Search results for "röntgenkristallografia"

showing 10 items of 57 documents

The Effect of the Side Chain on Gelation Properties of Bile Acid Alkyl Amides

2021

Abstract Six bile acid alkyl amide derivatives were studied with respect to their gelation properties. The derivatives were composed of three different bile acids with hexyl or cyclohexyl side chains. The gelation behaviour of all six compounds were studied for 36 solvents with varying polarities. Gelation was observed mainly in aromatic solvents, which is characteristic for bile‐acid‐based low molecular weight gelators. Out of 108 bile acid‐solvent combinations, a total of 44 gel systems were formed, 28 of which from lithocholic acid derivatives, only two from deoxycholic acid derivatives, and 14 from cholic acid derivatives. The majority of the gel systems were formed from bile acids with…

geelitintermolecular interactionssupramolecular gelssolvent influenceCholic AcidAmidesBile Acids and Saltssappihapotamiditbile acid amidessupramolekulaarinen kemiaLithocholic AcidGelsResearch ArticlesröntgenkristallografiaResearch ArticleX-ray crystallography
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Iodine(I) and Silver(I) Complexes of Benzoimidazole and Pyridylcarbazole Derivatives

2021

The synthesis of iodine(I) complexes with either benzoimidazole or carbazole-derived sp 2 N -containing Lewis bases is described, as well as their corresponding silver(I) complexes. The addition of elemental iodine to the linear two-coordinate Ag(I) complexes produces iodine(I) complexes with a three-center four-electron (3c-4e) [N — I — N] + bond. The 1 H and 1 H- 15 N HMBC NMR studies unambiguously confirm the formation of the complexes in all cases via the [N — Ag — N] + → [N — I — N] + cation exchange, with the 15 N NMR chemical shift change between 94 to 111 ppm when compared to the free ligand. The single crystal X-ray crystallographic studies on four I + complexes revealed highly sym…

halogeenitLigandChemical shiftOrganic ChemistrySupramolecular chemistrychemistry.chemical_elementGeneral ChemistryNuclear magnetic resonance spectroscopyhalogen(I)kompleksiyhdisteetIodineCatalysissupramolecular chemistryNMRCrystallographykemialliset sidoksetchemistryX-ray crystallographysupramolekulaarinen kemiahalogen bondLewis acids and basesNMR-spektroskopiaSingle crystalröntgenkristallografiaX-ray crystallography
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Design and construction of halogen-bonded capsules and cages

2017

This thesis describes the design, synthesis and characterization of supramolecular halogen-bonded capsules and cages from multivalent ligands. In the first part of the thesis, an overview to halogen bonding is provided. After discussing the general features of the halogen bonding, the most frequently used halogen bond donors are introduced and examples of their utilization in halogen-bonded systems are discussed. The chapter also presents recent advances made in the field of halogen-bonded supramolecular capsules. The first part of the thesis also includes a review of halogen-bonded complexes involving halonium ions, and a brief introduction to [N···X+···N] halogen bonds is provided along w…

halogeenitcation exchangemolekyylitkompleksiyhdisteetself-assemblycavitandssupramolecular chemistrykavitanditkemialliset sidoksetsupramolekyylikemiahalogen-bonded capsuleshalogen bondhalogeenisidoshalonium ionsmolekyylikapselitröntgenkristallografiaX-ray crystallography
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Comment on "Crystallographic Snapshot of an Arrested Intermediate in the Biomimetic Activation of CO2"

2015

Out of focus: A recent Communication published in this journal describes the synthesis of [nBu4N]HCO3. The authors performed a single-crystal X-ray study that revealed a putative species described as an incipient hydroxide ion engaging in a long, and presumably weak, interaction with CO2. Our recent exploration of the coordination chemistry of CO2 with small ions leads us to believe that such an exceptional bonding situation is unlikely. Instead, we argue that the crystal structure is that of [nBu4N]O2CCH3 and therefore not representative of the bulk powder from the synthesis. peerReviewed

hiilidioksidiX-ray crystallography [structure elucidation]kiderakenteen ratkaisulaskennallinen kemiaröntgenkristallografia
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Comment on “Crystallographic Snapshot of an Arrested Intermediate in the Biomimetic Activation of CO2”

2015

Out of focus: A recent Communication published in this journal describes the synthesis of [nBu4 N]HCO3 . The authors performed a single-crystal X-ray study that revealed a putative species described as an incipient hydroxide ion engaging in a long, and presumably weak, interaction with CO2 . Our recent exploration of the coordination chemistry of CO2 with small ions leads us to believe that such an exceptional bonding situation is unlikely. Instead, we argue that the crystal structure is that of [nBu4 N]O2 CCH3 and therefore not representative of the bulk powder from the synthesis.

