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Ethylenediamine ligand chelating to a metal with two bonds Cu 2+ complexes with nonchelating methylamine (left) and chelating ethylenediamine (right) ligands. The chelate effect is the greater affinity of chelating ligands for a metal ion than that of similar nonchelating (monodentate) ligands for the same metal.
In coordination chemistry, the bite angle is the angle on a central atom between two bonds to a bidentate ligand. This ligand–metal–ligand geometric parameter is used to classify chelating ligands, including those in organometallic complexes.
In coordination chemistry, clathrochelates are ligands that encapsulate metal ions. Chelating ligands bind to metals more strongly than related monodentate ligands, and macrocyclic ligands bind more strongly than typical chelating ligands. It follows that bi- or polymacrocyclic ligands would bind to metals particularly strongly.
Ligands that bind via more than one atom are often termed chelating. A ligand that binds through two sites is classified as bidentate, and three sites as tridentate. The "bite angle" refers to the angle between the two bonds of a bidentate chelate. Chelating ligands are commonly formed by linking donor groups via organic linkers.
The complex involved bidentate chelating ligands attached to the iron atoms in the Fe–N–N–Fe core, in which N 2 acts as a bridging ligand between two iron atoms. Increasing the coordination number of iron by modifying the chelating ligands and adding another ligand per iron atom showed an increase in the strength of the N–N bond in the ...
In chemistry, a transition metal pincer complex is a type of coordination complex with a pincer ligand. Pincer ligands are chelating agents that binds tightly to three adjacent coplanar sites in a meridional configuration. [1] [2] The inflexibility of the pincer-metal interaction confers high thermal stability to the resulting complexes.
Transition metal oxalate complexes are coordination complexes with oxalate (C 2 O 4 2−) ligands. Some are useful commercially, but the topic has attracted regular scholarly scrutiny. Oxalate (C 2 O 4 2-) is a kind of dicarboxylate ligand. [1] As a small, symmetrical dinegative ion, oxalate commonly forms five-membered MO 2 C 2 chelate rings.
Like most amino acid complexes, the glycinate forms a 5-membered chelate ring, with the glycinato ligand serving as a bidentate (κ 2 Ο,Ν) species. [2] [5] The chelating ligands assume a square planar configuration around the copper atom as is common for tetracoordinate d 9 complexes, calculated to be much lower in energy than the alternative tetrahedral arrangement.