0000000001304094

AUTHOR

Elina Sievänen

showing 40 related works from this author

Stimuli-responsive bile acid-based metallogels forming in aqueous media

2015

Abstract The synthesis and gelation properties of a picolinic acid conjugated bile acid derivative in the presence of metal salts along with the stimuli-responsiveness of the systems are reported. The gels are formed in the presence of Cu 2+ ions in the solvent systems composed of 30–50% of organic solvent (MeOH, acetonitrile, or acetone) in water. The gels respond to various stimuli: they can be formed upon sonication or shaking, and their gel–sol transformation can be triggered by a variety of chemical species. NMR, MS, and SEM techniques are exploited in order to gain a deeper insight on the self-assembled systems.

medicine.drug_classSonicationClinical BiochemistryConjugated systemPicolinic acidBiochemistrystimuli-responsiveBile Acids and Saltschemistry.chemical_compoundpicolinic acidEndocrinologyAcetonemedicineOrganic chemistrybile acidPicolinic AcidsAcetonitrileMolecular Biologyta116PharmacologyMolecular StructureBile acidOrganic Chemistryself-assemblyAmideschemistrySelf-assemblymetallogelGelsCopperDerivative (chemistry)Steroids
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First bisphosphonate hydrogelators: potential composers of biocompatible gels

2020

Recently, investigation of hydrogels has gained ever increasing attention mostly because of their biomedical and pharmaceutical properties, and novel hydrogelators are constantly studied to find functional applications. Bisphosphonates (BPs) are well-known compounds applicable in different fields but are mostly used in clinics as drugs for bone-related diseases. In this study, a novel class of BP-hydrogelators together with a BP-organogelator was found, and the gelating abilities of the compounds were studied. Several techniques to analyze the structure and the properties of the formed gels were used, including solid state 13C and 31P CPMAS and solution state NMR spectroscopy, IR spectrosco…

Materials scienceSolution stateSelf-healing hydrogelsBiomedical EngineeringSolid-stateInfrared spectroscopyGeneral Materials ScienceGeneral ChemistryGeneral MedicineNuclear magnetic resonance spectroscopyBiocompatible materialta116Combinatorial chemistryJournal of Materials Chemistry B
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Controlling the crystal growth of potassium iodide with a 1,1'-bis(pyridin-4-ylmethyl)-2,2'-biimidazole ligand (L) – formation of a linear [K4I4L4]n …

2018

The crystal growth of potassium iodide was controlled by using the neutral organic 1,1′-bis(pyridin-4-ylmethyl)-2,2′-biimidazole (L) ligand as a modifier. The selected modifier allows the preservation of original cubic [K4I4] units and their arrangement into a linear ligand-supported 1D chain. The supported [K4I4] cubes are only slightly distorted compared to the cubes found in pure KI salt. The N–K binding of the ligand to the KI salt, as well as weak I⋯H, N⋯H, and N⋯I interactions, stabilizes the structure to create a unique 1D polymer of neutral potassium iodide ionic salt inside the [K4I4L4]n complex.

saltsIonic bondingSalt (chemistry)chemistry.chemical_elementsuolat (yhdisteet)Crystal growth02 engineering and technology010402 general chemistryIodine01 natural sciencescrystalsGeneral Materials Sciencepolymeeritta116polymerschemistry.chemical_classificationLigandGeneral ChemistryPolymer021001 nanoscience & nanotechnologyCondensed Matter Physicskiteet0104 chemical sciencesCrystallographychemistry0210 nano-technologyCrystEngComm
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Self-assembly properties of bile acid derivatives of L-cysteine, L-valine and L-serine alkyl esters

2012

Comprehensive self-assembly studies for nine bile acid amides of amino acid esters are reported. The number of the hydroxyl groups attached to the steroidal skeleton and the character of the amino acid ester moiety were used as variables when examining the self-assembly properties of the compounds. Two of the compounds were shown to undergo self-assembly leading to organogelation. In addition, preliminary self-assembly studies in aqueous mixtures of polar organic solvents were conducted. Microscopic methods (optical microscopy and scanning electron microscopy) were utilised in order to gain a deeper insight into the self-assembled structures. Furthermore, single-crystal X-ray structures for…

chemistry.chemical_classificationAqueous solutionBile acidmedicine.drug_classStereochemistryGeneral ChemistryAmino acidchemistryValineX-ray crystallographymedicineOrganic chemistryMoietySelf-assemblyta116AlkylSupramolecular Chemistry
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High-Resolution Solid-State NMR Spectroscopy of Steroids and Their Derivatives

