In Crystallo Snapshots of Rh2-Catalyzed C-H Amination

被引:41
|
作者
Das, Anuvab [1 ]
Wang, Chen-Hao [1 ]
Van Trieste, Gerard P., III [1 ]
Sun, Cheng-Jun [2 ]
Chen, Yu-Sheng [3 ]
Reibenspies, Joseph H. [1 ]
Powers, David C. [1 ]
机构
[1] Texas A&M Univ, Dept Chem, College Stn, TX 77843 USA
[2] Argonne Natl Lab, Adv Photon Source, Argonne, IL 60439 USA
[3] Univ Chicago, ChemMatCARS, Argonne, IL 60439 USA
基金
美国国家科学基金会;
关键词
AB-INITIO PSEUDOPOTENTIALS; SET MODEL CHEMISTRY; X-RAY; SPECTROSCOPIC CHARACTERIZATION; TRANS-INFLUENCE; TOTAL ENERGIES; BOND; COMPLEX; FUNCTIONALIZATION; CATALYST;
D O I
10.1021/jacs.0c09842
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
While X-ray crystallography routinely provides structural characterization of kinetically stable pre-catalysts and intermediates, elucidation of the structures of transient reactive intermediates, which are intimately engaged in bond-breaking and -making during catalysis, is generally not possible. Here, we demonstrate in crystallo synthesis of Rh-2 nitrenoids that participate in catalytic C-H amination, and we characterize these transient intermediates as triplet adducts of Rh-2. Further, we observe the impact of coordinating substrate, which is present in excess during catalysis, on the structure of transient Rh-2 nitrenoids. By providing structural characterization of authentic C-H functionalization intermediates, and not kinetically stabilized model complexes, these experiments provide the opportunity to define critical structure-activity relationships.
引用
收藏
页码:19862 / 19867
页数:6
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