Search results for "kiteet"

showing 10 items of 33 documents

Strong absorption and ultrafast localisation in NaBiS2 nanocrystals with slow charge-carrier recombination.

2022

Funder: AiF Project, no: ZIM-KK5085302DF0

NaBiS2 I V VI2 chalcogenides nanocrystals/639/638/298/917/147/3/145nanomateriaalitGeneral Physics and AstronomyGeneral Biochemistry Genetics and Molecular BiologyGeneticsvalokennot/128/140/146/140/125Multidisciplinary34 Chemical SciencesarticleGeneral Chemistrykiteet/119/118/147/28/639/301/299/946vismuttiFOS: Biological sciences3406 Physical Chemistryohutkalvot51 Physical Sciences/147/143
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Polymorphism in a π stacked Blatter radical: structures and magnetic properties of 3-(phenyl)-1-(pyrid-2-yl)-1,4-dihydrobenzo[ e ][1,2,4]triazin-4-yl

2020

International audience; 3-(Phenyl)-1-(pyrid-2-yl)-1,4-dihydrobenzo[e][1,2,4]triazin-4-yl (2) demonstrates the first example of polymorphism in the family of Blatter radicals. Two polymorphs, 2α and 2β, have been identified and characterized by single crystal X-ray diffractometry and magnetic susceptibility measurements to investigate their magnetism–structure correlations. Both polymorphs form one-dimensional (1D) π stacks of evenly spaced radicals with distinctly different π–π overlap modes. Within the 1D π stacks, radicals are located at evenly interplanar distances, 3.461 Å for 2α and 3.430 Å for 2β. Magnetic susceptibility studies indicate that both polymorphs exhibit antiferromagnetic …

Phase transitionmagneettiset ominaisuudetMaterials scienceSpins010405 organic chemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryRadicalGeneral Chemistryvapaat radikaalitkiteet010402 general chemistryCondensed Matter Physics01 natural sciencesMagnetic susceptibility0104 chemical sciencesCrystallographyPolymorphism (materials science)[CHIM.CRIS]Chemical Sciences/CristallographyAntiferromagnetismGeneral Materials ScienceSingle crystalQuantumorgaaniset yhdisteet
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The Importance of Electronic Dimensionality in Multiorbital Radical Conductors.

2019

The exceptional performance of oxobenzene-bridged bis-1,2,3-dithiazolyls 6 as single-component neutral radical conductors arises from the presence of a low-lying π-lowest unoccupied molecular orbital, which reduces the potential barrier to charge transport and increases the kinetic stabilization energy of the metallic state. As part of ongoing efforts to modify the solid-state structures and transport properties of these so-called multiorbital materials, we report the preparation and characterization of the acetoxy, methoxy, and thiomethyl derivatives 6 (R = OAc, OMe, SMe). The crystal structures are based on ribbonlike arrays of radicals laced together by S···N' and S···O' secondary bondin…

Steric effects010405 organic chemistryChemistryRadicalElectronic structureCrystal structuremultiorbital radical conductors010402 general chemistryvapaat radikaalitkiteet01 natural sciencessähkönjohtavuus0104 chemical sciencesInorganic ChemistryCrystallographyelectronic dimensionalityElectronic effectAntiferromagnetismMolecular orbitalDensity functional theoryPhysical and Theoretical Chemistryta116Inorganic chemistry
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Stacking of Sterically Congested Trifluoromethylated Aromatics in their Crystals – The Role of Weak F···π or F···F Contacts

2020

European journal of organic chemistry : EurJOC 2020(38), 6073-6077 (2020). doi:10.1002/ejoc.202001008

Steric effectsaromaattiset yhdisteetChemistryOrganic ChemistryStackingstacking interactionskiteet540fluoriCrystallographyddc:540solid-state structurescrystalssupramolekulaarinen kemiafluorinated compoundsPhysical and Theoretical Chemistryröntgenkristallografiatrifluoromethyl substituents
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Nonlinear optical properties of diaromatic stilbene, butadiene and thiophene derivatives

