取代基效应对脂肪醇^(13)C NMR化学位移的影响  

Influence of Substituent Effects on the ^(13)C NMR Chemical Shifts of Aliphatic Alcohols

作　　者：易贵元[1] 曹晨忠[1] 

机构地区：[1]湖南科技大学化学化工学院,湖南湘潭411201

出　　处：《波谱学杂志》2009年第1期58-74,共17页Chinese Journal of Magnetic Resonance

基　　金：国家自然科学基金资助项目(20772028);湖南省自然科学基金(06JJ2002);湖南省教育厅资助项目

摘　　要：用原子电负性、静电作用、极化度作为基本参数,并结合表征原子空间连接方式的立体效应参数,对醇分子中不同环境碳原子的化学位移进行关联,将120个模型化合物(91个脂肪一元醇,29个二元醇)中747个碳原子相关参数值和化学位移值带入模型中得到如下估算方程:δC=42.9479+63.0640Qi-3.6286F+5.1213Σαx-6.5848QiΣαx-4.8427NαH-0.5855NγH-4.1046NγOH(R=0.9981R2=0.9961S=1.14F=27125.2n=747)方程中各参数物理意义比较明确.通过用"留一法"(LOO)检验(Rcv=0.9980,Rc2v=0.9960,Scv=1.16)及对样本外5个化合物69个碳原子化学位移的预测值和实验值比较,结果表明模型方程具有很好的稳定性和预测精度,该模型的提出为以后计算更加复杂化合物的13CNMR化学位移奠定了良好的基础.An empirical model for calculating ^13C chemical shifts of aliphatic alcohols was proposed, in which the parameters describing the chemical environment of the focused carbon atoms are in were used as the independent variables. The parameters included electronegativity, atomic polarizability and those representing the sterie effects. The experimentally-measured ^13C NMR chemical shifts of 747 carbon atoms in 120 model compounds （91 alcohols and 29 diols） were used as the training set to derive the weights for the independent variables. The correlation coefficient R of the model was found to be 0. 998. Leave-one-out cross-validation demonstrated good predictive ability and stability of the model. The model proposed was used to calculate the ^13C chemical shifts of 69 different carbon atoms in 5 compounds that were not included in results proven to be satisfactory. The proposed model may be NMR chemical shifts in alcohols with complex structures. the training set, and the useful for calculating ^13C NMR chemical shifts in alcohols with complex structures.

关 键 词：核磁共振(NMR) 13C化学位移 电负性 静电场 原子极化度 立体效应 脂肪醇 

分 类 号：O482.53[理学—固体物理]