Search results for "Benzene"

showing 10 items of 1701 documents

Divulging the various chemical reactivity of trifluoromethyl-4-vinyl-benzene as well as methyl-4-vinyl-benzene in [3+2] cycloaddition reactions.

2020

Abstract In the present paper, an investigation about the [3 + 2]cycloaddition (32 C A) reactions of benzonitrile oxide with 1-trifluoromethyl-4-vinyl-benzene, and with 1-methyl-4-vinyl-benzene, using the Molecular Electron Density Theory (MEDT) through DFT/B3LYP/6–311++G (d,p), is performed. A deep mechanistic study beside an accurate electronic description of different stationary points along the IRC paths of the two 32 C A reactions have performed by examining the two competitive regioisomericortho/metareaction pathways, and providing the mechanism associated with them. The presence of the CF3 group reduces the activation energy, which makes it possible to increase the experimental yield…

Models MolecularTrifluoromethylCycloaddition Reaction010405 organic chemistryRegioselectivityBenzeneElectrons010402 general chemistry01 natural sciencesComputer Graphics and Computer-Aided DesignMedicinal chemistryCycloaddition0104 chemical sciencesSolventBenzonitrilechemistry.chemical_compoundchemistryYield (chemistry)Materials ChemistrySolventsSingle bondPhysical and Theoretical ChemistryBenzeneSpectroscopyJournal of molecular graphicsmodelling
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Nebenreaktionen der radikalisch ausgelösten Cyclisierung von 2,2′-Methylen-bis(4-methyl-1,2-phenylen)-dimethacrylat

1979

2,2′-Methylene-bis(4-methyl-1,2-phenylene) dimethacrylate (1) was reacted with an excess of 2,2′-azoiso-butyronitrile (mole ratio 1:15) highly diluted in boiling benzene. The reaction products were separated by column chromatography. It was found that the 1-cyano-1-methylethyl radical induced the cyclization of 1 to yield the product of a head to tail addition (2) in 55% yield. In addition, the product of a head to head addition (3) was isolated in 4% yield. 35% of 1 reacted in the same way as it has already been observed as suppression of polymerization in the case of p-tolyl methacrylate to give the products 4 and 5. The structures of the products were confirmed by elemental analyses, by …

Mole ratioPolymers and PlasticsChemistryHead to headMethacrylateMedicinal chemistrychemistry.chemical_compoundColloid and Surface ChemistryColumn chromatographyPolymerizationYield (chemistry)Polymer chemistryMaterials ChemistryProton NMRPhysical and Theoretical ChemistryBenzeneColloid and Polymer Science
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A Dendrimer Chiroptical Switch Based on the Reversible Intramolecular Photoreaction of Anthracene and Benzene Rings

2010

A series of Fréchet-type dendrimers with 9-benzyloxymethylanthracene cores were synthesized and characterized. The chiral source for the dendrimers was an (S)-2-methyl-1-butoxy group in the 3-position of the benzene ring. Irradiation at 366 nm of a dilute benzene solution led to the formation of two diastereomers (1:1) through a quantitative intramolecular [4pi+4pi] cycloaddition between the central anthracene ring and the neighboring benzene ring. The process can be reversed with 254 nm UV light or heat. The benzene rings in the dendrons work as a light-harvesting system. The optical rotation values measured for the reversible process showed fatigue resistance. Thus, a promising new type o…

Molecular switchAnthraceneOrganic ChemistryGeneral ChemistryRing (chemistry)PhotochemistryBiochemistryCycloadditionchemistry.chemical_compoundchemistryIntramolecular forceDendrimerOptical rotationBenzeneChemistry - An Asian Journal
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Reversible and Efficient Light-Induced Molecular Switching on an Insulator Surface

2018

Prototypical molecular switches such as azobenzenes exhibit two states, i.e., trans and cis, with different characteristic physical properties. In recent years various derivatives were investigated on metallic surfaces. However, bulk insulators as supporting substrate reveal important advantages since they allow electronic decoupling from the environment, which is key to control the switching properties. Here, we report on the light-induced isomerization of an azobenzene derivative on a bulk insulator surface, in this case calcite (101̅4), studied by atomic force microscopy with submolecular resolution. Surprisingly, cis isomers appear on the surface already directly after preparation, indi…

Molecular switchMaterials sciencePhotoisomerizationGeneral EngineeringGeneral Physics and AstronomyInsulator (electricity)02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology53001 natural sciences0104 chemical sciencesMetalchemistry.chemical_compoundAzobenzenechemistryChemical physicsvisual_artvisual_art.visual_art_mediumMoleculeGeneral Materials Science0210 nano-technologyIsomerizationCis–trans isomerismACS Nano
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Novel Domino Oxidative Coupling: C−C Bond Formation Sequence to Highly Functionalized Dibenzo[a,c]cycloheptenes

2011

A domino sequence involving various MoCl(5)-mediated oxidations followed by trapping and supposed [3,3]-sigmatropic rearrangement provides a fast access to the full carbon skeleton of metasequirin-B. A variety of different moieties R(1) and R(2) are tolerated.

