N-phosphinoamidinato silylene- and phosphine-borylborylene complexes
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...
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Main Authors: | , , , |
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Other Authors: | |
Format: | Article |
Language: | English |
Published: |
2023
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Subjects: | |
Online Access: | https://hdl.handle.net/10356/168936 |
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Institution: | Nanyang Technological University |
Language: | English |
Summary: | 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. |
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