C. Shalini, M. Akilesh, G. Sathiyaraj, N. S. P. Bhuvanesh, K. S. Neethu, M. V. Kaveri, N. Dharmaraj
{"title":"通过 N∩O 螯合肼的钯络合物的位点选择性 CCl 键活化从 3-氯香豆素和芳基硼酸制备 3-芳香豆素支架","authors":"C. Shalini, M. Akilesh, G. Sathiyaraj, N. S. P. Bhuvanesh, K. S. Neethu, M. V. Kaveri, N. Dharmaraj","doi":"10.1002/aoc.7709","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>Using palladium hydrazone complex as a homogeneous catalyst for SMC, we synthesized a library of 15 variant 3-arylcoumarins. In this context, we report a set of four coordinated palladium(II) hydrazone complexes <b>1</b> and <b>2</b> having the general formula [Pd(L)(Cl)(PPh<sub>3</sub>)] by reacting the precursor complex [PdCl<sub>2</sub>(PPh<sub>3</sub>)<sub>2</sub>] with the hydrazone ligands <b>HL</b><sub><b>1</b></sub> or <b>HL</b><sub><b>2</b></sub>. Single crystal XRD and conventional spectroscopic techniques were employed to characterize both complexes. From the catalytic application point of view, the new complexes <b>1</b> and <b>2</b> were tested as homogeneous catalysts towards the conversion of 3-chlorocoumarins into 3-arylcoumarins by activating the challenging C<span></span>Cl functionality. A minimal catalyst loading of complex <b>2</b> (0.01 mol%), afforded a series of 3-arylcoumarins with a maximum of 92% yield and reusability up to five cycles. The present methodology is simple and easy to carry out at room temperature utilizing a green solvent (ethanol) in an open flask with a spectrum of aryl boronic acids.</p>\n </div>","PeriodicalId":8344,"journal":{"name":"Applied Organometallic Chemistry","volume":"38 12","pages":""},"PeriodicalIF":3.7000,"publicationDate":"2024-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"3-Arylcoumarin Scaffolds From 3-Chlorocoumarin and Arylboronic Acids via Site-Selective CCl Bond Activation With Palladium Complexes of N∩O Chelating Hydrazones\",\"authors\":\"C. Shalini, M. Akilesh, G. Sathiyaraj, N. S. P. Bhuvanesh, K. S. Neethu, M. V. Kaveri, N. Dharmaraj\",\"doi\":\"10.1002/aoc.7709\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n <p>Using palladium hydrazone complex as a homogeneous catalyst for SMC, we synthesized a library of 15 variant 3-arylcoumarins. In this context, we report a set of four coordinated palladium(II) hydrazone complexes <b>1</b> and <b>2</b> having the general formula [Pd(L)(Cl)(PPh<sub>3</sub>)] by reacting the precursor complex [PdCl<sub>2</sub>(PPh<sub>3</sub>)<sub>2</sub>] with the hydrazone ligands <b>HL</b><sub><b>1</b></sub> or <b>HL</b><sub><b>2</b></sub>. Single crystal XRD and conventional spectroscopic techniques were employed to characterize both complexes. From the catalytic application point of view, the new complexes <b>1</b> and <b>2</b> were tested as homogeneous catalysts towards the conversion of 3-chlorocoumarins into 3-arylcoumarins by activating the challenging C<span></span>Cl functionality. A minimal catalyst loading of complex <b>2</b> (0.01 mol%), afforded a series of 3-arylcoumarins with a maximum of 92% yield and reusability up to five cycles. The present methodology is simple and easy to carry out at room temperature utilizing a green solvent (ethanol) in an open flask with a spectrum of aryl boronic acids.</p>\\n </div>\",\"PeriodicalId\":8344,\"journal\":{\"name\":\"Applied Organometallic Chemistry\",\"volume\":\"38 12\",\"pages\":\"\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2024-08-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Applied Organometallic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/aoc.7709\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applied Organometallic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/aoc.7709","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
3-Arylcoumarin Scaffolds From 3-Chlorocoumarin and Arylboronic Acids via Site-Selective CCl Bond Activation With Palladium Complexes of N∩O Chelating Hydrazones
Using palladium hydrazone complex as a homogeneous catalyst for SMC, we synthesized a library of 15 variant 3-arylcoumarins. In this context, we report a set of four coordinated palladium(II) hydrazone complexes 1 and 2 having the general formula [Pd(L)(Cl)(PPh3)] by reacting the precursor complex [PdCl2(PPh3)2] with the hydrazone ligands HL1 or HL2. Single crystal XRD and conventional spectroscopic techniques were employed to characterize both complexes. From the catalytic application point of view, the new complexes 1 and 2 were tested as homogeneous catalysts towards the conversion of 3-chlorocoumarins into 3-arylcoumarins by activating the challenging CCl functionality. A minimal catalyst loading of complex 2 (0.01 mol%), afforded a series of 3-arylcoumarins with a maximum of 92% yield and reusability up to five cycles. The present methodology is simple and easy to carry out at room temperature utilizing a green solvent (ethanol) in an open flask with a spectrum of aryl boronic acids.
期刊介绍:
All new compounds should be satisfactorily identified and proof of their structure given according to generally accepted standards. Structural reports, such as papers exclusively dealing with synthesis and characterization, analytical techniques, or X-ray diffraction studies of metal-organic or organometallic compounds will not be considered. The editors reserve the right to refuse without peer review any manuscript that does not comply with the aims and scope of the journal. Applied Organometallic Chemistry publishes Full Papers, Reviews, Mini Reviews and Communications of scientific research in all areas of organometallic and metal-organic chemistry involving main group metals, transition metals, lanthanides and actinides. All contributions should contain an explicit application of novel compounds, for instance in materials science, nano science, catalysis, chemical vapour deposition, metal-mediated organic synthesis, polymers, bio-organometallics, metallo-therapy, metallo-diagnostics and medicine. Reviews of books covering aspects of the fields of focus are also published.