Szynkiewicz Natalia, Chojnacki Jarosław, Grubba Rafał
Department of Inorganic Chemistry, Faculty of Chemistry, Gdańsk University of Technology, 11/12 Gabriela Narutowicza Str., 80-233 Gdańsk, Poland.
Inorg Chem. 2022 Jun 27;61(25):9523-9532. doi: 10.1021/acs.inorgchem.2c00589. Epub 2022 Jun 14.
We present a comprehensive study on the diphosphanation of iso(thio)cyanates by unsymmetrical diphosphanes. The reactions involving unsymmetrical diphosphanes and phenyl isocyanate or phenyl thioisocyanate gave rise to phosphanyl, phosphoryl, and thiophosphoryl derivatives of amides, imines, and iminoamides. The structures of the diphosphanation products were confirmed through NMR spectroscopy, IR spectroscopy, and single-crystal X-ray diffraction. We showed that unsymmetrical diphosphanes could be used as building blocks to synthesize phosphorus analogues of important classes of organic molecules. The described transformations provided a new methodology for the synthesis of organophosphorus compounds bearing phosphanyl, phosphoryl, or thiophosphoryl functional groups. Moreover, theoretical studies on diphosphanation reactions explained the influence of the steric and electronic properties of the parent diphosphanes on the structures of the diphosphanation products.
我们展示了一项关于不对称双膦对异(硫)氰酸酯进行双膦化反应的全面研究。涉及不对称双膦与苯基异氰酸酯或苯基硫代异氰酸酯的反应生成了酰胺、亚胺和亚氨基酰胺的膦基、磷酰基和硫代磷酰基衍生物。通过核磁共振光谱、红外光谱和单晶X射线衍射确定了双膦化产物的结构。我们表明,不对称双膦可用作构建单元来合成重要类别的有机分子的磷类似物。所描述的转化为合成带有膦基、磷酰基或硫代磷酰基官能团的有机磷化合物提供了一种新方法。此外,对双膦化反应的理论研究解释了母体双膦的空间和电子性质对双膦化产物结构的影响。