hiilidioksidichemistry.chemical_classificationMolecular StructureGeneral ChemistryCrystal structureCarbon Dioxidelaskennallinen kemiaCrystallography X-Raycomputational chemistryCatalysisstructure elucidation: X-ray crystallographyCoordination complexchemistry.chemical_compoundCrystallographychemistryBiomimeticsX-ray crystallographyHydroxideMoleculekiderakenteen ratkaisuta116röntgenkristallografiaAngewandte Chemie International Edition
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Efficient Consecutive Synthesis of Ethyl-2-(4-Aminophenoxy) Acetate, a Precursor for Dual GK and PPARγ Activators, X-ray Structure, Hirshfeld Analysi…

2022

Herein, we report a facile synthesis of ethyl-2-(4-aminophenoxy)acetate 4 as a building synthon for novel dual hypoglycemic agents. This building template was synthesized by alkylation of 4-nitrophenol with ethyl bromo-acetate followed by selective reduction of the nitro group. This reduction methoddoes not require nascent hydrogen or any reaction complexity; it goes easily via consecutive reaction in NH4Cl/Fe to yield our target synthon as very pure crystals. This product was characterized by 1HNMR, 13CNMR, COSY, NOESY NMR spectroscopy, and elemental analysis. Additionally, its structure was studied and approved by X-ray single crystal structure determination. The unit cell parameters are …

hypoglycemicX-raykemiallinen synteesiconsecutive reactionbioaktiiviset yhdisteettiheysfunktionaaliteoriaglukoosiaineenvaihduntaaminophenoxyHirshfeld analysisheterosykliset yhdisteetröntgenkristallografia
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Structural studies on filamin domain interactions

2015

immunoglobulin-like domainrakennesmall-angle x-ray scatteringmechanosensingfilamiinitproteiinitliganditfilaminmutaatiotproteiinidomeenitröntgenkristallografiax-ray crystallographyinter-domain interactions
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Dynamic Refolding of Ion-Pair Catalysts in Response to Different Anions.

2019

Four distinct folding patterns were identified in two foldamer-type urea-thiourea catalysts bearing a basic dimethylamino unit by a combination of X-ray crystallography, solution NMR studies, and computational studies (DFT). These patterns are characterized by different intramolecular hydrogen bonding schemes that arise largely from different thiourea conformers. The free base forms of the catalysts are characterized by folds where the intramolecular hydrogen bonds between the urea and the thiourea units remain intact. In contrast, the catalytically relevant salt forms of the catalyst, where the catalyst forms an ion pair with the substrate or substrate analogues, appear in two entirely dif…

inorganic chemicalsBearing (mechanical)anionitcatalysis010405 organic chemistryChemistryorganic chemicalsOrganic Chemistryfolding anion bindingIon pairs010402 general chemistrykidetiede01 natural sciences0104 chemical sciencesCatalysislaw.inventionFolding (chemistry)X-rayCrystallographyconformational changelawkatalyysisolution structuresröntgenkristallografiaThe Journal of organic chemistry
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Halogen bonding and host–guest chemistry between N-alkylammonium resorcinarene halides, diiodoperfluorobutane and neutral guests

2019

Single crystal X-ray structures of halogen-bonded assemblies formed between host N-hexylammonium resorcinarene bromide (1) or N-cyclohexylammonium resorcinarene chloride (2), and 1,4-diiodooctafluorobutane and accompanying small solvent guests (methanol, acetonitrile and water) are presented. The guests’ inclusion affects the geometry of the cavity of the receptors 1 and 2, while the divalent halogen bond donor 1,4-diiodooctafluorobutane determines the overall nature of the halogen bond assembly. The crystal lattice of 1 contains two structurally different dimeric assemblies A and B, formally resulting in the mixture of a capsular dimer and a dimeric pseudo-capsule. 1H and 19F NMR analyses …

inorganic chemicalscapsuleDimerHalideFluorine-19 NMRCrystal structurelcsh:QD241-441kemialliset sidoksetchemistry.chemical_compoundlcsh:Organic chemistryBromidesupramolekulaarinen kemiahost-guest chemistryhost–guest chemistrylcsh:ScienceHost–guest chemistryta116Biochemistry Biophysics and Structural BiologyX-ray crystallographyresorcinarene saltsHalogen bondChemistryOrganic ChemistryResorcinareneChemistryCrystallographyhalogen bondinglcsh:Qröntgenkristallografiadimeric assembliesBeilstein Journal of Organic Chemistry
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Ion pair recognition by ditopic crown ether based bis-urea and uranyl salophen receptors

2016

ionition pair bindingcrown ethersuranyl salophensureatitraussupramolecular chemistryditopic receptorsionisidosanion bindinguranyylisalofeenitkemialliset sidoksetkruunueetteritsupramolekyylikemia¹H NMR titrationsNMR-spektroskopiaorgaaniset yhdisteetröntgenkristallografiaX-ray crystallography
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