Abstract
The reaction of Cp*Ir(CO)2 (1) with pentafluorobenzontrile in the presence of a base afforded the diaryl complex Cp*Ir(CO)(p-C 6F4CN)2 (4). The reaction proceeds via the metallacarboxylic acid Cp*Ir(CO)(p- C6F4CN)(COOH) (2). The latter can be decarboxylated in the presence of a base to the hydrido species Cp*Ir(CO)(p-C6F4CN)(H) (5), which can then undergo hydrideechloride exchange to Cp*Ir(CO)(p-C6F 4CN)(Cl) (6a). In the presence of air and water, the reaction of 1 with pentafluorobenzontrile afforded a complex formulated as Cp*Ir(CO)(p-C6F4CN){C(OH)(NH2)C 6F5} (7a); this is also available from the reaction of 2 with pentafluorobenzamide in the presence of aqueous NaOH.
Original language | English |
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Pages (from-to) | 176-180 |
Number of pages | 5 |
Journal | Journal of Organometallic Chemistry |
Volume | 741-742 |
Issue number | 1 |
DOIs | |
Publication status | Published - 2013 |
Externally published | Yes |
ASJC Scopus Subject Areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry
- Inorganic Chemistry
- Materials Chemistry
Keywords
- Iridium
- Pentafluorobenzonitrile
- Restricted rotation