Search results for "cyclic"

showing 10 items of 2439 documents

Water-soluble hyperbranched polyglycerol photosensitizer for enhanced photodynamic therapy

2020

Porphyrin and its derivatives as promising photosensitizers have been widely utilized in photodynamic therapy (PDT). However, the water-solubility and biocompatibility of porphyrins are the typical bottlenecks in clinical PDT processes. Herein, we successfully fabricated a new type of water-soluble, hyperbranched polyglycerol photosensitizer through one-step esterification between water-soluble hyperbranched polyglycerol (hbPG) and fluorophenylporphyrin (FP). Compared with the linear control polymer, i.e., FP covalently connected with linear polyethylene glycol (LPEG), the hyperbranched structures bearing multiple porphyrin units generated more singlet oxygen and exhibited higher cytotoxici…

chemistry.chemical_classificationPolymers and PlasticsBiocompatibilitySinglet oxygenmedicine.medical_treatmentOrganic ChemistryBioengineeringPhotodynamic therapyPolymerBiochemistryCombinatorial chemistryPorphyrinchemistry.chemical_compoundchemistryCovalent bondpolycyclic compoundsmedicinePhotosensitizerCytotoxicityPolymer Chemistry
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Polycyclic Aromatic Hydrocarbons in Sediments of Marine Coastal Lagoons in Messina, Italy: Extraction and GC/MS Analysis, Distribution and Sources

2004

The content of 21 polycyclic aromatic hydrocarbons (PAHs) has been determined in 16 samples of sediments collected from Ganzirri and Faro marine coastal lagoons in Messina (Italy). Analysis was performed by gas chromatography/mass spectrometry (GC/MS) in selected ion monitoring (SIM) mode. The total concentration of polycyclic aromatic hydrocarbons (PAHs) ranged from 74 to 5755 ...g/Kg of dry matrix. The resulting distributions and molecular ratios of specific compounds have been discussed in terms of sampling location and origin of organic matter. The results obtained show that levels of contamination are not homogeneous throughout the stations, while the relative distributions of PAH are…

chemistry.chemical_classificationPolymers and PlasticsChemistryOrganic ChemistryExtraction (chemistry)ContaminationMass spectrometrypolycyclic aromatic hydrocarbons sediments organic matter content coastal marine lagoonsSettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni CulturaliMatrix (chemical analysis)Environmental chemistryMaterials ChemistrySettore CHIM/01 - Chimica AnaliticaSelected ion monitoringOrganic matterGas chromatographyGas chromatography–mass spectrometryPolycyclic Aromatic Compounds
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Poly(phosphonate)-mediated Horner–Wadsworth–Emmons reactions

2015

A novel, general protocol for a polymer-mediated Horner–Wadsworth–Emmons (HWE) reaction is reported. The polyvalent polymeric reagent was prepared via acyclic diene metathesis (ADMET) polymerization. Homo- and copolymers of reactive poly(phosphonate)s with molecular weights up to 40 000 g·mol−1 and molecular weight dispersities Đ < 2 were successfully synthesized. Subsequent application of these polymers in the HWE reaction to prepare a library of aromatic α,β-unsaturated ketones (chalcons) has proven to be an efficient synthetic pathway to minimize purification efforts, as the polymeric side-product can be removed by simple precipitation. In this paper we also demonstrate for the first tim…

chemistry.chemical_classificationPolymers and PlasticsMolecular massPolyphosphateOrganic ChemistryBioengineeringPolymerBiochemistryPhosphonatechemistry.chemical_compoundchemistryPolymerizationReagentCopolymerOrganic chemistryAcyclic diene metathesisPolymer Chemistry
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Influence of preparation conditions of nano-crystalline ceria catalysts on the total oxidation of naphthalene, a model polycyclic aromatic hydrocarbon

2007

Abstract Nano-crystalline ceria catalysts prepared by homogeneous precipitation with urea were tested for the total oxidation of naphthalene, a model polycyclic aromatic hydrocarbon (PAH). Systematic variation of preparation conditions, including calcination temperature, calcination time and aging time, resulted in differences in surface area, reducibility, morphology and crystallite size of the CeO 2 catalyst and hence differences in catalytic performance. A combination of high surface area, small crystallite size and high oxygen defect concentration was found to favor the efficiency of the ceria catalysts for the total oxidation of naphthalene. Optimum preparation conditions for this stud…

chemistry.chemical_classificationProcess Chemistry and TechnologyInorganic chemistryPolycyclic aromatic hydrocarbonHeterogeneous catalysisCatalysisCatalysislaw.inventionchemistry.chemical_compoundHydrocarbonCatalytic oxidationchemistrylawCalcinationCrystalliteGeneral Environmental ScienceNaphthaleneApplied Catalysis B: Environmental
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The role of potassium and hydrogen ions in the Prussian Blue ⇆ Everitt's Salt process

1998

Cyclic voltammetry experiments have proved very useful in the knowledge and understanding of the role of the potassium and hydrogen ions during the Prussian Blue ⇄ Everitt's Salt process. While potassium ions act as a stoichiometric reactant, the hydrogen ions play a very important role in the kinetics of the electron-hopping process. The entropy change for the reaction PB ⇄ ES has proved to be dependent on the degree of crystallinity of the film, indicating that this entropy change is related to the fixation of inner counterions on the crystal structure of the films.

chemistry.chemical_classificationPrussian blueAqueous solutionHydrogenGeneral Chemical EngineeringPotassiumInorganic chemistrychemistry.chemical_elementElectrochemistrychemistry.chemical_compoundchemistryElectrochemistrysense organsCounterionCyclic voltammetryStoichiometry
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Electrochemical study of dinuclear ruthenium(II)—arene compounds: Electrogeneration of Ru(II)—Ru(I) species