2021

Series of highly polar stilbene (1a–e), diphenylbutadiene (2a–c) and phenylethenylthiophene (3a–c) derivatives were prepared via Horner–Wadsworth–Emmons method with a view to produce new and efficient materials for second harmonic generation (SHG) in the solid-state. The single-crystal X-ray structures of compounds 1–3 reveal extensive polymorphism and a peculiar photodimerization of the 2-chloro-3,4-dimethoxy-4′-nitrostilbene derivative 1a to afford two polymorphs of tetra-aryl cyclobutane 4. The stilbene congeners 2-chloro-3,4-dimethoxy-4′-nitrostilbene (1a·non-centro), 5-bromo-2-hydroxy-3-nitro-4′-nitrostilbene (1b) and 4-dimethylamino-4′-nitrostilbene (1e), as well as 4′-fluoro-4′′-nitr…

aromaattiset yhdisteet010405 organic chemistrySecond-harmonic generationbutadieeniGeneral ChemistryConjugated systemChromophoreoptiset ominaisuudetkiteet010402 general chemistry01 natural sciencesFluorescenceCatalysis0104 chemical sciencesCyclobutaneCrystallographychemistry.chemical_compoundNonlinear opticalPolymorphism (materials science)chemistrystilbeenitMaterials ChemistryUreaorgaaniset yhdisteetNew Journal of Chemistry
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Assembly and dichroism of a four-component halogen-bonded metal-organic cocrystal salt solvate involving dicyanoaurate(I) acceptors

2017

We describe the use of dicyanoaurate ions as linear ditopic metal–organic acceptors for the halogen bond-driven assembly of a dichroic metal–organic cocrystal based on azobenzene chromophores. Structural analysis by single crystal X-ray diffraction revealed that the material is a four-component solid, consisting of anticipated anionic metal–organic halogen-bonded chains based on dicyanoaurate ions, as well as complex potassium-based cations and discrete molecules of the crown ether 15-crown-5. Importantly, the structural analysis revealed the parallel alignment of the halogen-bonded chains required for dichroic behaviour, confirming that crystal engineering principles developed for the desi…

chemistry.chemical_classification010405 organic chemistryContext (language use)Dichroismorganometalliyhdisteet010402 general chemistryDichroic glassCrystal engineeringkiteet01 natural sciencesCocrystal0104 chemical scienceschemistry.chemical_compoundCrystallographyAzobenzenechemistryorganometallic compoundscrystalsMoleculePhysical and Theoretical Chemistryta116Crown etherFaraday Discussions
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Computational and theoretical studies on lattice thermal conductivity and thermal properties of silicon clathrates

2016

The lattice thermal conductivity is usually an intrinsic property in the study of thermoelectricity. In particular, relatively low lattice thermal conductivity is usually a desired feature when higher thermoelectric efficiency is pursued. The mechanisms which lower the lattice thermal conductivity are not known in sufficient detail and deeper understanding about the phenomena is needed and if such understanding is achieved it can be used to design more efficient thermoelectric materials. In this thesis, the lattice thermal conductivity and other thermal properties of several silicon clathrates, which are known to be promising candidates for the thermoelectric applications, are studied by theoreti…

clathratespiiphononsmany-body perturbation theorykiteetCondensed Matter::Materials Sciencehilarakenneklatraatitpuolijohteetlämmön johtuminenthermal conductivityGreen's functionslattice dynamicslämpösähköiset materiaalitlämpölaajeneminenthermal expansionfononit
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Role of Weak Hydrogen Bonds and Halogen Bonds in 5-Halo-1,3-dimethyluracils and Their Cocrystals—A Combined Experimental and Computational Study

