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21.
Hexaphyrin(1.0.1.0.0.0) (isoamethyrin) undergoes a significant color change in the presence of UO22+, PuO22+, and NpO22+. The complexation of the first of these dioxo actinide cations was studied in semi-quantitative fashion in 1:1 MeOH-CH2Cl2. Under these conditions, the detection limit for UO22+ was found to be ca. 5.8 ppm by naked eye monitoring and <28 ppb by UV-vis spectroscopy. Isoamethyrin does not undergo a color change in the presence of most transition metals or when exposed to Gd(III). Isoamethyrin thus constitutes an attractive alternative to 2,2′(1,8-dihydroxy-3,6-disulfonaphthylene-2,7-bisazo)-bisbenzenarsonic acid (AzIII) and 2-(5-bromo-2-pyridylazo)-5-(diethylamino)phenol (BrPADAP), systems currently used as actinide cation sensors.  相似文献   
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Poly(ethylene isophthalate) (PEI) was synthesized for this research with essentially a condensation polymerization of isophthalic acid and ethylene glycol catalyzed by zinc acetate and antimony trioxide. Several samples were obtained, and their characteristics were observed and compared with poly(ethylene terephthalate) (PET). The synthesized PEI samples were chemically identified by 1H NMR. Thermal analysis with differential scanning calorimetry (DSC) yielded results that indicate the samples were primarily amorphous, with a glass‐transition temperature of 55–60 °C. Molecular weights of these PEI samples were also obtained through intrinsic viscosity measurements (Mark–Houwink equation). Molecular weights varied with conditions of the polymerization, and the highest molecular weight achieved was 21,000 g/mol. Finally, the diffusion coefficient, solubility, and permeability of CO2 gas in PEI were measured and found to be substantially lower than in PET, as anticipated from their isomeric chemical structures. This is because in PET the phenyl rings are substituted in the para (1,4) positions, which allows for their facile flipping, effectively permitting gases to pass through. However, the meta‐substituted phenyl rings in PEI do not permit such ring flipping, and thus PEI may be more suitable for barrier applications. © 2004 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 42: 4247–4254, 2004  相似文献   
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NaBH4 reduction of a cage dione proceeds in a stereospecific fashion to give theendo,endo-diol. This reactivity is related to the crystal structure.  相似文献   
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This author wants to express his thanks to the School of Information Engineering at Teesside Polytechnic, Middlesbrough, England, for its support and hospitality during a visiting appointment of 3 months in 1989, when this paper was written.  相似文献   
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The concept of backward extension for subnormal weighted shifts is generalized to arbitrary subnormal operators. Several differences and similarities in these contexts are explored, with emphasis on the structure of the underlying measures.

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Bies et al. (J. Sound Vib. 204(4) (1997) 631) investigated Curle's theory (Proc. R. Soc. Ser. A 231 (1955) 505) published in 1955 over a wide range of flow speeds from about 50-200 m/s and found only partial agreement with the experimental data. Here the experimental investigation has been repeated allowing the data to be recorded in a format amenable to analysis, which was not previously possible.Reintroduction of a term neglected by Curle has been found necessary as Curle's compact source condition ensures so low a radiation impedance that the effect cannot be detected in the jet background noise. The reintroduction of the term, which has been neglected, allows his analysis to include radiation from sources not compact but less than half a wavelength in characteristic dimension. It is shown that the power ratio defined as the measured sound power divided by Curle's amended prediction converges to about 3 whereas Curle predicts that the power ratio should converge to 1 as the wave number converges to zero. The introduction of the empirically determined constant 3 into Curle's prediction brings the measurements into very good agreement with prediction over the entire range of the non-dimensional wave numbers from about 0.4 to 3.2.  相似文献   
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