Absorption Bands Research Articles

Spectator Exciton Effects in Nanocrystals III: Unveiling the Stimulated Emission Cross Section in Quantum Confined CsPbBr3 Nanocrystals.

Quantifying stimulated emission in semiconductor nanocrystals (NCs) remains challenging due to masking of its effects on pump-probe spectra by excited state absorption and ground state bleaching signals. The absence of this defining photophysical parameter in turn impedes assignment of band edge electronic structure in many of these important fluorophores. Here we employ a generally applicable 3-pulse ultrafast spectroscopic method coined the "Spectator Exciton" (SX) approach to measure stimulated-emission efficiency in quantum confined inorganic perovskite CsPbBr3 NCs, the band edge electronic structure of which is the subject of lively ongoing debate. Our results show that in 5-6 nm CsPbBr3 NCs, a single exciton bleaches more than half of the intense band edge absorption band, while the cross section for stimulated emission from the same state is nearly 6 times weaker. Discussion of these findings in light of several recent electronic structure models for this material proves them unable to simultaneously explain both measures, proving the importance of this new input to resolving this debate. Along with femtosecond time-resolved photoluminescence measurements on the same sample, SX results also verify that biexciton interaction energy is intensely attractive with a magnitude of ∼80 meV. In light of this observation, our previous suggestion that biexciton interaction is repulsive is reassigned to hot phonon induced slowdown of carrier relaxation leading to direct Auger recombination from an excited state. The mechanism behind the extreme slowing of carrier cooling after several stages of exciton recombination remains to be determined.

Infrared Spectroscopy of SARS-CoV-2 Viral Protein: from Receptor Binding Domain to Spike Protein.

Spike (S) glycoprotein is the largest structural protein of SARS-CoV-2 virus and the main one involved in anchoring of the host receptor ACE2 through the receptor binding domain (RBD). S protein secondary structure is of great interest for shedding light on various aspects, from functionality to pathogenesis, finally to spectral fingerprint for the design of optical biosensors. In this paper, the secondary structure of SARS-CoV-2 S protein and its constituting components, namely RBD, S1 and S2 regions, are investigated at serological pH by measuring their amide I infrared absorption bands through Attenuated Total Reflection Infrared (ATR-IR) spectroscopy. Experimental data in combination with MultiFOLD predictions, Define Secondary Structure of Proteins (DSSP) web server and Gravy value calculations, provide a comprehensive understanding of RBD, S1, S2, and S proteins in terms of their secondary structure content, conformational order, and interaction with the solvent.

Growth, thermal, spectroscopy and 2.8 μm laser performance of Er:LuYGG crystal

A novel mid-infrared (Er0.3Lu0.1Y0.6)3Ga5O12 laser crystal is successfully grown by the Czochralski method, the crystal structure, segregation coefficient, thermal performance, spectroscopy and 2.8 μm laser performance are studied systematically. The crystal possesses a pure garnet phase with a thermal conductivity of 4.54 W m−1 K−1. It exhibits a broader absorption band around 966 nm and some strong emission peaks at 2.6–3 μm, corresponding to the absorption cross-section of 1.39 × 10−21 cm2 at 966 nm and emission cross-section of 1.25 × 10−20 cm2 at 2822 nm, respectively. The level lifetimes of 4I11/2 and 4I13/2 are fitted to be 0.885 and 3.203 ms. A LD end-pumped Er:LuYGG laser has been demonstrated, achieving a maximum output power of 339 mW and a slope efficiency of 17.77 %. The primary laser wavelength is centered at 2824.76 nm. All the results indicate that the Er:LuYGG crystal is a novel and promising crystal material to realize the 3 μm laser.

First-Principles Modeling of the Absorption Spectrum of Crystal Violet in Solution: The Importance of Environmentally Driven Symmetry Breaking.

