Journal of Organometallic Chemistry最新文献

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Synthesis and properties of diphenylphosphanyl and di-isopropylphosphanyl triphenylsilanes and pentaphenyldisilanes
IF 2.1 3区 化学
Journal of Organometallic Chemistry Pub Date : 2025-02-06 DOI: 10.1016/j.jorganchem.2025.123555
Mike Friebel , Uwe Böhme , Edwin Kroke
{"title":"Synthesis and properties of diphenylphosphanyl and di-isopropylphosphanyl triphenylsilanes and pentaphenyldisilanes","authors":"Mike Friebel ,&nbsp;Uwe Böhme ,&nbsp;Edwin Kroke","doi":"10.1016/j.jorganchem.2025.123555","DOIUrl":"10.1016/j.jorganchem.2025.123555","url":null,"abstract":"<div><div>A new, less hazardous synthetic pathway to chloropentaphenyldisilane, ClSi<sub>2</sub>Ph<sub>5</sub>, has been developed. Starting from this compound and lithium diorganophosphides, the two previously unknown diorganophosphanyldisilanes (diphenylphosphanyl)pentaphenyldisilane, Ph<sub>2</sub>PSi<sub>2</sub>Ph<sub>5</sub>, and (di-isopropylphosphanyl)pentaphenyldisilane, (<em>i</em>-Pr)<sub>2</sub>PSi<sub>2</sub>Ph<sub>5</sub>, were prepared. To compare these compounds with the corresponding monosilanes, the known (diphenylphosphanyl)triphenylsilane, Ph<sub>2</sub>PSiPh<sub>3</sub>, and the unknown (di-isopropylphosphanyl)triphenylsilane, (<em>i</em>-Pr)<sub>2</sub>PSiPh<sub>3</sub>, were prepared, too. The former was prepared via new synthetic routes. The compounds were characterized with IR-, Raman-, <sup>31</sup>P-, <sup>29</sup>Si-, and <sup>1</sup>H NMR spectroscopy and melting point determination. Single crystal structure analyses of ClSi<sub>2</sub>Ph<sub>5</sub> and (<em>i</em>-Pr)<sub>2</sub>PSiPh<sub>3</sub> were carried out and confirm the results presented.</div></div>","PeriodicalId":374,"journal":{"name":"Journal of Organometallic Chemistry","volume":"1029 ","pages":"Article 123555"},"PeriodicalIF":2.1,"publicationDate":"2025-02-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143388049","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Investigations into the reactivity of a molybdenocene formamidinate complex
IF 2.1 3区 化学
Journal of Organometallic Chemistry Pub Date : 2025-02-05 DOI: 10.1016/j.jorganchem.2025.123556
Joscha Nellesen, Christian Ganter
{"title":"Investigations into the reactivity of a molybdenocene formamidinate complex","authors":"Joscha Nellesen,&nbsp;Christian Ganter","doi":"10.1016/j.jorganchem.2025.123556","DOIUrl":"10.1016/j.jorganchem.2025.123556","url":null,"abstract":"<div><div>A cationic molybdenocene amidinate complex was investigated in view of its suitability to serve as a precursor for a metalla-N-heterocyclic carbene. Upon deprotonation, an amidinate complex with a cyclopenatdiene substituent at the amidinate C atom was identified. This points to the intermediate formation of the sought-after carbene which nucleophilicly attacks a Cp ring of the remaining cationic molybdenocene precursor and subsequent fragmentation. In contrast, the nucleophilic attack of standard imidazolylidenes to the cationic molybdenocene amidinate yields stable adducts with a η<sup>4</sup>-cyclopentadiene ligand. The rotational dynamics of this structure has been studied by variable temperature NMR studies. The experimental findings are supported by DFT calculations.</div></div>","PeriodicalId":374,"journal":{"name":"Journal of Organometallic Chemistry","volume":"1029 ","pages":"Article 123556"},"PeriodicalIF":2.1,"publicationDate":"2025-02-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143348749","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Synthesis of rhodium complexes with chiral diene ligands based on R-carvone
IF 2.1 3区 化学
Journal of Organometallic Chemistry Pub Date : 2025-02-03 DOI: 10.1016/j.jorganchem.2025.123554
Tatiana N. Petrushina, Alexey N. Rodionov, Yulia V. Nelyubina, Dmitry S. Perekalin
