Publications by authors named "P K Hota"

Article Synopsis
  • The design and study of synthetic copper-dioxygen complexes help understand the structure and function of various copper-based metalloenzymes, like dopamine monooxygenase and tyrosinase.
  • Creating ligands that accurately replicate the diverse active sites of these enzymes is a significant challenge for chemists in the field of synthetic bioinorganic chemistry.
  • This review discusses different ligand systems that stabilize copper-dioxygen species, outlines their synthesis and characterization, and examines their reactivity patterns, including electrophilic arene hydroxylation and the associated thermodynamic-kinetic relationships.
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The chemistry of copper-dioxygen complexes is relevant to copper enzymes in biology as well as in (ligand)Cu-O (or Cu-O) species utilized in oxidative transformations. For overall energy considerations, as applicable in chemical synthesis, it is beneficial to have an appropriate atom economy; both O-atoms of O are transferred to the product(s). However, examples of such dioxygenase-type chemistry are extremely rare or not well documented.

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Synthetic side-on peroxide-bound dicopper(II) () complexes are important for understanding the active site structure/function of many copper-containing enzymes. This work highlights the formation of new {Cu(μ-η:η-O)Cu} complexes (with electronic absorption and resonance Raman (rR) spectroscopic characterization) using tripodal NArOH ligands at -135 °C, which spontaneously participate in intramolecular phenolic H-atom abstraction (HAA). This results in the generation of bis(phenoxyl radical)bis(μ-OH)dicopper(II) intermediates, substantiated by their EPR/UV-vis/rR spectroscopic signatures and crystal structural determination of a diphenoquinone dicopper(I) complex derived from ligand -C═C coupling.

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Copper ion is a versatile and ubiquitous facilitator of redox chemical and biochemical processes. These include the binding of molecular oxygen to copper(I) complexes where it undergoes stepwise reduction-protonation. A detailed understanding of thermodynamic relationships between such reduced/protonated states is key to elucidate the fundamentals of the chemical/biochemical processes involved.

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In recent years, advancements in chemistry have allowed the tailoring of materials at the nanoscopic level as needed. There are mainly four main types of nanomaterials used as drug carriers:metal-based nanomaterials, organic nanomaterials, inorganic nanomaterials, and polymer nanomaterials. The nanomaterials as a drug carrier showed advantages for decreased side effects with a higher therapeutic index.

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