Triazole Groups Research Articles

Crystal structure of bis{5-(4-chlorophenyl)-3-[6-(1H-pyrazol-1-yl)pyridin-2-yl]-1H-1,2,4-triazol-1-ido}nickel(II) methanol disolvate

The unit cell of the title compound, [Ni(C16H10ClN6)2]·2CH3OH, consists of a neutral complex and two methanol molecules. In the complex, the two tridentate 2-(3-(4-chlorophenyl)-1H-1,2,4-triazol-5-yl)-6-(1H-pyrazol-1-yl)pyridine ligands coordinate to the central NiII ion through the N atoms of the pyrazole, pyridine and triazole groups, forming a pseudooctahedral coordination sphere. Neighbouring tapered molecules are linked through weak C—H(pz)...π(ph) interactions into monoperiodic chains, which are further linked through weak C—H...N/C interactions into diperiodic layers. The intermolecular contacts were quantified using Hirshfeld surface analysis and two-dimensional fingerprint plots, revealing the relative contributions of the contacts to the crystal packing to be H...H 32.8%, C...H/H...C 27.5%, N...H/H...N 15.1%, and Cl...H/H...Cl 14.0%. The average Ni—N bond distance is 2.095 Å. Energy framework analysis at the HF/3–21 G theory level was performed to quantify the interaction energies in the crystal structure.

A convenient approach for generating dimeric nucleic acid dyes via click-chemistry.

Fluorescent dyes are essential tools for visualizing DNA and RNA. Dimeric dyes like GelGreen have gained popularity as safer alternatives to ethidium bromide (EB) due to their reduced mutagenicity and genotoxicity. In this study, we present a straightforward method to synthesize novel acridine orange (AO)-based dimeric dyes using click chemistry. Starting from acridine orange, these dyes can be synthesized in just two steps. Compared to GelGreen, these new dyes incorporate additional triazole groups in their linkers. They exhibit a maximum absorption wavelength of approximately 472 nm, which shifts to around 503 nm upon binding with DNA, allowing excitation by blue light. These dyes show minimal fluorescence in aqueous solutions, indicating that they adopt a closed conformation where the fluorescence of acridine orange is quenched due to intramolecular aggregation. The presence of DNA significantly enhances their fluorescence at around 526 nm, suggesting that DNA binding induces an open conformation. This "light-up" property makes them highly sensitive DNA dyes with a strong signal-to-noise ratio. We successfully applied these novel dyes in agarose gel electrophoresis, where they demonstrated excellent performance.

Taming of Triazole, Tetrazole, and Azido Groups: Nitrogen-Rich Energetic Materials with High Thermal Stabilities.

Nitrogen-rich energetic materials are of interest due to their potential use as high-energy-density materials in various applications. However, most compounds with a high nitrogen content show poor thermal stabilities, which may limit their use in certain applications. In pursuit of nitrogen-rich energetic materials, this study presents the synthesis and characterization of two nitrogen rich energetic compounds, namely 3-azido-1-(1H-tetrazol-5-yl)-1H-1,2,4-triazol-5-amine (3, C3H3N11, N%: 79.78) and (E)-1,2-bis(3-azido-1-(1H-tetrazol-5-yl)-1H-1,2,4-triazol-5-yl) diazene (7, C6H2N22, N%: 80.62). Compounds 3 and 7 have high thermal stabilities of 216 and 221 °C, respectively, making them the most thermally stable among metal-free primary explosives. Additionally, they show good energetic performance (vD: 8345 m s-1; P: 25.17 GPa; vD: 8275 m s-1; P: 25.57 GPa), making them potential candidates for metal-free high energy primary explosive. The energetic salts of 3 and 7 were also investigated. Among them, hydrazinium salt 11 displays better energetic performance (vD: 9089 m s-1; P: 30.55 GPa), which was on par with those of cyclotetramethylene tetranitramine (HMX). This research contributes to the exploration of nitrogen-rich energetic materials with potential applications in various fields.

Heteroleptic Triazole-Bisoxazoline Iron Complexes Reveal Lability of the Iron-Carbene Bond Even Within a Chelating Scaffold.

