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7738390 
Journal Article 
COORDINATION OF POLYTHIAETHER MACROCYCLES TO METAL CLUSTER COMPLEXES .2. COORDINATION OF POLYTHIAETHER MACROCYCLES TO HEXARUTHENIUM CARBIDO CARBONYL CLUSTERS 
Adams, RD; Falloon, SB; Mcbride, KT; Yamamoto, JH 
1995 
1 
Organometallics
ISSN: 0276-7333
EISSN: 1520-6041 
AMER CHEMICAL SOC 
WASHINGTON 
14 
4 
1739-1747 
English 
WOS:A1995QT98000029 
The synthesis and structural characterizations of Ru6(μ6-C) cluster complexes containing the polythiaether macrocycle ligands 1,5,9-trithiacyclododecane (12S3), 1,5,9,13-tetrathiacyclohexadecane (16S4), and 1,4,7-trithiacyclononane (9S3) are reported. The reactions of Ru6(CO)17(μ6-C), 1, with 12S3 and 16S4 in refluxing octane solvent have yielded the new cluster complexes Ru6(CO)13(μ-η3-12S3)(μ6-C), 2, in 78% yield, and Ru6(CO)15(μ-η2-16S4)(μ6-C), 3, in 58% yield, respectively. The reaction of 1 with 9S3 in refluxing hexane solvent has yielded the new cluster complex Ru6(CO)14(η3-9S3) (μ6-C). 4, in 93% yield. All three products were characterized by a combination of IR, 1H NMR, and single crystal X-ray diffraction analyses. All three compounds contain octahedral Ru6 clusters with a carbido ligand in the center. In compound 2 the three sulfur atoms of the 12S3 ligand are coordinated to one ruthenium atom but one of the sulfur atoms simultaneously serves as a bridge to an adjacent ruthenium atom. In compound 3 only two of the four sulfur atoms of the 16S4 ligand are coordinated to the cluster and they are coordinated to two adjacent ruthenium atoms. In compound 4 the three sulfur atoms of the 9S3 ligand are coordinated to one ruthenium atom only. When heated to 105 °C for 18 h, compound 4 was converted to the new compound Ru6(CO)14(μ3-η3-SCH2CH2SCH2CH2S)(μ5-C), 5, in 68% yield. The evolution of ethylene was observed by 1H NMR spectroscopy. Compound 5 was obtained in one step from the reaction of 1 with 9S3 in refluxing octane solvent in 36% yield. Compound 5 was characterized crystallographically and was shown to consist of a “spiked” square pyramidal cluster of six metal atoms with the carbido ligand in the center of the base of the square pyramid. The spike is bonded to one of the metal atoms in the base of the square pyramid. The 9S3 ligand was converted into a triply bridging 3-thiapentane-1,5-dithiolato ligand. All three sulfur atoms form bridges between the ruthenium spike and the Ru5 square pyramid. Crystal data: for 2·C6H6, space group = P1̅, a = 16.755(2) Å, b = 11.647(2) Å, c = 11.355(2) Å, α = 61.30(1)°, β= 89.78(1)°, γ = 101.76(2)°, Z = 2, 2648 reflections, R = 0.032; for 3: space group = Pnma, a = 23.373(3) Å, b = 17.643(2) Å, c = 9.453(2) Å, Z = 4, 1854 reflections, R = 0.030; for 4.C6H6, space group = P21/a, a = 13.366(2) Å, b = 20.746(6) Å, c = 13.059(3) Å, β = 90.75(1)°, Z = 4, 3345 reflections, R = 0.025; for 5·CH2Cl2, space group = P21/c, a = 13.669(2) Å, b = 15.610(3) Å, c = 15.476(2) Å, β= 92.46(1)°, Z = 4, 4526 reflections, R = 0.033. © 1995, American Chemical Society. All rights reserved.