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Single crystals of a metal organic complex ce{(C5H12N)CuBr3} (ce{C5H12N} = piperidinium, pipH for short) have been synthesized and the structure was determined by single-crystal X-ray diffraction. ce{(pipH)CuBr3} crystallizes in the monoclinic group $C$2/$c$. Edging-sharing ce{CuBr5} units link to form zigzag chains along the $c$ axis and the neighboring Cu(II) ions with spin-1/2 are bridged by bi-bromide ions. Magnetic susceptibility data down to 1.8 K can be well fitted by the Bonner-Fisher formula for antiferromagnetic spin-1/2 chain, giving the intrachain magnetic coupling constant $J$ $sim$ 17 K. At zero field, ce{(pipH)CuBr3} shows three-dimensional (3D) order below $T_N$ = 1.68 K. Calculated by the mean-field theory, the interchain coupling constant $J$ = 0.65 K is obtained and the ordered magnetic moment $m_0$ is about 0.20 $mu_B$. This value of $m_0$ makes ce{(pipH)CuBr3} a rare compound suitable to study the dimensional crossover problem in magnetism, since both 3D order and one-dimensional (1D) quantum fluctuations are prominent. In addition, specific heat measurements reveal two successive magnetic transitions with lowering temperature when external field $H geq$ 3 T is applied along the $a$ axis. The $H$ - $T$ phase diagram of ce{(pipH)CuBr3} is roughly constructed. The interplay between exchange interactions, dimensionality, Zeeman energy and possible Dzyaloshinkii-Moriya interaction should be the driving force for the multiple phase transitions.
We report inelastic time-of-flight and triple-axis neutron scattering measurements of the excitation spectrum of the coupled antiferromagnetic spin-1 Heisenberg chain system CsNiCl3. Measurements over a wide range of wave-vector transfers along the c
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