Structural diversity in pyridine-N-functionalized carbene copper(I) complexes
Structural diversity in pyridine-N-functionalized carbene copper(I) complexes
The use of the versatile pyridine N-functionalized carbene ligands has allowed the isolation and structural characterization of copper(I) imidazol-2-ylidene complexes of the type ([(3-R)(1-L)imidazol-2-ylidene] CuBr}, where L = 2-picolyl, R = 2,4,6-trimethylphenyl (mesityl), 2,6-(Pr2C6H3)-C-i; L = 2-pyridyl, R = 2,6-(Pr2C6H3)-C-i. They were prepared by interaction of the corresponding imidazolium bromides with Cu2O in chlorinated solvents in the presence of molecular sieves. In the solid state the 2-picolyl derivatives crystallize as dimers or polymers depending on the crystallization conditions, while the 2-pyridyl derivative crystallizes as monomer.
heterocyclic carbene, olefin metathesis, catalysts, palladium
2027-2031
Tulloch, Arran A. D.
8fe08eb4-a6f5-4ebb-b0a4-19fc745a018a
Danopoulos, Andreas A.
4919c13e-ebe4-4456-b329-c806c8e22236
Kleinhenz, Sven
24f0e096-1f4a-4589-8378-d53720994426
Light, Mark E.
cf57314e-6856-491b-a8d2-2dffc452e161
Hursthouse, Michael B.
57a2ddf9-b1b3-4f38-bfe9-ef2f526388da
Eastham, Graham
b5a80d7f-914e-4e5b-b3de-8e9944ca95d8
14 May 2001
Tulloch, Arran A. D.
8fe08eb4-a6f5-4ebb-b0a4-19fc745a018a
Danopoulos, Andreas A.
4919c13e-ebe4-4456-b329-c806c8e22236
Kleinhenz, Sven
24f0e096-1f4a-4589-8378-d53720994426
Light, Mark E.
cf57314e-6856-491b-a8d2-2dffc452e161
Hursthouse, Michael B.
57a2ddf9-b1b3-4f38-bfe9-ef2f526388da
Eastham, Graham
b5a80d7f-914e-4e5b-b3de-8e9944ca95d8
Tulloch, Arran A. D., Danopoulos, Andreas A., Kleinhenz, Sven, Light, Mark E., Hursthouse, Michael B. and Eastham, Graham
(2001)
Structural diversity in pyridine-N-functionalized carbene copper(I) complexes.
Organometallics, 20 (10), .
(doi:10.1021/om010014t).
Abstract
The use of the versatile pyridine N-functionalized carbene ligands has allowed the isolation and structural characterization of copper(I) imidazol-2-ylidene complexes of the type ([(3-R)(1-L)imidazol-2-ylidene] CuBr}, where L = 2-picolyl, R = 2,4,6-trimethylphenyl (mesityl), 2,6-(Pr2C6H3)-C-i; L = 2-pyridyl, R = 2,6-(Pr2C6H3)-C-i. They were prepared by interaction of the corresponding imidazolium bromides with Cu2O in chlorinated solvents in the presence of molecular sieves. In the solid state the 2-picolyl derivatives crystallize as dimers or polymers depending on the crystallization conditions, while the 2-pyridyl derivative crystallizes as monomer.
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Published date: 14 May 2001
Keywords:
heterocyclic carbene, olefin metathesis, catalysts, palladium
Identifiers
Local EPrints ID: 19625
URI: http://eprints.soton.ac.uk/id/eprint/19625
ISSN: 0276-7333
PURE UUID: 775f7deb-9ea9-4ed9-b525-b8e8d1f2fa96
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Date deposited: 13 Feb 2006
Last modified: 16 Mar 2024 03:04
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Author:
Arran A. D. Tulloch
Author:
Andreas A. Danopoulos
Author:
Sven Kleinhenz
Author:
Graham Eastham
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