Tris Iron Research Articles

Effect of Film Thickness on the Electrical Resistivity and Optical Functions Distribution of Iron Tris(8-hydroxyquinoline) Thin Films

Iron tris(8-hydroxyquinoline) (Feq3) was synthesized and investigated by X-ray photoemission spectroscopy. It crystalizes in triclinic polycrystalline structure in powder form, whereas the Feq3 films, with different thickness values (12, 20, 35, and 42 nm), have an amorphous structure. The influence of film thickness on the electrical resistivity and the optical properties is reported. The morphology of Feq3 was investigated in terms of field-emission scanning electron microscope. Electrical resistivity measurements indicate an inverse proportionality to the film thickness. The optical properties of Feq3 films were investigated in terms of photoluminescence spectra and spectrophotometric measurements of transmittance and reflectance. The optical functions such as absorption coefficient and refractive index of the films were calculated. The dependence of the Feq3 film thickness on the optical energy band gap and dispersion parameters was studied. The outcomes indicate that the Feq3 films are of great importance for applications in organic solar cells and light emitting diodes.

Electrical conduction and photodiode properties of Au/Feq3/p-Si/al hybrid heterostructure

Thin films of iron tris(8-hydroxyquinoline) (Feq3) are prepared on p-Si substrates by thermal deposition under high vacuum. The current-voltage (I–V) curves of Au/Feq3/p-Si/Al heterojunction are recorded as a function of temperature range from 303 to 383 K at 20 K interval. The device shows rectification behavior, with room temperature ideality factor (n) and barrier height (φ) values of 2.30 and 0.81 eV, respectively. The temperature dependence of φ and n is explained in terms of barrier inhomogeneity, in which the homogenous φ value is estimated as 0.97 eV. The conduction mechanisms of the diode are determined and related parameters are evaluated The series resistance of the diode is estimated as a function of temperature. Up on illuminating the diode, the reverse current of the diode increases with increasing the impinging light intensity, from which the photosensitivity and photoconduction are determined.

A High Potential, Low Capacity Fade Rate Iron Complex Posolyte for Aqueous Organic Flow Batteries

AbstractAn iron complex, tris(4,4′‐bis(hydroxymethyl)‐2,2′‐bipyridine) iron dichloride is reported, which operates at near‐neutral pH with a redox potential of 0.985 V versus SHE. This high potential compound is employed in the posolyte of an aqueous flow battery, paired with bis(3‐trimethylammonio)propyl viologen tetrachloride in the negolyte, exhibiting an open‐circuit voltage of 1.3 V at near‐neutral pH. It demonstrates excellent cycling performance with a low temporal capacity fade rate of 0.07% per day over 35 days of cycling. The extended cycling lifetime is the result of low permeability and improved structural stability of the newly developed iron complex compared to that of the iron tris(bipyridine) complex. The combination of high redox potential and low capacity fade rate compares favorably with those of all previously demonstrated organic and organometallic aqueous posolytes. Extensive investigation into the possible degradation mechanisms, including post‐mortem chemical and electrochemical analyses, indicates that stepwise ligand dissociations of the iron complex are responsible for the reported capacity loss during cell cycling. This investigation provides unprecedented insight to guide further improvements of such metalorganic compounds for energy storage and conversion applications.

Weak Coordinating Character of Organosulfonates in Oriented Silica Films: An Efficient Approach for Immobilizing Cationic Metal-Transition Complexes.

Iron (II) tris(2,2′-bipyridine) complexes, [Fe(bpy)3]2+, have been synthesized and immobilized in organosulfonate-functionalized nanostructured silica thin films taking advantage of the stabilization of [Fe(H2O)6]2+ species by hydrogen bonds to the anionic sulfonate moieties grafted to the silica nanopores. In a first step, thiol-based silica films have been electrochemically generated on indium tin oxide (ITO) substrates by co-condensation of 3-mercaptopropyltrimethoxysilane (MPTMS) and tetraethoxysilane (TEOS). Secondly, the thiol function has been modified to sulfonate by chemical oxidation using hydrogen peroxide in acidic medium as an oxidizing agent. The immobilization of [Fe(bpy)3]2+ complexes has been performed in situ in two consecutive steps: (i) impregnation of the sulfonate functionalized silica films in an aqueous solution of iron (II) sulfate heptahydrate; (ii) dipping of the iron-containing mesostructures in a solution of bipyridine ligands in acetonitrile. The in situ formation of the [Fe(bpy)3]2+ complex is evidenced by its characteristic optical absorption spectrum, and elemental composition analysis using X-ray photoelectron spectroscopy. The measured optical and electrochemical properties of immobilized [Fe(bpy)3]2+ complexes are not altered by confinement in the nanostructured silica thin film.