{"title":"Synthesis of rhodium complexes with chiral diene ligands based on R-carvone","authors":"Tatiana N. Petrushina,&nbsp;Alexey N. Rodionov,&nbsp;Yulia V. Nelyubina,&nbsp;Dmitry S. Perekalin","doi":"10.1016/j.jorganchem.2025.123554","DOIUrl":"10.1016/j.jorganchem.2025.123554","url":null,"abstract":"<div><div>Allylic chlorination of <em>R</em>-carvone and subsequent nucleophilic substitution produced chiral diene ligands with additional pyrazole, phthalimide, or diethyl phosphonate coordinating groups. Reactions of these ligands with [(C<sub>2</sub>H<sub>4</sub>)<sub>2</sub>RhCl]<sub>2</sub> produced the corresponding 16-electron rhodium complexes (carvone-L)RhCl. The pyrazole-based ligand formed the most stable complex, which was characterized by the X-ray diffraction. This complex catalyzed the insertion of aryldiazoacetates into <em>B</em>−<em>H</em> bond and cyclopropanation of 2,3-dihydrofurane but gave only racemic products.</div></div>","PeriodicalId":374,"journal":{"name":"Journal of Organometallic Chemistry","volume":"1029 ","pages":"Article 123554"},"PeriodicalIF":2.1,"publicationDate":"2025-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143268357","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A convenient synthesis of Os3(CO)12 from OsO4 and formic acid
IF 2.1 3区 化学
Journal of Organometallic Chemistry Pub Date : 2025-02-01 DOI: 10.1016/j.jorganchem.2024.123480
Elumalai Kumaran, Weng Kee Leong
{"title":"A convenient synthesis of Os3(CO)12 from OsO4 and formic acid","authors":"Elumalai Kumaran,&nbsp;Weng Kee Leong","doi":"10.1016/j.jorganchem.2024.123480","DOIUrl":"10.1016/j.jorganchem.2024.123480","url":null,"abstract":"<div><div>A convenient synthesis of the osmium carbonyl cluster Os<sub>3</sub>(CO)<sub>12</sub> starting from osmium tetroxide and the <em>in-situ</em> generation of gaseous carbon monoxide via the decomposition of formic acid, is reported.</div></div>","PeriodicalId":374,"journal":{"name":"Journal of Organometallic Chemistry","volume":"1025 ","pages":"Article 123480"},"PeriodicalIF":2.1,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143139406","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Transesterification of glycerol with dimethyl carbonate for the synthesis of glycerol carbonate and glycidol by Iron (III) salen complex
IF 2.1 3区 化学
Journal of Organometallic Chemistry Pub Date : 2025-02-01 DOI: 10.1016/j.jorganchem.2024.123467
Long-Yat Lai, Pak-Chung Lau, Tsz-Lung Kwong, Ka-Fu Yung
{"title":"Transesterification of glycerol with dimethyl carbonate for the synthesis of glycerol carbonate and glycidol by Iron (III) salen complex","authors":"Long-Yat Lai,&nbsp;Pak-Chung Lau,&nbsp;Tsz-Lung Kwong,&nbsp;Ka-Fu Yung","doi":"10.1016/j.jorganchem.2024.123467","DOIUrl":"10.1016/j.jorganchem.2024.123467","url":null,"abstract":"<div><div>The transesterification of glycerol and dimethyl carbonate (DMC) was investigated in the presence of <span><math><mi>μ</mi></math></span>-oxo-Fe(salen)<sub>2</sub> under the optimal reaction condition. Several transition metal(salen) were tested, and only Fe (salen) shows an excellent results towards transesterification of glycerol. Therefore, Fe (salen) was characterized by IR, elemental analysis, MS, XPS and Surface Basicity test, and it can be confirmed that the as-synthesized Fe(salen) was existed in the form of <span><math><mi>μ</mi></math></span>-oxo-Fe(salen)<sub>2</sub>. It was proposed that the <span><math><mi>μ</mi></math></span>-oxo-Fe(salen)<sub>2</sub> can provide two different reaction pathway based on its molecular structures and the electronic configuration of iron itself. <span><math><mi>μ</mi></math></span>-oxo-Fe(salen)<sub>2</sub> was reacted with the mixture of glycerol and DMC under microwave-heating in 60 min at 100 °C and at the molar ratio of glycerol:DMC:<span><math><mi>μ</mi></math></span>-oxo-Fe(salen)<sub>2</sub> of 1:2:0.01 and obtaining the highest glycerol carbonate yield of 93.8 %.</div></div>","PeriodicalId":374,"journal":{"name":"Journal of Organometallic Chemistry","volume":"1025 ","pages":"Article 123467"},"PeriodicalIF":2.1,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143138864","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Sequential phase transfer catalysis–hydrosilylation as an efficient method for the synthesis of polyfluorinated triethoxysilanes
