Science. 1993 Oct 15;262(5132):402-4. doi: 10.1126/science.262.5132.402.
The crystal structure of the tri-isopropyl silyl species, i-Pr(3)Si(Br(6)-CB(11)H(6)), where the brominated carborane Br(6)-CB(11) H(6)(-) is perhaps the least nucleophilic anion presently known, has revealed the highest degree of silylium cation character (R(3)Si(+)) yet observed. The average C-Si-C angle is 117 degrees , only 3 degrees short of the planarity expected of a pure silylium ion(120 degrees ). This value compares to 114 degrees recently reported for a toluene-solvated silyl cation, Et(3)Si(toluene) by Lambert and co-workers. The greater silylium ion character of i-Pr(3)Si(Br(6)-CB(11)H(6)) versus i-Pr(3)Si(toluene) is also reflected in the larger downfield shift of the silicon-29 nuclear magnetic resonance, 109.8 versus </=94.0 parts per million. The unusual bonding of toluene to R(3)Si(+) in Lambert's compound is reinterpreted as a significant covalent pi interaction.
三异丙基硅基溴代笼形倍半硅氧烷(i-Pr(3)Si(Br(6)-CB(11)H(6)))的晶体结构,其中溴代笼形倍半硅氧烷 Br(6)-CB(11) H(6)(-) 可能是目前已知的最非亲核性的阴离子,具有迄今为止观察到的最高程度的硅鎓阳离子特征(R(3)Si(+))。平均 C-Si-C 角为 117 度,仅比纯硅鎓离子(120 度)预期的平面性短 3 度。这一数值与 Lambert 及其同事最近报道的甲苯溶剂化硅鎓阳离子 Et(3)Si(toluene) 的 114 度相比有所增加。与 i-Pr(3)Si(toluene)相比,i-Pr(3)Si(Br(6)-CB(11)H(6))具有更强的硅鎓离子特征,这也反映在硅-29 核磁共振的更大的场位移上,为 109.8 对 </=94.0 百万分之一。在 Lambert 的化合物中,甲苯与 R(3)Si(+)的异常键合被重新解释为显著的共价 pi 相互作用。