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911.
Michael Hengge Paul Hänsch Daniel Ehjeij Frank S. Benneckendorf Jan Freudenberg Uwe H. F. Bunz Klaus Müllen Emil J. W. List-Kratochvil Felix Hermerschmidt 《Journal of polymer science. Part A, Polymer chemistry》2022,60(12):1878-1886
An increasing number of organic light-emitting diodes (OLEDs) is nowadays based on the use of polymers as the emissive material. For this material class in particular, solution-processing of the OLEDs has gained traction in both research and industry. However, in order to access multilayer material systems, orthogonal solvents must be used to prevent dissolution of previously prepared layers. The use of crosslinkers can facilitate this production method by reducing the number of orthogonal solvents needed since insoluble networks are generated. In this work, a novel bisazide crosslinker is employed to insolubilize Super Yellow, a polyphenylene-vinylene emitter. This allows the use of an additional poly[bis(4-phenyl)(2,4,6-trimethylphenyl)amine electron blocking layer (EBL) from the same solvent. Devices including the blocking layer show improved efficacies compared to reference devices without the additional EBL, while also maintaining the emission spectrum. Using the upscalable technique of doctor blading, OLEDs were fabricated which showed a particularly noticeable effect of the blocking layer with a nearly twofold increase in luminance and a 56% increase in current efficacy. 相似文献
912.
A new NMR-based method for the discrimination of olive oils of any grade from seed oils and mixtures thereof was developed with the aim of allowing the verification of olive oil authenticity. Ten seed oils and seven monovarietal and blended extra virgin olive oils were utilized to develop a principal component analysis (PCA) based analysis of 1H NMR spectra to rapidly and accurately determine the authenticity of olive oils. Another twenty-eight olive oils were utilized to test the principal component analysis (PCA) based analysis. Detection of seed oil adulteration levels as low as 5% v/v has been shown using simple one-dimensional proton spectra obtained using a 400 MHz NMR spectrometer equipped with a room temperature inverse probe. The combination of simple sample preparation, rapid sample analysis, novel processing parameters, and easily interpreted results, makes this method an easily accessible tool for olive oil fraud detection by substitution or dilution compared to other methods already published. 相似文献
913.
Hilary E. Kent Terence H. Lilley Peter J. Milburn Michael Bloemendal Gus Somsen 《Journal of solution chemistry》1985,14(2):101-115
Enthalpies of dilution of the N-acetyl amides of glycine, L-alanine, L-valine, L-leucine, and L-phenylalanine, dissolved in N,N-dimethylformamide (DMF) as a solvent have been measured at 25°C. The results obtained have been analyzed to give the enthalpic interaction (or virial) coefficients of the solutes and these are compared with information previously obtained in aqueous systems. There are marked differences in the interaction properties in the two solvents and, while the additivity approach of Savage and Wood is applicable to the solutes in water it is not suitable for representing the interactions in DMF. A correlation is presented between the enthalpic second virial coefficients in DMF and the propensity of side-chains to be in proximity in globular proteins. 相似文献
914.
The cycloaddition of Cr-co-ordinated alkyne, carbene and carbonyl ligands provides a variable route to the anthracyclinone skeleton. The key step of a formal total synthesis of4-demethoxydaunomycinone (1) is based on the reaction of carbonyl-carbene complex 15—used as a CD ring synthon—and alkyne 9 leading to the formation of ring B. 相似文献
915.
A. Stanley Jones Michael J. McClean Hironichi Tanaka Richard T. Walker Jan Balzarini Erik De Clercq 《Tetrahedron》1985,41(24):5965-5972
Reaction of 2',3'-secouridine with acetone gave the 3',5'--isopropylidene derivative (1) which upon treatment with mesylchloride gave the 2'--mesyl compound (2). Replacement of the mesyl group of 2 with halide could be effected by reaction with a metal halide in DMF. The 3',5'--isopropylidene group was removed simultaneously to give a 2'-halogeno-2'-deoxy-2',3'-secouridine. 2',3'-Dichloro-2',3'-dideoxy-2',3'-secouridine upon treatment with base gave 6()-chloromethyl-2()-(uracil-1-yl)-1,4-dioxane in addition to O2,2'-anhydro-3'-chloro-3'-deoxy-2',3'-secouridine, as previously reported. 2',3'-Dichloro-2',3'-dideoxy-5'-0-trityl-2',3'-secouridine was converted to 2',3'-dichloro-2',3'-dideoxy-2',3'-secocytidine (16) a triazole derivative. Compound 16 was unstable and appeared to form O2,2'-anhydro-3'-chloro-3'-deoxy-2,3'-secocytidine upon standing at room temperature. 5-Vinyl- and 5-() (2-bromovinyl) uridine dialdehydes have been made, as well as a number of other 5-substituted 2',3'-secouridine derivatives. None of the compounds obtained showed significant activity against a number of virus strains or tumor cell lines, except for 5-()(2-bromovinyl) uridine dialdehyde, which was inhibitory to the growth of human lymphoblast (Raji, Namalva) cells at a concentration of 28 μ/ml. 相似文献
916.