Chiral control of spin-crossover dynamics in Fe(II) complexes.

Iron-based spin-crossover complexes hold tremendous promise as multifunctional switches in molecular devices. However, real-world technological applications require the excited high-spin state to be kinetically stable-a feature that has been achieved only at cryogenic temperatures. Here we demonstrate high-spin-state trapping by controlling the chiral configuration of the prototypical iron(II)tris(4,4'-dimethyl-2,2'-bipyridine) in solution, associated for stereocontrol with the enantiopure Δ- or Λ-enantiomer of tris(3,4,5,6-tetrachlorobenzene-1,2-diolato-κ2O1,O2)phosphorus(V) (P(O2C6Cl4)3- or TRISPHAT) anions. We characterize the high-spin-state relaxation using broadband ultrafast circular dichroism spectroscopy in the deep ultraviolet in combination with transient absorption and anisotropy measurements. We find that the high-spin-state decay is accompanied by ultrafast changes of its optical activity, reflecting the coupling to a symmetry-breaking torsional twisting mode, contrary to the commonly assumed picture. The diastereoselective ion pairing suppresses the vibrational population of the identified reaction coordinate, thereby achieving a fourfold increase of the high-spin-state lifetime. More generally, our results motivate the synthetic control of the torsional modes of iron(II) complexes as a complementary route to manipulate their spin-crossover dynamics.

Crystal Structure of a Mononuclear Iron(III) Complex, Hexakis(dimethylformamide-κ<i>O</i>)iron(III) Tris(hexafluoridophosphate)

Crystal Structure of a Mononuclear Iron(III) Complex, Hexakis(dimethylformamide-κ<i>O</i>)iron(III) Tris(hexafluoridophosphate)

Benchmarking Plane Waves Quantum Mechanical Calculations of Iron(II) Tris(2,2′-bipyridine) Complex by X-ray Absorption Spectroscopy

In this work, we used, for the first time, a computational Self-Consistent Field procedure based on plane waves to describe the low and high spin conformational states of the complex [Fe(bpy)3]2+. The results obtained in the study of the minimum energy structures of this complex, a prototype of a wide class of compounds called Spin Cross Over, show how the plane wave calculations are in line with the most recent studies based on gaussian basis set functions and, above all, reproduce within acceptable errors the experimental spectra of X-ray absorption near-edge structure spectroscopy (XANES). This preliminary study shows the capabilities of plane wave methods to correctly describe the molecular structures of metal-organic complexes of this type and paves the way for future even complex computational simulations based on the energy gradient, such as Nudge Elastic Band or ab-initio Born-Oppenheimer molecular dynamics.

Switching of shifting and relaxational NMR-thermosensor properties of iron (II) tris-(pyrazol-1-yl) methane complexes due to spin-crossover

The processes of spin-crossover (SCO) transition in the solid phase and in the solution for complexes of [Fe(HC(Pz)3)2](CF3SO3)2 and [Fe(HC(Pz)3)2]SiF6 were studied by UV–vis-spectrometry and NMR methods. According to NMR, the both complexes in solution showed the monotonic decrease in the fraction of the low-spin (LS) state and the increase in the fraction of the high-spin (HS) state when the temperature increases from 295 to 360 K. The observed chemical shifts and signal half-widths change significantly on temperature, despite the fact that the fraction of the HS form increases with rising temperature not so sharp as in the solid phase. The increased in temperature sensitivity of the observed chemical shifts in comparison with the temperature sensitivity of the “pure” HS and LS forms is caused by a growth in the relative population of the HS form with temperature rising. The significant temperature dependences of the observed chemical shifts and signal half-widths are suggested to use for temperature control in liquid media using NMR and MRI.

