Repozytorium

On rhodium complexes bearing H-spirophosphorane derived ligands : Synthesis, structural and catalytic properties.

Autorzy

Anna Skarżyńska

Ewa Mieczyńska

Miłosz Siczek

Rok wydania

2013

Czasopismo

Journal of Organometallic Chemistry

Numer woluminu

743

Strony

179-186

DOI

10.1016/j.jorganchem.2013.06.020

Kolekcja

Naukowa

Język

Angielski

Typ publikacji

Artykuł

Streszczenie

We investigated the coordination properties of H-spirophosphoranes towards rhodium ion. Symmetrical phosphorus ligands: HP(OCH2CH2NH)2 L1, HP(OCH2CMe2NH)2 L2, HP(OCMe2CMe2O)2 L3, HP(OC6H4NH)2 L4, and unsymmetrical phosphorus ligands: HP(OCMe2CMe2O)(OCH2CMe2NH) L5, HP(OCMe2CMe2O)(OC6H4NH) L6 were found to coordinate to rhodium precursor [Rh(CO)2Cl]2 exclusively in protonated κ2-P,E (E = N, O) bidentate fashion, yielding complexes [Rh(CO)ClL] 16. The complexes were characterised by spectroscopic methods. The molecular structures of the ligand L6 complexes 3, 5 and 6 were determined by single-crystal X-ray diffraction. The catalytic activity of the complexes was determined in hydroformylation reaction of 1-hexene. Complexes 1 and 2 appeared to be active in isomerisation reactions yielding 76 and 62% of 2-hexene. When used with six-fold excess of triphenylphosphite P(OPh)3 as a modified ligand, the most active catalyst 1 in hydroformylation reaction produced 66% of aldehydes and 22% of 2-hexene.

Słowa kluczowe

H-spirophosphorane ligands, Phosphorus ligands, Rhodium complexes, Hydroformylation reactions, Catalysis, X-ray structure

Adres publiczny

http://dx.doi.org/10.1016/j.jorganchem.2013.06.020

Strona internetowa wydawcy

http://www.elsevier.com

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