The coordination chenistry of iminooxosulphuranes. III. Synthesis of the ruthenium complexes (L=CO, CNtBu, CNC6H3Me2-2,6; R=C6H4Me-2, C6H4Me-4)

DOI: 10.1016/0022-328X(89)80123-8

Source and publish data:

Journal of Organometallic Chemistry p. 111 - 118 (1989)

Update date:2022-08-04

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Authors:

Herberhold, Max

Hill, Anthony F.

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Article abstract of DOI:10.1016/0022-328X(89)80123-8

The tris(phosphine) complexes (L=CO, CN^tBu, CNC6H3Me2-2,6) react with iminooxosulphuranes, RN=S=O, (R=C6H4Me-2, C6H4Me-4) by a displacement of one labile phosphine ligand to provide .Spectroscopic data indicate that the heterocumulenes are bound to ruthenium through both nitrogen and sulphur.Sulphur dioxide coordinates in a similar bidentate mode, through sulphur and oxygen, in the complexes that are obtained upon treatment of the corresponding tris(phosphine) precursors with gaseous sulphur dioxide.

Full text of DOI:10.1016/0022-328X(89)80123-8

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