Dynamic nuclear polarization effects

Chemically Induced Dynamic Nuclear Polarization Effects. 132... 

The first discovery of chemically induced dynamic electron polarization (CIDEP) was made by Fessenden and Schuler in 1963 (58). These authors observed the abnormal spectra of the H atoms produced during the irradiation of liquid methane. The low-field line in the esr spectrum was inverted compared to the corresponding high-field line. The related chemically induced dynamic nuclear polarization effect (CIDNP) was reported independently four years later by Bargon et al. (22) and by Ward and Lawler (134). Because of the wider application of nmr in chemistry, the CIDNP effect immediately attracted considerable theoretical and experimental attention, and an elegant theory based on a radical-pair model (RPM) was advanced to explain the effect. The remarkable development of the radical-pair theory has obviously brought cross-fertilization to the then-lesser-known CIDEP phenomenon. 

In 1969, Jemison and Morris followed the Stevens rearrangement of A, iV-dimethyl-4-nitrobenzylamine acetamide by NMR and noted a chemically induced dynamic nuclear polarization effect on benzylic protons consistent with a benzyl radical. They postulated that this Stevens-type rearrangement of a benzyl group from an ammonium center to a negatively-charged nitrogen center occurred via a homolytic dissociation... 

Methods of disturbing the Boltzmann distribution of nuclear spin states were known long before the phenomenon of CIDNP was recognized. All of these involve multiple resonance techniques (e.g. INDOR, the Nuclear Overhauser Effect) and all depend on spin-lattice relaxation processes for the development of polarization. The effect is referred to as dynamic nuclear polarization (DNP) (for a review, see Hausser and Stehlik, 1968). The observed changes in the intensity of lines in the n.m.r. spectrum are small, however, reflecting the small changes induced in the Boltzmann distribution. 

Further evidence for the formation of alkene radical cations derives from the work of Giese, Rist, and coworkers who observed a chemically induced dynamic nuclear polarization (CIDNP) effect on the dihydrofuran 6 arising from fragmentation of radical 5 and electron transfer from the benzoyl radical within the solvent cage (Scheme 6) [67]. 

Hence, provided that I g is known and that R has been determined by means of an independent experiment, provides the cross-relaxation rate ct. This enhancement is called nuclear Overhauser effect (nOe) (17,19) from Overhauser (20) who was the first to recognize that, by a related method, electron spin polarization could be transferred to nuclear spins (such a method can be worked out whenever EPR lines are relatively sharp it is presently known as DNP for Dynamic Nuclear Polarization). This effect is usually quantified by the so-called nOe factor p... 

Among NMR methods providing insight into radical ions, chemically induced dynamic nuclear polarization (CIDNP) has proved especially useful it results in enhanced transient signals, in absorption or emission CIDNP effects were first reported in 1967 their application was soon extended to radical ions. The method lends itself to modest time resolution. 

Chemically induced dynamic nuclear polarization (CIDNP) was first reported in 1967 in independent work from three different laboratories. The effects of free radicals on NMR spectra were revealed (Fig. 6) in studies of radicals from peroxides (equation 62) and azo compounds, as well as radicals generated from the reaction of alkyl halides and organolithium compounds. ... 

The second approach is the use of the dynamic nuclear polarization (DNP) detection principle. Dorn and co-workers have pioneered the application of this technique [9,10], Whereas the NOE enhancement of 13C nuclei in the conventional 13C H recording is dependent upon the 7h/7c ratio (NOE = Th/ Tc = 2 1), the DNP enhancement relates to the ye/yuc ratio (2640 1). In an electron-nucleus spinsystem, the electron-electron transitions are saturated by microwave irradiation and magnetization transfer from electron to nucleus (Overhauser effect) occurs via a scalar and/or dipolar mechanism. The DNP enhancement, A, is described by the following equation ... 

Key Words Dynamic nuclear polarization, DNP, Overhauser effect, Hyperpolarization, Sensitivity enhancement,... 

The ion pair spin multiplicity may be a valuable tool to affect the BET rates and to probe the ion pair dynamics via magnetic field effects [36], Even weak magnetic fields are known to influence relative probabilities of singlet and triplet reactions [34], Chemically induced dynamic nuclear polarization (CIDNP) is a particularly informative technique [12]. Many bond scission reactions and rearrangements in cyclic radical ions have been successfully explored using this approach. Both structural data (spin densities) and approximate kinetic informations are indirectly available from such experiments [12]. 

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