Search results for "surface modification"

showing 10 items of 417 documents

Growth Mechanism and Surface Functionalization of Metal Chalcogenides Nanostructures

2014

Following the discovery of carbon fullerenes and nanotubes (NTs), nanostructured materials and their synthesis have attracted tremendous attention due to their superior mechanical properties, their unique electronic behavior, and their high potential in making technologically advanced nanodevices. Among different classes, layered metal chalcogenides nanostructures are of interest for a variety of applications ranging from nanoelectronics or as source materials for energy applications, nanotribology and in heterogeneous catalysis. These nanoparticles are metastable phases. Therefore, equilibrium methods are necessary to prevent the formation of the thermodynamically stable bulk phase. On the…

chemistry.chemical_classificationchemistry.chemical_compoundMaterials sciencechemistryNanoelectronicsChalcogenideBiomoleculeParticleNanoparticleSurface modificationNanotechnologyNanoengineeringNanomaterials
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Defect-Free Chemical Functionalization of Magnetic Monolayers Based on Coordination Polymers

2018

<p>Chemical functionalization has demonstrated to be a powerful approach to tailor the physical and chemical properties of two-dimensional (2D) materials, to increase their processability and</p> <p>stability, to add new functionalities and, even, to create new 2D materials. However, this post synthetic method – which involves the anchoring of molecules on the surface of an exfoliated 2D crystal – inevitably leads to defective materials, which lack long-range structural order. If defect-free functionalized monolayers are required, a radically new approach needs to be developed. Here we present a pre-synthetic method based on coordination chemistry that affords the isolatio…

chemistry.chemical_classificationchemistry.chemical_compoundMembraneMaterials scienceFerrocenechemistryLigandMonolayerMoleculeSurface modificationNanotechnologyPolymerCoordination complex
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Functionalization of P3HT with Various Mono- and Multidentate Anchor Groups

2018

Due to its favorable optoelectronic properties and the accessibility via Grignard metathesis (GRIM) polymerization, poly(3-hexylthiophene) (P3HT) is one of the most applied conjugated polymers. The ‘living' nature of GRIM polymerization enables the modification of the polymer and the installation of desired properties. In the present study, two versatile approaches for the synthesis of anchor group-modified P3HT have been developed, which enable the functionalization of various inorganic nanoparticles. Depending on the polymerization conditions, mono- and bifunctional ethynyl-terminated P3HT or solely monofunctionalized aldehyde-terminated P3HT was synthesized. Afterwards, the quantitative …

chemistry.chemical_classificationhybrid nanocompositesChemistryImineGeneral ChemistryPolymerConjugated systemGRIMMetathesisP3HTchemistry.chemical_compoundPolymerizationPolymer chemistryclick chemistryClick chemistryconjugated polymersSurface modificationBifunctional
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Post-synthetic methods for functionalization of imidazole-fused porphyrins

2018

Several methods for the post-synthetic modification of imidazo[4,5-[Formula: see text]]porphyrins are reported. First, a synthetic approach to the isomeric difunctionalized porphyrins, containing two [Formula: see text]-fused 2-aryl-1[Formula: see text]-imidazole cycles at adjacent or opposite pyrrole rings of the macrocycle is developed. The core chemistry of this synthetic route is the transformation of 2-aryl-1[Formula: see text]-imidazo[4,5-[Formula: see text]]porphyrins into corresponding imidazodioxochlorins followed by Debus–Radziszewski condensation with aromatic aldehyde. Next, 2-(4-bromophenyl)-1[Formula: see text]-imidazo[4,5-[Formula: see text]]-5,10,15,20-tetramesitylporphyrin…

chemistry.chemical_compound010405 organic chemistryChemistrySurface modificationImidazoleGeneral Chemistry010402 general chemistry01 natural sciencesCombinatorial chemistryCoupling reaction0104 chemical sciencesJournal of Porphyrins and Phthalocyanines
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How do different surface modification strategies affect the properties of MnO nanoparticles for biomedical applications? Comparison of PEGylated and …

