Zhiqiang Wu, Yuan Min, Yongqin Li, Fang Qian, Lin-an Cao, Rong Tan, Enke Feng, Jiya Ding and Pengxi Jiang
{"title":"机械化学介导十二烷基硫酸铅纳米棒材料的制备及绿色无溶剂催化合成杂环衍生物","authors":"Zhiqiang Wu, Yuan Min, Yongqin Li, Fang Qian, Lin-an Cao, Rong Tan, Enke Feng, Jiya Ding and Pengxi Jiang","doi":"10.1039/D4MR00123K","DOIUrl":null,"url":null,"abstract":"<p >In this work, the lead dodecyl sulfate material (Pb(DS)<small><sub>2</sub></small>) was successfully synthesized for the first time <em>via</em> a mechanochemical ball milling method. The synthesized material was comprehensively analyzed using scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), Fourier transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), thermogravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS) and nuclear magnetic resonance (NMR) spectroscopy. The results demonstrate that the Pb(DS)<small><sub>2</sub></small> catalyst, synthesized <em>via</em> solvent-free mechanical ball milling, possesses a distinctive solid nanorod morphology. Furthermore, the catalyst efficiently promotes the synthesis of heterocyclic derivatives in a solvent-free environment within 20 minutes, achieving a target product yield of up to 98%. Specifically, it produced bis(indolyl)methane derivatives with yields ranging from 78% to 98%, and quinoxaline derivatives with yields ranging from 87% to 98% within the same timeframe. The Pb(DS)<small><sub>2</sub></small> catalyst also exhibits remarkable catalytic activity in the Biginelli reaction. Notably, the catalyst maintains excellent and stable performance over eight recycling cycles.</p>","PeriodicalId":101140,"journal":{"name":"RSC Mechanochemistry","volume":" 4","pages":" 584-597"},"PeriodicalIF":0.0000,"publicationDate":"2025-05-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/mr/d4mr00123k?page=search","citationCount":"0","resultStr":"{\"title\":\"Preparation of lead dodecyl sulfate nanorod materials mediated by mechanochemistry and green solvent-free catalytic synthesis of heterocyclic derivatives†\",\"authors\":\"Zhiqiang Wu, Yuan Min, Yongqin Li, Fang Qian, Lin-an Cao, Rong Tan, Enke Feng, Jiya Ding and Pengxi Jiang\",\"doi\":\"10.1039/D4MR00123K\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >In this work, the lead dodecyl sulfate material (Pb(DS)<small><sub>2</sub></small>) was successfully synthesized for the first time <em>via</em> a mechanochemical ball milling method. The synthesized material was comprehensively analyzed using scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), Fourier transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), thermogravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS) and nuclear magnetic resonance (NMR) spectroscopy. The results demonstrate that the Pb(DS)<small><sub>2</sub></small> catalyst, synthesized <em>via</em> solvent-free mechanical ball milling, possesses a distinctive solid nanorod morphology. Furthermore, the catalyst efficiently promotes the synthesis of heterocyclic derivatives in a solvent-free environment within 20 minutes, achieving a target product yield of up to 98%. Specifically, it produced bis(indolyl)methane derivatives with yields ranging from 78% to 98%, and quinoxaline derivatives with yields ranging from 87% to 98% within the same timeframe. The Pb(DS)<small><sub>2</sub></small> catalyst also exhibits remarkable catalytic activity in the Biginelli reaction. Notably, the catalyst maintains excellent and stable performance over eight recycling cycles.</p>\",\"PeriodicalId\":101140,\"journal\":{\"name\":\"RSC Mechanochemistry\",\"volume\":\" 4\",\"pages\":\" 584-597\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-05-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.rsc.org/en/content/articlepdf/2025/mr/d4mr00123k?page=search\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"RSC Mechanochemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2025/mr/d4mr00123k\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"RSC Mechanochemistry","FirstCategoryId":"1085","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/mr/d4mr00123k","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Preparation of lead dodecyl sulfate nanorod materials mediated by mechanochemistry and green solvent-free catalytic synthesis of heterocyclic derivatives†
In this work, the lead dodecyl sulfate material (Pb(DS)2) was successfully synthesized for the first time via a mechanochemical ball milling method. The synthesized material was comprehensively analyzed using scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), Fourier transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), thermogravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS) and nuclear magnetic resonance (NMR) spectroscopy. The results demonstrate that the Pb(DS)2 catalyst, synthesized via solvent-free mechanical ball milling, possesses a distinctive solid nanorod morphology. Furthermore, the catalyst efficiently promotes the synthesis of heterocyclic derivatives in a solvent-free environment within 20 minutes, achieving a target product yield of up to 98%. Specifically, it produced bis(indolyl)methane derivatives with yields ranging from 78% to 98%, and quinoxaline derivatives with yields ranging from 87% to 98% within the same timeframe. The Pb(DS)2 catalyst also exhibits remarkable catalytic activity in the Biginelli reaction. Notably, the catalyst maintains excellent and stable performance over eight recycling cycles.