2013

Abstract: Steroids are an important class of organic compounds containing a vast array of biologically and physiologically essential molecules. Due to their availability, relatively straightforward derivatizability, and endogeneity, they are widely used in pharmacological applications. The investigation of molecular and physicochemical properties of active pharmaceutical ingredients (APIs) in the solid state is important, because these properties are directly related to their pharmacological activity. Several methods are available for this purpose. Solid-state NMR spectroscopy offers a nondestructive and flexible technique, providing both structural and dynamic information. It can be applie…

Active ingredientSolid-state nuclear magnetic resonancePolymorphism (materials science)ChemistryMoleculeOrganic chemistryHigh resolutionNuclear magnetic resonance spectroscopySpectroscopyInstrumentationCombinatorial chemistrySpectroscopyAmorphous solidApplied Spectroscopy Reviews
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Steroidal supramolecular metallogels

2020

The review deals with an expanding number of steroidal compounds that are capable of forming a metallogel providing a multitude of novel materials rich in their properties. The future of steroidal metallogels holds a myriad of potential applications as new intelligent materials. Detection of potentially harmful compounds without expensive instrumentation, entrapment of environmentally hazardous substances, and sensitive and selective nanomaterials represent only a few of these potential applications. This article reviews the design, synthesis, characterization, and applications of steroidal metallogels. peerReviewed

steroidal metallogelsMaterials sciencesteroidal compoundssupramolekulaarinen kemiaSupramolecular chemistryNanotechnologyGeneral ChemistryInstrumentation (computer programming)metallogelsChemical Society Reviews
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Synthesis, Characterization, and Saccharide Binding Studies of Bile Acid − Porphyrin Conjugates

2007

Synthesis and characterization of bile acid-porphyrin conjugates (BAPs) are reported. Binding of saccharides with BAPs in aqueous methanol was studied by monitoring changes in the visible absorption spectral of the porphyrin-moieties. Although these studies clearly showed absorbance changes, suggesting quite high if non-selective binding, the mass spectral studies do not unambiguously support these results.

Spectrometry Mass Electrospray IonizationMagnetic Resonance SpectroscopyPorphyrinsmedicine.drug_classElectrospray ionizationCarbohydratesPharmaceutical ScienceESI MS.ArticleAnalytical ChemistryAbsorbanceBile Acids and Saltslcsh:QD241-441chemistry.chemical_compoundUltraviolet visible spectroscopylcsh:Organic chemistryHeterocyclic Compoundsvisible spectroscopyDrug Discoverymedicinepolycyclic compoundsOrganic chemistryPhysical and Theoretical ChemistrysaccharideAqueous solutionBile acidMolecular StructureOrganic Chemistry1H-NMRPorphyrinCombinatorial chemistryBile acidschemistryChemistry (miscellaneous)Proton NMRMolecular Medicinesense organsporphyrinConjugateMolecules
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Novel Porphyrin-cholic Acid Conjugates as Receptors for Biologically Important Anions

2007

chemistry.chemical_compoundChemistrySupramolecular chemistryCholic acidGeneral ChemistryReceptorPorphyrinCombinatorial chemistryConjugateSupramolecular Chemistry
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Novel lithocholaphanes: Syntheses, NMR, MS, and molecular modeling studies

2007

Abstract Novel head-to-head lithocholaphanes 6 and 11 have been synthesized via precursors 1 – 5 and 7 – 10 with overall good yields, and characterized by 1 H, 13 C, and 15 N NMR spectroscopy, ESI-TOF mass spectrometry, thermal analysis, and molecular modeling. In addition, the binding abilities of 6 and 11 towards alkali metal cations have been investigated via competitive complexation studies using equimolar mixtures of Li + , Na + , K + , and Rb + -cations, and cholaphanes 6 and 11 . The formation of cation–cholaphane adducts was detected by ESI-TOF mass spectrometry. The trends in these comparative binding studies are nicely reproduced theoretically with PM3 energetically optimized stru…

Coordination sphereMolecular modelChemistryOrganic ChemistryAnalytical chemistrychemistry.chemical_elementNuclear magnetic resonance spectroscopyAlkali metalAnalytical ChemistryRubidiumAdductInorganic ChemistryCrystallographyMoietyLithiumSpectroscopyJournal of Molecular Structure
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A computationally feasible quantum chemical model for 13C NMR chemical shifts of PCB-derived carboxylic acids.

