Synthesis and some properties of binuclear ruthenocenes bridged by oligoynes: formation of bis(cyclopentadienylidene)cumulene diruthenium complexes in the two-electron oxidation

Masaru Sato; Yusuke Kubota; Yasushi Kawata; Takashi Fujihara; Kei Unoura; Aiko Oyama

doi:10.1002/chem.200500926

Synthesis and some properties of binuclear ruthenocenes bridged by oligoynes: formation of bis(cyclopentadienylidene)cumulene diruthenium complexes in the two-electron oxidation

Chemistry. 2006 Mar 1;12(8):2282-92. doi: 10.1002/chem.200500926.

Authors

Masaru Sato¹, Yusuke Kubota, Yasushi Kawata, Takashi Fujihara, Kei Unoura, Aiko Oyama

Affiliation

¹ Department of Chemistry, Faculty of Science, Saitama University, Saitama, Saitama 338-8570, Japan. msato@chem.saitama-u.ac.jp

PMID: 16342316
DOI: 10.1002/chem.200500926

Abstract

The monoynes [Rc*C[triple bond]CRc*] and [Rc'C[triple bond]CRc'] were obtained in improved yields using [Mo(CO)6]/2-FC6H5OH as a catalyst in the alkyne metathesis of [Rc*C[triple bond]CMe] and [Rc'C[triple bond]CMe], respectively (Rc = ruthenocenyl, Rc* = 1'',2'',3'',4'',5''-pentamethylruthenocenyl, and Rc' = 2',3',4',5'-tetramethylruthenocenyl groups). The diynes [Rc*(C[triple bond]C)2Rc*] and [Rc'(C[triple bond]C)2Rc'] were synthesized by the oxidative coupling of the corresponding terminal ethynes in good yields. The triyne [Rc*(C[triple bond]C)3Rc*] and the tetrayne [Rc*(C[triple bond]C)4Rc*] were prepared by the hetero- and homocoupling of [Rc*C[triple bond]CC[triple bond]CH], which was obtained from the reaction of [Rc*C[triple bond]CCHO] with Li[N2CSiMe3], respectively. Although the oxidation waves did not always exhibit a clear two-electron oxidation process, the oxidation potentials shifted to a lower potential with an increase in the number of methyl substituents on the ruthenocenyl ring, and shifted to a higher potential with the increase in the number of C[triple bond]C units; this result is in contrast to that found in the [Rc(CH=CH)(n)Rc] series. The chemical oxidation of [Rc'C[triple bond]CRc'] yielded a stable two-electron-oxidized species, the structure of which was confirmed by X-ray crystallography to be [Ru2(mu2-eta(6):eta(6)-C5Me4C=CC5Me4)(eta-C5H5)2](BF4)2. Changing the substituents (Rc, Rc*, and Rc') had no effect on the chemical oxidation, but in the case of the Rc' series the Me substituent increased the stability of the two-electron-oxidized species in solution. The diyne [Rc*(C[triple bond]C)2Rc*] and the triyne [Rc*(C[triple bond]C)3Rc*] also gave a similar but unstable two-electron-oxidized species. In acetone or acetonitrile, the two-electron-oxidized species of [Rc*C[triple bond]CRc*] and [Rc*(C[triple bond]C)2Rc*] gradually formed the corresponding bis(fulvene)-type complexes. This implies that the two-electron-oxidized species of [Rc*(C[triple bond]C)(n)Rc*] are destabilized with the increasing n.