Search results for "Ruth"

showing 10 items of 661 documents

Ruthenium Janus-Head Complexes with a Triazolediylidene Ligand. Structural Features and Catalytic Applications

2007

The use of the ligand triazolediylidene (ditz), has afforded the preparation of two new complexes of Ru in which the ligand is bridging two metal fragments in a facially opposed (Janus-head) disposition. One of the complexes is dinuclear (2) and the other tetranuclear (3). The tetranuclear compound displays interesting structural features, as shown by the X-ray diffraction studies. The two complexes have been tested in the catalytic β-alkylation of secondary alcohols with primary alcohols, providing high activities when both aliphatic and aromatic alcohols are used.

Inorganic ChemistryMetalChemistryvisual_artOrganic Chemistryvisual_art.visual_art_mediumchemistry.chemical_elementJanusPhysical and Theoretical ChemistryCombinatorial chemistryCatalysisRutheniumOrganometallics
researchProduct

Selective area vapor-phase epitaxy and structural properties of Hg1 − xCdxTe on sapphire

1997

Selective area (SA) Hg1 − xCdxTesapphire layers have been grown using the recently developed technique of the vapor-phase epitaxy (VPE) of Hg1 − xCdxTe layers on CdTesapphire heteroepitaxial substrates (HS), which we have called “VPE on HS technique” (Sochinskii et al., J. Crystal Growth 149 (1995) 35; 161 (1996) 195). First, planar CdTe (1 1 1) 5–7 μm thick layers were grown on sapphire (0 0 0 1) wafers by metalorganic vapor-phase epitaxy (MOVPE) at 340°C for 1–2.5 h using dimethylcadmium and di-isopropyltellurium as precursors. Second, CdTe/sapphire mesas were formed using standard photolithography in the form of alternating parallel linear arrays consisting of 500 × 70 μm2 elements. Thir…

Inorganic ChemistryScanning electron microscopeChemistryMaterials ChemistryAnalytical chemistrySapphireCrystal growthMetalorganic vapour phase epitaxySubstrate (electronics)Condensed Matter PhysicsEpitaxyRutherford backscattering spectrometryCadmium telluride photovoltaicsJournal of Crystal Growth
researchProduct

Anchor‐Functionalized Push‐Pull‐Substituted Bis(tridentate) Ruthenium(II) Polypyridine Chromophores: Photostability and Evaluation as Photosensitizers

2014

Stable push-pull substituted heteroleptic bis(tridentate) ruthenium(II) polypyridine complexes with COOH or 2,2′-bipyridine anchor groups have been prepared and characterized by 1H, 13C and 15N NMR 1D and 2D spectroscopy, infrared spectroscopy, elemental analysis, high-resolution ESI mass spectrometry, electrochemistry, UV/Vis absorption spectroscopy, luminescence spectroscopy, and density functional calculations. The complexes feature a pronounced electronic directionality and high absorption wavelengths up to λmax = 544 nm extending to 720 nm as a result of favorable push-pull substitutions. A remarkable photostability in the presence of water and coordinating ions (I–) was discovered for…

Inorganic ChemistrychemistryAbsorption spectroscopyPhotodissociationchemistry.chemical_elementInfrared spectroscopyChromophorePhotochemistryElectrochemistryLuminescenceSpectroscopyRutheniumEuropean Journal of Inorganic Chemistry
researchProduct

Carbonyl Transition Metal Complexes of a Silaborate Ligand

1998

Reaction between three equivalents of the silaborate [NEt4][MeSiB10H12] (2) and one equivalent of [Ru3(CO)12] resulted in almost quantitative formation of the mononuclear transition metal complex [NEt4][Ru(CO)3(η5-MeSiB10H10)] (5), which was characterized by X-ray structure analysis. The trinuclear ruthenium complex [NEt4][Ru3(CO)8(η5-MeSiB10H10)] (7) was synthesized in high yield from the reaction of one equivalent of 2 and [Ru3(CO)12]. The cluster 7 reacts with two equivalents of PMe2Ph with substitution of two carbonyl groups to give the substitution product [NEt4][Ru3(CO)6(PMe2Ph)2(η5-MeSiB10H10)] (8).

