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Organometallic macrocycle chemistry. 5.<sup>1</sup> σ-vinyl and σ-aryl complexes of ruthenium(II) ligated by 1,4,7-trithiacyclononane: X-ray crystal structure of [Ru(CH=CH<sub>2</sub>)(CO)(PPh<sub>3</sub>)([9]aneS <sub>3</sub>)]PF6·2CH<sub>2</sub>Cl<sub>2</sub>

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Cannadine, Jason C.
Hill, Anthony F.
White, Andrew J.P.
Williams, David J.
Wilton-Ely, James D.E.T.

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The reaction of coordinatively unsaturated σ-vinyl complexes [Ru(CR=CHR′)Cl(CO)(PPh3)2] with 1,4,7-trithiacyclononane ([9]aneS3) provides chiral salts of the "half-sandwich" complexes [Ru(CR=CHR′)(CO)(PPh3)([9]aneS3)]+. The synthesis of the σ-aryl complex [Ru(C6H4Me-4)(CO)(PPh3)([9]aneS 3)]+ is also described. A representative NMR study of one example allowed the assignment of individual chemical shifts for the 12 diastereotopic proton environments of the macrocycle. The crystal structure of [Ru(CH=CH2)(CO)(PPh3)-([9]aneS3)]PF 6·2CH2Cl2 is also reported.

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Organometallics

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