X-band Electron Paramagnetic Resonance Spectroscopy Research Articles

Distribution of Radiation-Induced Defects in Quartz at the ACKIO Uranium Prospect, Athabasca Basin, Saskatchewan: Tracing Uranium-Bearing Fluids

Abstract Quartz grains from the ACKIO uranium prospect, located near the eastern margin of the Athabasca Basin, Saskatchewan, have been investigated using powder X-band electron paramagnetic resonance (EPR) spectroscopy. The EPR spectra of quartz separates from samples systematically collected from the Athabasca Supergroup sandstones and the underlying metamorphosed basement reveal a suite of silicon-vacancy hole centers, which were formed by the bombardment of alpha particles emitted from the radioactive decay of uranium, thorium, and their unstable progeny. The differences in EPR signal intensities of these hole centers indicate that quartz grains received different accumulative doses of alpha particle irradiation in different locations within the ACKIO prospect. For example, quartz extracted from a mineralized sample has the highest EPR signal intensity due to the presence of disseminated uraninite. For quartz sampled at distance from uranium mineralization, the elevated intensities of the silicon-vacancy hole centers most likely indicate a temporary source of radiation, such as ancient uranium-bearing fluids. The median EPR intensities of quartz from the basement rocks at ACKIO are an order of magnitude higher than those of its counterpart from the Athabasca sandstones. Also, the EPR intensities of quartz along the sandstone–basement contact at ACKIO differ by more than two orders of magnitude, suggesting limited migration of uranium-bearing fluids along this contact in the study area. Instead, anomalously high EPR intensities in quartz close to the sandstone–basement contact and elsewhere are restricted to fault gouges and brecciated areas, suggesting that they are the structural pathways for channelized migration of ancient uranium-bearing fluids. A three-dimensional distribution model of the EPR signal intensities has been constructed to define conduits for the migration of ancient uranium-bearing fluids at ACKIO and suggest favorable targets for further exploration. These findings demonstrate the power of EPR spectroscopy in delineating pathways of uranium-bearing fluids and predicting potential mineralization targets.

Solvent Controlled Generation of Spin Active Polarons in Two-Dimensional Material under UV Light Irradiation.

Polarons belong to a class of extensively studied quasiparticles that have found applications spanning diverse fields, including charge transport, colossal magnetoresistance, thermoelectricity, (multi)ferroism, optoelectronics, and photovoltaics. It is notable, though, that their interaction with the local environment has been overlooked so far. We report an unexpected phenomenon of the solvent-induced generation of polaronic spin active states in a two-dimensional (2D) material fluorographene under UV light. Furthermore, we present compelling evidence of the solvent-specific nature of this phenomenon. The generation of spin-active states is robust in acetone, moderate in benzene, and absent in cyclohexane. Continuous wave X-band electron paramagnetic resonance (EPR) spectroscopy experiments revealed a massive increase in the EPR signal for fluorographene dispersed in acetone under UV-light irradiation, while the system did not show any significant signal under dark conditions and without the solvent. The patterns appeared due to the generation of transient magnetic photoexcited states of polaronic character, which encompassed the net 1/2 spin moment detectable by EPR. Advanced ab initio calculations disclosed that polarons are plausibly formed at radical sites in fluorographene which interact strongly with acetone molecules in their vicinity. Additionally, we present a comprehensive scenario for multiplication of polaronic spin active species, highlighting the pivotal role of the photoinduced charge transfer from the solvent to the electrophilic radical centers in fluorographene. We believe that the solvent-tunable polaron formation with the use of UV light and an easily accessible 2D nanomaterial opens up a wide range of future applications, ranging from molecular sensing to magneto-optical devices.

Application of electron paramagnetic resonance spectroscopy to examine free radicals formed in indapamide and torasemide storage under UV irradiation and at the higher temperatures which appear under light exposition

