Search results for "Spectrum"
showing 10 items of 2043 documents
Hantzsch Ester-Mediated Photochemical Transformations in the Ketone Series: Remote C(sp3)–H Arylation and Cyclopentene Synthesis through Strain Relea…
2021
A metal-free Hantzsch ester-mediated synthesis of cyclopentenylketones as well as γ-hetarylketones starting from ketocyclopropanes under eco-friendly conditions was developed. The versatility of the developed conditions is shown by reacting ketocyclopropanes in both a formal [3 + 2] cycloaddition with terminal alkynes (further investigated using theoretical calculations) and a radical C-C-coupling with cyanopyridines. The newly developed methodologies were later on utilized as a downstream reaction for photogenerated cyclopropanes combining UV and visible light photochemistry. Following this procedure, a UV-driven Norrish-Yang-type reaction induces the ring strain of the intermediates, whic…
Single-Molecule Spectroscopy of MEH-PPV Polymer Molecules in Different Host Matrices
2009
Fluorescence emission and excitation spectra of single MEH-PPV molecules dispersed in three different host polymers (PMMA, PS, and Zeonex) have been recorded at 1.2 K. We observed only minor effects of the host matrix on the following parameters: the ratios of single-chromophoric to multichromophoric emission, the widths of the distributions of emission maxima, and the (generally very low) fraction of emission spectra with sharp zero-phonon lines. The differences are tentatively attributed to different conformations of MEH-PPV chains, subtle variations in local chromophore−matrix interactions, and/or different distributions of conjugation lengths of emitting chromophores, respectively. Usin…
Red-light-emitting electrochemical cell using a polypyridyl iridium(III) polymer.
2009
A deep-red phosphorescent ionic iridium(III) complex is prepared and incorporated into a polymer. Both the complex (1) and the polymer (2) were used as the single active material in solid-state light-emitting electrochemical cells (LECs). The devices built up using 1 and 2 emit in the deep-red region of the visible spectrum with CIE coordinates x = 0.710; y = 0.283 and x = 0.691; y = 0.289, respectively, making them one of the deepest-red emitting LECs reported. It is the first example of a polymeric LEC incorporating an ionic iridium complex, which exhibits increased stabilities compared with the device based on the small molecular weight complex.
Low-dimensional iodide perovskite nanocrystals enable efficient red emission
2019
We report herein a simple ligand-assisted reprecipitation method at room temperature to synthesize mixed-cation hybrid organic–inorganic perovskite nanocrystals with low structural dimensionality.
<title>Effect of light exposure on dislocation mobility in fullerite C60 crystals</title>
2001
The illumination-time evolution and the wavelength dependence of the photoinduced changes in dislocation mobility on the (111) face of C60 single crystals in air for the wavelength range 150 - 900 nm and power densities 0.2 - 2 mW/cm2 has been investigated. The results show that the light exposure in air leads to the decrease of the dislocation mobility. The magnitude of the effect as a function of the illumination time was investigated and a two-stage relationship was obtained. The ultraviolet light was found to be more effective than the visible light in the photoinduced reduction of dislocation mobility and solubility. In the wavelength range of 150 - 700 nm, the reduction of dislocation…
Carbon nitride as photocatalyst in organic selective transformations
2020
Abstract Graphitic carbon nitride (g-C3N4) is a metal-free conjugated polymer which has become a new research hotspot in photocatalysis. It can be used for solar energy exploitation like in solar energy organic synthesis, one of the most new and appealing green applications of heterogeneous photocatalysis. This chapter resumes the state-of-the-art and progresses in the application of heterogeneous visible light photocatalysis in organic selective transformations by using C3N4 as photocatalyst.
Mass spectra of halogenated esters 6—Methyl esters of some trihalogenated propanoic and butanoic acids
1984
The mass spectral fragmentation of trihalogenated methyl esters, formed in the reactions of monochlorinated methyl propenoates and 2-butenoates with Cl2, BrCl and Br2, have been investigated. In most cases α-cleavage gives the base peak, [COOCH3]+, the peaks originating from the subsequent losses of one or two halogen atoms also being abundant. The primary loss of a halogen atom is more prominent in the C4 derivatives, Br˙ and Cl˙ being preferentially lost from the 2- and 3-positions, respectively. The McLafferty rearrangement yields in one case the base peak; the 2-halo compounds could in general be distinguished by that fragmentation. Typical for all 2-bromo-substituted methyl butanoates …
ChemInform Abstract: Preparation and Structural Characterization of (Me3SiNSN)2Se, a New Synthon for Sulfur-Selenium Nitrides.
2010
The reaction of (Me(3)SiN)(2)S with SeCl(2) (2:1 ratio) in CH(2)Cl(2) at -70 degrees C provides a route to the novel mixed selenium-sulfur-nitrogen compound (Me(3)SiNSN)(2)Se (1). Crystals of 1 are monoclinic and belong the space group P2(1)/c, with a = 7.236(1) A, b = 19.260(4) A, c = 11.436(2) A, beta = 92.05(3) degrees, V = 1592.7(5) A(3), Z = 4, and T = -155(2) degrees C. The NSNSeNSN chain in 1 consists of Se-N single bonds (1.844(3) A) and S=N double bonds (1.521(3)-1.548(3) A) with syn and anti geometry at the N=S=N units. The N-Se-N bond angle is 91.8(1) degrees. The EI mass spectrum shows a molecular ion with good agreement between the observed and calculated isotopic distributions…
Photon yields and decay times of cross luminescence in ionic crystals
1992
The authors report on the scintillation properties of the ternary inorganic crystals KMgF/sub 3/, KYF/sub 4/:Rb, K/sub 2/YF/sub 5/, KLuF/sub 4/, RbMgF/sub 3/, KZnF/sub 3/, BaTm/sub 2/F/sub 8/, LiYF/sub 4/:Nd, and BaF/sub 2/:Rb. The scintillation light output of these crystals was estimated from the X-ray-induced emission spectra. Optical absorption spectra and decay time spectra were also measured and are presented. The first four crystals produced cross-luminescence (CL) with a decay time of about 1.5 ns. CL was not observed for the other crystals. >
Pyrrole Studies XXVII.1Utilisation of 1-Methyl-2-pyrrolyl Lithium in the Synthesis of 1-Methyl-2-substituted Pyrroles
1982
Abstract Although metallation of 1-substituted pyrroles with alkyl lithium reagents to give the lithiated derivatives has been recorded by several research groups,4–6 only limited use has been made of these derivatives in the synthesis of 1,2-disubstituted pyrroles. Subsequent to ourinitial studies,7 it was reported that tetrahydrofuran was the solvent of choice for the formation of the mono-lithiated pyrrole derivative and that the rate of the metallation was accelerated by the presence of TMEDA.6 We had noted,7 however, that prolonged reaction of n-butyl lithium with 1-methylpyrrole in a 2:1 mixture of tetrahydrofuran:hexaneat ca 18°C in the absence of TMEDA gave 1-methyl-2-pyrrolyl lithi…