N-Heterocyclic carbenes have proven to be excellent ligands for transition metals, with numerous applications in catalysis and beyond. However, they have also displayed lability with first row transition metals, largely due to the hard-soft mismatch of the metal-carbon bond. Chelation is often considered a suitable methodology for supporting the labile M-C bond through the introduction of a strongly coordinating donor site such as hard phenolates. Herein, we demonstrate that chelating phenolate-carbene ligands are kinetically labile in iron(II) complexes. Specifically, heteroleptic iron complexes [Fe(C^O)(N^N)] were synthesized composed of a phenolate-functionalized triazolylidene (CO) ligand and N,N-bidentate coordinating bisoxazoline ligand (N^N). Stability studies by 1H NMR spectroscopy showed that the heteroleptic complexes preferentially convert to their corresponding homoleptic complexes [Fe(C^O)2] and [Fe(N^N)2], indicating reversible decoordination of the carbene phenolate chelate from the iron center. The rate of this rearrangement is dependent on the substituents on the ligands and increases for triazolylidene wingtip groups mesityl (Mes) < di(isopropyl)aryl (DIPP) < adamantyl (Ad), with significant ligand redistribution for DIPP and Ad systems observed even at room temperature. The most stable heteroleptic complex featured mesityl wingtips on the triazole and phenyl groups as oxazoline substituents and displayed signs of ligand exchange only after 16 h at room temperature. This substitutional lability of carbene ligands even when supported by a phenolate chelating group has direct consequences when designing iron complexes for catalytic applications.

Bioisosteres at C9 of 2-Deoxy-2,3-didehydro-N-acetyl Neuraminic Acid Identify Selective Inhibitors of NEU3.

Human neuraminidases play critical roles in many physiological and pathological processes. Humans have four isoenzymes of NEU, making selective inhibitors important tools to investigate the function of individual isoenzymes. A typical scaffold for NEU inhibitors is 2-deoxy-2,3-didehydro-N-acetylneuraminic acid (DANA) where C9 modifications can be critical for potency and selectivity against human NEU. To design improved DANA analogues, we generated a library of compounds with either a short alkyl chain or a biphenyl substituent linked to the C9 position through one of six amide bioisosteres. Bioisostere linkers included triazole, urea, thiourea, carbamate, thiocarbamate, and sulfonamide groups. Within this library, we identified a C9 biphenyl carbamate derivative (963) that showed high selectivity and potency for NEU3 (Ki = 0.12 ± 0.01 μM). In contrast, NEU1 and NEU4 isoenzymes preferred amide and triazole linkers, respectively. Finally, analogues with urea, sulfonamide, and amide linkers showed enhanced inhibitory activity for a bacterial NEU, NanI from Clostridium perfringens.

Effect of “corona-core” structuring of poly(1-vinyl-1,2,4-triazole)–poly(acrylic acid)-Ag(I) interpolymer complexes on the radiation-induced preparation and stability of silver nanoparticles

Interpolymer complexes (IPC) of water-soluble polymers can be promising matrices for the synthesis of metal colloids. In this work, silver nanoparticles were obtained via radiation-induced reduction (under X-ray irradiation) of complexes based on poly (1-vinyl-1,2,4-triazole) (PVT) and poly (acrylic acid) (PAA) containing Ag+ ions. Particular attention was paid to the role of the supramolecular structure in the formation of nanoparticles. Combined dynamic light scattering and electrophoretic mobility measurements have revealed that, in pH range 5.5–7, micro-scale aggregates of the initial PVT-PAA-Ag(I) IPC transform into nano-sized particles consisting of a PVT-Ag(I) core electrostatically stabilized by PAA loops and tails forming a corona. It was explicitly demonstrated for the first time that such transformation of IPC aggregates can significantly enhance the efficiency of AgNPs formation. In particular, using UV-VIS spectroscopy and transmission electron microscopy, we have shown that at pH 7.0 the core of the “corona-like” form of the PVT-PAA-Ag(I) complex ensures the radiation-induced generation of AgNPs with a narrow size distribution due to the strong affinity of triazole groups to the metal surface. At the same time, the localization of the excessive negatively charged carboxylate groups in the outer part of the complex provides a long-term colloidal stability of the prepared AgNPs.

