Phosphinine-Based Ligands in Gold-Catalyzed Reactions.
Massimo RigoEvi R M HabrakenKoyel BhattacharyyaManuela WeberAndreas W EhlersNicolas MézaillesJ Chris SlootwegChristian MüllerPublished in: Chemistry (Weinheim an der Bergstrasse, Germany) (2019)
A series of substituted phosphinines, 1-phosphabarrelenes and 5-phosphasemibullvalenes were synthesized and evaluated for their potential application as ligands in homogeneous catalytic reactions. While their buried volume (%Vbur ) was calculated to get insight into the steric properties, [LNi(CO)3 ] complexes were prepared in order to determine the corresponding Tolman electronic parameter. ETS-NOCV (extended-transition-state natural orbital for chemical valence) calculations on [LAuCl] complexes further allowed an estimation of the σ- and π-contributions to the L-M interaction. AuI coordination compounds of selected examples were prepared and characterized by single crystal X-ray diffraction. Finally, the three classes of PIII compounds were successfully used in the AuI -catalyzed cycloisomerization of N-2-propyn-1-ylbenzamide, showing very good activities and selectivities, which are comparable with the reported data of cationic phosphorus-based gold catalysts.
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