Analytical derivation of multiple spin echo amplitudes with arbitrary refocusing angle.
Explicit non-recursive expressions for spin echo amplitudes have been derived for CPMG sequences with arbitrary refocusing flip angle.
Biomedical subjects
Publications and source records attributed to N N Lukzen.
Explicit non-recursive expressions for spin echo amplitudes have been derived for CPMG sequences with arbitrary refocusing flip angle.
The double-channel recombination and separation of the photochemically created singlet radical pair is investigated, taking into account the spin conversion in a zero magnetic field and the arbitrary initial distance between the radicals. The quantum yields of the singlet and triplet products and the free radicals production are found analytically, assuming that the recombination of the diffusing radicals occurs at contact. All the yields are related to the singlet and triplet populations of the recombining radical pair, subjected to spin conversion and contact exchange interaction. The general analytical expressions for the quantum yields are specified for the particular limits of the weak and strong exchange. They are greatly simplified in the case of polar solvents, especially at the contact start. A close similarity is obtained with the results of a previously developed incoherent model of spin conversion, provided that the conversion rate is appropriately related to the hyperfine coupling constant.
Analytical solution is obtained for time-resolved magnetic field effects (TR-MFE) on recombination fluorescence of radical-ion pair (RIP) containing radical ion with two groups of magnetically equivalent nuclei. The present theoretical approach is applied to three experimental systems: RIPs containing radical cations of 2,3-dimethylbutane, 2,2,6,6-tetramethylpiperidine, or diisopropylamine and radical anion of p-terphenyl-d14 in nonpolar alkane solutions. Good agreement between theory and experiment is found for all the three systems, hyperfine coupling constants of radical cations are obtained by fitting the experimental TR-MFE traces. The potential of the TR-MFE technique for studying radical ions with nonequivalent nuclei is discussed in detail. The wide applicability of the theoretical model and the experimental technique make them useful for studying short-lived radical species that are often beyond the reach of the conventional electron paramagnetic resonance spectroscopy.
The electron self-exchange between a neutral molecule and its charged radical, which is part of a spin-correlated radical ion pair, gives rise to line width effects in the fluorescence-detected MARY (magnetic field effect on reaction yield) spectrum similar to those observed in EPR spectroscopy. An increasing self-exchange rate (i.e., a higher concentration of the neutral molecule) leads to broadening and subsequent narrowing of the spectrum. Along with a series of MARY spectra recorded for several systems (the fluorophores pyrene, pyrene-d(10) and N-methylcarbazole in combination with 1,2- and 1,4-dicyanobenzene) in various solvents, a theoretical model is developed that describes the spin evolution and the diffusive recombination of the radical pair under the influence of the external magnetic field and electron self-exchange, thereby allowing the simulation of MARY spectra of the systems investigated experimentally. The spin evolution of the radicals in the pair is calculated separately using spin correlation tensors, thereby allowing rigorous quantum mechanical calculations for real spin systems. It is shown that the combination of these simulations with high resolution, low noise experimental spectra makes the MARY technique a novel, quantitative method for the determination of self-exchange rate constants. In comparison to a simple analytical formula which estimates the self-exchange rate constant from the slope of the linear part of a line width vs concentration plot, the simulation method yields more reliable and accurate results. The correctness of the results obtained by the MARY method is proved by a comparison with corresponding data from the well-established EPR line broadening technique. With its less stringent restrictions on radical lifetime and stability, the MARY technique provides an alternative to the classical EPR method, in particular for systems involving short-lived and unstable radicals.
An image postprocessing technique that is based on the relaxation properties of tissues and that can produce MR images with increased contrast is proposed. The technique involves no a priori assumptions concerning the form of the relaxation decay. An arbitrary number of postprocessed images, each emphasizing a selected tissue type, is obtained from the original images of a multiecho acquisition. It is shown with examples that the technique allows more complete utilization of relaxation information for tissue differentiation.