Turkish Journal of Chemistry最新文献

{"title":"Removal of heavy metal iron(II) ions from wastewater using an ultrasonic system with climbazole-alcohol.","authors":"Melek Gökmen Karakaya, Bahdişen Gezer, Abdullah Menzek, Özlem Gündoğdu Aytaç","doi":"10.55730/1300-0527.3729","DOIUrl":"10.55730/1300-0527.3729","url":null,"abstract":"<p><p>Climbazole (CBZ) is an antifungal active pharmaceutical ingredient often used in antidandruff products. In this study, the ketone group in the racemic CBZ molecule was reduced to synthesize CBZ-alcohol, named 1-(4-chlorophenoxy)-1-(1<i>H</i>-imidazol-1-yl)-3,3-dimethylbutan-2-ol, and the optimum adsorption conditions were investigated for removing iron(II) (Fe²⁺) ions from wastewater by adsorption from aqueous solutions using the economical and environmentally friendly ultrasonic method. The parameters and levels used in the study were designed using response surface methodology and model equations were derived to optimize the results. The independent variables selected were the initial pH (1, 3, and 5), adsorption time (30, 45, and 60 min), adsorption temperature (40, 60, and 80 °C), and Fe²⁺ ions consumption percentage from the wastewater. Experiments were conducted on a real wastewater sample taken from the Uşak Organized Industrial Zone. Conditions that maximize each dependent variable were specified separately and verification experiments were conducted under these conditions. Maximum Fe²⁺ ion consumption was 91.83%. The R² value of the model was 0.9598. The findings demonstrate that CBZ-alcohol was effective as an adsorbent in Fe²⁺ ion removal from aqueous solution.</p>","PeriodicalId":23367,"journal":{"name":"Turkish Journal of Chemistry","volume":"49 3","pages":"279-292"},"PeriodicalIF":1.3,"publicationDate":"2025-03-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12253972/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144627197","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Ecofriendly synthesis and characterization of oxygen-enriched g-C₃N₄ from diverse precursors for efficient organic dye decontamination.","authors":"Muchammad Tamyiz","doi":"10.55730/1300-0527.3724","DOIUrl":"10.55730/1300-0527.3724","url":null,"abstract":"<p><p>Industrial wastewater from sectors such as textiles, printing, and pharmaceuticals contain harmful pollutants, including nonbiodegradable dyes, which pose significant challenges for environmental safety. Neutral red, a cationic dye commonly found in wastewater, obstructs photosynthesis in aquatic ecosystems and carries potential toxicity. Traditional methods of dye removal often prove ineffective due to the chemical stability of these compounds. In this study, oxygen-doped graphitic carbon nitride (O-doped g-C₃N₄) was synthesized as an innovative photocatalyst for the degradation of neutral red dye under visible light. The material was synthesized through a sustainable process involving the calcination of urea, dicyandiamide, and oxalic acid, and its characteristics were evaluated using various techniques, including XRD, FT-IR, UV-Vis spectroscopy, and SEM. Photocatalytic degradation of neutral red was analysed using a custom photoreactor under visible light. The results demonstrated that O-doped g-C₃N₄ exhibited enhanced photocatalytic efficiency compared to pure g-C₃N₄, reducing the recombination of electron-hole pairs and effectively degrading the dye. Adsorption kinetics followed a pseudo-2nd-order model, while adsorption isotherms suggested that the Langmuir model best described the adsorption process, indicating monolayer adsorption. The maximum adsorption capacity of O-doped g-C₃N₄ for neutral red was 9.643 mg g^-1, surpassing pure g-C₃N₄. The photocatalytic performance of OCN-UD was assessed under visible light, revealing a significant degradation efficiency of 86% for neutral red after 60 min, compared to 51% for pure g-C₃N₄. Kinetic studies indicated that the adsorption of neutral red onto OCN-UD primarily followed a pseudo-2nd-order model, demonstrating chemical adsorption processes. The synergistic effects of adsorption and photocatalysis were evident, as the initial adsorption phase concentrated dye molecules near active sites, facilitating efficient photocatalytic degradation through reactive oxygen species generation. This study highlights the potential of O-doped g-C₃N₄ as an efficient, eco-friendly solution for the treatment of dye-laden wastewater.