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Although nuclear magnetic resonance in low fields around or below the Earth's magnetic field is almost as old as nuclear magnetic resonance itself, the recent years have experienced a revival of this technique that is opposed to the common trend towards higher and higher fields. The background of this development is the expectation that the low-field domain may open a new window for the study of molecular structure and dynamics. Here, we will give an overview on the specific features in the low-field domain, both from the technical and from the physical point of view. In addition, we present a short passage on the option of magnetic resonance imaging in fields of the micro-Tesla range. 相似文献
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P. K. Claus H. A. Schwarz W. Rieder W. Vycudilik 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1):11-18
Abstract N-Aryl-S,S-dialkylsulfimides, 1, with R1 = alkyl other than CH3, have been rearranged by heating in ethanol yielding o-alkylthiomethyl-anilines, 2, as main products. Isomeric o-methylthioalkyl-anilines, 14, are formed in minor amounts only. Reactions of sulfimides, 1, with R1 = CH3, with certain alkylating or acylating agents yielded o-methylthiomethylated, N-alkylated or -acylated products 9. Mechanistic considerations are discussed. The rearrangement of sulfimides 1 has been assumed to occur via [2,3]-sigmatropic reactions of intermediate azasulfonium ylids 3. Attempts to resolve (+)-camphor-10-sulfonates of N-aryl sulfimides failed, but optically active N-aryl sulfimides could be obtained by reaction of anilines with optically active sulfoxides and P4O10. Optically active 2,6-disubstituted sulfimides, 1, could be rearranged in ethanolic KOH to yield optically active cyclohexadienimines 12, indicating a transfer of asymmetry from sulfur to carbon and supporting the assumption of a sigmatropic rearrangement. 相似文献
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Dietrich Gudat Asadollah Haghverdi Timo Gans-Eichler Martin Nieger 《Phosphorus, sulfur, and silicon and the related elements》2013,188(6-7):1637-1640
The high intrinsic stability of 1,3,2-diazaphospholenium cations enhances ionic polarization of covalent P--X bonds in P -halogeno- and P -hydrido-diazaphospholenes. The physical properties of the latter suggest a hydridic nature of the P--H bond, and their reactivities display an "Umpolung" as compared to known reaction patterns of phosphines. 相似文献
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Martin Pomerantz Jiping Wang Seeyearl Seong Kyle P. Starkey Long Nguyen Dennis S. Marynick 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1-4):507-508
Abstract Poly(benzo[1,2-b:4,5-b′]dithiophene-4,8-diyl vinylene) (1) has been prepared by the pyrolysis of the precursor polymer 2 and studied. Quantum mechanical calculations on the aromatic and quinoid monomers, oligomers and polymers indicate that 1 is a planar aromatic polymer. 相似文献
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