Abstract— Time-resolved fluorescence microscopy using excitation by actively mode-locked dye lasers and analysis by time-correlated single photon counting is shown to be an effective way of obtaining a high degree of spatial and temporal resolution. The imaging capabilities of the microscope make for optimal instrument response functions even with inexpensive photomultiplier tubes. Thus far limited (by the laser source) to long wavelength visible excitation, the excellent light collection and imaging, coupled with the sensitivity of single photon counting make it highly probable that the much weaker U-V second harmonics of the visible dyes will be useable. Certainly the potential of using the third harmonic line (355 nm) of a mode-locked c.w. Nd: YAG laser, or fundamental lines from mode-locked c.w. ion lasers as excitation sources will enhance the technique. Nevertheless, with visible-absorbing dyes only it is possible to excite such fluorochromes as chlorophylls, porphyrins, xanthenes (rose bengal, erythrosin B), phycobiliproteins, thionine dyes, ethidium bromide, and so on. Furthermore, this technique can be straightforwardly extended for polarized light measurements thereby allowing determinations of rotational diffusion of fluorochromes in cells and organelles. The extension to variable temperature situations is easy to conceive. In addition to its use for examination of cellular and sub-cellular entities, the equipment described can be profitably employed wherever spatial resolution may provide extra information, such as studies of powders and the structures of surfaces and interfaces. 相似文献
917.
简要总结了我们在C=C及C=O双键低温加氢双金属催化剂方面的最新研究成果. 首先, 我们以环己烯加氢为探针反应, 证明了平行使用多种研究手段的重要性, 包括单晶表面的基础研究与DFT计算, 多晶表面的合成与表征, 负载型催化剂的制备与性能测试等. 其次, 总结了双金属催化剂在其他加氢反应, 如丙烯醛C=O双键的选择性加氢, 苯的低温加氢, 以及乙炔的选择性加氢等反应中的应用. 最后, 讨论了利用金属碳化物代替贵金属Pt以减少双金属催化剂中Pt用量的可能性. 相似文献
918.
Michael I. Bruce Omar bin Shawkataly Brian K. Nicholson 《Journal of organometallic chemistry》1985,286(3):427-437
H2Ru3(μ3-S)(CO)9 is deprotonated by K[HBBus3] to give cluster anions which react with [O{Au(PPh3)}3]+ or with AuCl(PPh3)/T1+ to give HRu3Au(μ3-S)(CO)9(PPh3) (1) and Ru3Au2(μ3-S)(CO)9(PPh3)2 (3). A similar sequence with HRu3(μ3-SBut)(CO)9 leads to Ru3Au(μ3-SBut)(CO)9(PPh3) (2) as the main product although some 1 also forms, indicating SC cleavage competes with deprotonation of HRu3(μ3-SBut)(CO)9 by [HBBus3]?. The X-ray crystal structures of 1, 2 and 3 are described; (1) and (2) have “butterfly” AuRu3 cores with markedly different hinge angles of 119 and 148° respectively, while 3 has a trigonal-bipyramidal Au2Ru3 skeleton. All three clusters have the sulphur atom symmetrically bridging the Ru3 triangular face. 相似文献
919.
Peter Bougeard Christopher J. Cooksey Michael D. Johnson Melanie J. Lewin Stewart Mitchell Paul A. Owens 《Journal of organometallic chemistry》1985,288(3):349-358
Under irradiation by tungsten light in pyridine solution, several substituted alkylcobaloximes undergo rearrangement to more stable substituted alkyl- or alkenyl-cobaloximes. When the same reactions are carried out in the presence of carbon tetrachloride or chloroform, no rearranged organocobaloximes are obtained, but a variety of organic products are obtained derived from the interception of transient organic radicals by the halogenated solvent. The rearrangements are rationalised in terms of a reversible homolysis of the carbon-cobalt bond, rearrangement of the organic radical and recapture by the cobalt(II) fragment to give complexes that are more stable to irradiation than their precursors. 相似文献
920.
Alan W. Duff Peter B. Hitchcock Michael F. Lappert Richard G. Taylor John A. Segal 《Journal of organometallic chemistry》1985,293(3):271-283
n-Heptane-soluble “di-butylmagnesium” (I) (a commercially available material, prepared by addition of LiBus to MgBunCl, and subsequent addition of ca. 5% MgOct2n) has been found to be a useful starting material for obtaining numerous organic magnesium compounds. This is illustrated by its reaction with a number of protic compounds HA to give in good yields Mg(C5H5)2, Mg(C5H4Me)2, or the new compounds MgA2: IV (A = C5H4SiMe3), V [A = C5H3(SiMe3)2], VII (A = OC6H2Bu2t-2,6-Me-4), and X [A2 = N(SiMe3)C6H4N(SiMe3)-o(OEt2)]. The value of such compounds MgA2 as mild ligand transfer reagents is illustrated by the synthesis of Zr(C5H3X2)Cl3 (X = H or SiMe3). Compound X was isolated from OEt2 solution as the crystalline dimer with two o-(SiMe3)C6H4(SiMe3) ligands bridging two magnesium atoms and a terminal OEt2 ligand completing a distorted tetrahedral environment around each Mg. Some key parameters are: MgNt 1.997(7), MgNb 2.083(8), MgO 2.041(7) Å; OMgNt 112.1(3), OMgNb 119.7(3), and NtMgNb 118.5(3)°. 相似文献