ЕFFECT OF IRON AND NICKEL DITHIOCARBAMATES ON THE PROPERTIES OF MODIFIED POLYURETHANES

The effect of modifiers - nickel bis(N,N-dimethyldithiocarbamate) (DTC-Ni) and iron tris(N, N-dimethyldithiocarbamate) (DTC-Fe) depending on their content on the structural peculiarities of polyurethane matrix based on polyoxytetramethylene glycol-1000 4,4’-diphenylmethane diisocyanate and 1,4-butanediol has been studied. The method of IR spectroscopy according to the results of NH groups’, C = O- and COC fragments’ association has shown the structuring effect of modifiers due to the PU matrix coordination. The processes of photolysis occurred as a result of exposure of PU under the conditions of the climate chamber have been also studied by IR spectroscopy method. The influence of modifiers and their content on the modified polyurethanes density has been investigated. The planar structure of DTC-Ni has shown to contribute to the density increase of modified PU as the result of polymer chain coordination, while the spherical structure of DTC-Fe - causes a density decrease due to steric hindrances in the implementation of H-bonds. Modification of polyurethanes with both nickel bis (N, N-dimethyldithiocarbamate) and iron tris (N, N-dimethyldithiocarbamate) as well as UV irradiation and moisture under the conditions of the climatic chamber contribute to the increase of water absorption. Studies of the strength properties of modified polyurethanes in comparison with the matrix under the conditions of the climate chamber have established the photosensitizing effect of nickel and iron dithiocarbamates. By studying the mass of samples of PU-DTС-Fe/Ni after extraction with dimethylformamide in the Soxhlet apparatus it has been found an increase in the level of gel fraction (0.29 - 1.58%) with increasing the modifier content, which confirms the presence of a network structure of modified PU due to radical processes taking place during destruction with the modifier participation. The influence of alkaline and acidic media on the destruction level of both modified polyurethanes and their analogues depending on the modifier content under the influence of climatic chamber conditions has been studied. Comparative derivatographic studies in air of weight loss of modified polyurethanes have confirmed the structuring and thermostabilizing effect of DTC-Ni on the PU matrix due to the probable difficulty of oxygen diffusion to the polymer volume, while the spatial structure of PU-DTC-Fe reduces the thermal stability.

Reductions of M{N(SiMe3)2}3 (M = V, Cr, Fe): Terminal and Bridging Low-Valent First-Row Transition Metal Hydrido Complexes and "Metallo-Transamination".

The reaction of the vanadium(III) tris(silylamide) V{N(SiMe3)2}3 with LiAlH4 in diethyl ether gives the highly unstable mixed-metal polyhydride [V(μ2-H)6[Al{N(SiMe3)2}2]3][Li(OEt2)3] (1), which was structurally characterized. Alternatively, performing the same reaction in the presence of 12-crown-4 affords a rare example of a structurally verified vanadium terminal hydride complex, [VH{N(SiMe3)2}3][Li(12-crown-4)2] (2). The corresponding deuteride 2D was also prepared using LiAlD4. In contrast, no hydride complexes were isolated by reaction of M{N(SiMe3)2}3 (M = Cr, Fe) with LiAlH4 and 12-crown-4. Instead, these reactions afforded the anionic metal(II) complexes [M{N(SiMe3)2}3][Li(12-crown-4)2] (3, M = Cr; 4, M = Fe). The reaction of the iron(III) tris(silylamide) Fe{N(SiMe3)2}3 with lithium aluminum hydride without a crown ether gives the "hydrido inverse crown" complex [Fe(μ2-H){N(SiMe3)2}2(μ2-Li)]2 (5), while treatment of the same trisamide with alane trimethylamine complex gives the iron(II) polyhydride complex Fe(μ2-H)6[Al{N(SiMe3)2}2]2[Al{N(SiMe3)2}(NMe3)] (6). Complexes 2-6 were characterized by X-ray crystallography, as well as by infrared, electronic, and 1H and 13C (complex 6) NMR spectroscopies. Complexes 1 and 6 are apparently formed by an unusual "metallo-transamination" process.

