Search results for "CRO"

showing 10 items of 40106 documents

Efficient and simple synthesis of novel 1,2,3-triazolyl-linked benzimidazolone, molecular docking and evaluation of their antimicrobial activity

2020

In this study, a novel series of 1,2,3-triazolyl-benzimidazolone derivatives have been synthesized by click reaction of azides with benzimidazolones 2a–b. The latter compounds were prepared with excellent yields (85–97%), the structures of products were determined by spectral analysis. Then, the X-rays crystallographic analysis of compound 7a revealed the self-assembling properties. The new heterocycles were evaluated for their in vitro antimicrobial activities against Gram-positive and Gram-negative bacteria and against fungi strains. The most tested synthesized compounds showed potent antibacterial and antifungal activities against all tested strains. The compound 6c was found to be the m…

010405 organic chemistrySimple (abstract algebra)ChemistryOrganic ChemistryClick chemistryRegioselectivity010402 general chemistryAntimicrobial01 natural sciencesCombinatorial chemistry0104 chemical sciences
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Photo-Chromium: Sensitizer for Visible-Light-Induced Oxidative C−H Bond Functionalization-Electron or Energy Transfer?

2017

The chromium(III) sensitizer [Cr(ddpd)2]3+ - based on an earth-abundant metal center - possesses a unique excited state potential energy landscape (ddpd = N,N'-dimethyl-N,N'-dipyridine-2-ylpyridine-2,6-diamine). The very large energy gap between the redox active and substitutionally labile 4T2 state and the long-lived low-energy 2E spin-flip state enables a selective, efficient sensitization of triplet dioxygen to give singlet dioxygen. Ultrafast intersystem crossing after the Franck Condon point from the 4T2 to the 2E excited state within 3.5 ps precludes intermolecular electron transfer pathways from the ultrashort-lived excited 4T2 state. This specific excited state reactivity enables a …

010405 organic chemistrySinglet oxygenOrganic ChemistryIntermolecular forcechemistry.chemical_element010402 general chemistryPhotochemistry01 natural sciences0104 chemical sciencesAnalytical Chemistrychemistry.chemical_compoundChromiumElectron transferIntersystem crossingchemistryExcited stateSinglet fissionReactivity (chemistry)Physical and Theoretical ChemistryChemPhotoChem
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Co–Co and Co–Fe cyano-bridged pentanuclear clusters based on a methylpyrazinyl-diamine tetradentate ligand: spin crossover and metal substitution eff…

2017

A pentanuclear [CoII3CoIII2] cluster complex has been developed by a solvothermal synthesis. Its highly stable metal-mixed Fe–Co derivatives display robust spin crossover (T1/2 = 268 K) controlled by the degree of substitution.

010405 organic chemistrySolvothermal synthesisSubstitution (logic)General Chemistry010402 general chemistryCondensed Matter PhysicsPhotochemistry01 natural sciences0104 chemical sciencesMetalCrystallographychemistry.chemical_compoundDegree of substitutionchemistrySpin crossovervisual_artDiaminevisual_art.visual_art_mediumCluster (physics)General Materials ScienceTetradentate ligandCrystEngComm
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Three Co(II) Metal-Organic Frameworks with Diverse Architectures for Selective Gas Sorption and Magnetic Studies.

2019

Three Co(II) metal–organic frameworks, namely, {[Co2(L)2(OBA)2(H2O)4]·xG}n (1), {[Co(L)0.5(OBA)]·xG}n (2), and {[Co2(L)2(OBA)2(H2O)]·DMA·xG}n (3) [where L = 2,5-bis(3-pyridyl)-3,4-diaza-2,4-hexadiene, H2OBA = 4,4′-oxybisbenzoic acid, DMF = dimethylformamide, DMA = dimethylacetamide, and G denotes disordered guest molecules], have been synthesized under diverse reaction conditions through self-assembly of a bent dicarboxylate and a linear spacer with a Co(II) ion. While 1 is crystallized at room temperature in DMF to form a 2D layer structure, 2 is formed by the assembly of similar components under solvothermal conditions with a 3D network structure. On the other hand, changing the solvent t…

