Search results for "Side-Chains"

showing 5 items of 5 documents

From an epoxide monomer toolkit to functional PEG copolymers with adjustable LCST behavior.

2011

The lower critical solution temperature (LCST) behavior of novel poly(ethylene glycol) (PEG)-based copolymers bearing multiple functional groups, obtained by anionic ring-opening (co)polymerization (AROP), has been investigated. Variable comonomer ratios of ethylene oxide (EO) and the corresponding oxiranes isopropylidene glyceryl glycidyl ether (IGG), ethoxyl vinyl glycidyl ether (EVGE), allyl glycidyl ether (AGE), or N,N-dibenzyl amino glycidyl (DBAG), particularly designed to implement functional groups at the PEG backbone, were found to influence the LCST behavior. Sharp transitions from translucent to opaque solutions, comparable to other well-established stimuli-responsive polymers, w…

Ethylene OxideMaterials scienceHot TemperaturePolymers and PlasticsPolymersAllyl glycidyl etherpolyethersEpoxideLower critical solution temperaturePolymerizationPolyethylene Glycolschemistry.chemical_compoundPolymer chemistrycopolymersMaterials ChemistryCopolymerPoly(Ethylene Glycol) CopolymersSide-ChainsAqueous-SolutionEthylene oxideComonomerstimuli-sensitiveOrganic ChemistryPegchemistryPolymerizationGlycidolLcstEthylene glycolHydrophobic and Hydrophilic InteractionsMacromolecular rapid communications
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Direct experimental observation of mesoscopic fluorous domains in fluorinated room temperature ionic liquids

2017

Fluorinated room temperature ionic liquids (FRTILs) represent a class of solvent media that are attracting great attention due to their IL-specific properties as well as features stemming from their fluorous nature. Medium-to-long fluorous tails constitute a well-defined apolar moiety in the otherwise polar environment. Similarly to the case of alkyl tails, such chains are expected to result in the formation of self-assembled fluorous domains. So far, however, no direct experimental observation has been made of the existence of such structural heterogeneities on the nm scale. We report here the first experimental evidence of the existence of mesoscopic spatial segregation of fluorinated dom…

General Physics and AstronomyNanotechnology02 engineering and technologyNeutron scattering010402 general chemistryLAYER CAPACITOR APPLICATIONS; PERFLUOROALKYL SIDE-CHAINS; ANGLE NEUTRON-SCATTERING; PARTICLE MESH EWALD; PHYSICOCHEMICAL PROPERTIES; FORCE-FIELD; CATION SYMMETRY; STRUCTURAL-CHARACTERIZATION; AMMONIUM TETRAFLUOROBORATE; MOLECULAR SIMULATION01 natural sciencesionic liquidsionic liquids SANS nanostructuration fluorous domains NMR NOEchemistry.chemical_compoundMolecular dynamicsPhysics and Astronomy (all)nanostructurationMoietyPhysical and Theoretical ChemistryAlkylNOEchemistry.chemical_classificationfluorous domainsMesoscopic physicsSANSNuclear magnetic resonance spectroscopy021001 nanoscience & nanotechnologyNMR0104 chemical sciencesfluorinated ionic liquids neutron scattering x-ray diffraction structurechemistryChemical physicsIonic liquidPolar0210 nano-technology
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A Very Low Band Gap Diketopyrrolopyrrole-Porphyrin Conjugated Polymer

2017

International audience; A porphyrin-diketopyrrolopyrrole-containing polymer (poly(porphyrin-diketopyrrolopyrrole) (PPDPP)) shows impressive molar absorption coefficients from lambda=300 to 1000 nm. The photophysical and structural properties of PPDPP have been studied. With PPDPP as the electron donor and [ 6,6]phenyl C-71 butyric acid methyl ester (PC71BM) as the electron acceptor, the bulk heterojunction polymer solar cell showed overall power conversion efficiencies of 4.18 and 6.44% for as-cast and two-step annealing processed PPDPP: PC71BM (1: 2) active layers, respectively. These results are quite impressive for porphyrin-containing polymers, especially when directly included in the p…

Materials scienceBand gapbuilding-blockporphyrinoidsElectron donorthin-film transistors02 engineering and technologyConjugated system010402 general chemistryPhotochemistry[ CHIM ] Chemical Sciences01 natural sciencesPolymer solar cellheterojunction solar-cellschemistry.chemical_compound[CHIM]Chemical Sciencessmall-moleculepolymerschemistry.chemical_classificationsemiconducting polymerscharge transferGeneral ChemistryPolymerChromophoreElectron acceptorside-chains021001 nanoscience & nanotechnologyPorphyrinphotovoltaic properties0104 chemical sciencesphotodynamic therapychemistryorganic photovoltaics0210 nano-technologyabsorptionperformanceconjugationChemPlusChem
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Genomic determinants of protein folding thermodynamics in prokaryotic organisms.

2004

Here we investigate how thermodynamic properties of orthologous proteins are influenced by the genomic environment in which they evolve. We performed a comparative computational study of 21 protein families in 73 prokaryotic species and obtained the following main results. (i) Protein stability with respect to the unfolded state and with respect to misfolding are anticorrelated. There appears to be a trade-off between these two properties, which cannot be optimized simultaneously. (ii) Folding thermodynamic parameters are strongly correlated with two genomic features, genome size and G+C composition. In particular, the normalized energy gap, an indicator of folding efficiency in statistical…

Models MolecularProtein DenaturationProtein FoldingProtein familyArchaeal ProteinsThermodynamicsdeleterious mutationsthermophilic proteinsBiologymonte-carlo algorithmGenomeNegative selectionBacterial ProteinsStructural BiologyMolecular evolutionGenome ArchaealevolutionbuchneraMolecular BiologyGenome sizeGeneticsPrincipal Component Analysisacid side-chainsBacteriaSequence Homology Amino Acidreplica approachComputational BiologystabilityGenetic codeArchaeaPRI BioscienceFolding (chemistry)endosymbiotic bacteriacation-pi interactionsThermodynamicsProtein foldingHydrophobic and Hydrophilic InteractionsGenome BacterialJournal of molecular biology
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The pentafluorophenyl group as π-acceptor for anions: a case study

2015

Chemical science 6(1), 354-359 (2015). doi:10.1039/C4SC02762K

positive chargesChemistryStereochemistryChemieSolid-stateGeneral Chemistryhapticities540side-chainsstructural dataAcceptor3. Good healthIonevaluation criteriakey elementsComputational chemistryGroup (periodic table)pentafluorophenylddc:540HapticitySide chainStatistical analysiselectron-deficientta116Chemical Science
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