Search results for "YIELD"

showing 10 items of 1338 documents

Toward luminescence vapochromism of tetranuclear AuI-Cu I clusters

2013

A family of triphosphine gold–copper clusters bearing aliphatic and hydroxyaliphatic alkynyl ligands of general formula [HC(PPh2)3Au3Cu(C2R)3]+ (R = cyclohexyl (1), cyclopentyl (2), But (3), cyclohexanolyl (4), cyclopentanolyl (5), 2,6-dimethylheptanolyl (6), 2-methylbutanolyl (7), diphenylmethanolyl (8)) was synthesized via a self-assembly protocol, which involves treatment of the (AuC2R)n acetylides with the (PPh2)3CH ligand in the presence of Cu+ ions and NEt3. Addition of Cl– or Br– anions to complex 8 results in coordination of the halides to the copper atoms to give neutral HC(PPh2)3Au3CuHal(C2COHPh2)3 derivatives (Hal = Cl (9), Br (10)). The title compounds were characterized by NMR …

ChemistryLigandStereochemistryOrganic ChemistryQuantum yieldchemistry.chemical_elementHalideCopperIonInorganic ChemistryCrystallographyPhysical and Theoretical ChemistrySpectroscopyLuminescencePhosphorescenceta116Organometallics
researchProduct

Preparative, structural, and electrochemical investigations on peralkylated niobocene dichlorides and difluorides

1994

CP(dagger)2NbCl2 (CP(dagger) = 175-C5Me4Et) (1b) was synthesized from NbCl5 and a slight excess of Cp(dagger)Li and NaBH4. Its electrochemical (2 e-, E1/2 = -1.6 V) and chemical reduction (2 equiv of Na/Hg) was studied showing that peralkylation of the Cp ligand facilitates two-electron reduction compared to less substituted CP2NbHal2 derivatives. The reduced solutions of CP*2NbCl2 (CP* = C5Me5) (1a) and of lb were shown by means of EPR spectroscopy to contain two new paramagnetic species 1A,B for which bent niobocene (A(Nb) = 100 G) and fulvene-like structures (A(Nb) = 55 G) are proposed. The high reduction potential of these species led in their reaction with HPF6 to the first stable difl…

ChemistryLigandStereochemistryddc:540Organic ChemistryCrystal structureElectrochemistrylaw.inventionInorganic Chemistrychemistry.chemical_compoundCrystallographylawYield (chemistry)540 ChemieX-ray crystallographyMoleculePhysical and Theoretical ChemistryElectron paramagnetic resonanceMetallocene
researchProduct

Installation of Amine Moieties into a Polycyclic Anodic Product Derived from 2,4-Dimethylphenol

2011

When 2,4-dimethylphenol is anodically treated, a dehydrotetramer with four contiguous stereocentres is readily obtained on a multi-gram scale. The substitution of a 2,4-dimethyl-phenoxy fragment by several amines was demonstrated, and the best results were obtained with primary amines. Optically pure α-chiral aliphatic amines yield diastereomeric mixtures that can be separated in most cases. The basic amine causes a partial hemiketal-opening of the bisbenzofuran moiety leading to an equilibrium within an α,β-unsaturated cyclohexenone. This dynamic behaviour occurs on the time scale of NMR spectroscopy and is also found by X-ray analysis providing a consistent picture.

ChemistryOrganic ChemistryDiastereomerGeneral ChemistryNuclear magnetic resonance spectroscopyCatalysisChiral resolutionchemistry.chemical_compoundCyclohexenoneYield (chemistry)MoietyOrganic chemistryAmine gas treatingAminationChemistry - A European Journal
researchProduct

Catalytic Enantioselective α-Oxysulfonylation of Ketones Mediated by Iodoarenes

2008

The alpha-oxysulfonylation of ketones catalysed by enantioenriched iodoarenes using mCPBA as stoichiometric oxidant is reported to give useful synthetic intermediates in good yield and modest enantioselectivity. We believe this to be the first report of an enantioselective organocatalytic reaction involving hypervalent iodine reagents which should open up a new field for enantioselective organocatalysis of oxidation reactions.

ChemistryOrganocatalysisReagentYield (chemistry)Organic ChemistryEnantioselective synthesisHypervalent moleculeOrganic chemistryPhysical and Theoretical ChemistryRedoxStoichiometryCatalysisEuropean Journal of Organic Chemistry
researchProduct

Isolation of Free Phenylide-like Carbanions with N-Heterocyclic Carbene Frameworks

2009

A series of 1,3-bis(2,6-diisopropylphenyl)-5-methyl-1,3-diaza-4,6-diborabenzenes with methyl, phenyl, and dimethylamino substituents on the ring boron atoms were prepared using the cyclocondensation reaction between N,N'-bis(2,6-diisopropylphenyl)trimethylsilylformamidine and the appropriately substituted 1,1-bis(organochloroboryl)ethane, followed by deprotonation of the cationic ring intermediate. The planar, heterocyclic benzene analogues could be further deprotonated at the other ring carbon using an additional equivalent of potassium hexamethyldisilazide to yield organometallic derivatives akin to the potassium phenylide. The potassium cations could be efficiently sequestered in both so…

ChemistryPotassiumCationic polymerizationchemistry.chemical_elementGeneral ChemistryRing (chemistry)PhotochemistryBiochemistryMedicinal chemistryCatalysischemistry.chemical_compoundColloid and Surface ChemistryDeprotonationYield (chemistry)BenzeneCarbeneCarbanionJournal of the American Chemical Society
researchProduct

Energy transfer rates and pathways of single donor chromophores in a multichromophoric dendrimer built around a central acceptor core.

