Abstract
The tricobalt enneacarbonyl-ethynylestradiol derivative Co3(CO)9C-C≢C-E (E=estradiol) proved to be elusive, due to the strong electron-withdrawing properties of both the 17β OH and the Co3(CO)9C groups. However, the advantage of introducing the Co3C core, which undergoes a reversible 1 e reduction, can be achieved by the interposition of a spacer arm, namely -C(O)NHC6H4-, generated in situ during the synthesis in the appropriate experimental conditions. The corresponding bioorganometallic product Co3(CO)9C-C(O)NHC6H4-C≢;C-E retains an acceptable relative binding affinity for estradiol receptor affording a new electrochemical marker suitable for biochemical analyses.
| Lingua originale | Inglese |
|---|---|
| pagine (da-a) | 232-239 |
| Numero di pagine | 8 |
| Rivista | Journal of Organometallic Chemistry |
| Volume | 593-594 |
| DOI | |
| Stato di pubblicazione | Pubblicato - 15 gen 2000 |
| Pubblicato esternamente | Sì |
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