Search results for "Elf"

showing 10 items of 5893 documents

Self-assembly of small gold colloids with functionalized gold nanorods.

2007

We present a general strategy to stabilize gold nanorod suspensions with mono- and bifunctional polyethylene glycol (PEG) and to attach a controlled number of nanoparticles or biomolecules. Characterization by gel electrophoresis, transmission electron microscopy (TEM), and optical dark-field microscopy show the specific binding of functionalized nanorods to their target while avoiding nonspecific binding to substrates, matrices, and other particles. Such nanorods are well suited for self-assembly of nanostructures and single-molecule labeling.

chemistry.chemical_classificationNanostructureMaterials scienceMechanical EngineeringBiomoleculeNanoparticleBioengineeringNanotechnologyGeneral ChemistryPolyethylene glycolCondensed Matter Physicschemistry.chemical_compoundchemistryTransmission electron microscopyGeneral Materials ScienceNanorodSelf-assemblyBifunctionalNano letters
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Porphyrin-Polymer Networks, Worms, and Nanorods: pH-triggerable Hierarchical Self-assembly

2011

In this study, we present a novel, multifaceted pH-triggerable system of self-organized hierarchical nanostructures. The system consists of meso-tetrakis(4-sulfonatophenyl)porphyrin (TPPS) and poly(2-vinylpyridine) cylindrical brushes (PVP brushes) and can yield polymer-porphyrin networks, porphyrin loaded polymer brushes and pure porphyrin nanorods. In addition, the polymer influences the pK(a) and the mutual TPPS stacking geometry. Structures were characterized by AFM, dynamic light scattering using an IR laser, UV-Vis spectroscopy and small-angle neutron scattering (SANS). Supramolecular composite porphyrin structures that can be switched through external triggers have potential in photo…

chemistry.chemical_classificationNanostructureMaterials sciencePolymers and PlasticsOrganic ChemistryStackingNanoparticleNanotechnologyPolymerPorphyrinchemistry.chemical_compoundchemistryDynamic light scatteringMaterials ChemistryNanorodSelf-assemblyMacromolecular Rapid Communications
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Living Light-Induced Crystallization-Driven Self-Assembly for Rapid Preparation of Semiconducting Nanofibers.

2018

Well-defined nanostructures composed of conjugated polymers have attracted significant attention due to their intriguing electronic and optical properties. However, precise control of the size and uniformity of these semiconducting nanostructures is still rare and challenging, despite recent advances in strategies to obtain self-assembled nanostructures with narrow dispersions. Herein, we demonstrate the preparation of fluorescent conjugated block copolymers by one-shot polymerization and rapid formation of nanofibers in a few minutes via light-induced crystallization-driven self-assembly, driven by facile cis-to- trans photoisomerization of its poly( p-phenylenevinylene) blocks. Furthermor…

chemistry.chemical_classificationNanostructurePhotoisomerizationNanotechnology02 engineering and technologyGeneral ChemistryPolymerConjugated system010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesBiochemistryCatalysis0104 chemical sciencesColloid and Surface ChemistryPolymerizationchemistryNanofiberCopolymerSelf-assembly0210 nano-technologyJournal of the American Chemical Society
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Nanotube Friendly Poly(N-isopropylacrylamide).

2010

Poly(N-ispropylacrylamide) [PNIPAM] is a widely studied polymer for use in biological applications due to its lower critical solution temperature (LCST) being so close to the human body temperature. Unfortunately, attempts to combine carbon nanotubes (CNTs) with PNIPAM have been unsuccessful due to poor interactions between these two materials. In this work, a PNIPAM copolymer with 1 mol-% pyrene side group [p-PNIPAM] was used to produce a thermoresponsive polymer capable of stabilizing both single and multi-walled carbon nanotubes (MWNTs) in water. The presence of pyrene in the polymer chain lowers the LCST less than 4 °C and the interaction with nanotubes does not show any influence on LC…

chemistry.chemical_classificationNanotubeMaterials sciencePolymers and PlasticsOrganic ChemistryPolymerCarbon nanotubeExfoliation jointLower critical solution temperaturelaw.inventionchemistry.chemical_compoundchemistryChemical engineeringlawSelf-healing hydrogelsPolymer chemistryMaterials ChemistryPoly(N-isopropylacrylamide)CopolymerMacromolecular rapid communications
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From Bowls to Capsules: Assembly of Hexanuclear Ni II Rings Tailored by Alkali Cations

2020

An anionic hexanuclear NiII metallamacrocycle with endo and exo linking sites has been employed as a building block to generate a series of capsules and bowls of nanometric size. The supramolecular arrangement of the {Ni6 } rings was tailored by the size of the alkali cations, showing the transition from {Ni6 -M2 -Ni6 } capsules (M=LiI and NaI ) to {Ni6 -M} bowls (M=KI and CsI ). The alkyl co-cations are determinant to stabilize the assemblies by means of CH⋅⋅⋅π interactions on the exo side of the metallamacrocycles. The effect on the topology of the supramolecular assemblies of the cation size, cation charge, Et3 NH+ or Me4 N+ counter cations has been analyzed. Magnetic measurements reveal…

chemistry.chemical_classificationNíquelPropietats magnètiques010405 organic chemistryOrganic ChemistrySupramolecular chemistrychemistry.chemical_elementGeneral Chemistry010402 general chemistryBlock (periodic table)Alkali metal01 natural sciencesCatalysisAnàlisi de conglomerats0104 chemical sciencesCrystallographyNickelCluster analysischemistryNickelMagnetic propertiesAntiferromagnetismSelf-assemblyGround stateAlkylChemistry – A European Journal
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Macrocyclic (1,3)- and (1,4)-benzena-(1,4)-piperazinacyclophanes