</p>","PeriodicalId":23367,"journal":{"name":"Turkish Journal of Chemistry","volume":"49 2","pages":"228-240"},"PeriodicalIF":1.3,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12068676/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144043956","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"1,3,4-thiadiazole derivatives as PI3Ks inhibitor: design, in silico studies, synthesis, characterization, and antimicrobial evaluation.","authors":"Dharmvir Singh, Pankaj Kumar, Anoop Kumar, Vivek V Bhosale, Kalicharan Sharma, Deepak Kumar, Ramchander Khatri, Tanuj Hooda, Amit Lather","doi":"10.55730/1300-0527.3732","DOIUrl":"10.55730/1300-0527.3732","url":null,"abstract":"<p><p>Since PI3Ks are targeted by a variety of bacterial pathogens, they represent a promising target for host-directed immune therapy and may be beneficial in managing persistent bacterial infections. In the present study, computational studies of 5-(pyridin-4-yl)-1,3,4-thiadiazol-2-amine derivatives for phosphoinositide-3-kinases (PI3Ks) inhibitors were carried out using dock scores, Glide scores, and the MMGBSA dG method, with comparison to standard drugs (ofloxacin and fluconazole). A series of 5-(pyridin-4-yl)-1,3,4-thiadiazol-2-amine derivatives (D1-D17) were synthesized and evaluated for their in vitro antimicrobial activity against both gram-positive and gram-negative bacterial strains, as well as fungal strains, using the tube dilution method. The synthesized compounds were characterized based on their physicochemical properties, and spectral data confirmed consistency with the proposed molecular structures. Docking studies, the MMGBSA analyses, and in vitro antimicrobial activity results indicated that compounds D₄, D₆, D₈, and D₁₂ were the most active against different microbial species and also showed favorable docking results in comparison with the PDB ligand and standard antimicrobial drugs (ofloxacin and fluconazole). This study highlights the potential of these compounds for future in vivo antimicrobial and anticancer investigations.</p>","PeriodicalId":23367,"journal":{"name":"Turkish Journal of Chemistry","volume":"49 3","pages":"325-335"},"PeriodicalIF":1.3,"publicationDate":"2025-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12253968/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144627188","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"WO₃/α-Fe₂O₃/Bi₂S₃ ternary photoanode for improved oxygen evolution reaction in photoelectrochemical water splitting.","authors":"Fatih Tezcan, Abrar Ahmad, Gülfeza Kardaş","doi":"10.55730/1300-0527.3720","DOIUrl":"10.55730/1300-0527.3720","url":null,"abstract":"<p><p>This study presents a ternary WO₃/α-Fe₂O₃/Bi₂S₃ photoanode system suitable for photoelectrochemical water-splitting applications. WO₃/α-Fe₂O₃ heterojunction is obtained using a hydrothermal approach, while Bi₂S₃ is deposited onto WO₃/α-Fe₂O₃ via the successive ionic layer adsorption and reaction (SILAR) method. The cycle count is adjusted to determine the optimal photocatalytic photoanode. X-ray diffraction analysis confirms different morphologies and phases for the photoelectrodes: WO₃ is deposited as plates with monoclinic phases, α-Fe₂O₃ as nanorods with hexagonal phases, and Bi₂S₃ in the form of nanoparticles (NPs) with orthorhombic phases. Solar light absorption spectra indicate that ternary WO₃/α-Fe₂O₃/Bi₂S₃ photoanodes absorb a larger portion of the solar spectrum and display a large red shift in wavelength compared to binary WO₃/α-Fe₂O₃ photoanodes. Chronoamperometric and electrochemical impedance spectroscopy measurements indicate that the as-prepared WO₃/α-Fe₂O₃/Bi₂S₃ photoanode exhibits notable stability and low charge transfer resistance (R_ct) compared to binary electrodes and pristine WO₃ plates in faradaic photoelectrochemical conversion for the oxygen evolution reaction and S^-2/S² processes. Linear sweep voltammetry studies show that the WO₃/α-Fe₂O₃/Bi₂S₃ photoanode, sensitized with 8 SILAR cycles, achieves the maximum photocurrent density of 5.777 mA.cm^-2 at 1.0 V vs. RHE under 100 mW cm^-2 simulated solar irradiation.