IF 2.1 3区 化学
Journal of Organometallic Chemistry Pub Date : 2025-02-01 DOI: 10.1016/j.jorganchem.2024.123483
M.A. Stepanov, Yu.I. Bolgova, O.M. Trofimova, E.F. Belogolova, A.I. Emel'yanov, A.I. Albanov, A.S. Pozdnyakov
{"title":"Sequential phase transfer catalysis–hydrosilylation as an efficient method for the synthesis of polyfluorinated triethoxysilanes","authors":"M.A. Stepanov,&nbsp;Yu.I. Bolgova,&nbsp;O.M. Trofimova,&nbsp;E.F. Belogolova,&nbsp;A.I. Emel'yanov,&nbsp;A.I. Albanov,&nbsp;A.S. Pozdnyakov","doi":"10.1016/j.jorganchem.2024.123483","DOIUrl":"10.1016/j.jorganchem.2024.123483","url":null,"abstract":"<div><div>An efficient approach to obtain of polyfluorinated triethoxysilanes H(CF<sub>2</sub>)<sub>n</sub>CH<sub>2</sub>O(CH<sub>2</sub>)<sub>3</sub>Si(OEt)<sub>3</sub> with high yields, is presented using a sequential reactions of phase transfer catalysis and hydrosilylation. Tetrabutylammonium bromide and Speier's catalyst (200 ppm) were used as catalysts. The hydrosilylation reaction proceeds rather quickly within 1–3 h under mild conditions at room temperature. <sup>1</sup>H NMR monitoring indicates a selective process with the formation of only the main γ-addition product. The individuality of the synthesized triethoxy(polyfluoroalkoxy)propyl silanes have been confirmed by FTIR, <sup>1</sup>H, <sup>13</sup>C, <sup>19</sup>F, and <sup>29</sup>Si NMR spectroscopy and elemental analysis. Quantum chemical calculations have shown that with a decrease in the number of electronegative fragments CF<sub>2</sub> in the molecule, an increase in the energetic favorability of the hydrosilylation reaction is observed. The prospects for using the obtained fluorosilanes in polymer systems are discussed.</div></div>","PeriodicalId":374,"journal":{"name":"Journal of Organometallic Chemistry","volume":"1025 ","pages":"Article 123483"},"PeriodicalIF":2.1,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143138992","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A comparative study of CH and mCH mechanisms in hydrosilylation reactions
IF 2.1 3区 化学
Journal of Organometallic Chemistry Pub Date : 2025-02-01 DOI: 10.1016/j.jorganchem.2024.123451
Manxin Hong , Zhengjian Qi , Yu Sun
{"title":"A comparative study of CH and mCH mechanisms in hydrosilylation reactions","authors":"Manxin Hong ,&nbsp;Zhengjian Qi ,&nbsp;Yu Sun","doi":"10.1016/j.jorganchem.2024.123451","DOIUrl":"10.1016/j.jorganchem.2024.123451","url":null,"abstract":"<div><div>The cyclic process of Si-H oxidation addition, olefin insertion, and reductive elimination was discussed by density functional theory (DFT) and high-precision quantum chemical calculations. All the calculations were performed at the B3LYP-D3/def2-TZVP level. Two fundamental mechanisms of Chalk-Harrod (CH) and modified Chalk-Harrod (mCH) were explored, in the perspective of computational chemistry. Pt(PH<sub>3</sub>)<sub>2</sub> was used as model for the renowned Speier's catalyst, while HSiR (R=(CH<sub>3</sub>)<sub>3</sub> and CH<sub>3</sub>(OSi(CH<sub>3</sub>)<sub>3</sub>)<sub>2</sub> and CH<sub>2</sub>=CHR’ (R’=<em>H</em>, CH<sub>2</sub>OH and CH<sub>2</sub>OCH<sub>2</sub>CH<sub>2</sub>OH) were used as the reactant models. Significant findings include the identification of the olefin insertion as the rate-determining step in both mechanisms.The energy barrier of rate-determining step was 27.6 kcal/mol