Institute of Organic Chemistry, Justus Liebig University, Heinrich-Buff-Ring 17, 35392, Giessen, Germany.
Angew Chem Int Ed Engl. 2020 Jul 20;59(30):12445-12449. doi: 10.1002/anie.202004172. Epub 2020 May 8.
The structures and reactivities of organic phosphinidene chalcogenides have been mainly inferred from trapping or complexation experiments. Phosphinidene chalcogenide derivatives appear to be an elusive family of molecules that have been suggested as reactive intermediates in multiple organophosphorus reactions. The quest to isolate "free" phosphinidene chalcogenides remains a challenge in the field. Here, we present the synthesis, IR, and UV/Vis spectroscopic identification of hitherto elusive phenylphosphinidene oxide and phenylphosphinidene sulfide from the corresponding phosphonic diazide precursors. We isolated these higher congeners of nitroso- and thionitrosobenzene in argon matrices at 10 K. The spectral assignments are supported by B3LYP/6-311++G(3df,3pd) and MP2/cc-pVTZ computations.
有机膦亚硒化物和亚碲化物的结构和反应性主要是通过捕获或络合实验推断出来的。膦亚硒化物和亚碲化物衍生物似乎是一类难以捉摸的分子,它们被认为是多种有机磷反应中的反应中间体。分离“游离”膦亚硒化物和亚碲化物仍然是该领域的一个挑战。在这里,我们从相应的膦叠氮前体出发,通过合成、IR 和 UV/Vis 光谱鉴定,首次得到了迄今难以捉摸的苯膦亚硒氧化物和苯膦亚碲化物。我们在 10 K 的氩基质中分离出这些亚硝基亚苯和硫代亚硝苯的更高同系物。光谱分配得到了 B3LYP/6-311++G(3df,3pd)和 MP2/cc-pVTZ 计算的支持。