Copper-based Compounds Research Articles

Current Market Potential and Prospects of Copper-based Pyridine Derivatives: A Review.

Nicotine, minodronic acid, nicotinamide (niacin), zolpidem, zolimidine, and other pyridine-based chemicals play vital roles in medicine and biology. Pyridinecontaining drugs are widely available on the market to treat a wide range of human ailments. As a result of these advances, pyridine research is continually expanding, and there are now higher expectations for how it may aid in the treatment of numerous ailments. This evaluation incorporates data acquired from sources, like PubMed, to provide a thorough summary of the approved drugs and bioactivity data for compounds containing pyridine. Most of the reactions discussed in this article will provide readers with a deeper understanding of various pyridine-related examples, which is necessary for the creation of copper catalysis-based synthetic processes that are more accessible, secure, environmentally friendly, and practical, and that also have higher accuracy and selectivity. This paper also discusses significant innovations in the multi-component copper-catalyzed synthesis of N-heterocycles (pyridine), with the aim of developing precise, cost-effective, and environmentally friendly oxygenation and oxidation synthetic methods for the future synthesis of additional novel pyridine base analogs. Therefore, the review article will serve as a novel platform for researchers investigating copperbased pyridine compounds.

Harnessing phages as biocontrol agents against common bacterial blight diseases in plants

Bacterial blight diseases in plants are caused by various bacterial pathogens such as Dickeya, Pectobacterium, Xanthomonas, and others. They infect a wide range of crops including potatoes, tomatoes, apples, and citrus. The impact of these diseases includes reduced crop yields, lower quality produce, and economic losses for farmers. Traditional control methods like antibiotics and copper-based compounds are becoming less effective due to the development of resistance and environmental concerns. As a result, there is growing interest in alternative strategies such as biocontrol agents (BCAs), particularly bacteriophages. Bacteriophages are viruses that infect bacteria, they offer a promising solution to agricultural disease management. Their specificity and ability to target pathogenic bacteria make them an environmentally friendly alternative to chemical interventions. By optimizing phage formulations and application protocols, bacteriophages have the potential to contribute to healthier crops, increased yields, and a more sustainable agricultural system.

Accelerating alcohol oxidation kinetics for electrochemical biomass upgrading via photoinduced active CuIII-O generation

Copper-based compounds exhibit broad prospects in the electrocatalytic oxidation of biomass for sustainable production of high-value-added chemicals due to their passivated oxygen evolution reaction (OER) competitiveness. However, the sluggish reaction kinetics remain the main challenge in constraining their scalable application. Herein, a highly selective electrooxidation of 5-hydroxymethylfurfural (HMF) to 2, 5-furandicarboxylic acid (FDCA) on CuO is achieved via photoinduced surface reconstruction. The experimental results confirmed that the photogenerated hole accumulation on the surface of CuO with matched valence band position can promote the CuOOH active phase generation. Density functional theory (DFT) calculations and the overall relationship between structure and selectivity indicate the CuOOH species can accelerate the spontaneous dehydrogenation process of hydroxyl group. Therefore, the activated CuO electrode under illumination can effectively regulate the conversion of 5-Hydroxymethyl-2-furancarboxylic acid (HMFCA) key intermediates and exhibits accelerated reaction kinetics, FDCA yield increased by 17.79 % compared to dark condition. Additionally, a general enhancement effect on the oxidation of benzyl alcohol and furfuryl alcohol was also revealed. This work introduces photoassistance effect for the first time in HMF oxidation, opening up prospects for the application of photoelectric synergy in biomass value-added conversion and providing insights into the activity mechanism of Cu-based catalysts in organic oxidation.

Cu(II) complexes using acylhydrazones or cyclen for biocidal antifouling coatings

Abstract Copper and copper-based compounds have broad spectrum antimicrobial activity, but concerns about leaching into the environment and toxicity on non-target organisms is leading the use of copper-based coatings being restricted. Our objective was to develop coatings that used the biocidal activity of copper, but with low negative impacts by reducing its leaching into the environment. This study reports the synthesis and characterisation of copper coordinating ligands, their formulation into coatings and testing of their antibacterial activity. A polyacylhydrazone and a series of simple acylhydrazones were synthesised and coordinated to Cu(II), but were considered unsuitable due to either their poor water-solubility or high levels of copper leaching. In an alternative approach, copper was successfully chelated to the tetraazamacrocycle, cyclen, and used to synthesise Cu(II)-cyclen functionalised silica particles, which were successfully combined with commercial paint formulations. These functionalised products showed poor antibacterial activity when incorporated into epoxy coatings, probably due to the low copper content of the formulations. However, these ligands may have other applications, such as removal of heavy metals from contaminated effluent steams.

