2018
DOI: 10.1088/2053-1591/aaf083
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Hydrogen-bonded and supramolecular ferroelectricity in a new hybrid (C12H25NH3)2CoCl4

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Cited by 6 publications
(5 citation statements)
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“…1 H spin–lattice relaxation time in the studied compounds consists of two contributions: the first one, 1 H– 1 H, results from the dipole–dipole interactions between protons of the pyrrolidinium cations and the second one, the 1 H– 59 Co relaxation pathway, results from the dipole–dipole couplings of protons with the unpaired electron spin of 59 Co. 22,24,28,34,55–57 where the J ( ω ) are the spectral density functions being Fourier transforms of time correlation functions describing the stochastic fluctuations of the dipole–dipole interaction. The spectral densities taken at ω H and ω S are associated with different correlation times, τ eff,1 and τ eff,2 , respectively, defined as τ eff,1 −1 = τ c −1 + 1/ T 1,e and τ eff,2 −1 = τ c −1 + 1/ T 2,e , where T 1,e and T 2,e are electron spin–lattice and electron spin–spin relaxation rates, respectively.…”
Section: Resultsmentioning
confidence: 99%
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“…1 H spin–lattice relaxation time in the studied compounds consists of two contributions: the first one, 1 H– 1 H, results from the dipole–dipole interactions between protons of the pyrrolidinium cations and the second one, the 1 H– 59 Co relaxation pathway, results from the dipole–dipole couplings of protons with the unpaired electron spin of 59 Co. 22,24,28,34,55–57 where the J ( ω ) are the spectral density functions being Fourier transforms of time correlation functions describing the stochastic fluctuations of the dipole–dipole interaction. The spectral densities taken at ω H and ω S are associated with different correlation times, τ eff,1 and τ eff,2 , respectively, defined as τ eff,1 −1 = τ c −1 + 1/ T 1,e and τ eff,2 −1 = τ c −1 + 1/ T 2,e , where T 1,e and T 2,e are electron spin–lattice and electron spin–spin relaxation rates, respectively.…”
Section: Resultsmentioning
confidence: 99%
“…The spectral densities taken at ω H and ω S are associated with different correlation times, τ eff,1 and τ eff,2 , respectively, defined as τ eff,1 −1 = τ c −1 + 1/ T 1,e and τ eff,2 −1 = τ c −1 + 1/ T 2,e , where T 1,e and T 2,e are electron spin–lattice and electron spin–spin relaxation rates, respectively. 22,24,28,34,55–57 C HH and C HCo are relaxation dipole–dipole constants. The C HCo relaxation constant is defined as:where r HCo is an effective inter atomic distance, γ H is the proton gyromagnetic ratio and γ s is the electron gyromagnetic ratio, and S is the electron spin quantum number for Co( ii ) S = 3/2.…”
Section: Resultsmentioning
confidence: 99%
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