Structural diversity and properties of four coordination polymers based on a heterofunctional ligand containing both triazole and carboxyl groups

A heterofunctional ligand containing both triazole and carboxyl groups namely 5-((4-(4H-1,2,4-triazol-4-yl)phenoxy)methyl) isophthalic acid (H2L) was designed. Four CPs based on H2L have been assembled. Structural analysis indicates that [(CuL)3]·CH3OH (1) displays a three-dimensional (3D) structure with the (3,6)-connected (42.6)2(44.62.86.103) topology. [Cu(HL)2] (2) shows a (2, 4)-connected 3-fold interpenetrating grids with (82)(8.8.8.8) topology. [Zn(L)] (3) and [Cd2(L)2(H2O)0.2]·H2O (4) possesses 3D frameworks with 4, 4-connected (4·73·82)2 topology and 3, 4, 7-connected (43)(44·62)(3·46·52·67·74·8) topology, respectively. The reasons for structural diversity are analyzed in detail. In addition, the magnetic properties of 1, 2 and the fluorescence of 3 have been investigated.

Fabrication of microfibrillated cellulose from biomass by use of carbon nitride with high nitrogen/carbon ratio

Microfibrillated cellulose (MFC) as an attractive green bio-based material has attracted widespread attention in recent years due to its non-toxicity, degradability, excellent performance, and high aspect ratio. In this study, the g-C3N5 with a high nitrogen/carbon ratio was prepared as a catalyst through the self-polymerization of a nitrogen-rich precursor. The triazole groups at the edges of g-C3N5 were proven to exhibit strong adsorption to biomass and strong alkalinity. In a low-acidic aqueous system with g-C3N5, MFC with diameters of 100–200 nm and lengths up to 100 μm was fabricated from various biomasses within 5 min under microwave radiation. The ultimate yield of the MFC produced from viscose reached 90 %. Young's modulus of the MFC reaches 3.7 GPa. This work provides a particular method with high efficiency to prepare MFC with excellent properties from biomass by chemical method.

Biodegradation of Difenoconazole Using Fungal-Bacterial Consortia

Abstract Pesticides are used all over the world in agricultural operations to reduce the damage of pests and to improve the productivity of agricultural crops. The excessive use of these chemical compounds has led to the deterioration of soil and increase the level of pollution of water and air resources. Moreover, the continuous use and non-target toxicity of pesticides has become a major concern to the agricultural ecosystem that directly hinders the productivity of agricultural products. Therefore, this study aimed to isolate and identify fungal and bacterial species with the ability to biodegrade fungicide via conducting preliminary tests to find out which of them have the ability to grow in a treated medium with a fungicide Difenoconazole, which belongs to the group of the pesticides Triazoles. The fungi and bacteria that succeeded in growing were as follow Aspergillus flavus, Aspergillus ochraceus, Bacillus cereus S1 and Bacillus cereus S2 were identified by extracting their genomic DNA and applying the primers ITS and 16s rRNA for both examined fungi and bacteria, respectively. The fungi were laboratory adapted to multiple concentrations reaching the highest concentration of 550 mgL-1, while bacteria reached 1200 mgL-1 laboratory to break down the pesticide. The results of the combinations tested as the B. cereus S1 and B. cereus S2 were the fastest growing in the liquid medium PDB at the concentration of 325 mgL-1. While the combination A. flavus and B. cereus S1 had the highest biodegrading ability at the same concentration, which led to the disappearance of the pesticide Difenoconazole turbidity in the liquid medium as a result of its consumption by fungal and bacterial isolates. As for the treatment of the pesticide in the solid PDA medium to know its effect on the growth of fungi and the formation of spores, the results revealed that fungal isolates increase their vegetative growth when the concentration increases, the production of fungal spores decreases, and indicates the ability of the fungi to use the pesticide as an energy source.

Synthesis, Spectral and Electrochemical Properties, and Theoretical Studies of Highly Functionalized Fused Triazole-Isoindoline Derivatives as a Donor-Acceptor System

Triazole and propargyl group functionalities are frequently utilized in the construction of efficient blue-emitting materials, serving as acceptors and donors, respectively. Leveraging the synergistic effect of donor-acceptor coupling between these moieties, three new compounds, namely CB-But-I2, Ph-But-I2, and DP-But-I2, were synthesized. Given the advantageous strategy of combining electron donors and acceptors to optimize carrier injection and transport, CB-But-I2, Ph-But-I2, and DP-But-I2 demonstrate remarkable capabilities in both hole and electron transportation. A metal-free synthesis approach was employed to produce highly functionalized 1,2,3-triazole cores incorporating electronic donor and acceptor functionalities. This synthesis method involved the “Click reaction” ring formation between acetylene and azide compounds of 2-(4-bromobutyl) isoindoline-1,3-dione, catalyzed by copper sulfate pentahydrate and assisted by ascorbic acid as a base. The process boasts several advantages, including mild reaction conditions, accessibility of precursors, metal-free synthesis, straightforward setup, and the generation of various substituted regioselective triazole compounds in satisfactory yields. All synthesized compounds were found to possess thermal stability and exhibited fluorescence within the 292–355 nm range. Moreover, a significant positive solvato-chromic behavior was noted across different solvents with varying polarities, and the theoretical values were compared against experimental data for validation.

