- Abstract:
-
Treatment of [(PPh3)2Ir(COD)][closo-CB11H6 Br6] with H2 in CH2Cl2 solution affords crystallographically characterized (PPh3)2Ir(H)2(closo-CB11 H6Br6), in which the weakly coordinating carborane anion is bound to the metal center. In solution the anion rapidly dissociates/recombines with the metal center, and this process can be frozen out at -50°C. At lower temperatures (-80°C) a solvent-stabilized complex [(PPh3)2Ir(H)2 (CH2Cl2)][closo-CB11H6Br6 ] is suggested to also be present. (PPh3)2Ir(H...
Expand abstract - Publication status:
- Published
- Publisher copy:
- 10.1021/om034177o
-
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- Journal:
- ORGANOMETALLICS
- Volume:
- 23
- Issue:
- 3
- Pages:
- 428-432
- Publication date:
- 2004-02-02
- DOI:
- EISSN:
-
1520-6041
- ISSN:
-
0276-7333
- URN:
-
uuid:1304df12-b6d0-435a-baad-419f9ed10795
- Source identifiers:
-
51706
- Local pid:
- pubs:51706
- Copyright date:
- 2004
Journal article
Cationic iridium phosphines partnered with [closo-CB11H6Br6](_): (PPh3)(2)Ir(H)(2)(closo-CB11H6Br6) and [(PPh3)(2)Ir(eta(2)-C2H4)(3)][closo-CB11H6Br6]. Relevance to counterion effects in olefin hydrogenation
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