</p>","PeriodicalId":23367,"journal":{"name":"Turkish Journal of Chemistry","volume":"49 2","pages":"176-190"},"PeriodicalIF":1.3,"publicationDate":"2025-02-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12068670/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144012042","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Investigation of the interaction conditions of As₂S₅ and CuCl₂ compounds in water and ethylene glycol medium.","authors":"Huseyn Imanov, Mahnur Jafarli","doi":"10.55730/1300-0527.3722","DOIUrl":"10.55730/1300-0527.3722","url":null,"abstract":"<p><p>The article presents the results of the interaction conditions of CuCl₂ and As₂S₅ in ethylene glycol and aquatic medium. Besides, the results of the obtained samples' physicochemical properties are given by X-ray diffraction (XRD), differential thermogravimetric (DTG), thermogravimetric (TG), elemental, and scanning electron microscope (SEM) methods. It was found that when ethylene glycol and water are used as a solvent and CuCl₂ and As₂S₅ as the initial components, Cu₃AsS₄ is obtained at a temperature of 323-353 K. According to the results of DTA analysis, it was found that the melting point of obtained samples was 964.4 K contrary to the reactions carried out to obtain Cu₃(AsS₄)₂ compounds both in ethylene glycol and water medium. Elemental analysis of the compounds was carried out, energy-dispersion spectrum, mass, and atomic ratios of copper, arsenic, and sulfur were determined, and the stoichiometric composition of Cu₃AsS₄ was determined. Furthermore, X-ray analysis of the obtained samples confirmed that peaks on the graphs correspond to the standard intensity maxima of the Cu₃AsS₄ compound.</p>","PeriodicalId":23367,"journal":{"name":"Turkish Journal of Chemistry","volume":"49 2","pages":"204-214"},"PeriodicalIF":1.3,"publicationDate":"2025-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12068193/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143988357","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Synthesis of thiazole-integrated pyrrolotriazinones: evaluations of cytotoxicity and effects on PI3K levels in cancer cells.","authors":"Eylem Kuzu, Ege Arzuk, Fuat Karakuş, Burak Kuzu, Hasan Genç","doi":"10.55730/1300-0527.3723","DOIUrl":"10.55730/1300-0527.3723","url":null,"abstract":"<p><p>The synthesis of novel heterocyclic compounds, particularly those targeting critical signaling pathways in cancer, represents a promising approach to drug development. In this study, we designed and synthesized a series of thiazole-integrated pyrrolotriazinone derivatives, aiming to combine the antiproliferative properties of thiazole with the PI3K inhibitory activity of pyrrolotriazinones. The PI3K pathway, which plays a critical role in regulating cell growth, proliferation, and survival, is frequently dysregulated in cancer, making it an attractive target for therapeutic intervention. The synthesized derivatives were evaluated for their cytotoxic activities against MCF-7, A549, and HepG2 cancer cell lines. Their effect on PI3K protein levels was assessed to evaluate their potential as PI3K inhibitors. Preliminary results indicate that these thiazole-pyrrolotriazinone hybrids exhibit significant cytotoxic effects and may reduce PI3K protein levels in cancer cells. Furthermore, drug-likeness assessments and pre-ADMET evaluations demonstrated that the compounds exhibited promising characteristics, supporting their potential as viable drug candidates. Overall, this study highlights the potential of these novel compounds in cancer therapy and provides valuable insights into the design of small molecules that can target key regulatory pathways involved in cancer progression.