Seliger J, Zagar V, Asaji T, Konnai A
Jozef Stefan Institute, Jamova 39, 1000 Ljubljana, Slovenia.
Magn Reson Chem. 2008 Aug;46(8):756-60. doi: 10.1002/mrc.2249.
The reorientation of a pyridinium ion in the paraelectric and antiferroelectric phase of PyHICl(4) is investigated using (1)H-(14)N nuclear quadrupole double resonance (NQDR). The (14)N nuclear quadrupole resonance frequencies are measured. The temperature variations of the principal values of the time-averaged electric-field-gradient (EFG) tensor at the nitrogen position are used to determine the occupation probabilities of the six orientations of a pyridinium ion in both crystallographic phases. The energy difference between various orientations is determined. The molar transition entropy associated with the reorientation of the pyridinium ions is calculated and compared to the experimental value.
利用氢-氮核四极双共振(NQDR)研究了PyHICl(4)顺电相和反铁电相中吡啶鎓离子的重新取向。测量了氮的核四极共振频率。利用氮位置处时间平均电场梯度(EFG)张量主值的温度变化来确定吡啶鎓离子在两个晶体学相中六种取向的占据概率。确定了不同取向之间的能量差。计算了与吡啶鎓离子重新取向相关的摩尔转变熵,并与实验值进行了比较。