19-electron intermediates in the ligand substitution of CpW(CO)3* with a Lewis base.

The photochemical reactions of [CpW(CO)3]2 with the Lewis base P(OMe)3 are examined on the nanosecond and microsecond time scales using step-scan FTIR spectroscopy. Photolysis at 532 nm produces the 17-electron (17e) radicals CpW(CO)3*, which are in equilibrium with the 19-electron (19e) radicals CpW(CO)3P(OMe)3* on the nanosecond time scale. The reactions of the 19e radical are directly observed for the first time; the major reaction pathway is spontaneous loss of a carbonyl to form the 17e species CpW(CO)2P(OMe)3*, with a barrier of 7.6 +/- 0.3 kcal/mol for this process. The minor reaction pathway (<20%) at this concentration of P(OMe)3 (85 mM) is disproportionation to form the products CpW(CO)3P(OMe)3+ and CpW(CO)3-. On the microsecond time scale, the 17e radicals CpW(CO)2P(OMe)3* dimerize to form the ligand substitution product [CpW(CO)2P(OMe)3]2. These results indicate that the 19e species is a stable intermediate rather than transition state in the ligand substitution reaction, and this type of reactivity is likely to be typical of 17e organometallic radicals which undergo associative substitution mechanisms.