Department of Chemistry, University of California , Irvine, California 92697-2025, United States.
J Am Chem Soc. 2015 Nov 25;137(46):14716-25. doi: 10.1021/jacs.5b08597. Epub 2015 Nov 12.
(C5Me5)2Y(μ-Ph)2BPh2, 1, reacted with ethyllithium at -15 °C to make (C5Me5)2Y(CH2CH3), 2, which is thermally unstable at room temperature and formed the C-H bond activation product, (C5Me5)2Y(μ-H)(μ-η(1):η(5)-CH2C5Me4)Y(C5Me5), 3, containing a metalated (C5Me5)(1-) ligand. Spectroscopic evidence for 2 was obtained at low temperature, and trapping experiments with (i)PrNCN(i)Pr and CO2 gave the Y-CH2CH3 insertion products, (C5Me5)2Y[(i)PrNC(Et)N(i)Pr-κ(2)N,N'], 4, and [(C5Me5)2Y(μ-O2CEt)]2, 5. Although 2 is highly reactive, low temperature isolation methods allowed the isolation of single crystals which revealed an 82.6(2)° Y-CH2-CH3 bond angle consistent with an agostic structure in the solid state. Complex 2 reacted with benzene and toluene to make (C5Me5)2YPh, 7, and (C5Me5)2YCH2Ph, 8, respectively. The reaction of 2 with [(C5Me5)2YCl]2 formed (C5Me5)2Y(μ-Cl)(μ-η(1):η(5)-CH2C5Me4)Y(C5Me5) in which a (C5Me5)(1-) ligand was metalated. C-H bond activation also occurred with methane which reacted with 2 to make [(C5Me5)2YMe]2, 9.
(C5Me5)2Y(μ-Ph)2BPh2,1,与乙基锂在-15°C反应生成(C5Me5)2Y(CH2CH3),2,其在室温下不稳定,形成 C-H 键活化产物(C5Me5)2Y(μ-H)(μ-η(1):η(5)-CH2C5Me4)Y(C5Me5),3,其中含有一个金属化的(C5Me5)(1-)配体。在低温下获得了 2 的光谱证据,并用(i)PrNCN(i)Pr 和 CO2进行的捕获实验得到了 Y-CH2CH3 插入产物(C5Me5)2Y[(i)PrNC(Et)N(i)Pr-κ(2)N,N'],4,和[(C5Me5)2Y(μ-O2CEt)]2,5。尽管 2 具有很高的反应性,但低温分离方法允许分离出单晶,单晶显示出在固态中具有 82.6(2)°的 Y-CH2-CH3 键角,与桥接配位的结构一致。化合物 2 与苯和甲苯反应生成(C5Me5)2YPh,7,和(C5Me5)2YCH2Ph,8,分别。2 与[(C5Me5)2YCl]2的反应形成(C5Me5)2Y(μ-Cl)(μ-η(1):η(5)-CH2C5Me4)Y(C5Me5),其中一个(C5Me5)(1-)配体被金属化。C-H 键活化也发生在甲烷与 2 反应生成[(C5Me5)2YMe]2,9。