دورية أكاديمية

Expanding the Coordination of f-Block Metals with Tris[2-(2-methoxyethoxy)ethyl]amine: From Molecular Complexes to Cage-like Structures.

التفاصيل البيبلوغرافية
العنوان: Expanding the Coordination of f-Block Metals with Tris[2-(2-methoxyethoxy)ethyl]amine: From Molecular Complexes to Cage-like Structures.
المؤلفون: Bokouende SS; Department of Chemistry, Wayne State University, 5101 Cass Avenue, Detroit, Michigan 48202, United States., Kulasekara DN; Department of Chemistry, Wayne State University, 5101 Cass Avenue, Detroit, Michigan 48202, United States., Worku SA; Department of Chemistry, Wayne State University, 5101 Cass Avenue, Detroit, Michigan 48202, United States., Ward CL; Lumigen Instrument Center, Wayne State University, 5101 Cass Avenue, Detroit, Michigan 48202, United States., Kajjam AB; Department of Chemistry, Wayne State University, 5101 Cass Avenue, Detroit, Michigan 48202, United States., Lutter JC; Department of Chemistry, Wayne State University, 5101 Cass Avenue, Detroit, Michigan 48202, United States., Allen MJ; Department of Chemistry, Wayne State University, 5101 Cass Avenue, Detroit, Michigan 48202, United States.
المصدر: Inorganic chemistry [Inorg Chem] 2024 May 27; Vol. 63 (21), pp. 9434-9450. Date of Electronic Publication: 2023 Nov 28.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: American Chemical Society Country of Publication: United States NLM ID: 0366543 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1520-510X (Electronic) Linking ISSN: 00201669 NLM ISO Abbreviation: Inorg Chem Subsets: PubMed not MEDLINE; MEDLINE
أسماء مطبوعة: Original Publication: [Easton, Pa.] American Chemical Society.
مستخلص: Low-valent f-block metals have intrinsic luminescence, electrochemical, and magnetic properties that are modulated with ligands, causing the coordination chemistry of these metals to be imperative to generating critical insights needed to impact modern applications. To this end, we synthesized and characterized a series of twenty-seven complexes of f-metal ions including Eu II , Yb II , Sm II , and U III and hexanuclear clusters of La III and Ce III to study the impact of tris[2-(2-methoxyethoxy)ethyl]amine, a flexible acyclic analogue of the extensively studied 2.2.2-cryptand, on the coordination chemistry and photophysical properties of low-valent f-block metals. We demonstrate that the flexibility of the ligand enables luminescence tunability over a greater range than analogous cryptates of Eu II in solution. Furthermore, the ligand also displays a variety of binding modes to f-block metals in the solid state that are inaccessible to cryptates of low-valent f-block metals. In addition to serving as a ligand for f-block metals of various sizes and oxidation states, tris[2-(2-methoxyethoxy)ethyl]amine also deprotonates water molecules coordinated to trivalent triflate salts of f-block metal ions, enabling the isolation of hexanuclear clusters containing either La III or Ce III . The ligand was also found to bind more tightly to Yb II and U III in the solid state compared to 2.2.2-cryptand, suggesting that it can play a role in the isolation of other low-valent f-block metals such Cf II , Np III , and Pu III . We expect that our findings will inspire applications of tris[2-(2-methoxyethoxy)ethyl]amine in the design of light-emitting diodes and the synthesis of extremely reducing divalent f-block metal complexes that are of interest for a wide range of applications.
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معلومات مُعتمدة: R01 EB027103 United States EB NIBIB NIH HHS
تواريخ الأحداث: Date Created: 20231128 Latest Revision: 20240529
رمز التحديث: 20240529
مُعرف محوري في PubMed: PMC11129929
DOI: 10.1021/acs.inorgchem.3c02752
PMID: 38016147
قاعدة البيانات: MEDLINE
الوصف
تدمد:1520-510X
DOI:10.1021/acs.inorgchem.3c02752