Search results for "Cyclohexane"

showing 10 items of 295 documents

CCDC 938974: Experimental Crystal Structure Determination

2014

Related Article: Lena Kaufmann, Nora L. Traulsen, Andreas Springer, Hendrik V. Schröder, Toni Mäkelä, Kari Rissanen, Christoph A. Schalley|2014|Org.Chem.Front.|1|521|doi:10.1039/C4QO00077C

N-(2-(hexanoyl(methyl)amino)ethyl)-N-methylbenzamide 11'-iodo-5'17'23'35'38'40'43'45'-octamethyl-7'15'25'33'39'-pentaazadispiro[cyclohexane-12'-heptacyclo[32.2.2.2^36^.2^1619^.2^2124^.1^913^.1^2731^]hexatetracontane-20'1''-cyclohexane]-1'(36')3'5'9'(44')10'12'16'18'21'23'27'(39')28'30'34'37'40'42'45'-octadecaene-8'14'26'32'-tetroneSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Conformational changes in Cmethyl-resorcinarene pyridine N -oxide inclusion complexes in the solid state

2016

Aromatic N-oxides interact with Cmethyl-resorcinarene resulting in marked changes in the conformation of the host resorcinarene. In the solid state, 2- and 3-methylpyridine N-oxides form pseudo-capsular 2 : 2 endo host-guest complexes with Cmethyl-resorcinarene stabilized by C-H⋯π interactions. The Cmethyl-resorcinarene·2-methylpyridine N-oxide complex has a C4v crown conformation, while the Cmethyl-resorcinarene·3-methylpyridine N-oxide complex has a slightly open C2v boat conformation. On the contrary, other para-substituted and benzo-fused pyridine N-oxides form only exo complexes with Cmethyl-resorcinarene. In the exo complexes, the asymmetry of the guest, conformational flexibility and…

N-oxidesHydrogenta114010405 organic chemistryChemistryStereochemistryHydrogen bondCyclohexane conformationSolid-statechemistry.chemical_elementPyridine-N-oxidemacromolecular substancesGeneral ChemistryResorcinarene010402 general chemistryCondensed Matter Physics01 natural sciences0104 chemical sciencesCrystallographychemistry.chemical_compoundPyridineGeneral Materials ScienceN-oxide inclusion complexesta116CRYSTENGCOMM
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Physicochemical characterization of octakis(alkyloxy)-substituted Zn(ii)-phthalocyanines non-covalently incorporated into an organogel and their rema…

2007

A series of octakis(alkyloxy)-substituted Zn(II)-phthalocyanines were efficiently incorporated into an organogel made of (1R,2R)-trans-1,2-bis(dodecanoylamino)cyclohexane by means of multiple cooperative non-covalent interactions, and SEM revealed the formation of unique brush-like nanostructures.

NanostructureCyclohexaneChemistryMetals and AlloysGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCharacterization (materials science)chemistry.chemical_compoundCovalent bondPolymer chemistryMaterials ChemistryCeramics and CompositesNanoscopic scaleChem. Commun.
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Phosphorescence emission and polarization of quinoline 3-carbonitrile

1993

Abstract The phosphorescence emission and excitation spectra and their polarization have been studied for quinoline 3-carbonitrile in methylcyclohexane and ethanol glasses at 77 K. From the results obtained in this molecule (τ=1.15 sec in ethanol, τ=1.04 sec in methylcyclohexane and out-of-plane polarization) it is concluded that the emission is orginated from a triplet state of 3 ππ * character. The two major spin-orbit coupling mechanisms through which the ππ * state of quinoline 3-carbonitrile acquires dipole-allowed character via nπ * states are: 1. In ethanol glass: 2. In methylcyclohexane glass:

NitrileOrganic ChemistryQuinolinePhotochemistryAnalytical ChemistryInorganic Chemistrychemistry.chemical_compoundchemistryMoleculeEmission spectrumMethylcyclohexaneTriplet statePolarization (electrochemistry)PhosphorescenceSpectroscopyJournal of Molecular Structure
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Comparison of the Photoelectronic and Photocatalytic Activities of Various Anatase and Rutile Forms of Titania in Pure Liquid Organic Phases and in A…

1996

Various titania samples of industrial origin (Degussa and Tioxide) have been characterized by electrical photoconductance measurements and tested as photocatalysts in various liquid media (either pure organic liquids or aqueous solutions) as a function of their structure (anatase versus rutile). Anatase was constantly found more active than rutile, whatever the reaction chosen (mild oxidation of pure cyclohexane and 2-propanol; total degradation of phenol and nitrophenol isomers in water). In identical conditions, Degussa was found more active, but the intrinsic activity, expressed in moles converted per hour and per square meter of active surface, was found slightly higher for anatase Tiox…

