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Digging the Sigma‐Hole of Organoantimony Lewis Acids by Oxidation
Author(s) -
Yang Mengxi,
Tofan Daniel,
Chen ChangHong,
Jack Kevin M.,
Gabbaï François P.
Publication year - 2018
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.201808551
Subject(s) - lewis acids and bases , chemistry , catalysis , reagent , antimony , medicinal chemistry , stereochemistry , inorganic chemistry , organic chemistry
The development of group 15 Lewis acids is an area of active investigation that has led to numerous advances in anion sensing and catalysis. While phosphorus has drawn considerable attention, emerging research shows that organoantimony(III) reagents may also act as potent Lewis acids. Comparison of the properties of SbPh 3 , Sb(C 6 F 5 ) 3 , and SbAr F 3 with those of their tetrachlorocatecholate analogues SbPh 3 Cat, Sb(C 6 F 5 ) 3 Cat, and SbAr F 3 Cat (Cat= o ‐O 2 C 6 Cl 4 , Ar F =3,5‐(CF 3 ) 2 C 6 H 3 ) demonstrates that the Lewis acidity of electron deficient organoantimony(III) reagents can be readily enhanced by oxidation to the +V state—as verified by binding studies, organic reaction catalysis, and computational studies. The results are rationalized by explaining that oxidation of the antimony center leads to a lowering of the accepting σ* orbital and a deeper carving of the associated σ‐hole.