Two New Mononuclear Mn(II) and Cu(II) Mixed-Ligand Complexes Incorporating 2,6-Di(1H-pyrazol-1-yl)pyridine and 2-Hydroxy Naphthaldehyde-Derived Schiff Base: Structural, Theoretical, and Phenoxazinone Synthase Mimicking Activity

IF 3.7 2区 化学 Q2 CHEMISTRY, APPLIED Applied Organometallic Chemistry Pub Date : 2024-08-26 DOI:10.1002/aoc.7668
Aly Abdou
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Abstract

The current investigation involved the synthesis and detailed characterization of novel mixed-ligand complexes of Mn(II) (MnDPPNPH) and Cu(II) (CuDPPNPH). These complexes incorporate 2,6-di(1H-pyrazol-1-yl)pyridine (DPP) and a Schiff base derived from 2-hydroxy naphthaldehyde (NPH). The synthesized complexes revealed a stoichiometric ratio of 1:1:1 (metal:DPP:NPH), indicative of an octahedral coordination geometry around the Mn(II) and Cu(II) centers, as represented by the chemical formula [M (DPP)(NPH)(Cl)]. To elucidate their structural and electronic properties, theoretical calculations were performed. These calculations facilitated the optimization of the geometrical structures and provided insights into the molecular orbital characteristics of the complexes. The MnDPPNPH and CuDPPNPH complexes demonstrated potential phenoxazinone synthase mimicking activity by catalyzing aerial coupling of o-aminophenol (OAPh) to form phenoxazine-2-one (phenox). The mimicking activity of these complexes was quantitatively assessed using Michaelis–Menten enzymatic kinetics. Various enzyme kinetics plots were employed to determine several kinetic parameters, including the specificity constant and turnover number (kcat), which are crucial for understanding the efficiency of the catalytic cycles. Remarkably, the synthesized MnDPPNPH and CuDPPNPH complexes exhibited significantly higher turnover numbers (kcat) compared to previously reported complexes. This finding suggests that these new complexes possess superior catalytic activity, highlighting their potential as effective catalysts for reactions mimicking the function of phenoxazinone synthase.

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加入 2,6-二(1H-吡唑-1-基)吡啶和 2-Hydroxy Naphthaldehyde-Derived Schiff Base 的两种新单核 Mn(II) 和 Cu(II) 混合配体:结构、理论和苯并噁嗪酮合成酶模拟活性
目前的研究涉及新型锰(II)(MnDPPNPH)和铜(II)(CuDPPNPH)混合配体配合物的合成和详细表征。这些配合物包含 2,6-二(1H-吡唑-1-基)吡啶(DPP)和由 2-羟基萘(NPH)衍生的希夫碱。合成的配合物显示出 1:1:1 的化学计量比(金属:DPP:NPH),表明 Mn(II) 和 Cu(II) 中心周围存在八面体配位几何,化学式为[M (DPP)(NPH)(Cl)]。为了阐明它们的结构和电子特性,我们进行了理论计算。这些计算有助于优化这些配合物的几何结构,并深入了解了它们的分子轨道特性。MnDPPNPH 和 CuDPPNPH 复合物通过催化邻氨基苯酚(OAPh)的架空偶联生成吩嗪-2-酮(phenox),显示出潜在的吩嗪酮合成酶模拟活性。利用 Michaelis-Menten 酶动力学对这些复合物的模拟活性进行了定量评估。利用各种酶动力学图确定了几个动力学参数,包括特异性常数和周转次数(kcat),这些参数对于了解催化循环的效率至关重要。值得注意的是,与之前报道的复合物相比,合成的 MnDPPNPH 和 CuDPPNPH 复合物表现出明显更高的周转次数(kcat)。这一发现表明这些新复合物具有更高的催化活性,突出了它们作为模拟苯并噁嗪酮合成酶功能的反应的有效催化剂的潜力。
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来源期刊
Applied Organometallic Chemistry
Applied Organometallic Chemistry 化学-无机化学与核化学
CiteScore
7.80
自引率
10.30%
发文量
408
审稿时长
2.2 months
期刊介绍: All new compounds should be satisfactorily identified and proof of their structure given according to generally accepted standards. Structural reports, such as papers exclusively dealing with synthesis and characterization, analytical techniques, or X-ray diffraction studies of metal-organic or organometallic compounds will not be considered. The editors reserve the right to refuse without peer review any manuscript that does not comply with the aims and scope of the journal. Applied Organometallic Chemistry publishes Full Papers, Reviews, Mini Reviews and Communications of scientific research in all areas of organometallic and metal-organic chemistry involving main group metals, transition metals, lanthanides and actinides. All contributions should contain an explicit application of novel compounds, for instance in materials science, nano science, catalysis, chemical vapour deposition, metal-mediated organic synthesis, polymers, bio-organometallics, metallo-therapy, metallo-diagnostics and medicine. Reviews of books covering aspects of the fields of focus are also published.
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Issue Information Issue Information One-Pot Multicomponent Synthesis of Substituted 1,6-Naphthyridine Derivatives Employing 4-Aminocumarin The Role of L-Ligands in Silica-Supported Ti Oxo/Imido Heterometathesis Catalysts Cover Image
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