Cu(I) Coordination Compounds Conjugated to Au Nanorods for Future Applications in Drug Delivery: Insights in Molecular, Electronic and Cu Local Structure in Solid and Liquid Phase.

In the framework of the design, synthesis and testing of a library of copper complexes and nanostructured assemblies potentially endowed with antitumor and antiviral activity and useful for several applications, from drugs and related delivery systems to the development of biocidal nanomaterials, we present the detailed spectroscopic investigation of the molecular and electronic structure of copper-based coordination compounds and of a new conjugated system obtained by grafting Cu(I) complexes to gold nanorods. More in detail, the electronic and molecular structures of two Cu complexes and one AuNRs/Cu-complex adduct were investigated by X-ray photoelectron spectroscopy (XPS), synchrotron-induced XPS (SR-XPS) and near edge X-ray absorption spectroscopy (NEXAFS) in solid state, and the local structure around copper ion was assessed by X-ray absorption spectroscopy (XAS) both in solid state and water solution for the AuNRs/Cu-complex nanoparticles. The proposed multi-technique approach allowed to properly define the coordination geometry around the copper ion, as well as to ascertain the molecular structures of the coordination compounds, their stability and modifications upon interaction with gold nanoparticles, by comparing solid state and liquid phase data.

Designed Synthesis and Electrochemical Performance Regulation of the Hierarchical Hollow Structure Cu2S/Cu7S4/NC Anode for Hybrid Supercapacitors.

Copper-based compounds have attracted increasing attention as electrode materials for rechargeable devices, but their poor conductivity and insufficient stability inhibit their further development. Herein, an effective method has been proposed to improve the electrochemical properties of the copper-based electrodes by coating carbon materials and generating unique micro/nanostructures. The prepared Cu2S/Cu7S4/NC with hierarchical hollow structure possesses excellent electrochemical performance, attributing to the composition and structure optimization. The superior charge storage performance has been assessed by theoretical and experimental research. Specifically, the Cu2S/Cu7S4/NC exhibits remarkably higher electrical conductivity and lower adsorption-free energy for O* and OH* than those of Cu2O. Moreover, the Cu2S/Cu7S4/NC delivers a high specific capacitance of 1261.3 F·g-1 at the current density of 1 A·g-1 and also has great rate performance at higher current densities, which are much better than those of the Cu2O nanocubes. In addition, the assembled hybrid supercapacitor using Cu2S/Cu7S4/NC as the anode exhibits great energy density, power density, and cycling stability. This study has proposed a novel and feasible method for the synthesis of high-performance copper-based electrodes and their electrochemical performance regulation, which is of great significance for the advancement of high-quality electrode materials and rechargeable devices.

Photoassisted activation of persulfate by Cu2(OH)2CO3 for the degradation of tetracycline hydrochloride

Cu2(OH)2CO3 (cupric carbonate basic, CCB) is a common copper-based semiconductor compound that can absorb the visible light due to its suitable bandgap structure. Here, CCB was synthesized by a one-pot hydrothermal strategy. The catalyst exhibited excellent activation activity of persulfate (PS) supported by visible light irradiation and can degrade tetracycline hydrochloride (TCH) over a wide pH range from 3.0 to 10.0. Under the condition of 0.1 g/L catalyst and 2 mM PS, the removal rate of TCH (30 mg/L) reached 96% after 60 min of visible light irradiation. Coexisting anions (Cl- , HCO3 - , SO4 2- ) had little effect on the TCH degradation. The synergistic effects of CCB combined with PS and visible light were beneficial for the separation of photogenerated hole-electrons and the generation of more free radicals. Electron paramagnetic resonance (EPR) experiments and quenching experiments show that HO∙ and h+ are the predominant species in the catalytic reaction. Thus, this study proposes a promising approach using the CCB/PS/Vis system for wastewater remediation.

No- or Low-Content Copper Compounds for Controlling Venturia oleaginea, the Causal Agent of Olive Leaf Spot Disease.

