Search results for "periodi"

showing 10 items of 1017 documents

"Płynie Wisła, płynie..." : motyw rzeki w literaturze międzywojennego "Płomyka" (1917-1939)

2017

"Płomyk" (1917-1939)periodical pressmotif ot riveryouth literature
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A half-metallic half-Heusler alloy having the largest atomic-like magnetic moment at optimized lattice constant

2016

For half-Heusler alloys, the general formula is XYZ, where X can be a transition or alkali metal element, Y is another transition metal element, typically Mn or Cr, and Z is a group IV element or a pnicitide. The atomic arrangements within a unit-cell show three configurations. Before this study, most of the predictions of half-metallic properties of half-Heusler alloys at the lattice constants differing from their optimized lattice constant. Based on the electropositivity of X and electronegativity of Z for half-Heusler alloys, we found that one of the configurations of LiCrS exhibits half-metallic properties at its optimized lattice constant of 5.803Å, and has the maximum atomic-like magn…

010302 applied physicsCondensed matter physicsMagnetic momentChemistryAlloyGeneral Physics and Astronomy02 engineering and technologyengineering.material021001 nanoscience & nanotechnologyAlkali metal01 natural scienceslcsh:QC1-999ElectronegativityMetalCondensed Matter::Materials ScienceLattice constantTransition metalGroup (periodic table)visual_art0103 physical sciencesengineeringvisual_art.visual_art_medium0210 nano-technologylcsh:PhysicsAIP Advances
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Structure and dielectric properties of Na0.5Bi0.5TiO3-CaTiO3 solid solutions

2016

Despite wide studies of Na0.5Bi0.5TiO3, structure of this material and its connection with the observed physical properties still raise numerous questions due to mutually contradicting results obtained. Here, structure and dielectric properties of poled and unpoled Na0.5Bi0.5TiO3-CaTiO3 solid solutions are studied, projecting the obtained concentration dependence of structure and dielectric properties on pure Na0.5Bi0.5TiO3 as the end member of this material group. X-ray diffraction patterns for Na0.5Bi0.5TiO3-CaTiO3 solid solutions reveal dominating of an orthorhombic Pnma phase, even for the compositions approaching the end composition (Na0.5Bi0.5TiO3), whereas structure of pure Na0.5Bi0.…

010302 applied physicsDiffractionMaterials scienceCondensed matter physicsStructure (category theory)General Physics and Astronomy02 engineering and technologyDielectric021001 nanoscience & nanotechnology01 natural sciencesCrystallographyGroup (periodic table)Phase (matter)Distortion0103 physical sciencesOrthorhombic crystal system0210 nano-technologySolid solutionJournal of Applied Physics
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Assembling Halogen-Bonded Capsules via Cation Exchange

2017

Dr. Lotta Turunen is currently a postdoctoral researcher within Acad. Prof. Kari Rissanen's research group at the University of Jyvaskyla in Finland. Under his supervision, she obtained her MSc in organic chemistry and completed her PhD in chemistry in late September 2017. Her research focused on designing, synthesizing, and characterizing halogen-bonded supramolecular assemblies, capsules, and cages.

010405 organic chemistryChemistryGeneral Chemical EngineeringBiochemistry (medical)Supramolecular chemistryNanotechnologyGeneral Chemistry010402 general chemistry01 natural sciencesBiochemistry0104 chemical sciencesGroup (periodic table)HalogenMaterials ChemistryEnvironmental ChemistryOrganic chemistryChem
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Towards the synthesis of substituted porphyrins by a pyridyl group bearing a reactive functionality

2010

Pyridyl-substituted porphyrins bearing a reactive functionality were prepared via Suzuki cross-coupling reactions and resulted in very good yields. These compounds are precursors of new porphyrin architectures able to coordinate two metals: one in the porphyrin core and the second around the pyridyl moiety. During the coupling reactions, a higher reactivity of a chloro picolyl group was evidenced compared to a bromo function on the same reacting molecule.

010405 organic chemistryChemistryStereochemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryGeneral Chemistry010402 general chemistry01 natural sciencesPorphyrinCoupling reaction0104 chemical sciencesA3B-porphyrinschemistry.chemical_compoundSuzuki reactionGroup (periodic table)[ CHIM.ORGA ] Chemical Sciences/Organic chemistryPolymer chemistrypolycyclic compoundsMoietyMoleculeheterocyclic compoundsReactivity (chemistry)meso-functionalizationSuzuki couplingpyridyl substituted porphyrinsComputingMilieux_MISCELLANEOUS
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A polar/π model of interactions explains face-to-face stacked quinoid rings: a case study of the crystal of potassium hydrogen chloranilate dihydrate

