Evidence for Solution-State Nonlinearity of sp-Carbon Chains Based on IR and Raman Spectroscopy: Violation of Mutual Exclusion
作者:Andrea Lucotti、Matteo Tommasini、Daniele Fazzi、Mirella Del Zoppo、Wesley A. Chalifoux、Michael J. Ferguson、Giuseppe Zerbi、Rik R. Tykwinski
DOI:10.1021/ja078198b
日期:2009.4.1
violations of the mutual-exclusion principle between IR and Raman spectroscopy, spectral evidence demonstrates that these molecules possess a noncentrosymmetric molecular structure in both the solid and solution states. This premise is supported by X-ray crystallographic analysis of C12, which shows a bent, noncentrosymmetric structure in the solid state. Density functional theory (DFT) calculations
已经合成了具有 4、6、8、10、12、16 和 20 sp 杂化碳 (C4-C20) 链的金刚烷基封端的聚炔,并获得了它们的红外和拉曼光谱。在违反 IR 和拉曼光谱之间的互斥原理的基础上,光谱证据表明这些分子在固体和溶液状态下都具有非中心对称的分子结构。这一前提得到了 C12 的 X 射线晶体学分析的支持,该分析显示出固态弯曲的非中心对称结构。与氢封端的聚炔相比,金刚烷基封端的聚炔的密度泛函理论 (DFT) 计算表明,观察到的互斥违反与聚炔链的端基无关(即,金刚烷基与H)。