Solid-state multinuclear magnetic resonance and X-ray crystallographic investigation of the phosphorus...iodine halogen bond in a bis(dicyclohexylphenylphosphine)(1,6-diiodoperfluorohexane) cocrystal.

D. Zheng, Patrick M. J. Szell, Safaa Khiri, Jeffrey S. Ovens, D. L. Bryce
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Abstract

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 [dI...P = 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. 13C, 19F, and 31P magic angle spinning solid-state NMR spectra are reported. A 31P 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.
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磷的固态多核磁共振和x射线晶体学研究。二(双环己基苯基膦)(1,6-二碘过氟己烷)共晶中的碘卤素键。
卤素与磷原子成键仍然不常见,文献中报道的例子相对较少。本文用x射线晶体学和固态多核磁共振波谱法研究了双(双环己基苯基膦)(1,6-二碘过氟己烷)共晶的制备和研究。晶体结构具有两个晶体学上独特的C-I…P卤素键[dI…]P = 3.090 (5) Å, 3.264 (5) Å]和其中一个1,6-二碘过氟己烷分子的晶体结构紊乱。第一个是最短和最线性的I。迄今为止报道的P卤键。报道了13C、19F和31P魔角旋转固体核磁共振谱。与纯双环己基苯基膦相比,共晶发生了-7.0 p.p.m.的31P化学位移变化,与卤素键形成一致。本研究建立了碘过氟烷烃与磷受体配对时作为可行的卤素键供体,并表明二环己基苯基膦可以作为实际的卤素键受体。
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