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https://elib.bsu.by/handle/123456789/288737Полная запись метаданных
| Поле DC | Значение | Язык |
|---|---|---|
| dc.contributor.author | Erb, W. | - |
| dc.contributor.author | Wen, M. | - |
| dc.contributor.author | Pierre Hurvois, J. | - |
| dc.contributor.author | Mongin, F. | - |
| dc.contributor.author | Halauko, Y.S. | - |
| dc.contributor.author | Ivashkevich, O.A. | - |
| dc.contributor.author | Matulis, V.E. | - |
| dc.contributor.author | Roisnel, T. | - |
| dc.date.accessioned | 2022-11-10T07:50:08Z | - |
| dc.date.available | 2022-11-10T07:50:08Z | - |
| dc.date.issued | 2021 | - |
| dc.identifier.citation | Eur J Inorg Chem 2021;2021(31):3165-3176 | ru |
| dc.identifier.uri | https://elib.bsu.by/handle/123456789/288737 | - |
| dc.description.abstract | Few 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.sponsorship | This 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.iso | en | ru |
| dc.publisher | John Wiley and Sons Inc CODEN EJICF | ru |
| dc.rights | info:eu-repo/semantics/openAccess | ru |
| dc.subject | ЭБ БГУ::ЕСТЕСТВЕННЫЕ И ТОЧНЫЕ НАУКИ::Химия | ru |
| dc.subject | ЭБ БГУ::ТЕХНИЧЕСКИЕ И ПРИКЛАДНЫЕ НАУКИ. ОТРАСЛИ ЭКОНОМИКИ::Химическая технология. Химическая промышленность | ru |
| dc.title | O-Isopropylferrocenesulfonate: Synthesis of Polysubstituted Derivatives and Electrochemical Study | ru |
| dc.type | article | ru |
| dc.rights.license | CC BY 4.0 | ru |
| dc.identifier.DOI | 10.1002/ejic.202100448 | - |
| dc.identifier.scopus | 85111915659 | - |
| Располагается в коллекциях: | Статьи сотрудников НИИ ФХП | |
Полный текст документа:
| Файл | Описание | Размер | Формат | |
|---|---|---|---|---|
| Erb et al-2021-O-Isopropylferrocenesulfonate.pdf | 1,72 MB | Adobe PDF | Открыть |
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