2011

ABSTRACTMnO nanoparticles (NPs) were surface functionalized by two different approaches, (1) using a dopamine-poly(ethylene glycol) (PEG) (DA-PEG) ligand and (2) by encapsulation within a thin silica shell applying a novel approach. Both MnO@DA-PEG and MnO@SiO2 NPs exhibited excellent long-term stability in physiological solutions. In addition, the cytotoxic potential of both materials was comparatively low. Furthermore, owing to the magnetic properties of MnO NPs, both MnO@DA-PEG and MnO@SiO2 lead to a shortening of the longitudinal relaxation time T1 in MRI. In comparison to the PEGylated MnO NPs, the presence of a thin silica shell led to a greater stability of the MnO core itself by pre…

chemistry.chemical_compoundAqueous solutionMaterials sciencechemistryChemical engineeringPEG ratioSurface modificationNanoparticleNanotechnologyLeaching (metallurgy)Ethylene glycolLongitudinal Relaxation TimeIonMRS Proceedings
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Synthesis of small carboranylsilane dendrons as scaffolds for multiple functionalizations.

2006

Small carbosilane dendrons in which a closo-carborane is located at the focal point have been prepared by a sequence of steps involving hydrosilylation and reduction reactions. These compounds are used as scaffolds for peripheral functionalization with styrene, chlorovinylstyrene, or suitable carboranes, while keeping the C(cluster)-Si (C(c)-Si) bond. Modification of the core by reduction of the carborane with Mg/BrCH2CH2Br was also achieved.

chemistry.chemical_compoundChemistryHydrosilylationOrganic ChemistryCarboraneOrganic chemistrySurface modificationSequence (biology)Physical and Theoretical ChemistryBiochemistryCombinatorial chemistryStyreneOrganic letters
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From Single Molecules to Nanoscopically Structured Functional Materials

2006

AbstractThe synthesis of MS2 (M = Mo, W) onion-like nanoparticles by means of a high temperature MOCVD process starting from W(CO)6 and elemental sulfur is reported. The reaction can also be carried out in two steps where the intermediate amorphous WS2 nanoparticles formed through the high temperature reaction of tungsten and sulfur in the initial phase of the reaction are isolated and converted in a separate annealing step to onion-type WS2 nanoparticles. Based on a study of the temperature dependence of the reaction a set of conditions could be derived where onion-like structures were formed in a one-step reaction. Onion-like structures obtained in the single-step process were filled, whe…

chemistry.chemical_compoundMaterials scienceNanostructurechemistryChemical engineeringAnnealing (metallurgy)ChalcogenideMoleculechemistry.chemical_elementNanoparticleSurface modificationTungstenAmorphous solidMRS Proceedings
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Organic Field Effect Transistors: Noncovalent Functionalization and Passivation of Black Phosphorus with Optimized Perylene Diimides for Hybrid Field…

2020

chemistry.chemical_compoundMaterials sciencePassivationchemistryMechanics of MaterialsMechanical EngineeringSurface modificationField-effect transistorNanotechnologyBlack phosphorusPeryleneAdvanced Materials Interfaces
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Process Development for Wet-Chemical Surface Functionalization of Gallium Arsenide Based Nanowires

2019

chemistry.chemical_compoundMaterials sciencechemistryProcess developmentNanowireSurface modificationNanotechnologyCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsGallium arsenideElektrotechnik
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ChemInform Abstract: Palladium-Polypyrrole Nanocomposites Pd@PPy for Direct C-H Functionalization of Pyrroles and Imidazoles with Bromoarenes.

2016

Palladium–polypyrrole nanocomposites (Pd@PPy) with unique combination of high palladium dispersion (nanoparticle size 2.4 nm) and high palladium content (35 wt%) are efficient catalysts for the selective arylation of substituted pyrroles and imidazoles with either activated or deactivated aryl bromides. The performances of the recoverable supported palladium catalyst matches the best performances of homogeneous systems based on Pd(OAc)2 at 0.5–0.2 mol%, and largely overwhelm the classical Pd/C catalyst.

chemistry.chemical_compoundNanocompositechemistryArylPolymer chemistrySurface modificationchemistry.chemical_elementNanoparticleGeneral MedicinePolypyrroleDispersion (chemistry)CatalysisPalladiumChemInform
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