Free radical formation in two diuretics: indapamide and torasemide was examined during UV irradiation and storage at higher temperatures using X-band (9.3 GHz) electron paramagnetic resonance spectroscopy (EPR). The aim of this study was to investigate the possibility of storing indapamide and torasemide under UV irradiation and at higher temperatures, which may occur during exposure to light. The diuretic samples were exposed to UVA irradiation for 15, 30 and 45 minutes, and stored at temperatures of 40 °C and 50 °C by 30 minutes. The EPR spectra were analyzed to determine the amplitudes (A), linewidths (ΔBpp), and integral intensities (I) and g factors. The concentrations of free radical (N) in the diuretic samples were also determined. The influence of microwave power on amplitudes, linewidths and the asymmetry parameter were evaluated. The result showed that the tested indapamide and torasemide samples exhibited high free radical concentrations in the range of 1018-1019 spin/g after UV irradiation and heat treatment. Therefore, due to the significant free radical formation indapamide and torasemide should not be stored under UV light and at temperatures of 40 °C and 50 °C. The complex character of free radical systems in the diuretic samples was proved as evidenced by the changes of the asymmetry parameters of the EPR lines with increasing microwave power. Fast spin-lattice relaxation processes were observed in all tested diuretic samples, regardless of the storage conditions. Electron paramagnetic resonance spectroscopy is proposed as a useful method in pharmacy to determine the appropriate storage conditions for diuretics.

Spin-labeling Insights into How Chemical Fixation Impacts Glycan Organization on Cells.

As new methods to interrogate glycan organization on cells develop, it is important to have a molecular level understanding of how chemical fixation can impact results and interpretations. Site-directed spin labeling technologies are well suited to study how the spin label mobility is impacted by local environmental conditions, such as those imposed by cross-linking effects of paraformaldehyde cell fixation methods. Here, we utilize three different azide-containing sugars for metabolic glycan engineering with HeLa cells to incorporate azido glycans that are modified with a DBCO-based nitroxide moiety via click reaction. Continuous wave X-band electron paramagnetic resonance spectroscopy is employed to characterize how the chronological sequence of chemical fixation and spin labeling impacts the local mobility and accessibility of the nitroxide-labeled glycans in the glycocalyx of HeLa cells. Results demonstrate that chemical fixation with paraformaldehyde can alter local glycan mobility and care should be taken in the analysis of data in any study where chemical fixation and cellular labeling occur.

Structures and catalytic properties of Cu(II) complex with chelating fluorinated ligands

Structure of Cu(II) complex with chelating fluorinated ligands were studied at 298 K and 90 K using CW X-band electron paramagnetic resonance (EPR) spectroscopy and density functional theory (DFT). Spin-Hamiltonian and structural parameters have been determined and the latter were compared with the X-ray data showing good similarity. A phase transition occurred at 360 K in solid crystalline sample was observed by EPR and discussed. Qualitative kinetic analysis of the catalytic behavior of Cu(II) complex upon H2O2 decomposition in acetonitrile-aqueous solutions at 313 K was studied using EPR and UV–visible spectroscopy.

Unexplored Facet of Pincer Ligands: Super-Reductant Behavior Applied to Transition-Metal-Free Catalysis.

Pincer ligands are well-established supporting ancillaries to afford robust coordination to metals across the periodic table. Despite their widespread use in developing homogeneous catalysts, the redox noninnocence of the ligand backbone is less utilized in steering catalytic transformations. This report showcases a trianionic, symmetric NNN-pincer to drive C-C cross-coupling reactions and heterocycle formation via C-H functionalization, without any coordination to transition metals. The starting substrates are aryl chlorides that can tease the limit of a catalyst's ability to promote a reductive cleavage at a much demanding potential of -2.90 V vs SCE. The reducing power of the simple trianionic ligand backbone has been tremendously amplified by shining visible light on it. The catalyst's success relies on its easy access to the one-electron oxidized iminosemiquinonate form that has been thoroughly characterized by X-band electron paramagnetic resonance spectroscopy through spectroelectrochemical experiments. The moderately long-lived excited-state lifetime (10.2 ns) and such a super-reductive ability dependent on the one-electron redox shuttle between the bisamido and iminosemiquinonato forms make this catalysis effective.