Inorganic ChemistrychemistryTransition metalStructure analysisLigandYield (chemistry)Inorganic chemistryCluster chemistryCluster (physics)chemistry.chemical_elementMedicinal chemistryRutheniumEuropean Journal of Inorganic Chemistry
researchProduct

Observation of electroluminescence at room temperature from a ruthenium(II) bis-terpyridine complex and its use for preparing light-emitting electroc…

2005

A terpyridine ruthenium (II) complex containing a substituted and an unsubstituted terpyridine ligand was synthesized, and its luminescence properties were studied in a solid-state single-layer light-emitting electrochemical cell. The obtained devices emitted light of a very deep red color (CIE, x = 0.717 y = 0.282) at low external applied bias. It is the first example of an electroluminescence device based on a bis-chelated ruthenium complex. Its ambient atmosphere decay is remarkably different from analogous devices using tris-chelated ruthenium complexes.

Inorganic Chemistrychemistry.chemical_compoundchemistryLigandchemistry.chemical_elementPhysical and Theoretical ChemistryTerpyridineElectroluminescenceLuminescencePhotochemistryRed ColorElectrochemical cellRutheniumInorganic chemistry
researchProduct

Synthesis and structural studies of TiRu polymetallic systems

2000

Abstract The reaction of the titanocene monophosphines 1 and 2 with the dimer [( p -cymene)RuCl 2 ] 2 give the heterobimetallic compounds ( p -cymene)[(η 5 -C 5 H 4 )(μ-η 5 :η 1 -C 5 H 4 PPh 2 )TiCl 2 ]RuCl 2 and ( p -cymene)[(η 5 -C 5 H 4 )(μ-η 5 :η 1 -C 5 H 4 CH 2 CH 2 PPh 2 )TiCl 2 ]RuCl 2 , respectively. Both structures have been confirmed by X-ray diffraction. By using same procedure, the synthesis of a trimetallic complex RuTiRu has been achieved.

Inorganic Chemistrychemistry.chemical_compoundchemistryStereochemistryDimerOrganic ChemistryMaterials Chemistrychemistry.chemical_elementPhysical and Theoretical ChemistryBiochemistryMedicinal chemistryRutheniumJournal of Organometallic Chemistry
researchProduct

Ruthenium‐assisted tellurium abstraction in bis(thiophen‐2‐yl) ditelluride

2023

The reaction of [RuCl2(CO)3]2 and Te2Tpn2 (Tpn = thiophen-2-yl, C4H3S) in the absence of light resulted in the formation of cct-[RuCl2(CO)2(TeTpn2)2] (1) [cis(Cl)-cis(CO)-trans(TeTpn2)] and TeTpn2 (2) together with the precipitation of tellurium. The complex 1 and the monotelluride 2 were characterized by NMR spectroscopy and single-crystal X-ray diffraction. The decomposition of Te2Tpn2 to TeTpn2 has been monitored by 125Te NMR spectroscopy and seemed to be faster than the ligand substitution in [RuCl2(CO)3]2 by TeTpn2. A catalytic cycle is proposed for the decomposition of Te2Tpn2 to TeTpn2 based on the PBE0-D3/def2-TZVP calculations. peerReviewed

Inorganic Chemistrycrystal structurestelluuriBis(thiophen-2-yl) ditellanedicarbonyldichloridobis[bis(thiophen-2-yl)tellane]rutheniumreaction pathwaykompleksiyhdisteetorganometalliyhdisteettellurium abstraction
researchProduct

Fluorescent organometallic rhodium(I) and ruthenium(II) metallodrugs with 4-ethylthio-1,8-naphthalimide ligands: Antiproliferative effects, cellular …

