Non-innocent ligand

In chemistry, a (redox) non-innocent ligand is a ligand in a metal complex where the oxidation state is not clear. Typically, complexes containing non-innocent ligands are redox active at mild potentials. The concept assumes that redox reactions in metal complexes are either metal or ligand localized, which is a simplification, albeit a useful one. Redox non-innocent ligands have been intensively investigated spectroscopically. Redox non-innocent ligands play a crucial role in the mechanism of catalytic processes mediated by several metalloenzymes, including galactose oxidase and cytochrome P450. In chemistry, a (redox) non-innocent ligand is a ligand in a metal complex where the oxidation state is not clear. Typically, complexes containing non-innocent ligands are redox active at mild potentials. The concept assumes that redox reactions in metal complexes are either metal or ligand localized, which is a simplification, albeit a useful one. Redox non-innocent ligands have been intensively investigated spectroscopically. Redox non-innocent ligands play a crucial role in the mechanism of catalytic processes mediated by several metalloenzymes, including galactose oxidase and cytochrome P450. C.K. Jørgensen first described ligands as 'innocent' and 'suspect': 'Ligands are innocent when they allow oxidation states of the central atoms to be defined. The simplest case of a suspect ligand is NO...' Conventionally, redox reactions of coordination complexes are assumed to be metal-centered. The reduction of MnO4− to MnO42− is described by the change in oxidation state of manganese from 7+ to 6+. The oxide ligands do not change in oxidation state, remaining 2- (a more careful examination of the electronic structure of the redox partners reveals however that the oxide ligands are affected by the redox change). Oxide is an innocent ligand. Another example of conventional metal-centered redox couple is3+/2+. Ammonia is innocent in this transformation. Redox non-innocent behavior of ligands is illustrated by z, which exists in three oxidation states: z = 2-, 1-, and 0. If the ligands are always considered to be dianionic (as is done in formal oxidation state counting), then z = 0 requires that that nickel has a formal oxidation state of +IV. The formal oxidation state of the central nickel atom therefore ranges from +II to +IV in the above transformations (see Figure). However, the formal oxidation state is different from the real (spectroscopic) oxidation state based on the (spectroscopic) metal d-electron configuration. The stilbene-1,2-dithiolate behaves as a redox non-innocent ligand, and the oxidation processes actually take place at the ligands rather than the metal. This leads to the formation of ligand radical complexes. The charge-neutral complex (z =0) is therefore best described as a Ni2+ derivative of S2C2Ph2−. The diamagnetism of this complex arises from anti-ferromagnetic coupling between the unpaired electrons of the two ligand radicals. Ligands with extended pi-delocalization such as porphyrins, phthalocyanines, and corroles and ligands with the generalised formulas n− (D = O, S, NR’ and R, R' = alkyl or aryl) are often non-innocent. In contrast, − such as NacNac or acac are innocent. In certain enzymatic processes, redox non-innocent cofactors provide redox equivalents to complement the redox properties of metalloenzymes. Of course, most redox reactions in nature involve innocent systems, e.g. clusters. Porphyrin ligands can be innocent (2-) or noninnocent (1-). In the enzymes chloroperoxidase and cytochrome P450, the porphyrin ligand sustains oxidation during the catalytic cycle, notably in the formation of Compound I. In other heme proteins, such as myoglobin, ligand-centered redox does not occur and the porphyrin is innocent. The catalytic cycle of galactose oxidase (GOase) illustrates the involvement of non-innocent ligands. GOase oxidizes primary alcohols into aldehydes using O2 and releasing H2O2. The active site of the enzyme GOase features a tyrosyl coordinated to a CuII ion. In the key steps of the catalytic cycle, a cooperative Brønsted-basic ligand-site deprotonates the alcohol, and subsequently the oxygen atom of the tyrosinyl radical abstracts a hydrogen atom from the alpha-CH functionality of the coordinated alkoxide substrate. The tyrosinyl radical participates in the catalytic cycle: 1e-oxidation is effected by the Cu(II/I) couple and the 1e oxidation is effected by the tyrosyl radical, giving an overall 2e change. The radical abstraction is fast. Anti-ferromagnetic coupling between the unpaired spins of the tyrosine radical ligand and the d9 CuII center gives rise to the diamagnetic ground state, consistent with synthetic models.