Novel series of hydrazones carrying pyrazole and triazole moiety: Synthesis, structural elucidation, quantum computational studies and antiviral activity against SARS-Cov-2

The novel series of hydrazones carrying both pyrazole and triazole moiety were synthesized and characterized using single crystal X-ray diffraction studies. It is found that the compound crystallizes in the triclinic system in the space group P1̅. Hirshfeld analysis was carried out to visualize the noncovalent intermolecular interactions which are responsible for molecular packing in the crystal. Further, density functional theory (DFT) calculations were used to calculate optimized molecular structure, stability, and a few of the quantum chemical parameters. Derived results are in good agreement with the experimentally obtained results. Analysis of frontier molecular orbitals (HOMO and LUMO) and their energy gap of the optimized structure revealed that the compound is stable in the gaseous state. Molecular electron densities, and electrostatic potential maps provide the reactive site and charge distribution of triazole group. Quantum theory of atoms in molecules (QTAIM) and reduced density gradient (RDG) analysis were carried out to explore the weak interactions present in the molecule. In addition, the synthesized compound was investigated as an inhibitor for SARS CoV-2 protease using in-silico molecular docking analysis to understand the mode of binding. The docking results showed the good binding score with Mpro protease 6LU7. Further, molecular dynamics (MD) were carried out for the best hit docked complexes.

Module-combinatorial design and screening of multifunctional polymers based on polyaspartic acid for DNA delivery

It is crucial to develop non-viral gene vectors that can efficiently and safely transfect plasmid DNA into cells. Low transfection efficiency and high cytotoxicity of cationic polymers hinder their application as gene carriers. Modification of cationic polymers has emerged as an attractive strategy for efficient and safe nucleic acids delivery. In this study, a simple and rapid method is developed to synthesize a series of multifunctional polymers by utilizing biodegradable polyaspartic acid as the backbone and modifying it with three modules. This one-component polymer possesses capabilities for nucleic acid condensation, cellular uptake, and endosomal escape. Polymers containing imidazole, triazole, or pyridine group exhibited promising transfection activity. Substituted with dodecylamine or 2-hexyldecan-1-amine enhance cellular uptake and subsequent transfection. Furthermore, the influence of ionizable amine side chains on gene delivery is investigated. Two optimal polymers, combined with the avian encephalomyelitis virus (AEV) plasmid vaccine, induced robust specific antibody responses and cellular immune responses in mice and chickens. Through module-combination design and screening of polyaspartamide polymers, this study presents a paradigm for the development of gene delivery vectors.

Synthesis of a charring-foaming agent containing triazine and triazole groups and its flame retardancy in PP

Synthesis of a charring-foaming agent containing triazine and triazole groups and its flame retardancy in PP

A cyanide-bridged FeII/FeIII mixed-valence chain exhibiting spin transition in the Fe(II) sites

A cyanide-bridged {FeIII2FeII}n one-dimensional chain {[Fe(Tp)(CN)3]2Fe(btb)}n (1) (Tp = hydrotris(pyrazolyl)borate, btb = 1,4-(1H-1,2,4-triazole)butane) has been synthesized via the hydrothermal reaction of Li[Fe(Tp)(CN)3], btb, and FeII(ClO4)2·6H2O at 120 °C. Single-crystal X-ray analysis reveals that compound 1 is an isolated neutral mixed-valence {FeIII2FeII}n double-zigzag chain with each [FeIII(Tp)(CN)3]− unit connecting with two Fe(II) centres via two of its three CN− groups in the cis-positions, and two triazole groups from btb coordinated with Fe(II) ion in its axial positions. Single-crystal data obtained at different temperature together with magnetic data indicate that complex 1 exhibits thermal induced spin transition in the Fe(II) sites with T1/2 ≈ 165 K. Additionally, light-induced excited spin-state trapping (LIESST) of 1 was also observed at low temperature.