010405 organic chemistrySorptionMicroporous material010402 general chemistry01 natural sciencesDimethylacetamide0104 chemical sciencesInorganic ChemistrySolventchemistry.chemical_compoundCrystallographychemistryDimethylformamideMoleculeMetal-organic frameworkPhysical and Theoretical ChemistryBET theoryInorganic chemistry
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A spin-crossover complex based on a 2,6-bis(pyrazol-1-yl)pyridine (1-bpp) ligand functionalized with a carboxylate group

2014

Combining Fe(ii) with the carboxylate-functionalized 2,6-bis(pyrazol-1-yl)pyridine (bppCOOH) ligand results in the spin-crossover compound [Fe(bppCOOH)2](ClO4)2 which shows an abrupt spin transition with a T1/2 of ca. 380 K and a TLIESST of 60 K due to the presence of a hydrogen-bonded linear network of complexes.

010405 organic chemistryStereochemistryLigandSpin transition010402 general chemistry01 natural sciencesMedicinal chemistry3. Good health0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundLinear networkBPP ligandchemistrySpin crossoverGroup (periodic table)PyridineCarboxylateDalton Transactions
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Nonanuclear Spin-Crossover Complex Containing Iron(II) and Iron(III) Based on a 2,6-Bis(pyrazol-1-yl)pyridine Ligand Functionalized with a Carboxylat…

2016

The synthesis and magnetostructural characterization of [Fe(III)3(μ3-O)(H2O)3[Fe(II)(bppCOOH)(bppCOO)]6](ClO4)13·(CH3)2CO)6·(solvate) (2) are reported. This compound is obtained as a secondary product during synthesis of the mononuclear complex [Fe(II)(bppCOOH)2](ClO4)2 (1). The single-crystal X-ray diffraction structure of 2 shows that it contains the nonanuclear cluster of the formula [Fe(III)3(μ3-O)(H2O)3[Fe(II)(bppCOOH)(bppCOO)]6](13+), which is formed by a central Fe(III)3O core coordinated to six partially deprotonated [Fe(II)(bppCOOH)(bppCOO)](+) complexes. Raman spectroscopy studies on single crystals of 1 and 2 have been performed to elucidate the spin and oxidation states of iron …

010405 organic chemistryStereochemistryTrimer010402 general chemistry01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundsymbols.namesakeCrystallographyDeprotonationchemistrySpin crossoverCluster (physics)symbolsAntiferromagnetismCarboxylatePhysical and Theoretical ChemistrySpin (physics)Raman spectroscopyInorganic chemistry
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Microporous Triptycene‐Based Affinity Materials on Quartz Crystal Microbalances for Tracing of Illicit Compounds

2019

Triptycene-based organic molecules of intrinsic microporosity (OMIMs) with extended functionalized π-surfaces are excellent materials for gas sorption and separation. In this study, the affinities of triptycene-based OMIM affinity materials on 195 MHz high-fundamental-frequency quartz crystal microbalances (HFF-QCMs) for hazardous and illicit compounds such as piperonal and (-)-norephedrine were determined. Both new and existing porous triptycene-based affinity materials were investigated, resulting in very high sensitivities and selectivities that could be applied for sensing purposes. Remarkable results were found for safrole - a starting material for illicit compounds such as ecstasy. A …

010405 organic chemistrySupramolecular chemistrySorptionGeneral ChemistryMicroporous material010402 general chemistry01 natural sciencesCombinatorial chemistry0104 chemical sciencesCrystalchemistry.chemical_compoundPiperonalchemistryTriptycenePorosityQuartzChemPlusChem
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Theoretical investigation of the spin crossover transition states of the addition of methane to a series of Group 6 metallocenes using minimum energy…

2016

International audience; Density functional calculations are reported on the addition of methane to Group 6 metallocenes, M(η-C5H5)2 (M), M(CH2(η-C5H4)2) (a-M) and M(η-C5Me5)2 (M*) where M = Mo and W. Full geometry optimisations were carried out on the singlet and triplet 16 electron complexes, 1[M] and 3[M], the η2-methane complexes, 1[M(η2-CH4)], and the hydridomethyl adducts, 1[M(CH3)(H)]. The triplet state for [M] was found to be more stable for all six metallocenes, the difference being least in the case of the ansa-bridged system. Formation of the hydridomethyl complexes was exoenergetic for all tungsten systems and for a-Mo, the other two Mo systems being endoenergetic. Minumum energy…