Theoretical spectroscopy plays a crucial role in understanding the properties of the materials and molecules. One of the most promising methods for computing optical spectra of chromophores embedded in complex environments from the first principles is the cumulant approach, where both (generally anharmonic) vibrational degrees of freedom and environmental interactions are explicitly accounted for. In this work, we verify the capabilities of the cumulant approach in describing the effect of complex environmental interactions on linear absorption spectra by studying Crystal Violet (CV) in different solvents. The experimental absorption spectrum of CV strongly depends on the nature of the solvent, indicating strong coupling to the condensed-phase environment. We demonstrate that these changes in absorption line shape are driven by an increased splitting between absorption bands of two low-lying excited states that is caused by a breaking of the D3 symmetry of the molecule and that in polar solvents, this symmetry breaking is mainly driven by electrostatic interactions with the condensed-phase environment rather than distortion of the structure of the molecule, in contrast with conclusions reached in a number of previous studies. Our results reveal the importance of explicitly including a counterion in the calculations in nonpolar solvents due to electrostatic interactions between CV and the ion. In polar solvents, these interactions are strongly reduced due to solvent screening effects, thus minimizing the symmetry breaking. Computed spectra in methanol are found to be in reasonable agreement with the experiment, demonstrating the strengths of the outlined approach in modeling strong environmental interactions.

Mechanism and kinetics of polycarbonate synthesized from isosorbide: Identification on the reactivity of terminal groups

AbstractChallenges in the mechanistic and kinetic study on the polymerization with multiple functional monomers hinder the scale‐up for the controllable reaction process. Herein, poly (isosorbide carbonate) synthesized from isosorbide (ISB) was employed to investigate the reaction behavior of functional monomers during polymerization. DFT calculations not only determined the energetically preferable pathways but also provided explanations for the significant differences between terminal groups at the molecular level. Subsequently, the characteristic absorption bands were detected from 1000 to 1100 cm−1 for hydroxyls on ISB, providing a quantitative measure for asymmetric hydroxyls. The reaction network indicated that the reactivity was dominated by the types of terminal groups instead of the chain length. Thereafter, a functional group model with six kinetic parameters was built, acting a crucial role in reaction control and reactor design. This method can be promoted to other functional monomers, conducing to the industrialization of high‐performance polymers.

An Ultra-Wideband Frequency Selective Rasorber with Low Infrared Emissivity

The paper proposes an ultra-wideband frequency selective rasorber (FSR) with low infrared emissivity for the composite detection threat of both radars and infrared sensors. Firstly, the equivalent circuit (EC) method based on transmission line (TL) theory is utilized to analyze the absorption/transmission conditions. Then, based on the analysis above, sinusoidal microstrip lines with non-frequency-varying characteristics are adopted in the design, which significantly enhances the transmission bandwidth of FSR. The FSR demonstrates an absorption band ranging from 2.65 GHz to 8.80 GHz and a transmission band ranging from 9.15 GHz to 17.71 GHz. Furthermore, an infrared shielding layer (IRSL) exhibiting low emissivity in the infrared band and high transmittance in the microwave band is applied to the FSR. The simulation and experiment results verify that the IRSL-FSR demonstrates an ultra-wide transmission band ranging from 9.16 GHz to 17.94 GHz and an ultra-wide absorption band ranging from 2.66 GHz to 8.01 GHz. Additionally, it exhibits a low emissivity value (0.23) in 8–14 μm, providing a viable solution to the formidable challenge of radar-infrared bistealth for satellites and other communication-enabled flying platforms.

Non-destructive diagnosis of Inflammatory Bowel Disease by near-infrared spectroscopy and aquaphotomics

