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C.F. Griffin R.B. Creel J. Worth E. von Meerwall 《Journal of Physics and Chemistry of Solids》1974,35(1):71-76
The exact theory for the frequency of transition between the two lowest levels of a spin nucleus experiencing a large asymmetric electric field gradient, an applied magnetic field, and an anistropic chemical interaction was presented in an earlier paper. Using the assumption that the quadrupolar and chemical shift tensors have the same principal axis system, the Hamiltonian was solved exactly — analytically for the applied field aligned along each of the three axes of the quadrupolar principal axis system, and numerically for arbitrary orientations.This theory is reviewed here and applied to our room-temperature experiments in single-crystal paradibromobenzene. The self-consistent least-squares fit to the field-dependencies and simultaneously the angular dependence (rotational pattern) of the resonance frequency was performed using the literature value for the pure quadrupole frequency . The fit yielded values for the quadrupolar asymmetry η = 0·0461 ± 0·0004 and the chemical shift components σx = ?0·001 ± 0·001, σv = σz = 0·000 ± 0·001. Our value for η is in good agreement with values determined by other methods; it and our shift values are consistent with the information obtained by this method using a powdered specimen.The process of using the NMR signal itself to align the specimen yielded sufficient information for an unambiguous determination of the Euler angles of orientation of the crystal in its mounting within ± 0.6°. 相似文献
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Using complementary experiments we show that the room temperature ferromagnetism observed in anatase Co:TiO(2) films is not carrier mediated, but coexists with the dielectric state. TEM and x-ray absorption spectroscopy reveal a solid solution of Co in anatase, where Co is not metallic but in the +2 state substituting for Ti. Measurements at 300 K yield a M(S) of 1.1 mu(B)/Co atom, while all films are highly insulating. The evidence of intrinsic ferromagnetism in the dielectric ground state of Co:TiO(2) leads to new considerations for the origin of ferromagnetism in transition metal doped oxides. 相似文献
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We describe new correlation experiments suitable for determining long-range 1H-1H distances in 2H,15N-labeled peptides and proteins. The approach uses perdeuteration together with back substitution of exchangeable protons during sample preparation as a means of attenuating the strong 1H-1H dipolar couplings that broaden 1H magic angle spinning (MAS) spectra of solids. In the approach described here, we retain 100% of the 1H sensitivity by labeling and detecting all exchangeable sites. This is in contrast to homonuclear multiple pulse decoupling sequences that are applied during detection and that compromise sensitivity because of the requirement of sampling between pulses. As a result 1H detection provides a gain in sensitivity of >5 compared to the 15N detected version of the experiment (at a MAS frequency of 13.5kHz). The pulse schemes make use of the favorable dispersion of the amide 15Ns resonances in the protein backbone. The experiments are demonstrated on a sample of the uniformly 2H,15N-labeled dipeptide N-Ac-Val-Leu-OH and are analogous to the solution-state suite of HSQC-NOESY experiments. In this compound the 1H amide linewidths at 750MHz vary from approximately 0.67 ppm at omega(r)/2pi approximately 5kHz to approximately 0.20 ppm at omega(r)/2pi approximately 30kHz, indicating that useful resolution is available in the 1H spectrum via this approach. Since the experiments circumvent the problem of dipolar truncation in the 1H-1H spin system, they should make it possible to measure long-range distances in a uniformly labeled environment. Thus, we expect the experiments to be useful in constraining the global fold of a protein. 相似文献
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Costa PR Sun B Griffin RG 《Journal of magnetic resonance (San Diego, Calif. : 1997)》2003,164(1):92-103
The solid state NMR technique of rotational resonance (R2) has been used extensively to measure distances approaching 5-6 A between 13C nuclei in a variety of compounds including amyloidogenic peptides and membrane proteins. The accuracy of the distance information extracted from the time-dependent spin dynamics at R2 is often limited by the accuracy with which the relevant zero-quantum lineshape parameters are estimated. Here we demonstrate that measurement of spinning frequency dependent magnetization exchange dynamics provides data from which both distance and zero-quantum relaxation parameters can be extracted independently. In addition to providing more accurate distance information, this technique allows examination of the zero-quantum lineshape, which can indicate the presence of correlated relaxation or chemical shift distributions between dipolar-coupled sites. With this approach we have separated the contribution of dipolar couplings and zero quantum relaxation to R2 exchange curves. Thus, we have significantly improved the accuracy of the measurement of the intramolecular, internuclear distances between a pair of 13C's in two model compounds (N-acetyl-D,L-valine and glycylglycine.HCl) that lie in the distance range 4.6-4.7 A. 相似文献