Search results for "Medium"

showing 10 items of 3746 documents

ChemInform Abstract: New Binary Antimonide Hf5Sb3 - Differences and Similarities to the Zr Antimonides.

2010

Abstract Hf5Sb3 can be prepared by arc-melting of hafnium and previously synthesized HfSb2. It crystallizes like the high-temperature modification of Zr5Sb3 in the Y5Bi3 structure type, space group Pnma, Z=4, a=740.75(9) pm, b=871.8(1) pm, c=1073.6(1) pm, V=693.3(1) 106pm3. An antimonide analogous to the low-temperature form of Zr5Sb3 was not obtained during our investigations. In the structure of Hf5Sb3, the Hf atoms form a three-dimensional network with numerous short Hf–Hf contacts, including the Sb atoms in severely distorted two- and three-capped trigonal prismatic voids. Calculations of the electronic structure, performed with the extended Huckel approximation as well as the TB-LMTO-A…

chemistry.chemical_elementBinary numberGeneral MedicineElectronic structureStructure typeTrigonal prismatic molecular geometryHafniumMetalCrystallographychemistryGroup (periodic table)visual_artAntimonidevisual_art.visual_art_mediumChemInform
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Crystal structure, spectroscopic characterisation and magnetic properties of [Cu(BIP)(N3)]·H2O (BIP=3,3-bis(2-imidazolyl)propionate), a copper(II) po…

2001

Abstract The structure and the spectroscopic and magnetic properties of [3,3-bis(2-imidazolyl)propionato]azidocopper(II) monohydrate are described. The compound is built of [Cu(BIP)N3] entities which are connected through carboxylate groups from the BIP molecules —which act as a tridentate ligand—and asymmetrical μ-1,3-azido bridges, leading to a polymeric sheet-like structure. The copper atom is involved in a CuN3ON′ chromophore and lies in a distorted square-pyramidal environment. Both electronic and EPR spectra are indicative of an essentially dx2−y2 ground state for the copper(II) ions. Magnetic susceptibility measurements in the range 1.8–200 K show very weak antiferromagnetic exchange…

chemistry.chemical_elementCrystal structureChromophoreCopperMagnetic susceptibilitylaw.inventionInorganic ChemistryMetalCrystallographychemistry.chemical_compoundchemistrylawvisual_artMaterials Chemistryvisual_art.visual_art_mediumMoleculeCarboxylatePhysical and Theoretical ChemistryElectron paramagnetic resonanceInorganica Chimica Acta
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Synthesis, structure, spectral characterization and DNA binding affinity of new water soluble trinuclear copper(II) complexes with partial cubane Cu3…

2015

Two new water soluble trinuclear copper(II) complexes, [Na 6 (H 3 O) 4 ][Cu 3 (cbal) 3 (μ 3 -OH)(H 2 O) 3 ] 4 (ClO 4 ) 6 ·3H 2 O ( 1 ) and [K(H 2 O) 2 ][Cu 3 (cbal) 3 (μ 3 -OH)(H 2 O)]·3.75H 2 O ( 2 ) have been synthesized in good yield via the reaction of an unsymmetrical amino dicarboxylic ligand, N-(2-carboxybenzomethyl)-β-alanine (H 2 cbal), Cu(ClO 4 ) 2 ·6H 2 O and NaOH/K 2 CO 3 in methanol at room temperature. Complexes 1 and 2 have been characterized by elemental analysis, room temperature magnetic susceptibility measurements, FTIR, UV–Vis, mass spectrometry and single crystal X-ray crystallography. Both complexes contain a partial cubane [Cu 3 O 4 ] core consisting of the trinuclear…

chemistry.chemical_elementCrystal structureCopperSquare pyramidal molecular geometryInorganic ChemistryMetalchemistry.chemical_compoundCrystallographyTrigonal bipyramidal molecular geometrychemistryCubanevisual_artOctahedral molecular geometryMaterials Chemistryvisual_art.visual_art_mediumPhysical and Theoretical ChemistrySingle crystalPolyhedron
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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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Competence needs of older worker in small and medium size enterprises

2000

competencecompetence needchanges in working lifeparticipation in trainingolder workersmall and medium size enterprise
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Ethical Behavior and Organizational Innovation: Analysis of Small and Medium-Sized Enterprises in Latvia

2018

Abstract Innovations can provide small and medium-sized enterprises (SMEs) a significant competitive advantage considering the ambiguous business environment. SMEs may face lower capacity and more constrained funding for long-term investments, however, understanding innovation in a broader sense and looking into organizational structures, behaviors and processes, SMEs have an opportunity to become more competitive. This study analyzes the impact of ethical behavior as a part of an organizational culture on organizational innovation performance in SMEs. Six hundred SMEs in Latvia were surveyed to assess whether employees follow the principles of business ethics in their work and what is the …

competitivenessOrganizational innovationComputingMilieux_THECOMPUTINGPROFESSIONorganizational cultureHF5001-6182ethical behavior05 social sciencessmall and medium-sized enterprisesOrganizational cultureFace (sociological concept)Ethical behaviorCompetitive advantageEconomics as a scienceWork (electrical)organizational innovation0502 economics and businessBusinessOrganizational structureBusiness050207 economicsBusiness ethicsHB71-74050203 business & managementIndustrial organizationEconomics and Business
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