Narinderjit Singh Sawaran Singh , Alejandro Pérez-Larios , Syed Waheedullah Ghori , Rekha M M , Carlos Soto-Robles , Subhashree Ray , Kattela Chennakesavulu , Renu Sharma , Osmin Áviles-García , Layth Hussen , M.A. Diab , Heba A. El-Sabban
{"title":"绿色负载的金纳米颗粒在锌铝层状双氧根上作为Suzuki-Miyaura偶联反应的有效纳米催化剂","authors":"Narinderjit Singh Sawaran Singh , Alejandro Pérez-Larios , Syed Waheedullah Ghori , Rekha M M , Carlos Soto-Robles , Subhashree Ray , Kattela Chennakesavulu , Renu Sharma , Osmin Áviles-García , Layth Hussen , M.A. Diab , Heba A. El-Sabban","doi":"10.1016/j.jorganchem.2025.123840","DOIUrl":null,"url":null,"abstract":"<div><div>This research explains a strategy for decoration of gold nanoparticles over the surface of Zn–Al Layered Double Hydroxide mediated by <em>Pistacia</em> bark extract as natural raducing and coating agent. The existence of phytomolecules in the Zn-Al LDH/<em>Pistacia</em> helped create a safe way to change gold ions into gold particles without using harmful substances. To study the structure of the Zn-Al LDH/<em>Pistacia</em>/Au NPs composite, a wide array of advanced techniques were applied, including FESEM-elemental mapping, EDX, TEM, ICP-OES, and XRD. The new produced nanocatalyst was tested in the Suzuki-Miyaura coupling to generate C–C bonds. The Zn-Al LDH/<em>Pistacia</em>/Au NPs illustrated a high level of catalytic activity with various aryl halides. Moreover, the catalyst shown good recyclability, keeping its performance even after 8 reaction runs. The heterogeneous nature of the catalyst was confirmed by a hot filtration method, as no leaching was observed during the reaction process.</div></div>","PeriodicalId":374,"journal":{"name":"Journal of Organometallic Chemistry","volume":"1041 ","pages":"Article 123840"},"PeriodicalIF":2.1000,"publicationDate":"2025-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Green supported of gold nanoparticles over Zn–Al Layered Double Hydroxide as an effective nanocatalyst for Suzuki-Miyaura coupling reactions\",\"authors\":\"Narinderjit Singh Sawaran Singh , Alejandro Pérez-Larios , Syed Waheedullah Ghori , Rekha M M , Carlos Soto-Robles , Subhashree Ray , Kattela Chennakesavulu , Renu Sharma , Osmin Áviles-García , Layth Hussen , M.A. Diab , Heba A. El-Sabban\",\"doi\":\"10.1016/j.jorganchem.2025.123840\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>This research explains a strategy for decoration of gold nanoparticles over the surface of Zn–Al Layered Double Hydroxide mediated by <em>Pistacia</em> bark extract as natural raducing and coating agent. The existence of phytomolecules in the Zn-Al LDH/<em>Pistacia</em> helped create a safe way to change gold ions into gold particles without using harmful substances. To study the structure of the Zn-Al LDH/<em>Pistacia</em>/Au NPs composite, a wide array of advanced techniques were applied, including FESEM-elemental mapping, EDX, TEM, ICP-OES, and XRD. The new produced nanocatalyst was tested in the Suzuki-Miyaura coupling to generate C–C bonds. The Zn-Al LDH/<em>Pistacia</em>/Au NPs illustrated a high level of catalytic activity with various aryl halides. Moreover, the catalyst shown good recyclability, keeping its performance even after 8 reaction runs. The heterogeneous nature of the catalyst was confirmed by a hot filtration method, as no leaching was observed during the reaction process.</div></div>\",\"PeriodicalId\":374,\"journal\":{\"name\":\"Journal of Organometallic Chemistry\",\"volume\":\"1041 \",\"pages\":\"Article 123840\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2025-08-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Organometallic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0022328X25003328\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Organometallic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0022328X25003328","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
Green supported of gold nanoparticles over Zn–Al Layered Double Hydroxide as an effective nanocatalyst for Suzuki-Miyaura coupling reactions
This research explains a strategy for decoration of gold nanoparticles over the surface of Zn–Al Layered Double Hydroxide mediated by Pistacia bark extract as natural raducing and coating agent. The existence of phytomolecules in the Zn-Al LDH/Pistacia helped create a safe way to change gold ions into gold particles without using harmful substances. To study the structure of the Zn-Al LDH/Pistacia/Au NPs composite, a wide array of advanced techniques were applied, including FESEM-elemental mapping, EDX, TEM, ICP-OES, and XRD. The new produced nanocatalyst was tested in the Suzuki-Miyaura coupling to generate C–C bonds. The Zn-Al LDH/Pistacia/Au NPs illustrated a high level of catalytic activity with various aryl halides. Moreover, the catalyst shown good recyclability, keeping its performance even after 8 reaction runs. The heterogeneous nature of the catalyst was confirmed by a hot filtration method, as no leaching was observed during the reaction process.
期刊介绍:
The Journal of Organometallic Chemistry targets original papers dealing with theoretical aspects, structural chemistry, synthesis, physical and chemical properties (including reaction mechanisms), and practical applications of organometallic compounds.
Organometallic compounds are defined as compounds that contain metal - carbon bonds. The term metal includes all alkali and alkaline earth metals, all transition metals and the lanthanides and actinides in the Periodic Table. Metalloids including the elements in Group 13 and the heavier members of the Groups 14 - 16 are also included. The term chemistry includes syntheses, characterizations and reaction chemistry of all such compounds. Research reports based on use of organometallic complexes in bioorganometallic chemistry, medicine, material sciences, homogeneous catalysis and energy conversion are also welcome.
The scope of the journal has been enlarged to encompass important research on organometallic complexes in bioorganometallic chemistry and material sciences, and of heavier main group elements in organometallic chemistry. The journal also publishes review articles, short communications and notes.