Understanding the Photocatalytic Activity of Sodium Hexatitanate Nanoparticles for Pollutants Degradation: A Spectroscopic Insight

Sodium hexatitanate (Na2Ti6O13) nanoparticles have been synthesized by the hydrothermal method with microwave and conventional heating, after which their photocatalytic properties toward an azo dye pollutant degradation have been investigated. Insights into the dynamics and reactivity of the species involved in the photocatalytic mechanism of the (Na2Ti6O13) samples were precisely investigated, for the first time, by X-band electron paramagnetic resonance (EPR) spectroscopy under different experimental conditions. X-ray diffraction structural analysis revealed that all samples crystallized in a monoclinic C2/m structure, with different short-range structural order according to the employed heating, as indicated by Raman. Field-emission scanning electron microscopy and transmission electron microscopy results revealed the formation of rod- and fiber-like nanoparticles with different diameters and lengths. EPR measurements indicated the presence of different Ti3+ point defects and F centers in the samples. X-ray photoelectron spectroscopy analysis proved the presence of oxygen-related defects, but no Ti3+ was detected on the surface. Spin trapping experiments monitored the generation of hydroxyl (OH·) radicals over UV-irradiation time. Various parameters contribute to the photocatalytic activity of the samples; however, the type of defect and particle morphology appeared as key factors for enhanced efficiency. Our study provides significant information about paramagnetic defects in Na2Ti6O13 materials and their role in photocatalysis to design other Ti-based photocatalysts.

Two-Electron Mixed Valency in a Heterotrimetallic Nickel–Vanadium–Nickel Complex

Mixed-valence complexes represent an enticing class of coordination compounds to interrogate electron transfer confined within a molecular framework. The diamagnetic heterotrimetallic anion, [V(SNS)2{Ni(dppe)}2]-, was prepared by reducing (dppe)NiCl2 in the presence of the chelating metalloligand [V(SNS)2]- [dppe = bis(diphenylphosphino)ethane; (SNS)3- = bis(2-thiolato-4-methylphenyl)amide]. Vanadium-nickel bonds span the heterotrimetallic core in the structure of [V(SNS)2{Ni(dppe)}2]-, with V-Ni bond lengths of 2.78 and 2.79 Å. One-electron oxidation of monoanionic [V(SNS)2{Ni(dppe)}2]- yielded neutral, paramagnetic V(SNS)2{Ni(dppe)}2. The solid-state structure of V(SNS)2{Ni(dppe)}2 revealed that the two nickel ions occupy unique coordination environments: one nickel is in a square-planar S2P2 coordination environment (τ4 = 0.19), with a long Ni···V distance of 3.45 Å; the other nickel is in a tetrahedral S2P2 coordination environment (τ4 = 0.84) with a short Ni-V distance of 2.60 Å, consistent with a formal metal-metal bond. Continuous-wave X-band electron paramagnetic resonance spectroscopy, electrochemical investigations, and density functional theory computations indicated that the unpaired electron in the neutral V(SNS)2{Ni(dppe)}2 cluster is localized on the bridging [V(SNS)2] metalloligand, and as a result, V(SNS)2{Ni(dppe)}2 is best described as a two-electron mixed-valence complex. These results demonstrate the important role that metal-metal interactions and flexible coordination geometries play in enabling multiple, reversible electron transfer processes in small cluster complexes.

Hyperfine interactions and coherent spin dynamics of isotopically purified 167Er3+ in polycrystalline Y2O3

167Er3+ doped solids are a promising platform for quantum technology due to erbium’s telecom C-band optical transition and its long hyperfine coherence times. We experimentally study the spin Hamiltonian and dynamics of 167Er3+ spins in Y2O3 using electron paramagnetic resonance (EPR) spectroscopy. The anisotropic electron Zeeman, hyperfine and nuclear quadrupole matrices are fitted using data obtained by X-band (9.5 GHz) EPR spectroscopy. We perform pulsed EPR spectroscopy to measure spin relaxation time T 1 and coherence time T 2 for the 3 principal axes of an anisotropic g tensor. Long electronic spin coherence time up to 24.4 μs is measured for lowest g transition at 4 K, exceeding previously reported values at much lower temperatures. Measurements of decoherence mechanism indicates T 2 limited by spectral diffusion and instantaneous diffusion. Long spin coherence times, along with a strong anisotropic hyperfine interaction makes 167Er3+:Y2O3 a rich system and an excellent candidate for spin-based quantum technologies.

Domain-Specific Phase Transitions in a Supramolecular Nanostructure.