Cellulose-based adsorbent using in mercury detection and removal from water via an efficient grafting strategy of fluorometric sensors by click reaction

Mercury pollution in waters attracts lots of attention due to its serious toxicity and high bioenrichment and many efforts have been devoted in the development of adsorbents for mercury detection and removal. Herein, a cellulose-based adsorbent Cell-TriA-HQ is functionalized with quinoline fluorophore by covalent immobilization through “Click reaction” with high yield. In addition to the admirable adsorptive performance, the prepared adsorbent exhibits excellent selectivity and sensitivity towards Hg (II) in water that the detection limit for Hg (II) is determined to be as low as 1.92 × 10−7 M. The sensitive fluorescence enhancement response is considered to be resulted from the inhibition of photo-induced electron transfer between triazole and quinoline groups and the reinforcement of structural rigidity. The easy manipulation along with excellent performance of adsorption capacity, detective ability and reusability for the multifunctional adsorbent makes it potential in mercury monitoring and removal from aqueous solutions in the field of water treatment.

Tuning C-N Ullmann coupling with anion-exchanged ionic liquid-functionalized nanoparticle catalysts

Modern organic chemistry demands efficient and sustainable synthetic methods. Copper-catalyzed Ullmann coupling reactions, adept at constructing biaryl and aryl-heteroaryl motifs, have gained significant traction. However, traditional methods suffer from limitations. Nanoparticle catalysts, particularly copper nanoparticles (CuNPs), offer improved efficiency, but their performance is hampered by agglomeration and leaching. Hybrid supports incorporating ionic liquids (ILs) address this issue by providing a polar environment stabilizing CuNPs and enhancing catalytic activity and selectivity. This study investigates the impact of anion exchange in ionic liquids on the catalytic performance of C-N Ullmann couplings. Anion exchange modifies interionic interactions, hydrogen bonding, and dipolar properties, ultimately influencing the reaction's outcome. We synthesized CuNPs impregnated in silica supports functionalized with a triazolium-based ionic liquid possessing different anions (BF4−, PF6−, NTf2−) to elucidate the effect of anion exchange.Characterization techniques like FT-IR, XPS, TGA, and XPS confirmed successfully incorporating the triazole group and varying anions onto the material. TEM analysis showed the presence of CuNPs (4.5–5.7 nm) impregnated on the triazole functionalized silica supports.Catalytic studies yielded fascinating insights into the impact of different anions on conversion and selectivity. Iodide (I−) promoted higher conversion (100%), while tetrafluoroborate (BF4−) offered superior selectivity (57%). Computational studies provided valuable explanations, shedding light on the reactivity of the nanostructures and the interaction mechanism between substrates and the nanocatalyst. The theoretical results suggest that coordinative covalent bonds and highly polarized interactions govern the substrate interaction, with the aniline path achieving higher stabilization.Furthermore, the choice of anion influences the reactivity, substrate stabilization, and spin density distribution. These properties directly correlate with the conversion and selectivity observed in the catalytic studies.

Intramolecular cooperation and biphasic flame retardant mode of action: Effectiveness of hexa(1,2,4-triazol-3-ylamine) cyclotriphosphazene in epoxy resin

The substitutional structure of cyclotriphosphazene derivatives significantly influences their flame-retardant effectiveness. A cyclotriphosphazene derivative with triazole group, referred to as hexa(1,2,4-triazol-3-ylamine) cyclotriphosphazene (HATA), was utilized to improve the flame retardancy of epoxy resin (EP). Differential scanning calorimetry, thermogravimetric analysis, and dynamic mechanical analysis were employed to characterize the thermal properties of EP/HATA thermosets. HATA facilitated the curing of EP due to its triazole and secondary amine structure. EP/HATA thermosets exhibited improved char-forming ability and storage modulus, attributed to the rigid cyclophosphonitrile structure of HATA. As a result of incorporating 5% HATA with 0.73 wt% phosphorus, EP passed UL-94 V-0 level. Subsequent analysis using a cone calorimeter revealed obvious reductions in the peak heat release rate, fire growth rate, and total smoke production of EP with the addition of HATA. Simultaneously, there was a significant enhancement in the char yield of EP during combustion, indicating notable improvements in fire safety. Additional investigations, including X-ray photoelectron spectroscopy, scanning electron microscopy, TG-FTIR, and pyrolysis gas chromatography/mass spectrometry, were employed to analyze the char residue and gaseous volatiles. HATA promoted the formation of a dense, continuous, and intumescent char layer containing cyclophosphonitrile structure in EP. Moreover, the decomposition of HATA released a notable quantity of nitrogen-containing volatiles, effectively mitigating flammable gases originating from the EP matrix in gaseous phase. A biphasic flame-retardant mode of action was proposed, underscoring cooperative flame-retardant effects arising from the interaction between triazole substituents and cyclophosphonitrile structure in HATA molecular for EP.

