Abstract
This work describes a straightforward method to synthesize a borylborylene without proceeding via the rearrangement of a diborene. An amidinato amidosilylene [LSiNMe2] (L = PhC(NtBu)2) and PMe3 were reacted with an N-phosphinoamidinato diborane 1 and KC8 to form a stable silylene-borylborylene 2 and a persistent phosphine-borylborylene 3, respectively. Compound 2 is stable as the borylene center is well stabilized by the silylene donor and boryl substituent, whereas compound 3 is unstable in solution due to labile PMe3. The latter was illustrated by reacting compound 3 with Ar’NC (Ar’ = 2,6-Me2C6H3), where Ar’NC displaced PMe3 and inserted into the N-phosphinoamidinate ligand and B-B bond to form compound 4.
Original language | English |
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Pages (from-to) | 863-870 |
Number of pages | 8 |
Journal | Inorganic Chemistry |
Volume | 62 |
Issue number | 2 |
DOIs | |
Publication status | Published - Jan 16 2023 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2023 American Chemical Society.
ASJC Scopus Subject Areas
- Physical and Theoretical Chemistry
- Inorganic Chemistry