Browse by author
Lookup NU author(s): Emeritus Professor Bill CleggORCiD,
Dr Luca Russo
Full text for this publication is not currently held within this repository. Alternative links are provided below where available.
The cleavage of ethers is commonly encountered in organometallic chemistry, although rarely studied in the context of new, emerging bimetallic reagents. Recently, it was reported that a bimetallic sodium-zinc base can deprotonate cyclic tetrahydrofuran under mild conditions without opening its heterocyclic (OC4) ring. In marked contrast to this synergic sedation, herein we show that switching to the more reactive sodium-magnesium or sodium-manganese bases promotes cleavage of at least six bonds in tetrahydrofuran, but uniquely the ring fragments are captured in separate crystalline complexes. Oxide fragments occupy guest positions in bimetallic, inverse crown ethers and C-4 fragments ultimately appear in bimetallated butadiene molecules. These results demonstrate the special synergic reactivity that can be executed by bimetallic reagents, which include the ability to capture and control, and thereby study, reactive fragments from sensitive substrates.
Author(s): Mulvey RE, Blair VL, Clegg W, Kennedy AR, Klett J, Russo L
Publication type: Article
Publication status: Published
Journal: Nature Chemistry
Print publication date: 23/05/2010
ISSN (print): 1755-4330
Publisher: Nature Publishing Group
Altmetrics provided by Altmetric