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M. V. FEDIN H. YASHIRO P. A. PURTOV E. G. BAGRYANSKAYA M. D. E. FORBES 《Molecular physics》2013,111(8):1171-1180
Chemically induced electron-nuclear polarization at low magnetic fields is considered theoretically for a radical with one magnetic nucleus. It is shown that large non-equilibrium populations of the radical spin levels are expected to exist under low magnetic fields. This large electron-nuclear polarization has been observed experimentally during the photolysis of two phosphine oxides using a modified L-band TREPR setup. The TREPR spectra and kinetics of dimethoxyphosphonyl and diphenylphosphonyl radicals have been measured and analysed in low magnetic fields, and excellent agreement between experiment and theory has been achieved. 相似文献
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The photochemical reaction of tetraphenylhydrazine in an SDS micellar solution is studied using a transient absorption detected magnetic resonance (ADMR) method. This system is photo-dissociated via the singlet excited state and forms a transient radical pair. Strong microwave irradiation of this system under an × band EPR magnetic field provides an ADMR spectrum of the singlet born radical pair as the optical absorbance change of the diphenylaminyl radical. The employment of a short duration microwave pulse that efficiently flips the electron spin quantum (Δm s = 1) controls the reaction of the radical pair, and the reaction rate constant of this system is determined. Furthermore, changing the microwave duration shows the quantum beat of this system induced by the electromagnetic field. This beat signal carries both a single beat that corresponds to the Rabi frequency and a double-frequency beat that is due to simultaneous two-spin controlling. 相似文献
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