12H-Quinoxalino[2,3-b]phenoxazinium complexes with CoII and ZnII hexafluoroacetylacetonates: synthesis, structure, and properties

IF 1.7 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY Russian Chemical Bulletin Pub Date : 2024-07-26 DOI:10.1007/s11172-024-4273-z
V. I. Minkin, S. M. Aldoshin, N. I. Omelichkin, G. V. Shilov, D. V. Korchagin, E. I. Kunitsyna, N. I. Makarova, A. G. Starikov, G. S. Borodkin, P. A. Knyazev, E. P. Ivakhnenko
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Abstract

Reactions of 12H-quinoxaline[2,3-b]phenoxazine (QOPO) derivatives with the CoII and ZnII hexafluoroacetylacetonates accompanied by protonation of the starting bases result in stable complexes [QOPOH]+[M(hfac)3] whose structure was determined by X-ray diffraction and by 1H and 15N NMR spectroscopy. The complexes are characterized by long-wavelength absorption (560–664 nm) and fluorescence in the red region (λfl = 674–805 nm). The relative energies of the protonated tautomers N(14)—H and N(7)—H were determined using the results of B3LYP–D3BJ/6-311G++(d,p) density functional calculations with inclusion of D3BJ dispersion correction. A SQUID magnetometry study of the static and dynamic magnetic properties of the CoII complex revealed that it behaves as a field-induced single-ion magnet.

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12H-喹喔啉并[2,3-b]苯并噁嗪与 CoII 和 ZnII 六氟乙酰丙酮络合物:合成、结构和性质
12H-喹喔啉并[2,3-b]吩噁嗪(QOPO)衍生物与 CoII 和 ZnII 六氟乙酰丙酮酸盐的反应以及起始碱的质子化反应产生了稳定的络合物 [QOPOH]+[M(hfac)3]-,其结构由 X 射线衍射以及 1H 和 15N NMR 光谱确定。这些复合物具有长波长吸收(560-664 nm)和红色区域荧光(λfl = 674-805 nm)的特点。质子化同系物 N(14)-H 和 N(7)-H 的相对能量是通过 B3LYP-D3BJ/6-311G++(d,p) 密度泛函计算并加入 D3BJ 色散校正确定的。对 CoII 复合物的静态和动态磁性进行的 SQUID 磁力测量研究表明,它表现为一种场致单离子磁体。
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来源期刊
Russian Chemical Bulletin
Russian Chemical Bulletin 化学-化学综合
CiteScore
2.70
自引率
47.10%
发文量
257
审稿时长
3-8 weeks
期刊介绍: Publishing nearly 500 original articles a year, by leading Scientists from Russia and throughout the world, Russian Chemical Bulletin is a prominent international journal. The coverage of the journal spans practically all areas of fundamental chemical research and is presented in five sections: General and Inorganic Chemistry; Physical Chemistry; Organic Chemistry; Organometallic Chemistry; Chemistry of Natural Compounds and Bioorganic Chemistry.
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