Search results for "nimi"

showing 10 items of 596 documents

CCDC 1414523: Experimental Crystal Structure Determination

2016

Related Article: Vanessa Soto-Cerrato, Pilar Manuel-Manresa, Elsa Hernando, Silvia Calabuig-Fariñas, Alicia Martínez-Romero, Víctor Fernández-Dueñas, Kristoffer Sahlholm, Thomas Knöpfel, María García-Valverde, Ananda M. Rodilla, Eloisa Jantus-Lewintre, Rosa Farràs, Francisco Ciruela, Ricardo Pérez-Tomás, and Roberto Quesada|2015|J.Am.Chem.Soc.|137|15892|doi:10.1021/jacs.5b09970

(5-(1H-indol-2-yl)-3-methoxy-1H-pyrrol-2-yl)-N-(2-phenylethyl)methaniminium chlorideSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 986951: Experimental Crystal Structure Determination

2014

Related Article: Ivan I. Eliseev, Pavel V. Gushchin, Yi-An Chen, Pi-Tai Chou, Matti Haukka, Galina L. Starova, Vadim Yu. Kukushkin|2014|Eur.J.Inorg.Chem.||4101|doi:10.1002/ejic.201402364

(N-(Anilino(phenylamino)methylene)ethanimidamidato)-(bis(2-pyridyl)amine-NN')-platinum trifluoromethanesulfonateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1835082: Experimental Crystal Structure Determination

2018

Related Article: Jamal Lasri, Ali I. Ismail, Matti Haukka, Saied M. Soliman|2015|Spectrochim.Acta,Part A|136|1857|doi:10.1016/j.saa.2014.10.096

(Z)-N-methyl(246-trimethylphenyl)methanimine N-oxideSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1919442: Experimental Crystal Structure Determination

2019

Related Article: Jana Anhäuser, Rakesh Puttreddy, Lukas Glanz, Andreas Schneider, Marianne Engeser, Kari Rissanen, Arne Lützen|2019|Chem.-Eur.J.|25|12294|doi:10.1002/chem.201903164

(rac)-hexakis(mu-NN'-[tricyclo[8.2.2.247]hexadeca-1(12)46101315-hexaene-512-diylbis(41-phenylene)]bis[1-(pyridin-2-yl)methanimine])-tetra-iron(ii) octakis(trifluoromethanesulfonate) unknown solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1919440: Experimental Crystal Structure Determination

2019

Related Article: Jana Anhäuser, Rakesh Puttreddy, Lukas Glanz, Andreas Schneider, Marianne Engeser, Kari Rissanen, Arne Lützen|2019|Chem.-Eur.J.|25|12294|doi:10.1002/chem.201903164

ΔΔΔ)-hexakis(mu-(RP)-NN'-[tricyclo[8.2.2.247]hexadeca-1(12)46101315-hexaene-512-diylbis(41-phenylene)]bis[1-(pyridin-2-yl)methanimine])-tetra-iron(ii) octakis(trifluoromethanesulfonate) acetonitrile unknown solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Cryo-EM structure of ssDNA bacteriophage ΦCjT23 provides insight into early virus evolution.

2022

AbstractThe origin of viruses remains an open question. While lack of detectable sequence similarity hampers the analysis of distantly related viruses, structural biology investigations of conserved capsid protein structures facilitate the study of distant evolutionary relationships. Here we characterize the lipid-containing ssDNA temperate bacteriophage ΦCjT23, which infects Flavobacterium sp. (Bacteroidetes). We report ΦCjT23-like sequences in the genome of strains belonging to several Flavobacterium species. The virion structure determined by cryogenic electron microscopy reveals similarities to members of the viral kingdom Bamfordvirae that currently consists solely of dsDNA viruses wit…

/631/326/1321bacteriophagesviruksetcryoelectron microscopyevoluutioGeneral Physics and AstronomyelektronimikroskopiaDNA Single-Stranded/45/23FlavobacteriumGeneral Biochemistry Genetics and Molecular Biologybakteriofagit/631/45/535/1258/1259viral evolution/631/326/596/2554BacteriophagesMultidisciplinaryfylogenia/45fylogenetiikkaCryoelectron Microscopy/101/28articleGeneral Chemistryperimä1182 Biochemistry cell and molecular biologyCapsid Proteins
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Enhanced loss model algorithm for interior permanent magnet synchronous machines

2017

This paper presents an experimental study on the impact of the parameter variations over the performances of a LMA (Loss Model Algorithm) designed for an IPMSM (Interior Permanent Magnet Synchronous Machine). In a previous work, the characterization was carried out by assessing, for several working conditions, the motor parameters that influence the motor efficiency. The proposed enhanced loss model algorithm is implemented in a rapid prototyping system and its performances, in term of efficiency, are compared with other control systems, obtaining promising results.

