Quentin Gaydon, Raluca Malacea-Kabbara, Jérôme Bayardon, Laurent Plasseraud, Michel Picquet, Pierre Le Gendre, Benoit Legras, Johann Kieffer
{"title":"苯氧亚胺锌与苯氧亚胺配合物催化酯交换反应合成N,N-二甲基氨基丙烯酸乙酯","authors":"Quentin Gaydon, Raluca Malacea-Kabbara, Jérôme Bayardon, Laurent Plasseraud, Michel Picquet, Pierre Le Gendre, Benoit Legras, Johann Kieffer","doi":"10.1002/aoc.70387","DOIUrl":null,"url":null,"abstract":"<p>Heteroleptic and homoleptic complexes of zinc with phenoxyimine and phenoxyamidine ligands are used as alternatives to currently used tin catalysts in the transesterification reaction of methyl acrylate and <i>N,N-</i>dimethylethanolamine in the synthesis of <i>N,N-</i>dimethylaminoethyl acrylate. A large screening of phenoxyimine and three generations of phenoxyamidine ligands has been undertaken and used to determine the best catalysts in terms of conversion and selectivity. All of the catalysts tested show significant improvement in activity over catalysts currently well-established in industrial processes such as dibutyltin oxide or Ti(O<sup><i>i</i></sup>Pr)<sub>4</sub>. The catalytic charges can be decreased significantly (10–20×) still affording good conversions and selectivities. A series of heteroleptic and homoleptic zinc complexes with phenoxyimine and phenoxyamidine ligands have been tested for the transesterification of methyl acrylate with <i>N,N</i>-dimethylethanolamine. All the catalysts demonstrated a substantial increase in activity compared to dibutyltin oxide, a well-established catalyst that is currently used in industry for this reaction.</p>","PeriodicalId":8344,"journal":{"name":"Applied Organometallic Chemistry","volume":"39 11","pages":""},"PeriodicalIF":3.7000,"publicationDate":"2025-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/aoc.70387","citationCount":"0","resultStr":"{\"title\":\"Synthesis of N,N-Dimethylaminoethyl Acrylate via a Zinc Phenoxyimine and Phenoxyamidine Complexes Catalyzed Transesterification Reaction\",\"authors\":\"Quentin Gaydon, Raluca Malacea-Kabbara, Jérôme Bayardon, Laurent Plasseraud, Michel Picquet, Pierre Le Gendre, Benoit Legras, Johann Kieffer\",\"doi\":\"10.1002/aoc.70387\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Heteroleptic and homoleptic complexes of zinc with phenoxyimine and phenoxyamidine ligands are used as alternatives to currently used tin catalysts in the transesterification reaction of methyl acrylate and <i>N,N-</i>dimethylethanolamine in the synthesis of <i>N,N-</i>dimethylaminoethyl acrylate. A large screening of phenoxyimine and three generations of phenoxyamidine ligands has been undertaken and used to determine the best catalysts in terms of conversion and selectivity. All of the catalysts tested show significant improvement in activity over catalysts currently well-established in industrial processes such as dibutyltin oxide or Ti(O<sup><i>i</i></sup>Pr)<sub>4</sub>. The catalytic charges can be decreased significantly (10–20×) still affording good conversions and selectivities. A series of heteroleptic and homoleptic zinc complexes with phenoxyimine and phenoxyamidine ligands have been tested for the transesterification of methyl acrylate with <i>N,N</i>-dimethylethanolamine. All the catalysts demonstrated a substantial increase in activity compared to dibutyltin oxide, a well-established catalyst that is currently used in industry for this reaction.</p>\",\"PeriodicalId\":8344,\"journal\":{\"name\":\"Applied Organometallic Chemistry\",\"volume\":\"39 11\",\"pages\":\"\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2025-10-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/aoc.70387\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Applied Organometallic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/aoc.70387\",\"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.70387","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
Synthesis of N,N-Dimethylaminoethyl Acrylate via a Zinc Phenoxyimine and Phenoxyamidine Complexes Catalyzed Transesterification Reaction
Heteroleptic and homoleptic complexes of zinc with phenoxyimine and phenoxyamidine ligands are used as alternatives to currently used tin catalysts in the transesterification reaction of methyl acrylate and N,N-dimethylethanolamine in the synthesis of N,N-dimethylaminoethyl acrylate. A large screening of phenoxyimine and three generations of phenoxyamidine ligands has been undertaken and used to determine the best catalysts in terms of conversion and selectivity. All of the catalysts tested show significant improvement in activity over catalysts currently well-established in industrial processes such as dibutyltin oxide or Ti(OiPr)4. The catalytic charges can be decreased significantly (10–20×) still affording good conversions and selectivities. A series of heteroleptic and homoleptic zinc complexes with phenoxyimine and phenoxyamidine ligands have been tested for the transesterification of methyl acrylate with N,N-dimethylethanolamine. All the catalysts demonstrated a substantial increase in activity compared to dibutyltin oxide, a well-established catalyst that is currently used in industry for this reaction.
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.