with peak at 4.7 eV and halfwidth 0.94 eV is identified in F2 laser - irradiated (photon energy=7.9 eV) synthetic silica glass bearing both interstitial O2 and Cl2 molecules. Alongside with intrinsic defects, this OA band can contribute to solarization of silica glasses produced from SiCl4. While the formation of ClClO is confirmed by its Raman signature, its structural isomer ClOCl may also contribute to this induced OA band. Thermal destruction of this band between 300C and 400C almost completely restores the pre-irradiation concentration of interstitial Cl2. An additional weak OA band at 3.5 eV is tentatively a…

optical absorptionMaterials scienceInfraredinterstitial chlorinemedicine.medical_treatmentFOS: Physical sciencesPhoton energyPhotochemistrysinglet oxygenchemistry.chemical_compoundsymbols.namesakesilica glassMaterials ChemistrymedicineElectrical and Electronic Engineering[PHYS]Physics [physics]Condensed Matter - Materials ScienceExcimer laserSinglet oxygenMaterials Science (cond-mat.mtrl-sci)Surfaces and InterfacesCondensed Matter PhysicsSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsDichlorine monoxidechemistryglass nanovoidssymbolschlorine oxidesluminescenceactivationAbsorption (chemistry)Raman spectroscopyLuminescence
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Donor-π-acceptors containing the 10-(1,3-dithiol-2-ylidene)anthracene unit for dye-sensitized solar cells

2012

Two donor-acceptor molecular tweezers incorporating the 10-(1,3-dithiol-2-ylidene)anthracene unit as donor group and two cyanoacrylic units as accepting/anchoring groups are reported as metal-free sensitizers for dye-sensitized solar cells. By changing the phenyl spacer with 3,4-ethylenedioxythiophene (EDOT) units, the absorption spectrum of the sensitizer is red-shifted with a corresponding increase in the molar absorptivity. Density functional calculations confirmed the intramolecular charge-transfer nature of the lowest-energy absorption bands. The new dyes are highly distorted from planarity and are bound to the TiO(2) surface through the two anchoring groups in a unidentate binding for…

optical propertiesAbsorption spectroscopypigments010402 general chemistryPhotochemistrydyes01 natural sciences7. Clean energyCatalysischemistry.chemical_compound[CHIM]Chemical SciencesComputingMilieux_MISCELLANEOUSAnthracene010405 organic chemistryOrganic ChemistryDithiolGeneral ChemistryMolar absorptivity0104 chemical sciencesDye-sensitized solar cellchemistryIntramolecular forcesensitizerssolar cellsAbsorption (chemistry)absorptionMolecular tweezers
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Silver Sulfide Nanoclusters and the Superatom Model

2015

The superatom model of electron-shell closings has been widely used to explain the stability of noble-metal nanoclusters of few nanometers, including thiolate-protected Au and Ag nanoclusters. The presence of core sulfur atoms in silver sulfide (Ag–S) nanoclusters renders them a class of clusters with distinctive properties as compared to typical noble-metal clusters. Here, it is natural to ask whether the superatom model is still applicable for the Ag–S nanoclusters with mixed metal and nonmetal core atoms. To address this question, we applied density functional simulations to analyze a series of Ag–S nanoclusters: Ag14S(SPh)12(PPh3)8, Ag14(SC6H3F2)12(PPh3)8, Ag70S16(SPh)34(PhCO2)4(triphos…

optical propertiesElectron densitySilver sulfideInorganic chemistryNanoclusterschemistry.chemical_compoundAtomic orbitalNonmetalCluster (physics)Physical and Theoretical Chemistryta116electromagnetic wave absorptionconduction bandsatomsta114ChemistrySuperatomprecious metalsmolecular orbitalsTriphosSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialsenergy gapCrystallographyGeneral Energysulfurlight absorptionThe Journal of Physical Chemistry C
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Long-transient conoscopic pattern technique

1999

0038-1098; Recent results on laser induced anisotropy in terbium gallium garnet are extended to the dynamic regime. We observed that the characteristic conoscopic pattern formation time presents a quadratic dependence on the beam size. The observed pattern intensity is accounted for by a simple analytical formula. The transient refractive index change due to thermal stress in the terbium gallium garnet is determined. (C) 1999 Elsevier Science Ltd. All rights reserved.

optical propertiesheat capacityPhysics::OpticsPattern formation02 engineering and technologyTERBIUM-GALLIUM GARNET01 natural sciencesTerbium gallium garnetlaw.invention010309 opticsCondensed Matter::Materials Sciencechemistry.chemical_compoundOpticslaw0103 physical sciencesMaterials ChemistryBirefringenceCondensed matter physicsbusiness.industrynonlinear opticsNonlinear opticsGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsLaserIntensity (physics)chemistryTransient (oscillation)0210 nano-technologybusinessRefractive index
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4,4'-[Thiophene-2,5-diylbis(ethyne-2,1-diyl)]dibenzonitrile

2008

In the solid state, the title compound, C(22)H(10)N(2)S, forms centrosymmetric dimers by pairs of non-classical C-H⋯S hydrogen bonds linking approximately coplanar mol-ecules. The benzene ring involved in this inter-action makes a dihedral angle of only 7.21 (16)° with the thio-phene ring, while the other benzene ring is twisted somewhat out of the plane, with a dihedral angle of 39.58 (9)°. The hydrogen-bonded dimers stack on top of each other with an inter-planar spacing of 3.44 Å. C-H⋯N hydrogen bonds link together stacks that run in approximately perpendicular directions. Each mol-ecule thus inter-acts with 12 adjacent mol-ecules, five of them approaching closer than the sum of the van …

optoelectronicsmolecular electronicsSolid-state.Dihedral angle010402 general chemistryRing (chemistry)BioinformaticsOrganic Papers01 natural sciencesnanoelectronicsFaculdade de Ciências Exatas e da Engenhariasymbols.namesakechemistry.chemical_compound44000-[Thiophene-25-diylbis(ethyne-21diyl)]dibenzonitrilePerpendicularPhysics::Atomic and Molecular ClustersGeneral Materials ScienceVan der Waals radiusPhysics::Chemical PhysicsBenzene010405 organic chemistryChemistryHydrogen bondGeneral ChemistryCondensed Matter Physics3. Good health0104 chemical sciencesCrystallographysymbolsorganic compoundsActa Crystallographica Section E: Crystallographic Communications
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New simple hydrophobic proline derivatives as highly active and stereoselective catalysts for the direct asymmetric aldol reaction in aqueous medium

2008

New 4-substituted acyloxyproline derivatives with different hydrophobic properties of the acyl group were easily synthesized and used as catalysts in the direct asymmetric aldol reaction between cyclic ketones (cyclohexanone and cyclopentanone) and several substituted benzaldehydes. Reactions were carried out using water, this being the best reaction medium examined. Screening of these catalysts showed that compounds bearing the most hydrophobic acyl chains [4-phenylbutanoate and 4-(pyren-1-yl)butanoate] provided better results. The latter catalysts were successfully used in only 2 mol% at room temperature without additives to give aldol products in excellent stereoselectivities. These resu…

or-ganic catalysiorganic chemicalsOrganic ChemistryketoneSubstituentCyclohexanoneSettore CHIM/06 - Chimica OrganicaCyclopentanoneCatalysisaldehydeCatalysischemistry.chemical_compoundchemistryAldol reactionMoietyOrganic chemistryaldol reactionStereoselectivityprolineAcyl group
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