Search results for "center"

showing 10 items of 1724 documents

First principles hybrid Hartree-Fock-DFT calculations of bulk and (001) surface F centers in oxide perovskites and alkaline-earth fluorides

2020

Valuable discussions with E. A. Kotomin are gratefully acknowledged. Research contribution of R. E. and A. I. P. has been performed within the framework of the EUROfusion Enabling Research project: ENR-MFE19.ISSP-UL-02 “Advanced experimental and theoretical analysis of defect evolution and structural disordering in optical and dielectric materials for fusion applications.” The views and opinions expressed herein do not necessarily reflect those of the European Commission.

010302 applied physicsAlkaline earth metalMaterials sciencePhysics and Astronomy (miscellaneous)F centerperovskitesGeneral Physics and AstronomyIonic bondingElectronic structure7. Clean energy01 natural sciencesCrystallographic defectCrystallographyAb initio quantum chemistry methodsVacancy defect0103 physical sciences:NATURAL SCIENCES:Physics [Research Subject Categories]Ab initio calculations010306 general physicsShallow donorPerovskite (structure)
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Efficiency of H center stabilization in alkali halide crystals at low-temperature uniaxial deformation

2020

The efficiency of stabilization of H centers as well as its dependence on the degree of uniaxial deformation are considered within the framework of the modified geometric model of alkali halides. It is shown that stabilization of H centers is difficult in KI and RbI crystals, while in other NaCl-type crystals it becomes quite probable. Under uniaxial deformation, the interstitial space, in which the defect will be located, decreases, and the efficiency decrease. In the case of cesium halides, the orientation of the H centers takes place predominantly in the direction; therefore, the criteria for their stabilization differ from the NaCl-type alkali halide crystals. According to calculations,…

010302 applied physicsMaterials sciencePhysics and Astronomy (miscellaneous)General Physics and AstronomyHalideUniaxial compressionchemistry.chemical_elementCenter (group theory)Deformation (meteorology)Alkali metal01 natural sciencesMolecular physicsIonchemistryCaesium0103 physical sciences010306 general physicsLow Temperature Physics
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An Energy Saving Mechanism Based on Vacation Queuing Theory in Data Center Networks

2018

To satisfy the growing need for computing resources, data centers consume a huge amount of power which raises serious concerns regarding the scale of the energy consumption and wastage. One of the important reasons for such energy wastage relates to the redundancies. Redundancies are defined as the backup routing paths and unneeded active ports implemented for the sake of load balancing and fault tolerance. The energy loss may also be caused by the random nature of incoming packets forcing nodes to stay powered on all the times to await for incoming tasks. This paper proposes a re-architecturing of network devices to address energy wastage issue by consolidating the traffic arriving from di…

010302 applied physicsQueueing theorybusiness.industryComputer scienceNetwork packet020206 networking & telecommunicationsFault tolerance02 engineering and technologyEnergy consumptionData center networksLoad balancing (computing)01 natural sciencesNetworking hardwareBackupPower consumption0103 physical sciencesVacation queuing theory0202 electrical engineering electronic engineering information engineeringData centerbusinessComputer network
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The history and future challenges associated with the hydrogenation of vinyl fluorides

2018

Abstract Catalytic hydrogenation is one of the most powerful transformations available in synthetic chemistry; there have been three Nobel Laureates rewarded for their work in the field. Despite the advances in substrate scope and the development of enantioselective versions of this transformation, vinyl fluorides remain somewhat underrepresented. Successful hydrogenation of vinyl fluorides can give rise to a fluorine-containing stereocenter, an important feature which has great potential in many areas of chemistry. This review aims to explore the history of vinyl fluorides as substrates in hydrogenation reactions, and to highlight modern day challenges and unresolved issues regarding this …

010405 organic chemistryChemistryOrganic ChemistryEnantioselective synthesisNanotechnology010402 general chemistry01 natural sciencesBiochemistry0104 chemical sciencesStereocenterInorganic ChemistryEnvironmental ChemistryPhysical and Theoretical ChemistryCatalytic hydrogenationJournal of Fluorine Chemistry
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Proline-Modified Porphyrin Catalysts for Enantioselective Epoxidations: Design, Synthesis, and Reactivity

2004

International audience; The syntheses of various strapped and −picket-fence× chiral porphyrins are described, and their reactivities towards the enantioselective epoxidation of alkenes are reported. Four L-proline residues provide the chiralityfor the various meso-substituted catalysts, which differ by either the spatial arrangement of the stereogenic centers or the nature and length of the straps. The resulting bridged structures possess four amide linkages ineach strap, leading to highly rigid molecules with well-defined geometries whereas the strapped Fe catalysts gave rise to only moderate enantioselectivities, the C2-symmetrical ones being superior to the D2-symmetrical compounds. The …

010405 organic chemistryChemistryStereochemistryOrganic ChemistryEnantioselective synthesis010402 general chemistry01 natural sciencesBiochemistryPorphyrin[ CHIM ] Chemical SciencesCatalysis0104 chemical sciencesStereocenterCatalysisInorganic Chemistrychemistry.chemical_compoundAmideDrug DiscoveryMolecule[CHIM]Chemical SciencesReactivity (chemistry)Physical and Theoretical ChemistryChirality (chemistry)
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The Fluoro-Pauson-Khand Reaction in the Synthesis of Enantioenriched Nitrogenated Bicycles Bearing a Quaternary C-F Stereogenic Center

2019

The authors are grateful to the Spanish MICINN and the AEI (CTQ2017-84249-P) for financial support, the SCSIE (Universitat de Valencia) for access to instrumental facilities, and M. ̀ R. Pedrosa (Universidad de Burgos) for providing us with MoO2Cl2. The technical and human support provided by SGIker (UPV/EHU, MINECO, GV/DJ, ERDF, and ESF) is also gratefully acknowledged. P.B. thanks the Spanish Ministry of Economy for a Ramon y Cajal contract (RyC-2016-20951). ́ The authors are also grateful to Jose Cabeza for assistance in the synthesis of certain starting materials.

