Organisch-Chemisches Institut der Universität Münster, Corrensstrasse 40, 48149 Münster, Germany.
Chemistry. 2012 Feb 6;18(6):1826-30. doi: 10.1002/chem.201101937. Epub 2012 Jan 3.
The frustrated Lewis pair Mes(2)PCH(2)CH(2)B(C(6)F(5))(2) reacts readily with 6-dimethylamino-6-methylfulvene at room temperature to yield the trans-1-[B(C(6)F(5))(2)]-2-[CH(2)CH(2)PMes(2)] disubstituted fulvene derivative 9 that features an internal N-B contact. Thermolysis (80 °C in toluene) results in a complete isomerization to the respective 1-[B(C(6)F(5))(2)]-3-[CH(2)CH(2)PMes(2)] isomer 10. Both compounds were characterized by using X-ray diffraction. A reaction scheme is formulated to rationalize the specific formation of these compounds, involving a retro-hydroboration/hydroboration sequence. The reaction of the 6-dimethylaminofulvene with HB(C(6)F(5))(2) yielded the corresponding parent compound 13 that was also characterized by X-ray diffraction.
受挫的路易斯对 Mes(2)PCH(2)CH(2)B(C(6)F(5))(2) 很容易与 6-二甲氨基-6-甲基芐基反应,在室温下生成反式 1-[B(C(6)F(5))(2)]-2-[CH(2)CH(2)PMes(2)]取代芐基衍生物 9,其具有内部 N-B 接触。热解(在甲苯中 80°C)导致完全异构化为相应的 1-[B(C(6)F(5))(2)]-3-[CH(2)CH(2)PMes(2)]异构体 10。这两种化合物均通过 X 射线衍射进行了表征。提出了一个反应方案来合理化这些化合物的特定形成,涉及反氢硼化/氢硼化序列。6-二甲氨基芐基与 HB(C(6)F(5))(2)的反应生成了相应的母体化合物 13,也通过 X 射线衍射进行了表征。