Synthesis and solution structure of desoxotungsten(IV) and monooxotungsten(VI) benzenedithiolate complexes containing two intramolecular NH⋯S hydrogen bonds
| Autor: | Kiyotaka Onitsuka, Yui Omi, Taka-aki Okamura |
|---|---|
| Rok vydání: | 2017 |
| Předmět: |
Silylation
010405 organic chemistry Hydrogen bond Chemistry Stereochemistry Bailar twist 010402 general chemistry 01 natural sciences 0104 chemical sciences Inorganic Chemistry Crystallography Intramolecular force Materials Chemistry Proton NMR Molecule Physical and Theoretical Chemistry Enantiomer Cis–trans isomerism |
| Zdroj: | Inorganica Chimica Acta. 467:379-384 |
| ISSN: | 0020-1693 |
| DOI: | 10.1016/j.ica.2017.08.036 |
| Popis: | Desoxotungsten(IV) and monooxotungsten(VI) benzenedithiolate complexes containing two intramolecular NH⋯S hydrogen bonds, (NEt4)[WIV{OSi(tBu)Ph2}(1,2-S2-3-tBuCONHC6H3)2] (1) and (NEt4)[WVIO{OSi(tBu)Ph2}(1,2-S2-3-tBuCONHC6H3)2] (2), were synthesized by silylation of the parent mono- and di-oxo compounds. The geometrical isomers, trans- and cis-1, were present at room temperature without any interconversion. 1H NMR spectra of 2 showed only one set of signals at room temperature, which were separated into two sets of distinct signals upon cooling down to lower temperatures. These results suggest that only one pair of enantiomers is present in solution, which are exchanged rapidly in the NMR time scale via Bailar twist at room temperature. Subsequent structural analysis demonstrates that the isomer is 2tc, where, one NH⋯S hydrogen bond is trans to the terminal W O and the other is cis to W O. Theoretical calculations revealed the contribution of the hydrogen bond to the molecular structure and indicate that 2tc is the most stable isomer. |
| Databáze: | OpenAIRE |
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