Search results for "Benzene"

showing 10 items of 1701 documents

Thermische Autoxydation und thermische Polymerisation des Styrols. Der Mechanismus der Startreaktion

1964

Die thermische Autoxydation des Styrols wurde bei verschiedenen Sauerstoffpartial drucken und in verschieden konzentrierten Losungen in Chlorbenzol mit Hilfe einer WARBURG-Apparatur gemessen. Aus den kinetischen Beziehungen folgt, das sich zuerst aus swei Styrolmolekulen ein Zwischenprodukt bildet, das von molekularem Sauerstoff unter Radikalbildung dehydriert wird. The thermal autoxidation of styrene was carried out in a WARBURG apparatus in different concentrations in chlorobenzene and under different partial pressures of oxygen. In consequence of the kinetic relations an intermediate is formed by two styrene molecules and this intermediate is dehydrated by molecular oxygen under the form…

chemistry.chemical_compoundchemistryAutoxidationChlorobenzeneRadicalPolymer chemistryMoleculechemistry.chemical_elementMolecular oxygenPartial pressureOxygenStyreneDie Makromolekulare Chemie
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Comparison of the molecular structure and spectra of benzene and borazine

1970

Ab initio SCF MO and CI calculations for two different gaussian basis sets are carried out for the isoelectronic molecules benzene C6H6 and borazine B3N3H3 in order to investigate the effect of increasing the flexibility in the representation of their respective π systems. In the process it is found from comparison of orbital charge density contour diagrams and inner shell orbital energies of borazine with analogous data for other systems that the BN bonds of this compound are considerably less polar (B+N−) than that of ammonia borane BNH6 (B−N+). CI calculations employing the larger basis set produce generally better agreement with the experimental transition energies of benzene than do th…

chemistry.chemical_compoundchemistryBorazineAb initioCharge densityMoleculeChiropracticsPhysical and Theoretical ChemistryAtomic physicsBenzeneExcitationBasis setSpectral lineTheoretica Chimica Acta
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Photochemical generation of benzene–naphthalene biplanemers

2005

Abstract A direct biplanemer synthesis could be achieved by a quantitative [4π+4π]photocycloaddition of benzyloxy substituted benzene and naphthalene rings ( 3d , e  ⇄  4d , e ). Since the products do not show a thermal Cope rearrangement—in contrast to the related longicyclic conjugated 9,10-benzotricyclo[4.2.2.2 2,5 ]dodeca-3,7,9-trienes—but a quantitative reverse reaction, they are interesting systems for an optical switching.

chemistry.chemical_compoundchemistryOrganic ChemistryDrug DiscoveryConjugated systemPhotochemistryBenzeneBiochemistryReversible reactionCycloadditionNaphthaleneTetrahedron Letters
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Mononuclear heterocyclic rearrangements 5. Kinetic Investigation of the behaviour of (e)- and (z)-phenylhydrazones of 3-benzoyl-5-phenyl-1,2,4-oxadia…

1980

The kinetic behaviour of the geometrical isomers I-E and I-Z of the title compound in the presence of piperidine in benzene has been investigated. The kinetic results suggest that I-Z rearranges directly into 2,5-diphenyl-4-benzoylamino-1,2,3-triazole (II), whereas I-E probably rearranges only through the intermediate I-Z formed by isomerization. All the reactions studied are piperidine-catalyzed.

chemistry.chemical_compoundchemistryOrganic ChemistryOxadiazolePiperidinePhotochemistryKinetic energyBenzeneMedicinal chemistryIsomerizationCis–trans isomerismJournal of Heterocyclic Chemistry
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Die Reaktion von 1,4-Bis(1-phenylvinyl)benzol mit Lithium

1975

Die Reaktion von 1,4-Bis(1-phenylvinyl)benzol (1) mit Lithium in THF, die vorwiegend zu einem dimeren α,ω-Dien-dianion 3 fuhrt, wird diskutiert. Die durch Umsetzung des Dianions 3 mit Methanol, Kohlendioxid und Methyljodid erhaltenen Reaktionsprodukte 4, 6 und 7 werden durch ihre IR-, NMR- und Massenspektren charakterisiert. The reaction of 1,4-bis(1-phenylvinyl)benzene (1) with lithium in THF yielding predomaintly the dimeric α,ω-diene dianion 3 is discussed. The products 4, 6, and 7 resulting from the reaction of the dianion 3 with methanol, carbon dioxide and methyl iodide are characterized by IR, NMR and mass spectra.

chemistry.chemical_compoundchemistryPolymer chemistryMass spectrumchemistry.chemical_elementLithiumMethanolBenzeneMethyl iodideDie Makromolekulare Chemie
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Phosphororganische Verbindungen. 60. Mitt. Aufbau und Eigenschaften eines optisch aktiven Anionenaustauschers mit identischem Chiralitäts- und Ladung…

