Department of Chemistry and Biomolecular Sciences, University of Ottawa, 10 Marie Curie Private, Ottawa, Ontario K1N 6N5, Canada.
Acta Crystallogr B Struct Sci Cryst Eng Mater. 2022 Jun 1;78(Pt 3 Pt 2):557-563. doi: 10.1107/S2052520622004322. Epub 2022 May 28.
Halogen bonding to phosphorus atoms remains uncommon, with relatively few examples reported in the literature. Here, the preparation and investigation of the cocrystal bis(dicyclohexylphenylphosphine)(1,6-diiodoperfluorohexane) by X-ray crystallography and solid-state multinuclear magnetic resonance spectroscopy is described. The crystal structure features two crystallographically unique C-I...P halogen bonds [d = 3.090 (5) Å, 3.264 (5) Å] and crystallographic disorder of one of the 1,6-diiodoperfluorohexane molecules. The first of these is the shortest and most linear I...P halogen bond reported to date. C, F, and P magic angle spinning solid-state NMR spectra are reported. A P chemical shift change of -7.0 p.p.m. in the cocrystal relative to pure dicyclohexylphenylphosphine, consistent with halogen bond formation, is noted. This work establishes iodoperfluoroalkanes as viable halogen bond donors when paired with phosphorus acceptors, and also shows that dicyclohexylphenylphosphine can act as a practical halogen bond acceptor.
磷原子上的卤素键合仍然很少见,文献中报道的例子相对较少。在这里,通过 X 射线晶体学和固态多核磁共振波谱学描述了双(二环己基膦基)(1,6-二碘全氟己烷)的制备和研究。晶体结构具有两个结晶学上独特的 C-I…P 卤素键[ d = 3.090(5)Å,3.264(5)Å]和一个 1,6-二碘全氟己烷分子的结晶学无序。其中第一个是迄今为止报道的最短和最线性的 I…P 卤素键。报道了 C、F 和 P 魔角旋转固态 NMR 谱。在配合物中相对于纯二环己基膦的 P 化学位移变化为-7.0 p.p.m.,这与卤素键的形成一致。这项工作确立了碘全氟链烷烃与磷受体配对时是可行的卤素键供体,同时也表明二环己基膦基可以作为实用的卤素键受体。