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The magnetic behavior of the low-dimensional phosphates (Sr,Ba)_2 Cu(PO_4)_2 and BaCuP_2O_7 was investigated by means of magnetic susceptibility and ^{31}P nuclear magnetic resonance (NMR) measurements. We present here the NMR shift K(T), the spin-lattice 1/T_1 and spin-spin 1/T_2 relaxation-rate data over a wide temperature range 0.02 K < T < 300 K. The T-dependence of the NMR K(T) is well described by the S=1/2 Heisenberg antiferromagnetic chain model with an intrachain exchange of J/k_B = 165 K, 151 K, and 108 K in Sr_2Cu(PO_4)_2, Ba_2Cu(PO_4)_2, and BaCuP_2O_7, respectively. Our measurements suggest the presence of magnetic ordering at 0.8 K in BaCuP_2O_7 (J/k_B = 108 K). For all the samples, we find that 1/T_1 is nearly T-independent at low-temperatures (1 K < T < 10 K), which is theoretically expected for 1D chains when relaxation is dominated by fluctuations of the staggered susceptibility. At high temperatures, 1/T_1 varies nearly linearly with temperature.
The magnetic properties of Na2CuP2O7 were investigated by means of 31P nuclear magnetic resonance (NMR), magnetic susceptibility, and heat capacity measurements. We report the 31P NMR shift, the spin-lattice 1/T1, and spin-spin 1/T2 relaxation-rate d
We have employed first principles calculations to study the electronic structure and magnetic properties of the low-dimensional phosphates, Ba2Cu(PO4)2 and Sr2Cu(PO4)2. Using the self-consistent tight-binding lin- earized muffin-tin orbital method an
Quasi-one-dimensional iron-based ladders and chains, with the 3$d$ iron electronic density $n = 6$, are attracting considerable attention. Recently, a new iron chain system Ba$_2$FeS$_3$, also with $n = 6$, was prepared under high-pressure and high-t
Rb-NMR study has been performed on the quasi-one dimensional competing spin chain Rb2Cu2Mo3O12 with ferromagnetic and antiferromagnetic exchange interactions on nearest neighboring and next nearest neighboring spins, respectively. The system changes
Magnetic properties in the quasi-one-dimensional organic salt (TMTTF)2SbF6 are investigated by 13C NMR under pressures. Antiferromagnetic phase transition at ambient pressure (AFI) is confirmed. Charge-ordering is suppressed by pressure and is not ob