Search results for "Organo"

showing 10 items of 1460 documents

An efficient method for selective oxidation of (oxime)Pt(II) to (oxime)Pt(IV) species using N,N-dichlorotosylamide

2016

The oxidation of (oxime)PtII species using the electrophilic chlorine-based oxidant N,N-dichlorotosylamide (4-CH3C6H4SO2NCl2) was studied. The reactions of trans-[PtCl2(oxime)2] (where oxime = acetoxime, cyclopentanone oxime, or acetaldoxime) with this oxidant led to trans-[PtCl4(oxime)2] products. The oxidation of trans-[Pt(o-OC6H4CH = NOH)2] at room temperature gave trans-[PtCl2(o-OC6H4CH = NOH)2], whereas the same reaction upon heating was accompanied by electrophilic substitution of the benzene rings. peerReviewed

oxidation010405 organic chemistryoxime ligandsMetals and Alloyschemistry.chemical_elementoxidative chlorination010402 general chemistryOxime01 natural sciencesMedicinal chemistry0104 chemical sciencesCatalysisInorganic ChemistryElectrophilic substitutionchemistry.chemical_compoundchemistryElectrophileMaterials ChemistryChlorineOrganic chemistryAcetaldoximeBenzeneOrganometallic chemistryplatinum complexesTransition Metal Chemistry
researchProduct

Mukaiyama-Michael reactions with α-substituted acroleins - a useful tool for the synthesis of the pectenotoxins and other natural product targets

2013

pektenotoksiini25-diphenylpyrrolidinepectenotoxinMukaiyama-Michael reactionorganocatalysistotal synthesisluonnonaineetreaktiomekanismitmyrkylliset aineet
researchProduct

Designing P-Chirogenic 1,2-Diphosphinobenzenes at Both P-Centers Using P(III)-Phosphinites

2016

International audience; A new enantiodivergent synthesis of P-chirogenic 1,2-diphosphinobenzenes (DP*B) bearing the chirality on one or both phosphorus centers is reported using aryne chemistry. The principle is based on successive reactions of 1,2-dibromobenzene with sec-phosphide boranes, then DABCO to remove the borane, and finally with chlorophosphines or P(III)-chirogenic phosphinites. The efficiency of this synthesis was demonstrated by the stereoselective preparation of (S,S)-1,2-bis(o-anisylphenylphosphino)benzene. A comparison of DIPAMP and homochiral DP*B ligands in asymmetric Rh- or Pd-catalyzed reactions was reported.

phosphine-ligandsDIPAMPketonesStereochemistryBoranesDABCOBorane010402 general chemistry[ CHIM ] Chemical Sciences01 natural sciencesBiochemistryArynecatalyzed asymmetric hydrogenationchemistry.chemical_compoundfunctionalized alkenes[ CHIM.ORGA ] Chemical Sciences/Organic chemistry[CHIM]Chemical SciencesorganocatalysisPhysical and Theoretical Chemistryhydroformylation010405 organic chemistryChemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic Chemistrycarbon-monoxide0104 chemical scienceshighly enantioselective hydrogenationOrganocatalysisderivativesStereoselectivityChirality (chemistry)phospholane ligands
researchProduct

The clavecins a maillets of Marius and Veltman: new observations on some of the first pianos in France

2011

In 1716, Jean Marius submitted several projects for his clavecins à maillet to the Academy of Sciences in Paris. Short descriptions and plates of four of Marius’s actions were published in 1735 after his death. Even though Marius is well known as the first French piano-maker, a large part of his handwritten reports and descriptions on his clavecins à maillet remain unpublished. These descriptions give a number of details about the first piano actions devised in France some 15 years after Cristofori’s invention of his "arpicimbalo che fa il piano e il forte" in about 1700. These documents, which are published for the first time in this article, were not quoted in the 1735 printed version tha…

pianofortemedia_common.quotation_subjectPianoSettore L-ART/07 - Musicologia E Storia Della MusicaArt historyorganologiaArtMusicMarius JeanVeltman Andriemedia_common
researchProduct

High-Level Ab Initio Predictions of Thermochemical Properties of Organosilicon Species: Critical Evaluation of Experimental Data and a Reliable Bench…

2022

A high-level composite quantum chemical method, W1X-1, is used herein to calculate the gas-phase standard enthalpy of formation, entropy, and heat capacity of 159 organosilicon compounds. The results set a new benchmark in the field that allows, for the first time, an in-depth assessment of existing experimental data on standard enthalpies of formation, enabling the identification of important trends and possible outliers. The calculated thermochemical data are used to determine Benson group additivity contributions for 60 Benson groups and group pairs involving silicon. These values allow fast and accurate estimation of thermochemical parameters of organosilicon compounds of varying comple…

piilämpökemiakvanttikemiaorganometalliyhdisteetPhysical and Theoretical ChemistryThe Journal of Physical Chemistry A
researchProduct

