Search results
Results From The WOW.Com Content Network
The term is mainly used in coordination chemistry. The template effects emphasizes the pre-organization provided by the coordination sphere, although the coordination modifies the electronic properties (acidity, electrophilicity, etc.) of ligands. [1] An early example is the dialkylation of a nickel dithiolate: [2]
In coordination chemistry, a coordinate covalent bond, [1] also known as a dative bond, [2] dipolar bond, [1] or coordinate bond [3] is a kind of two-center, two-electron covalent bond in which the two electrons derive from the same atom. The bonding of metal ions to ligands involves this kind of interaction. [4]
In coordination chemistry, a macrocyclic ligand is a macrocyclic ring having at least nine atoms (including all hetero atoms) and three or more donor sites that serve as ligands. [1] Crown ethers and porphyrins are prominent examples. Macrocyclic ligands often exhibit high affinity for metal ions, the macrocyclic effect.
Template: Periodic table (electron configuration) 5 languages. ... Download as PDF; Printable version; In other projects Wikidata item; Appearance. move to sidebar hide
Most are anions. Cyanide is a highly basic and small ligand, hence it readily saturates the coordination sphere of metal ions. The resulting cyanometallate anions are often used as building blocks for more complex structures called coordination polymers, the best known example of which is Prussian blue, a common dyestuff. [2]
Another example is [Co(H 2 O) 6] 2+. [14] Note that the ligand is the same as the last example. Here the cobalt ion has the oxidation state of +2, and it is a d 7 ion. From the high-spin (left) side of the d 7 Tanabe–Sugano diagram, the ground state is 4 T 1 (F), and the spin multiplicity is a quartet.
For simple carboxylates, the acetate complexes are illustrative. Most transition metal acetates are mixed ligand complexes. One common example is hydrated nickel acetate, Ni(O 2 CCH 3) 2 (H 2 O) 4, which features intramolecular hydrogen-bonding between the uncoordinated oxygens and the protons of aquo ligands. Stoichiometrically simple ...
This template for writing a metal complex also allows for a better comparison of molecules with different charges. This can happen when the assignment is reduced to its “equivalent neutral class". The equivalent neutral class is the classification of the complex if the charge was localized on the ligand as opposed to the metal center. [1]