and 41.0 kcal/mol, respectively, according to the CH mechanism and the mCH mechanism, when HSi(CH<sub>3</sub>)<sub>3</sub> and CH<sub>2</sub>=CH<sub>2</sub> were used as the reactant models. But the barrier of rate-determining step become to 27.2 kcal/mol and 28.4 kcal/mol, when HSiCH<sub>3</sub>(OSi(CH<sub>3</sub>)<sub>3</sub>)<sub>2</sub> and CH<sub>2</sub>=CHCH<sub>2</sub>OCH<sub>2</sub>CH<sub>2</sub>OH were used as the reactant models. The difference in energy barriers betweeen the CH and mCH mechanisms become closer as the reactant models increase. The reaction between polyhydrosiloxane and allyl polyether may very potentially follow the mCH mechanism rather than CH mechanism.</div></div>","PeriodicalId":374,"journal":{"name":"Journal of Organometallic Chemistry","volume":"1025 ","pages":"Article 123451"},"PeriodicalIF":2.1,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143139469","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Application of supported palladium nanoparticles over chitosan-agarose encapsulated Fe3O4 microspheres as efficient catalyst in the Sonogashira cross-coupling reactions
IF 2.1 3区 化学
Journal of Organometallic Chemistry Pub Date : 2025-02-01 DOI: 10.1016/j.jorganchem.2025.123553
Ali Kakanejadifard , Parisa Safarimehr , Bikash Karmakar , Mozhgan Pirhayati , Hojat Veisi
{"title":"Application of supported palladium nanoparticles over chitosan-agarose encapsulated Fe3O4 microspheres as efficient catalyst in the Sonogashira cross-coupling reactions","authors":"Ali Kakanejadifard ,&nbsp;Parisa Safarimehr ,&nbsp;Bikash Karmakar ,&nbsp;Mozhgan Pirhayati ,&nbsp;Hojat Veisi","doi":"10.1016/j.jorganchem.2025.123553","DOIUrl":"10.1016/j.jorganchem.2025.123553","url":null,"abstract":"<div><div>In this work, a simple and modified method for immobilizing Pd(0) NPs on the surface of dual functionalized magnetic Fe<sub>3</sub>O<sub>4</sub> microspheres with chitosan-agarose (CS-Agar) has been used. The high area surface showed a dispersion of the minuscule Pd NPs. The key role of the CS-Agar hydrogel is to reduce Pd ions via a green pathway, stabilizing them via capping in the process. In order to determine the morphological aspects of the synthesized material, it was subjected to a variety of physicochemical techniques, including FE-SEM (Field Emission Scanning Electron Microscopy) and TEM (Transmission Electron Microscopy). The new material was studied catalytically as a reusable heterogeneous nanocatalyst that is effective in phosphine-free production of a variety of stilbene derivatives using the Sonogashira coupling method. Excellent results were obtained in every reaction, with the exception of chloroarenes and sterically hindered substrates. Without seeing a discernible decline in activity, the catalyst was reused seven times in a row.</div></div>","PeriodicalId":374,"journal":{"name":"Journal of Organometallic Chemistry","volume":"1029 ","pages":"Article 123553"},"PeriodicalIF":2.1,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143268005","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Recent progress in palladium-catalyzed reduction with organosilanes
IF 2.1 3区 化学
Journal of Organometallic Chemistry Pub Date : 2025-02-01 DOI: 10.1016/j.jorganchem.2024.123484
Maryam Mirza-Aghayan , Amir Sepehr Moieni
