Loading...
|
Please use this identifier to cite or link to this item:
http://ir.ncue.edu.tw/ir/handle/987654321/10107
|
| Title: | Reactions of Dimeric Aluminium Hydride Compounds Containing Bidentate Dianionic Pyrrolyl Ligands and Their Applications in Ring-Opening Polymerization of ε-Caprolactone |
| Authors: | Chen, Ya-Chi;Lin, Che-Yu;Huang, Wen-Yen;Datta, Amitabha;Huang, Jui-Hsien;Tsai, Meng-Shiue;Lee, Ting-Yu;Tu, Cheng-Yi;Hu;Ching-Han |
| Contributors: | 化學系 |
| Keywords: | Aluminium;Hydrides;N ligands;Ring-opening polymerization |
| Date: | 2011-05
|
| Issue Date: | 2012-05-03T06:18:33Z
|
| Publisher: | John Wiley & Sons, Inc. |
| Abstract: | A series of dimeric aluminium compounds containing substituted bidentate dianionic pyrrolyl ligands have been synthesized and their reactivity and application in the ring-opening polymerization of ϵ-caprolactone have been studied. The reactions of [{C4H3N(2-CH2NtBu)}AlH]2 (1) with 2 equiv. of 1-indanone and 9-fluorenone in dichloromethane generated [{C4H3N(2-CH2NtBu)}Al(μ-OC9H9)]2 (2) and [{C4H3N(2-CH2NtBu)}Al{μ-OCH(C12H8)}]2 (3), respectively, by hydroalumination. Similarly, the reactions of 1 with 2 equiv. of 2-cyclohexen-1-one, 1-(2,4,6-trimethylphenyl)-1-ethanone, benzophenone, and 1,1-diphenylacetone in dichloromethane afforded NtBu-bridged dialuminium compounds 4–7, [{C4H3N(2-CH2NtBu)}Al(OR)]2 [4, R = C6H9; 5, R = CH(Me)(C6H2-2,4,6-Me3); 6, R = CHPh2; 7, R = CH(Me)(CHPh2)] by insertion. A similar insertion occurred when 1 was treated with 2 equiv. of 2,4-pentandione and dibenzoylmethane in dichloromethane to yield NtBu-bridged dioxylate aluminium dimeric compounds 8 and 9, respectively. The Al atoms in compounds 2 and 4–7 possess a distorted tetrahedral geometry whereas the Al atoms in 8 and 9 have a square-pyramidal environment. All the compounds have been well characterized by NMR spectroscopy and compounds 2 and 4–9 in the solid state were subjected to X-ray diffraction analysis. A study of the polymerization of ϵ-caprolactone revealed that the activity of the Al complexes is largely reliant on the steric nature of the substituents of their alkoxide groups. |
| Relation: | Eur. J. Inorg. Chem., 2011(15): 2459-2469 |
| Appears in Collections: | [化學系] 期刊論文
|
Files in This Item:
| File |
Size | Format | |
|---|
| index.html | 0Kb | HTML | 814 | View/Open |
|
All items in NCUEIR are protected by copyright, with all rights reserved.
|
