P. Munín, Francisco Reigosa, F. Lucio, Pablo Romarís, J. M. Ortigueira, J. M. Vila, M. Pereira
{"title":"Synthesis and study of the stability of phosphane palladacycles","authors":"P. Munín, Francisco Reigosa, F. Lucio, Pablo Romarís, J. M. Ortigueira, J. M. Vila, M. Pereira","doi":"10.3390/ecsoc-22-05765","DOIUrl":null,"url":null,"abstract":": The chemistry of phosphane palladacycles[1] has been amply developed in last years. This kind of chemistry results interesting due to their applications in numerous fields such as organic synthesis[2], catalysis[3] or as potential biologically active materials[4]. Palladacycles bearing the diphosphine dppm have been described before[5] and we now report a new behavior shown by palladacycles of the type [Pd 2 (Ph 2 PCH 2 PPh 2 −P,P) 2 (C,N:C,N)]. In this case the coordination of dppm spontaneously shifts from chelate to bridging mode in solution giving a core A-frame conformation with two palladium atoms with a chlorido or bromido ligand between them.","PeriodicalId":448277,"journal":{"name":"Proceedings of The 22nd International Electronic Conference on Synthetic Organic Chemistry","volume":"19 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-22-05765","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
: The chemistry of phosphane palladacycles[1] has been amply developed in last years. This kind of chemistry results interesting due to their applications in numerous fields such as organic synthesis[2], catalysis[3] or as potential biologically active materials[4]. Palladacycles bearing the diphosphine dppm have been described before[5] and we now report a new behavior shown by palladacycles of the type [Pd 2 (Ph 2 PCH 2 PPh 2 −P,P) 2 (C,N:C,N)]. In this case the coordination of dppm spontaneously shifts from chelate to bridging mode in solution giving a core A-frame conformation with two palladium atoms with a chlorido or bromido ligand between them.