In chemistry, ligand theory is one among numerous theories that describe the electronic structure of coordination or complex compounds, particularly transition metal complexes, which have a core metal atom surrounded by electron-rich atoms or molecules referred to as ligands. The ligand theory investigates the origins and effects of metal–ligand interactions to know their magnetic, optical, and chemical properties.
Unidentate or monodentate ligand
The term “monodentate” means “one tooth,” pertaining to the very fact that the ligand binds to the centre with just one atom. Chloride ions (referred to as chloro when it’s a ligand), water (referred to as aqua when it’s a ligand), hydroxide ions (referred to as hydroxo when it’s a ligand), and ammonia are all instances of monodentate ligands (referred to as ammine when it’s a ligand).
Ligands
To produce the complex ion, each ligand only forms one bond with the centre metal ion. Unidentate ligands are described intrinsically . That basically implies it’s just one tooth! It can only attach to the metal with one pair of electrons; the other lone pairs are pointing within the incorrect direction. Some ligands, on the opposite hand, have tons more teeth! These ligands are mentioned as multidentate or polydentate ligands, however there are several different forms.
Identification of a unidentate ligand as compared to bidentate, polydentate, and chelating ligands
The number of locations at which ligands are linked to, or bonded to, the metal centre is the commonest means of classifying them. The denticity is that this . Monodentate ligands have just one possible donor atom. A polydentate ligand is one that has bonds from two or more donor atoms to a central metal ion. Ambidentate ligands are people who have quite one potential donor atom, like the thiocyanate ion, NCS-, which may bind to the metal centre with either the nitrogen or the sulphur atoms. Chelating ligands are polydentate ligands with the power to make a hoop around a metal atom.
Only one donor atom is employed to attach to the centre metal atom or ion during a monodentate ligand. Because they only bind to the core metal atom at one place, monodentate ligands are frequently mentioned as “one toothed.” Chloride ions (referred to as chloro when it’s a ligand), water (referred to as aqua when it’s a ligand), hydroxide ions (referred to as hydroxo when it’s a ligand), and ammonia are all instances of monodentate ligands (referred to as ammine when it’s a ligand).
Bidentate ligands feature two donor atoms, allowing them to connect to a core metal atom or ion from two different angles. Ethylenediamine (en) and therefore the oxalate ion are two samples of bidentate ligands (ox).
More than two Lewis base sites, like several lone pair donating sites utilised to attach to a core atom or ion, distinguish a polydentate ligand. A polydentate ligand is EDTA, which may be a hexadentate ligand. EDTA comprises six electron-paired donor atoms which will attach to a core metal atom or ion.
Multiple lone pair sites are going to be present during a chelating ligand, but they need to be orientated in such a way that they will interact with the metal’s d-orbitals.
Example of monodentate ligand
There are many various sorts of ligands, which are classed consistent with the amount of donor atoms they include. they will have one or more donor atoms.
Unidentate or monodentate ligands are people who have just one donor atom within the molecule (or atom or ion) which will coordinate.
A monodentate ligand has just one atom that coordinates directly with the central atom of a posh .
The core metal atoms or ions share a lone pair of electrons with ammonia. Because NH3 can only share one pair of electrons, it’s classified as a monodentate ligand.
H2O may appear to be a bidentate ligand since oxygen has two lone pairs of electrons, but it’s not because a ligand must have two donor atoms to be bidentate. As a result, water is simply a monodentate ligand.
Because ligands contain lone pairs of electrons, they’re often mentioned as Lewis bases.
Ligand theory
The structure of crystals containing a transition metal ion surrounded by nonmetallic ions is described by Ligand theory (ligands). It supported the formation of molecular orbitals involving the core metal ion’s d-orbitals and combinations of ligand atomic orbitals.
Conclusion
The design of ligands lies at the guts of recent coordination chemistry. There would be no coordination chemistry without ligands. Almost any conceivable atom, molecule, or ion can act as a ligand in some scenario, and it’s probably correct to say that nearly any conceivable atom, molecule, or ion can act as a ligand in some circumstance.