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对三氟甲基化的洞察——Togni试剂I的实验电子密度

Insight into trifluoromethylation - experimental electron density for Togni reagent I.

作者信息

Wang R, Kalf I, Englert U

机构信息

Institute of Inorganic Chemistry, RWTH Aachen University Landoltweg 1 52074 Aachen Germany

Institute of Molecular Science, Shanxi University Taiyuan Shanxi 030006 P. R. China.

出版信息

RSC Adv. 2018 Oct 5;8(60):34287-34290. doi: 10.1039/c8ra07187j. eCollection 2018 Oct 4.

Abstract

3,3-Dimethyl-1-(trifluoromethyl)-1,3-dihydro-1-λ3,2-benziodoxole represents a popular reagent for trifluoromethylation. The σ hole on the hypervalent iodine atom in this "Togni reagent" is crucial for adduct formation between the reagent and a nucleophilic substrate. The electronic situation may be probed by high resolution X-ray diffraction: the experimental charge density thus derived shows that the short intermolecular contact of 3.0 Å between the iodine and a neighbouring oxygen atom is associated with a local charge depletion on the heavy halogen in the direction of the nucleophile and visible polarization of the O valence shell towards the iodine atom. In agreement with the expectation for λ3-iodanes, the intermolecular O⋯I-C halogen bond deviates significantly from linearity.

摘要

3,3-二甲基-1-(三氟甲基)-1,3-二氢-1-λ3,2-苯并碘杂环戊二烯是一种常用的三氟甲基化试剂。这种“托格尼试剂”中高价碘原子上的σ空穴对于试剂与亲核底物之间加合物的形成至关重要。电子情况可通过高分辨率X射线衍射进行探测:由此得到的实验电荷密度表明,碘与相邻氧原子之间3.0 Å的短分子间接触与重卤素在亲核试剂方向上的局部电荷耗尽以及氧价层向碘原子的明显极化有关。与对λ3-碘烷的预期一致,分子间O⋯I-C卤键明显偏离线性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28aa/9087471/19cad6ec63dd/c8ra07187j-s1.jpg

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