Search results for "element"

showing 10 items of 13601 documents

Understanding the ring current effects on magnetic shielding of hydrogen and carbon nuclei in naphthalene and anthracene

2008

The local response to an external magnetic field normal to the molecular plane of naphthalene and anthracene was investigated via current density and magnetic shielding density maps. The Biot-Savart law shows that the deshielding caused by pi-ring currents in naphthalene is stronger for alpha- than for beta-protons due to geometrical factors. The shielding tensor of the carbon nuclei in both molecules is strongly anisotropic and its out-of-plane component determines the up-field chemical shift of (13)C in nuclear magnetic resonance spectra. The pi-ring currents flowing beyond the C-skeleton in front of a probe carbon nucleus, and on remote parts of the molecular perimeter, yield positive co…

AnthraceneHydrogennaphthalenechemistry.chemical_elementGeneral ChemistryAromatic ring currentMagnetic fieldComputational Mathematicschemistry.chemical_compoundchemistrycurrent density mapsElectromagnetic shieldingproton and carbon chemical shiftAtomic physicsnaphthalene; ring currents; proton and carbon chemical shift; current density mapsCarbonCurrent densityring currentsRing currentJournal of Computational Chemistry
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Effect of molecular geometry and extended conjugation on the performance of hydrogen-bonded semiconductors in organic thin-film field-effect transist…

2021

A general synthetic method has been used for the condensation of the 7-azaindole substructure at both extremes of centrosymmetric fused polyheteroaromatic systems. Four different aromatic spacers (benzene, naphthalene, anthracene and pyrene) that modify the molecular geometry and the π-conjugated surface have proved the ability of 7-azaindole to work as a building block that can control the crystal packing through reciprocal hydrogen bond interactions. Two possible self-assembled columnar arrangements have been observed as a result of the π–π interactions between hydrogen-bonded ribbon-like supramolecular structures. A detailed comparative analysis of the molecular organisation driven by hy…

AnthraceneMaterials scienceHydrogenHydrogen bondSupramolecular chemistrychemistry.chemical_elementGeneral ChemistryCrystalchemistry.chemical_compoundMolecular geometrychemistryChemical physicsMaterials ChemistryPyreneThin filmJournal of Materials Chemistry C
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Radioactively labelled epoxides. part V. Tritium labelled K-region oxides and trans-dihydrodiols of pyrene, benzo[a]pyrene and dibenz[a, h]anthracene

1987

Tritium labelled K-region oxides of pyrene, benzo[a]pyrene and dibenz[a,h]anthracene have been prepared by cyclization of the corresponding trans-dihydrodiols which were obtained by reduction of K-region quinones with sodium borotritide in the presence of oxygen. This synthetic pathway not only yields two metabolically important radioactively labelled derivatives of polycyclic aromatic hydrocarbons in a simple and efficient manner, but also requires a rather inexpensive source of tritium.

AnthraceneOrganic Chemistrychemistry.chemical_elementBiochemistryMedicinal chemistryOxygenAnalytical Chemistrychemistry.chemical_compoundchemistryBenzo(a)pyreneDrug Discoverypolycyclic compoundsDibenz(ah)anthracenePyreneOrganic chemistryRadiology Nuclear Medicine and imagingTritiumSpectroscopySodium borotritideJournal of Labelled Compounds and Radiopharmaceuticals
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Synthesis of an anthracenyl bridged porphyrin–corrole bismacrocycle. Physicochemical and electrochemical characterisation of the biscobalt μ-superoxo…

2001

Abstract Dicobalt or heterobimetallic cofacial bisporphyrins are up till now amongst the very few molecular electrocatalysts able to promote the direct reduction of dioxygen to water via a four-electron process in acidic medium. Numerous studies have been devoted to elucidate the key steps of this catalytic reaction and an important result has revealed an unexpected high dioxygen affinity for a mixed valence Co(II)/Co(III) cofacial porphyrin, the key intermediate complex being a μ-superoxo derivative. At the same time, the great importance assumed by ‘Pacman’ porphyrins and the recent developments in corrole chemistry have provided the stimulation to synthesise porphyrin–corrole dyads which…

