Search results for "ELECTRONICS"

showing 10 items of 4340 documents

Electrically Conductive Phthalocyanine Assemblies. Structural and Non-Integer Oxidation Number Considerations

1990

Aggregation is a well-known phenomenon in phthalocyanine chemistry. Interactions can occur between adjacent phthalocyanine rings, both in organic and aqueous phases, resulting in coupling between the electronic states of two, or more, phthalocyanine units [1].

Coupling (electronics)chemistry.chemical_compoundAqueous solutionMaterials sciencechemistryPolymer chemistryPhthalocyanineMolecular planeElectrically conductivePhotochemistryElectric chargeInteger (computer science)Electronic states
researchProduct

ChemInform Abstract: Palladium-Catalyzed Suzuki-Miyaura Cross-Coupling of α-Halomethyl Oxime Ethers and Site-Selective Cross-Coupling of Dihalo Deriv…

2014

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 selectivechemistry.chemical_elementGeneral MedicineOximeMedicinal chemistryCatalysisPalladiumChemInform
researchProduct

Evaluation of Cyclic Amides as Activating Groups in N-C Bond Cross-Coupling: Discovery of N-Acyl-δ-valerolactams as Effective Twisted Amide Precursor…

2021

The development of efficient methods for facilitating N-C(O) bond activation in amides is an important objective in organic synthesis that permits the manipulation of the traditionally unreactive amide bonds. Herein, we report a comparative evaluation of a series of cyclic amides as activating groups in amide N-C(O) bond cross-coupling. Evaluation of N-acyl-imides, N-acyl-lactams, and N-acyl-oxazolidinones bearing five- and six-membered rings using Pd(II)-NHC and Pd-phosphine systems reveals the relative reactivity order of N-activating groups in Suzuki-Miyaura cross-coupling. The reactivity of activated phenolic esters and thioesters is evaluated for comparison in O-C(O) and S-C(O) cross-c…

Coupling (electronics)chemistry.chemical_compoundChemistryStereochemistryAmideOrganic ChemistryElectrophilePeptide bondReactivity (chemistry)Organic synthesisResonance (chemistry)Coupling reactionJournal of Organic Chemistry
researchProduct

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
researchProduct

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
researchProduct

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
researchProduct

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
researchProduct

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
researchProduct

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
researchProduct

13C NMR study of some polychloro-isobutane and -isobutene compounds

1984

The 13C chemical shifts and the carbon–proton coupling constants have been determined for some chlorinated isobutane and isobutene compounds. The one-bond coupling constants in isobutane derivatives showed a regular increase with an increasing number of γ-chlorine substituents. The three-bond coupling constant of the methyl carbon decreased from 4.2 to 2.0 Hz as the number of chlorine substituents in the γ-position increased. In the isobutene compounds, the vicinal coupling of C-1 was larger to protons in a group that is trans with respect to a chlorine substituent on C-1 than to those in the corresponding group cis to the chlorine. The vicinal coupling constants between atoms in geminal gr…

Coupling constantGeminalChemical shiftchemistry.chemical_elementGeneral ChemistryCarbon-13 NMRMedicinal chemistryCoupling (electronics)chemistry.chemical_compoundchemistrypolycyclic compoundsIsobutaneChlorineOrganic chemistryGeneral Materials ScienceVicinalOrganic Magnetic Resonance
researchProduct