2004

Two quantum chemical models have been derived for the prediction of 13C NMR chemical shifts of novel PCB acids obtained from PCBs by catalytic carbonylation. 13C isotropic shielding constants were calculated employing the GIAO (gauge-independent atomic orbital) method with density functional theory (DFT). The best results were obtained by cluster calculations, which took the solvent effects into account properly. In this approach, a solvent molecule (acetone) was attached by a hydrogen bond to every hydrogen atom present in a PCB acid, and the geometry of the molecular cluster was optimized employing the AM1 method. For 158 chemical shifts, the cross-validated standard error was 2.8 ppm and…

Models MolecularEnvironmental EngineeringMagnetic Resonance SpectroscopyHealth Toxicology and MutagenesisCarboxylic AcidsQuantum chemistryAtomic orbitalEnvironmental ChemistryQuantitative Biology::BiomoleculesCarbon IsotopesMolecular StructureHydrogen bondChemistryChemical shiftPublic Health Environmental and Occupational HealthGeneral MedicineGeneral ChemistryHydrogen atomCarbon-13 NMRPollutionPolychlorinated BiphenylsModels ChemicalSolventsPhysical chemistryQuantum TheoryDensity functional theoryEnvironmental PollutantsSolvent effectsSoftwareChemosphere
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Spectral and microscopic study of self-assembly of novel cationic spermine amides of betulinic acid

2016

Supramolecular characteristics of two spermine amides of betulinic acid (1 and 2) were studied by measuring and evaluating their UV-VIS-NIR spectra in aqueous acetonitrile and DOSY-NMR spectra in tetradeuteromethanol, accompanied by atomic force microscopy (AFM) images, scanning electron microscopy (SEM) micrographs, and transmission electron microscopy (TEM) micrographs. Fibrous supramolecular self-assembly of 1 and 2 was observed by AFM images, as well as by the SEM and TEM micrographs. Bathochromic shifts of the absorbance maximum at 870nm to 1015-970nm in the UV-VIS-NIR spectra were observed with increasing water content in the acetonitrile/water systems, indicating formation of fibrous…

Magnetic Resonance SpectroscopyScanning electron microscopeClinical BiochemistrySupramolecular chemistrymacromolecular substancesDOSY-NMRMicroscopy Atomic Force010402 general chemistry01 natural sciencesBiochemistryAbsorbancechemistry.chemical_compoundEndocrinologyMicroscopy Electron TransmissionBathochromic shiftBetulinic AcidAcetonitrileta116Molecular BiologyPharmacologyAqueous solutionMolecular Structure010405 organic chemistryChemistryOrganic Chemistryta1182technology industry and agricultureAmidesTriterpenes0104 chemical sciencesCrystallographyTransmission electron microscopySEMTEMSpermineMicroscopy Electrochemical ScanningAFMPentacyclic TriterpenesChirality (chemistry)Steroids
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Novel Porphyrin-Cholic Acid Conjugates as Receptors for Biologically Important Anions

2005

A series of novel receptors showing high binding affinity in aqueous media for biologically important anions are reported. These naturally chromophoric porphyrin-based receptors contain cholic acids connected via quaternary alkyl ammonium amido linkages.

chemistry.chemical_classificationchemistry.chemical_compoundAqueous mediumChemistryStereochemistrypolycyclic compoundsCholic acidAmmoniumGeneral ChemistryReceptorPorphyrinAlkylConjugateSupramolecular Chemistry
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Bile acid–cysteamine conjugates: Structural properties, gelation, and toxicity evaluation