010405 organic chemistryChemistryStereochemistryPauson–Khand reactionOrganic ChemistryPhysical and Theoretical Chemistry010402 general chemistry01 natural sciencesBiochemistry0104 chemical sciencesStereocenter
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Asymmetric Synthesis of Spiro β-Lactamsviaa Squaramide- Catalyzed Sulfa-Michael Addition/Desymmetrization Protocol

2016

An efficient asymmetric synthesis of spirocyclohexenone β-lactams bearing three contiguous stereocenters has been achieved in moderate to good yields and high stereoselectivities. The protocol involves the combination of a squaramide-catalyzed sulfa-Michael addition under desymmetrization via a dynamic kinetic resolution of racemic 2,5-cyclohexadienones.

010405 organic chemistryChemistryStereochemistrybeta-lactamsasymmetric synthesisEnantioselective synthesisSquaramideGeneral Chemistry010402 general chemistry01 natural sciencesDesymmetrization0104 chemical sciencesKinetic resolutionStereocenterCatalysisOrganocatalysisMichael reactionta116Advanced Synthesis & Catalysis
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Squaramide-Catalyzed Asymmetric aza-Friedel-Crafts/N,O-Acetalization Domino Reactions Between 2-Naphthols and Pyrazolinone Ketimines

2017

N-Boc ketimines derived from pyrazolin-5-ones were explored to develop an unprecedented domino aza-Friedel-Crafts/N,O-acetalization reaction with 2-naphthols. The novel method requires a catalyst loading of only 0.5 mol % of a bifunctional squaramide catalyst, is scalable to gram amounts, and provides a new series of furanonaphthopyrazolidinone derivatives bearing two vicinal tetra-substituted stereogenic centers in excellent yields (95-98 %) and stereoselectivity (>99:1 d.r. and 97-98 % ee). A different reactivity was observed in the case of 1-naphthols and other electron-rich phenols, which led to the aza-Friedel-Crafts adducts in 70-98 % yield and 47-98 % ee.

010405 organic chemistryChemistrydomino reactionsEnantioselective synthesisSquaramideGeneral MedicineGeneral Chemistry010402 general chemistry01 natural sciencesMedicinal chemistryCatalysisDomino0104 chemical sciencesStereocenterCatalysischemistry.chemical_compoundOrganocatalysisYield (chemistry)StereoselectivityReactivity (chemistry)Bifunctionalta116Friedel–Crafts reactionAngewandte Chemie International Edition
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Enantioselective synthesis of chiral oxazolines from unactivated ketones and isocyanoacetate esters by synergistic silver/organocatalysis

2018

[EN] A multicatalytic approach that combines a bifunctional Brønsted base¿squaramide organocatalyst and Ag+ as Lewis acid has been applied in the reaction of unactivated ketones with tert-butyl isocyanoacetate to give chiral oxazolines bearing a quaternary stereocenter. The formal [3+2] cycloaddition provided high yields of the corresponding cis-oxazolines with good diastereoselectivity and excellent enantioselectivity, being applied to aryl¿alkyl and alkyl¿alkyl ketones.

010405 organic chemistryMetals and AlloysEnantioselective synthesisGeneral Chemistry010402 general chemistry01 natural sciencesCombinatorial chemistryCatalysisCycloaddition0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsStereocenterchemistry.chemical_compoundchemistryCatàlisiFISICA APLICADAOrganocatalysisMaterials ChemistryCeramics and CompositesLewis acids and basesBifunctionalQuímica orgànica
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Amino‐Substituted Ferra‐bis(tricarbollides) − Metallatricarbaboranes Designed for Linear Molecular Constructions

2004

Reactions between high purity FeCl2 and the anion [nido-7-(tBuHN)-7,8,9-C3B8H10)]− (1−) have been used for efficient syntheses of the twelve-vertex double-cluster metallatricarbollide complexes of the para,para (p,p) type [closo-9,9′(RHN)2-commo-2,2′-FeII-1,7,9-(C3B8H10)-1′,7′,9′-(C3B8H10)] (2) (2a, R = tBu and 2b, R = H) (yields 42−45% for 2a). Compound 2b, which contains two reactive amino substituents conveniently attached to the tricarbollide subclusters in p-positions with respect to the metal center, was prepared via facile cleavage of the tBu substituent in 2a either by AlCl3 or by thermal means. The structure of 2b constitutes a good setting for the synthesis of building blocks for …

010405 organic chemistryStereochemistryCenter (category theory)SubstituentBoranes010402 general chemistryCleavage (embryo)01 natural sciencesMedicinal chemistry0104 chemical sciencesIonInorganic ChemistryMetalchemistry.chemical_compoundchemistryvisual_artReagentvisual_art.visual_art_mediumEuropean Journal of Inorganic Chemistry
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