0000000001268219

AUTHOR

Elina I. Sievänen

showing 9 related works from this author

Solid‐state NMR Spectroscopy of Iodine(I) Complexes

2023

Solid-state NMR has been applied to a series of Barluenga-type iodine(I) [L-I-L]PF6 (L=pyridine, 4-ethylpyridine, 4-dimethylaminopyridine, isoquinoline) complexes as their hexafluorophosphate salts, as well as their respective non-liquid ligands (L), their precursor silver(I) complexes, and the respective N-methylated pyridinium and quinolinium hexafluorophoshate salts. These results are compared and contrasted to the corresponding solution studies and single-crystal X-ray structures. As the first study of its kind on the solid-state NMR behavior of halogen(I) complexes, practical considerations are also discussed to encourage wider utilization of this technique in the future. peerReviewed

jodihalogenbondBarluengareagentOrganic Chemistrykiinteän olomuodon kemiaGeneral Chemistrycationexchangeiodine(I)Biochemistrysolid-stateChemistry – An Asian Journal
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Systematic Modulation of the Supramolecular Gelation Properties of Bile Acid Alkyl Amides

2018

The self-assembly properties of nine low-molecular-weight gelators (LMWGs) based on bile acid alkyl amides were studied in detail. Based on the results, the number of hydroxyl groups attached to the steroidal backbone plays a major role in the gelation, although the nature of the aliphatic side chain also modulates the gelation abilities. Of the 50 gel systems studied, 35 are based on lithocholic acid and 15 on cholic acid derivatives. The deoxycholic acid derivatives did not form any gels. The gelation occurred primarily in aromatic solvents and the gels manifested typical fibrous or spherical morphologies. The 13C cross-polarized magic angle spinning (CPMAS) NMR spectra measured on the cr…

Lithocholic acidSupramolecular chemistry02 engineering and technology010402 general chemistry01 natural sciencesCatalysischemistry.chemical_compoundAmidebile acid amidesPolymer chemistrysupramolekulaarinen kemiaSide chainMagic angle spinningNMR-spektroskopiata116AlkylX-ray crystallographygeelitchemistry.chemical_classificationintermolecular interactionsOrganic ChemistryDeoxycholic acidsupramolecular gelsCholic acidGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical scienceschemistryamidit0210 nano-technologyröntgenkristallografiaChemistry – A European Journal
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Biocompatible Hydrogelators Based on Bile Acid Ethyl Amides

2016

Four novel bile acid ethyl amides were synthetized using a well-known method. All the four compounds were characterized by IR, SEM, and X-ray crystal analyses. In addition, the cytotoxicity of the compounds was tested. Two of the prepared compounds formed organogels. Lithocholic acid derivative 1 formed hydrogels as 1% and 2% (w/v) in four different aqueous solutions. This is very intriguing regarding possible uses in biomedicine. peerReviewed

Models MolecularLithocholic acidBiocompatibilitymedicine.drug_classClinical Biochemistrysupramolecular hydrogelMolecular ConformationBiocompatible Materials02 engineering and technology010402 general chemistry01 natural sciencesBiochemistryMicechemistry.chemical_compoundEndocrinologybiocompatibilityAmidemedicineAnimalsOrganic chemistrybile acidMolecular Biologyta116PharmacologyAqueous solutionBile acidOrganic Chemistryta1182WaterHydrogels3T3 Cellsself-assembly021001 nanoscience & nanotechnologyAmidesamide0104 chemical scienceschemistryBiochemistrySelf-healing hydrogelsLithocholic AcidSelf-assembly0210 nano-technologyDerivative (chemistry)
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Two-component self-assembly with solvent leading to "wet" and microcrystalline organogel fibers

2014

Abstract Hypothesis The microcrystalline fibers of N -(2-aminoethyl)-3α-hydroxy-5β-cholan-24-amide 1 provided a useful model system for studying the complex relationship between morphology, experimental parameters, solvent, and the phenomenon of organogelation. The presence of solvents in the solid forms of 1 along with crystallization behavior suggested solvate formation and polymorphic behavior. Experiments Forty solid state- and xerogel samples of 1 formed in organic solvents and in three categories of experimental conditions were analyzed with single crystal X-ray diffraction (XRD), powder X-ray diffraction (PXRD), Raman microscopy, and attenuated total reflection Fourier-transform infr…