2011

Abstract Design, synthesis, and characterization of six novel bile acid–cysteamine conjugates together with investigation of their structural studies, gelation properties, and preliminary toxicity evaluation, are reported. Solid state properties of selected compounds were studied by means of X-ray diffraction and 13C CPMAS NMR spectroscopy. N-(2-thioethyl)-3α,7α,12α-trihydroxy-5β-cholan-24-amide was shown to exhibit (pseudo)polymorphism, and a single crystal structure of its non-stoichiometric hydrate is reported herein. Cholyl and dehydrocholyl derivatives bearing three functionalities in their steroidal backbone were shown to undergo self-assembly leading to gelation in certain organic so…

BALB 3T3 CellsMagnetic Resonance Spectroscopymedicine.drug_classCysteamineClinical BiochemistryCholic AcidBiochemistryBile Acids and SaltsInhibitory Concentration 50Micechemistry.chemical_compoundEndocrinologyX-Ray DiffractionmedicineAnimalsOrganic chemistryta116Molecular BiologyPharmacologyBile acidUrsodeoxycholic AcidOrganic ChemistryHydrogen BondingNuclear magnetic resonance spectroscopyFibroblastsAmidesCombinatorial chemistrychemistrySolid-state nuclear magnetic resonancePolymorphism (materials science)SolventsLithocholic AcidCysteamineHydrateSingle crystalDeoxycholic AcidConjugateSteroids
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Structural, Thermoanalytical and Molecular Modeling Studies on N-(3-hydroxypropyl) 3a,12a-Dihydroxy-5b-cholan-24-amide and Its Monohydrates

2007

The synthetic method for preparing N-(3-hydroxypropyl) 3 alpha,12 alpha-dihydroxy-5 beta-cholan-24-amide can lead to formation of at least three different crystal forms - an anhydrous compound and two monohydrates. The structural and thermal properties of these forms have been characterized by 13C-CP/MAS-NMR and IR spectroscopy, thermo- gravimetry, differential scanning calorimetry and by powder and single crystal x-ray crystallography. In addition, theoretical 13C-NMR chemical shift calculations were also performed for the anhydrous compound and for the first monohydrate, starting from single crystal structures and the structures of these species have now been verified. The first monohydra…

Models MolecularMagnetic Resonance Spectroscopysolid state structure.termoanalyysiPharmaceutical ScienceInfrared spectroscopy13C-CP/MAS-NMR spectroscopy13C-CP/MAS-NMR spektroskopiaFull Research PaperAnalytical ChemistryCrystallcsh:QD241-441Differential scanning calorimetrylcsh:Organic chemistryX-Ray DiffractionDrug Discoverykiinteän tilan rakenneSolid state structurePhysical and Theoretical ChemistrycrystallographyCarbon Isotopeskristallografiathermal Bile acidsCalorimetry Differential ScanningChemistryHydrogen bondOrganic ChemistryTemperatureWaterHydrogen BondingkidetiedeAmidesBile acidsCrystallographysappihapotChemistry (miscellaneous)X-ray crystallographyThermogravimetryAnhydrousCholanesMolecular MedicineOrthorhombic crystal systemSingle crystalthermal analysis
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Bile acid alkylamide derivatives as low molecular weight organogelators: systematic gelation studies and qualitative structural analysis of the syste…

2011

A series of amino- and hydroxyalkyl amides of bile acids have been synthesized and characterized by Fourier transform infrared spectroscopy (FTIR), (1)H and (13)C nuclear magnetic resonance spectroscopy (NMR), as well as electrospray ionization mass spectrometry (ESI-MS) measurements. The ability of the synthesized molecules to promote gel formation was systematically investigated. Out of 396 combinations formed by 11 compounds and 36 different solvents, 22 gel-containing systems were obtained with 1% (w/v) gelator concentration. Apart from one exception, the gelator compounds were lithocholic acid derivatives. This challenges the general trend of bile acid-based physical gelators, accordin…

Lithocholic acidmedicine.drug_classSurface PropertiesElectrospray ionizationAnalytical chemistryInfrared spectroscopyMass spectrometryBiomaterialsBile Acids and Saltschemistry.chemical_compoundColloid and Surface ChemistrymedicineOrganic chemistryFourier transform infrared spectroscopyParticle SizeBile acidMolecular StructureStereoisomerismNuclear magnetic resonance spectroscopyAmidesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsSolventMolecular WeightchemistryGelsJournal of colloid and interface science
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ChemInform Abstract: High-Resolution Solid-State NMR Spectroscopy of Steroids and Their Derivatives

