Search results for "transition-metal"

showing 4 items of 24 documents

Origin of the large spectral shift in electroluminescence in a blue light emitting cationic iridium(III) complex

2007

A new, but archetypal compound [ Ir( ppy- F-2) (2)Me(4)phen] PF6, where ppy- F2 is 2-(2',4'- fluorophenyl) pyridine and Me(4)phen is 3,4,7,8- tetramethyl- 1,10- phenanthroline, was synthesized and used to prepare a solid-state light-emitting electrochemical cell (LEEC). This complex emits blue light with a maximum at 476 nm when photoexcited in a thin film, with a photoluminescence quantum yield of 52%. It yields an efficient single-component solid-state electroluminescence device with a current efficiency reaching 5.5 cd A(-1) and a maximum power efficiency of 5.8 Lm Watt(-1). However, the electroluminescence spectrum is shifted with respect to the photoluminescence spectrum by 80 nm resul…

education.field_of_studyFunctional Response TheoryPhotoluminescenceExcitation-EnergiesTransition-Metal-ComplexesChemistryPopulationQuantum yieldSolid-StateGeneral ChemistryExcited-State PropertiesElectroluminescencePhotochemistryOptical SpectroscopyExcited stateMaterials ChemistryLight emissionEmission spectrumElectrochemical-CellsTriplet stateeducationRoom-TemperatureSingle-LayerPhotophysical Properties
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Aqueous-phase reactive species formed by fine particulate matter from remote forests and polluted urban air

2021

In the aqueous phase, fine particulate matter can form reactive species (RS) that influence the aging, properties, and health effects of atmospheric aerosols. In this study, we explore the RS yields of aerosol samples from a remote forest (Hyytiälä, Finland) and polluted urban locations (Mainz, Germany; Beijing, China), and we relate the RS yields to different chemical constituents and reaction mechanisms. Ultra-high-resolution mass spectrometry was used to characterize organic aerosol composition, electron paramagnetic resonance (EPR) spectroscopy with a spin-trapping technique was applied to determine the concentrations of ⚫OH, O2⚫-, and carbon- or oxygen-centered organic radicals, and a …

humic-like substancesAtmospheric ScienceReaction mechanism010504 meteorology & atmospheric sciencesQC1-999Radicalchemistry.chemical_element010501 environmental sciences01 natural scienceswater-soluble pm2.5114 Physical scienceselectron-paramagnetic-resonance11. Sustainabilitypersistent free-radicalsQD1-999Chemical compositionScavenging0105 earth and related environmental sciencespolycyclic aromatic-hydrocarbonsatmospheric hydrogen-peroxideAqueous solutionChemistryhydroxyl radicalsPhysicstransition-metalsParticulatesoxalic-acidAerosolChemistry13. Climate actionEnvironmental chemistryCarbonsecondary organic aerosol
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Density-Functional Tight-Binding Simulations of Curvature-Controlled Layer Decoupling and Band-Gap Tuning in Bilayer MoS2

2014

Monolayer transition-metal dichalcogenides (TMDCs) display valley-selective circular dichroism due to the presence of time-reversal symmetry and the absence of inversion symmetry, making them promising candidates for valleytronics. In contrast, in bilayer TMDCs both symmetries are present and these desirable valley-selective properties are lost. Here, by using density-functional tight-binding electronic structure simulations and revised periodic boundary conditions, we show that bending of bilayer MoS2 sheets breaks band degeneracies and localizes states on separate layers due to bendinginduced strain gradients across the sheets. We propose a strategy for employing bending deformations in b…

transition-metal dichalcogenidesaugmented-wave method
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Cleavage of Ge–Ge and Sn–Sn Triple Bonds in Heavy Group 14 Element Alkyne Analogues (EAriPr4)2 (E = Ge, Sn; AriPr4 = C6H3-2,6(C6H3-2,6-iPr2)2) by Rea…

2016

The reactions of heavier group 14 element alkyne analogues (EAriPr4)2 (E = Ge, Sn; AriPr4 = C6H3-2,6-(C6H3-2,6-iPr2)2) with the group 6 transition-metal carbonyls M(CO)6 (M = Cr, Mo, W) under UV irradiation resulted in the cleavage of the E–E triple bond and the formation of the complexes {AriPr4EM(CO)4}2 (1–6), which were characterized by single crystal X-ray diffraction as well as by IR and multinuclear NMR spectroscopy. Single-crystal X-ray structural analyses of 1–6 showed that the complexes have a nearly planar rhomboid M2E2 core with three-coordinate group 14 atoms. The coordination geometry at the group 6 metals is distorted octahedral formed by four carbonyl groups as well as two br…

triple bondkoordinaatiokompleksitalkyne analoguessiirtymämetallien karbonyylikompleksittransition-metal carbonylssidosten hajoaminenkolmoissidoksetkompleksiyhdisteetalkyynianalogitbond cleavage
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