Understanding thermal phase behavior within nanomaterials can inform their rational design for medical technologies like drug delivery systems and vaccines, as well as for energy technologies and catalysis. This study resolves thermal phases of discrete domains within a supramolecular aramid amphiphile (AA) nanoribbon. Dynamics are characterized by X-band EPR spectroscopy of spin labels positioned at specific sites through the nanoribbon cross-section. The fitting of the electron paramagnetic resonance (EPR) line shapes reveals distinct conformational dynamics, with fastest dynamics at the surface water layer, intermediate dynamics within the flexible cationic head group domain, and slowest dynamics in the interior aramid domain. Measurement of conformational mobility as a function of temperature reveals first- and second-order phase transitions, with melting transitions observed in the surface and head group domains and a temperature-insensitive crystalline phase in the aramid domain. Arrhenius analysis yields activation energies of diffusion at each site. This work demonstrates that distinct thermal phase behaviors between adjacent nanodomains within a supramolecular nanostructure may be resolved and illustrates the utility of EPR spectroscopy for thermal phase characterization of nanostructures.

Electron spin resonance (ESR) spectroscopy study of gamma-irradiated dried white mulberry (Morus Alba L.) fruits

Two different groups of dried fruits of white mulberry (Morus Alba L.) sold in Turkish markets were investigated by the X-band ESR spectroscopy technique for irradiation detection purposes. No resonance signals were detected in the ESR spectra of the un-irradiated samples. After irradiation, identical multi-line resonance signals were induced in the ESR spectra of both types of samples, except for the intensities. At doses of 2 and 10 kGy, the long-term stabilities of the radiation-induced radicals at room temperature were investigated over a storage period of about 100 days. The results obtained show that the ESR technique can be used to distinguish irradiated white mulberry fruits from un-irradiated ones.

Quantifying the Number and Affinity of Mn2+-Binding Sites with EPR Spectroscopy.

During the last decades, various functional oligonucleotides have been discovered including DNAzymes, ribozymes, and riboswitches. Their function is based on their ability to form and change their three-dimensional structure. Binding of divalent ions to specific binding pockets was found to be important for the global structure and function. Here, we present a protocol that allows counting the number of Mn2+-binding sites and to determine their dissociation constants by means of continuous wave X-band Electron Paramagnetic Resonance (EPR) spectroscopy. In this method, Mn2+ is titrated into the oligonucleotide-containing sample and the intensity of the EPR spectrum is recorded. By comparison with a Mn2+-only reference sample, the binding isotherm can be constructed and fitted to binding models yielding the number and affinities of the binding sites. This method has been successfully applied to several functional oligonucleotides.

Flagellin lysine methyltransferase FliB catalyzes a [4Fe-4S] mediated methyl transfer reaction.

The methyltransferase FliB posttranslationally modifies surface-exposed ɛ-N-lysine residues of flagellin, the protomer of the flagellar filament in Salmonella enterica (S. enterica). Flagellin methylation, reported originally in 1959, was recently shown to enhance host cell adhesion and invasion by increasing the flagellar hydrophobicity. The role of FliB in this process, however, remained enigmatic. In this study, we investigated the properties and mechanisms of FliB from S. enterica in vivo and in vitro. We show that FliB is an S-adenosylmethionine (SAM) dependent methyltransferase, forming a membrane associated oligomer that modifies flagellin in the bacterial cytosol. Using X-band electron paramagnetic resonance (EPR) spectroscopy, zero-field 57Fe Mössbauer spectroscopy, methylation assays and chromatography coupled mass spectrometry (MS) analysis, we further found that FliB contains an oxygen sensitive [4Fe-4S] cluster that is essential for the methyl transfer reaction and might mediate a radical mechanism. Our data indicate that the [4Fe-4S] cluster is coordinated by a cysteine rich motif in FliB that is highly conserved among multiple genera of the Enterobacteriaceae family.

Free Radical Scavenging Activity of Infusions of Different Medicinal Plants for Use in Obstetrics.