2004

An artificial light-harvesting dendrimer showing highly efficient electronic excitation energy transfer from four peripheral donors to one central acceptor has been investigated by single-molecule spectroscopy at low temperatures. Confocal imaging in combination with frequency selective excitation spectroscopy gives direct access to energy transfer rates of individual donors and allows the determination of energy transfer pathways within a single multichromophoric aggregate.

ChemistryQuantum yieldGeneral ChemistryChromophorePhotochemistryBiochemistryAcceptorCatalysisFluorescence spectroscopyCore (optical fiber)Colloid and Surface ChemistryDendrimerSpectroscopyExcitationJournal of the American Chemical Society
researchProduct

Synthesis ofo-thiatelluraphenylenezirconocenes. X-ray crystal structure of

1992

o-Thiatelluraphenylenezirconocene complexes were obtained in good yield by reaction of dilithiumo-benzenthiatelluride with zirconocene dichlorides. These compounds represent the first examples of heterodichalcogenaphenylene bent metallocences. They were characterized by spectroscopic methods and the effect on the n.m.r. results of stepwise substitution of one and two Te atoms for S is discussed.

ChemistryStereochemistryBent molecular geometryMetals and AlloysCrystal structureMetallacycleInorganic ChemistryCrystallographychemistry.chemical_compoundYield (chemistry)X-ray crystallographyMaterials ChemistryMoleculeMetalloceneOrganometallic chemistryTransition Metal Chemistry
researchProduct

ortho-metallation of P(m-MeC6H4)3 in dirhodium(II) tetraacetate. Molecular structure of Rh2(O2CCH3)2[(m-MeC6H3)P(m-MeC6H4)2]2(HO2CCH3)2·CH3CO2H

1990

Abstract The thermal reaction of Rh2(O2CCH3)4(MeOH)2 and P(m-MeC6H4)3 in a 1:2 molar ratio in acetic acid yielded Rh2(O2CCH3)2[(m-MeC6H3)P(m -MeC6H4)2]2(HO2CCH3)2. Purple monoclinic crystals of this compound and one molecule of acetic acid, space group P21/c, were obtained by evaporation of a solution of the original reaction product in acetic acid/CH2Cl2 mixture. The unit cell parameters are a = 21.346(3), b = 11.909(2), c = 20.071 A, β = 97.98(1)° and Z = 4. The structure consists of a dinuclear rhodium core bridged by cisoid acetate groups and two ortho-metallated phosphine ligands. The ortho-metallation occurs at the least sterically hindered carbon atom which is trans to the methyl sub…

ChemistryStereochemistryDimerSubstituentchemistry.chemical_elementCrystal structureMedicinal chemistryRhodiumInorganic ChemistryAcetic acidchemistry.chemical_compoundYield (chemistry)Materials ChemistryCarboxylatePhysical and Theoretical ChemistryPhosphineInorganica Chimica Acta
researchProduct

Influence of Micromixing on Microorganisms and Products

2001

The influence of mixing intensity as well as physical and chemical parameters on the cells of different microorganisms and the biosynthesis process is examined in this paper. Some reactions of cells effecting mixing intensity are described, such as retarded biomass growth, changes in aggregation and mutual arrangement of cells, morphological changes of cells and decreasing of biological activity, caused by an increased intensity of turbulence (turbohypobiosis). Several methods for investigating the local energy in reactors are compared. It is concluded that conventional methods of hydrodynamic analysis do not always allow valid results for the optimization of the mixing regime to be obtaine…

ChemistryStereochemistryMixing (process engineering)BiomassBioengineeringApplied Microbiology and BiotechnologyMicromixingYield (chemistry)Scientific methodProcess optimizationAerationBiological systemIntensity (heat transfer)BiotechnologyActa Biotechnologica
researchProduct

Selective derivatisations of resorcarenes - 2. Multiple regioselective ring closure reactions

1997

Abstract The condensation of the C-pentyl resorcarene 1 with long chain aliphatic diamines 3a-d and excess formaldehyde leads under high dilution conditions to tetrabenzoxazine derivatives 4a-d in which pairs of adjacent oxazine rings are connected by an aliphatic chain. Six new rings are formed per resorcarene molecule during this reaction in a regioselective way. For one example (4a) the chiral cleft-like structure with C2 symmetry was proved by single crystal X-ray analysis. Hydrolysis of the oxazine rings gives the secondary amine derivatives 5a,b with C2v symmetry in high yield.

ChemistryStereochemistryOrganic ChemistryCondensationRegioselectivityResorcinareneRing (chemistry)BiochemistryHydrolysisYield (chemistry)Drug DiscoveryPolymer chemistryMoleculeSingle crystalTetrahedron
researchProduct