2013

Abstract: Steroids are an important class of organic compounds containing a vast array of biologically and physiologically essential molecules. Due to their availability, relatively straightforward derivatizability, and endogeneity, they are widely used in pharmacological applications. The investigation of molecular and physicochemical properties of active pharmaceutical ingredients (APIs) in the solid state is important, because these properties are directly related to their pharmacological activity. Several methods are available for this purpose. Solid-state NMR spectroscopy offers a nondestructive and flexible technique, providing both structural and dynamic information. It can be applie…

Active ingredientSolid-state nuclear magnetic resonanceChemistrySolid-stateMoleculeHigh resolutionGeneral MedicineNuclear magnetic resonance spectroscopySpectroscopyCombinatorial chemistryAmorphous solidChemInform
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Porphyrin-bile acid conjugates: from saccharide recognition in the solution to the selective cancer cell fluorescence detection.

2008

This paper describes the preparation and use of conjugates of porphyrins and bile acids as ligands to bind to tumor expressed saccharides. Bile acid-porphyrin conjugates were tested for recognition of saccharides that are typically present on malignant tumor cells. Fluorescence microscopy, in vitro PDT cell killing, and PDT of subcutaneous 4T1 mouse tumors is reported. High selectivity for saccharide cancer markers and cancer cells was observed. This in vivo and in vitro study demonstrated high potential use for these compounds in targeted photodynamic therapy.

GlycosylationPorphyrinsmedicine.drug_classmedicine.medical_treatmentCarbohydratesPhotodynamic therapyApoptosisDNA FragmentationLigandsBiochemistrySensitivity and SpecificityCell LineBile Acids and Saltschemistry.chemical_compoundMiceStructure-Activity RelationshipIn vivoNeoplasmsmedicineFluorescence microscopeBiomarkers TumorAnimalsHumansPhysical and Theoretical ChemistryCell Line TransformedCell ProliferationMice Inbred BALB CBinding SitesBile acidDose-Response Relationship DrugMolecular StructureChemistryOrganic ChemistryCancer3T3 Cellsmedicine.diseasePorphyrinSolutionsCell killingBiochemistryMicroscopy FluorescencePhotochemotherapyCancer cellDrug Screening Assays AntitumorHeLa CellsOrganicbiomolecular chemistry
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Dissolution behavior of co-amorphous amino acid-indomethacin mixtures: The ability of amino acids to stabilize the supersaturated state of indomethac…

2017

Article

Magnetic Resonance SpectroscopyArgininesupersaturationIndomethacinCo-amorphousbiorelevantPharmaceutical ScienceExcipientPhenylalanine02 engineering and technologyPrecipitationprecipitation030226 pharmacology & pharmacy03 medical and health sciences0302 clinical medicineco-amorphousSpectroscopy Fourier Transform InfraredmedicineAmino AcidsSolubilityDissolutionta116Chromatography High Pressure LiquidSupersaturationChromatographyAqueous solutionCalorimetry Differential ScanningChemistryAnti-Inflammatory Agents Non-SteroidalTryptophanGeneral Medicine021001 nanoscience & nanotechnologyAmino acidSupersaturationSolubilityBiorelevant0210 nano-technologyPowder Diffractionamino acidBiotechnologymedicine.drug
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1 H,13 C, 19 F NMR, and ESI mass spectral characterization of two geminal difluorosteroids

2008

Two geminal difluorosteroids, 3,3-difluoro-5β-cholan-24-oic acid (1) and 3,3-difluoro-5α-androstan-17-one (2), have been prepared from corresponding ketosteroids with diethylaminosulphurtrifluoride (DAST) treatment in moderate yields. The structures of 1 and 2 have been characterized by 1H, 13C, 19F NMR, and ESI mass spectral techniques. Copyright © 2008 John Wiley & Sons, Ltd.

