Abstract
The solid state structure of (cyclohexadiene)Fe(CO)2P(o-tolyl)3 reveals an exo2 conformation for the phosphine. In solution, arene ring exchange in the phosphine and exchange of phosphine between equivalent basal positions of the square pyramid occur at equal rates. In solution, (cycloheptadiene)Fe(CO)2(+)-PPh2(neomenthyl) exhibits a diastereoselection between basal isomers, and crystallizes as a single diastereoisomer which has been structurally characterized.
| Original language | English (Ireland) |
|---|---|
| Number of pages | 18 |
| Journal | Journal Of Organometallic Chemistry |
| Volume | 413 |
| Publication status | Published - 1 Aug 1991 |
Authors (Note for portal: view the doc link for the full list of authors)
- Authors
- HOWELL, JAS,PALIN, MG,TIRVENGADUM, MC,CUNNINGHAM, D,MCARDLE, P,GOLDSCHMIDT, Z,GOTTLIEB, HE
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Dive into the research topics of 'EVIDENCE FOR CORRELATED ROTATION AND DIASTEREOISOMER DISCRIMINATION IN (ETA-4-DIENE)FE(CO)2L COMPLEXES - THE CRYSTAL AND SOLUTION STRUCTURES OF (CYCLOHEXADIENE)FE(CO)2P(ORTHO-TOLYL)3 AND (CYCLOHEPTADIENE)FE(CO)2(+)-PPH2(NEOMENTHYL)'. Together they form a unique fingerprint.Cite this
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