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Highly Efficient Synthesis of (Phosphinodihydrooxazole)(1,5-cyclooctadiene) Iridium Complexes

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2009

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Zeitschrift fur Naturforschung B: Journal of Chemical Sciences. 2009, 64b(10), pp. 1147-1158

Zusammenfassung

A highly efficient one-pot procedure for the synthesis of complexes of the type [Ir(COD)(Phox)]X, where Phox is a (chiral) phosphinooxazoline ligand, X = PF6 or B[(3,5-(CF3)2C6H3)]4 (BARF), is developed. Former reported syntheses demanded the isolation of pure ligands by column chromatography, but the ligands tend to adsorb irreversibly on silica. Moreover, the chromatography has to be performed with careful exclusion of air. The present method avoids this difficulties. The yields of the syntheses are comparable with those starting from the pure ligands. The method is also suitable for the preparation of complexes of the type [Rh(COD)(Phox)]BARF and [Rh(Phox)2]BARF.

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540 Chemie

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Iridium, Rhodium, Chiral Ligand, Homogeneous Catalysis, Heterocycles

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ISO 690SEMENIUCHENKO, Volodymyr, Volodymyr KHILYA, Ulrich GROTH, 2009. Highly Efficient Synthesis of (Phosphinodihydrooxazole)(1,5-cyclooctadiene) Iridium Complexes. In: Zeitschrift fur Naturforschung B: Journal of Chemical Sciences. 2009, 64b(10), pp. 1147-1158
BibTex
@article{Semeniuchenko2009Highl-1033,
  year={2009},
  title={Highly Efficient Synthesis of (Phosphinodihydrooxazole)(1,5-cyclooctadiene) Iridium Complexes},
  number={10},
  volume={64b},
  journal={Zeitschrift fur Naturforschung B: Journal of Chemical Sciences},
  pages={1147--1158},
  author={Semeniuchenko, Volodymyr and Khilya, Volodymyr and Groth, Ulrich}
}
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    <dcterms:abstract xml:lang="eng">A highly efficient one-pot procedure for the synthesis of complexes of the type [Ir(COD)(Phox)]X, where Phox is a (chiral) phosphinooxazoline ligand, X = PF6 or B[(3,5-(CF3)2C6H3)]4 (BARF), is developed. Former reported syntheses demanded the isolation of pure ligands by column chromatography, but the ligands tend to adsorb irreversibly on silica. Moreover, the chromatography has to be performed with careful exclusion of air. The present method avoids this difficulties. The yields of the syntheses are comparable with those starting from the pure ligands. The method is also suitable for the preparation of complexes of the type [Rh(COD)(Phox)]BARF and [Rh(Phox)2]BARF.</dcterms:abstract>
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