Iron-Based, Symmetric, Non-Aqueous Redox Flow Battery

The redox flow battery (RFB) is a promising technology for the long-duration storage of energy from domestic- to utility-scale. A RFB stores charge in a liquid electrolyte that is charged and discharged in an electrochemical cell reactor. Since storage and reaction site are separated, energy and power of the system can be scaled independently via electrolyte tank and cell stack dimensions. Iron as one of earth’s most abundant elements is an attractive active material, especially in symmetric RFBs using the same electrolyte on both negative and positive side of the battery. One way to realize such a system is by combining iron with redox-active ligands in non-aqueous solvents.[1],[2] We study the iron tris(2,2’-bipyridine) complex which shows a metal-centred reversible oxidation and three ligand-based reductions that are solvent-dependent.[3] The influence of electrolyte composition on charge and discharge reactions as well as on viscosity and conductivity is further investigated. Charge-discharge cycling experiments are carried out in 3-electrode H-cell and flow cell setups. We determine failure modes for the positive side due to electrode kinetics and for the negative side due to solubility changes. We propose improvements to this non-aqueous RFB system based on the selection of electrode materials and cycling conditions.[1] J. Mun et al., J. Electrochem. Soc. 2018, 165, 215-219.[2] C. X. Cammack et al., DaltonTrans . 2021, 50, 858.[3] D. M. Cabral, P. C. Howlett, D. R. MacFarlane, Electrochim. Acta 2016, 220, 347-353.

Enhanced Fe3+ binding through cooperativity of 3-hydroxypyridin-4-one groups within a linear co-polymer: wrapping effect leading to superior antimicrobial activity.

To tackle the rise of antibiotic resistant pathogenic microbes, iron withdrawal agents have shown considerable promise as antibiotic alternatives due to the microbes' irreplaceable metabolic need for the essential element iron. DIBI is a water-soluble, linear co-polymer functionalized with 3-hydroxy-pyridin-4-one (HPO) chelators that selectively and strongly bind iron(III) in biological environments. Compared to HPO congeners, DIBI has over 1000 times higher antimicrobial activity against a broad-spectrum of Gram-(+) and Gram-(-) bacteria including highly antibiotic resistant clinical isolates. Herein, we explain the enhanced antimicrobial activity of DIBI by a cooperativity effect of the linear co-polymer wrapping around three iron(III) centres. DIBI's structural and iron(III) binding properties were investigated by comparative experiments against HPO monomer and deferiprone using chemical and physical characterization methods with direct biological implications such as pH stability, reductive off-loading of bound iron(III), trans-membrane permeability, and competition experiments with vertebrate transferrin class iron carrier. The three iron(III) ions bound to DIBI are preferentially incorporated into a tris-bidentate chelates, which forces the linear backbone of the polymer to wrap around the complexes, as the bound iron was much less susceptible to dithionite reduction than the tris iron(III) complexes of HPO monomers and deferiprone. The results suggest a high degree of cooperativity of the polymer-bound HPO groups to effect a wrapping of the polymer backbone around the chelated iron, shielding the iron(III) centres from ready access by microbes. The structural effect of DIBI is compared to polymers containing 3-hydroxy-pyridin-4-one chelators that do not undergo this wrapping effect.

Quantification and spatial resolution of silver nanoparticles in cotton textiles by surface-enhanced Raman spectroscopy (SERS)

For its powerful antimicrobial properties, nanosilver is the most widely used nanoparticle in commercial odor-neutralizing and anti-infective textiles. However, the recent prevalent use of nanosilver has prompted concerns for the potential adverse human and environmental effects caused from the leaching of nanosilver during usage and laundering, necessitating innovative strategies in characterizing nanosilver on textile substrates. This study investigated the viability of surface-enhanced Raman spectroscopy (SERS) as an analytical method for the characterization and quantification of nanosilver (silver nanoparticles, 12.4 ± 5.1 nm) in cotton. Two indicators, iron (III) tris (dimethyldithiocarbamate) (ferbam) and rhodamine 6G (R6G) were used to compare how efficiently they bind onto nanosilver incorporated into cotton (nanosilver-cotton) and exhibit signature SERS responses. Comparing the SERS spectra of the two indicators, R6G was found to be more appropriate for nanosilver-cotton. The solvent system for R6G was important in enhancing the SERS intensity in the cotton medium – the intensity obtained from water was nearly threefold greater than those from methanol and the 50:50 mixture of water and methanol. A linear correlation (R2 = 0.9761) between the intensity at 1503 cm−1 of R6G and the concentration of nanosilver in cotton was developed and was validated by analyzing the washing stability of nanosilver-cotton fabrics through simulated laundering cycles. The technique was also successfully applied to spatially resolve the distribution and aggregation of nanosilver on textile fabrics by mapping a coffee-ring deposition produced by the surface application of nanosilver to textile samples of raw cotton, scoured raw cotton, and 50:50 and 80:20 blends of polyester-cotton. These results validate SERS as a rapid and facile tool for monitoring the dispersion and concentration of nanosilver on textiles after application and laundering.