The efficacy of using a synthetic (azoxystrobin + difenoconazole), copper-based (copper oxychloride) and low-content copper compound (copper complexed with gluconate and lignosulphonate) fungicides for controlling Venturia oleaginea, the causal agent of olive spot disease, was evaluated in an olive (cv. Nabali) orchard located in the Kafr Qud area (Palestine) in 2017-2018. Treatments were applied at three different times (February, April, and August). In January 2017, at the beginning of the experiment, about 90% of the leaves grown in 2016 were infected. Defoliation was determined by counting the leaves on the labeled branches initially and then periodically. It increased gradually in both the control and treated trees, but those treated with azoxystrobin + difenoconazole or with copper complexed with gluconate and lignosulphonate showed a slower defoliation rate. During 2017, new shoots grew and new leaves developed. All treatments reduced the drop of new leaves with respect to the control, with positive effects on the reproductive activity (inflorescence growth and yield). Overall, all treatments significantly reduced the disease, thus indicating the possibility of greatly reducing infections if treatments are regularly applied each year, also with traditional (copper-based) fungicides. Due to their capability of penetrating inside the vegetative tissue, azoxystrobin + difenoconazole or copper complexed with gluconate and lignosulphonate reduced/slowed down the drop of infected leaves. The use of these fungicides is therefore particularly recommended when olive leaf spot disease is severe. The use of low-content copper compounds allows the amount of metallic copper used for the treatments against V. oleaginea to be greatly reduced.

Multifunctional electrodes based on brochantite/malachite/polyaniline on Ni foam for the fabrication of binder-free supercapacitors and pyrimethanil/carbendazim fungicide electrochemical sensors

In this work, multifunctional electrode materials based on copper-based compounds and polyaniline were applied for binder-free supercapacitors and pyrimethanil/carbendazim fungicide sensors for the first time. Brochantite and malachite were synthesized on Ni foam via a one-step solvothermal method. Polyaniline (PANI) was electrochemically polymerized as inner and outer layers. PANI as the inner layer for the brochantite/malachite@Ni foam was found to enhance conductivity and cycling stability. The composite electrodes synergistically provided a specific capacitance as high as 737 F g−1 and a capacitance retention of 83.15 % after 10,000 cycles, which are much better than each of its parent compounds. During the in-situ fabrication of supercapacitor electrode on Ni foam, the powder form of brochantite/malachite mixture was also recovered from the reaction mixture, which was then used to prepare the composite electrodes with PANI. These fabricated electrodes demonstrated superb electrochemical sensing activity for the detection of pyrimethanil and carbendazim fungicides, giving the limits of detection of 29 and 10 nM, respectively. These fungicides were successfully determined in fruits, vegetables, and water sources, yielding satisfactory recovery between 99.8 and 107.5 %. The high-performance electrochemical electrodes based on copper-based compounds developed in this study hold significant potential for a variety of electrochemical applications.

Realizing Persistent Zero Area Compressibility over a Wide Pressure Range in Cu2 GeO4 by Microscopic Orthogonal-Braiding Strategy.

Zero area compressibility (ZAC) is an extremely rare mechanical response that exhibits an invariant two-dimensional size under hydrostatic pressure. All known ZAC materials are constructed from units in two dimensions as a whole. Here, we propose another strategy to obtain the ZAC by microscopically orthogonal-braiding one-dimensional zero compressibility strips. Accordingly, ZAC is identified in a copper-based compound with a planar [CuO4 ] unit, Cu2 GeO4 , that possesses an area compressibility as low as 1.58(26) TPa-1 over a wide pressure range from ≈0 GPa to 21.22 GPa. Based on our structural analysis, the subtle counterbalance between the shrinkage of [CuO4 ] and the expansion effect from the increase in the [CuO4 ]-[CuO4 ] dihedral angle attributes to the ZAC response. High-pressure Raman spectroscopy, in combination with first-principles calculations, shows that the electron transfer from in-plane bonding dx 2 -y 2 to out-of-plane nonbonding dz 2 orbitals within copper atoms causes the counterintuitive extension of the [CuO4 ]-[CuO4 ] dihedral angle under pressure. Our study provides an understanding on the pressure-induced structural evolution of copper-based oxides at an electronic level and facilitates a new avenue for the exploration of high-dimensional anomalous mechanical materials.

New mononuclear Cu(i) compounds: synthesis, characterization, and application to the electroreduction of CO2

We disclose the preparation and complete characterization of four new copper-based compounds used in the selective electrocatalytic activation of CO2 to produce oxalate. Additionally, key mechanistic insights are included.

