Search results for "Ylide"

showing 10 items of 1084 documents

A remarkable rearrangement during reaction between triazolopyridinium ylides and dimethyl acetylenedicarboxylate

1991

Abstract The ylides from 2-acylmethyltriazolopyridinium salts ( 1 ) react with dimethyl acetylenedicarboxylate in toluene solution to give the 7-pyrroleninylpyrazolo[1,5-a]pyridines ( 5 ).

Dimethyl acetylenedicarboxylatechemistry.chemical_classificationChemistryOrganic ChemistryBiochemistryMedicinal chemistryTolueneCycloadditionchemistry.chemical_compoundYlideDrug DiscoveryMoleculeOrganic chemistrySolvent effectsTetrahedron Letters
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Copolymerization of VDF and HFP in Supercritical Carbon Dioxide: A Robust Approach for Modeling Precipitation and Dispersion Kinetics

2012

A kinetic model is developed for the heterogeneous free-radical copolymerization of vinylidene fluoride and hexafluoropropylene in supercritical CO 2. The model accounts for polymerization in both the dispersed (polymer-rich) phase and in the continuous (polymer-free) supercritical phase, for radical interphase transport, diffusion limitations, and chain-length-dependent termination in the polymer-rich phase. A parameter evaluation strategy is developed and detailed to estimate most of the kinetic parameters a priori while minimizing their evaluation by direct fitting. The resulting model predictions compare favorably with the experimental results of conversion and MWD at varying monomer fe…

Dispersion kineticChain-length-dependent terminationDiffusionSupercritical carbon dioxideSupercritical phaseCopolymerCopolymerizationKineticRobust approacheHexafluoropropyleneModel predictionFree radical polymerizationFree radical copolymerizationKinetic modelPolymers Supercritical fluid extractionSettore ING-IND/27 - Chimica Industriale E TecnologicaDiffusion limitationFluorine containing polymerMonomerParameter evaluationVinylidene fluoride Carbon dioxideHeterogeneous polymerizationMonomer concentrationFeed compositionSupercritical COModel
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Dispersion Polymerization of Vinylidene Fluoride in Supercritical Carbon Dioxide

2006

The dispersion polymerization of vinylidene fluoride in supercritical carbon dioxide is investigated using two ammonium carboxylate perfluoropolyether stabilizers of different molecular weights. Under suitable operating conditions a polymer made of well-dispersed spherical particles has been obtained up to relatively high conversion. The experimental data of polymerization rate and molecular weight distribution are in good agreement with the predictions of a model previously developed. Such an agreement supports the conclusion that the polymerization kinetics is dominated by the interphase transport of the active radicals between the continuous phase and the polymer particles.

Dispersion polymerizationSupercritical carbon dioxidePolymers and PlasticsChemistryPolymerization vinylideneOrganic ChemistryRadical polymerizationSettore ING-IND/27 - Chimica Industriale E TecnologicaInorganic ChemistryEnd-groupChain-growth polymerizationPolymerizationChemical engineeringPolymer chemistryMaterials ChemistryMolar mass distributionAddition polymerMacromolecules
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A combined experimental and theoretical study of the thermal [3+2] cycloaddition of carbonyl ylides with activated alkenes

2018

International audience; 4-Benzoyl-3,5-diaryltetrahydrofuran-2,2-dicarbonitriles were first synthesized from 2,2-dicyano-3-aryloxiranes and chalcones at toluene reflux; the 4,5-cis products proved to be predominantly formed and were isolated. Whereas shortened reaction times were observed by using microwave irradiation or catalytic cuprous chloride, no significant stereoselectivity change was in general noticed. Reacting 2,2-dicyano-3-aryloxiranes with 2-cyclopentenone next afforded 3-aryl-4-oxohexahydro-1H-cyclopenta[c]furan-1,1-dicarbonitriles, and the endo stereoisomers were isolated. That no stereoselectivity change was noticed in the presence of cuprous chloride rather suggests an impac…

Epoxide010402 general chemistryenones01 natural sciencesMedicinal chemistryAnalytical ChemistryCatalysisInorganic Chemistrychemistry.chemical_compound[SDV.SP.MED]Life Sciences [q-bio]/Pharmaceutical sciences/MedicationCascade reaction[3+2] cycloadditionEnamines[CHIM]Chemical SciencesTetrahydrofuransSpectroscopytheoretical calculationschemistry.chemical_classification[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryOrganic ChemistryRegioselectivityCycloaddition0104 chemical sciencescarbonyl ylideschemistryYlide[SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/VirologyStereoselectivityCis–trans isomerismJournal of Molecular Structure
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Analytic CCSD(T) second derivatives

1997

A general-purpose implementation of analytic CCSD(T) second derivatives is presented. Its applicability is demonstrated by calculations of vibration-rotation interaction constants for the astrophysically important molecule cyclopropenylidene (C3H2) in which the required cubic force constants have been determined by numerical differentiation of analytically evaluated second derivatives of the energy.

