Tidey Jeremiah P, Wong Henry L S, McMaster Jonathan, Schröder Martin, Blake Alexander J
School of Chemistry, The University of Nottingham, University Park, Nottingham NG7 2RD, England.
Acta Crystallogr B Struct Sci Cryst Eng Mater. 2016 Jun 1;72(Pt 3):357-71. doi: 10.1107/S2052520616007435. Epub 2016 May 26.
The three reported phases of the mononuclear macrocyclic Pd(II) complex [PdCl2([9]aneS2O)] [(1); [9]aneS2O = 1-oxa-4,7-dithiacyclononane] were each studied up to pressures exceeding 9 GPa using high-pressure single-crystal X-ray diffraction. The α- and γ-phases both exhibit smooth compression of the unit-cell parameters with third-order Birch-Murnaghan bulk moduli of 14.4 (8) and 7.6 (6) GPa, respectively. Between 6.81 and 6.87 GPa β-[PdCl2([9]aneS2O)] was found to undergo a reversible transition to a phase denoted as β' and characterized by a tripling of the unit-cell volume. Across the phase transition, rearrangement of the conformation of the bound macrocycle at two of the resulting three unique sites gives rise to an extensively disordered structure.
使用高压单晶X射线衍射对单核大环钯(II)配合物[PdCl2([9]aneS2O)]((1); [9]aneS2O = 1-氧杂-4,7-二硫杂环壬烷)报道的三个相进行了研究,压力超过9 GPa。α相和γ相均表现出晶胞参数的平滑压缩,三阶Birch-Murnaghan体模量分别为14.4(8)和7.6(6) GPa。在6.81至6.87 GPa之间,发现β-[PdCl2([9]aneS2O)]可逆地转变为一个称为β'的相,其特征是晶胞体积增加两倍。在相变过程中,所得三个独特位点中的两个位点处结合大环的构象重排产生了一个高度无序的结构。