A Systematic Evaluation of the N-F Bond Strength of Electrophilic N-F Reagents: Hints for Atomic Fluorine Donating Ability

被引:42
|
作者
Yang, Jin-Dong [1 ]
Wang, Ya [1 ]
Xue, Xiao-Song [1 ]
Cheng, Jin-Pei [1 ,2 ]
机构
[1] Nankai Univ, Collaborat Innovat Ctr Chem Sci & Engn, Coll Chem, State Key Lab Elementoorgan Chem, Tianjin 300071, Peoples R China
[2] Tsinghua Univ, Dept Chem, Ctr Basic Mol Sci, Beijing 100084, Peoples R China
来源
JOURNAL OF ORGANIC CHEMISTRY | 2017年 / 82卷 / 08期
关键词
C-H BONDS; HYPERVALENT FLUOROIODANE REAGENT; LATE-STAGE FLUORINATION; ENANTIOSELECTIVE FLUORINATION; ASYMMETRIC FLUORINATION; HALOGENO-COMPOUNDS; FLUOROPYRIDINIUM TRIFLATE; DENSITY FUNCTIONALS; UNACTIVATED ALKENES; CINCHONA ALKALOIDS;
D O I
10.1021/acs.joc.7b00036
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The recent discovery of the radical reactivity of a few traditionally-electrophilic N-F reagents has sparked a renaissance of radical fluorination. A knowledge of the N-F bond dissociation enthalpies (BDE) of electrophilic N-F reagents is essential for understanding of their reactivities. However, a thorough literature survey revealed that such information is extremely sparse. This prompted us to carry out the first systematic computation on the N-F BDEs of electrophilic N-F reagents. The calculated N-F BDE scale of 88 electrophilic N-F reagents ranges from 49.3 to 80.0 kcal mol(-1) in acetonitrile. The large variety of N-F reagents and wide span of N-F BDEs make the scale a useful tool not only for the future rational design of novel reagents but also for judicious selection of appropriate ones to explore new radical fluorinations.
引用
收藏
页码:4129 / 4135
页数:7
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