</p>","PeriodicalId":23367,"journal":{"name":"Turkish Journal of Chemistry","volume":"49 2","pages":"215-227"},"PeriodicalIF":1.3,"publicationDate":"2025-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12068666/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144050325","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Pyrene-based hole transport materials for efficient perovskite solar cells.","authors":"Madiha Irfan, Aamer Saeed, Sania Tahir, Muhammad Rehman Yaqoob, Sohaib Ahmed Zia, Muhammad Usama, Junaid Mukhtar, Usama Farrukh, Sara Rehman","doi":"10.55730/1300-0527.3727","DOIUrl":"10.55730/1300-0527.3727","url":null,"abstract":"<p><p>In the past few years, perovskite solar cells (PSCs) have gained a lot of attention and become a well-known topic in solar studies due to their lower manufacturing costs and improved efficiencies. Previously utilized hole transport materials (HTMs), such as poly[bis(4-phenyl)(2,4,6-trimethylphenyl)amine] and 2,2',7,7'-tetrakis(N,N-di-p-methoxyphenylamine)-9,9'-spirobifluorene, are challenging due to their high price, complicated synthesis, limited carrier mobility, and poor device stability. Developing HTMs for PSCs that are inexpensive and high-performance has gained much interest. Currently, many HTMs of organic molecules are used to improve photovoltaic qualities and reduce synthesis costs. Effectively using HTMs is essential for producing the best photovoltaic efficiency in PSCs because they are essential in extracting and transporting charge carriers. Pyrene-based HTMs have excellent device performance, chemical stability, and photovoltaic qualities compared to the other organic moieties. The significant developments made in pyrene-based HTMs over the past five years are reported herein. This review analyzed the relationship between the molecular structure, hole mobility, highest occupied molecular orbital-lowest unoccupied molecular orbital energy levels, power conversion efficiency (PCE), and energy band gap of pyrene-based HTMs. It was revealed that PSC devices fabricated with pyrene-based HTMs have attained a PCE greater than 22%. It is hoped that this review will encourage more researchers to develop HTMs that have good performance, low cost, and high device stability.</p>","PeriodicalId":23367,"journal":{"name":"Turkish Journal of Chemistry","volume":"49 3","pages":"254-266"},"PeriodicalIF":1.3,"publicationDate":"2025-01-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12253967/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144627195","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"A hindered phenol containing PVC/CuO nanocomposites; study on the mechanical and thermooxidative properties.","authors":"Mohsen Hajibeygi, Alireza Ghasemi","doi":"10.55730/1300-0527.3708","DOIUrl":"10.55730/1300-0527.3708","url":null,"abstract":"<p><p>The effect of synthesized 5-((4-hydroxy-3,5-di-tert-butylphenyl)diazenyl)isophthalic acid (HBA) containing a hindered phenol derivative on the thermooxidation, hydrochloric acid release time, and mechanical strength of PVC/CuO nanocomposites was studied. Moreover, 5-((4-hydroxy-2,5-dimethylphenyl)diazenyl)isophthalic acid (HMA) was synthesized for comparison of corresponding PVC nanocomposite properties. PVC nanocomposite thin films were prepared through in situ surface modification of CuO nanoparticles with HBA and HMA, individually, in the PVC solution. The XRD and FE-SEM results clarified the desirable dispersion of CuO nanoparticles. The PVC sample with loading of 5 wt% from each HBA and CuO was found to be the most thermally stable, which was confirmed by thermogravimetric analysis in inert conditions. The thermooxidation and Congo red test results revealed that the simultaneous loading of HBA and CuO nanoparticles into the PVC matrix could increase the initial thermal degradation and the stability times. Moreover, the PVC sample containing 2.5 wt% each from HBA and CuO nanoparticles exhibited tensile strength almost 20 MPa more than that of neat PVC.