2015

International audience; The nature of interactions between face-to-face staggered stacked quinoid rings with pi-systems, observed with a short inter-ring centroid. centroid distance, is analyzed by experimental and theoretical methods. Charge density studies based on X-ray diffraction and DFT calculations, complemented by impedance spectroscopy, were employed to define the electronic and structural characteristics of the quinoid rings responsible for their interactions within the crystal packing. The crystal packing is mainly stabilized by strong electrostatic interactions between the K+ cation and the hydrogen chloranilate anion. The proximity and orientation of the stacked quinoid rings i…

010405 organic chemistryHydrogen bondChemistryStackingCharge densityGeneral ChemistryElectronic structure010402 general chemistryCondensed Matter PhysicsElectrostaticsCrystal engineeringpi-interactions ; chloranilic acid ; X-ray charge density ; periodic DFT ; intermolecular interaction01 natural sciences0104 chemical sciencesIon[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryCrystalCrystallography[CHIM.CRIS]Chemical Sciences/CristallographyGeneral Materials Science
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The Cu(II) complex of a C-lipophilized 13aneN4 macrocycle with an additional protonable amino group as micellar anion receptor.

2009

Three 13aneN4 macrocyclic ligands have been prepared bearing a -CH(2)NHR side arm (R = H, n-C(5)H(11), n-C(10)H(21)) on a carbon atom. When Cu(2+) is complexed in the macrocyclic ring, the amino group of the side arm undergoes an acid-base protonation equilibrium but it is not able to coordinate apically the metal cation even when it is deprotonated. The Cu(2+) complex with the ligand bearing the longest appended aliphatic chain is fully confined inside Triton X-100 micelles, and its ability to bind and sequestrate a series of anions inside micelles has been studied at two different pH values, i.e. both with protonated and neutral side-arm amino group. The favourable role played by the prot…

010405 organic chemistryLigandStereochemistryChemistryProtonation010402 general chemistryRing (chemistry)01 natural sciencesMicelle0104 chemical sciencesInorganic ChemistryMetalDeprotonationGroup (periodic table)visual_artvisual_art.visual_art_mediumAnion receptorDalton transactions (Cambridge, England : 2003)
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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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Substituent effect on the σ- and π-electron structure of the nitro group and the ring in meta- and para-substituted nitrobenzenes

2017

An application of quantum chemical modeling allowed us to investigate a substituent effect on a σ and π electron structure of a ring and the nitro group in a series of meta- and para-X-substituted nitrobenzene derivatives (X = NMe2, NHMe, NH2, OH, OMe, Me, H, F, Cl, CF3, CN, CHO, COMe, CONH2, COOH, NO2, and NO). The obtained pEDA and sEDA parameters (the π- and σ-electron structure characteristics of a given planar fragment of the system obtained by the summation of π- and σ-orbital occupancies, respectively) of the NO2 group and the benzene ring allowed us to reveal the impact of the substituents on their mutual relations as well as to analyze them from the viewpoint of substituent charact…

010405 organic chemistryStereochemistrySubstituent010402 general chemistryRing (chemistry)Resonance (chemistry)01 natural sciences0104 chemical sciencesNitrobenzeneElectronegativitychemistry.chemical_compoundCrystallographychemistryGroup (periodic table)NitroPhysical and Theoretical ChemistryBenzeneJournal of Physical Chemistry A
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Essential features of the polytypic charoite-96 structure compared to charoite-90

2011

AbstractCharoite, ideally (K,Sr,Ba,Mn)15–16(Ca,Na)32[(Si70(O,OH)180)](OH,F)4·nH20, is a rock-forming mineral from the Murun massif in Yakutia, Sakha Republic, Siberia, Russia, where it occurs in a unique alkaline intrusion. Charoite occurs as four different polytypes, which are commonly intergrown in nanocrystallme fibres. We report the structure of charoite-96(a =32.11(6),b =19.77(4),c =7.23(1) Å, β = 95.85(9)°,V =4565(24) Å3, space groupP21/m),which was solvedab initioby direct methods on the basis of 2676 unique electron diffraction reflections collected by automated diffraction tomography and refined toR1/wR2=0.34/0.37. The structure of charoite-96 is related to that of the charoite-90,…

010504 meteorology & atmospheric sciencesElectron crystallographyAb initiocrystal structure analysisengineering.material010502 geochemistry & geophysicscharoite polytypes01 natural sciencesSilicateNanocrystalline materialchemistry.chemical_compoundCrystallographyelectron crystallographychemistryOctahedronElectron diffractionGeochemistry and PetrologyGroup (periodic table)Charoitecharoite polytypes; crystal structure analysis; electron crystallography; electron diffraction; electron diffraction tomographyengineeringelectron diffractionelectron diffraction tomography0105 earth and related environmental sciences
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