Logo BSU

Пожалуйста, используйте этот идентификатор, чтобы цитировать или ссылаться на этот документ: https://elib.bsu.by/handle/123456789/288737
Полная запись метаданных
Поле DCЗначениеЯзык
dc.contributor.authorErb, W.-
dc.contributor.authorWen, M.-
dc.contributor.authorPierre Hurvois, J.-
dc.contributor.authorMongin, F.-
dc.contributor.authorHalauko, Y.S.-
dc.contributor.authorIvashkevich, O.A.-
dc.contributor.authorMatulis, V.E.-
dc.contributor.authorRoisnel, T.-
dc.date.accessioned2022-11-10T07:50:08Z-
dc.date.available2022-11-10T07:50:08Z-
dc.date.issued2021-
dc.identifier.citationEur J Inorg Chem 2021;2021(31):3165-3176ru
dc.identifier.urihttps://elib.bsu.by/handle/123456789/288737-
dc.description.abstractFew studies have been reported on the synthesis of ferrocenesulfonates up to now. Here, we describe the use of ortho-deprotometalation and “halogen dance” reactions to easily reach original derivatives. Further functionalizations using cross-coupling and metal/halogen exchange were also performed from iodinated derivatives. Finally, while the electrochemical properties of selected ferrocenesulfonates were evaluated and compared with the corresponding sulfonamide derivatives, halogen bonds were observed at the solid state for iodinated derivatives of ferrocenesulfonates.ru
dc.description.sponsorshipThis work was supported by the Agence Nationale de la Recherche (ANR; Ferrodance program) and the Université de Rennes 1. William Erb thanks Rennes Métropole. We gratefully acknowledge BASF (generous gift of (R,R)‐bis(1‐phenylethyl)amine), Thermofisher (generous gift of 2,2,6,6‐tetramethylpiperidine), and the Fonds Européen de Développement Régional (FEDER; D8 Venture Bruker AXS diffractometer). This work was supported by the Agence Nationale de la Recherche (ANR; Ferrodance program) and the Universit? de Rennes 1. William Erb thanks Rennes M?tropole. We gratefully acknowledge BASF (generous gift of (R,R)-bis(1-phenylethyl)amine), Thermofisher (generous gift of 2,2,6,6-tetramethylpiperidine), and the Fonds Europ?en de D?veloppement R?gional (FEDER; D8 Venture Bruker AXS diffractometer).ru
dc.language.isoenru
dc.publisherJohn Wiley and Sons Inc CODEN EJICFru
dc.rightsinfo:eu-repo/semantics/openAccessru
dc.subjectЭБ БГУ::ЕСТЕСТВЕННЫЕ И ТОЧНЫЕ НАУКИ::Химияru
dc.subjectЭБ БГУ::ТЕХНИЧЕСКИЕ И ПРИКЛАДНЫЕ НАУКИ. ОТРАСЛИ ЭКОНОМИКИ::Химическая технология. Химическая промышленностьru
dc.titleO-Isopropylferrocenesulfonate: Synthesis of Polysubstituted Derivatives and Electrochemical Studyru
dc.typearticleru
dc.rights.licenseCC BY 4.0ru
dc.identifier.DOI10.1002/ejic.202100448-
dc.identifier.scopus85111915659-
Располагается в коллекциях:Статьи сотрудников НИИ ФХП

Полный текст документа:
Файл Описание РазмерФормат 
Erb et al-2021-O-Isopropylferrocenesulfonate.pdf1,72 MBAdobe PDFОткрыть
Показать базовое описание документа Статистика Google Scholar



Все документы в Электронной библиотеке защищены авторским правом, все права сохранены.