2016

Seven single crystals containing either N,N-dimethyluracil (DMHU) or one of its 5-halogenated derivatives (DMXU; X = F, Cl, Br, I) were prepared using N,N-dimethylformamide as the crystallization solvent. Single crystal X-ray diffraction and quantum chemical calculations carried out at the spin component scaled local MP2 level of theory were then used to study the intramolecular halogen and nonconventional hydrogen bonds present in the structures. The results were compared to and contrasted with the previously reported data for uracil and its halogenated derivatives. In particular, the intermolecular interactions in DMIU were compared to the halogen and hydrogen bonds in 5-iodouracil that, …

computational studieshalogen bondsInorganic chemistryhydrogen bonds; computational analysis; computational studieschemistry010402 general chemistry01 natural sciencesGeneral Materials Sciencecocrystalsta116Degree of unsaturationvetysidoksetHalogen bondyhteiskiteet010405 organic chemistryHydrogen bondChemistryIntermolecular forceGeneral ChemistryCondensed Matter Physics0104 chemical sciencesSolventCrystallographycomputational analysisIntramolecular forcehydrogen bondsHalogenhalogeenisidoksetSingle crystalCrystal Growth & Design
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Host-guest complexes of C-propyl-2-bromoresorcinarene with aromatic N-oxides*

2018

The host-guest complexes of C-propyl-2-bromoresorcinarene with pyridine N-oxide, 3-methylpyridine N-oxide, quinoline N-oxide and isoquinoline N-oxide are studied using single crystal X-ray crystallography and 1H NMR spectroscopy. The C-propyl-2-bromoresorcinarene forms endo-complexes with the aromatic N-oxides in the solid-state when crystallised from either methanol or acetone. In solution, the endo-complexes were observed only in methanol-d4. In DMSO the solvent itself is a good guest, and crystallisation provides only solvate endo-complexes. The C-propyl-2-bromoresorcinarene shows remarkable flexibility when crystallised from either methanol or acetone, and packs into one-dimensional sel…

crystal structurekemiaSupramolecular chemistryCrystal structurechemistry010402 general chemistry01 natural scienceschemistry.chemical_compoundPolymer chemistryPyridinecrystalssupramolekulaarinen kemiaAcetoneresorcinarenesmoleculesIsoquinolineta116Biochemistry Biophysics and Structural Biologyvetysidoksetta114010405 organic chemistryHydrogen bondQuinolinemolekyylitGeneral Chemistrykiteet0104 chemical sciencesaromatic N-oxidesSolventChemistrychemistryvetyhydrogenhydrogen bondsSupramolecular chemistrySUPRAMOLECULAR CHEMISTRY
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A second solvatomorph of poly[[μ4-N,N′-(1,3,5-oxadiazinane-3,5-diyl)bis(carbamoylmethanoato)]nickel(II)dipotassium] : crystal structure, Hirshfeld su…

2021

The title compound, poly[triaquabis[μ4-N,N′-(1,3,5-oxadiazinane-3,5-diyl)bis(carbamoylmethanoato)]dinickel(II)tetrapotassium], [K4Ni2(C7H6N4O7)2(H2O)3] n , is a second solvatomorph of poly[(μ4-N,N′-(1,3,5-oxadiazinane-3,5-diyl)bis(carbamoylmethanoato)nickel(II)dipotassium] reported previously [Plutenko et al. (2021). Acta Cryst. E77, 298–304]. The asymmetric unit of the title compound includes two structurally independent complex anions [Ni(C7H6N4O7)]2−, which exhibit an L-shaped geometry and consist of two almost flat fragments perpendicular to one another: the 1,3,5-oxadiazinane fragment and the fragment including other atoms of the anion. The central Ni atom is in a square-planar N2O2 co…

crystal structureshape analysischemistry.chemical_elementCrystal structureEnergy minimizationIonpseudomacrocyclic ligandCrystalchemistry.chemical_compoundtemplate reactionSHAPE analysisAmidehirshfeld surface analysisAtomHirshfeld surface analysisGeneral Materials Sciencesemi-empirical geometry optimizationCrystallographynickel(ii) complexGeneral ChemistrykompleksiyhdisteetCondensed Matter Physicsnickel(II) complexkiteetTemplate reactionNickelCrystallographychemistryQD901-999nikkelihydrazide-based ligand
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