Metallocenes and post-metallocenes immobilized on ionic liquid-modified silica as catalysts for polymerization of ethylene

2014

Abstract The supported ionic liquid (SIL) strategy was used for the first time to metallocene and post-metallocene heterogeneous catalysts for olefin polymerization. The metal complexes: Cp2TiCl2, Cp2ZrCl2, FI–Ti, and Sal–Ti were immobilized in the 1-(3-triethoxysilyl)propyl-3-methylimidazolium alkylchloroaluminate ionic liquid, anchored on the surface of the mesoporous amorphous silica. The SIL systems were characterized by FTIR, 29Si NMR, N2 adsorption, EA, AAS, TG, and SEM techniques. The developed supported catalytic systems were found to be active in the ethylene polymerization and produce the polyethylene of various properties.

polyethyleneChemistryProcess Chemistry and TechnologyPost-metallocene catalystPolyethyleneCatalysischemistry.chemical_compoundAdsorptionPolymerizationsilicaIonic liquidPolymer chemistryorganometallic catalystCoordination polymerizationMesoporous materialMetalloceneionic liquidApplied Catalysis A : General : an International Journal Devoted to Catalytic Science and its Applications
researchProduct

Effect of catalyst composition on chain‐end‐group of polyethylene produced by salen‐type complexes of titanium, zirconium, and vanadium

2010

The chain end structures of polyethylenes produced by salen complexes of titanium, zirconium, and vanadium, activated by MAO or common alkylaluminium compounds were investigated by 1H NMR and FTIR spectroscopy. The polymerization process with the use of vanadium complexes was found to produce polymers with only vinyl end groups in practice. In the processes catalyzed by titanium and zirconium complexes activated by MAO or Et2AlCl, not only β‐hydrogen elimination and/or chain transfer to the monomer occurs but also the chain termination reaction takes place in which an organoaluminium cocatalyst is involved. That reaction proceed particularly easily in the systems: titanium complex/Et2AlCl.

polyethyleneFTIRorganometallic catalystsstructureNMRJournal of Polymer Science. Part A : Polymer Chemistry
researchProduct

The role of organoclay in the morphology modification and in the properties in polyethylene/polyamide blend systems

2009

polyethylene/polyamide blend systemsorganoclaymorphology modification
researchProduct

Weryfikacja kinetycznego modelu polimeryzacji etylenu wobec metaloorganicznych katalizatorów wanadowych na nośniku magnezowym

1998

The kinetic studies are reviewed on low-pressure polymerization of ethylene over two types of organovanadium catalysts, viz., MgCl 2(THF) 2/VCl 4/Et 2AlCl and MgCl 2(THF) 2VOCl 3Et 2AlCl, each deposited on a magnesium carrier. The polymerization rate was found to be directly related to the catalyst and monomer concentrations (Figs. 2 and 3), unless when the access of the monomer to the reactive V-C bond is restricted by diffusion. Polymer chain termination step was found to result from the reaction of the transfer onto the monomer and to be associated with the regeneration of the active site on which a new macromolecule can be formed. A kinetic model was developed for the ethylene polymeriz…

polymerization of ethylenemechanism of termination reactionorganovanadium catalysts on carrierskinetic model of polymerizationPolimery
researchProduct

Selective Laser Sintering of Metal-Organic Frameworks: Production of Highly Porous Filters by 3D Printing onto a Polymeric Matrix.

2019

Metal‐organic frameworks (MOFs) have raised a lot of interest, especially as adsorbing materials, because of their unique and well‐defined pore structures. One of the main challenges in the utilization of MOFs is their crystalline and powdery nature, which makes their use inconvenient in practice. Three‐dimensional printing has been suggested as a potential solution to overcome this problem. We used selective laser sintering (SLS) to print highly porous flow‐through filters containing the MOF copper(II) benzene‐1,3,5‐tricarboxylate (HKUST‐1). These filters were printed simply by mixing HKUST‐1 with an easily printable nylon‐12 polymer matrix. By using the SLS, powdery particles were fused t…

porosityMaterials sciencematerials sciencelaser sinteringMixing (process engineering)3D printingNanotechnologyorganometalliyhdisteet010402 general chemistry01 natural scienceslaw.inventionMatrix (chemical analysis)huokoisuusAdsorptionlaw3D-tulostuspolymeeritmateriaalitiedePorosityta116metal-organic frameworkspolymerschemistry.chemical_classification010405 organic chemistrybusiness.industryGeneral ChemistryPolymer0104 chemical sciencesSelective laser sinteringchemistryadsorptionMetal-organic frameworkadsorptiobusinessChemPlusChem
researchProduct