Near-zero-field nuclear magnetic resonance

We investigate nuclear magnetic resonance (NMR) in near zero field, where the Zeeman interaction can be treated as a perturbation to the electron mediated scalar interaction (J?coupling). This is in stark contrast to the high-field case, where heteronuclear J?couplings are normally treated as a small perturbation. We show that the presence of very small magnetic fields results in splitting of the zero-field NMR lines, imparting considerable additional information to the pure zero-field spectra. Experimental results are in good agreement with first-order perturbation theory and with full numerical simulation when perturbation theory breaks down. We present simple rules for understanding the splitting patterns in near-zero-field NMR, which can be applied to molecules with nontrivial spectra.     

Double-resonance circuit for nuclear magnetic resonance spectroscopy

A new double-resonance probe circuit design is described. The circuit contains no quarter-wavelength elements or equivalents, yet nonetheless achieves adequate isolation between the two input channels. It contains relatively few components, and so is both compact and efficient. It has been incorporated in two solid-state nuclear magnetic resonance (NMR) probes, with excellent results.     

Basic concepts for nuclear magnetic resonance imaging

The basic concepts necessary to understand the physical basis of NMR imaging are presented in this didactic article. It is intended as a starting point for the radiologist or medical physicist who is addressing the topic of NMR for the first time. The basis of the NMR phenomena is described with introduction of the concepts of magnetic moment, magnetic fields, magnetic resonance, net magnetic moment of a sample, NMR excitation and NMR emission. The equipment necessary to observe these NMR properties of matter is summarized as well as the procedures for basic pulsed NMR experiments. The physical concepts for spatial localization of NMR emissions are introduced with physical analogies to stringed musical instruments. Several alternative imaging modalities are compared with greatest emphasis on the inversion recovery technique which yields images weighted by tissue T₁ values. The six subsystems of an NMR imaging device (primary magnet, computer, radio equipment, magnetic gradient, data storage and display subsystems) are described in an overview fashion. The paper is followed by a series of study questions to test the reader's comprehension of basic NMR imaging concepts.     

170 nm nuclear magnetic resonance imaging using magnetic resonance force microscopy

We demonstrate one-dimensional nuclear magnetic resonance imaging of the semiconductor GaAs with 170 nm slice separation and resolve two regions of reduced nuclear spin polarization density separated by only 500 nm. This was achieved by force detection of the magnetic resonance, magnetic resonance force microscopy (MRFM), in combination with optical pumping to increase the nuclear spin polarization. Optical pumping of the GaAs created spin polarization up to 12 times larger than the thermal nuclear spin polarization at 5K and 4T. The experiment was sensitive to sample volumes of 50 microm(3) containing approximately 4 x 10(11)71 Ga/Hz. These results demonstrate the ability of force-detected magnetic resonance to apply magnetic resonance imaging to semiconductor devices and other nanostructures.     

89Yttrium nuclear magnetic resonance studies

With a Fourier-transform spectrometer, especially developed for nuclei with weak NMR signals, the lines of⁸⁹Y have been investigated in aqueous solutions of Y(NO₃)₃, YCl₃, and Y(ClO₄)₃. The concentration dependence of the chemical shifts of the⁸⁹Y resonance frequencies in these solutions were measured. Using this dependence, the Larmor frequency of the⁸⁹Y³⁺ ion solely surrounded by water was determined by extrapolation. The Larmor frequency of⁸⁹Y was referred to those of²H,³⁹K, and⁷³Ge with high accuracy. The magnetic moment of the⁸⁹Y³⁺ ion purely surrounded by H₂O molecules is μ(⁸⁹Y³⁺) = ?0.1368523(4) μ_N. The concentration dependence of Y(NO₃)₃ solutions in D₂O yields the solvent isotope effect δ(⁸⁹Y³⁺ in D₂O)?δ(⁸⁹Y³⁺ in H₂O)= ?(4.3±0.5)ppm. The⁸⁹Y relaxation times T₁ and T₂ of a 3 molal aqueous Y(NO₃)₃ solution were determined in the pH range ?0.5...+1.25. T₁ 190...90 s is nearly constant in this range, whereas the transverse relaxation rate T₂ ^?1 increases strongly with increasing pH; this effect seems to be due to the chemical exchange of the hydrated Y³⁺ ion between a monomer and a polymer site.