Tactic poly(crown ether)s with pendant benzocrown ethers

Summary Tactic and atactic poly(crown ether)s, poly(methacryloyloxymethylbenzo-15-crown-5), were synthesized by polymer reaction of the respective poly(methacrylic acid) with chloromethylbenzo-15-crown-5 and radical polymerization of methacryloyloxymethylbenzo-15-crown-5. By solvent extraction of alkali metal picrates with these poly(crown ether)s, the isotactic poly(crown ether) was found to be a little more selective for K⁺ and Rb⁺ than the syndiotactic and atactic ones.     

Electron spin resonance study of Langmuir-Blodgett films of N-docosylpyridinium- di(tetracyanoquinodimethane)

An electron spin resonance (ESR) investigation is performed on Langmuir-Blodgett films consisting of a surface-active 1:2 complex of N-docosylpyridinium and tetracyanoquinodimethane (TCNQ), whose temperature-dependent spin susceptibility has been so far found to be consistent with the random-exchange Heisenberg antiferromagnetic chain (REHAC) model of Soos and Bondeson. An out-of-plane anisotropy in the ESR spectra shows that the long axes of TCNQ molecules are preferentially oriented along the plane normal to the sample, where the negligible in- plane anisotropy indicates the random distribution of the short and the pπ orbital axes in the film plane. A heat treatment applied to the samples results in an increase in the concentration of disorder, showing the possibility of controlling it in the present REHAC system.     

Redox reaction of tri(2-deoxy-2-L-ascorbyl)amine. Formation of a persisting free radical species in water

Electrochemical studies showed that tri(2-deoxy-2-L-ascorbyl)amine ($\text{1}$), a new compound isolated as one of the products of reaction of dehydro-L-ascorbic acid with phenylalanine (with added L-ascorbic acid) in ethanol, is oxidized in aqueous solution in two reversible one-electron transfer steps, on mercury or platinum electrode. The first step occurs through the dianion, and its product is an unusually stable blue anion radical giving a characteristic ESR signal. The product of the second step of oxidation is labile and is slowly converted into the oxidized form of di(2-deoxy-2-L-ascorbyl)amine, presumably by hydrolysis with splitting of L-ascorbic acid.     

An 18-ns 1-Mbit CMOS SRAM

A 1-Mb (256 K×4 b) CMOS static random-access memory with a high-resistivity load cell was developed with 0.7-μm CMOS process technology. This SRAM achieved a high-speed access of 18 ns. The SRAM uses a three-phase back-bias generator, a bus level-equalizing circuit and a four-stage sense amplifier. A small 4.8×8.5-μm² cell was realized by the use of a triple-polysilicon structure. The grounded second-polysilicon layer increases cell capacitance and suppresses α-particle-induced soft errors. The chip size measures 7.5×12 mm²     

In vivo fluoride profiles at different sites of buccal and lingual enamel surfaces obtained by enamel biopsy of human maxillary first permanent molars in young adults

Twenty male volunteers, average age 24 years, participated in this study. Specimens were obtained by enamel biopsy using 5 microliters of 0.5 M HClO4 for 30 s. Using a regression curve, comparisons of fluoride concentrations were made at different depths. The fluoride concentrations (mean +/- SE) at a depth of 5 microns were highest in the distobuccal (1698 +/- 136), high in the mesiobuccal (1343 +/- 122), low in the distolingual (1119 +/- 107), and lowest in the mesiolingual sites (819 +/- 78). Of the interior enamels (> or = 10 microns in depth), the distobuccal site (1330 +/- 88 parts/10(6) F at 10 microns) had a higher-concentration than all other sites. The fluoride profiles were steepest to shallowest in the order: distobuccal, mesiobuccal, distolingual and mesiolingual. There were no correlations between the enamel fluoride concentrations and the fluoride concentration in parotid saliva. It was concluded that in vivo fluoride profiles of maxillary first molars reflect the wear of the tooth surface with age and the condition of dental plaque deposition, and, to some extent, the site-specific distribution of saliva between buccal and lingual surfaces.     

Repetition bend properties of Cu-Cr and Cu-Cr-Sn alloys

Repetition numbers of bending of Cu-0.81 wt% Cr, Cu-0.81 wt% Cr-0.14 wt% Sn and Cu-0.26 wt% Cr-0.10 wt% Sn alloys were investigated. After solution treatment, the first two types of copper alloys have a primary chromium phase; this is not so in the last alloy. The primary chromium phase does not influence the repetition numbers of bending of cold-rolled specimens; the repetition numbers of bending of specimens aged at 723 K for 1.8 × 10³ sec after cold rolling are higher than those of cold-rolled specimens. The cause of this is considered to be a recovery of work-hardening during ageing.     

Photoresponsive liquid membrane transport of alkali metal ions using crowned spirobenzopyrans

Several azacrown ether derivatives, which are monoaza-12-crown-4, -15-crown-5, and -18-crown-6 and diaza-12-crown-4 and -18-crown-6, bearing one or two spirobenzopyran(s), which we call crowned spirobenzopyran or crowned bis(spirobenzopyran), were synthesized and were used as carriers for liquid membrane transport of alkali metal ions. The passive alkali metal transports through liquid membranes containing crowned spirobenzopyrans were carried out under dark, and UV- and visible-light irradiation conditions. The metal ion transport was accelerated and retarded by UV- and visible-light irradiation, respectively. On the other hand, the photoresponse of the metal ion selectivity in membrane transport by crowned spirobenzopyrans was different, depending on the kind of crown ether units. Especially, diaza-12-crown-4-bis(spirobenzopyran) exhibited an excellently selective and effective transporting ability for Li(+). The uphill transports of Li(+) through a liquid membrane containing monoaza-12-crown-4-spirobenzopyran or diaza-12-crown-4-bis(spirobenzopyran) were realized under the conditions where the same aqueous solution was used as the source and receiving phases with UV and visible lights being irradiated onto the boundary phases between the source and membrane phases and between the receiving and membrane phases, respectively. The uphill transport of Li(+) from the source to receiving phases through a liquid membrane containing a crowned spirobenzopyran was also attained by the proton-concentration gradient between the source and receiving phases under dark conditions, and the transporting ability was remarkably increased by photoirradiation.