010302 applied physicsRapid prototypingInterior permanent magnet synchronous motorComputer science020208 electrical & electronic engineeringWork (physics)02 engineering and technologySettore ING-IND/32 - Convertitori Macchine E Azionamenti Elettrici01 natural sciencesDC motorTerm (time)Settore ING-IND/31 - Elettrotecnicaspeed control drive systemsMagnetControl system0103 physical sciences0202 electrical engineering electronic engineering information engineeringTorquepower loss minimizationSettore ING-INF/07 - Misure Elettriche E ElettronicheAlgorithmPermanent magnet synchronous machine2017 AEIT International Annual Conference
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Recent progress in the application of fluorinated chiral sulfinimine reagents

2018

Abstract The development of synthetic methodology allowing for a strategic incorporation of fluorine into target compounds is in a high demand in many areas of the chemical and pharmaceutical industries. In this regard, application of fluorinated chiral sulfinimine reagents, in particularly, N-tert-butylsulfinyl-3,3,3-trifluoroacetaldimine, is one of the most general and practical approaches for preparation of compounds containing pharmacophoric fluoro-amino-keto/hydroxy moieties. This article provides a timely and comprehensive overview of the recent synthetic applications of fluorinated chiral sulfinimine reagents for asymmetric synthesis of fluoro-containing polyfunctional amino-compound…

010405 organic chemistryChemistryOrganic ChemistryEnantioselective synthesisAsymmetric synthesisFluoro-imineAmino compounds010402 general chemistry01 natural sciencesBiochemistryCombinatorial chemistry0104 chemical sciencesInorganic ChemistrySulfinimineReagentEnvironmental ChemistryPhysical and Theoretical ChemistryAmino compounds; Asymmetric synthesis; Fluoro-imine; Sulfinimine; Biochemistry; Environmental Chemistry; Physical and Theoretical Chemistry; Organic Chemistry; Inorganic ChemistryJournal of Fluorine Chemistry
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Aqua Mater: On the Meaning of the Theonym Betatun

2021

La aparición en el entorno del santuario tardoibérico de Las Atalayuelas (Fuerte del Rey – Torredelcampo, Jaén) de una inscripción en la que se documenta el teónimo ibérico Betatun abre nuevas perspectivas en el estudio de la religión ibérica. Con el presente artículo intentamos demostrar que en el nombre de la divinidad está implícito un elemento común que lo relacionaría con una serie de topónimos e hidrónimos, tanto antiguos como modernos, y que no es otro que el agua. The finding of an inscription containing the Iberian theonym Betatun in the surrounding area of the Late Iberian sanctuary in Las Atalayuelas site (Fuerte del Rey – Torredelcampo, Jaén) opens up new perspectives for the st…

010506 paleontologyArcheologyHistory05 social sciencessincretismos050109 social psychologyToponímiaHistòria antigaToponymysantuarios ibéricos01 natural sciencesIberian ShrinesSyncretismsdioses ibéricosHydronymy0501 psychology and cognitive scienceshidronimiaClassicsIberian Godstoponimia0105 earth and related environmental sciences
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Leaf-Level Spectral Fluorescence Measurements : Comparing Methodologies for Broadleaves and Needles

2019

Successful measurements of chlorophyll fluorescence (ChlF) spectral properties (typically in the wavelength range of 650–850 nm) across plant species, environmental conditions, and stress levels are a first step towards establishing a quantitative link between solar-induced chlorophyll fluorescence (SIF), which can only be measured at discrete ChlF spectral bands, and photosynthetic functionality. Despite its importance and significance, the various methodologies for the estimation of leaf-level ChlF spectral properties have not yet been compared, especially when applied to leaves with complex morphology, such as needles. Here we present, to the best of our knowledge, a first comparison of …

0106 biological sciencesCorrection methodMaterials science010504 meteorology & atmospheric sciencesSciencesun-induced fluorescenceAnalytical chemistryleaf morphology01 natural sciencesSpectral lineFluoWatlingonberryLEAVESChlorophyll fluorescence0105 earth and related environmental sciences4112 Forestryphotosynthesischlorophyll fluorescencesilver birchQSpectral propertiesSpectral bandsOPTICAL-PROPERTIESA FLUORESCENCECANOPY-LEVELFluorescencebaseline correctionRATIO F690/F730Integrating sphereLIGHTPHOTOSYSTEM-IPlant speciesScots pineINDUCED CHLOROPHYLL FLUORESCENCEMINIMIZING MEASUREMENT UNCERTAINTIESREVISED MEASUREMENT METHODOLOGYGeneral Earth and Planetary Sciencesbaseline correction; chlorophyll fluorescence; FluoWat; leaf morphology; lingonberry; photosynthesis; Scots pine; silver birch; sun-induced fluorescence010606 plant biology & botany
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