</p>","PeriodicalId":23367,"journal":{"name":"Turkish Journal of Chemistry","volume":"49 1","pages":"29-44"},"PeriodicalIF":1.3,"publicationDate":"2024-12-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11913362/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143658741","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Enhanced and proficient chitosan membranes embedded with polyaniline-TiO₂ core-shell nanocomposites for fuel-cell hydrogen storage.","authors":"Mallikarjunagouda B Patil, Shridhar N Mathad, Arun Y Patil, Abdulaziz Abdulah Al-Kheraif, Sachin Naik, Sajith Vellapally","doi":"10.55730/1300-0527.3730","DOIUrl":"10.55730/1300-0527.3730","url":null,"abstract":"<p><p>This study investigates the preparation and properties of aniline polymerized in situ onto a nanosized TiO₂ surface to form core-shell nanoparticles at ambient temperatures. The in situ polymerization of aniline to polyaniline (PANI), in conjunction with the utilization of an anionic surfactant, was employed in this investigation. The prepared PANI-TiO₂ core-shell nanoparticles were integrated with chitosan at a gravimetric ratio and cast as core-shell nanocomposite membranes. The nanocomposites were subjected to structural analysis using Fourier transform infrared spectroscopy and X-ray diffraction patterns. The surface morphologies of the PANI and its nanocomposites were analyzed using scanning electron microscopy. Direct current conductivity studies revealed three discrete tiers of conductivity intrinsic to a semiconductor material. The nanocomposite, comprising a chitosan membrane embedded with 4 wt.% PANI-TiO₂, demonstrated peak direct current conductivity of 5.7 S/cm. The properties of the core-shell nanocomposite membranes could be elucidated using cyclic voltammetry, a technique that allowed for the observation of redox peaks occurring at 0.94 V and 0.25 V. The presence of both peaks was due to the redox transition of the prepared nanocomposite membranes from a semiconducting to a conductive state. At room temperature, the hydrogen absorption capacity was approximately 4.5 wt.%, but when the temperature was raised to 65 °C, it doubled to about 7.5 wt.%. In comparison to other nanocomposites, the 4 wt.% PANI-TiO₂ core-shell embedded chitosan membrane exhibited significantly higher absorption capacity of 10.5 wt.%.</p>","PeriodicalId":23367,"journal":{"name":"Turkish Journal of Chemistry","volume":"49 3","pages":"293-309"},"PeriodicalIF":1.3,"publicationDate":"2024-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12253973/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144627192","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Fabrication of Au-Pd bimetallic dendrites and their catalytic application for 4-nitrophenol reduction.","authors":"Jun Liu, Xuanyan Liu, Hongguang Liao","doi":"10.55730/1300-0527.3721","DOIUrl":"10.55730/1300-0527.3721","url":null,"abstract":"<p><p>Bimetal nanocatalysts hold significant application potential in catalytic reactions due to their compositions, morphologies, and electronic structures. In the present work, a series of AuPd alloy dendrites were successfully prepared using sodium formate, without surfactants or templates. A systematic investigation was then conducted to analyze the composition of the AuPd bimetallic dendrites and the effects of preparation conditions on their structure and catalytic performance. The AuPd alloy dendrites were characterized through various techniques, including scanning electron microscopy, transmission electron microscopy, X-ray energy scattering spectroscopy, X-ray diffraction, and X-ray photoelectron spectroscopy. The results showed that the Au:Pd ratio in the AuPd alloy dendrites closely matched the initial feeding ratio. The catalytic activity and stability of the AuPd alloy dendrites towards 4-nitrophenol reduction were remarkably higher compared to those of the single metal Au and Pd nanocatalysts. Specifically, the Au₁Pd₁ alloy dendrites exhibited the highest catalytic reduction activity for 4-nitrophenol, with a reaction rate constant of 1.05 × 10^-2. Moreover, the stability of the Au₁Pd₁ alloy dendrites was also examined. The results demonstrated that the catalytic stability of the Au₁Pd₁ alloy dendrites did not experience a significant decrease even after five cycles of operation.</p>","PeriodicalId":23367,"journal":{"name":"Turkish Journal of Chemistry","volume":"49 2","pages":"191-203"},"PeriodicalIF":1.3,"publicationDate":"2024-12-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12068668/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144034034","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}