“…Synthesis of [Cr(2)(CO) 4 ] (6)[Cr(NBD)(CO) 4 ] (109 mg, 0.427 mmol) and one equivalent of 2 (126 mg, 0.427 mmol) were reacted as above at 65°C for 24 h yielding the product as red crystals (62 mg, 0.135 mmol, 32%) 1. H NMR (400 MHz, C 6 D 6 ): δ = 7.71-7.61 (m, 1H, 6-H), 7.55-7.51 (m, 4H, o-PPh 2 ), 7.13-6.99 (m, 7H, 5-H & m,p-PPh 2 ), 6.37 (bs, 1H, 4-H), 1.52 (s, 3H, 3-CH 3 ); 13 C NMR (100 MHz, C 6 D 6 ,): δ = 230.3 (d, J = 13.6 Hz, CO), 228.4 (dd, J = 11.2, 3.2 Hz, CO), 223.0 (dd, J = 17.6, 11.2 Hz, CO), 166.9 (dd, J = 15.2, 1.6 Hz, phosphinine C) 149.6 (dd, J = 28.0, 20.0 Hz, phosphinine CH), 146.9 (dd, J = 12.8, 7.2 Hz, phosphinine C), 140.6 (dd, J = 16.0, 3.2 Hz, phosphinine CH), 133.5 (dd, J = 28.8, 10.4 Hz, ipso-Ph C), 132.1 (d, J = 12.0 Hz, PPh 2 ), 130.8 (d, J = 2.4 Hz, PPh 2 ), 129.5 (d, J = 9.6 Hz, PPh 2 ), 128.6-128.2 (m, phosphinine CH and C 6 D 6 overlapping), 21.9 (t, J = 7.2 Hz CH 3 ); 31 P NMR (162 MHz, C 6 D 6 ): δ = 250.3 (d, 2 J PP = 33.8 Hz, 1-P), 41.8 (d, 2 J PP = 33.P); HRMS (ASAP/QTof) m/z Calc.…”