Six polyoxotungstate-based transition metal compounds for electrochemical capacitor application and a comparative analysis of factors affecting capacitances.

Six different polyoxotungstate-based transition metal complexes were synthesized, namely [Cu5(2,2'-bpy)5(μ2-Cl)2(PO4)2(H2O)2][HPW12O40]·2H2O (1), [Cu1.5(2,2'-bpy)1.5(inic)2(H2O)1.5]3[H1.5PW12O40]2·16.25H2O (2), [Cu(2,2'-bpy)2]2[SiW12O40]·10H2O (3), [Zn(phen)3]2[PWVWVI11O40]·5H2O (4), [Zn(phen)2(H2O)]2[SiW12O40]·2H2O (5), and [Zn(2,2'-bpy)2]2[SiW12O40] (6) (2,2'-bpy = 2,2'-bipyridine, inic = isonicotinic acid, phen = 1,10-phenanthroline). Compound 1 is based on [HPW12O40]2- anions, which are accommodated within the open channels of a supramolecular network formed by novel Cu-P-Cl coordination clusters. Compound 2 is constructed from [H1.5PW12O40]1.5- and novel [Cu1.5(2,2'-bpy)1.5(inic)2(H2O)1.5]+ coordination fragments, and polyoxoanions are encapsulated within the pores created by the copper coordination fragments, resulting in a unique three-dimensional supramolecular architecture. Compound 3 is a two-dimensional structure formed through the covalent linkage between [SiW12O40]4- and [Cu(2,2'-bpy)2]2+. Compound 4 is a supramolecular architecture formed by [PWVWVI11O40]4- and [Zn(phen)3]2+ coordination fragments, while compound 5 is a supramolecular structure based on POM bi-supported Zn coordination complexes. Compound 6 is a two-dimensional framework structure constituted by [SiW12O40]4- and [Zn(2,2'-bpy)2]2+via covalent interactions. In addition, electrochemical measurement results show that the copper-based tungstate compounds 1-3 and zinc-based tungstate compounds 4-6 exhibit different performances and durabilities as electrochemical capacitors (compound 1 shows the highest specific capacitance of 94.0 F g-1 at 1.5 A g-1, whereas compound 6 maintains the best cycling stability with the capacity retention of 80.7% after 1000 cycles at 4 A g-1.). This study contributes to the development of POM-based transition metal complexes with high capacitance by providing insights into the design and synthesis process.

Novel metabolite madeirone and neomarinone extracted from Streptomyces aculeoletus as marine antibiofilm and antifouling agents.

Introduction: Biofouling poses a significant economic threat to various marine industries, leading to financial losses that can reach billions of euros annually. This study highlights the urgent need for effective alternatives to traditional antifouling agents, particularly following the global ban on organotin compounds. Material and methods: Streptomyces aculeolatus PTM-346 was isolated from sediment samples on the shores of the Madeira Archipelago, Portugal. The crude extract was fractionated using silica flash chromatography and preparative HPLC, resulting in two isolated marinone compounds: madeirone (1), a novel marinone derivative discovered in this study, and neomarinone (2). The antifouling activities of these compounds were tested against five marine bacterial species and the larvae of the mussel Mytilus galloprovincialis. Additionally, in silico and in vivo environmental toxicity evaluations of madeirone (1) and neomarinone (2) were conducted. Results: Madeirone (1) demonstrated significant antibiofilm efficacy, inhibiting Phaeobacter inhibens by up to 66%, Marinobacter hydrocarbonoclasticus by up to 60%, and Cobetia marina by up to 40%. Neomarinone (2) also exhibited substantial antibiofilm activity, with inhibition rates of up to 41% against P. inhibens, 40% against Pseudo-oceanicola batsensis, 56% against M. hydrocarbonoclasticus, 46% against C. marina, and 40% against Micrococcus luteus. The growth inhibition activity at the same concentrations of these compounds remained below 20% for the respective bacteria, highlighting their effectiveness as potent antibiofilm agents without significantly affecting bacterial viability. Additionally, both compounds showed potent effects against the settlement of Mytilus galloprovincialis larvae, with EC50 values of 1.76µg/mL and 0.12µg/mL for compounds (1) and (2), respectively, without impairing the viability of the targeted macrofouling species. In silico toxicity predictions and in vivo toxicity assays both support their potential for further development as antifouling agents. Conclusion: The newly discovered metabolite madeirone (1) and neomarinone (2) effectively inhibit both micro- and macrofouling. This distinct capability sets them apart from existing commercial antifouling agents and positions them as promising candidates for biofouling prevention. Consequently, these compounds represent a viable and environmentally friendly alternative for incorporation into paints, primers, varnishes, and sealants, offering significant advantages over traditional copper-based compounds.

