Orientation, zinc

If the electrolysis parameters (precursor concentrations, pH, temperature, cur-rent/potential, substrate) be defined in a precise manner, a self-regulated growth of the compound can be established, and highly (111 )-oriented zinc blende (ZB) deposits up to several p,m thickness are obtained at potentials lying at the anodic limit of the diffusion range (Fig. 3.3) [60]. Currently, the typical method of cathodic electrodeposition has been developed to yield quite compact and coherent, polycrystalline, ZB n-CdSe films of well-defined stoichiometry. The intensity of the preferred ZB(f 11) orientation obtained with as-deposited CdSe/Ni samples has been quite high [61]. 

A unique feature of the interaction of the hormone and PLR is at the beginning of the F-G loop in the C-terminal domain. In HGR the sequence is Arg-Asn-Ser whereas in PLR it is Asp-His-deletion. This loop interacts with His 18 and Glu 174 of the hormone. In PLR the orientation of this loop is such that the Asp and His residues, in combination with His and Glu from the hormone, form a strong binding site for a zinc atom that links the hormone and the receptor (Figure 13.23b). The presence of zinc increases the affinity of the hormone for the receptor in vitro by a factor of 10,000. As shown by mutagenesis studies His 18 and Glu 174 of the hormone are important for the tight binding to PRL but not to GHR. 

Further examination of the chiral ketals reveals that the lone pairs available for reagent coordination are oriented either in a syw or an anti relationship to the neighboring methyl substituents. The influence of the chiral auxiliary over the reaction is now clear. If zinc coordination must occur proximal to the double bond. 

Since the system is processed as thermoplastics are processed, its reprocessability was studied under repeated cycles of extrusion in the MPT. Results of reprocessability studies are shown in Table 5. It is evident that after the first cycle viscosity increased slightly, which may be due to the orientation effect. In the subsequent cycles viscosity remained almost constant. Therefore, it is concluded that the zinc stearate plasticized zinc salt of m-EPDM is melt processable just as thermoplastics. 

It was noted (23) that the NMR spectrum of compound 32 was identical with that published (34) for the third product (assigned structure 29) isolated from the reaction of tetra-O-acetyl-2-hydroxy-D-glucal with acetic anhydride and zinc chloride. The identity of the compounds was fully established and a revised structure proposed for this third product. In the presence of zinc chloride, therefore, epimerization can occur at an allylic site and the quasi-equatorial C-4 acetoxy group in the erythro isomers 27 and 28 can assume the favored quasi-axial orientation (24). 

Fig. 3.6 XRD patterns (CuKa source) of equally thick deposits prepared on Ti at-1.2 V/SSEfromaO.5 x 10-3 M Se02, 0.2 M ZnS04, pH 2.5 solution at various temperatures (25-85 °C). Increase of bath temperature promotes the formation of zinc blende ZnSe crystallites, exhibiting a random orientation. The semimetallic, hexagonal phase of Se unavoidably forms together with the selenide compound. (With kind permission from Springer Science+Business Media [105])...

Epitaxial effects are not limited to single-crystalline substrates. The possibility for substrate-induced epitaxial development in the difficult case of ZnSe (cf. conventional electrodeposition) has been established also by using strongly textured, albeit polycrystalline, zinc blende (111) CdSe electrolytic films to sustain monolithic growth of ZnSe in typical acidic selenite baths [16]. Investigation of the structural relations in this all-electrodeposited ZnSe/CdSe bilayer revealed that more than 30-fold intensification of the (111) ZnSe XRD orientation can be obtained on the textured (111) CdSe films, compared to polycrystalline metal substrates (Fig. 4.2). The inherent problems of deposition from the Se(IV) bath, i.e., formation of... 

Significant improvements in ECALE deposit morphology and quality were reported as achieved by switching from a thin layer cell to a thick layer H-form cell, integrated in an automated deposition system [46]. Thin epitaxial films of zinc blende CdTe, CdSe, and CdS with predominate (111) orientations were grown. 

A similar one-step process was employed successfully [66] to prepare well-crystallized CdS thin films of optical quality on Au(lll) from an aqueous solution of CdSOa, EDTA, and Na2S at room temperature. A phase transition from cubic (zinc blende) to hexagonal (wurtzite) CdS structure was observed with decreasing pH below 5, while highly preferential orientation along [11.0] directions for the... 

Photoelectrochemical studies with ternary chalcogenide systems containing zinc as one of the components have been published however, such investigations on bulk or thin film binary ZnS and ZnTe electrodes are practically absent from the literature or may be found fragmentary in electrosynthesis-oriented works. ZnTe has been studied as a possible candidate for a photocathode in the photoelectrochemical production of hydrogen. Related information will be given in the relevant section. 

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