Search results for "Química de superfícies"

showing 3 items of 3 documents

Rapid Surface Functionalization of Hydrogen-Terminated Silicon by Alkyl Silanols

2017

Surface functionalization of inorganic semiconductor substrates, particularly silicon, has focused attention toward many technologically important applications, involving photovoltaic energy, biosensing and catalysis. For such modification processes, oxide-free (H-terminated) silicon surfaces are highly required, and different chemical approaches have been described in the past decades. However, their reactivity is often poor, requiring long reaction times (2-18 h) or the use of UV light (10-30 min). Here, we report a simple and rapid surface functionalization for H-terminated Si(111) surfaces using alkyl silanols. This catalyst-free surface reaction is fast (15 min at room temperature) and…

HydrogenSiliconSilici Compostoschemistry.chemical_element02 engineering and technology010402 general chemistryPhotochemistry01 natural sciencesBiochemistryCatalysisArticleQuímica de superfíciesCatalysisColloid and Surface ChemistryMonolayerLife ScienceOrganic chemistryReactivity (chemistry)AlkylVLAGchemistry.chemical_classificationOrganic ChemistryGeneral ChemistryPolymer021001 nanoscience & nanotechnologyOrganische Chemie0104 chemical scienceschemistrySurface modification0210 nano-technologyJournal of the American Chemical Society
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Rapid and Complete Surface Modification with Strain-Promoted Oxidation-Controlled Cyclooctyne-1,2-Quinone Cycloaddition (SPOCQ)

2017

Abstract Strain‐promoted oxidation‐controlled cyclooctyne‐1,2‐quinone cycloaddition (SPOCQ) between functionalized bicyclo[6.1.0]non‐4‐yne (BCN) and surface‐bound quinones revealed an unprecedented 100 % conjugation efficiency. In addition, monitoring by direct analysis in real time mass spectrometry (DART‐MS) revealed the underlying kinetics and activation parameters of this immobilization process in dependence on its microenvironment.

Kinetics02 engineering and technologyMetal-free click chemistry010402 general chemistryMass spectrometry01 natural sciencesCatalysisQuímica de superfíciesVLAGMass spectrometryStrain (chemistry)Bicyclic moleculeChemistryCommunicationOrganic ChemistryGeneral MedicineGeneral ChemistryCyclooctynes021001 nanoscience & nanotechnologyOrganische ChemieSurface chemistryCombinatorial chemistryCommunicationsCycloaddition0104 chemical sciencesQuinoneKineticsSurface modification0210 nano-technologyQuímica orgànicaAngewandte Chemie International Edition
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Organic Monolayers by B(C6F5)3-Catalyzed Siloxanation of Oxidized Silicon Surfaces

2017

Inspired by the homogeneous catalyst tris(pentafluorophenyl) borane [B(C6F5)3], which acts as a promotor of Si-H bond activation, we developed and studied a method of modifying silicon oxide surfaces using hydrosilanes with B(C6F5)3 as the catalyst. This dedihydrosiloxanation reaction yields complete surface coverage within 10 min at room temperature. Organic monolayers derived from hydrosilanes with varying carbon chain lengths (C8-C18) were prepared on oxidized Si(111) surfaces, and the thermal and hydrolytic stabilities of the obtained monolayers were investigated in acidic (pH 3) medium, basic (pH 11) medium, phosphate-buffered saline (PBS), and deionized water (neutral conditions) for …

SiliconInorganic chemistrySilici Compostoschemistry.chemical_elementHomogeneous catalysis02 engineering and technologyBorane010402 general chemistry01 natural sciencesQuímica de superfíciesCatalysischemistry.chemical_compoundHydrolysisMonolayerElectrochemistryLife ScienceGeneral Materials ScienceSilicon oxideSpectroscopyVLAGOrganic ChemistrySurfaces and Interfaces021001 nanoscience & nanotechnologyCondensed Matter PhysicsOrganische ChemieSilane0104 chemical scienceschemistry0210 nano-technologyQuímica orgànicaLangmuir
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