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 |
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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 | ||||
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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
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:
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