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131.
Three new complexes, [Zn(dbsf)2(dmf)2] · 5.5dmf (dbsf = 4,4′-sulfonyldibenzoate) (1β), [Cu(tdsa)(phen)2] · 1.5EtOH (tdsa = 5,5′-thiodisalicylate, phen = 1,10-phenanthroline) (2), and [Cu(sdp)(phen) · Cu(Hsdp)(phen)(CH3COO)] · 3EtOH (sdp = 4,4′-sulfonyldiphenolate) (3) were prepared and structurally characterized. Complex 1β shows a one-dimensional coordination framework constructed from bridges between Zn(II) centers with two ligands. Complex 2 is a monomeric complex, which assembles by π–π interactions. Complex 3 shows a unique two-dimensional coordination framework that is constructed from two Cu(II) centers, sdp, and Hsdp. The redox properties of these three complexes were characterized by solid-state cyclic voltammetry. Complexes 1β and 3 show irreversible reduction waves because of the reduction of their sulfone sites. Complex 2 shows an irreversible oxidation wave because of oxidation of the sulfide site.  相似文献   
132.
A polyvinyl chloride (PVC, [CH2CHCl]n) sample was ground with one of the following oxide samples, lanthanum oxide (La2O3) and calcium oxide (CaO), as a reference, to investigate its mechanochemical (MC) decomposition. According to the XRD patterns for the ground products, peaks of lanthanum oxy-chloride, LaOCl which is water insoluble, were observed to appear in the patterns of the mixture samples at a molar ratio of (PVC: La2O3 = 1:2) and (1:4), after 20 min grinding, while the patterns of the ground PVC-CaO mixtures show the formation of CaOHCl, which is water soluble, in the products after 2 h grinding. TG patterns taken for the PVC-La2O3 mixtures ground for different periods of time do not indicate significant weight loss in the range from 200 to 300 degrees C, and this suggests that La2O3 is more effective additive than CaO in the MC decomposition for PVC. FT-IR patterns for organic phases in the ground mixture show the reduction of CCl bindings in the PVC structure. The MC reaction between PVC and La2O3 is accompanied by the formation of C-O single bonds, to form LaOCl, which is insoluble in water at ambient condition. This is the reason why the yield of Cl extracted by the water leaching reaches only less than 50%, while it reaches almost 100% in the yield of Cl from the PVC-CaO mixture ground for 2 h or more.  相似文献   
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134.
Ten-eleven translocation (TET) proteins, a family of Fe2+- and 2-oxoglutarate-dependent dioxygenases, are involved in DNA demethylation. They also help regulate various cellular functions. Three TET paralogs have been identified (TET1, TET2, and TET3) in humans. This study focuses on the evolution of mammalian TET genes. Distinct patterns in TET1 and TET2 vs. TET3 were revealed by codon-based tests of positive selection. Results indicate that TET1 and TET2 genes have experienced positive selection more frequently than TET3 gene, and that the majority of codon sites evolved under strong negative selection. These findings imply that the selective pressure on TET3 may have been relaxed in several lineages during the course of evolution. Our analysis of convergent amino acid substitutions also supports the different evolutionary dynamics among TET gene subfamily members. All of the five amino acid sites that are inferred to have evolved under positive selection in the catalytic domain of TET2 are localized at the protein’s outer surface. The adaptive changes of these positively selected amino acid sites could be associated with dynamic interactions between other TET-interacting proteins, and positive selection thus appears to shift the regulatory scheme of TET enzyme function.  相似文献   
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136.
In recent years, the expansion of demand for lithium ion batteries has resulted in soaring prices of the constituent resources. From the viewpoint of safety, studies on all-solid-state batteries are actively being carried out. In this study, we succeeded in driving all-solid-state batteries derived from nontoxic oxide glasses at room temperature without requiring scarce resources such as lithium and cobalt. The main structure of the ceramic batteries with a simple structure in which Na2FeP2O7 crystallized glass and β″-alumina solid solution are joined by pressureless cofiring at 550°C. During the crystallization of Na2O-Fe2O3-P2O5 glass, fusion with the β″-alumina solid solution is achieved. Reversible charge and discharge of 80 mAh/g were achieved at room temperature. It is not necessary to apply pressure during cell preparation or the use of the batteries. Furthermore, the strong junction at the cathode and electrolyte interface does not peel off during charge and discharge over a long period of 623 cycles. Ex situ X-ray photoelectron spectroscopy revealed partial Fe4+ induction and a reversible charge and discharge reaction even after overcharging to 9 V. It was demonstrated that Na2FeP2O7 is very stable against overcharging to 9 V.  相似文献   
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138.
This paper presents the results of a series of experiments performed to examine the validity of a theoretical model for evaluation of cutting forces and machining error in ball end milling of curved surfaces. The experiments are carried out at various cutting conditions, for both contouring and ramping of convex and concave surfaces. A high precision machining center is used in the cutting tests. In contouring, the machining error is measured with an electric micrometer, while in ramping it is measured on a 3-coordinate measuring machine. The results show that in contouring, the cutting force component that influences the machining error decreases with an increase in milling position angle, while in ramping, the two force components that influence the machining error are hardly affected by the milling position angle. Moreover, in contouring, high machining accuracy is achieved in “Up cross-feed, Up cut” and “Down cross-feed, Down cut” modes, while in ramping, high machining accuracy is achieved in “Left cross-feed, Downward cut” and “Right cross-feed, Upward cut” modes. The theoretical and experimental results show reasonably good agreement.  相似文献   
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140.
The pervaporation behaviors of methanol–water by poly(γ-methyl L -glutamate) (PMLG) membrane at non-steady- and steady-state permeation were investigated. The values of t1/2 (time required to reach a half value of steady-state permeation flux) for methanol and water changed and did not change with the component in feed, respectively. Both of the average diffusion coefficients for methanol–and water–PMLG from the mixture changed exponentially with the sorption amount of methanol by the synergetic effect on diffusion. The difference in behavior of non-steady and steady state diffusion was explained by whether Do (diffusion coefficient at zero penetrant concentration) was influenced by the concentration distribution of penetrant in PMLG membrane.  相似文献   
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