Search results for "synthesis"

showing 10 items of 2844 documents

Hydrogen Bonding Donor–Acceptor Carbon Nanostructure

2012

The natural process of photosynthesis is paradigmatic in converting sunlight into energy. This complicated process requires a cascade of energy- and electron-transfer events in a highly organised matrix of electron–donor, electron–acceptor and antennae units and has prompted researchers to emulate it. In fact, energy- and electron-transfer processes play a pivotal role in molecular-scale optoelectronics. In this chapter we compile a number of remarkable examples of noncovalent aggregates formed by the combination of carbon-based electroactive species (fullerenes and carbon nanotubes) hydrogen bonded with a variety of moieties. We will show that: (a) the connection of complementary electroac…

Hydrogen bond Fullerene carbon nanotubes polymers synthesisSettore CHIM/06 - Chimica Organica
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Enantioselective Strecker Reaction Catalyzed by an Organocatalyst Lacking a Hydrogen-Bond-Donor Function

2007

Hydrogen bondChemistryOrganocatalysisStrecker amino acid synthesisEnantioselective synthesisOrganic chemistryGeneral ChemistryPlanar chiralityCatalysisCatalysisAngewandte Chemie International Edition
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Ni and Ni-Pd nanostructures electrodes for water-alkaline electrolyses

2017

Hydrogen production by water electrolysis (WE) is a very promising technology because it is a pollution free-process specially if renewable energy are employed. Up to day, the cost of hydrogen production by WE is higher than other available technologies, making WE not competitive. Many efforts have been made to improve WE performance, through the use of electrodes made of transition metal alloys (Pt2Mo, TiPt) as a cathode or pyrochlore type oxide (Tl2RuxIr2-xO7) as an anode [1]. In the field of water-alkaline electrolyzer, the development of cheap nanoporous nickel electrodes with high electrocatalytic features is one of the potential approaches to increase the WE performance [2]., A facile…

Hydrogen gas water splitting Ni nanowire template electrosynthesis alkaline solutionSettore ING-IND/23 - Chimica Fisica Applicata
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Hydrogen: a good partner for rhodium-catalyzed hydrosilylation

2014

The influence of hydrogen pressure on the hydrosilylation of ketones catalyzed by [((S)-SYNPHOS)Rh(nbd)]OTf has been studied. We have notably demonstrated that hydrogen significantly affected the outcome of the reaction while not being consumed as stoichiometric reducing agent. In THF, diethyl ether or toluene, the hydrogen pressure exceedingly accelerated the hydrosilylation reaction and preserved or even improved the enantioselectivity of the process. In CH2Cl2, the rhodium catalyst also showed generally higher catalytic activity under hydrogen pressure. Most serendipitously, several ketones were found to give products of absolute opposite configuration upon performing the hydrosilylation…

HydrogenHydrosilylationReducing agentEnantioselective synthesischemistry.chemical_elementGeneral ChemistryMedicinal chemistryRhodiumCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryDiethyl etherStoichiometryApplied Organometallic Chemistry
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Stabilized Ru[(H2O)(6)](3+) in Confined Spaces (MOFs and Zeolites) Catalyzes the lmination of Primary Alcohols under Atmospheric Conditions with Wide…

2018

[EN] Imines are ubiquitous intermediates in organic synthesis, and the metal-mediated imination of alcohols is one of the most direct and simple methods for their synthesis. However, reported protocols lack compatibility with many other functional groups since basic supports/media, pure oxygen atmospheres, and/or released hydrogen gas are required during reaction. Here we show that, in contrast to previous metal-catalyzed methods, hexa-aqueous Ru(III) catalyzes the imination of primary alcohols with very wide functional group tolerance, at slightly acid pH and under low oxygen atmospheres. The inorganic metal complex can be supported and stabilized, integrally, within either faujasite-type …

HydrogenMetal-organic frameworkIminechemistry.chemical_element02 engineering and technology010402 general chemistryHeterogeneous catalysis01 natural sciencesRutheniumCatalysisCatalysischemistry.chemical_compoundQUIMICA ORGANICAImineZeoliteZeoliteGeneral Chemistry021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical sciencesRutheniumchemistryMetal-organic frameworkOrganic synthesis0210 nano-technology
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Effect of a Rigid Sulfonamide Bond on Molecular Folding: A Case Study

2015

A disulfonamide compound with bulky aromatic side chains was prepared, and its properties as a potential building block for foldamers were evaluated. Two different solvate crystal forms of the compound were identified and compared to the structures of an analogous oligoamide and related disulfonamides. The disulfonamide is unfolded in one of the solvates, whereas in the other one, a loosely folded conformer stabilized by an intramolecular hydrogen bond is found. Density functional calculations indicated that the loosely folded conformer is slightly more stable than its unfolded isomer. The calculations also identified a third, more tightly folded and more extensively hydrogen bonded, confor…