Electrocatalytic Ammonia Oxidation Mediated by a Polypyridyl Iron Catalyst

Electrocatalytic ammonia oxidation (AO) mediated by iron(II) tris(2-pyridylmethyl)amine (TPA) bis-ammine triflate, [(TPA)Fe(NH3)2]OTf2, is reported. Interest in (electro)catalytic AO is growing rap...

Dynamic Light Scattering and Image Analysis of FePt Based Nanoparticles from Size-Selective Precipitation

Nanoseparation was performed on iron-platinum based nanoparticles from the reaction between iron(III) tris(2,2,6,6-tetramethyl-3,5-heptanedionate) and platinum(II) acetylacetonate. Dynamic Light Scattering (DLS) provided a rapid and effective technique to monitor the classification of these polydisperse nanoparticles. After the size-selective precipitation, the nanoparticles were separated into 2 groups with different hydrodynamic diameters. In additions, the storage time and additional surfactants also increased the size distribution of nanoparticles. After the repeated size-selective precipitation, the hydrodynamic diameter was reduced to 7.8 nm and the particle diameter of 3.4 nm was averaged from Transmission Electron Microscopy (TEM). Furthermore, the TEM image processing was used to demonstrate the correlation between the size distribution of nanoparticles from the repeated size-selective precipitation and their self-assembly on liquid as well as solid substrates.

Nitrogenase-Relevant Reactivity of a Synthetic Iron-Sulfur-Carbon Site.

Simple synthetic compounds with only S and C donors offer a ligation environment similar to the active site of nitrogenase (FeMoco) and thus demonstrate reasonable mechanisms and geometries for N2 binding and reduction in nature. We recently reported the first example of N2 binding at a mononuclear iron site supported by only S and C donors. In this work, we report experiments that examine the mechanism of N2 binding in this system. The reduction of an iron(II) tris(thiolate) complex with 1 equiv of KC8 leads to a thermally unstable intermediate, and a combination of Mössbauer, EPR, and X-ray absorption spectroscopies identifies it as a high-spin (S = 3/2) iron(I) species that maintains coordination of all three sulfur atoms. DFT calculations suggest that this iron(I) intermediate has a pseudotetrahedral geometry that resembles the S3C iron coordination environment of the belt iron sites in the resting state of the FeMoco. Further reduction to the iron(0) oxidation level under argon causes the dissociation of one of the thiolate donors and gives an η6-arene species which reacts with N2. Thus, in this system the loss of thiolate and binding of N2 require reduction beyond the iron(I) level to the iron(0) level. Further reduction of the iron(0)-N2 complex gives a reactive, formally iron(-I) species. Treatment of the putative iron(-I) complex with weak acids gives low yields of ammonia and hydrazine, demonstrating that these nitrogenase products can be generated from N2 at a synthetic Fe-S-C site. Catalytic N2 reduction is not observed, which is attributed to protonation of the supporting ligand and degradation of the complex via ligand dissociation. Identification of the challenges in this system gives insight into the design features needed for functional biomimetic complexes.

Crystal structures and spectroscopic characterization of MBr2(CNXyl)n (M = Fe and Co, n = 4; M = Ni, n = 2; Xyl = 2,6-dimethylphenyl), and of formally zero-valent iron as a cocrystal of Fe(CNXyl)5 and Fe2(CNXyl)9.

Structures and spectroscopic characterization of the divalent complexes cis-dibromidotetrakis(2,6-dimethylphenyl isocyanide)iron(II) dichloromethane 0.771-solvate, [FeBr2(C9H9N)4]·0.771CH2Cl2 or cis-FeBr2(CNXyl)4·0.771CH2Cl2 (Xyl = 2,6-dimethylphenyl), trans-dibromidotetrakis(2,6-dimethylphenyl isocyanide)iron(II), [FeBr2(C9H9N)4] or trans-FeBr2(CNXyl)4, trans-dibromidotetrakis(2,6-dimethylphenyl isocyanide)cobalt(II), [CoBr2(C9H9N)4] or trans-CoBr2(CNXyl)4, and trans-dibromidobis(2,6-dimethylphenyl isocyanide)nickel(II), [NiBr2(C9H9N)2] or trans-NiBr2(CNXyl)2, are presented. Additionally, crystals grown from a cold diethyl ether solution of zero-valent Fe(CNXyl)5 produced a structure containing a cocrystallization of mononuclear Fe(CNXyl)5 and the previously unknown dinuclear [Fe(CNXyl)3]2(μ2-CNXyl)3, namely pentakis(2,6-dimethylphenyl isocyanide)iron(0) tris(μ2-2,6-dimethylphenyl isocyanide)bis[tris(2,6-dimethylphenyl isocyanide)iron(0)], [Fe(C9H9N)5][Fe2(C9H9N)9]. The (M)C-N-C(Xyl) angles of the isocyanide ligand are nearly linear for the metals in the +2 oxidation state, for which the ligands function essentially as pure donors. The νCN stretching frequencies for these divalent metal isocyanides are at or above that of the free ligand. Relative to FeII, in the structure containing iron in the formally zero-valent oxidation state, the Fe-C bond lengths have shortened, the C[triple-bond]N bond lengths have elongated, the (M)C-N-C(Xyl) angles of the terminal CNXyl ligands are more bent, and the νCN stretching frequencies have shifted to lower energies, all indicative of substantial M(dπ)→π* backbonding.