010405 organic chemistrychemistry.chemical_elementGeneral ChemistryElectronTungsten010402 general chemistry7. Clean energy01 natural sciencesTransition stateMethane0104 chemical sciencesAdduct[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistry.chemical_compoundchemistry13. Climate actionSpin crossoverComputational chemistryPhysical chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistrySinglet stateTriplet stateJOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS
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Intercomparison of Soil Moisture Retrieved from GNSS-R and from Passive L-Band Radiometry at the Valencia Anchor Station

2019

In this paper, the SOMOSTA (Soil Moisture Monitoring Station) experiment on the intercomparison of soil moisture monitoring from Global Navigation Satellite System Reflectometry (GNSS-R) signals and passive L-band microwave radiometer observations at the Valencia Anchor Station is introduced. The GNSS-R instrument has an up-looking antenna for receiving direct signals from satellites, and a dual-pol down-looking antenna for receiving LHCP (left-hand circular polarization) and RHCP (right-hand circular polarization) reflected signals from the soil surface. Data were collected from the three different antennas through the two channels of Oceanpal GNSS-R receiver and, in addition, calibration …

010504 meteorology & atmospheric sciences0211 other engineering and technologies02 engineering and technologyELBARA-II radiometerlcsh:Chemical technology01 natural sciencesBiochemistryArticleAnalytical Chemistrylcsh:TP1-1185L-band radiometryElectrical and Electronic EngineeringOceanpalReflectometryInstrumentationWater content021101 geological & geomatics engineering0105 earth and related environmental sciencesRemote sensingValencia Anchor StationRadiometerMoistureGNSS-RMicrowave radiometerAtomic and Molecular Physics and OpticsGNSS applicationsSoil waterEnvironmental scienceRadiometrysoil moistureSensors
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The global forest above-ground biomass pool for 2010 estimated from high-resolution satellite observations

2021

Funding Information: We are thankful to the GlobBiomass project team and Frank Martin Seifert (ESA) for valuable suggestions and stimulating scientific discussions. We are thankful to Takeo Tadono (JAXA EORC), Masato Hayashi, (JAXA EORC), Kazufumi Kobayashi (RESTEC), Åke Rosenqvist (soloEO), and Josef Kellndorfer (EBD) for support with the use and interpretation of the ALOS PALSAR mosaics. Support by the CCI Land Cover project team, in particular Sophie Bontemps (UCL), is greatly acknowledged. The help from Martin Jung (MPI-BGC) in feature selection and Ulrich Weber (MPI-BGC) for data processing for the GSV-to-AGB conversions is greatly acknowledged. Forest inventory data for the validation…

010504 meteorology & atmospheric sciencesALOS PALSAR0211 other engineering and technologies02 engineering and technology01 natural sciencesLaboratory of Geo-information Science and Remote SensingSDG 13 - Climate ActionGE1-350BiomassEMISSIONSSDG 15 - Life on LandQE1-996.5GROWING STOCK VOLUMETaigaGeologyPE&RCPlant Production SystemsMAPbiomaCARBON-CYCLECrop and Weed EcologySynthetic aperture radarPhysical geographyRETRIEVALUNITED-STATESEarth and Planetary Sciences(all)Synthetic aperture radarSubtropicsSpatial distributionEnvironmental scienceCarbon cycletropicsTemperate climateBOREAL FORESTSMANAGEMENTLife ScienceSpatial ecologySpatial distributionLaboratorium voor Geo-informatiekunde en Remote Sensing021101 geological & geomatics engineering0105 earth and related environmental sciencesForest inventoryRadarTemperate climateEnvironmental sciencesSatelliteEarth and Environmental SciencesDENSITYPlantaardige ProductiesystemenSpatial ecologyEnvironmental scienceGeneral Earth and Planetary SciencescavelabPhysical geographyForest inventory
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