Search results for "visual_art.visual_art_medium"

showing 10 items of 2982 documents

Electrochemistry and spectroelectrochemistry of heterobimetallic porphyrin-corrole dyads. Influence of the spacer, metal ion, and oxidation state on …

2005

Combined electrochemical and UV-visible spectroelectrochemical methods were utilized to elucidate the prevailing mechanisms for electroreduction of previously synthesized porphyrin-corrole dyads of the form (PCY)H2Co and (PCY)MClCoCl where M = Fe(III) or Mn(III), PC = porphyrin-corrole, and Y is a bridging group, either biphenylenyl (B), 9,9-dimethylxanthenyl (X), anthracenyl (A), or dibenzofuranyl (O). These studies were carried out in pyridine, conditions under which the cobalt(IV) corrole in (PCY)MClCoCl is immediately reduced to its Co(III) form, thus enabling direct comparisons with the free-base porphyrin dyad, (PCY)H2Co(III) under the same solution conditions. The compounds are all r…

chemistry.chemical_elementElectrochemistryPhotochemistryRedoxPorphyrinInorganic ChemistryMetalchemistry.chemical_compoundchemistryOxidation statevisual_artPolymer chemistryPyridinevisual_art.visual_art_mediumPhysical and Theoretical ChemistryCorroleCobaltInorganic chemistry
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The Aluminyl Anion : A New Generation of Aluminium Nucleophile

2020

Trivalent aluminium compounds are well known for their reactivity as Lewis acids/electrophiles, a feature that is exploited in many pharmaceutical, industrial and laboratory-based reactions. Recently, a series of isolable aluminium(I) anions ('aluminyls') have been reported, which offer an alternative to this textbook description: these reagents behave as aluminium nucleophiles. This minireview covers the synthesis, structure and reactivity of aluminyl species reported to date, together with their associated metal complexes. The frontier orbitals of each of these species have been investigated using a common methodology to allow for a like-for-like comparison of their electronic structure a…

chemistry.chemical_elementElectronic structureorganometalliyhdisteet010402 general chemistryreaktiivisuus01 natural sciencesCatalysisMetalmain groupNucleophileAluminiumnucleophile organometallicReactivity (chemistry)Lewis acids and basesalumiini010405 organic chemistryaluminiumGeneral MedicineGeneral ChemistrykompleksiyhdisteetCombinatorial chemistry0104 chemical scienceschemistryReagentvisual_artElectrophilevisual_art.visual_art_mediumaluminylalumiiniyhdisteet
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Titanium dioxide in dental enamel as a trace element and its variation with bleaching

2017

Background Titanium is a less studied trace element in dental enamel. Literature relates an increased Titanium concentration with a decreased enamel crystal domain size, which in turn is related to a higher color value. The aim of our study was to analyze the effect of tooth bleaching agents on its concentration in dental enamel by means of confocal Raman spectroscopy. Material and methods Human teeth were randomly distributed in six experimental groups (n=10) and submitted to different bleaching protocols according to the manufacturer´s instructions. Confocal Raman spectroscopy was carried out in order to identify and quantify the presence of titanium dioxide molecules in enamel prior to a…

chemistry.chemical_elementOdontología01 natural sciences010309 optics03 medical and health sciencessymbols.namesakechemistry.chemical_compound0302 clinical medicinestomatognathic systemwhitening0103 physical sciencesHydrogen peroxideGeneral DentistryTooth Bleaching AgentsEnamel painttitanium dioxidecarbamide peroxideChemistryDental enameltechnology industry and agricultureTrace elementbleaching030206 dentistryHydrogen peroxide:CIENCIAS MÉDICAS [UNESCO]stomatognathic diseasesvisual_artRaman spectroscopyUNESCO::CIENCIAS MÉDICASTitanium dioxidevisual_art.visual_art_mediumsymbolsRaman spectroscopyNuclear chemistryTitaniumJournal of Clinical and Experimental Dentistry
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Solubility-Driven Isolation of a Metastable Nonagold Cluster with Body-Centered Cubic Structure.

