State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Nanjing University , Nanjing 210093, China.
J Am Chem Soc. 2014 Apr 30;136(17):6251-4. doi: 10.1021/ja502675d. Epub 2014 Apr 16.
Two phosphorus-containing four-membered ring radical cations 1(•+) and 2(•+) have been isolated and characterized by UV-vis absorption spectroscopy, electron paramagnetic resonance (EPR), and single-crystal X-ray diffraction. Compared with neutral molecules 1 and 2, radical 1(•+) has elongated P-P bonds and more pyramidalized phosphorus atoms, while shortened P-Nring distances and larger angles around phosphorus centers are observed for 2(•+). EPR studies indicate that for 1(•+) spin density mainly resides on the exocyclic nitrogen atoms with very minor contribution from endocyclic phosphorus atoms, while the situation is opposite for 2(•+). Such an inverse spin density distribution is controlled by the exocyclic substituents, which is supported by DFT calculations.
两种含磷的四元环自由基阳离子 1(•+) 和 2(•+) 已通过紫外-可见吸收光谱、电子顺磁共振(EPR)和单晶 X 射线衍射进行了分离和表征。与中性分子 1 和 2 相比,自由基 1(•+) 的 P-P 键被拉长,磷原子的金字塔化程度更高,而 2(•+) 的 P-N 环距离缩短,磷中心周围的角度增大。EPR 研究表明,对于 1(•+),自旋密度主要位于杂环氮原子上,而来自环内磷原子的贡献很小,而对于 2(•+) 则相反。这种反自旋密度分布由外消旋取代基控制,这得到了 DFT 计算的支持。