摘要
Reduction of the group 4 transition metal precursors [(PN)(2)MCl2] (M = Zr (1), and Hf (2)); PN similar to = (N-(2-(diisopropylphosphino)-4-methylphenyl)-2,4,6-trimethylanilide), both readily prepared by transmetallation of 2 LiPN with [MCl4(THF)(2)], with a slight excess of KC8, resulted in the isolation of the trivalent complexes [(PN)(2)MCl] (M = Zr (3), and Hf (4)). Complexes 1-4 were all identified by solidstate X-ray diffraction analysis, whereas in the case of 3 and 4 low temperature X-band EPR spectroscopy allowed for the identification of these metal-centered d1 radicals. A comparison with the isostructural and isoelectronic but more stable [(PN)(2)TiCl] is also presented.
- 出版日期2018-2-25