Nitrophenolchemistry.chemical_compoundAnataseAqueous solutionchemistryCyclohexaneRutileInorganic chemistryGeneral EngineeringPhotocatalysisPhenolPhysical and Theoretical ChemistryActive surfaceThe Journal of Physical Chemistry
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Trends of organochlorine compounds in Finnish inland waters

2001

Caged common lake mussels (Anodonta piscinalis) have been used in the monitoring of organochlorine compounds in pulp and paper mill recipient watercourses of Finland annually from 1984 to 1998. Statistically significant decreasing trends of chlorophenols and chloroguaiacols originating from chlorobleaching were observed in all recipients in parallel with the decreasing discharges from the mills. Metabolites of chlorophenols, chloroanisoles and chloroveratroles had no or slightly increasing trends. Elevated PCB concentrations were measured in four watercourses. In two areas, PCBs were found to be significantly increasing, in two other cases they showed no trend. A mill producing recycled pap…

PaperAnodontaWater flowHealth Toxicology and MutagenesisFresh WaterAnisolesWaste Disposal FluidDDTAnimalsIndustryEnvironmental ChemistryEcotoxicologyLongitudinal StudiesOrganic ChemicalsIncubationFinlandbiologyChemistrybusiness.industryfood and beveragesPaper millGeneral MedicineMusselbiology.organism_classificationPolychlorinated BiphenylsPollutionBivalviaData Interpretation StatisticalEnvironmental chemistrySuspended matterChlorine CompoundsbusinessHexachlorocyclohexaneWater Pollutants ChemicalChlorophenolsEnvironmental MonitoringEnvironmental Science and Pollution Research
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Full band spectroscopic studies on the molecular mobility of diluted alcohols

1991

Abstract Static permittivity has been determinded for pure n-decanol and cyclohexanol and their solutions in cyclohexane up to very dilute solutions, the dipole moment is found to decrease with the increase in concentration to a minimum, then it increases continuously. At a certain concentration range, no effect of temperature on the measured dipole moments could be observed, within the observed temperature interval. The dielectric loss was measured in the frequency range from o.1 GHz to 670 GHz. The data are analysed in several Debye and Frohlich terms and the results are discussed.

PermittivityCondensed matter physicsCyclohexaneCyclohexanolAnalytical chemistryCondensed Matter PhysicsAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic Materialschemistry.chemical_compoundsymbols.namesakeDipoleViscositychemistryMoment (physics)Materials ChemistrysymbolsDielectric lossPhysical and Theoretical ChemistrySpectroscopyDebyeJournal of Molecular Liquids
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On structural phase transitions in the (C 5 H 12 N) 2 SbCl 5 crystals

2000

Abstract The results of the X-ray (at 295 and 355 K), dilatometric, differential scanning calorimetry and dielectric studies on a new piperidinium crystal, (C5H12N)2SbCl5, are presented. The anionic sublattice of the crystal is built up of infinite (SbCl52−)n chains composed of SbCl63− distorted octahedra connected with each other by corners. In voids of anionic sublattice two crystallographically independent piperidinium cations are located. At 295 K they are both in chair conformation. The compound undergoes three first-order phase transitions at 378.5 K (I→II), 339.5 K (II→III) and 205 K (III→IV). The mechanism of the (II→III) transition (Pna21→P212121) was proposed based on the X-ray da…

Phase transitionChemistryOrganic ChemistryCyclohexane conformationDielectricAnalytical ChemistryInorganic ChemistryCrystalCrystallographyDifferential scanning calorimetryOctahedronPhase (matter)X-ray crystallographySpectroscopyJournal of Molecular Structure
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Acute toxicity of organochlorined pesticides to the European eel,Anguilla anguilla: The dependency on exposure time and temperature

1987

PollutantInsecticidesEelsTime FactorsHealth Toxicology and MutagenesisTemperatureGeneral MedicinePesticideBiologyToxicologyPollutionAcute toxicityToxicologychemistry.chemical_compoundchemistryToxicityAnimalsEcotoxicologyWater PollutantsLindaneHexachlorocyclohexaneWater Pollutants ChemicalDependency (project management)Bulletin of Environmental Contamination and Toxicology
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Myrcenol-Based Monomer for Carbanionic Polymerization: Functional Copolymers with Myrcene and Bio-Based Graft Copolymers

2020

A bio-based hydroxyl group-containing diene monomer, silyl-protected β-myrcenol (MyrOSi), is introduced to the field of carbanionic polymerization. Polymerization in cyclohexane, using sec-butyllit...

Polymers and PlasticsCyclohexaneDieneOrganic ChemistryBio based02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundMonomerchemistryPolymerizationMyrcenePolymer chemistryMaterials ChemistryCopolymerMyrcenol0210 nano-technologyMacromolecules
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