Materials sciencecrystallizationbile acid amideInfrared spectroscopylaw.inventioninclusion crystalBiomaterialsCrystalColloid and Surface Chemistrysolvatelawmicrocrystalline fiberCrystallizationIsostructuralta116x-ray crystallographyorganogelxerogelraman microscopySurfaces Coatings and FilmsElectronic Optical and Magnetic Materialsfourier transform infrared spectroscopyCrystallographyMicrocrystallineAttenuated total reflectionSingle crystalPowder diffractionJournal of Colloid and Interface Science
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Insights into localized manipulation of organogel-related microcrystalline spherulite formation

2015

Abstract The formation processes of microcrystalline spherulitic fiber systems related to bile acid amides were determined to include dominant interface-related aspects, the role of which were studied in terms of potential manipulation and increased control over the overall structure of the networks. The nucleation and growth properties and aggregation of two lithocholyl amide derivatives were studied in several organic solvents using thermomicroscopy, as well as thermal control at macroscopic level. Nucleation/crystallization at interfaces was observed to act as the main route for the formation of microcrystalline fibers/solids in six gelator–solvent systems, in which spherulite formation …

Materials scienceSpheruliteOrganogelNucleationFiber networkSpherulite (polymer physics)InterfaceThermal controllaw.inventionCrystallographyColloid and Surface ChemistryMicrocrystallineChemical engineeringlawBile acid amideNucleationFiberCrystallizationCrystallizationta116Topology (chemistry)Colloids and Surfaces A: Physicochemical and Engineering Aspects
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Pot-Economy Autooxidative Condensation of 2-Aryl-2-lithio-1,3-dithianes

2018

The autoxidative condensation of 2-aryl-2-lithio-1,3-dithianes is here reported. Treatment of 2-aryl-1,3-dithianes with n-BuLi in the absence of any electrophile leads to condensation of three molecules of 1,3-dithianes and formation of highly functionalized α-thioether ketones orthothioesters in 51-89% yields upon air exposure. The method was further expanded to benzaldehyde dithioacetals, affording corresponding orthothioesters and α-thioether ketones in 48-97% yields. The experimental results combined with density functional theory studies support a mechanism triggered by the autoxidation of 2-aryl-2-lithio-1,3-dithianes to yield a highly reactive thioester that undergoes condensation wi…

116 Chemical sciencesorganometalliyhdisteet010402 general chemistryThioester01 natural sciencesMedicinal chemistryBenzaldehydechemistry.chemical_compoundorganometallic compoundsMoleculeta116chemistry.chemical_classificationAutoxidation010405 organic chemistryoxidation (passive)ArylOrganic ChemistryCondensationhapettuminenautooxidative condensation0104 chemical scienceslitiumchemistrylithiumYield (chemistry)ElectrophileThe Journal of Organic Chemistry
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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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CCDC 872741: Experimental Crystal Structure Determination

2014

Related Article: Kari V. Ahonen, Manu K. Lahtinen, Miika S. Löfman, Anniina M. Kiesilä, Arto M. Valkonen, Elina I. Sievänen, Nonappa, Erkki T. Kolehmainen|2012|Steroids|77|1141|doi:10.1016/j.steroids.2012.06.003

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersN-(Pyridin-4-yl) 3alpha7beta-dihydroxy-5beta-cholan-24-amideExperimental 3D Coordinates
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CCDC 2178008: Experimental Crystal Structure Determination

2023

Related Article: Jas S. Ward, Elina I. Sievänen, Kari Rissanen|2023|Chem.Asian J.|18|e202201203|doi:10.1002/asia.202201203

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters2-methylisoquinolin-2-ium hexafluorophosphateExperimental 3D Coordinates
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