Study on the catalysis of copper-based compounds on coal spontaneous combustion and its mechanism

ABSTRACTTo study the effect of the copper element in coal on the spontaneous combustion process of coal, corresponding copper-containing compounds were added to the coal-based on their occurrence state, and thermodynamic experiments and in-situ diffuse reflectance infrared spectroscopy experiments were conducted. Thermodynamic oxidation experiments have shown that the catalytic effects of Cu (NO3)2, CuCl2, CuCl, and Cu2O on three types of coal with different degrees of metamorphism are mainly reflected in the accelerated oxidation stage. After adding copper-containing compounds, the ignition temperature of coal decreased by 22.1°C to 134.4°C, the heat release increased by 1.33 to 3.19 times, and the CO emission and oxygen consumption rate also increased. CuCl has the greatest impact on the ignition point temperature of coal and increases the oxygen consumption rates of DNH and TS by 2.32 and 1.51 times that of raw coal. CuCl2 has the strongest catalytic effect on coal oxidation heat release. Through in-situ diffuse reflectance infrared spectroscopy experiments, it was found that the reaction rate of fatty hydrocarbons in the oxidation process of three types of coal with the addition of copper-containing compounds increased to 1.3–3 times that of raw coal, and the oxidation rate of oxygen-containing functional groups also significantly increased, while the cracking temperature of aromatic structures significantly decreased. This is because copper ions, as strong free radicals, induce free radical chain reactions in coal and exhibit a strong promoting effect on the coal oxygen reaction process.

Comparison of the accumulation and effects of copper pyrithione and copper sulphate on rainbow trout larvae

Copper pyrithione (CuPT) is used as a co-biocide in new antifouling paints but its toxicity remains little known. To compare the toxicity of copper-based compounds, rainbow trout (Oncorhynchus mykiss) larvae were exposed for 8-day to CuPT and CuSO4 at equivalent copper concentrations. CuPT exposure led to the greatest accumulation of Cu in larvae. Exposure to 10 µg.L−1 CuPT induced 99% larval mortality but only 4% for CuSO4-exposed larvae. The larval development and growth were affected by CuPT (from 0.5 µg.L−1 Cu) but not by CuSO4. Lipid peroxidation was not induced by either contaminant. The expression of genes involved in oxidative stress defence, detoxification and copper transport was induced in larvae exposed to CuSO4 and CuPT but at higher concentrations for CuPT. This study highlights the marked toxicity of CuPT for early life stages of fish and raises the question of the possible environmental risks of this antifouling compound.

Comparison between laboratory and synchrotron X-ray absorption spectroscopy setup examination of Cu(II) complexes with prospective anticancer properties

From the commonly known metal-based chemotherapeutics, like cisplatin, there is ongoing interest in searching for some of their alternatives, including copper complexes containing organic groups. In this paper, we report the results of the preliminary examination of copper-based compounds, which are studied with the use of the laboratory XAS setup, that are compared with data obtained at the synchrotron facility. Identification of spectral features and oxidation state of copper was successfully performed based only on the laboratory data, however, some limitation of this test apparatus is also reported. Additionally, we performed first testing of the laboratory XAS spectrometer to study more complex compounds, which could be used in anticancer therapy, than metallic foils, which are usually used to estimate the experimental capabilities of such setups.

Targeting copper metabolism: a promising strategy for cancer treatment.

Copper is an essential micronutrient that plays a critical role in many physiological processes. However, excessive copper accumulation in cancer cells has been linked to tumor growth and metastasis. This review article explores the potential of targeting copper metabolism as a promising strategy for cancer treatment. Excessive copper accumulation in cancer cells has been associated with tumor growth and metastasis. By disrupting copper homeostasis in cancer cells and inducing cell death through copper-dependent mechanisms (cuproplasia and cuprotosis, respectively), therapies can be developed with improved efficacy and reduced side effects. The article discusses the role of copper in biological processes, such as angiogenesis, immune response, and redox homeostasis. Various approaches for targeting copper metabolism in cancer treatment are examined, including the use of copper-dependent enzymes, copper-based compounds, and cuprotosis-related genes or proteins. The review also explores strategies like copper chelation therapy and nanotechnology for targeted delivery of copper-targeting agents. By understanding the intricate network of cuprotosis and its interactions with the tumor microenvironment and immune system, new targets for therapy can be identified, leading to improved cancer treatment outcomes. Overall, this comprehensive review highlights the significant potential of targeting copper metabolism as a promising and effective approach in cancer treatment, while providing valuable insights into the current state of research in this field.

