Search results for "Propane"

showing 10 items of 486 documents

CCDC 1955601: Experimental Crystal Structure Determination

2020

Related Article: Lucia Volbach, Niklas Struch, Fabian Bohle, Filip Topić, Gregor Schnakenburg, Andreas Schneider, Kari Rissanen, Stefan Grimme, Arne Lützen|2020|Chem.-Eur.J.|26|3335|doi:10.1002/chem.201905070

catena-[[(propane-13-diyl)bis(diphenylphosphine)]-[mu-tricyclo[8.2.2.247]hexadeca-1(12)46101315-hexaene-512-dicarbonitrile]-palladiumbis( trifluoromethanesulfonate) dichloromethane solvate]Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1449686: Experimental Crystal Structure Determination

2016

Related Article: Kaisa Helttunen, Maija Nissinen|2016|CrystEngComm|18|4944|doi:10.1039/C6CE00243A

catena-[bis(mu-281420-tetrapentyl-6121824-tetramethoxy-410:1622-bis(22'-(propane-13-diyldisulfanediyl)di(ethoxy))calix[4]arene)-tetrakis(mu-trifluoroacetato)-(trifluoroacetato)-penta-silver ethanol solvate monohydrate]Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1547125: Experimental Crystal Structure Determination

2017

Related Article: Alokesh Hazari, Carlos J. Gómez-García, Michael G.B. Drew, Ashutosh Ghosh|2017|Polyhedron|138|145|doi:10.1016/j.poly.2017.09.012

catena-[octakis(mu-22'-[propane-13-diylbis(azanediylmethylene)]diphenolato)-tetraazido-tetra-iron(iii)-octa-nickel(ii) methanol solvate dihydrate]Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Rigid biobased polycarbonates with good processability based on a spirocyclic diol derived from citric acid

2020

Introducing biobased polymers from renewable sources for use as high-performance thermoplastics with high demands on mechanical rigidity, transparency, thermal stability, as well as good processability, is a significant challenge. In the present work we have designed and prepared a rigid biobased bis-spirocylic diol by di-cycloketalization of a bicyclic diketone (cis-bicyclo[3.3.0]octane-3,7-dione, obtained from citric acid) using trimethylolpropane. This spiro-diol monomer has two reactive primary hydroxyl groups and the synthesis from inexpensive biobased starting materials is straightforward and readily upscalable, involving no chromatographic purification. In order to explore the useful…

chemistry.chemical_classificationCondensation polymerMaterials scienceDiolThermal decompositionPolymerPollutionchemistry.chemical_compoundMonomerchemistryRheologyChemical engineeringEnvironmental ChemistryThermal stabilityTrimethylolpropaneGreen Chemistry
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Non-classical CH⋯O hydrogen-bond determining the regio- and stereoselectivity in the [3 + 2] cycloaddition reaction of (Z)-C-phenyl-N-methylnitrone w…

2015

The role of the ester groups in the regio- and stereoselectivities of the zw-type [3 + 2] cycloaddition (32CA) reaction of C-phenyl-N-methylnitrone with dimethyl 2-benzylidenecyclopropane-1,1-dicarboxylate (BCPC) has been studied using DFT methods at the MPWB1K/6-31G(d) level. The possible ortho/meta regioisomeric channels and the endo/exo stereoselective approach modes were explored and characterized. Analysis of the relative energies associated with the different reaction pathways indicates that the presence of the two CO2Me groups in the cyclopropane ring has a remarkable effect on selectivities favouring the ortho/endo path, in good agreement with the experimental data. Inclusion of sol…

chemistry.chemical_classificationHydrogen bondChemistryStereochemistryGeneral Chemical EngineeringGeneral ChemistryActivation energyTopologyCycloadditionNitroneCyclopropanechemistry.chemical_compoundStereoselectivitySolvent effectsSelectivityRSC Advances
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A unified synthetic approach to trachylobane-, beyerane-, atisane- and kaurane-type diterpenes

2006

A general synthetic approach to the polycyclic carbon skeleton of biogenetically related trachylobane, beyerane, atisane, and kaurane diterpenes from carvone is described. The skeleton of these diterpenes is prepared from a common intermediate, that is, 25, readily prepared from carvone using an IMDA reaction and an intramolecular diazo ketone cyclopropanation of an unsaturated ketone as key steps. The tetracyclic diterpene ring systems are obtained from this key trachylobane-type intermediate through the regioselective reductive cleavage of the cyclopropane ring, after adequate modification of the functionalization around the tricyclo[3.2.1.02,7]octane moiety.

chemistry.chemical_classificationKetoneCyclopropanationStereochemistryOrganic ChemistryRegioselectivityRing (chemistry)BiochemistryCyclopropanechemistry.chemical_compoundchemistryDrug DiscoveryOrganic chemistryMoietyDiazoDiterpeneTetrahedron
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Part II. Chiral dirhodium (II) catalysts with ortho-metalated arylphosphane ligands in the enantioselective intramolecular cyclopropanation of a race…

