## Abstract Chemically induced dynamic nuclear polarization (CIDNP) observed during electron transfer (ET) reactions of tertiary amines such as DABCO (**1**) or Et~3~N (**2**) with a wide range of electron acceptors support the involvement of amine radicalβcations (__e.g.__, **1^.^**^**+**^ or **2^
Single-phase primary electron spin polarization transfer in spin-trapping reactions
β Scribed by Nicholas J. Turro; Igor V. Khudyakov
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- English
- Weight
- 592 KB
- Volume
- 193
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
Time-resolved (TR) ESR was employed to investigate the reaction of diphenylphosphinoyl reactive free radicals with N-phenyltert-butylnitrone (PBN), which were produced by laser flash photolysis (YAG laser, 355 nm) of diphenyl-2,4,6-trimethylbenzoyl phosphine oxide (DPO). The TR ESR and continuous wave (cw) ESR spectra of the nitroxide spin adduct ojdiphenylphosphinoyl radicals and PBN were investigated, and both spectra of the adduct show the same hyperfine-splitting and relative line intensities. The TR ESR spectra of the spin adduct as well as the initial diphenylphosphinoyl radicals are absorptively polarized, corresponding to a net electron spin polarization transfer. The requirements for spin polarization transfer in radical addition reactions and the TR and cw ESR spectrum of the spin adduct are discussed.
π SIMILAR VOLUMES
The nuclear spin polarization resulting from optical pumping of molecular triplet states, ONP, has been studied in a timeresolving experiment by synchronized irradiation of light and rfpulses. After laser flash excitation of T, triplet states of actidine doped into a fluorene crystal, an rf pulse of
It is ~'now~ that electron polarization can be transmitted along a reactton pathway and that the observed poIarkation of a radical may result from both primary and secondary processes. These secondary processes affect measurement of polarization ratios, and hence experimental tests of poiarization t