HydrogenStereochemistrychemistry.chemical_elementmolecular foldingkonformeeritorgaaninen synteesiCrystalSide chainmolecular conformersGeneral Materials Sciencemolekyylien laskostuminenta116sulfonamidisidosConformational isomerismX-ray crystallographychemistry.chemical_classificationHydrogen bondsulfonamide bondGeneral Chemistryorganic synthesisCondensed Matter PhysicsSulfonamideFolding (chemistry)chemistryIntramolecular forceröntgenkristallografiaCrystal Growth & Design
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Sensitivity of scope modelled GPP and fluorescence for different plant functional types

2014

This study addresses the question which factors are responsible for reported positive correlations between solar induced fluorescence (SIF) and gross primary production (GPP). A sensitivity analysis of the model SCOPE, which simulates photosynthesis, fluorescence emission and radiative transfer in canopies, has been carried out for four different plant functional types (PFT): tropical rainforest, C4 crops, C3 crops, and tundra, located in distinct climate zones: tropical everwet (Af), tropical with seasonal drought (savannah, Aw), temperate (Cf), and continental tundra (Dfd). Literature values for structural and physiological parameters and climate reanalysis data were used as input. The ef…

HydrologyIrradianceTropicsHumidityPrimary productionsensitivity analysiAtmospheric sciencesPhotosynthesisgross primary productionTundraSCOPESignal ProcessingTemperate climateEnvironmental sciencefluorescenceplant functional typeTropical rainforest1707
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Microreactor processing for the aqueous Kolbe-Schmitt synthesis of hydroquinone and phloroglucinol

2007

Hydroquinone and phloroglucinol were used as substrates for the aqueous Kolbe-Schmitt synthesis, using a novel processing methodology, termed high-p,T processing, recently demonstrated for the carboxylation of resorcinol. By the high-p,T approach, the temperature limitations of classical batch synthesis, e.g., set by reflux conditions (solvent boiling point), can be overcome by simple technical expenditure, e.g., the use of a few microstructured components, a capillary, and a needle valve at very low internal holdup. In this way, favorable speed-up of chemical reaction is achieved at temperatures normally outside the useful range for organic synthesis. While the hydroquinone synthesis gave …

HydroquinoneChemistryDecarboxylationGeneral Chemical EngineeringPhloroglucinolGeneral ChemistryIndustrial and Manufacturing EngineeringReaction ratechemistry.chemical_compoundCarboxylationYield (chemistry)Organic chemistryOrganic synthesisMicroreactorChemical Engineering & Technology
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Deoxygenative Divergent Synthesis : En Route to Quinic Acid Chirons

2020

The installation of vicinal mesylate and silyl ether groups in a quinic acid derivative generates a system prone for stereoselective borane-catalyzed hydrosilylation through a siloxonium intermediate. The diversification of the reaction conditions allowed the construction of different defunctionalized fragments foreseen as useful synthetic fragments. The selectivity of the hydrosilylation was rationalized on the basis of deuteration experiments and computational studies. peerReviewed

Hydrosilylation010402 general chemistry01 natural sciencesBiochemistrySilyl etherchemistry.chemical_compoundredox reactionsPhysical and Theoretical Chemistryhapetus-pelkistysreaktioorgaaniset yhdisteeteetteritkemiallinen synteesi010405 organic chemistryreaction productsOrganic ChemistryhydrosilylationQuinic acidCombinatorial chemistry0104 chemical sciencesbond cleavageetherschemistryStereoselectivitySelectivityDivergent synthesisDerivative (chemistry)Vicinal
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AICA-ribosiduria due to ATIC deficiency: Delineation of the phenotype with three novel cases, and long-term update on the first case.

2020

5-Amino-4-imidazolecarboxamide-ribosiduria (AICA)-ribosiduria is an exceedingly rare autosomal recessive condition resulting from the disruption of the bifunctional purine biosynthesis protein PURH (ATIC), which catalyzes the last two steps of de novo purine synthesis. It is characterized biochemically by the accumulation of AICA-riboside in urine. AICA-ribosiduria had been reported in only one individual, 15 years ago. In this article, we report three novel cases of AICA-ribosiduria from two independent families, with two novel pathogenic variants in ATIC. We also provide a clinical update on the first patient. Based on the phenotypic features shared by these four patients, we define AICA-…

Hydroxymethyl and Formyl TransferasesMalemedicine.medical_specialtyCyclohydrolase activityBioinformaticsCongenital AbnormalitiesEpilepsyMultienzyme ComplexesIntellectual DisabilityGeneticsmedicineHumansBifunctional Purine Biosynthesis Protein PURHChildGenetics (clinical)ATIC DEFICIENCYEpilepsybusiness.industryInfant NewbornInfantmedicine.diseaseAminoimidazole CarboxamidePhenotypePhenotypeNucleotide DeaminasesChild PreschoolMutationMedical geneticsFemaleRibonucleosidesNephrocalcinosisbusinessRare diseaseJournal of inherited metabolic diseaseREFERENCES
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