Abstract
The elucidation of the crystal structure of one isomer of the mixed metal boride [HFe4(CO)12{AuPEt3}2B] illustrates that the geometry of the hexametal atom core and the location of the endohydrogen atom depend upon the steric, rather than electronic, requirements of the gold(I) phosphine substituents. Electronic effects, however, are responsible for the AuPR3 fragment interacting with Fe-B rather than Fe-Fe bonds of the core cluster.
| Original language | English |
|---|---|
| Pages (from-to) | 1885-1887 |
| Number of pages | 3 |
| Journal | Organometallics |
| Volume | 7 |
| Issue number | 8 |
| Publication status | Published - 1988 |
ASJC Scopus subject areas
- Inorganic Chemistry
- Organic Chemistry
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Housecroft, C. E., Shongwe, M. S., & Rheingold, A. L. (1988). An appraisal of the steric versus electronic requirements of gold(I) phosphine substituents in clusters: The crystal structure of [HFe4(CO)12{AuPEt3}2B]. Organometallics, 7(8), 1885-1887.