1995

New large, up to 45-membered macrocycles were synthesised from piperazine and m- and p-2,6-bis(bromomethyl)xylene under high dilution conditions. X-ray structures of compounds 3a, 4a, 5a, and 8b were determined. Surprisingly, none of the macrocycles prepared showed any inclusion properties towards small guest molecules. Instead, the compounds were found to self-organize during the packing process into larger structures due to the complementary of the molecular skeletons. In the crystalline state 3a forms nets, where the macrocycles are bound by HCH…N interactions to each other. 4a exits in a dimeric structure, which, in turn, further extends to a sheet structure. The positively charged phan…

chemistry.chemical_classificationOrganic ChemistryXyleneSalt (chemistry)ProtonationGeneral ChemistryTurn (biochemistry)Piperazinechemistry.chemical_compoundCrystallographychemistrySheet structureMoleculeSelf-assemblyPhysical and Theoretical ChemistryLiebigs Annalen
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Temperature triggered self-assembly of polypeptides into multivalent spherical micelles.

2007

We report herein thermally responsive elastin-like polypeptides (ELPs) in a linear AB diblock architecture with an N-terminal peptide ligand that self-assemble into spherical micelles when heated slightly above body temperature. A series of 10 ELP block copolymers (ELP(BC)'s ) with different molecular weights and hydrophilic-to-hydrophobic block ratios were genetically synthesized by recursive directional ligation. The self-assembly of these polymers from unimers into micelles was investigated by light scattering, fluorescence spectroscopy, and cryo-TEM. These ELP(BC)'s undergo two phase transitions as a function of solution temperature: a unimer-to-spherical micelle transition at an interm…

chemistry.chemical_classificationPhase transitionHot TemperatureLightChemistryCryoelectron MicroscopyTemperatureGeneral ChemistryPolymerBiochemistryKrafft temperatureMicelleCatalysisFluorescence spectroscopyArticleElastinCrystallographyColloid and Surface ChemistrySpectrometry FluorescenceCritical micelle concentrationCopolymerScattering RadiationSelf-assemblyPeptidesMicellesJournal of the American Chemical Society
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Molecular Weight Distribution of Hyperbranched Polymers Generated by Self-Condensing Vinyl Polymerization in Presence of a Multifunctional Initiator

1999

The molecular weight distribution (MWD) is derived for polymers generated by self-condensing vinyl polymerization (SCVP) of a monomer having a vinyl and an initiator group (“inimer”) in the presence of a multifunctional initiator. If the monomer is added slowly to the initiator solution (semi-batch process), this leads to hyperbranched polymers with a multifunctional core. If monomer and initiator are mixed simultaneously (batch process), even at vinyl group conversions as high as 99%, the total MWD consists of polymers which have grown via reactions between inimer molecules (i.e., the normal SCVP process) and those which have reacted with the initiator. Consequently, the weight distributio…

chemistry.chemical_classificationPolymers and PlasticsBulk polymerizationOrganic ChemistryPolymerSelf-condensationInorganic Chemistrychemistry.chemical_compoundMonomerchemistryPolymerizationPolymer chemistryWeight distributionMaterials ChemistryMolar mass distributionMoleculeMacromolecules
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Spectroscopic and structural characterization of pure and FeCl3-containing tri-n-butyl phosphate

2014

The spectroscopic properties and liquid structure of pure tri-n-butyl phosphate (TBP) and FeCl3/TBP solutions have been investigated by Uv–Vis and Raman spectroscopies, X-ray diffraction and conductometry. Uv–Vis and Raman spectra, supported by conductometric measurements, consistently indicate that the solubilized salt is present mostly as TBP n [FeCl3 − n ] n+ and FeCl4 − complex ions due to specific interaction with the TBP phosphate group. Thanks to this interaction, a high amount of salt (up to 13 % w/w) can be dissolved despite the relatively low dielectric constant of TBP. The X-ray diffractogram of pure TBP has been interpreted in terms of three main contributions which can be attri…

chemistry.chemical_classificationPolymers and PlasticsConductometryChemistryInorganic chemistryTri-N-butyl PhosphateFeCl3 . Tri-n-butyl phosphate . Self-assembling . Local structures .Amphiphilic solventsNanoparticleSalt (chemistry)Ionic bondingTri-n-butyl phosphatePhosphatesymbols.namesakechemistry.chemical_compoundColloid and Surface ChemistryFeCl3Materials ChemistrysymbolsMoleculeSelf-assemblingAmphiphilic solventsPhysical and Theoretical ChemistryLocal structuresRaman spectroscopy
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Topology-Dependent Swichability of Peptide Secondary Structures in Bioconjugates with Complex Architectures

2013

Peptide sequences, which exhibit a reversible pH-responsive coil to α-helix secondary structure transition, are conjugated to polymer precursors to yield linear AB and graft ABA peptide-poly(ethylene oxide) conjugates. While the PEO B-block is comparable, the conjugates differ in topologies of the peptide bearing A-blocks. The influences of topology on the structure transitions in the peptide segments are investigated, comparing linear AB-bioconjugates with graft ABA-bioconjugates having multiple peptide segments combined in star or pom-pom topologies.

chemistry.chemical_classificationPolymers and PlasticsEthylene oxideOrganic ChemistryPeptidePolymerConjugated systemMicroscopy Atomic ForceTopologyCombinatorial chemistryProtein Structure SecondaryPolyethylene Glycolschemistry.chemical_compoundchemistryMaterials ChemistrySelf-assemblyPeptidesProtein secondary structureTopology (chemistry)ConjugateMacromolecular Rapid Communications
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