Search results for " modifica"

showing 10 items of 817 documents

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
researchProduct

Concave Tetrathiafulvalene-Type Donors as Supramolecular Partners for Fullerenes

2007

The cap fits! A new class of concave π-extended tetrathiafulvalene (TTF) derivatives, truxene-TTFs, were prepared and characterized, and their self-assembly with fullerenes was investigated (see picture). Truxene-TTFs represent the first example of TTF-related electron donors that serve, without chemical modification, as monotopic receptors for fullerenes in solution. (Chemical Equation Presented). © 2007 Wiley-VCH Verlag GmbH & Co. KGaA.

chemistry.chemical_compoundCrystallographyFullerenechemistryStereochemistrySupramolecular chemistryChemical modificationGeneral ChemistrySelf-assemblyGeneral MedicineChemical equationCatalysisTetrathiafulvaleneAngewandte Chemie
researchProduct

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
researchProduct

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
researchProduct

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
researchProduct

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
researchProduct

1988

chemistry.chemical_compoundPhenylacetylenechemistryHead to headDopingAnalytical chemistryChemical modificationInfrared spectroscopyDehydrogenationPhotochemistryElectrical conductorDie Makromolekulare Chemie, Rapid Communications
researchProduct

Thermoresponsive hyperbranched polyethylenimines with isobutyramide functional groups

2007

chemistry.chemical_compoundPolyethylenimineCloud pointAqueous solutionPolymers and PlasticschemistryOrganic ChemistryPolymer chemistryMaterials ChemistryChemical modificationIsobutyramideLower critical solution temperatureJournal of Polymer Science Part A: Polymer Chemistry
researchProduct

Functionalization with silyl enol ethers, VI Zinc chloride mediated alkoxyalkylation of O-methyl-O-trimethylsilyl) keten acetals with 2-alkoxy-1,3-di…

1987

O-Methyl-O-(trimethylsilyl) keten acetals2 were regioselectively alkoxyalkylated by 2-alkoxy-1,3-dioxolanes1 in the presence of zinc chloride. This method represents a good way for synthesis of α-protected β-keto carbonic esters4.

chemistry.chemical_compoundSilylationTrimethylsilylChemistryAlkoxy groupSurface modificationchemistry.chemical_elementOrganic chemistryGeneral ChemistryZincEnolMonatshefte für Chemie - Chemical Monthly
researchProduct

ChemInform Abstract: Approaches for the Introduction of Fluorinated Substituents into [1,2,3]Triazolo[1,5-a]pyridines.

2014

Functionalization of [1,2,3]triazolo[1,5-a]pyridines with a trifluoromethyl group is achieved for the first time.

chemistry.chemical_compoundTrifluoromethylchemistryGroup (periodic table)Triazole derivativesSurface modificationOrganic chemistryGeneral MedicineChemInform
researchProduct