Search results for " Crystal Engineering"

showing 4 items of 4 documents

Aurophilicity as a cofactor in crystal engineering. Dicyanoaurate(I) anion as a building block in a novel Co(II)–Au(I) bimetallic assembly

2002

A 2D grid-shaped cyanide-bridged Co(II)–Au(I) bimetallic coordination polymer, [Co(DMF)2{Au(CN)2}2], has been prepared from the [Au(CN)2]2 building block; sheets associate pair-wise by aurophilic interactions and the compound exhibits zeolite-like properties. Lloret Pastor, Francisco, Francisco.Lloret@uv.es

AurophilicityStereochemistryCoordination polymerZeolite-like propertiesUNESCO::QUÍMICACrystal engineering010402 general chemistryCrystal engineering01 natural sciencesAurophilicity:QUÍMICA [UNESCO]CatalysisCofactorIonchemistry.chemical_compoundMaterials ChemistryBimetallic stripAurophilicity ; Crystal engineering ; Bimetallic ; Zeolite-like propertiesBimetallicbiologyUNESCO::QUÍMICA::Química inorgánica010405 organic chemistryChemistryMetals and AlloysGeneral ChemistryBlock (periodic table):QUÍMICA::Química inorgánica [UNESCO]3. Good health0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyCeramics and Compositesbiology.protein
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Naturally occurring polyphenols as building blocks for supramolecular liquid crystals – substitution pattern dominates mesomorphism

2021

A modular supramolecular approach towards hydrogen-bonded liquid crystalline assemblies based on naturally occurring polyphenols is reported. The combination of experimental observations, crystallographic studies and semi-empirical analyses of the assemblies provides insight into the structure–property relationships of these materials. Here a direct correlation of the number of donor OH-groups as well as their orientation with the mesomorphic behavior is reported. We discovered that the number and orientation of the OH-groups have a stronger influence on the mesomorphic behavior of the supramolecular assemblies than the connectivity (e.g. stilbenoid or chalconoid) of the hydrogen bond donor…

ChemistryHydrogen bondLiquid crystallineProcess Chemistry and TechnologyChemieBiomedical EngineeringSupramolecular chemistryEnergy Engineering and Power Technology02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesIndustrial and Manufacturing Engineering0104 chemical sciencesCrystallographyChemistry (miscellaneous)Liquid crystalSupramolecular Chemistry Liquid Crystals Crystal Engineering Hydrogen BondingMaterials ChemistryChemical Engineering (miscellaneous)Settore CHIM/07 - Fondamenti Chimici Delle Tecnologie0210 nano-technologyMolecular Systems Design & Engineering
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Chiral mesophases of hydrogen-bonded liquid crystals

2020

The chiral induction in hydrogen-bonded liquid crystals is investigated. The experimental study was accompanied by detailed density functional theory calculations and variable-temperature solid-state deuteron NMR measurements indicating that interactions between the linking groups of the hydrogen-bond accepting unit play a key role in the chiral induction.

Materials scienceHydrogenProcess Chemistry and TechnologyBiomedical EngineeringChemieEnergy Engineering and Power Technologychemistry.chemical_element02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesIndustrial and Manufacturing Engineering0104 chemical sciencesCrystallographychemistryDeuteriumChemistry (miscellaneous)Liquid crystalMaterials ChemistryChemical Engineering (miscellaneous)Supramolecular Chemistry Liquid Crystals Chirality Hydrogen Bonding Crystal EngineeringDensity functional theorySettore CHIM/07 - Fondamenti Chimici Delle Tecnologie0210 nano-technologyChiral induction
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6-Methyluracil: a redetermination of polymorph (II)

2019

6-Methyluracil, C5H6N2O2, exists in two crystalline phases: form (I), monoclinic, space group P21/c [Reck et al. (1988). Acta Cryst. A44, 417–421] and form (II), monoclinic, space group C2/c [Leonidov et al. (1993). Russ. J. Phys. Chem. 67, 2220–2223]. The structure of polymorph (II) has been redetermined providing a significant increase in the precision of the derived geometric parameters. In the crystal, molecules form ribbons approximately running parallel to the c-axis direction through N—H...O hydrogen bonds. The radical differences observed between the crystal packing of the two polymorphs may be responsible in form (II) for an increase in the contribution of the polar canonical forms…

supramolecular chemistry; crystal engineering; nucleobasecrystal structure010405 organic chemistryChemistryHydrogen bondUracilCrystal structurenucleobases010402 general chemistry01 natural sciencessupramolecular chemistry0104 chemical sciencesNucleobaseCrystalchemistry.chemical_compoundCrystallographycrystal engineeringGroup (periodic table)lcsh:QD901-999Canonical formlcsh:CrystallographynucleobaseMonoclinic crystal systemIUCrData
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