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1.
This study investigates a holographic recording effect of biphotonic polarization gratings (BPGs) written on dye-doped liquid crystal (DDLC) films. One linearly polarized green light (λG = 514.5 nm) and a polarization-modulated interference pattern formed by two mutually coherent orthogonal (±45° with respect to the polarization of the green light) polarized red lights simultaneously excite the DDLC films to generate a BPG. The formation of BPGs depends primarily on the dichroism of the dye molecules and a sequence of mechanisms: photoisomerization, anisotropic adsorption and inhibition of dye adsorption. The cis-isomer absorbance-modulated distribution associated with the red polarization-modulation pattern induces the dye adsorption-modulated pattern, in turn, yielding the permanent BPG which generates a modulated twisted nematic (TN) structure pattern in the sample. It is found that each BPG is verified to be electrically switchable and thermally erasable. The switching time is in the order of milliseconds. Additionally, the recording time to form a BPG decreases with increasing intensity of the green pump beam. 相似文献
2.
Dorris Heiligmann und L. Acker 《Fresenius' Journal of Analytical Chemistry》1955,144(4):291-294
Ohne Zusammenfassung 相似文献
3.
The chemical etching of silicon using HF-HNO3 mixtures is a widely used process in the processing of silicon wafers for microelectronic or photovoltaic applications. The control of the etch bath composition is the necessary condition for an effective bath utilization, for the replenishment of the consumed acids, and to maintain a certain etch rate. The present paper describes two methods for the total analysis of the individual etch bath constituents HF, HNO3, and H2SiF6. Both methods start with an aqueous acid-base titration determining the total acid concentration and the concentration of H2SiF6. The first method is an acid-base titration using a 0.1 mol L−1 methanolic solution of cyclohexylamine (CHA) as non-aqueous titrant to determine the content of nitric acid. Then, the amount of hydrofluoric acid is calculated from the difference between the total acid and nitric acid content. The second method is based on the determination of the total fluoride concentration using a fluoride ion-selective electrode (F-ISE). The content of hydrofluoric acid is obtained from the difference between the total fluoride content and the amount of fluoride bound as H2SiF6. The amount of nitric acid results finally calculated as difference to the total acid content. 相似文献
4.
L. Acker 《Fresenius' Journal of Analytical Chemistry》1960,173(2):168
Ohne Zusammenfassung 相似文献
5.
L. Acker 《Fresenius' Journal of Analytical Chemistry》1960,178(3):228
Ohne Zusammenfassung 相似文献
6.
L. Acker 《Fresenius' Journal of Analytical Chemistry》1960,178(1):80
Ohne Zusammenfassung 相似文献
7.
L. Acker 《Fresenius' Journal of Analytical Chemistry》1960,176(2):143
Ohne Zusammenfassung 相似文献
8.
Ermann M Simkovsky NM Roberts SM Parry DM Baxter AD 《Journal of combinatorial chemistry》2002,4(4):352-358
A solid-phase synthesis of substituted cyclic urea derivatives as potential heterocyclic library scaffolds is described. 2-Amino-3-nitropyridine is attached to Wang resin via a carbamate linkage. Reduction of the nitro group was achieved with SnCl(2).2H(2)O. Reductive alkylation with a range of substituted benzaldehydes followed by cyclative cleavage afforded a small library of 3-substituted imidazo[4,5-b]pyridine-2-ones in 33-45% yield and 59-88% purity. Subsequently, this methodology was applied to the synthesis of 3-substituted imidazo[4,5-f]quinolin-2-ones. 相似文献
9.
Thilo Berkenbusch Andy Ch. Laungani Reinhard Brückner Manfred Keller 《Tetrahedron letters》2004,45(52):9517-9520
4-tert-Butyl-2-cyclohexen-1-one dimerizes in THF solution via its kinetic enolate, leading to di-tert-butylditwistane 8 in up to 36% yield (−78 °C → room temp., protonolysis, flash chromatography). X-ray crystallography shows that 8 incorporates one R and one S enantiomer of the starting ketone; none of the diastereomeric ditwistanes epi-8, epi’-8 or iso-8 was isolated. This means that the formation of 8 proceeds with mutual kinetic resolution and 100% induced diastereoselectivity. 相似文献
10.