Crystal Structure of a Mononuclear Iron(III) Complex, Hexakis(dimethylsulfoxide-κ<i>O</i>)iron(III) Tris(hexafluoridophosphate)

Crystal Structure of a Mononuclear Iron(III) Complex, Hexakis(dimethylsulfoxide-κ<i>O</i>)iron(III) Tris(hexafluoridophosphate)

Characterization of the Earliest Intermediate of Fe-N2Protonation: CW and Pulse EPR Detection of an Fe-NNH Species and Its Evolution to Fe-NNH2+

Iron diazenido species (Fe(NNH)) have been proposed as the earliest intermediates of catalytic N2-to-NH3 conversion (N2RR) mediated by synthetic iron complexes and relatedly as intermediates of N2RR by nitrogenase enzymes. However, direct identification of such iron species, either during or independent of catalysis, has proven challenging owing to their high degree of instability. The isolation of more stable silylated diazenido analogues, Fe(NNSiR3), and also of further downstream intermediates (e.g., Fe(NNH2)), nonetheless points to Fe(NNH) as the key first intermediate of protonation in synthetic systems. Herein we show that low-temperature protonation of a terminally bound Fe-N2- species, supported by a bulky trisphosphinoborane ligand (ArP3B), generates an S = 1/2 terminal Fe(NNH) species that can be detected and characterized by continuous-wave (CW) and pulse EPR techniques. The 1H-hyperfine for ArP3BFe(NNH) derived from the presented ENDOR studies is diagnostic for the distally bound H atom ( aiso = 16.5 MHz). The Fe(NNH) species evolves further to cationic [Fe(NNH2)]+ in the presence of additional acid, the latter being related to a previously characterized [Fe(NNH2)]+ intermediate of N2RR mediated by a far less encumbered iron tris(phosphine)borane catalyst. While catalysis is suppressed in the present sterically very crowded system, N2-to-NH3 conversion can nevertheless be demonstrated. These observations in sum add support to the idea that Fe(NNH) plays a central role as the earliest intermediate of Fe-mediated N2RR in a synthetic system.

Determination of Adsorbates on the Surface of Polymer with Low Absorption Capacity by Thermal Lens Spectrometry

Thermal lens spectrometry in a coaxial configuration is used for the direct determination of adsorbates on a planar surface of polyethylene terephthalate (PET). A possibility of the direct measurement of the rate of adsorption from solutions and the determination of the parameters of the adsorbed layer is demonstrated by the example of an investigation of the adsorption of iron(II) tris(1,10-phenantrolinate) on a PET surface. The adsorption isotherm of iron(II) tris(1,10-phenantrolinate) on the PET surface is described by the Langmuir equation and is linear in the concentration range in solution from 0.02 to 0.7 mM. The method for calculating the thermal perturbation in surface-absorbing solids was used to interpret the results of the adsorption study, and a possibility of determining iron(II) tris(1,10-phenantrolinate) on the surface at a level smaller than a monolayer was shown. Thermal lens spectrometry enables the determination of the absorption of the surface layer at a level up to 5 × 10–5 absorbance units, which corresponds to the surface concentration of iron(II) tris(1,10-phenanthrolinate) 2 × 10–13 mol/cm2. Using the example of the adsorption of 4-(2-pyridylazo) resorcinol on the PET surface, it is demonstrated that, in the case of strong absorption of the surface layer, the thermal destruction of substance and the deformation of the substrate may occur. A local increase in temperature in the layer is also confirmed by theoretical calculations.