2007
DOI: 10.1070/rc2007v076n06abeh003715
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Quantum beats in radical pairs

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2007
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Cited by 54 publications
(70 citation statements)
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“…The time dependence of the spin density operator in the absence of spin relaxation and chemical reactions was obtained from the von Neumann equation, and the chemical fate of the RP was modeled by means of separate first-order spin-selective reactions of the singlet and triplet pairs. Spin relaxation was introduced phenomenologically following Bagryansky et al [ 35 ]. The derivation of Eq 6 has been given below.…”
Section: Methodsmentioning
confidence: 99%
“…The time dependence of the spin density operator in the absence of spin relaxation and chemical reactions was obtained from the von Neumann equation, and the chemical fate of the RP was modeled by means of separate first-order spin-selective reactions of the singlet and triplet pairs. Spin relaxation was introduced phenomenologically following Bagryansky et al [ 35 ]. The derivation of Eq 6 has been given below.…”
Section: Methodsmentioning
confidence: 99%
“…For example, a bimolecular electron transfer reaction between an excited triplet electron donor and a closed shell acceptor would produce a pair of ion radicals in a triplet state. However, singlet and triplet are rarely eigenstates of the spin Hamiltonian, with the consequence that the spin state of the radical pair evolves coherently at frequencies and with amplitudes determined by the internal and external magnetic interactions of the electron spins [3]. Simultaneously, the singlet and triplet radical pairs react at different rates to form distinct reaction products.…”
Section: Introductionmentioning
confidence: 99%
“…Spin relaxation was introduced phenomenologically (compare equation (19) of Bagryansky et al, 2007) as:true0pT(t) = 34 + (pTnormal′(t)34)exp(rt),where true0r is the relaxation rate constant.…”
Section: Methodsmentioning
confidence: 99%