Coupling reaction between the uncoordinated acetylenic bond of [Ru3(CO)103-FcC2 C≡CFc}] and FcC≡CC≡CFc to form [Ru2(CO)6{C4Fc2(C≡CFc)2}2], [Ru2(CO)6[μ-η1122-{FcC≡CCC(Fc)-C(O)-C(Fc)CC≡CFc}] and [Ru2(CO)6[μ-η11: η22-{FcC≡CCC(Fc)-C(O)-C(-C≡CFc)C(Fc)}]

Mathur, Pradeep ; Das, Atanu ; Chatterjee, Saurav ; Mobin, Shaikh M. (2008) Coupling reaction between the uncoordinated acetylenic bond of [Ru3(CO)103-FcC2 C≡CFc}] and FcC≡CC≡CFc to form [Ru2(CO)6{C4Fc2(C≡CFc)2}2], [Ru2(CO)6[μ-η1122-{FcC≡CCC(Fc)-C(O)-C(Fc)CC≡CFc}] and [Ru2(CO)6[μ-η11: η22-{FcC≡CCC(Fc)-C(O)-C(-C≡CFc)C(Fc)}] Journal of Organometallic Chemistry, 693 (10). pp. 1919-1926. ISSN 0022-328X

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Official URL: http://www.sciencedirect.com/science/article/pii/S...

Related URL: http://dx.doi.org/10.1016/j.jorganchem.2008.02.021

Abstract

Low temperature photolysis of a hexane solution of [Ru3(CO)12] and FcC≡CC≡CFc provides a convenient route to the diyne-bridged cluster [Ru3(CO)103-FcC2C≡CFc}] (1). When a toluene solution containing 1 and diferrocenyldiacetylene was heated at 80 °C three compounds formed: the ruthenacyclopentadiene complex [Ru2(CO)6{C4Fc2(C≡CFc)2}2], and two isomers of the diruthenacycloheptadienone complex, [Ru2(CO)6[μ-η1122-{FcC≡CCC(Fc)-C(O)-C(Fc)CC≡CFc}] (3), [Ru2(CO)6[μ-η1122-{FcC≡CCC(Fc)-C(O)-C(-C≡CFc)C(Fc)}] (4). Compounds 2-4 have been characterized spectroscopically and their structures established crystallographically. Consistent with structural reports on metallacyclic compounds bearing bulky substituents, in 2 and 3, the bulkier of the two types of substituents, the C≡CFc groups are located on the carbon atoms adjacent to the metal atoms, whereas in compound 4, only one of the two C≡CFc groups is on the α-carbon atom of the ruthenacyclopentadienone ring.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
Keywords:Ruthenium Carbonyl; Cluster; Coupling; Diacetylene; Ferrocenyl
ID Code:83071
Deposited On:16 Feb 2012 07:54
Last Modified:16 Feb 2012 07:54

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