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Controllable Solid-State Transformations and Enhanced Luminescence of Labile Lanthanide(III) Aquanitrato Complexes Anchored within a Hydrogen-Bonded Organic Matrix Научная публикация

Журнал Inorganic Chemistry
ISSN: 0020-1669 , E-ISSN: 1520-510X
Вых. Данные Год: 2026, Том: 65, Номер: 31, Страницы: 18334–18345 Страниц : 12 DOI: 10.1021/acs.inorgchem.6c02905
Ключевые слова Lanthanides, Luminescence, Solvents, Anions, Phase Transitions.
Авторы Ushakov Daniil A. 1 , Ryadun Alexey A. 1 , Demakov Pavel A. 1 , Fedin Vladimir P. 1
Организации
1 Nikolaev Institute of Inorganic Chemistry, Siberian Branch of the Russian Academy of Sciences, 630090 Novosibirsk, Russia

Информация о финансировании (1)

1

Реферат: Two structural types of lanthanide (Ln) aquanitrato complexes incorporating 1,4-diazabicyclooctane-N,N′-dioxide (odabco) were synthesized and structurally characterized by single-crystal X-ray diffraction (SCXRD). Phase 1Ln comprises (Hodabco)3[Ln(H2O)2(NO3)4](NO3)2 (Ln3+ = Eu3+, Gd3+, (Eu/Gd)3+, Tb3+) while phase 2Ln represents (Hodabco)3[Ln(H2O)(NO3)5](NO3) (Ln3+ = Eu3+, (Eu/Gd)3+). Due to a shared cationic network composition and coordination isomerism, these Ln-based phases exhibit reversible, solvent-driven structural transitions, fully confirmed by powder XRD. Despite the presence of quenching aqua ligands, the complexes display remarkable photoluminescence with quantum yields up to 40%. The structural transitions induce a 4- fold modulation of photoluminescence quantum yields and a 2-fold variation in excited-state lifetimes. These findings establish a robust strategy for the targeted control of Ln(III) emission via simple chemical stimuli, offering strong potential for chemical sensing and luminescent device design.
Библиографическая ссылка: Ushakov D.A. , Ryadun A.A. , Demakov P.A. , Fedin V.P.
Controllable Solid-State Transformations and Enhanced Luminescence of Labile Lanthanide(III) Aquanitrato Complexes Anchored within a Hydrogen-Bonded Organic Matrix
Inorganic Chemistry. 2026. V.65. N31. P.18334–18345. DOI: 10.1021/acs.inorgchem.6c02905 WOS Scopus
Даты:
Поступила в редакцию: 5 июн. 2026 г.
Принята к публикации: 17 июл. 2026 г.
Опубликована online: 28 июл. 2026 г.
Опубликована в печати: 10 авг. 2026 г.
Идентификаторы БД:
≡ Web of science: WOS:001834474200001
≡ Scopus: 2-s2.0-105046778049
Альметрики: