Abstract
The complexes [Ru{(Z)-HCCHPh}(CO)2(η5-C 5Ph5)] (1) and [Ru{(Z)-HCCHC6H 4NO2}(CO)2(η5-C 5Ph5)] (2) have been synthesized and their identity confirmed by single-crystal X-ray diffraction studies. Reaction of 2 with PMe2Ph and Me3NO in tetrahydrofuran afforded [Ru{(Z)-HCCHC6H4NO2}(CO)(PMe 2Ph)(η5-C5Ph5)] (3). Cyclic voltammetry confirms the expected increase in ease of oxidation on proceeding from 2 to 1 and from 2 to 3. Hyper-Rayleigh scattering studies at 1064 nm reveal a dramatic increase in quadratic non-linearity on co-ligand replacement of CO by PMe2Ph, in proceeding from 2 to 3. Z-scan studies at 800 nm are consistent with significant contribution from two-photon states, and with an increase in γreal on co-ligand replacement of CO by PMe 2Ph in proceeding from 2 to 3.
| Original language | English |
|---|---|
| Pages (from-to) | 1663-1672 |
| Number of pages | 10 |
| Journal | Inorganica Chimica Acta |
| Volume | 358 |
| Issue number | 5 SPEC. ISS. |
| DOIs | |
| Publication status | Published - 15 Mar 2005 |
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