کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1338612 | 979672 | 2013 | 8 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Dioxomolybdenum(VI) complexes with linear and tripodal tetradenate ligands: Synthesis, structures and their use as olefin epoxidation catalysts Dioxomolybdenum(VI) complexes with linear and tripodal tetradenate ligands: Synthesis, structures and their use as olefin epoxidation catalysts](/preview/png/1338612.png)
A series of linear and tripodal tetradentate ligands containing an amine-bis(phenolate) core were synthesized by Mannich condensations. Treatment of these ligands with MoO2(acac)2 (acac = acetylacetonate) in dichloromethane and methanol at room temperature gave the corresponding cis-dioxomolybdenum(VI) complexes in good yields. All these complexes were characterized by a wide range of spectroscopic methods (NMR, IR, and UV–Vis) and elemental analysis. The molecular structures of complexes MoO2(Ln) (n = 1–3, 5) were confirmed by single-crystal X-ray diffraction analysis. The catalytic activities of all complexes towards the epoxidation of styrene by tert-butyl hydroperoxide have also been investigated.
Several dioxomolybdenum(VI) complexes with linear and tripodal tetradentate amine-bis(phenolate) ligands were synthesized in good yields. Their X-ray structures show cis-dioxo distorted octahedral geometry. The catalytic activities of these complexes towards the epoxidation of styrene by tert-butyl hydroperoxide have been investigated.Figure optionsDownload as PowerPoint slideHighlights
► Several linear and tripodal tetradentate amine-bis(phenolate) ligands were synthesized.
► Dioxomolybdenum(VI) complexes with above ligands were prepared in good yields.
► All these complexes were characterized by NMR, IR, UV–Vis, and elemental analysis.
► X-ray structures of these complexes show cis-dioxo distorted octahedral geometry.
► All these complexes were evaluated as catalysts for the epoxidation of styrene.
Journal: Polyhedron - Volume 49, Issue 1, 25 January 2013, Pages 244–251