GeminalChemistryComputational chemistryElectrospray ionizationOrganic chemistryGeneral Materials ScienceGeneral ChemistryFluorine-19 NMRCharacterization (materials science)Magnetic Resonance in Chemistry
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Comparative NMR and IR spectral, X-ray structural and theoretical studies of eight 6-arylidenedibenzo[b,e]thiepin-11-one-5,5-dioxides

2007

Abstract Eight 6-arylidenedibenzo[b,e]thiepin-11-one-5,5-dioxides are characterized by NMR and IR spectroscopy. Single crystal X-ray structures for three congeners are reported. In addition, the transmission of substituent effects in conjugated double bond system of 6-arylidenedibenzo[b,e]thiepin-11-one-5,5-dioxide framework has been evaluated by calculating the correlations between selected 13C NMR chemical shifts and IR stretching wave numbers and Hammett constants of the substituents locating in the phenyl ring of the arylidene moiety.

Chemical shiftOrganic ChemistrySubstituentInfrared spectroscopyCarbon-13 NMRRing (chemistry)Analytical ChemistryInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryComputational chemistryProton NMRMoietySingle crystalSpectroscopyJournal of Molecular Structure
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Structural studies of five novel bile acid-4-aminopyridine conjugates

2012

Abstract Synthesis and solid-state structural characterization of five bile acid amides of 4-aminopyridine (4-AP) are reported. Systematic crystallization experiments revealed a number of structural modifications and/or solvate/hydrate systems for these conjugates. Particularly, cholic acid conjugate exhibited five distinct structure modifications, including one anhydrous form, mono- and dihydrates, as well as ethanol and 2-butanol solvates. The obtained crystal forms were examined extensively with various analytical methods, including solid-state NMR, Raman, and IR spectroscopies, powder and single crystal X-ray diffraction methods, thermogravimetry, and differential scanning calorimetry. …

Models MolecularMagnetic Resonance Spectroscopymedicine.drug_classButanolsClinical BiochemistryCrystallography X-RaySpectrum Analysis RamanBiochemistrylaw.inventionBile Acids and Saltschemistry.chemical_compoundEndocrinologylawmedicineOrganic chemistry4-AminopyridineCrystallizationta116Molecular BiologyPharmacologyCalorimetry Differential ScanningEthanolBile acidOrganic ChemistryCholic acidAmidesThermogravimetryCrystallographychemistryPolymorphism (materials science)ThermogravimetrySolventsCrystallizationHydrateSingle crystalConjugateSteroids
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Bile acid–amino acid ester conjugates: gelation, structural properties, and thermoreversible solid to solid phase transition

2010

Design, synthesis, and gelation properties of three novel biocompatible bile acid–L-methionine methyl ester conjugates are presented. Two of the conjugates have been shown to undergo self-assembly leading to organogelation in certain aromatic solvents. The properties of these gels have been investigated by conventional methods typical for molecular gel studies along with 13C CPMAS NMR spectroscopic studies of the native gel. In addition, properties in solid and solution states for all three compounds have been investigated, and single crystal X-ray structures of all compounds determined. Furthermore, powder X-ray diffraction studies have revealed that compound 1 undergoes a dynamic and reve…

chemistry.chemical_classificationDiffractionConformational changePhase transitionBile acidmedicine.drug_classChemistryGeneral ChemistryCondensed Matter PhysicsAmino acidPolymer chemistrymedicineOrganic chemistrySingle crystalConformational isomerismConjugateSoft Matter
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Secondary interactions as driving force in heterocomplex formation of 2,7-disubstituted-1,8-naphthyridines: Quantum chemical, NMR and mass spectral i…

2009

Abstract Tautomerism and dimerization of 2,7-disubstituted-1,8-naphtyridines has been studied theoretically by quantum chemical methods and experimentally by liquid and solid state NMR and ESI-TOF mass spectral techniques. The heterocomplex formation has been proven in solution by variable temperature 1H NMR and in solid state by 13C CPMAS NMR spectra of a grinded mixture of two congeners. Secondary interactions have been proposed as driving forces in the heterocomplex formation. The energy differences between homo- and heterocomplexes were calculated with recently developed DFT + D methods. The energy data obtained by the quantum chemical methods are in agreement with the concept of second…

Quantum chemicalChemistryOrganic ChemistryAb initioTautomerAnalytical ChemistryInorganic ChemistryNMR spectra databaseSolid-state nuclear magnetic resonanceAb initio quantum chemistry methodsProton NMRPhysical chemistrySelf-assemblySpectroscopyJournal of Molecular Structure
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Novel two-step synthesis of gold nanoparticles capped with bile acid conjugates

