Woodall Christopher H, Christensen Jeppe, Skelton Jonathan M, Hatcher Lauren E, Parlett Andrew, Raithby Paul R, Walsh Aron, Parker Stephen C, Beavers Christine M, Teat Simon J, Intissar Mourad, Reber Christian, Allan David R
Department of Chemistry, University of Bath, Bath BA2 7AY, UK.
Research Complex at Harwell, Rutherford Appleton Laboratory, Harwell Oxford, Didcot, Oxfordshire, OX11 0FA, UK.
IUCrJ. 2016 Aug 18;3(Pt 5):367-376. doi: 10.1107/S2052252516013129. eCollection 2016 Sep 1.
We report a molecular crystal that exhibits four successive phase transitions under hydro-static pressure, driven by aurophilic interactions, with the ground-state structure re-emerging at high pressure. The effect of pressure on two polytypes of tris(μ-3,5-diiso-propyl-1,2,4-triazolato-κ:)trigold(I) (denoted Form-I and Form-II) has been analysed using luminescence spectroscopy, single-crystal X-ray diffraction and first-principles computation. A unique phase behaviour was observed in Form-I, with a complex sequence of phase transitions between 1 and 3.5 GPa. The ambient 2/ mother cell transforms to a 2/ phase above 1 GPa, followed by a 2/ phase above 2 GPa and a large-volume 2/ supercell at 2.70 GPa, with the previously observed 2/ phase then reappearing at higher pressure. The observation of crystallographically identical low- and high-pressure 2/ phases makes this a rare example of a re-entrant phase transformation. The phase behaviour has been characterized using detailed crystallographic theory and modelling, and rationalized in terms of molecular structural distortions. The dramatic changes in conformation are correlated with shifts of the luminescence maxima, from a band maximum at 14040 cm at 2.40 GPa, decreasing steeply to 13550 cm at 3 GPa. A similar study of Form-II displays more conventional crystallographic behaviour, indicating that the complex behaviour observed in Form-I is likely to be a direct consequence of the differences in crystal packing between the two polytypes.
我们报道了一种分子晶体,在静水压下,受亲金相互作用驱动,它呈现出四个连续的相变,且基态结构在高压下重新出现。利用发光光谱、单晶X射线衍射和第一性原理计算,分析了压力对三(μ - 3,5 - 二异丙基 - 1,2,4 - 三唑合 - κ)三(金(I))的两种多晶型(表示为晶型I和晶型II)的影响。在晶型I中观察到了独特的相行为,在1至3.5 GPa之间有复杂的相变序列。常压下的2/母晶胞在1 GPa以上转变为2/相,在2 GPa以上转变为另一种2/相,在2.70 GPa时转变为大体积的2/超晶胞,然后在更高压力下先前观察到的2/相再次出现。晶体学上相同的低压和高压2/相的观察结果,使其成为重入相变的罕见例子。利用详细的晶体学理论和建模对相行为进行了表征,并根据分子结构畸变进行了合理化解释。构象的显著变化与发光最大值的位移相关,从2.40 GPa时14040 cm处的带最大值,在3 GPa时急剧下降到13550 cm。对晶型II的类似研究显示出更常规的晶体学行为,表明在晶型I中观察到的复杂行为可能是这两种多晶型在晶体堆积上差异的直接结果。