Lang Jun, Sloop David J, Lin Tien-Sung
Department of Chemistry, Washington University, St. Louis, Missouri 63130-4899, USA.
J Phys Chem A. 2007 Jun 7;111(22):4731-6. doi: 10.1021/jp070251v. Epub 2007 May 11.
Pulsed zero-field electron paramagnetic resonance free induction decay (ZF EPR FID) techniques are employed to study the phase transition of p-terphenyl crystals (Tc = 193 K) by measuring selectively populated photoexcited triplet ZF transitions of dilute pentacene molecules in p-terphenyl single crystals. The sensitivity of ZF spectroscopy to small shifts in local magnetic fields enables the studies of guest-host configuration changes over a wide temperature range. Here we report the observation of guest pentacene (-h(14) and -d(14)) triplet ZF EPR FID spectra that disappear abruptly at Tc and of spectral broadening and shift below Tc. We interpret these spectral changes as evidence for guest couplings to host phenyl rings. Further, these data allow assignments of spectroscopic sites to crystallographic sites that occur in the phase transition.
采用脉冲零场电子顺磁共振自由感应衰减(ZF EPR FID)技术,通过测量对三联苯单晶中稀并五苯分子选择性填充的光激发三重态ZF跃迁,来研究对三联苯晶体(Tc = 193 K)的相变。ZF光谱对局部磁场微小变化的敏感性使得能够在很宽的温度范围内研究客体-主体构型的变化。在此,我们报告了客体并五苯(-h(14)和-d(14))三重态ZF EPR FID光谱在Tc时突然消失以及在Tc以下光谱展宽和位移的观测结果。我们将这些光谱变化解释为客体与主体苯环耦合的证据。此外,这些数据允许将光谱学位点分配到相变中出现的晶体学位点。