1987

Abstract The preparation and characterization of Ru(II)—arene compounds [{RuCl2(p-cym)}2(μ-L-L)] where p-cym = p-MeC6H4CHMe2; and L-L = diphenylphosphinomethane (I), 1,1′-bisdiphenylphosphinoferrocene (II), pyrazine (III) and 4,4′-bipyridine (IV), are described. Electrochemical data for these compounds obtained by cyclic voltammetry and coulometry are reported. The electrochemical reduction of compounds I or II yields ruthenium(O) species. However, compounds III or IV containing ligands with delocalized Π orbitals undergo one-electron reduction. The ESR signal detected during the electrolysis of compounds III or IV is consistent with one delocalized electron through the whole dinuclear unit.

chemistry.chemical_classificationPyrazineInorganic chemistrychemistry.chemical_elementElectrochemistryMedicinal chemistryRutheniumInorganic ChemistryCoulometrychemistry.chemical_compoundDelocalized electronHydrocarbonchemistryMaterials ChemistryPhysical and Theoretical ChemistryCyclic voltammetryMetallocenePolyhedron
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UV-B-Induced acute toxicity of pyrene to the waterflea Daphnia magna in natural freshwaters.

1999

Abstract The effects of various water characteristics in natural freshwaters on the acute toxicity of one polycyclic aromatic hydrocarbon (PAH), pyrene, to a pelagic invertebrate Daphnia magna was studied under ultraviolet B (UV-B) radiation and in the dark. Pyrene was photoactivated and was more toxic to D. magna in the presence of UV-B radiation. Dissolved organic material (DOM), measured as dissolved organic carbon (DOC), significantly reduced the photoenhanced toxicity of pyrene. Under UV-B radiation the EC50 values were lower and in relation to the amount of DOM, ranging from 3.0 to 30.0 μg/L pyrene, whereas in the dark they were between 29.2 and 54.8 μg/L and not related to the amount…

chemistry.chemical_classificationPyrenesbiologyDose-Response Relationship DrugUltraviolet RaysHealth Toxicology and MutagenesisDaphnia magnaPublic Health Environmental and Occupational HealthPolycyclic aromatic hydrocarbonFresh WaterGeneral Medicinebiology.organism_classificationPollutionAcute toxicitychemistry.chemical_compoundchemistryCladoceraDaphniaEnvironmental chemistryDissolved organic carbonToxicityPyreneAnimalsOrganic matterOrganic ChemicalsEcotoxicology and environmental safety
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Radiolabeling of DOTATOC with the long-lived positron emitter 44Sc.

2010

Abstract The positron-emitting radionuclide 44 Sc with a half-life of 3.97 h and a β + branching of 94.3% is of potential interest for clinical PET. As so far it is available from a 44 Ti/ 44 Sc generator in Mainz, where long-lived 44 Ti decays to no-carrier-added (nca) 44 Sc. The 44 Sc is a trivalent metal cation and should be suitable for complexation with many well established bifunctional chelators conjugated to peptides or other molecular targeting vectors. Thus, the aim of this work was to investigate the potential of 44 Sc for labeling of DOTA-conjugated peptides. DOTA-D-Phe 1 -Tyr 3 -octreotide (DOTATOC) was used as a model molecule to study and optimize labeling procedure. Reaction…

chemistry.chemical_classificationRadioisotopesRadiationRadiochemistryAnalytical chemistryContrast MediaPeptideConjugated systemOctreotideMetalchemistry.chemical_compoundchemistryvisual_artIsotope LabelingPositron-Emission Tomographyvisual_art.visual_art_mediumMoleculeDOTAMacrocyclic ligandRadiopharmaceuticalsBifunctionalAmmonium acetateScandiumApplied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine
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A study on the aminomercuration-nucleophilic demercuration of --1,5-cyclooctadiene; stereoselective synthesis of 2,6-disubstituted-9-aza bicyclo[3.3.…

1992

Abstract The aminomercuration of cis - cis -1,5-Cyclooctadiene with a series of mercury(II) salts followed by nucleophilic displacement of mercury by aromatic amines, water and nitrate ion has been studied. As a result, bicyclic triamines, aminoalcohols and nitrate esters have been obtained respectively in clean processes which occur under total stereoelectronic control by involvement of a tricyclic aziridium ion to afford a single stereoisomer in each case. The influence of the counter ion and the basicity of the amine on the tandem aminomercuration-demercuration is discussed.

chemistry.chemical_classificationReaction mechanismBicyclic molecule15-CyclooctadieneOrganic ChemistryBiochemistrychemistry.chemical_compoundchemistryNucleophileDrug DiscoveryOrganic chemistryAmine gas treatingStereoselectivityCounterionAminationTetrahedron
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Cyclodextrins in Polymer Synthesis: Enantiodiscrimination in Free-Radical Polymerization of Cyclodextrin-Complexed Racemic N -Methacryloyl-D,L -pheny…

2003

The enantiodiscriminating polymerization of racemic cyclodextrin-complexed N-methacryloylphenylalanine methyl ester is investigated 1 H NMR spectra of the complexes with methylated β-cyclodextrin in D 2 O manifest splittings due to chiral recognition. The different stabilities of the diastereomeric complexes influence the kinetics of the homopolymerization, particularly at 0°C. An enrichment of the residual N-methacryloyl-L-phenylalanine methyl ester of 14% was achieved after 21 h of polymerization.

chemistry.chemical_classificationReaction mechanismPolymers and PlasticsCyclodextrinOrganic ChemistryRadical polymerizationtechnology industry and agricultureDiastereomerPolymerchemistry.chemical_compoundMonomerchemistryPolymerizationPolymer chemistrypolycyclic compoundsMaterials ChemistryProton NMRMacromolecular Rapid Communications
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