“…After purification (silicapacked column chromatography), 3 was obtained as a deep red solid together with trace amounts of 2-(2,4,6-tri-tertbutylphenyl)-1-(2,4,6-tri-tert-butylphenylphosphanyl)acetylene (6), 1-(2,4,6-tri-tert-butylphenyl)-1-phosphaacetylene (7), [5±7, 9] and 6,8-di-tert-butyl-4,4-dimethyl-1-phospha-3,4-dihydronaphthalene (8). [5,6,10] The 31 P NMR spectrum of 3 shows an ABX system. The signal of the exocyclic phosphorus atom P X (d P X 313.8) is positioned downfield compared to ring atoms P A and P B but similar to that found for 9 (d 321.5), [11] due to the electron-withdrawing effects of the 1,3-diphosphacyclopentadiene moiety.…”