Ruthenium carbonyl cluster complexes with oxygen ligands. Part 2. Auration of a hexaruthenium 'raft' cluster; Crystal structures of [Ru63-H)(μ-H)(μ-O:μ-C:η 6-OC6H3OMe-4)(CO)16] and [AuRu63-H)(μ-O:μ-C:η6-OC 6H3OMe-4)(CO)16...

Marie P. Cifuentes, Tyrone P. Jeynes, Mark G. Humphrey*, Brian W. Skelton, Allan H. White

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

11 Citations (Scopus)

Abstract

Full title: Ruthenium carbonyl cluster complexes with oxygen ligands. Part 2. Auration of a hexaruthenium 'raft' cluster; Crystal structures of [Ru63-H)(μ-H)(μ-O:μ-C:η 6-OC6H3OMe-4)(CO)16] and [AuRu63-H)(μ-O:μ-C:η6-OC 6H3OMe-4)(CO)16(PPh3)]. The hexaruthenium raft cluster [Ru63-H)(μ-H)(μ-O:μ-C:η 6-OC6H3OMe-4)(CO)16] 1 is smoothly deprotonated by K-Selectride {K[B(CHMeEt)3H] in tetrahydrofuran}, the resulting cluster anion being aurated by [AuCl(PPh3)] to afford the mixed-metal cluster [AuRu63-H)(μ-O:μ-C:η6-OC 6H3OMe-4)(CO)16(PPh3)] 2 as the major product in moderate yield. The crystal structures of both 1 and 2 have been determined. The structural studies have revealed that isostructural replacement of H by isolobal Au(PPh3) has not occurred; rather, an edge-bridging hydride has been replaced by a face-capping (phosphine)aurio moiety. In an analogous fashion to the auration, sequential reaction of 1 with K-Selectride and H3PO4 regenerated 1. By contrast, hydrogenation [1 atm (ca. 105Pa) H2, refluxing cyclohexane] of 1 resulted in expulsion of the -OC6H3OMe-4 ligand and formation of [Ru4(μ-H)4(CO)12].

Original languageEnglish
Pages (from-to)925-930
Number of pages6
JournalJournal of the Chemical Society, Dalton Transactions
Issue number6
DOIs
Publication statusPublished - 1994
Externally publishedYes

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