An X-band (9.3 GHz) electron paramagnetic resonance (EPR) spectroscopy was used to examine the free radical scavenging activity of the following infusions, which were nonirradiated and exposed to UVA: root of Asparagus racemosus and herbs of Mitchella repens, Cnicus benedictus L., Galega officinalis L., and Eupatorium cannabinum L. The plant materials for obstetrics applications were chosen for analysis. The aims of these studies were to compare the free radical scavenging ability of the tested infusions and to determine the influence of UVA irradiation of the plant materials on interactions of these infusions with free radicals. Both the magnitude and kinetics of the interactions of the infusions with the model DPPH free radicals were examined. The ability to quench the free radicals for the examined plant infusions increases in the following order: Asparagus racemosus (root) < Mitchella repens (herb) < Cnicus benedictus L. (herb) < Galega officinalis L. (herb) < Eupatorium cannabinum L. (herb). The analyzed infusions differ in the kinetics of the interactions with free radicals. The fastest interactions with free radicals characterize the infusions of Galega officinalis L. herb and Eupatorium cannabinum L. herb. The infusion of Mitchella repens herb interacts with free radicals in the slowest way. UVA radiation reduces the antioxidant interactions of all tested infusions, especially the infusion of Eupatorium cannabinum L. herb, which should be protected against UVA radiation during storage. The weakest decrease of free radical scavenging activity was observed for the infusion of the root of Asparagus racemosus exposed to UVA radiation. UVA radiation affected the speed of the free radical interactions of the infusions, depending on the type of plant materials. EPR spectroscopy is useful to examine the free radical scavenging activity of plant infusions, which is helpful to find effective antioxidants for applications in obstetrics and their optimal storage conditions.

Cu(II) complex based on lemofloxacin and N,N-donor ligand: Synthesis, crystal structure, DFT calculations, and in vitro antimicrobial evaluation

Cu(II) complex of second-generation quinolone lemofloxacin with 2,2′-bipyridylamine formulated as [Cu(lmx)(bipym)Cl](CH3OH)·3H2O (1) [lmx = lemofloxacin, bipym = 2,2′-bipyridylamine] has been synthesized and characterized utilizing X-ray single-crystal diffraction and spectroscopic methods. The crystal structure of [Cu(lmx)(bipym)Cl](CH3OH).3H2O has been determined via X-ray diffraction and the result showed that Cu (II) ion is coordinated by two oxygen atoms from lmx ligand and two nitrogen atoms from bipym ligand in a slightly distorted square pyramidal arrangement. The X-ray structural analysis shows that the complex crystallizes in the monoclinic system with a = 15.031(3), b = 14.2647(13), c = 16.687(4) Å, and space group P21/n. Thermal analysis studies was used to determine the decomposition pattern of the complex, also confirm the presence of lattice water molecules and the metal oxide which is the final product. X-band electron paramagnetic resonance (EPR) spectroscopy at liquid nitrogen temperature (LNT) from solution indicates the presence of a monomeric unit in the crystal structure. The Density functional theory (DFT) studies revealed that the Cu(II) complex is a soft molecule with high chemical reactivity and low kinetic stability as indicated by the low values of the global hardness (η = 1.063), energy gap (ΔE = 2.126 eV) and chemical potential (µ = -5.304).Furthermore, the ligand and complex were also subjected to antimicrobial activity against three (3) Gram (+) and two (2) Gram (-) bacterial strains by using the agar disk diffusion method and the findings indicated that the complex possesses a better activity compared to the parent ligand lmx while a decreased antimicrobial activity was observed against E. coli.

Rotation of a Charged Spin Probe in Room-Temperature Ionic Liquids.

X-band electron paramagnetic resonance spectroscopy has been used to investigate the rotational diffusion of a stable, positively charged nitroxide 4-trimethylammonium-2,2,6,6-tetramethylpiperidine-1-oxyl iodide (Cat-1) in a series of 1-alkyl-3-methylimidazolium tetrafluoroborate room-temperature ionic liquids (RTILs) having alkyl chain lengths from two to eight carbons. The rotation of Cat-1 is anisotropic with the preferential axis of rotation along the NO• moiety. The Stokes-Einstein-Debye law describes the mean rotational correlation time of Cat-1, assuming that the hydrodynamic radius is smaller than the van der Waals radius of the probe. This implies that the probe rotates freely, experiencing slip boundary condition, which is solvent-dependent. The rotational correlation time of Cat-1 in RTILs can very well be fitted to a power-law functionality with a singular temperature, which suggests that the apparent activation energy of rotation exhibits non-Arrhenius behavior. Compared to the rotation of perdeuterated 2,2,6,6-tetramethyl-4-oxopiperidine-1-oxyl (pDTO), which is neutral, the rotation of Cat-1 is several times slower. The rotational anisotropy, the ratio of the rotational times of pDTO and Cat-1, and the apparent activation energy indicate the transition from a homogeneously globular structure to a spongelike structure when the alkyl chain has four carbons, which is also observed in molecular dynamics computational studies. For the first time, we have been able to show that the rotational correlation time of a solute molecule can be analyzed in terms of the Cohen-Turnbull free volume theory. The Cohen-Turnbull theory fully describes the rotation of Cat-1 in all ionic liquids in the measured temperature range.