2008

Bile acids and their conjugates are physiologically important molecules. Syntheses and structure elucidation combined with investigation of properties and applications of bile acids and their derivatives are of academic interest. The concept of using bile acids and their conjugates in nanoscience is a novel idea, which opens up fascinating prospects. In this article, an easy and simple route for obtaining N-lithocholyl-L-(cysteine ethyl ester) (3), capable of effectively capping and stabilizing metal nanoparticles, is described. The whole synthetic route needs only two steps giving a moderate to good yield. The gold NPs are characterized by elemental analysis, UV spectroscopy, and TEM. Addi…

Lithocholic acidBile acidChemistryLigandmedicine.drug_classBioengineeringBiomaterialschemistry.chemical_compoundUltraviolet visible spectroscopyMechanics of MaterialsColloidal goldYield (chemistry)medicineMoleculeOrganic chemistryConjugateMaterials Science and Engineering: C
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Recent advances in steroidal supramolecular gels

2020

During the last decade or two the interest towards small molecules capable of self-assembly leading to gelation has increased intensively. The investigation of these supramolecular gels aims not only at understanding the fundamental processes underlying gel formation but also at development of new materials with a myriad of applications. Steroids are widely-spread natural products with a large and rigid steroidal nucleus combined with derivatizable functional groups leading to an adjustable polarity profile, which makes them attractive building blocks when designing novel low molecular weight gelators. Due to their unique properties, steroid-based supramolecular gels may find use in applica…

ChemistryGeneral Chemical EngineeringDrug deliverySupramolecular chemistryNew materialsNanotechnologyGeneral Chemistry
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Structural studies of homoisoflavonoids: NMR spectroscopy, X-ray diffraction, and theoretical calculations

2010

Abstract In this article we present a detailed structural investigation for five homoisoflavonoids, molecules important from the pharmacological point of view. For studying the electron distribution as well as its influence on the physicochemical properties, NMR spectroscopy, X-ray diffraction, and theoretical calculations have been used. Nuclear magnetic shieldings obtained by using DFT calculations for optimized molecular geometries are correlated with the experimentally determined chemical shifts. The theoretical data are well in agreement with the experimental values. The single crystal X-ray structures of homoisoflavonoid derivatives 1, 3, and 4 have been solved. The molecular geometri…

010405 organic chemistryChemistryChemical shiftOrganic ChemistryIntermolecular forceNuclear magnetic resonance spectroscopy010402 general chemistry01 natural sciences0104 chemical sciencesAnalytical ChemistryInorganic ChemistryCrystalMolecular geometryComputational chemistryX-ray crystallographyPhysical chemistryMoleculeSingle crystalSpectroscopyJournal of Molecular Structure
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Nanotutkimusta megahertseillä

2016

nanotutkimusspektroskopia
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CCDC 1550984: Experimental Crystal Structure Determination

2019

Related Article: Riikka Kuosmanen, Rakesh Puttreddy, Kari Rissanen, Elina Sievänen|2018|Chem.-Eur.J.|24|18676|doi:10.1002/chem.201803151

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters312-dihydroxy-N-(3-methylbutyl)cholan-24-amideExperimental 3D Coordinates
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CCDC 1550980: Experimental Crystal Structure Determination

2019

Related Article: Riikka Kuosmanen, Rakesh Puttreddy, Kari Rissanen, Elina Sievänen|2018|Chem.-Eur.J.|24|18676|doi:10.1002/chem.201803151

Space GroupCrystallographyCrystal SystemCrystal StructureN-butyl-3-hydroxycholan-24-amideCell ParametersExperimental 3D Coordinates
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CCDC 1550979: Experimental Crystal Structure Determination

2019

Related Article: Riikka Kuosmanen, Rakesh Puttreddy, Kari Rissanen, Elina Sievänen|2018|Chem.-Eur.J.|24|18676|doi:10.1002/chem.201803151

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters3712-trihydroxy-N-propylcholan-24-amideExperimental 3D Coordinates
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CCDC 1550977: Experimental Crystal Structure Determination

2019

Related Article: Riikka Kuosmanen, Rakesh Puttreddy, Kari Rissanen, Elina Sievänen|2018|Chem.-Eur.J.|24|18676|doi:10.1002/chem.201803151

