Experimental Evidence for Heavy-Atom Tunneling in the Ring-Opening of Cyclopropylcarbinyl Radical from Intramolecular 12C/13C Kinetic Isotope Effects

被引:74
作者
Gonzalez-James, Ollie M. [3 ]
Zhang, Xue [1 ,2 ]
Datta, Ayan [1 ,2 ]
Hrovat, David A. [1 ,2 ]
Borden, Weston Thatcher [1 ,2 ]
Singleton, Daniel A. [3 ]
机构
[1] Univ N Texas, Dept Chem, Denton, TX 76203 USA
[2] Univ N Texas, Ctr Adv Sci Comp & Modeling, Denton, TX 76203 USA
[3] Texas A&M Univ, Dept Chem, College Stn, TX 77842 USA
基金
美国国家科学基金会;
关键词
CARBON; AUTOMERIZATION; STATE; REARRANGEMENTS; MECHANISMS;
D O I
10.1021/ja1055593
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The intramolecular C-13 kinetic isotope effects for the ring-opening of cyclopropylcarbinyl radical were determined over a broad temperature range. The observed isotope effects are unprecedentedly large, ranging from 1.062 at 80 degrees C to 1.163 at -100 degrees C. Semiclassical calculations employing canonical variational transition-state theory drastically underpredict the observed isotope effects, but the predicted isotope effects including tunneling by a small-curvature tunneling model match well with experiment. These results and a curvature in the Arrhenius plot of the isotope effects support the recently predicted importance of heavy-atom tunneling in cyclopropylcarbinyl ring-opening.
引用
收藏
页码:12548 / 12549
页数:2
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