ArticleThe journal of physical chemistry. B2008
Theory of stochastic dipolar recoupling in solid-state nuclear magnetic resonance.
Article in The journal of physical chemistry. B, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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3 citing papers in PubMed.
- Zero-quantum stochastic dipolar recoupling in solid state nuclear magnetic resonance.The Journal of chemical physics · 2012Article
- Solid-state NMR studies of amyloid fibril structure.Annual review of physical chemistry · 2011Review
- A Monte Carlo/simulated annealing algorithm for sequential resonance assignment in solid state NMR of uniformly labeled proteins with magic-angle spinning.Journal of magnetic resonance (San Diego, Calif. : 1997) · 2010Article
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Abstract
Dipolar recoupling techniques in solid-state nuclear magnetic resonance (NMR) consist of radio frequency (rf) pulse sequences applied in synchrony with magic-angle spinning (MAS) that create nonzero average magnetic dipole-dipole couplings under MAS. Stochastic dipolar recoupling (SDR) is a variant in which randomly chosen rf carrier frequency offsets are introduced to cause random phase modulations of individual pairwise couplings in the dipolar spin Hamiltonian. Several aspects of SDR are investigated through analytical theory and numerical simulations: (1) An analytical expression for the evolution of nuclear spin polarization under SDR in a two-spin system is derived and verified through simulations, which show a continuous evolution from coherent, oscillatory polarization exchange to incoherent, exponential approach to equilibrium as the range of random carrier offsets (controlled by a parameter f(max)) increases; (2) in a many-spin system, polarization transfers under SDR are shown to be described accurately by a rate matrix in the limit of large f(max), with pairwise transfer rates that are proportional to the inverse sixth power of pairwise internuclear distances; (3) quantum mechanical interferences among noncommuting pairwise dipole-dipole couplings, which are a complicating factor in solid-state NMR studies of molecular structures by traditional dipolar recoupling methods, are shown to be absent from SDR data in the limit of large f(max), provided that coupled nuclei have distinct NMR chemical shifts.
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