Inflammatory Bowel Disease includes Crohn's Disease and Ulcerative Colitis. Currently, diagnosing involves a series of current diagnostic methods that are invasive, time-consuming, and expensive. Near-infrared spectroscopy and aquaphotomics can detect changes in biofluids and thus have the potential to diagnose disease. This study aimed to investigate the diagnostic ability of near infrared spectroscopy and aquaphotomics for Inflammatory Bowel Disease and its types. This method used blood plasma and saliva samples absorbance spectrum and multivariate analysis with the Principal Component Analysis and, Linear Discriminant Analysis, Quadratic Discriminant Analysis, and Support Vector Machine in the range 1300–1600 nm and 12 water absorbance bands in this range, separately. In the near-infrared range, total accuracy of 100% led to the separation of the healthy group and Inflammatory Bowel Disease and then the separation of the healthy group and patients with Ulcerative Colitis and Crohn's Disease. The aquaphotomics approach was used to investigate the changes in the 12 water absorbance bands and their impact on the accuracy of the diagnostic method. Aquaphotomics also detected 100% of the mentioned samples. We achieved a fast, accurate, non-invasive method based on near-infrared spectroscopy and aquaphotomics to diagnose Inflammatory Bowel Disease and its types using blood plasma or saliva samples. The current study found that monitoring blood plasma or saliva using near-infrared spectra offers an opportunity to thoroughly investigate biofluids and changes in their water spectral patterns caused by complex physiological changes due to Inflammatory Bowel Disease and its types, and to visualize these changes using aquagram.

Environmentally sensitive fluorescence of the topical retinoid adapalene

Intrinsic fluorescence of drugs brings valuable information on their localization in the organism and their interaction with key biomolecules. In this work, we investigate the absorption and emission properties of the topical retinoid adapalene in different solvents and biological media. While the UVA/UVB absorption band does not exhibit any significant solvent-dependent behavior, a strong positive solvatochromism is observed for the emission. These results are in line with molecular modeling and simulations that show the presence of two quasi-degenerate states, i.e., a local π-π* and an intermolecular charge-transfer (ICT) state. However, molecular modeling also revealed that, whatever the solvent, at the corresponding equilibrium geometry the lowest and emissive excited state is the local π-π*. Finally, the potential of adapalene to act as a biological probe is demonstrated using albumin, DNA and micelles.

Diagnostic features of rutile and cassiterite from heavy mineral concentrate samples, according to the IR microscopy data

Based on the study of rutile and cassiterite grains, using Fourier transform infrared microscopy, a new method for their determination in heavy mineral concentrate samples has been developed. The natural vibrations of the crystal lattice of these minerals are predominantly inactive in the infrared spectrum, which complicates their identification. Rutile is proposed to be determined by the absorption band ~ 1062 cm-1; and cassiterite, by the lines 1059–1065, ~ 1130, 1217–1220, and 1366–1373 cm-1. The characteristic absorption bands in the region of 3200–3400 cm-1, associated with vibrations of OH defects in the crystal lattice of these minerals, have been shown to be of particular importance for the diagnosis of rutile and cassiterite. Structural hydroxyl groups in the spectra are manifested in rutile by a line at about 3279–3283 cm-1; and in cassiterite, by lines at about 3254–3259 cm-1, ~ 3343 and ~ 3377 cm-1.

Environmentally sensitive fluorescence of the topical retinoid adapalene

Intrinsic fluorescence of drugs brings valuable information on their localization in the organism and their interaction with key biomolecules. In this work, we investigate the absorption and emission properties of the topical retinoid adapalene in different solvents and biological media. While the UVA/UVB absorption band does not exhibit any significant solvent-dependent behavior, a strong positive solvatochromism is observed for the emission. These results are in line with molecular modeling and simulations that show the presence of two quasi-degenerate states, i.e., a local π-π* and an intermolecular charge-transfer (ICT) state. However, molecular modeling also revealed that, whatever the solvent, at the corresponding equilibrium geometry the lowest and emissive excited state is the local π-π*. Finally, the potential of adapalene to act as a biological probe is demonstrated using albumin, DNA and micelles.