Anthracenechemistry.chemical_compoundValence (chemistry)chemistryStereochemistrychemistry.chemical_elementGeneral ChemistryCorroleElectrochemistryCobaltCombinatorial chemistryPorphyrinCatalysisComptes Rendus de l'Académie des Sciences - Series IIC - Chemistry
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Electrochemistry and spectroelectrochemistry of bismanganese biscorroles dyads

2011

Three manganese biscorrole dyads were synthesized, physicochemically characterized and investigated as to their electrochemistry and spectroelectrochemistry in nonaqueous media. Each dyad contained the same two corroles linked in a face-to-face arrangement via one of the three different linking groups, 9,9-dimethylxanthene, anthracene or diphenylether, the exact nature of which determined the distance and possible interaction between the two metallomacrocycles. The initial compounds contained Mn ( III ) in their air stable form and were shown to exhibit two major redox processes, one being a Mn (III)/ Mn (IV) conversion and the other being either Mn ( III )/ Mn ( II ) or reduction at the c…

Anthracenechemistry.chemical_elementGeneral ChemistryManganeseConjugated systemElectrochemistryPhotochemistryRedoxchemistry.chemical_compoundElectron transferchemistryPyridinePolymer chemistryCorroleJournal of Porphyrins and Phthalocyanines
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Electronic Interactions in a New π-Extended Tetrathiafulvalene Dimer

2006

The first pi-extended tetrathiafulvalene (exTTF) dimer in which the two exTTF units are covalently connected by 1,3-dithiole rings has been obtained in a multistep synthetic procedure involving the Ullmann cross-coupling reaction by using copper(I) thiophene-2-carboxylate (CuTC). The electronic spectrum reveals a significant electronic interaction between the exTTF units. The electrochemical study carried out by cyclic voltammetry in solution and in thin-layer conditions, and the electrochemical simulation and spectroelectrochemical (SEC) measurements confirm the electronic communication and show that the oxidation of dimer 14 occurs as two consecutive 2 e(-) processes D(0)-D(0)-->D(2+)-D(0…

AnthracenesAnthraceneDimerOrganic Chemistrychemistry.chemical_elementStereoisomerism[CHIM.MATE]Chemical Sciences/Material chemistryGeneral ChemistryPhotochemistryElectrochemistryCopperCatalysisDelocalized electronchemistry.chemical_compoundCrystallographyModels ChemicalchemistryHeterocyclic CompoundsCovalent bondElectrochemistryElectronicsCyclic voltammetryDimerizationOxidation-ReductionTetrathiafulvaleneChemistry - A European Journal
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Antimicrobial activity of biogenically produced spherical Se-nanomaterials embedded in organic material against Pseudomonas aeruginosa and Staphyloco…

2017

In an effort to prevent the formation of pathogenic biofilms on hydroxyapatite (HA)-based clinical devices and surfaces, we present a study evaluating the antimicrobial efficacy of Spherical biogenic Se-Nanostructures Embedded in Organic material (Bio Se-NEMO-S) produced by Bacillus mycoides SelTE01 in comparison with two different chemical selenium nanoparticle (SeNP) classes. These nanomaterials have been studied as potential antimicrobials for eradication of established HA-grown biofilms, for preventing biofilm formation on HA-coated surfaces and for inhibition of planktonic cell growth of Pseudomonas aeruginosa NCTC 12934 and Staphylococcus aureus ATCC 25923. Bio Se-NEMO resulted more e…

Anti-Infective Agent0301 basic medicineStaphylococcus aureusMetal Nanoparticleschemistry.chemical_elementBacillusBiocompatible MaterialsBioengineeringBacillus02 engineering and technologymedicine.disease_causeApplied Microbiology and BiotechnologyBiochemistrybiofilmantimicrobialsNanomaterialsMicrobiologyHydroxyapatiteSelenium03 medical and health sciencesAnti-Infective AgentsBiogenic Selenium nanoparticles (SeNPs) Hydroxyapatite Bacillus biofilm antimicrobials green synthesisOrganometallic CompoundsEnvironmental MicrobiologymedicineResearch ArticlesBiocompatible MaterialOrganometallic CompoundbiologyPseudomonas aeruginosagreen synthesisBiofilmBacillus mycoides021001 nanoscience & nanotechnologybiology.organism_classificationAntimicrobialBacilluDurapatite030104 developmental biologychemistryStaphylococcus aureusBiofilmsPseudomonas aeruginosaStaphylococcus aureu0210 nano-technologySeleniumResearch ArticleBiotechnologyBiogenic Selenium nanoparticles (SeNPs)
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Atomic fluorescence determination of total and inorganic arsenic species in beer