2006

Abstract In this report, chiral dirhodium (II) with ortho -metalated phosphane ligands, namely ( M )-Rh 2 (O 2 CR) 2 (PC) 2 [PC =  ortho -metalated aryl phosphane, O 2 CR = carboxylate bridging ligands) ( 1a–g ), have been used for the intramolecular cyclopropanation of racemic1-diazo-6-methyl-3-(2-propenyl)-5-hepten-2-one ( 2 ), containing both a tri- and monosubstituted carbon–carbon double bond, in pentane. The highest level of regiocontrol has been obtained with chiral catalyst Rh 2 (O 2 CCH 3 ) 2 [( p -MeC 6 H 3 )P( p -MeC 6 H 4 ) 2 ] 2 ( M )- 1c , affording favorably trisubstituted cyclopropane 3 versus monosubstituted cyclopropane 4 in 74:26 ratio. An exceptional diastereoselectivity…

chemistry.chemical_classificationKetoneDouble bondChemistryCyclopropanationStereochemistryArylEnantioselective synthesisCyclopropaneInorganic Chemistrychemistry.chemical_compoundIntramolecular forceMaterials ChemistryDiazoPhysical and Theoretical ChemistryInorganica Chimica Acta
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SiO2-supported vanadium magnesium mixed oxides as selective catalysts for the oxydehydrogenation of short chain alkanes

2001

Abstract Unsupported and SiO 2 -supported VMgO mixed oxides catalysts have been prepared, characterized and tested in the oxidation of propane, n -butane and propylene. Mg-vanadates are observed by XRD, IR and Raman spectroscopy in both pure and supported VMgO catalysts, although the effective Mg/V ratio, in the VMgO phases formed, depends on the silica content. Since SiO 2 reacts partially with MgO during the calcination step, forming Mg 2 SiO 4 , the effective Mg/V ratio depends on the silica content. In this sense, pyro -Mg 2 V 2 O 7 is mainly formed on supported catalysts with Mg/V atomic ratios lower than 4, while ortho -Mg 3 V 2 O 8 is observed on supported catalysts with Mg/V atomic …

chemistry.chemical_classificationProcess Chemistry and TechnologyInorganic chemistryVanadiumchemistry.chemical_elementButaneCatalysisCatalysisPropenechemistry.chemical_compoundHydrocarbonchemistryPropaneAtomic ratioPartial oxidationApplied Catalysis A: General
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Inhibitoren der Korrosion 10 (1). Nachweis der Sekundärinhibition durch Allyl-triphenyl-phosphonium- bzw. arsoniumbromid und N-Allyl-chinaldiniumbrom…

1971

Triphenyl-allyl-phosphonium- (1) und -arsoniumsalze (2) sowie Allyl-chinaldinium-bromid (4) sind Korrosionsinhibitoren mittlerer Wirksamkeit. Sie werden von Carbonyleisenpulver im sauren Medium zu Triphenylphosphin bzw. Triphenylarsin bzw. Chinaldin reduziert. Triphenylphosphin und Triphenylarsin, die sich als Schicht auf dem Carbonyleisenpulver befinden, konnen nach Extraktion dunnschichtchromatographisch identifiziert werden. Die Allylgruppe wird aus den Verbindungen 1, 2 und 4 durch Eisen als Propen, Propan und wahrscheinlich als Cyclopropan abgelost. Die gaschromatographisch bestimmten Mengen an Kohlenwasserstoffen stehen in guter Ubereinstim-mung mit den gravimetrisch ermittelten Werte…

chemistry.chemical_classificationSulfoniumMechanical EngineeringMetals and AlloysQuinaldineGeneral MedicineSurfaces Coatings and FilmsCyclopropanePropenechemistry.chemical_compoundHydrocarbonchemistryMechanics of MaterialsBromidePolymer chemistryMaterials ChemistryEnvironmental ChemistryPhosphoniumPhosphineMaterials and Corrosion/Werkstoffe und Korrosion
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Studies on the diurnal courses of the contents of abscisic acid, 1-aminocyclopropane carboxylic acid and its malonyl conjugate in needles of damaged …

1993

Summary The diurnal courses of the contents of 1-aminocyclopropane carboxylic acid (ACC), its malonyl conjugate (MACC) and abscisic acid (ABA) in the two-year-old needles of damaged and undamaged spruce trees (Picea abies L.) were investigated. The contents of ACC and MACC were significantly higher in the needles of the damaged trees as compared with the undamaged ones. In the needles of the damaged spruce trees, the ACC and MACC contents, and ABA contents as well, fluctuated to a greater extent than those in the undamaged spruce trees during the day. The relationships between ACC-ABA and MACC-ACC contents as well are also discussed.

chemistry.chemical_classificationbiologyPhysiologyChemistryCarboxylic acidfungiDiurnal temperature variationPicea abiesPlant Sciencebiology.organism_classificationbehavioral disciplines and activitiesstomatognathic diseaseschemistry.chemical_compoundBotany1-aminocyclopropanecarboxylic acidhuman activitiesAgronomy and Crop ScienceAbscisic acidpsychological phenomena and processesConjugateJournal of Plant Physiology
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