Here, we report the synthesis of the first phospha-palladacycle substituted with an acyclic carbene. The reaction of bis(dialkyl)aminocarbenes with the very stable phospha-palladacycles leads to metastable eta(1)-carbene complexes, which can be converted by intramolecular reduction to zero valent palladium complexes. (c) 2005 Elsevier B.V. All rights reserved.
Here, we report the synthesis of the first phospha-palladacycle substituted with an acyclic carbene. The reaction of bis(dialkyl)aminocarbenes with the very stable phospha-palladacycles leads to metastable eta(1)-carbene complexes, which can be converted by intramolecular reduction to zero valent palladium complexes. (c) 2005 Elsevier B.V. All rights reserved.
Unexpected thermal decomposition of the “Alder carbene” (iPr2N)2C
作者:Tim Schulz、Michael Leibold、Christian Färber、Martin Maurer、Timo Porsch、Max C. Holthausen、Ulrich Siemeling
DOI:10.1039/c2cc34208a
日期:——
The "Alder carbene" (iPr(2)N)(2)C undergoes a beta-fragmentation in solution already at room temperature, affording propene and N,N,N'-triisopropylformamidine. This stands in sharp contrast to the indefinite stability previously claimed for this iconic compound.