Abstract

The ability of an isolable N,N′‐diamidocarbene (DAC) to activate compounds containing early p‐block elements was explored. At ambient temperature, the DAC formally inserted into the Si–H bonds of various silanes to afford the corresponding DAC–silane adducts. The aforementioned adducts did not undergo intramolecular ring expansion as observed with other carbene–silane analogues. The DAC was also found to form a coordination complex with aluminum chloride, and a structurally rich, tris(aluminum) species was obtained upon exposure of the DAC to trimethylaluminum. The results gleaned from these studies are expected to facilitate the development of novel organometallic species as well as of new types of organocatalyzed silylations and aluminations. Copyright © 2014 John Wiley & Sons, Ltd.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call