0000000000392919

AUTHOR

Jarmo Ropponen

showing 10 related works from this author

Thermal and X-ray powder diffraction studies of aliphatic polyester dendrimers

2004

The syntheses and thermal and X-ray powder diffraction analyses of three sets of aliphatic polyester dendrimers based on 2,2-bis(hydroxymethyl)propionic acid as a repeating unit and 2,2-dimethyl-1,3-propanediol, 1,5-pentanediol, and 1,1,1-tris(hydroxymethyl)ethane as core molecules are reported. These dendritic polyesters were prepared in high yields with the divergent method. The thermal properties of these biodendrimers were evaluated with thermogravimetric analysis and differential scanning calorimetry. The thermal decomposition of the compounds occurred around 250 °C for the hydroxyl-ended dendrimers and around 150 °C for the acetonide-protected dendrimers. In addition, the crystallinit…

Thermogravimetric analysisDendrimersPolymers and PlasticsChemistryThermogravimetric analysis (TGA)2-bis(hydroxymethyl)propionic acid (bis-MPA)Organic ChemistryThermal decomposition2Differential scanning calorimetry (DSC)PolyesterCrystallinitychemistry.chemical_compoundDifferential scanning calorimetryDendrimerPolymer chemistryMaterials Chemistry22-bis(hydroxymethyl)propionic acid (bis-MPA)Physical chemistryAliphatic polyestersHydroxymethylPowder diffraction
researchProduct

Synthesis and Characterization of theO-Alkylation Products of Resorcinarene

2013

O-Substitution reactions of tetramethoxyresorcinarene with alkyl halides produced a variety of partially O-alkylated resorcinarene derivatives with terminal alkyne functionality. The degree of alkylation was affected by the reactivity of the alkylating halide used. NMR spectroscopy proved to be an ideal tool for analyzing the complex reaction mixtures and the isolated products based on the symmetry and degree of alkylation of the resorcinarene derivatives. Single-crystal X-ray diffraction studies furthermore showed diversity in the self-assembly of the various O-alkylation products that was greatly affected by the degree of alkylation, as well as the nature of the alkyne moiety.

chemistry.chemical_classificationOrganic ChemistrySupramolecular chemistryAlkyneNuclear magnetic resonance spectroscopyAlkylationResorcinarenechemistryMoietyOrganic chemistrylipids (amino acids peptides and proteins)Reactivity (chemistry)Physical and Theoretical ChemistryAlkylEuropean Journal of Organic Chemistry
researchProduct

Bisfunctionalized Janus Molecules

2004

[reaction: see text] Bisfunctionalized dendritic multiester molecules were synthesized by combined protection-deprotection and divergent-convergent-divergent sequences in high yields leading to dendritic molecules that combine two functionally different surfaces, polar aliphatic arborol and nonpolar gallate ether moieties, resulting in a two-faced Janus molecule.

chemistry.chemical_compoundchemistryStereochemistryOrganic ChemistryMoleculeEtherJanusGallatePhysical and Theoretical ChemistryBiochemistryCombinatorial chemistryOrganic Letters
researchProduct

Synthesis, thermal properties and X-ray structural study of weak C–H⋯OC hydrogen bonding in aliphatic polyester dendrimers

2004

Dendritic polyester compounds based on polyol with three, four and six reactive hydroxy groups as a molecular core, chloroacetyl chloride (or bromoacetyl bromide) and sodium metal enolate were prepared by a simple two-step synthetic procedure. The compounds were characterised by using the NMR and MS techniques, and the thermal properties were measured by differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). The structures of the crystalline compounds were determined by X-ray single crystal diffraction. Detailed analysis of the structures showed that the self-complementarity of the molecules together with a multitude of weak C-H⋯O=C hydrogen bonding results in crystal…

Thermogravimetric analysisHydrogen bondGeneral ChemistryCondensed Matter PhysicsChloroacetyl chloridePolyesterchemistry.chemical_compoundDifferential scanning calorimetrychemistryBromideDendrimerPolymer chemistryMoleculeGeneral Materials ScienceCrystEngComm
researchProduct

Synthesis, characterization and thermal properties of new aromatic quaternary ammonium bromides

2004

Series of new aromatic R 2R′ 2N +Br - (R=benzyl, 4-methylbenzyl, 2-phenylethyl, 3-phenylpropyl; R′=ethyl, methyl, isopropyl) or RR′ 2NH +Br --type (R=benzyl, R′=isopropyl) quaternary ammonium bromides were prepared by using novel synthetic route in which a formamide (N,N-diethylformamide, N,N-dimethylformamide, N,N-diisopropylformamide) is treated with aralkyl halide in presence of a weak base. The compounds were characterized by 1H-NMR and 13C-NMR spectroscopy and mass spectrometry. Structures of the crystalline compounds were determined by X-ray single crystal diffraction, and in addition the powder diffraction method was used to study the structural similarities between the single crysta…

FormamideAmmonium bromideInorganic chemistryTriclinic crystal systemIonic liquidCondensed Matter PhysicsQuaternary ammonium bromideElectronic Optical and Magnetic MaterialsInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryX-ray single crystal diffractionBromideX-ray powder diffractionIonic liquidMaterials ChemistryCeramics and CompositesOrthorhombic crystal systemThermal analysisPhysical and Theoretical ChemistryWeak interactionsIsopropylMonoclinic crystal systemJournal of Solid State Chemistry
researchProduct

