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Cubane-like tetranuclear Cu(II) complexes bearing a Cu4O4 core: crystal structure, magnetic properties, DFT calculations and phenoxazinone synthase like activity

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TLDR
Two new copper complexes 3a and 3b with a Cu4O4 cubane core are reported, and the first analysis of single crystal X-ray diffraction studies reveals that both molecules possess a [4 + 2] cubane-type core, and low temperature magnetic measurements show antiferromagnetic behaviour, in agreement with DFT calculations.
Abstract
In the present work, two new copper complexes 3a and 3b with a Cu4O4 cubane core are reported. Both complexes are obtained by means of the in situ conversion of the imine functionality of Schiff's base ligands 1a [(E)-4-chloro-2-((thiazol-2-ylimino)methyl)phenol] and 1b [(E)-4-bromo-2-((thiazol-2-ylimino)methyl)phenol] into amino alcohols 2a (4-chloro-2-(hydroxy(thiazol-2-ylamino)methyl)phenol) and 2b (4-bromo-2-(hydroxy(thiazol-2-ylamino)methyl)phenol), respectively. The ligand transformation may be metal assisted and the generated ligands show an interesting mode of coordination in which the alkoxo-O atom binds in a μ3-manner connecting simultaneously three copper centers and forming a Cu4O4 cubane core. The first analysis of single crystal X-ray diffraction studies reveals that both molecules possess a [4 + 2] cubane-type core, and low temperature magnetic measurements show antiferromagnetic behaviour, in agreement with DFT calculations. However, the best fit and DFT calculations point out three pairs of coupling constants, more coherent with a [2 + 2 + 2] situation, in accordance with the fine analysis of structural data. Finally, phenoxazinone synthase activity has been measured for both molecules, finding kcat = 86.3 h−1 for the chloride derivative copper(II) complex in methanol, whereas the bromide derivative copper(II) complex displays kcat = 3.4026 × 102 h−1 and 10.289 × 102 h−1 in methanol and DMSO, respectively.

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Citations
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Subtle Structural Changes in (CuIIL)2MnII Complexes To Induce Heterometallic Cooperative Catalytic Oxidase Activities on Phenolic Substrates (H2L = Salen Type Unsymmetrical Schiff Base).

TL;DR: The mechanisms of these biomimetic oxidase reactions are proposed for the first time involving any heterometallic catalyst on the basis of mass spectral analysis, EPR spectroscopy, and cyclic voltammetry.
Journal ArticleDOI

X-ray characterization, spectroscopic, DFT calculations and Hirshfeld surface analysis of two 3-D supramolecular mononuclear zinc(II) and trinuclear copper(II) complexes

TL;DR: In this article, two 3D mononuclear zinc and trinuclear copper complexes were synthesized via complexation of metal salts with based ligand HL1 (2-(3-bromo-5-chloro-2-hydroxyphenyl)-4-methyl-1,2-dihydroquinazoline 3-oxide, H is the deprotonatable hydrogen) originally.
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Antimicrobial activities of self-assembled copper(II), nickel(II), and cobalt(III) complexes combined with crystallographic, spectroscopic, DFT calculations and Hirshfeld surfaces analyses

TL;DR: The quinazoline-type ligand 2-(4methoxy-2-hydroxyphenyl)-4-methyl-1,2-dihydroquinazolin 3-oxide (HL1, H is the deprotonatable hydrogen) was synthesized as discussed by the authors.
Journal ArticleDOI

Ni(II) Complex of N2O3 Donor Unsymmetrical Ligand and Its Use for the Synthesis of NiII–MnII Complexes of Diverse Nuclearity: Structures, Magnetic Properties, and Catalytic Oxidase Activities

TL;DR: The mass spectral analyses suggest the probable intermediate formation and cyclic voltammetry measurement suggest the reduction of Ni(II) to Ni(I) during catalytic reaction.
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Mixed azido/phenoxido bridged trinuclear Cu(II) complexes of Mannich bases: Synthesis, structures, magnetic properties and catalytic oxidase activities

TL;DR: These are the first trinuclear Cu(ii) complexes of this type of Mannich base ligands and exhibited catecholase- like and phenoxazinone synthase-like activities towards the aerobic oxidation of 3,5-di-tert-butylcatechol and o-aminophenol, respectively.
References
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