کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1325611 | 977391 | 2006 | 11 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Theoretical studies on the protonation behavior of tropone and its metal complexes Theoretical studies on the protonation behavior of tropone and its metal complexes](/preview/png/1325611.png)
Density functional theory calculations were carried out to investigate structures and stabilities of tropone and troponeiron complexes, (tropone)Fe(CO)3, (tropone)Fe(CO)2(PH3) and (tropone)Fe(PH3)3, and their protonated species. The results show that the oxygen-protonated tropone is more stable than the carbon-protonated tropone. On the contrary, in the troponeiron complexes, the carbon protonated species are more stable than the oxygen protonated species. In the neutral and oxygen-protonated complexes, the tropone and oxygen-protonated tropone ligands are η4-coordinated. In the carbon-protonated complexes, the carbon-protonated tropone ligand is η5-coordinated. The results also show that the metal shift for complexes containing phosphine ligands is more difficult than that for those containing carbonyl ligands. For the neutral methyl-substituted troponeiron complexes, steric effect was found to play a key role in determining the relative stability of the regioisomers. For their protonated species, the electron-donating properties of the methyl substituent(s) were found to be important in determining the relative stability among the different regioiosmers.
Structures and stabilities of tropone and troponeiron complexes, (tropone)Fe(CO)3, (tropone)Fe(CO)2(PH3) and (tropone)Fe(PH3)3, and their protonated species have been theoretically investigated. While the oxygen-protonated tropone is more stable than the carbon-protonated tropone, on the contrary, the carbon-protonated species of the troponeiron complexes are more stable than the oxygen-protonated species.Figure optionsDownload as PowerPoint slide
Journal: Journal of Organometallic Chemistry - Volume 691, Issue 21, 15 October 2006, Pages 4545–4555