Ferritin and Free Radicals Species in Seeds by Electron Paramagnetic Resonance

Biodiesel is a relevant source of renewable energy which has received a lot of attention due to the need to create a renewable fuel matrix. An important source of raw material for the biodiesel production is oilseeds. Considering the lack of studies characterizing magnetic species present in seeds, different types of oilseed samples were characterized and compared using X-band Electron Paramagnetic Resonance spectroscopy, at room temperature and 30 K. It was identified the presence of the semiquinone radical in all seed’s samples. Besides the free radical resonance, the presence of ferritin was observed, that is an important Fe complex present in seeds and plants, which, although very studied, still lacks a precise description related with its storage and other processes. This study can potentially assist future research about biodiesel and other products that have seeds as raw material.

Photoreactivity of Hair Melanin from Different Skin Phototypes-Contribution of Melanin Subunits to the Pigments Photoreactive Properties.

Photoreactivity of melanin has become a major focus of research due to the postulated involvement of the pigment in UVA-induced melanoma. However, most of the hitherto studies were carried out using synthetic melanin models. Thus, photoreactivity of natural melanins is yet to be systematically analyzed. Here, we examined the photoreactive properties of natural melanins isolated from hair samples obtained from donors of different skin phototypes (I, II, III, and V). X-band and W-band electron paramagnetic resonance (EPR) spectroscopy was used to examine the paramagnetic properties of the pigments. Alkaline hydrogen peroxide degradation and hydroiodic acid hydrolysis were used to determine the chemical composition of the melanins. EPR oximetry and spin trapping were used to examine the oxygen photoconsumption and photo-induced formation of superoxide anion, and time-resolved near infrared phosphorescence was employed to determine the singlet oxygen photogeneration by the melanins. The efficiency of superoxide and singlet oxygen photogeneration was related to the chemical composition of the studied melanins. Melanins from blond and chestnut hair (phototypes II and III) exhibited highest photoreactivity of all examined pigments. Moreover, melanins of these phototypes showed highest quantum efficiency of singlet oxygen photogeneration at 332 nm and 365 nm supporting the postulate of the pigment contribution in UVA-induced melanoma.

Influence of Conditioning Temperature on Defects in the Double Al2O3/ZnO Layer Deposited by the ALD Method.

In this work, we present the results of defects analysis concerning ZnO and Al2O3 layers deposited by atomic layer deposition (ALD) technique. The analysis was performed by the X-band electron paramagnetic resonance (EPR) spectroscopy, transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS) methods. The layers were either tested as-deposited or after 30 min heating at 300 °C and 450 °C in Ar atmosphere. TEM and XPS investigations revealed amorphous nature and non-stoichiometry of aluminum oxide even after additional high-temperature treatment. EPR confirmed high number of defect states in Al2O3. For ZnO, we found the as-deposited layer shows ultrafine grains that start to grow when high temperature is applied and that their crystallinity is also improved, resulting in good agreement with XPS results which indicated lower number of defects on the layer surface.

Shedding Light on the Free Radical Nature of Sulfonated Melanins.

Melanin, an important class of natural pigment found in the human body, has stood out as a promising bioelectronic material due to its rather unique collection of electrical properties and biocompatibility. Among the available melanin derivatives, the sulfonated form has proven to not only be able to produce homogeneous device quality thin films with excellent adhesion, even on hydrophobic surfaces, but also to act as an ion to electron transducing element. It has recently been shown that the transport physics (and dominant carrier generation) may be related to a semiquinone free radical species in these materials. Hence, a better understanding of the paramagnetic properties of sulfonated derivatives could shed light on their charge transport behavior and thus enable improvement in regard to use in bioelectronics. Motivated by this question, in this work, different sulfonated melanin derivatives were investigated by hydration-controlled, continuous-wave X-band electron paramagnetic resonance spectroscopy and electronic structure calculations. Our results show that sulfonated melanin behaves similarly to non-functionalized melanin, but demonstrates a less pronounced response to humidity vis-à-vis standard melanin. We thus speculate on the structural and charge transport behavior in light of these differences with a view to further engineering structure-property relationships.