Battle, Andrew Raymond, Edwards, Peter Gerald ORCID: https://orcid.org/0000-0001-6999-753X, Haigh, Robert, Hibbs, David Edward, Li, Dong-Mei, Liddiard, Sam M. and Newman, Paul David ORCID: https://orcid.org/0000-0002-1808-1211
2006.
Synthesis and characterization of iron(II) complexes of 10- and 11-membered triphosphamacrocycles.
Organometallics
26
(2)
, pp. 377-386.
10.1021/om060798g
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Abstract
The complex [(η5-Me3SiC5H4)Fe(10aneP3-H2,C2H3)]+, where Me3SiC5H4 is trimethylsilylcyclopentadienyl and 10-aneP3-H2,C2H3 is 1-vinyl-1,4,8-triphosphacyclodecane, has been prepared by the base-catalyzed template cyclization of 1,3-bis(phosphino)propane (1,3-bpp) and trivinylphosphine (tvp) at the metal center. A related radical-initiated iron-template reaction between 1,2-bis(phosphino)ethane (1,2-bpe) and triallylphosphine (tap) gave [(η5-C5Me5)Fe(Me-10aneP3-H2,C3H5)]+, where C5Me5 is 1,2,3,4,5-pentamethylcyclopentadienyl and Me-10aneP3-H2,C3H5 is the unsymmetric 10-aneP3 derivative 1-allyl-3-methyl-1,4,7-triphosphacyclodecane. This macrocycle is the result of two intramolecular hydrophosphination reactions, one that generates a five-membered (chelate) ring with an exo-methyl group and one a six-membered chelate. The [(η5-CpR)Fe]+ fragment also controls the cyclization of 1,2-bis(diallylphosphino)ethane with phenylphosphine to give a ternary complex containing the symmetrical 11-membered macrocycle 1-phenyl-4,8-diallyl-1,4,8-triphosphacycloundecane, in addition to the unsymmetrical 10-aneP3 derivative.
| Item Type: | Article |
|---|---|
| Date Type: | Publication |
| Status: | Published |
| Schools: | Schools > Chemistry Research Institutes & Centres > Cardiff Catalysis Institute (CCI) |
| Subjects: | Q Science > QD Chemistry |
| Publisher: | American Chemical Society |
| ISSN: | 02767333 |
| Last Modified: | 17 Oct 2022 08:55 |
| URI: | https://orca.cardiff.ac.uk/id/eprint/1498 |
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