Schäfer Andreas, Golz Christopher, Preut Hans, Strohmann Carsten, Hiersemann Martin
Fakultät Chemie und Chemische Biologie, Technische Universität Dortmund, Otto-Hahn-Strasse 6, 44221 Dortmund, Germany.
Acta Crystallogr E Crystallogr Commun. 2015 Aug 29;71(Pt 9):o690-1. doi: 10.1107/S2056989015015698. eCollection 2015 Sep 1.
The title hydrate, C17H28O2·H2O, was synthesized in order to determine the relative configuration of the tetra-cyclic framework. The fused 5,6,7-tricarbocyclic core exhibits an entire cis-annulation, featuring a 1,4-cis-relation of the angular methyl groups in the six-membered ring. The oxa bridge of the ep-oxy-cyclo-heptane moiety is oriented towards the concave face of the boat-shaped mol-ecule, whereas the angular methyl groups are directed towards the convex face. The asymmetric unit of the crystal contains two nearly identical formula units, which are related via a pseudo-centre of symmetry. The structure could be solved in the space groups I-4 and I41/a. The refinement in the acentric space group, however, gave significantly better results and these are used in this paper. O-H⋯O hydrogen bonds are observed between the organic mol-ecules, between the organic mol-ecules and the water mol-ecules, and between the water mol-ecules, forming a chain along the c-axis direction.
合成了水合物C₁₇H₂₈O₂·H₂O,以确定四环骨架的相对构型。稠合的5,6,7-三环核心呈现出完全的顺式环合,六元环中角甲基具有1,4-顺式关系。环氧环庚烷部分的氧桥朝向船形分子的凹面,而角甲基则指向凸面。晶体的不对称单元包含两个几乎相同的化学式单元,它们通过一个假对称中心相关联。该结构可以在空间群I-4和I4₁/a中解析。然而,在非中心空间群中的精修给出了明显更好的结果,本文采用这些结果。在有机分子之间、有机分子与水分子之间以及水分子之间观察到O-H⋯O氢键,沿c轴方向形成一条链。