2020

The conventional synthetic methodology of atomically precise gold nanoclusters using reduction in solutions offers only thermodynamically most stable nanoclusters. We report herein a solubility‐driven isolation strategy to access the synthesis of a metastable gold cluster. The cluster, with the composition of [Au 9 (PPh 3 ) 8 ] + ( 1 ), displays an unusual, nearly perfect body‐centered‐cubic (bcc) structure. As revealed by ESI‐MS and UV/Vis measurement, the cluster is metastable in solution and converts to the well‐known [Au 11 (PPh 3 ) 8 Cl 2 ] + ( 2 ) within just 90 min. DFT calculations revealed that while both 1 and 2 are eight‐electron superatoms, there is a driving force to convert 1 …

cluster transformationBand gapnanoclusterCubic crystal system010402 general chemistry01 natural sciencesCatalysiskultaNanoclusterslaw.inventionMetalklusteritlawMetastabilityCluster (physics)metastable compoundsAu9CrystallizationGold cluster010405 organic chemistryChemistryOrganic ChemistryGeneral Chemistrygold0104 chemical sciencesCrystallographyvisual_artvisual_art.visual_art_mediumnanohiukkasetChemistry (Weinheim an der Bergstrasse, Germany)
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Metal Dependence on the Bidirectionality and Reversibility of the Singlet Energy Transfer in Artificial Special Pair-Containing Dyads

2017

International audience; The demetalation of a precursor dyad, 3, built upon a zinc(II)-containing artificial special pair and free-base antenna, leads to a new dyad, 4, for singlet energy transfer composed of cofacial free-base porphyrins (acceptor), [Fb](2) bridged by a 1,4-C6H4 group to a free-base antenna (donor), [Fb]. This dyad exhibits the general structure [M](2)-C6H4-[Fb], where [M](2) = [Fh](2), and completes a series reported earlier, where [M](2) = [Mg](2) (2) and [Zn](2) (3). The latter dyads exhibit a bidirectional energy-transfer process at 298 K for 2 and at 77 K for 3. Interestingly, a very scarce case of cycling process is observed for the zinc-containing dyad at 298 K. The…

cofacial bisporphyrin dyadsStereochemistryEnergy transferchemistry.chemical_elementZinc[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry01 natural sciencesphotoinduced electron-transferInorganic ChemistryMetalmolecular-orbital methodsMolecular orbitalSinglet statePhysical and Theoretical Chemistryphotosynthetic reaction-centerdensity-functional theoryvalence basis-setsbase hybrid diporphyrins010405 organic chemistry[ CHIM.INOR ] Chemical Sciences/Inorganic chemistryResonance (chemistry)Acceptor0104 chemical sciencesCrystallographychemistrylight-harvesting systemsvisual_artpolarizable continuum modelvisual_art.visual_art_mediumDensity functional theoryextended basis-sets
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Cytotoxicity investigations of plasma sprayed calcium phosphate coatings

1994

One potential alternative material to replace hydroxyapatite (HAp) as a coating material for plasma-sprayed coatings on implants for hip replacement is fluorapatite (FAp). FAp has advantages over HAp regarding the capability of being chemically stable during the coating process. This leads to surface coatings containing high apatite rates with a mechanical stability (bond strength, microhardness) comparable to HAp. From the technical point of view the production of FAp coatings is well investigated, although studies on biocompatibility of FAp coatings are fewer. This paper reports the production of HAp and FAp coatings with varying solubilities by plasma spraying and their in vitro cytotoxi…

congenital hereditary and neonatal diseases and abnormalitiesMaterials scienceBiocompatibilityBond strengthMetallurgyFluorapatiteBiomedical EngineeringBiophysicsBioengineeringElectrolyteengineering.materialCell morphologydigestive system diseasesApatiteBiomaterialschemistry.chemical_compoundstomatognathic systemchemistryChemical engineeringCoatingvisual_artvisual_art.visual_art_mediumengineeringFluorideJournal of Materials Science: Materials in Medicine
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Winter male plumage coloration correlates with breeding status in a cooperative breeding species

2007

The function of colored ornaments is usually related to the signaling of individual quality in intra- and intersexual interactions. In cooperative breeding species, where only a fraction of the male population access the breeding status and the other fraction has the option to help breeding pairs, colored traits might provide the females with a reliable information on the quality of potential mate. Males of the cooperative breeding azure-winged magpies (Cyanopica cyanus) display conspicuous blue plumage coloration. Here we explored the role played by structural blue coloration of males and the probability of becoming a breeder or a helper. Birds were trapped during 4 consecutive years, and …

cooperative breeding[ SDV.BDLR.RS ] Life Sciences [q-bio]/Reproductive Biology/Sexual reproductiongenetic structuresEcologyOrnamentsBody sizeBiologyPair formationPlumageFeathervisual_artCooperative breedingSexual selectionstructural colorationnonbreeding plumage[ SDV.EE.IEO ] Life Sciences [q-bio]/Ecology environment/Symbiosisvisual_art.visual_art_mediumsexual selectionAnimal Science and ZoologyCyanopica cyanusCyanopica cyanusEcology Evolution Behavior and SystematicsBehavioral Ecology
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The first copper(I)-olefin complexes bearing a 1,3,4-oxadiazole core: Alternating-current electrochemical crystallization, X-ray experiment and DFT s…

