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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]
In the covalent bond classification method, κ 1-carbonate is anX ligand and κ 2-carbonate is an X 2 ligand. With two metals, the number of bonding modes increases because carbonate often serves as a bridging ligand. It can span metal-metal bonds as in [Ru 2 (CO 3) 4 Cl 2] 5-, where again it functions as an (X) 2 ligand.
Complexes of phen and those of 2,2'-bipyridine (bipyr) are similar: the metal-ligand ensemble is planar, which facilitates electron delocalization. As a consequence of this delocalization, phen complexes often exhibit distinctive optical and redox properties.
Many rules in chemistry rely on electron-counting: Octet rule is used with Lewis structures for main group elements, especially the lighter ones such as carbon, nitrogen, and oxygen, 18-electron rule [2] in inorganic chemistry and organometallic chemistry of transition metals, Hückel's rule for the π-electrons of aromatic compounds,
In chemistry, pi backbonding or π backbonding is a π-bonding interaction between a filled (or half filled) orbital of a transition metal atom and a vacant orbital on an adjacent ion or molecule. [1] [2] In this type of interaction, electrons from the metal are used to bond to the ligand, which dissipates excess negative charge and
Prussian blue is intensely blue owing to an intervalence charge transfer band. Intervalence charge transfer (IVCT) is a type of charge-transfer band that is associated with mixed-valence compounds. Unlike the usual MLCT or LMCT bands, the IVCT bands are lower in energy, usually in the visible or near-infrared region of the spectrum and is broad ...
This gives the ligand a higher force constant. The resultant force constant found for a ligated carbonyl represents the same force constant for π ligands if they replaced the CO ligand in the same complex. Nucleophilic addition does not occur if kCO* (the effective force constant for the CO ligand) is below a threshold value [2]
In inorganic chemistry, the cis effect is defined as the labilization (or destabilization) of CO ligands that are cis to other ligands. CO is a well-known strong pi-accepting ligand in organometallic chemistry that will labilize in the cis position when adjacent to ligands due to steric and electronic effects.