Double- or Triple-Tiered Protection: Prospects for the Sustainable Application of Copper-Based Antimicrobial Compounds for Another Fourteen Decades

Copper (Cu)-based antimicrobial compounds (CBACs) have been widely used to control phytopathogens for nearly fourteen decades. Since the first commercialized Bordeaux mixture was introduced, CBACs have been gradually developed from highly to slightly soluble reagents and from inorganic to synthetic organic, with nanomaterials being a recent development. Traditionally, slightly soluble CBACs form a physical film on the surface of plant tissues, separating the micro-organisms from the host, then release divalent or monovalent copper ions (Cu2+ or Cu+) to construct a secondary layer of protection which inhibits the growth of pathogens. Recent progress has demonstrated that the release of a low concentration of Cu2+ may elicit immune responses in plants. This supports a triple-tiered protection role of CBACs: break contact, inhibit microorganisms, and stimulate host immunity. This spatial defense system, which is integrated both inside and outside the plant cell, provides long-lasting and broad-spectrum protection, even against emergent copper-resistant strains. Here, we review recent findings and highlight the perspectives underlying mitigation strategies for the sustainable utilization of CBACs.

Copper-Based Diamond-like Thermoelectric Compounds: Looking Back and Stepping Forward.

The research on thermoelectric (TE) materials has a long history. Holding the advantages of high elemental abundance, lead-free and easily tunable transport properties, copper-based diamond-like (CBDL) thermoelectric compounds have attracted extensive attention from the thermoelectric community. The CBDL compounds contain a large number of representative candidates for thermoelectric applications, such as CuInGa2, Cu2GeSe3, Cu3SbSe4, Cu12SbSe13, etc. In this study, the structure characteristics and TE performances of typical CBDLs were briefly summarized. Several common synthesis technologies and effective strategies to improve the thermoelectric performances of CBDL compounds were introduced. In addition, the latest developments in thermoelectric devices based on CBDL compounds were discussed. Further developments and prospects for exploring high-performance copper-based diamond-like thermoelectric materials and devices were also presented at the end.

Development of polyurethane antimicrobial coatings by composition with phenolic-, ionic- and copper-based agents

Microorganisms can be found in almost all environments with high-touch surfaces being an important fomite for microbial growth. Considering the health issues associated to acquired infection from inanimate surfaces, as well as the raising hygienic concerns, the incorporation of antimicrobial compounds in high-touch surfaces emerges as an effective solution for biomedical and common daily applications.In this work, we incorporated different antimicrobial agents (phenolic-, ionic- and copper-based compounds) into polyurethane commercial formulations to produce antimicrobial lacquer-films and evaluated not only their physical/chemical properties, but also their antimicrobial activity against bacteria (Staphylococcus aureus, Escherichia coli), fungi (Candida albicans), and virus (SARS-CoV-2).The incorporation of antimicrobial agents did not affect the performance of lacquer-films and the main properties were maintained, specifically the visual aspect, gloss values, optical properties and chemical stability.Among the different compounds tested, copper-based lacquer-films exhibited the strongest antibacterial and antifungal activity, with a >4 log reduction, but not against virus. Importantly, copper-based lacquer-films maintained their cytocompatibility, even at high concentrations. Regarding the ionic lacquer-films, the highest tested concentration also showed a strong antimicrobial action (5 log reduction) against fungi and gram-positive bacteria, but not against gram-negative bacteria and virus. However, at this concentration, the ionic-containing lacquer-films presented cytotoxic potential. The phenolic-based compounds were not associated with antimicrobial activity, regardless the concentrations tested.Collectively, these results highlight the potential of incorporating antimicrobial agents in polyurethane surface coatings as a promising strategy to avoid the microbial colonization on inanimate surfaces and, ultimately, prevent the spreading of potentially harmful pathogens among humans.