{"title":"Recent progress in palladium-catalyzed reduction with organosilanes","authors":"Maryam Mirza-Aghayan ,&nbsp;Amir Sepehr Moieni","doi":"10.1016/j.jorganchem.2024.123484","DOIUrl":"10.1016/j.jorganchem.2024.123484","url":null,"abstract":"<div><div>Reduction of unsaturated compounds using a standard method in laboratories as well as in industry to achieve valuable compounds is very important. The catalytic activity of various types of palladium (Pd) catalysts in the presence of organosilane for the reduction of unsaturated compounds has been proven over the years. As the main goal of the review, we present a comprehensive overview of the application of Pd catalysts in the presence of organosilane compounds for the reduction of organic building blocks such as thio esters, organic halides, acid chlorides, carboxylic acids, olefins, alkynes, ethers, α,β-unsaturated compounds, carbonyl compounds, alcohols, nitroaromatic derivatives, and imine compounds. We present the recent reports on the reduction of unsaturated compounds using the Pd catalyst/silane system. We briefly discuss the general mechanistic roles played by palladium and organosilane in the reduction reactions.</div></div>","PeriodicalId":374,"journal":{"name":"Journal of Organometallic Chemistry","volume":"1025 ","pages":"Article 123484"},"PeriodicalIF":2.1,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143139468","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Biosynthesis of Mikania micrantha mediated silver nanoparticles: Its application as a sustainable catalyst for Biginelli reaction and antioxidant capacity
IF 2.1 3区 化学
Journal of Organometallic Chemistry Pub Date : 2025-02-01 DOI: 10.1016/j.jorganchem.2024.123482
Manthae C. Phom , Betokali K. Zhimomi , Putusenla Imchen , Phitovili Sumi , Shisak Sharma , Khonzani Yanthan , Shokip Tumtin , Toka Swu , Tovishe Phucho
{"title":"Biosynthesis of Mikania micrantha mediated silver nanoparticles: Its application as a sustainable catalyst for Biginelli reaction and antioxidant capacity","authors":"Manthae C. Phom ,&nbsp;Betokali K. Zhimomi ,&nbsp;Putusenla Imchen ,&nbsp;Phitovili Sumi ,&nbsp;Shisak Sharma ,&nbsp;Khonzani Yanthan ,&nbsp;Shokip Tumtin ,&nbsp;Toka Swu ,&nbsp;Tovishe Phucho","doi":"10.1016/j.jorganchem.2024.123482","DOIUrl":"10.1016/j.jorganchem.2024.123482","url":null,"abstract":"<div><div>The current study focuses on the eco-friendly, bio-synthesis and of silver nanoparticles (AgNPs), utilizing an aqueous extract of <em>Mikania micrantha</em>. A rigorous analysis was performed to investigate the effects of several operational factors on the synthesis of AgNPs, including the various quantities of leaf extract, temperature, contact duration, and pH solution. The outcomes demonstrated that the optimal circumstances for producing nanoparticles are <em>Mikania micrantha</em> leaf extract dosage (5 % v/v), pH 9, and 80 °C temperature, with a duration of 60 min incubation time. The bio-synthesized AgNPs were examined using UV–Vis, FT-IR, X-ray diffraction (XRD), FE-SEM, EDX, TEM, and SAED studies. The FT-IR study proved that phytochemicals were involved in the AgNPs production process, and its spherical morphologies with the size range of 12.35 - 46.83 nm were apparent in the TEM images. The face-centered cubic structure of AgNPs was validated by the XRD spectrum. The XRD investigations also substantiated the SAED spectrum's indication that the AgNPs were crystalline. AgNPs were identified as an eco-friendly heterogeneous catalyst, demonstrating high catalytic efficiency in the Biginelli reaction under acid-free, mild conditions, achieving excellent yields in 30 s. 1,1-diphenyl- 2-picrylhydrazyl (DPPH) and Ferric reducing antioxidant power (FRAP) assays were used to assess the biological efficiency showing 89.8 % inhibition activity with an average IC<sub>50</sub> value of 24.99± 0.19 µg mL<sup>-1</sup> and higher reducing power than the positive control, respectively. This confirms that the leaf extract of <em>Mikania micrantha</em> and its biosynthesized nanoparticles also showed promising antioxidant capability.</div></div>","PeriodicalId":374,"journal":{"name":"Journal of Organometallic Chemistry","volume":"1025 ","pages":"Article 123482"},"PeriodicalIF":2.1,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143138862","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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