Two 2D inorganic—organic hybrid compounds containing Anderson—type polyoxometalate for electrocatalytic and capacitive performances

For constructing the compounds containing polyoxometalate with electrochemical properties, to employ 3,5 − di − [1,2,4]triazol − 1 − yl − benzonitrile (DTCN) as organic ligand, Anderson − type polyoxometalate {TeMo6O24}6− as inorganic building block, two inorganic–organic hybrid compounds were synthesized under hydrothermal condition, formulated as {M(H2O)4(DTCN)2}[M2(H2O)2(DTCN)2{TeMo6O24}]·2H2O [M = Co (1), Ni (2)]. Structural analysis indicated that two compounds have 2D structures. The {TeMo6O24}6− polyoxoanions were each other aggregated through paired transition metal centers to generate a 1D inorganic chain. The DTCN ligand played a role of bidentate linker, utilizing the nitrogen atoms of two triazole groups to link these inorganic chains into a 2D grid − like layer. Another kind of metal − organic fragments {M(H2O)4(DTCN)2}2+ were arranged in the grids. Compounds 1 and 2 displayed not only electrocatalytic activities for the reduction of Cr(VI), but also sensing activities with the limit of detection of 0.011 μM for 1 and 0.019 μM for 2, as well as capacitive performances with specific capacitances of 1297F·g−1 for 1 and 968F·g−1 for 2 at a current density of 1 A·g−1. The results might provide a potential approach for preparing polyoxometalate − based inorganic–organic hybrid compounds used as electrochemical materials.

A ratiometric fluorescent probe with 1,2,4-triazole recognition unit for fluoride ion detection based on synchronous fluorescence spectroscopy

As an important inorganic chemical with wide applications and high toxicity, the detection of fluoride-containing products and environmental samples has gained the most interest. In this work, a ratiometric fluorescent probe (NIN2) is constructed with a triazole group as the new recognition site for the detection of F−. The synchronous fluorescence technology was introduced to obtain the well discrimination of two emission bands. The value of wavelength intervals (Δλ = λem. - λex.) is optimized to be set as 70 nm with the minimized overlap of two emission bands centered around 380 nm and 470 nm, respectively. In this way, NIN2 can detect F− in the region of 0–0.2 μM with a good linear relationship (R2 = 0.9989) and low LOD value (36 nM). Only F− can induce obvious ratiometric response (I470nm/I380nm) from 0.2 to 3.4 while the ratios of the samples containing other cations and anions are as low as the blank sample. For investigating the recognition mechanism of triazole, 1H, 13C and 19F NMR spectral technologies were used to verify the interaction between triazole and F−. Furthermore, the DFT calculation was also performed to discuss the electronic transition of NIN2 before and after interaction with F−. We believe this work provides a new recognition moiety for detecting F−.

Semisynthesis and characterization of versatile azide intermediates using sodium alginate and its homopolymeric derivatives as starting material

Alginate, a polyuronic biopolymer composed of mannuronic and guluronic acid units, contain hydroxyl and carboxyl groups as targeting modification sites to obtain structures with new and/or improved biological properties. The copper-catalyzed azide-alkyne cycloaddition (CuAAC) is a versatile click reaction for polymer functionalization, but it typically requires a “pre-click” modification to introduce azide or alkyne groups. Here, we described a straightforward chemical path to selectively modify alginate carboxyl groups producing versatile azido derivatives through N-acylation using 3-azydopropylamine. The resulting azide-functionalized polysaccharides underwent click chemistry to yield amino derivatives, confirmed by NMR and FTIR analyses. The 1H NMR spectrum reveals a characteristic triazole group signal at 8.15 ppm. The absence of the azide FTIR band for all amino derivatives, previously observed for the N-acylation products, indicated reaction success. Antibacterial and antioxidant assessments revealed that the initial polysaccharide lacks E. coli inhibition, while the click chemistry-derived amine products exhibit growth inhibition at 5.0 mg/mL. Lower molecular weight derivatives demonstrate superior DPPH scavenging ability, particularly amino-derivatives (24–33 % at 1.2 mg/mL). This innovative chemical pathway offers a promising strategy for developing polysaccharide structures with enhanced properties, demonstrating potential applications in various fields.