Force constantCyclopropenylidenechemistry.chemical_compoundComputational chemistryChemistryNumerical differentiationGeneral Physics and AstronomyMoleculeThermodynamicsPhysics::Chemical PhysicsPhysical and Theoretical ChemistrySecond derivativeChemical Physics Letters
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Rainfall energy harvester

2015

This chapter provides a detailed study on the harvest of the energy contained in raindrops by means of piezoelectric transducers. The energy harvester has the role of an electric source, able to recharge storage devices of small electronic components, such wireless sensors, by using the vibrational energy released by the drops hitting the transducer, reducing in such a way the chemical waste of conventional batteries. In technical literature, diverse studies agree on the level of suitable generated voltage on the electrodes of a piezoelectric transducer subjected to rainfall, but a complete characterization on the supplied power is still missing. This work, also to limit optimistic forecast…

HydrologySettore ING-IND/31 - ElettrotecnicaEnvironmental scienceEnergy harvester piezoelectric effect lead zirconate titanate PZT polyvinylidene difluoride PVDF cantilever structureSettore ING-IND/32 - Convertitori Macchine E Azionamenti ElettriciEnergy harvester
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Synthesis of 2-anilinobenzimidates, anthranilamides, and 2,3-dihydroquinazolin-4(1H)-ones from N-heterocyclic carbenes of indazole

2015

N-Heterocyclic carbenes of indazole (indazol-3-ylidenes), which are substituted at N1 with aromatics were generated in situ from the corresponding indazolium salts. At 60 °C the indazol-3-ylidenes underwent a ring-opening under N–N bond cleavage to intermediary N-(6-methylenecyclohexa-2,4-dien-1-ylidene)anilines. Trapping of these intermediates by alcohols proved to be a convenient method for the preparation of 2-anilinobenzimidates, which have scarcely been described in the literature. The reaction temperature avoids carbene dimerization, which occurs at −80 °C or rearrangement of the ring-opened intermediate to acridines, which affords 100 °C. Water converted the ring-opened products into…

Indazole010405 organic chemistryCarbene dimerizationbenzamideOrganic Chemistryanthranilic acidFormaldehyde010402 general chemistry01 natural sciencesBiochemistryMedicinal chemistry0104 chemical sciencescarbenechemistry.chemical_compoundReaction temperaturechemistryDrug DiscoveryAnthranilic acidOrganic chemistryBenzamideCarbeneta116indazol-3-ylideneBond cleavagebenzenecarboximidic acidTetrahedron
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N-Heterocyclic carbenes from ylides of indolyl-imidazolium, azaindolyl-imidazolium, and indolyl-triazolium salts, and their borane adducts

2014

Abstract Indol-2-yl-imidazolium salts were deprotonated at N1 of the indole ring to give ylides. Their tautomeric N-heterocyclic carbenes (NHCs) were trapped by sulfur to give imidazole-2-thiones. Treatment of the ylides with triethylborane resulted in the formation of zwitterionic borane adducts. An analogous sequence of reactions was performed with 8-azaindol-2-yl-imidazolium salts, which served as precursor to prepare first representatives of a new heterocyclic ring system on reaction of their NHC-tautomers with triethylborane. Similarly, an indol-2-yl-1,2,4-triazolium salt was examined with respect to ylide–NHC tautomerism and trapping reactions. A nucleophilic ring transformation of in…

Indole testchemistry.chemical_classificationOrganic ChemistryTriethylboraneBoraneRing (chemistry)BiochemistryTautomerMedicinal chemistrychemistry.chemical_compoundchemistryNucleophileYlideDrug DiscoveryOrganic chemistryCarbeneta116Tetrahedron
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The equilibrium structure of propadienylidene

1999

Abstract A coupled-cluster study of the equilibrium geometry of propadienylidene (C3H2) is presented. Deviations between a recently reported experimental re structure and those computed at the CCSD(T)/cc-pVQZ and CCSD(T)/cc-pCVQZ levels are larger than expected. A closer analysis reveals that this discrepancy is due to inaccuracies in the cubic force field that was used to correct the measured rotational constants for vibrational effects. A satisfactory agreement between theory and experiment is obtained if the vibrational effects on the rotational constants are computed from harmonic and cubic force fields determined at either the CCSD(T)/cc-pVTZ and CCSD(T)/cc-pCVTZ levels. Revised values…

Inorganic ChemistryElectronic correlationChemistryOrganic ChemistryPhysics::Atomic and Molecular ClustersPhysics::Chemical PhysicsAtomic physicsEquilibrium geometryPropadienylideneSpectroscopyForce field (chemistry)Analytical ChemistryJournal of Molecular Structure
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CCDC 619596: Experimental Crystal Structure Determination

2006

Related Article: R.Corberan, M.Sanau, E.Peris|2006|Organometallics|25|4002|doi:10.1021/om060343r

Iodo-(eta^5^-pentamethyl-cyclopentadienyl)-(1-(diphenylmethyl)-3-methylimidazol-2-ylidenyl)-iridiumSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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