1968

Chlormethyliertes Polystyrol (vernetzt mit 0,5% Divinylbenzol) wird mit (+)-Methyl- n-propyl-phenyl-phosphin quartarisiert. Der entstehende Austauscher besitzt eine Kapazitat von 2,68 mVal/g. Mandelsaure, Atrolactinsaure und Traubensaure konnten an diesem Material nicht in die Antipoden gespalten werden. Chlormethylated polystyrene (crosslinked with 0.5% divinylbenzene) is quaternized with (+)-methyl-n-propyl-phenyl-phosphine. The resultant anion exchanger has a capacity of 2.68 m.equiv./g. Mandelic acid, atrolactic, and rac. tartaric acid could not be resolved into the antipodes on this material.

chemistry.chemical_compoundchemistryPolymer chemistryTartaric acidPolystyreneMandelic acidDivinylbenzeneAnion exchangerDie Makromolekulare Chemie
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N-(Diphenylmethylene)benzenesulfonamide andN-(Diphenylmethylene)-4-methylbenzenesulfonamide

2008

[10398-99-9] C19H15NO2S (MW 332.42) InChI = 1S/C19H15NO2S/c21-23(22,18-14-8-3-9-15-18)20-19(16-10-4-1-5-11-16)17-12-6-2-7-13-17/h1-15H InChIKey = LECLPBHPQOFADH-UHFFFAOYSA-N (reagent used as an activated imine) Physical Data: mp 119–120 °C. Form Supplied in: colorless crystals. Not commercially available. Purification: recrystalization from CH3OH. [10399-00-5] C20H17NO2S (MW 346.45) InChI = 1S/C20H17NO2S/c1-16-12-14-19(15-13-16)24(22,23)21-20(17-8-4-2-5-9-17)18-10-6-3-7-11-18/h2-15H,1H3 InChIKey = ODLFJRFKAOOIKO-UHFFFAOYSA-N (reagent used as an activated imine) Physical Data: mp 103–104 °C1; 102–103 °C2; 101–102 °C5; 103 °C6; 102–104 °C.7 Solubility: soluble in pyridine, dimethylformamide, …

chemistry.chemical_compoundchemistryReagentIminePyridineOrganic chemistryDimethylformamideSolubilityBenzeneAcetonitrileMedicinal chemistryTetrahydrofuran
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Durch elektronenübertragung initiierte diradikalische polykombination zu linearen und cyclischen polyanionen, 1. Umsetzung des protonierten dimeren v…

1975

Die Umsetzung von 1,4-Diphenyl-1,4-bis[4-(1-phenylvinyl)phenyl]butan (1)–des protonierten Dimeren des 1,4-Bis(1-phenylvinyl)benzols (2)–mit Natrium in THF wird beschrieben und diskutiert. Die Reaktionsprodukte werden durch GPC, NMR- und Massenspektren charakterisiert. The reactions of 1,4-diphenyl-1,4-bis[4-(1-phenylvinyl)phenyl]butane (1)—the protonized dimer of 1,4-bis(1-phenylvinyl)benzene (2)—with sodium in THF is described and discussed. The reaction products are characterized by GPC, NMR, and mass spectra.

chemistry.chemical_compoundchemistrySodiumDimerPolymer chemistryMass spectrumchemistry.chemical_elementButaneBenzeneDie Makromolekulare Chemie
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p-Di-(1-phenylvinyl)-Benzol und seine reaktion mit elektronenüberträgern

1972

p-Di-(1-phenylvinyl)-benzol (I) wurde, ausgehend von p-Diacetylbenzol und Phenylmagnesiumbromid, in hoher Reinheit und guter Ausbeute dargestellt und charakterisiert. I setzt sich spontan mit Elektronenubertragern (Natrium, Naphthalin-Natrium) unter Ausbildung einer tief violetten Farbung um. Es entstehen die Oligomeren bis zum Dekameren, wobei die geradzahligen Homologen in hoherer Konzentration vorliegen als die jeweils benachbarten ungeradzahligen. Die Ergebnisse werden diskutiert. p-Di-(1-phenylvinyl) benzene (I) was prepared from diacetyl benzene and phenyl magnesium bromide in high purity and with good yield. It was identified by IR, NMR, and elemental analysis. I reacts immediately w…

chemistry.chemical_compoundchemistrySodiumPolymer chemistryMagnesium bromidechemistry.chemical_elementBenzeneDie Makromolekulare Chemie
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Alkoxy-Substituted Hexastyrylbenzenes

2003

Star-shaped compounds 2a–e with a central benzene ring and six p-substituted, (E)-configured styryl groups have been prepared by a sequence of three-fold Heck and three-fold Wittig–Horner reactions. Alkoxy chains (OC3H7, OC6H13, OC10H21, OC12H25) on all six arms guarantee a good solubility of 2a–d, whereas the alternating hexyloxy and cyano substitution in 2e leads to an almost insoluble push-pull system. Irradiation into the long-wavelength absorption of 2a–d (with λmax values of 341–342 nm) results in a statistical photocross-linking, which is characterized by the complete degradation of all stilbene chromophores.

chemistry.chemical_compoundchemistryStereochemistryAlkoxy groupGeneral ChemistryChromophoreAbsorption (chemistry)SolubilityBenzeneRing (chemistry)Medicinal chemistryAdvanced Synthesis & Catalysis
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