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| Content Provider | Royal Society of Chemistry (RSC) |
|---|---|
| Author | Lu, Chengrong Ding, Hao Yao, Yingming Gong, Chao Zhao, Bei |
| Copyright Year | 2017 |
| Abstract | A divalent ytterbium amidate 1 ([Yb3L6]·2C7H8 for short) was synthesized via amine-elimination of Yb[N(SiMe3)2]2(TMEDA) with an amide proligand N-2,6-diisopropylphenylbenzamide HL (L = 2,6-iPr2C6H3NC(O)Ph) and structurally characterized to be a trinuclear symmetric cluster. Further studies on the reduction of iPrNCNiPr by complex 1 provide Yb(III) complex 2 in hexane–THF ([(YbL2)2(μ-NiPrCNiPr)][YbL3(THF)]·C7H8), which is composed of two subunits in a unit cell, one is a bridged Yb(III) carbene, just the same as complex 4 ([(YbL2)2(μ-NiPrCNiPr)]·3C7H8) obtained in the same reaction in toluene, and the other is a homoleptic monomeric Yb(III) amidate (YbL3). It is also found that complex 2 decomposed to complex 3 ([YbL3]2·2C7H8) and 4 at 90 °C in toluene. Complexes 1–4 were confirmed by X-ray structure determination. Furthermore, complex 4 was proved to be a more active species than its precursor 1 in the catalytic addition of amines to carbodiimides. Finally, complex 1 was found to be an excellent pre-catalyst for the guanylation reaction with a wide scope of substrates. |
| Starting Page | 6031 |
| Ending Page | 6038 |
| Page Count | 8 |
| File Format | HTM / HTML PDF |
| ISSN | 14779226 |
| Volume Number | 46 |
| Issue Number | 18 |
| Journal | Dalton Transactions |
| DOI | 10.1039/c7dt00871f |
| Language | English |
| Publisher | Royal Society of Chemistry |
| Access Restriction | Open |
| Subject Keyword | Ytterbium Tetramethylethylenediamine Amide Crystal structure Carbene Toluene Homoleptic X-ray crystallography |
| Content Type | Text |
| Resource Type | Article |
| Subject | Inorganic Chemistry |
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