SYNTHESIS, ISOLATION, AND SKELETAL INVERSION OF 5,10-DIHYDROPHOSPHANTHRENES

Two stereoisomers, the trans form 1a and the cis form 1b, of 2,3,7,8-tetramethyl-5,10-diphenyl-5,10-dihydrophosphanthrene dioxide (1) were formed by spontaneous oxidation in air of the corresponding 5,10-dihydrophosphanthrenes 2 and were separated by recrystallization. Both 1a and 1b were characterized by X-ray crystallographic analysis, which revealed configurations at the phosphorus and conformations of the central tricyclic system. The P-31 NMR of the reaction mixture showed at first two signals at - 15.3 and - 15.1 ppm, which shifted to 9.11 and 10.3 ppm after purification of the reaction mixture under aerobic conditions by oxidation of phosphorus atoms. The reaction of 1b with HSiCl3 in toluene-d(8) at 100 degrees C gave no change, whereas 1a reacted with HSiCl3 to give reduced compounds 2a and 2b under the same conditions. The trans-cis isomerization of 2 occurred via vertex inversion at phosphorus atom. VT-NMR, X-ray analysis, and density functional theory (DFT) calculation showed that the conformational exchange of the cis form 1b proceeded via skeletal inversion of the tricyclic ring.