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters3-hydroxy-N-propylcholan-24-amideExperimental 3D Coordinates
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CCDC 1550981: Experimental Crystal Structure Determination

2019

Related Article: Riikka Kuosmanen, Rakesh Puttreddy, Kari Rissanen, Elina Sievänen|2018|Chem.-Eur.J.|24|18676|doi:10.1002/chem.201803151

Space GroupCrystallographyN-butyl-312-dihydroxycholan-24-amideCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1550982: Experimental Crystal Structure Determination

2019

Related Article: Riikka Kuosmanen, Rakesh Puttreddy, Kari Rissanen, Elina Sievänen|2018|Chem.-Eur.J.|24|18676|doi:10.1002/chem.201803151

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersN-butyl-3712-trihydroxycholan-24-amideExperimental 3D Coordinates
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CCDC 1588805: Experimental Crystal Structure Determination

2018

Related Article: Margarita Bulatova, Rajendhraprasad Tatikonda, Pipsa Hirva, Evgeny Bulatov, Elina Sievänen, Matti Haukka|2018|CrystEngComm|20|3631|doi:10.1039/C8CE00483H

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameterscatena-[(mu-11'-bis[(pyridin-4-yl)methyl]-1H1'H-22'-biimidazole)-(mu-iodo)-potassium]Experimental 3D Coordinates
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CCDC 1438665: Experimental Crystal Structure Determination

2021

Related Article: Riikka Kuosmanen, Rakesh Puttreddy, Roosa-Maria Willman, Ilkka Aijalainen, Jitka Ulrichova, Adela Galandakova, Hannu Salo, Kari Rissanen and Elina Sievänen|2016|Steroids|108|7|doi:10.1016/j.steroids.2016.02.014

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersN-ethyl-3-hydroxycholan-24-amideExperimental 3D Coordinates
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CCDC 1550978: Experimental Crystal Structure Determination

2019

Related Article: Riikka Kuosmanen, Rakesh Puttreddy, Kari Rissanen, Elina Sievänen|2018|Chem.-Eur.J.|24|18676|doi:10.1002/chem.201803151

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters312-dihydroxy-N-propylcholan-24-amideExperimental 3D Coordinates
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CCDC 1438667: Experimental Crystal Structure Determination

2021

Related Article: Riikka Kuosmanen, Rakesh Puttreddy, Roosa-Maria Willman, Ilkka Aijalainen, Jitka Ulrichova, Adela Galandakova, Hannu Salo, Kari Rissanen and Elina Sievänen|2016|Steroids|108|7|doi:10.1016/j.steroids.2016.02.014

Space GroupCrystallographyCrystal SystemCrystal StructureN-ethyl-3712-trihydroxycholan-24-amide acetonitrile solvateCell ParametersExperimental 3D Coordinates
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CCDC 1438666: Experimental Crystal Structure Determination

2021

Related Article: Riikka Kuosmanen, Rakesh Puttreddy, Roosa-Maria Willman, Ilkka Aijalainen, Jitka Ulrichova, Adela Galandakova, Hannu Salo, Kari Rissanen and Elina Sievänen|2016|Steroids|108|7|doi:10.1016/j.steroids.2016.02.014

Space GroupCrystallographyCrystal SystemCrystal StructureN-ethyl-312-dihydroxycholan-24-amide acetonitrile solvateCell ParametersExperimental 3D Coordinates
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CCDC 1550985: Experimental Crystal Structure Determination

2019

Related Article: Riikka Kuosmanen, Rakesh Puttreddy, Kari Rissanen, Elina Sievänen|2018|Chem.-Eur.J.|24|18676|doi:10.1002/chem.201803151

Space GroupCrystallography3712-trihydroxy-N-(3-methylbutyl)cholan-24-amideCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1550983: Experimental Crystal Structure Determination

2019

Related Article: Riikka Kuosmanen, Rakesh Puttreddy, Kari Rissanen, Elina Sievänen|2018|Chem.-Eur.J.|24|18676|doi:10.1002/chem.201803151

Space GroupCrystallographyCrystal SystemCrystal Structure3-hydroxy-N-(3-methylbutyl)cholan-24-amideCell ParametersExperimental 3D Coordinates
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