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Tridentate facially chelating ligands

A.N. Vedernikov and co-workers designed and synthesized tridentate facially chelating ligands of the [2.n.1]-(2,6)-pyridinophane family. The key step in their synthesis of these tripyridine macrocycles was a double Chichibabin-type condensation of 1,2-b/s(2-pyridyl)ethanes with lithiated 2,6-dimethylpyridines. [Pg.81]

In the 2D polymer [Cd3(IDA)3(H20)]-3H20 n [138] the iminodiacetate dianions behave as tridentate chelating ligands and show both facial and meridional... [Pg.181]

See other pages where Tridentate facially chelating ligands is mentioned: [Pg.341]    [Pg.361]    [Pg.32]    [Pg.311]    [Pg.323]    [Pg.69]    [Pg.345]    [Pg.326]    [Pg.571]    [Pg.321]    [Pg.892]    [Pg.129]    [Pg.370]    [Pg.129]    [Pg.447]    [Pg.305]    [Pg.10]    [Pg.282]    [Pg.129]    [Pg.447]    [Pg.230]    [Pg.356]    [Pg.789]    [Pg.6592]    [Pg.34]   
See also in sourсe #XX -- [ Pg.81 ]



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Chelate ligands

Chelated ligand

Chelating tridentate

Chelators tridentate

Facial

Facial ligand

Ligands chelation

Tridentate

Tridentate ligand

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