Chirality at octahedral centres determined by tetradentate Schiff base ligands
نویسندگان
چکیده
منابع مشابه
Salan ligands assembled around chiral bipyrrolidine: predetermination of chirality around octahedral Ti and Zr centres.
The first synthesis of Salan ligands assembled around the chiral 2,2'-bipyrrolidine backbone is described; as chelation to a metal can only occur via specific faces of the two pyrrolidine nitrogens, these ligands lead to predetermined chirality at metal centres of octahedral titanium and zirconium complexes.
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The kinetics of a ligand exchange in the CuL4/H2Ln system, where H2Ln is the N,N'-alkylen-bis(salicyldimine) tetradentate Schiff base ligand (n = 2 or 3, CH2 groups in the chain length of the amine backbone) was studied spectrophotometrically in DMF solvent with or without triethylamine (NEt3) and H2O at 25 ± 0.1 °C and an ionic strength of 0.01 M NaNO3. The reaction rate was found to be first-...
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Contrary to the stereotype, Jacobsen's catalyst, chiral (salcy)Co(III)OAc adopts an unusual binding mode. The tetradentate {ONNO} ligand does not form a square plane but wraps cobalt in a cis-β fashion while acetate is chelating.
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The aim of the present study is to synthesize the oxovanadium complex of the V3+ ion with isatin sciff bases. Spectroscopic methods have been used to confirm these models of complexation and to understand the structures of the species formed in methanolic solution. We also have isolated a complex of Vanadium (III) with isatin schiff bases in the solid phase.
متن کاملBidentate Isatin Schiff Base Ligands Oxovanadium (IV) Complexes
The aim of the present study is to synthesize the oxovanadium complex of the V3+ ion with isatin sciff bases. Spectroscopic methods have been used to confirm these models of complexation and to understand the structures of the species formed in methanolic solution. We also have isolated a complex of Vanadium (III) with isatin schiff bases in the solid phase.
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ژورنال
عنوان ژورنال: Comptes Rendus Chimie
سال: 2015
ISSN: 1631-0748
DOI: 10.1016/j.crci.2014.06.002