Pablo Romarís, J. M. Vila, Fátima Lucio-Martínez, Francisco Reigosa, P. Munín, Paula Polo‐Ces, M. Pereira
{"title":"双金属配体双核钯环的合成及其对二膦的反应性","authors":"Pablo Romarís, J. M. Vila, Fátima Lucio-Martínez, Francisco Reigosa, P. Munín, Paula Polo‐Ces, M. Pereira","doi":"10.3390/ECSOC-22-05684","DOIUrl":null,"url":null,"abstract":": Palladacycles are an important class of organometallic compounds. They are interesting for their stability and for their important applications as catalysts in cross-coupling reactions. The work described herein relates to the synthesis of a dicyclometallated compound stemming from a diamine ligand, with a doubly metallated aromatic ring. Its reactivity towards a variety of tertiary diphosphines is also considered. The latter ligands show diverse coordination modes, opening the possibility of synthesizing quite different complex structures bearing transition metal atoms in close proximity to each other.","PeriodicalId":448277,"journal":{"name":"Proceedings of The 22nd International Electronic Conference on Synthetic Organic Chemistry","volume":"51 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis of a dinuclear palladacycle with a doubly metallated ligand and its reactivity towards diphosphines\",\"authors\":\"Pablo Romarís, J. M. Vila, Fátima Lucio-Martínez, Francisco Reigosa, P. Munín, Paula Polo‐Ces, M. Pereira\",\"doi\":\"10.3390/ECSOC-22-05684\",\"DOIUrl\":null,\"url\":null,\"abstract\":\": Palladacycles are an important class of organometallic compounds. They are interesting for their stability and for their important applications as catalysts in cross-coupling reactions. The work described herein relates to the synthesis of a dicyclometallated compound stemming from a diamine ligand, with a doubly metallated aromatic ring. Its reactivity towards a variety of tertiary diphosphines is also considered. The latter ligands show diverse coordination modes, opening the possibility of synthesizing quite different complex structures bearing transition metal atoms in close proximity to each other.\",\"PeriodicalId\":448277,\"journal\":{\"name\":\"Proceedings of The 22nd International Electronic Conference on Synthetic Organic Chemistry\",\"volume\":\"51 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-11-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Proceedings of The 22nd International Electronic Conference on Synthetic Organic Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3390/ECSOC-22-05684\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Proceedings of The 22nd International Electronic Conference on Synthetic Organic Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/ECSOC-22-05684","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Synthesis of a dinuclear palladacycle with a doubly metallated ligand and its reactivity towards diphosphines
: Palladacycles are an important class of organometallic compounds. They are interesting for their stability and for their important applications as catalysts in cross-coupling reactions. The work described herein relates to the synthesis of a dicyclometallated compound stemming from a diamine ligand, with a doubly metallated aromatic ring. Its reactivity towards a variety of tertiary diphosphines is also considered. The latter ligands show diverse coordination modes, opening the possibility of synthesizing quite different complex structures bearing transition metal atoms in close proximity to each other.