Synthesis, characterization, and thermal behavior of steroidal dendrons

2004

A series of novel dendritic steroidal polyesters of first and second generation has been synthesized in convergent fashion by the use of 2,2-bis(hydroxymethyl)propionic acid as a repeating unit. The first- and second-generation hydroxy-functionalized dendrons with a variety of surface modifications were produced through the use of four bile acids: lithocholic acid (LCA), ursodeoxycholic acid (UDCA), deoxycholic acid (DCA), and cholic acid (CA). The thermal behavior of the steroidal dendrons was characterized by differential scanning calorimetry (DSC) and by thermogravimetric analysis (TGA). Finally, quantum chemical calculation methods were used to study the geometries of the dendrons and t…

Aliphatic estersThermogravimetric analysisDendrimersLithocholic acidHydrogen bondOrganic ChemistryDeoxycholic acidCholic acidBile acidschemistry.chemical_compoundchemistryDendrimerPolymer chemistryOrganic chemistryMoleculeHydroxymethylSteroidsThermal analysisPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
researchProduct

Self-assembly of janus dendrimers into uniform dendrimersomes and other complex architectures

2010

Janus Drug Delivery Vehicle Efficient drug delivery vehicles need to be produced in a limited size range and with uniform size distribution. The self-assembly of traditional small-molecule and polymeric amphiphiles has led to the production of micelles, liposomes, polymeric micelles, and polymersomes for use in drug delivery applications. Now, Percec et al. (p. 1009 ) describe the self-assembly of Janus-type (i.e., two-headed) dendrimers to produce monodisperse supramolecular constructs, termed “dendrimersomes,” and other complex architectures. The structures, which showed long-term stability as well as very narrow size distributions, were easily produced by the injection of an ethanolic so…

Models MolecularDendrimersMaterials scienceSurface Propertiesta221Complex ArchitecturesNanotechnologyMolecular Dynamics SimulationSurface-Active AgentsBiomimetic MaterialsDendrimerAmphiphileJanusta218LiposomeDrug Carriersta214MultidisciplinaryAntibiotics Antineoplasticta114Molecular StructureVesicleCryoelectron MicroscopyWaterMembranes ArtificialNanostructuresJanus DendrimersSelf-AssemblyMembraneUniform DendrimersomesDoxorubicinPolymersomeSelf-assemblyHydrophobic and Hydrophilic InteractionsScience
researchProduct

High-Generation Amphiphilic Janus-Dendrimers as Stabilizing Agents for Drug Suspensions

2018

Pharmaceutical nanosuspensions are formed when drug crystals are suspended in aqueous media in the presence of stabilizers. This technology offers a convenient way to enhance the dissolution of poorly water-soluble drug compounds. The stabilizers exert their action through electrostatic or steric interactions, however, the molecular requirements of stabilizing agents have not been studied extensively. Here, four structurally related amphiphilic Janus-dendrimers were synthesized and screened to determine the roles of different macromolecular domains on the stabilization of drug crystals. Physical interaction and nanomilling experiments have substantiated that Janus-dendrimers with fourth gen…

Recrystallization (geology)huumeetPolymers and Plastics116 Chemical sciences02 engineering and technology01 natural sciencesdrugsContact angleMaterials ChemistryHUMAN LECTINSSurface plasmon resonanceta116chemistry.chemical_classificationChemistryBIOLOGICAL-MEMBRANES021001 nanoscience & nanotechnologyPROGRAMMABLE GLYCAN LIGANDSINDOMETHACIN317 PharmacyCLICK CHEMISTRYfarmaseuttinen kemia0210 nano-technologyHydrophobic and Hydrophilic InteractionsDendrimersSURFACEBioengineeringPoloxamer010402 general chemistryRSPOORLY SOLUBLE DRUGBiomaterialsHydrophobic effectSurface-Active AgentsSuspensionslääkeyhdisteetDendrimerAmphiphileGLYCODENDRIMERSOMESta216ta215AlkylMODULAR SYNTHESISWaterPoloxamerCombinatorial chemistry0104 chemical scienceslääkkeet1182 Biochemistry cell and molecular biologypharmaceutical nanosuspensionsCOMPLEX ARCHITECTURESBiomacromolecules
researchProduct

Novel one-pot synthesis of quaternary ammonium halides: new route to ionic liquids

2004

Treatment of an amide with an alkyl or substituted alkyl halide in the presence of a weak base in a one-pot reaction leads to crystalline quaternary ammonium halides with reasonable chemical yields; some of the compounds show low melting points and a liquid range of over 50–100 °C before decomposition.

chemistry.chemical_classificationInorganic chemistryOne-pot synthesisHalideGeneral ChemistryCatalysischemistry.chemical_compoundchemistryAmideIonic liquidMaterials ChemistryMelting pointAmmoniumWeak baseAlkylNew Journal of Chemistry
researchProduct

Improved Reactivity and Derivatization of Cellulose after Pre-Hydrolysis with Commercial Enzymes

2019

Reactivity is an important parameter when considering the chemical modification or dissolution of cellulose. Different pretreatment methods affect cellulose reactivity by decreasing its degree of polymerization (DP) and crystallinity. In this study, the molar mass of cellulose was decreased via enzymatic pretreatment. Three commercial endoglucanase-rich products were tested. The target was to reduce the viscosity of the pulp to below 200 mL/g and, thus, increase the reactivity of the cellulose. For comparison, cellulose was also pretreated with ozone, and the effects of each pretreatment method on crystallinity and monosaccharide composition of the resulting pulps were investigated. Both en…

stomatognathic diseasesentsyymitesteritstomatognathic systemenzymatic treatmentozone treatmentselluloosaotsonointiCellulosecellulose esters
researchProduct