2001

A simple and nearly direct procedure has been developed for the determination of As in beers, based on hydride generation and atomic fluorescence detection. Using 2 mol l−1 HCl with a carrier flow of 6 ml min−1, 3% m/v NaBH4 with a flow of 1.3 ml min−1, a reaction coil of 200 cm and an argon flow of 400 ml min−1, total arsenic in beer could be determined in samples diluted 1∶10 with a final concentration of 2 mol l−1 HCl, 1% m/v KI and 0.08% v/v of an antifoam agent. For the estimation of AsIII and AsV concentrations in beer samples, the difference between the analytical sensitivities of the fluorescence signals obtained for As hydride, without and with previous treatment of samples with KI…

Antifoam agentDetection limitAtomic fluorescenceAshingInorganic arsenicChemistryHydrideAnalytical chemistrychemistry.chemical_elementFluorescenceSpectroscopyArsenicAnalytical ChemistryJ. Anal. At. Spectrom.
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Synthesis and Influence of 3-Amino Benzoxaboroles Structure on Their Activity against Candida albicans

2020

Benzoxaboroles emerged recently as molecules of high medicinal potential with Kerydin&reg

Antifungal AgentsStereochemistrySubstituentPharmaceutical Sciencechemistry.chemical_elementMicrobial Sensitivity Tests01 natural sciencesArticleAnalytical Chemistrylcsh:QD241-441030207 dermatology & venereal diseases03 medical and health sciencesMinimum inhibitory concentrationchemistry.chemical_compound0302 clinical medicinebenzoxaboroleslcsh:Organic chemistryDrug DiscoveryCandida albicansformylPhysical and Theoretical ChemistryCandida albicanschemistry.chemical_classificationTavaboroleKerydinMolecular Structurebiology010405 organic chemistryChemistryOrganic Chemistrybiology.organism_classificationpiperazine0104 chemical sciences<i>Candida albicans</i>PiperazineChemistry (miscellaneous)Heterocyclic amineFluorineMolecular MedicineAmine gas treatingantifungalMolecules
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Synthesis and antifungal activity of new N-(1-phenyl-4-carbetoxypyrazol-5-yl)-, N-(indazol-3-yl)- and N-(indazol-5-yl)-2-iodobenzamides

2002

N-(1-Phenyl-4-carbetoxypyrazol-5-yl)-, N-(indazol-3-yl)- and N-(indazol-5-yl)-2-iodobenzamides 6, with a Benodanil-like structure, were synthesized by refluxing in acetic acid the corresponding benzotriazinones 5 with potassium iodide for 1 h in order to study the role on the antifungal activity of the N-substitution with an aromatic heterocyclic system on benzamide moiety. Among the tested iododerivatives, compounds 6d,f,g,h possess interesting activities toward some phytopathogenic fungal strains.

AntifungalAntifungal AgentsIndazolesMagnetic Resonance SpectroscopySpectrophotometry Infraredmedicine.drug_classStereochemistryColony Count MicrobialPharmaceutical Sciencechemistry.chemical_elementCarboxamideMicrobial Sensitivity TestsIodineChemical synthesisAcetic acidchemistry.chemical_compoundN-(1-phenyl-4-carbetoxypyrazol-5-yl)-2-iodobenzamides N-(indazol-3-yl)-2-iodobenzamides N-(indazol-3-yl)-2-iodobenzamides antifungal activityDrug DiscoverymedicineMoietyBenzamideChemistryFungiSettore CHIM/08 - Chimica FarmaceuticaBenzamidesPyrazolesIl Farmaco
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