Enhancing overall performance of thermophotovoltaics via deep reinforcement learning-based optimization

Thermophotovoltaic (TPV) systems can be used to harvest thermal energy for thermoelectric conversion with much improved efficiency and power density compared with traditional photovoltaic systems. As the key component, selective emitters (SEs) can re-emit tailored thermal radiation for better matching with the absorption band of TPV cells. However, current designs of the SEs heavily rely on empirical design templates, particularly the metal-insulator-metal (MIM) structure, and lack of considering the overall performance of TPV systems and optimization efficiency. Here, we utilized a deep reinforcement learning (DRL) method to perform a comprehensive design of a 2D square-pattern metamaterial SE, with simultaneous optimization of material selections and structural parameters. In the DRL method, only the database of refractory materials with gradient refraction indexes needs to be prepared in advance, and the whole design roadmap will automatically output the SE with optimal Figure-of-Merit (FoM) efficiently. The optimal SE is composed of a novel material combination of TiO2, Si, and W substrate, with its thickness and structure precisely optimized. Its emissivity spectra match well with the external quantum efficiency curve of the GaSb cell. Consequently, the overall performance of TPV is significantly enhanced with an output power density of 5.78 W/cm2, an energy conversion efficiency of 38.26%, and a corresponding FoM of 2.21, surpassing most existing designs. The underlying physics of optimal SE is explained by the coupling effect of multiple resonance modes. This work advances the practical application potential of TPV systems and paves the way for addressing other multi-physics optimization problems and metamaterial designs.

LOV1 protein of Pseudomonas cichorii JBC1 modulates its virulence and lifestyles in response to blue light

Bacteria perceive light signals via photoreceptors and modulate many physiological and genetic processes. The impacts played by light, oxygen, or voltage (LOV) and blue light (BL) photosensory proteins on the virulence-related traits of plant bacterial pathogens are diverse and complex. In this study, we identified LOV protein (Pc-LOV1) from Pseudomonas cichorii JBC1 (PcJBC1) and characterized its function using LOV1-deficient mutant (JBC1Δlov1). In the dark state, the recombinant Pc-LOV1 protein showed an absorption band in UV-A region with a double peak at 340 nm and 365 nm, and within the blue-region, it exhibited a main absorption at 448 nm along with two shoulder peaks at 425 nm and 475 nm, which is a typical feature of oxidized flavin within LOV domain. The adduct-state lifetime (τrec) of Pc-LOV1 was 67.03 ± 4.34 min at 25 °C. BL negatively influenced the virulence of PcJBC1 and the virulence of JBC1Δlov1 increased irrespective of BL, indicating that Pc-LOV1 negatively regulates PcJBC1 virulence. Pc-LOV1 and BL positively regulated traits relevant to colonization on plant surface, such as adhesion to the plant tissue and biofilm formation. In contrast, swarming motility, exopolysaccharide production, and siderophore synthesis were negatively controlled. Gene expression supported the modulation of bacterial features by Pc-LOV1. Overall, our results suggest that the LOV photosensory system plays crucial roles in the adaptive responses and virulence of the bacterial pathogen PcJBC1. The roles of other photoreceptors, sensing of other wavelengths, and signal networking require further investigation.

LOV1 protein of Pseudomonas cichorii JBC1 modulates its virulence and lifestyles in response to blue light

Bacteria perceive light signals via photoreceptors and modulate many physiological and genetic processes. The impacts played by light, oxygen, or voltage (LOV) and blue light (BL) photosensory proteins on the virulence-related traits of plant bacterial pathogens are diverse and complex. In this study, we identified LOV protein (Pc-LOV1) from Pseudomonas cichorii JBC1 (PcJBC1) and characterized its function using LOV1-deficient mutant (JBC1Δlov1). In the dark state, the recombinant Pc-LOV1 protein showed an absorption band in UV-A region with a double peak at 340 nm and 365 nm, and within the blue-region, it exhibited a main absorption at 448 nm along with two shoulder peaks at 425 nm and 475 nm, which is a typical feature of oxidized flavin within LOV domain. The adduct-state lifetime (τrec) of Pc-LOV1 was 67.03 ± 4.34 min at 25 °C. BL negatively influenced the virulence of PcJBC1 and the virulence of JBC1Δlov1 increased irrespective of BL, indicating that Pc-LOV1 negatively regulates PcJBC1 virulence. Pc-LOV1 and BL positively regulated traits relevant to colonization on plant surface, such as adhesion to the plant tissue and biofilm formation. In contrast, swarming motility, exopolysaccharide production, and siderophore synthesis were negatively controlled. Gene expression supported the modulation of bacterial features by Pc-LOV1. Overall, our results suggest that the LOV photosensory system plays crucial roles in the adaptive responses and virulence of the bacterial pathogen PcJBC1. The roles of other photoreceptors, sensing of other wavelengths, and signal networking require further investigation.

