Marquardt Christian, Hegen Oliver, Kahoun Tobias, Scheer Manfred
Institut für Anorganische Chemie, Universität Regensburg, 93040, Regensburg, Germany.
Chemistry. 2017 Mar 28;23(18):4397-4404. doi: 10.1002/chem.201605625. Epub 2017 Mar 8.
The elemental chalcogens sulfur, selenium, tellurium and bis(trimethylsilyl)peroxide as an oxygen source are applied for the oxidation of the phosphanylboranes Ph P-BH ⋅NMe (1) and tBuHP-BH ⋅NMe (2). The corresponding monooxidation products Ph P(X)-BH ⋅NMe (X=O-Te, 3 a-d) and tBuHP(X)-BH ⋅NMe (X=O-Te, 4 a-d) were obtained in good yields and comprehensively characterized by single crystal X-ray structure analysis, NMR, IR spectroscopy and mass spectrometry. The first oxidation step proceeds very selectively for all chalcogenides. For the tBu derivative, a further oxidation can be realised with O , S and Se yielding tBu(HX)P(X)-BH ⋅NMe (X=O, S, Se, 5 a-c). The telluride compounds presented herein are the first examples of neutral Te-substituted phosphanylboranes.
将元素硫族元素硫、硒、碲以及作为氧源的双(三甲基硅基)过氧化物用于膦硼烷PhP-BH·NMe(1)和tBuHP-BH·NMe(2)的氧化反应。相应的单氧化产物PhP(X)-BH·NMe(X = O-Te,3 a-d)和tBuHP(X)-BH·NMe(X = O-Te,4 a-d)以良好的产率得到,并通过单晶X射线结构分析、核磁共振、红外光谱和质谱进行了全面表征。对于所有硫族化物,第一步氧化反应都具有很高的选择性。对于tBu衍生物,可以用O、S和Se实现进一步氧化,生成tBu(HX)P(X)-BH·NMe(X = O、S、Se,5 a-c)。本文所呈现的碲化物化合物是中性Te取代膦硼烷的首例。