2018

Fluorescent 4-ethylthio-1,8-naphthalimides containing rhodium(I) N-heterocyclic carbene (NHC) and ruthenium (II) NHC fragments were synthesised and evaluated for their antiproliferative effects, cellular uptake and DNA-binding activity. Both types of organometallics triggered ligand dependent efficient cytotoxic effects against tumor cells with the rhodium(I) NHC derivatives causing stronger effects than the ruthenium (II) NHC analogues. Antiproliferative effects could also be observed against several pathogenic Gram-positive bacterial strains, whereas the growth of Gram-negative bacteria was not substantially affected. Cellular uptake was confirmed by atomic absorption spectroscopy as well…

Intercalation (chemistry)Fluorescent DyeLigands01 natural sciencesAntineoplastic Agentchemistry.chemical_compoundNeoplasmsDrug DiscoveryMoietyCell DeathBacterial InfectionsGeneral MedicineIntercalating AgentsNaphthalimideAnti-Bacterial AgentsRutheniumNaphthalimidesSettore CHIM/03 - Chimica Generale E InorganicaHumanStereochemistrychemistry.chemical_elementAntineoplastic AgentsLigandCarbene010402 general chemistryG-quadruplexBacterial InfectionRutheniumRhodiumCell Line TumorAnti-Bacterial AgentOrganometallic CompoundsG-QuadruplexeHumansRhodiumBioorganometallicFluorescent DyesGroup 2 organometallic chemistryCell ProliferationPharmacologyOrganometallic CompoundBacteria010405 organic chemistryLigandOrganic ChemistryIntercalating Agent0104 chemical sciencesG-QuadruplexeschemistryNeoplasmDrug Screening Assays AntitumorCarbene
researchProduct

Luminescent Ionic Transition-Metal Complexes for Light-Emitting Electrochemical Cells

2012

Higher efficiency in the end-use of energy requires substantial progress in lighting concepts. All the technologies under development are based on solid-state electroluminescent materials and belong to the general area of solid-state lighting (SSL). The two main technologies being developed in SSL are light-emitting diodes (LEDs) and organic light-emitting diodes (OLEDs), but in recent years, light-emitting electrochemical cells (LECs) have emerged as an alternative option. The luminescent materials in LECs are either luminescent polymers together with ionic salts or ionic species, such as ionic transition-metal complexes (iTMCs). Cyclometalated complexes of Ir(III) are by far the most util…

IonsMaterials scienceLuminescenceLightMolecular StructureIonic bondingNanotechnologycopper(I) complexes; electroluminescence; iridium(III) complexes; light-emitting electrochemical cells; ruthenium(II) complexesGeneral ChemistryElectrochemical TechniquesElectroluminescenceCatalysisElectrochemical celllaw.inventionTransition metallawOLEDOrganometallic CompoundsTransition ElementsLuminescenceLight-emitting diodeDiode
researchProduct

Reversible Colorimetric Probes for Mercury Sensing

2005

The selectivity and sensitivity of two colorimetric sensors based on the ruthenium complexes N719 [bis(2,2'-bipyridyl-4,4'-dicarboxylate)ruthenium(II) bis(tetrabutylammonium) bis(thiocyanate)] and N749 [(2,2':6',2' '-terpyridine-4,4',4' '-tricarboxylate)ruthenium(II) tris(tetrabutylammonium) tris(isothiocyanate)] are described. It was found that mercury ions coordinate reversibly to the sulfur atom of the dyes' NCS groups. This interaction induces a color change in the dyes at submicromolar concentrations of mercury. Furthermore, the color change of these dyes is selective for mercury(II) when compared with other ions such as lead(II), cadmium(II), zinc(II), or iron(II). The detection limit…

IronInorganic chemistrychemistry.chemical_elementBiosensing TechniquesBiochemistrySensitivity and SpecificityCatalysischemistry.chemical_compoundColloid and Surface ChemistryIsothiocyanatesOrganometallic CompoundsColoring AgentsIonsTitaniumAqueous solutionThiocyanateMolecular StructureChemistryGeneral ChemistryMercuryChemical sensorTransition metal ionsMercury (element)RutheniumZincLeadRuthenium CompoundsColorimetrySpectrophotometry UltravioletSelectivityThiocyanatesCadmium
researchProduct