MolybdenumMolecular StructureOxidative CouplingChemistryStereochemistryOrganic ChemistryCarbon skeletonSequence (biology)DibenzocycloheptenesBond formationBiochemistryCatalysisLignansDominoChloridesCyclizationBenzene DerivativesOxidative coupling of methanePhysical and Theoretical ChemistryOxidation-ReductionOrganic Letters
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Preparation of organic monolithic columns in polytetrafluoroethylene tubes for reversed-phase liquid chromatography

2017

[EN] In this work, a method for the preparation and anchoring of polymeric monoliths in a polytetrafluoroethylene (PTFE) tubing as a column housing for microbore HPLC is described. In order to assure a covalent attachment of the monolith to the inner wall of the PTFE tube, a two-step procedure was developed. Two surface etching reagents, a commercial sodium naphthalene solution (Fluoroetch®), or mixtures of H2O2 and H2SO4, were tried and compared. Then, the obtained hydroxyl groups on the PTFE surface were modified by methacryloylation. Attenuated total reflectance Fourier-transform infrared (ATR-FTIR) spectroscopy and scanning electron microscopy (SEM) confirmed the successful modification…

Monolithic HPLC columnMicrobore column02 engineering and technology01 natural sciencesBiochemistryAnalytical Chemistrychemistry.chemical_compoundSurface modificationQUIMICA ANALITICAEnvironmental ChemistryMonolith attachmentMonolithReversed-phase liquid chromatographyPolytetrafluoroethyleneSpectroscopychemistry.chemical_classificationChromatography Reverse-PhasegeographyChromatographygeography.geographical_feature_categoryPolytetrafluoroethyleneChemistry010401 analytical chemistryPolymer monolithEquipment DesignPolymer021001 nanoscience & nanotechnology0104 chemical sciencesChemical engineeringPolymerizationAttenuated total reflectionSurface modificationAlkylbenzenes0210 nano-technologyAnalytica Chimica Acta
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The role of water in the photocatalytic degradation of acetonitrile and toluene in gas-solid and liquid-solid regimes

2006

Photocatalytic degradation of acetonitrile and toluene was carried out both in gas-solid and in liquid-solid regimes by using commercialTiO2samples (Merck and Degussa P25). The investigation was mainly aimed to study the influence of water present in the reaction environment on the mechanism and degradation rate of two probe molecules. In gas-solid regime, the reacting mixture consisted of toluene or acetonitrile, oxygen, nitrogen, and water vapour. The main degradation product of toluene wasCO2with small amounts of benzaldehyde. In the presence of water vapour, the activity ofTiO2Merck remained stable but greatly decreased if water was absent.TiO2Degussa P25 continuously deactivated, even …

Muconic acidADSORPTIONBENZENEInorganic chemistrylcsh:TJ807-830lcsh:Renewable energy sourcesHUMIDIFIED AIRANATASE TIO2 CATALYSTOXIDATIONCH3CNBenzaldehydechemistry.chemical_compoundGeneral Materials ScienceFORMALDEHYDEBenzenePhotodegradationAcetonitrileBenzoic acidTITANIUM-DIOXIDERenewable Energy Sustainability and the EnvironmentGeneral ChemistryVAPOR-PHASETolueneAtomic and Molecular Physics and OpticsANATASE TIO2 CATALYST; TITANIUM-DIOXIDE; HUMIDIFIED AIR; VAPOR-PHASE; OXIDATION; ADSORPTION; BENZENE; CH3CN; FORMALDEHYDE; BEHAVIORchemistryBenzyl alcoholBEHAVIORInternational Journal of Photoenergy
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CCDC 684536: Experimental Crystal Structure Determination

2008

Related Article: A.Valkonen, R.Gawinecki, H.Janota, B.Osmialowski, E.Kolehmainen|2008|Acta Crystallogr.,Sect.E:Struct.Rep.Online|64|o737|doi:10.1107/S1600536808007435

N-(2-Benzoyl-4-chlorophenyl)-4-chlorobenzenesulfonamideSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1857204: Experimental Crystal Structure Determination

2019

Related Article: A. Sunil Kumar, Jyothi Kudva, Manu Lahtinern, Anssi Peuronen, Rajitha Sadashiva, Damodara Naral|2019|J.Mol.Struct.|1190|29|doi:10.1016/j.molstruc.2019.04.050

N-(4-methylphenyl)-4-[(quinazolin-4-yl)amino]benzene-1-sulfonamideSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 2034819: Experimental Crystal Structure Determination

2021

Related Article: Peng Shi, Yongliang Tu, Duo Zhang, Chenyang Wang, Khai‐Nghi Truong, Kari Rissanen, Carsten Bolm|2021|Adv.Synth.Catal.|363|2552|doi:10.1002/adsc.202100162

N-{[2-(4-t-butylphenyl)-2-chloroethenyl](oxo)phenyl-lambda6-sulfanyl}-4-methylbenzene-1-sulfonamideSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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