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| Content Provider | Royal Society of Chemistry (RSC) |
|---|---|
| Author | Yuan, Dan Wang, Yaorong Xu, Ya Yao, Yingming |
| Copyright Year | 2017 |
| Abstract | Different aluminum complexes were synthesized by the reaction of aluminum alkyls with a hexadentate salen-type Schiff base. The reaction of N,N′-bis(3,5-di-tert-butylsalicylidene)-2,2′-(ethylenedioxy)dianiline (LH2) with one equiv. of AlMe3 in toluene at 100 °C proceeded by methane elimination to produce the intermediate methyl complex [AlMeL] (1), and then subsequent intramolecular methyl migration to give the aluminum complex [AlL′] (2) [L′ = (2-O-3,5-tBu2C6H2)CHNC6H4OCH2CH2OC6H4NCH(Me)(2′-O-3′,5′-tBu2C6H2)]. The reaction of the same ligand with AlEt3 under the same experimental conditions involved ethane elimination, ethylene elimination and intramolecular hydrogen migration, and led to the complex [AlL′′] (3) [L′′ = (2-O-3,5-tBu2C6H2)CHNC6H4OCH2CH2OC6H4NCH2(2′-O-3′,5′-tBu2C6H2)]. However, the interaction of two equivalents of AlMe3 and AlEt3 afforded the corresponding binuclear complexes [(AlMe2)2L] (4) and [(AlEt2)2L] (5), respectively, and no methyl or hydrogen migration was found. The solid-state structures of aluminum complexes 1–3 were determined by single-crystal X-ray diffraction. It was found that complexes 2–5 show a very effective catalytic activity for the cycloaddition of epoxides and CO2 in the presence of NBu4Br as a cocatalyst at atmospheric pressure. |
| Starting Page | 5848 |
| Ending Page | 5855 |
| Page Count | 8 |
| File Format | HTM / HTML PDF |
| ISSN | 14779226 |
| Volume Number | 46 |
| Issue Number | 18 |
| Journal | Dalton Transactions |
| DOI | 10.1039/c7dt00789b |
| Language | English |
| Publisher | Royal Society of Chemistry |
| Access Restriction | Open |
| Subject Keyword | Schiff LH2 Schiff base Liquid hydrogen Toluene Methane Rearrangement reaction Ligand Ethylene X-ray crystallography Cycloaddition Atmospheric pressure |
| Content Type | Text |
| Resource Type | Article |
| Subject | Inorganic Chemistry |
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