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A Biomimetic System for Studying Salicylate Dioxygenase.

ABSTRACT: We report the characterization of [Fe(T1Et4iPrIP)(sal)] (2) (T1Et4iPrIP = tris(1-ethyl-4-isopropyl-imidazolyl)phosphine; sal^2- = salicylate dianion), which serves as a model for substrate-bound salicylate dioxygenase (SDO). Complex 2 crystallizes in the monoclinic space group P2₁/n with a = 10.7853(12) Å, b = 16.5060(19) Å, c = 21.217(2) Å, β = 94.489(2)°, and V = 3765.5(7) Å³. The structure consists of Fe^II bonded in distorted square pyramidal geometry (τ = 0.32) with two salicylate oxygens and two T1Et4iPrIP nitrogens serving as the base and the apical position occupied by the other ligand nitrogen. [Fe(T1Et4iPrIP)(OTf)₂] (1), the precursor for 2, catalyzes the cleavage of 1,4-dihydroxy-2-naphthoate in the presence of O₂. Complex 1 is also capable of cleaving the salicylate aromatic ring in the presence of H₂O₂. The progression of this reaction toward product formation involves an Fe^III-phenoxide species.

SUBMITTER: Banerjee A

PROVIDER: S-EPMC8101989 | biostudies-literature | 2019 Jan

REPOSITORIES: biostudies-literature

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A Biomimetic System for Studying Salicylate Dioxygenase.

Banerjee Atanu A Li Jia J Molenda Monika A MA Brennessel William W WW Chavez Ferman A FA

ACS symposium series. American Chemical Society 20190101 4

We report the characterization of [Fe(T1Et4iPrIP)(sal)] (2) (T1Et4iPrIP = tris(1-ethyl-4-isopropyl-imidazolyl)phosphine; sal2- = salicylate dianion), which serves as a model for substrate-bound salicylate dioxygenase (SDO). Complex 2 crystallizes in the monoclinic space group P21/n with a = 10.7853(12) Å, b = 16.5060(19) Å, c = 21.217(2) Å, β = 94.489(2)°, and V = 3765.5(7) Å3. The structure consists of Fe<s ...[more]

PMID: 33967356

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