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61.
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63.
Nancy C. Stoffel Edward J. Kramer Willi Volksen Thomas P. Russell 《Journal of Polymer Science.Polymer Physics》1998,36(13):2247-2258
Para-, meta-, and mixed isomeric poly(amic ethyl ester) precursors of the polyimide based on pyromellitic dianhydride (PMDA) and 3,4′-oxydianiline (3,4′-ODA) were synthesized. The intrinsic viscosity of each of the isomers was measured in an NMP solution and found to be less than corresponding isomers derived from PMDA and 4,4′-oxydianiline (4,4′-ODA) precursors with comparable molecular weight. The imidization and solvent retention were measured as a function of imidization temperatures, Ti using forward recoil spectrometry (FRES). For samples cast from a single solvent, either N-methyl pyrrolidone (NMP) or dimethyl sulfoxide (DMSO), no difference was observed in the temperature-dependent imidization behavior between the isomers. In all cases the imide fraction f increased as Ti increased, and reached a value of unity, i.e., full conversion at 400°C. At the same Ti, samples cast from DMSO showed a slightly higher f than samples cast from NMP. FRES and time of flight FRES (TOF-FRES) were used to measure the interdiffusion distance, w, of deuterium-labeled tracers into nondeuterated base layers of the polyimide of PMDA/3,4′-ODA treated at various Ti. The primary determinant of w for all isomers was Ti, and the particular isomer used as either the base or the tracer molecule did not seem to affect w. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 2247–2258, 1998 相似文献
64.
Perfluoro‐Tagged Benzyloxycarbonyl Protecting Group and Its Application in Fluorous Biphasic Systems
The synthesis of a new perfluoro‐tagged benzyloxycarbonyl protecting group is reported, as well as its application in the parallel protection of amines. Isolation of the protected amines was performed by simple liquid‐liquid extraction between perfluorinated and organic solvents. Deprotection was achieved by standard hydrogenolysis. The novel protecting group was also applied to cyclization protocols leading to quinazoline‐2,4‐diones. These products were isolated by simple extraction procedures 相似文献
65.
66.
An optimally capped duplex DNA (σ-DNA) was synthesized in which the cytosines in the homopyrimidine strand of σ-DNA 1 were replaced by 5-methylcytosine leading to σ-DNA 2 . Although only involving 13 base pairs, this modification resulted in very high melting temperatures above 90°. In addition, σ-DNA 2 was able to form triple helices with the corresponding homopyrimidine DNA or RNA even at neutral pH. This opens up the possibility to use σ-DNA in a triple-helix approach to modulate gene expressions on the level of the translation process. 相似文献
67.
We investigate the discrete chiral transformation of a Majorana fermion on a torus. Depending on the boundary conditions the integration measure can change sign. Taking this anomalous behavior into account we define a chiral order parameter as a ratio of partition functions with differing boundary conditions. Then the lattice realization of the Gross–Neveu model with Wilson fermions is simulated using the recent ‘worm’ technique on the loop gas or all-order hopping representation of the fermions. An algorithm is formulated that includes the Gross–Neveu interaction for N fermion species. The critical line mc(g) is constructed for a range of couplings at N=6 and for N=2, the Thirring model, as examples. 相似文献
68.
M. Borghesi T. Toncian J. Fuchs C. A. Cecchetti L. Romagnani S. Kar K. Quinn B. Ramakrishna P. A. Wilson P. Antici P. Audebert E. Brambrink A. Pipahl R. Jung M. Amin O. Willi R. J. Clarke M. Notley P. Mora T. Grismayer E. D’Humières Y. Sentoku 《The European physical journal. Special topics》2009,175(1):105-110
The acceleration of high-energy ion beams following the interaction of short (t < 1 ps) and intense (Iλ2 > 1018 W cm-2 μm2) laser pulses with solid targets is a field of research currently attracting high interest in the scientific community, due
to some of the unique properties of these ion sources, promising routes toward the optimization of their energy content, and
a number of possible, innovative applications in the scientific, technological and medical areas. Work on the characterization
and development of these sources has progressed enormously over the past few years, thanks to the contribution of many groups
worldwide. This paper will report some recent results, obtained in experiments carried out at the RAL and LULI laboratories,
in which we investigated the ion acceleration mechanism, developed a technique to control the ion beam divergence and energy
spectrum, and applied a proton radiography technique to investigate electric and magnetic field production following laser-matter
interaction. 相似文献
69.
70.
Willi A. Brand Tyler B. Coplen Anita T. Aerts‐Bijma J. K. Böhlke Matthias Gehre Heike Geilmann Manfred Gröning Henk G. Jansen Harro A. J. Meijer Stanley J. Mroczkowski Haiping Qi Karin Soergel Hilary Stuart‐Williams Stephan M. Weise Roland A. Werner 《Rapid communications in mass spectrometry : RCM》2009,23(7):999-1019
Internationally distributed organic and inorganic oxygen isotopic reference materials have been calibrated by six laboratories carrying out more than 5300 measurements using a variety of high‐temperature conversion techniques (HTC) a in an evaluation sponsored by the International Union of Pure and Applied Chemistry (IUPAC). To aid in the calibration of these reference materials, which span more than 125‰, an artificially enriched reference water (δ18O of +78.91‰) and two barium sulfates (one depleted and one enriched in 18O) were prepared and calibrated relative to VSMOW2 b and SLAP reference waters. These materials were used to calibrate the other isotopic reference materials in this study, which yielded:
The seemingly large estimated combined uncertainties arise from differences in instrumentation and methodology and difficulty in accounting for all measurement bias. They are composed of the 3‐fold standard errors directly calculated from the measurements and provision for systematic errors discussed in this paper. A primary conclusion of this study is that nitrate samples analyzed for δ18O should be analyzed with internationally distributed isotopic nitrates, and likewise for sulfates and organics. Authors reporting relative differences of oxygen‐isotope ratios (δ18O) of nitrates, sulfates, or organic material should explicitly state in their reports the δ18O values of two or more internationally distributed nitrates (USGS34, IAEA‐NO‐3, and USGS35), sulfates (IAEA‐SO‐5, IAEA‐SO‐6, and NBS 127), or organic material (IAEA‐601 benzoic acid, IAEA‐602 benzoic acid, and IAEA‐600 caffeine), as appropriate to the material being analyzed, had these reference materials been analyzed with unknowns. This procedure ensures that readers will be able to normalize the δ18O values at a later time should it become necessary. The high‐temperature reduction technique for analyzing δ18O and δ2H is not as widely applicable as the well‐established combustion technique for carbon and nitrogen stable isotope determination. To obtain the most reliable stable isotope data, materials should be treated in an identical fashion; within the same sequence of analyses, samples should be compared with working reference materials that are as similar in nature and in isotopic composition as feasible. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
Reference material | δ18O and estimated combined uncertainty c |
---|---|
IAEA‐602 benzoic acid | +71.28 ± 0.36‰ |
USGS35 sodium nitrate | +56.81 ± 0.31‰ |
IAEA‐NO‐3 potassium nitrate | +25.32 ± 0.29‰ |
IAEA‐601 benzoic acid | +23.14 ± 0.19‰ |
IAEA‐SO‐5 barium sulfate | +12.13 ± 0.33‰ |
NBS 127 barium sulfate | +8.59 ± 0.26‰ |
VSMOW2 water | 0‰ |
IAEA‐600 caffeine | ?3.48 ± 0.53‰ |
IAEA‐SO‐6 barium sulfate | ?11.35 ± 0.31‰ |
USGS34 potassium nitrate | ?27.78 ± 0.37‰ |
SLAP water | ?55.5‰ |