2017

By means of alternating-current electrochemical technique, four new π-complexes, namely [Cu2(C11H10N2OS)2Br1.91Cl0.09] (1), [Cu(C11H10N2OS)NO3] (2), [Cu2(C11H10N2OS)2(H2O)2](BF4)2 (3) and [Cu2(C11H10N2OS)2(H2O)2](ClO4)2 (4), were obtained using copper(II) salts and the 2-(allylthio)-5-phenyl-1,3,4-oxadiazole (C11H10N2OS) ligand. The metal and halogen centers in 1 form Cu2X2 dimers; the N-atom from the oxadiazole ring and the Cdouble bond; length as m-dashC bond of the allyl group from the same ligand complete the copper coordination environment, giving [Cu(C11H10N2OS)X]2 isolated fragments. The ligand plays the same chelating role in 2, whereas the O (NO3) atom occupies the third position i…

crystal structure3Stereochemistry1chemistry.chemical_elementOxadiazolekupariCrystal structure134-oxadiazole derivatives4-oxadiazole derivatives010402 general chemistryElectrochemistryRing (chemistry)DFT01 natural sciencesolefinpi-complexInorganic ChemistryMetalchemistry.chemical_compoundraman spectroscopyMaterials ChemistryMoleculePhysical and Theoretical Chemistryta116010405 organic chemistryLigandac-electrochemical techniquekompleksiyhdisteetCoppercopper(I)0104 chemical sciencesCrystallographychemistryvisual_artvisual_art.visual_art_mediumPolyhedron
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Double-CO32− Centered [CoII5] Wheel and Modeling of Its Magnetic Properties

2010

A high-spin Co(II) cluster with a rare pentagonal molecular structure and formula [Co(5)(CO(3))(2)(bpp)(5)]ClO(4) (1; Hbpp is 2,6-bis(phenyliminomethyl)-4-methylphenolate) has been synthesized and characterized by single-crystal X-ray diffraction. This topology arises from fusing five [Co(2)(bpp)] moieties in a cyclic manner around two CO(3)(2-) central ligands, resulting in propeller-like configuration. The irregular coordination of the carbonate ions to the metal centers results in a combination of coordination numbers (CNs) of the Co(II) ions of five and six. The bulk magnetization of this complicated magnetically exchanged system has been modeled successfully by employing a matrix diago…

crystal structureCoordination numberInorganic chemistrycarbonatesCatalysisIonCoordination complexMetalMagnetizationCluster (physics)Moleculecarbonate ligandschemistry.chemical_classificationOrganic Chemistrycarbonate ligands; carbonates; cobalt; coordination chemistry; density functional calculations; magnetic properties; spin-orbit coupling; crystal structure.General ChemistrySpin–orbit interactioncobaltspin-orbit couplingCrystallographychemistryvisual_artdensity functional calculationscoordination chemistryvisual_art.visual_art_mediummagnetic propertiesChemistry - A European Journal
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Ruthenium(II) carbonyl compounds with the 4′-chloro-2,2′:6′,2′′-terpyridine ligand

2017

The RuII atoms in the crystal structures of two new potential catalyst precursors, [Ru(Tpy-Cl)(CO)2Cl][Ru(CO)3Cl3] and [Ru(Tpy-Cl)(CO)2Cl2] (Tpy-Cl = 4′-chloro 2,2′:6′,2′′-terpyridine-κ3 N), exhibit distorted octa­hedral coordination spheres.

crystal structureCoordination spherechemistry.chemical_elementCrystal structurecarbonyl ligand010402 general chemistry01 natural sciencesResearch Communicationslcsh:ChemistryMetalchemistry.chemical_compoundAtomGeneral Materials Sciencerutheniumta116010405 organic chemistryLigandGeneral Chemistryterpyridine ligandCondensed Matter Physics0104 chemical sciences3. Good healthRutheniumCrystallographylcsh:QD1-999chemistryvisual_artvisual_art.visual_art_mediumTerpyridineActa Crystallographica Section E Crystallographic Communications
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