Photoluminescence emission enhancement in the LiSrVO4:Eu3+ vanadate phosphor by partial substitution of M+ ions (M+=Li+/Na+/K+); optical thermometry; and optical transition probabilities using Judd-Ofelt analysis

In solid state lighting (SSL), pcWLEDs gain more attention for various illumination applications. The Eu3+ activated LiSrVO4:xEu3+ (0–15 mol% in steps of 3) phosphors are prepared by the conventional solid state method and their phase formation is confirmed by PXRD. It suggest that the samples are in a monoclinic structure with P2/m space group. SEM results confirmed that the size of the prepared phosphor is in a micrometer range with an irregular spherical shape. The optical diffuse reflectance spectrum (DRS) consisted broad band absorption in the ultraviolet (UV) region (270–350 nm) and also, they are found to absorb strongly the NUV light (396 nm) and the blue light (466 nm). They exhibit the strongest emission at 617 nm for the samples under 326 nm excitation. The PL intensity of the phosphors are improved by co-doping. The optical transition probabilities of the LiSrVO4:9 mol% Eu3+ phosphor are also analyzed using the Judd-Ofelt theory. The optimized phosphor showed a good thermal stability and the lifetime values are in the millisecond range. The absolute and the relative sensitivities are obtained from the temperature dependent lifetime measurements. The LiSrVO4:9 mol%Eu3+ phosphor yielded CIE coordinates (x, y) of (0.5987, 0.4005), a low CCT of 1468K, and a color purity of 96.4 %. These results indicate the potential application of the LiSrVO4 based phosphors in WLEDs.

Surface mineral deposition and mechanical properties of one-step bonding agent with copper-modified niobium nanoparticles – An in vitro study

This study aimed to investigate the incorporation of copper-modified niobium (Nb/Cu) nanoparticles at concentrations of 0.1 % and 0.3 wt% in a one-step adhesive (PacBond Adhesive). Thirty sound human third molars were randomly divided into three groups: control, 0.1NbCu, and 0.3NbCu. Specimens were restored with PacBond and resin composite OptiComp, Composite LC. Stick specimens (0.64 mm2) were obtained and subjected to microtensile bond strength (MTBS) testing (n = 10) using a universal testing machine at a rate of 0.5 mm/min after 24 h and 6 months. Scanning electron microscope (SEM) analysis, microhardness after 24 h and immersion in ethanol (HK) (n = 7), degree of conversion (DC) (n = 6), and surface mineral deposition (n = 3) were also conducted. Data were analyzed using two-way ANOVA for MTBS and HK, and one-way ANOVA for %SHL and DC, all of them were followed by Tukey's test (p < 0.05). For MTBS, statistical difference in storage times was observed for 0.1NbCu after 24 h (p = 0.007). There was no statistical difference between the control and 0.3NbCu regarding time and materials after 24 h and 6 months (p = 0.065). There was no statistical difference among the groups for DC (p = 0.278), but there was a significant difference among the groups for the factor of time in HK measurements (p = 0.047). The 0.1NbCu and 0.3NbCu groups exhibited absorbance Bands indicative of surface mineral deposition after 14 and 21 days, and the 0.3NbCu interface showed better preservation in SEM analysis. The concentration of 0.3 % NbCu in a one-step adhesive appears promising and may offer enhanced longevity for the tooth/restoration interface.

A Donor-Acceptor Molecular Octopus and the CLICK Procedure in Columnar Liquid Crystal Phases.

