Search results for "Coupling"

showing 10 items of 1862 documents

Retraction notice to “trans-Tetrakis(pyridine)dichloroiron(II) as catalyst for Suzuki cross-coupling in ethanol and water” [Tetrahedron Lett. 49 (200…

2009

Coupling (electronics)chemistry.chemical_compoundEthanolchemistryOrganic ChemistryDrug DiscoveryPyridineInorganic chemistryPolymer chemistryTetrahedronBiochemistryCatalysisTetrahedron Letters
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ChemInform Abstract: Switchable Palladium-Catalyst Reaction of Bromomethyl Sulfoxides, CO, and N-Nucleophiles: Aminocarbonylation at Csp3versus Oxida…

2013

Pd2(dba)3/ Xantphos-catalyzed coupling of the sulfoxides (I) and (V) with amines and carbon monoxide allows a new and efficient access to amides of type (IV) and (VI).

Coupling (electronics)chemistry.chemical_compoundNucleophileChemistryOxidative carbonylationPolymer chemistryGeneral MedicinePalladium catalystPyrrole derivativesCarbon monoxideChemInform
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Transition-Metal-Free Decarboxylative Photoredox Coupling of Carboxylic Acids and Alcohols with Aromatic Nitriles.

2016

A transition-metal-free protocol for the redox-neutral light-induced decarboxylative coupling of carboxylic acids with (hetero)aromatic nitriles at ambient temperature is presented. A broad scope of acids and nitriles is accepted, and alcohols can be coupled in a similar fashion through their oxalate half esters. Various inexpensive sources of UV light and even sunlight can be used to achieve this C–C bond formation proceeding through a free radical mechanism.

Coupling (electronics)chemistry.chemical_compoundTransition metalchemistry010405 organic chemistryOrganic ChemistryOrganic chemistryBond formation010402 general chemistryPhotochemistry01 natural sciencesOxalate0104 chemical sciencesThe Journal of organic chemistry
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ChemInform Abstract: Transition-Metal-Free Decarboxylative Photoredox Coupling of Carboxylic Acids and Alcohols with Aromatic Nitriles.

2016

A transition-metal-free protocol for the redox-neutral light-induced decarboxylative coupling of carboxylic acids with (hetero)aromatic nitriles at ambient temperature is presented. A broad scope of acids and nitriles is accepted, and alcohols can be coupled in a similar fashion through their oxalate half esters. Various inexpensive sources of UV light and even sunlight can be used to achieve this C–C bond formation proceeding through a free radical mechanism.

Coupling (electronics)chemistry.chemical_compoundTransition metalchemistryOrganic chemistryGeneral MedicineBond formationOxalateChemInform
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Palladium-Catalyzed Suzuki-Miyaura Cross-Coupling of α-Halomethyl Oxime Ethers and Site-Selective Cross-Coupling of Dihalo Derivatives

2013

The Pd-catalyzed cross-coupling reaction of chloromethyl oxime ethers with a wide range of aryl-, heteroaryl-, and vinylboronic acids proceeds with good yields.

Coupling (electronics)chemistry.chemical_compoundchemistryArylSite selectiveOrganic chemistrychemistry.chemical_elementGeneral ChemistryOximeMedicinal chemistryCatalysisPalladiumAdvanced Synthesis & Catalysis
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ChemInform Abstract: Efficient Anodic and Direct Phenol-Arene C,C Cross-Coupling: The Benign Role of Water or Methanol.

2012

For the first time a significantly improved electrochemical C-C cross-coupling is reported.

Coupling (electronics)chemistry.chemical_compoundchemistryPhenolGeneral MedicineMethanolPhotochemistryElectrochemistryAnodeChemInform
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Evaluation of the Strength of Coupling Between a Vibrational Exciton and a Specific Low Frequency Mode

1993

In Davydov’s theory, one dimensional sub-systems within molecular crystals may exhibit self-trapping of some high frequency phonons as these travel by dipole resonance interaction, due to coupling to some specific soft oscillation mode1

Coupling (physics)DipoleNuclear magnetic resonancePhononChemistryOscillationExcitonTransition dipole momentResonanceLow frequencyMolecular physics
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Oscillatory Reactions in Heterogeneous Catalysis

1993

Publisher Summary This chapter focuses on the oscillatory reactions in heterogeneous catalysis. Oscillations are possible on all levels in a catalytic reactor, from the single-crystal plane to the crystallite to the catalyst pellet to the packed-bed reactor, and each level adds another degree of complexity. So, it is necessary to isolate the major influences at each level and to separate the characteristics of the oscillations on one level from the effects caused by coupling with other levels. Only when each level is well understood is it possible to fully understand the overall oscillatory behavior. Oscillations in heterogeneous catalysis, therefore, remain an intriguing and demanding prob…

Coupling (physics)Order (biology)ChemistryChemical physicsPhysical chemistrySurface reactionHeterogeneous catalysisBriggs–Rauscher reactionCatalysis
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Importance of Triples Contributions to NMR Spin–Spin Coupling Constants Computed at the CC3 and CCSDT Levels

2016

We present the first analytical implementation of CC3 second derivatives using the spin-unrestricted approach. This allows, for the first time, the calculation of nuclear spin–spin coupling constants (SSCC) relevant to NMR spectroscopy at the CC3 level of theory in a fully analytical manner. CC3 results for the SSCCs of a number of small molecules and their fluorine substituted derivatives are compared with the corresponding coupled cluster singles and doubles (CCSD) results obtained using specialized basis sets. For one-bond couplings the change when going from CCSD to CC3 is typically 1–3%, but much higher corrections were found for 1JCN in FCN, 15.7%, and 1JOF in OF2, 6.4%. The changes v…

Coupling constant010304 chemical physicsBasis (linear algebra)ChemistryNuclear magnetic resonance spectroscopy010402 general chemistry01 natural sciences0104 chemical sciencesComputer Science ApplicationsCoupled cluster0103 physical sciencesPhysical and Theoretical ChemistryAtomic physicsSpin-½Second derivativeJournal of Chemical Theory and Computation
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A Combined Experimental and Theoretical Study on the Magnetic Properties of a Family of Bis(μ‐phenoxido)dicopper(II) Complexes Bearing ω‐[Bis(2‐hydro…

2009

Five new neutral bis(μ-phenoxido)dicopper(II) complexes, [Cu2(μ-HL1)2]·3EtOH·H2O (1), [Cu2(μ-HL2)2]·1.65H2O (2), [Cu2(μ-HL3)2(μ-H2O)] (3), [Cu2(μ-HL4)2] (4) and [Cu2(μ-HL5)2(μ-H2O)] (5), were prepared from a family of ω-[bis(2-hydroxy-3,5-dimethylbenzyl)amino]alkan-1-ol ligands (H3L1–H3L5 derived from 2-aminoethanol, 3-aminopropanol, 4-aminobutanol, 5-aminopentanol and 6-aminohexanol, respectively) bearing a [O,N,O,O′] donor set. In complexes 3 and 5, there is also a bridging water molecule between the metallic centres. The copper(II) coordination planes of all these complexes form a roof-like structure (the bridging O atoms are located at the top of the roof). The structural differences fo…

Coupling constant010405 organic chemistryChemistryStereochemistrychemistry.chemical_element010402 general chemistry01 natural sciencesCopper0104 chemical sciencesMagnetic exchangeInorganic ChemistryMetalCrystallographyLinear relationshipFerromagnetismvisual_artvisual_art.visual_art_mediumAntiferromagnetismMoleculeEuropean Journal of Inorganic Chemistry
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