| Autor: |
Boumahdi Benkmil, Anne Kraft, Anna M. T. Erle, Harald Scherer, Ingo Krossing, Ulrich Preiss, Gunther Steinfeld |
| Rok vydání: |
2013 |
| Předmět: |
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| Zdroj: |
Zeitschrift für anorganische und allgemeine Chemie. 639:714-721 |
| ISSN: |
0044-2313 |
| DOI: |
10.1002/zaac.201300027 |
| Popis: |
The synthesis, spectroscopic and structural characterisation of a series of [M(hfip)6]– (M = Nb, Ta; hfip = O–C(H)(CF3)2) salts that are the typical starting materials to introduce these weakly coordinating anions by metathesis reactions into a given system is described. The salts Li[Nb(hfip)6] and Li[Ta(hfip)6] formed in 65 to 77 % yield from freshly sublimed MCl5 and Li[hfip]. By contrast, several attempts to synthesize Li[Sb(hfip)6] on the similar route (replace NbCl5 by SbCl5) failed to yield a pure product. Upon metathesis of the Li-niobate with AgF in CH2Cl2, the pure Ag[Nb(hfip)6] formed. Mixing Li[Nb(hfip)6] with an equimolar amount of Cl–CPh3 in CH2Cl2 gave the yellow [CPh3][Nb(hfip)6]. Several of the compounds were characterized by X-ray analysis. Thus, the crystal structures of the Li+- and Ag+-solvates 1, 2-C6H4F2{LiNb(hfip)6}2, [Li(H2O)][Ta(hfip)6], and [Ag(C6H5F)][Nb(hfip)6] as well as that of [CPh3][Nb(hfip)6] were solved and are described in this work. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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