Two star-shaped mesogens with a (meso-tetraphenylporphinato) zinc (II) core and bithiophene conjugated arms with 3,4,5-trisdodecyloxyphenyl periphery were synthesized. One of these molecules was decorated with four fullerenes via an aliphatic spacer. This is the sterically overcrowded compound with an octapodal morphology. The other star lacks the fullerenes and provides free space between the conjugated arms. This mesogen does not aggregate in solution, but in solid state it forms a hexagonal columnar and a highly ordered oblique helical columnar phase, while the octopus molecule assemble in an amorphous solid. Photophysical studies of the octapodal compound in solution and the solid thin film reveal the formation of J-type aggregates, in which the interaction between donors (porphyrin) and acceptors (fullerene) dominates leading to absorption bands in the NIR region of the spectra. The mixture of both compounds results in a self-assembly which is called the Click procedure. Fullerenes of the octopus nanosegregate in the pockets of the star mesogens generating hexagonal columnar structures with a regular stacking along the columnar axis. Thus providing free space is a tool to control the competition between supramolecular interactions and nanosegregation. Such liquid-crystalline donor-acceptor structures may play a role in future LC photovoltaic applications.

Coupling dielectric and magnetic components on a ternary composite for enhancing impedance matching and microwave absorption

Here in, a novel ternary manganese monoxide@nitrogen-doped carbon nanotube@cobalt composite was obtained via a scalable multistep reaction pathway. Mnganese monoxide (MnO) is adopted as the microwave transparent substrate to couple dielectric and magnetic components. The abundant internal voids of MnO and numerous interfaces between MnO and carbon can increase the dielectric loss to improve the microwave absorption (MA) performance, metal cobalt is employed as the magnetic component to enhance the magnetic loss. Benefiting from the synergistic effect of heterostructures, the ternary absorber exhibits the minimum reflection loss (RLmin) of −48.65 dB@8.1 GHz@2.8 mm and the effective absorption band (EAB) of 5.8 GHz with the thickness of 1.7 mm. Furthermore, the crystal structure, material components, surface element distribution and magnetic properties of the absorbers are characterized, the structure-performance correlation between “Physical properties” and “Electromagnetic performance” is established. Finally, the reliable MA mechanism based on “hierarchical component modulation” is summarized to guide the design of MnO-based absorbers.

Biological and Physicochemical Analysis of Sr-Doped Hydroxyapatite/Chitosan Composite Layers.

In this work results are presented on the evaluation of HAp, HApSr, HAp_CS, and HApSr_CS layers deposited on Ti substrates regarding L929 cell viability and cytotoxicity as well as antimicrobial activity against Staphylococcus aureus, in connection with their physicochemical properties. The HAp and HApSr layers generated by radio-frequency magnetron sputtering technique were further covered with chitosan by a matrix-assisted pulsed laser evaporation technique. During the plasma depositions, the Ti substrates were heated externally by a home-made oven above 100 °C. The HApSr_CS layers generated on the unpolished Ti substrates at 100 °C and 400 °C showed the highest biocompatibility properties and antimicrobial activity against Staphylococcus aureus. The morphology of the layer surfaces, revealed by scanning electron microscopy, is dependent on substrate temperature and substrate surface roughness. The optically polished surfaces of Ti substrates revealed grain-like and microchannel structure morphologies of the layers deposited at 25 °C substrate temperature and 400 °C, respectively. Chitosan has no major influence on HAp and HApSr layer surface morphologies. X-ray photoelectron spectroscopy indicated the presence of Ca 2p3/2 peak characteristic of the HAp structure even in the case of the HApSr_CS samples generated at a 400 °C substrate temperature. Fourier transform infrared spectroscopy investigations showed shifts in the wavenumber positions of the P-O absorption bands as a function of Sr or chitosan presence in the HAp layers generated at 25, 100, and 400 °C substrate temperatures.

