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On the Usability of Salt Metathesis Reactions for the Synthesis of Sterically Crowded tris-Formamidinate Ln(III) Complexes: Success and Limits. Spontaneous Reduction of Eu(III) to Eu(II) Full article

Journal New Journal of Chemistry
ISSN: 1144-0546 , E-ISSN: 1369-9261
Output data Year: 2022, Volume: 46, Number: 25, Pages: 11994-12001 Pages count : 8 DOI: 10.1039/d2nj01589g
Tags Europium compounds; Neodymium compounds; Synthesis (chemical); Toluene
Authors Bashirov Denis A. 1 , Kolybalov Dmitry S. 2 , Mironova Olga A. 1 , Sukhikh Taisiya S. 1 , Konchenko Sergey N. 1
Affiliations
1 Nikolaev Institute of Inorganic Chemistry SB RAS, Akademika Lavrentieva Ave. 3, 630090 Novosibirsk, Russia
2 Department of Natural Sciences, Novosibirsk State University, Pirogova St. 2, 630090 Novosibirsk, Russia

Abstract: Homoleptic [Ln(FormDipp)3] (FormDipp− = CH(NDipp)2− (Dipp = 2,6-diisopropylphenyl), Ln = Nd, Eu) complexes bearing three bulky formamidinate ligands were successfully obtained using the salt metathesis approach, viz. the reaction of [Ln(FormDipp)2Cl(thf)n] (Ln = Nd (n = 2), Ln = Eu (n = 1)) with K(FormDipp) in toluene at 100 °C. This method is not useful for the Ln smaller than Eu: all attempts to realize it for Gd and Tb were unsuccessful. In the case of Eu, the tris-formamidinate complex was obtained in toluene, but in a thf/toluene mixture, a spontaneous reduction of Eu(III) to Eu(II) leading to the formation of [Eu(FormDipp)2(thf)2] was observed. The Eu(III) to Eu(II) conversion is rather sterically induced. UV-Vis spectroscopy monitoring of the reaction indicates it to be a zero-order process. Possible routes of the reaction are proposed.
Cite: Bashirov D.A. , Kolybalov D.S. , Mironova O.A. , Sukhikh T.S. , Konchenko S.N.
On the Usability of Salt Metathesis Reactions for the Synthesis of Sterically Crowded tris-Formamidinate Ln(III) Complexes: Success and Limits. Spontaneous Reduction of Eu(III) to Eu(II)
New Journal of Chemistry. 2022. V.46. N25. P.11994-12001. DOI: 10.1039/d2nj01589g WOS Scopus РИНЦ ANCAN OpenAlex
Dates:
Submitted: Mar 31, 2022
Accepted: May 24, 2022
Published online: May 24, 2022
Published print: Jul 7, 2022
Identifiers:
Web of science: WOS:000806452600001
Scopus: 2-s2.0-85131968280
Elibrary: 48724467
Chemical Abstracts: 2022:1454008
Chemical Abstracts (print): 179:297717
OpenAlex: W4293193070
Citing: Пока нет цитирований
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