Abstract
The synthesis of mixed halo-phosphine isocyanide complexes of general formula [ReCl2(CNR)3(PMePh2)2] + is described. The crystal structure of a representative member of this class, [ReCl2(CN-t-Bu)3(PMePh2)2](SbF6) (1), has been determined. This complex adopts the C2v capped trigonal prismatic geometry with close nonbonded contacts of 2.341 (8) and 2.330 (9) Å between coordinated isocyanide carbon atoms. Such distances in seven-coordinate compounds reveal that they are good candidates for reductive coupling of the isocyanide ligands, a reaction previously studied for 1. The syntheses of [ReCI3(CN-t-Bu)2(PMePh2)2] and [ReCl3(CN-2,6-Me2Ph)3(PMePh2)] are also reported. Red crystals of [Re(O)(OEt)Cl2(PMePh2)2] (2) were isolated in 25% yield as a side product during the preparation of [ReCl3(PMePh2)3] starting material from AgReO4. The identity of 2 was established by IR spectroscopy, elemental analysis, and X-ray crystallography. The Re-O bond distance of 1.699 (5) Å is characteristic of a metal-oxygen triple bond. Crystal data: for.
| Original language | English |
|---|---|
| Pages (from-to) | 1221-1226 |
| Number of pages | 6 |
| Journal | Inorganic Chemistry |
| Volume | 30 |
| Issue number | 6 |
| DOIs | |
| Publication status | Published - 1 Mar 1991 |
| Externally published | Yes |