Solar light assisted enhanced photocatalytic activity of smart ternary ZnO:TiO2:SnO2 nanocomposites

In the present study, the smart combinations of metal oxide semiconductors (ZnO:TiO2)1-x(SnO2)x (ZTS) with different SnO2 loadings (as x = 0.0, 0.30, 0.25, 0.20, coded as ZTS0, ZTS1, ZTS2, and ZTS3) were synthesized by employing the simple sol-gel technique. The structural, morphological, optical properties and elemental composition were analyzed by using XRD, Raman spectroscopy, FE-SEM, BET, UV–Vis spectroscopy, IC-PMS, XPS and FTIR of ZTS nanocomposite and proved the formation of smart ternary combination of nanocomposites. Systematic investigation through the characterization emphasised that the acute interfacial combination was established between metal oxide semiconductors. The crystallite size was decreased on adding the amount of SnO2 in the pristine ZTS0 nanocomposites from 23.5 nm to 10.5 nm which was confirmed by Scherrer's equation. The optical energy band gap of the obtained ZTS nanocomposites was found to vary from 3.23 to 3.34 eV on adding the amount of SnO2. The performance of the ZTS nanocomposites as photocatalyst was examined towards organic dyes and the results shows highest degradation of MB and MO dyes with ZTS3 achieving 99 % and 97.3 % degradation efficiency with 1 g/L loading dose. The plausible mechanism was suggested considering the visible light absorption spectra and band diagram resulting in supressed of the recombination rate of charge carriers. The smart combination of ZTS nanocomposites makes it an ideal material for excellent photocatalytic activity for degrading organic contaminants in presence of solar light irradiation.

Synthesis and properties of N-(2,2,2-tribromoethylidene)-4-chlorobenzenesulfonamide

The present work continues a systematic study to find efficient and accessible methods for the synthesis ofN-sulfonylimines of polyhaloaldehydes and to analyze their properties. In the reaction of N,N-dichlorobenzene sulfon-amide with tribromoethylene, N-(2,2,2-tribromoethylidene)amide of 4-chlorobenzenesulfonic acid was obtained for the first time with a quantitative yield at boiling water bath temperature in carbon tetrachloride medium. The infrared spectra of N-(2,2,2-tribromoethylidene)-4-chlorobenzenesulfonamide reveal the absorption bands of sulfonic (1360 and 1165 cm-1) and NH (3275 cm-1) groups, while the 1H NMR spectra show a signal for azomethine protons within the region of 8.3–8.6 ppm. The 13C NMR spectra exhibit a signal for the CBr3 group within the region of ~31–43 ppm, while the signal characteristic of the CBr2Сl group within the region of ~53–56 ppm is absent. This means that no imine of dibromochloroacetic aldehyde is formed during the reaction. Thus, an efficient method for the synthesis of N-(2,2,2-tribromoethylidene)-4-chlorobenzenesulfonamide was developed, and the chemoselectivity of this reaction was found to depend on the process temperature. It was shown that N-(2,2,2-tribromoethylidene)-4-chlorobenzenesulfonamide has amidoalkylating properties. A reaction of N-(2,2,2-tribromoethylidene)-4-chlorobenzenesulfonamide with benzene, toluene, anisole, and 2-chlorothiophene in the presence of an acid catalyst yielded p-substituted aromatic derivatives and 2,5-substituted thiophene derivatives. Infrared spectroscopy and NMR spectroscopy (1H, 13C) revealed that the substitution reaction proceeds regioselectively. All the obtained products were isolated in pure form as powders soluble in polar organic solvents and insoluble in water. The yields of 4-chloro-N-(1-phenyl-2,2,2-tribromoethyl)-benzenesulfonamide, 4-chloro-N-[1-(4-methylphenyl)-2,2,2-tribromoethyl]-benzenesulfonamide, 4-chloro-N-[1-(4-methoxyphenyl)-2,2,2-tribromoethyl]-benzene-sulfonamide, and 4-chloro-N-[2,2,2-tribromoethyl-1-(5-chloro-2-thienyl)ethyl]-benzenesulfonamide amounted to 74, 72, 64, and 74 %, respectively.