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Influence of Neutral Auxiliary Ligands on Crystal Structure and Magnetic Behaviour of New [MnII2MnIII2] Clusters Supported by p-Adamantylcalix[4]arene Научная публикация

Журнал New Journal of Chemistry
ISSN: 1369-9261 , E-ISSN: 1144-0546
Вых. Данные Год: 2024, Том: 48, Номер: 1, Страницы: 203-215 Страниц : 13 DOI: 10.1039/d3nj04809h
Авторы Ovsyannikov Alexander 1 , Strelnikova Iuliia V. 2,1 , Samigullina Aida I. 3 , Islamov Daut 4 , Cherosov Mikhail 1 , Batulin Ruslan Germanovich 1 , Kiiamov Airat 1 , Gubaidullin Aidar Timergalievich 2 , Dorovatovskii Pavel 5 , Solovieva Svetlana 1 , Igor Antipin S. 1
Организации
1 Kazan Federal University, Kremlevskaya 18 str., 420008 Kazan, Russian Federation
2 A. E. Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center, Russian Academy of Sciences, Arbuzova 8 str., 420088 Kazan, Russian Federation
3 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Leninsky avenue 47, 119991 Moscow, Russian Federation
4 Laboratory for structural analysis of biomacromolecules, FRC Kazan Scientific Center, Russian Academy of Sciences, Lobachevskogo 2/31 str., 420111 Kazan, Russian Federation
5 National Research Center “Kurchatov Institute”, Acad. Kurchatov 1 Sq., 123182 Moscow, Russian Federation

Реферат: A series of new manganese complexes of general formula 32-Mn4Xn, displaying a highly-reproducible [MnII2MnIII2] cluster core formation, was observed when tetra-p-adamantylcalix[4]arene 3 was used in combination with N,N′-chelating auxiliary ligands, such as bipy (32-Mn4(bipy)2, bipy = 2,2′-bipyridyl) and phen (32-Mn4(phen)2, phen = 1,10-phenanthroline), as well as with DMF/H2O solvent molecules (32-Mn4(dmf)4, 32-Mn4(dmf)2(H2O)2), acting as O-donor coligands, in the crystalline phase. Single-crystal X-ray diffraction revealed that the involvement of auxiliary ligands in coordination with Mn-ions results in the distortion of their coordination sphere and leads to the controlled compression of the {Mn4}-cluster core of complexes. Moreover, the appearance of adamantyl groups at the upper rim of the macrocyclic backbone of 3 influences the crystalline self-assembly of obtained clusters, providing a preferable “side-to-head” orientation of the cluster molecules within the crystal, leading to the observation of relatively higher {Mn4}⋯{Mn4} distances than those revealed for the earlier reported calix[4]arene supported {Mn4} clusters. All 32-Mn4Xn clusters demonstrated ferromagnetic interactions between the metal atoms within the cluster core independent of the nature of the O-donor or N-donor auxiliary ligands.
Библиографическая ссылка: Ovsyannikov A. , Strelnikova I.V. , Samigullina A.I. , Islamov D. , Cherosov M. , Batulin R.G. , Kiiamov A. , Gubaidullin A.T. , Dorovatovskii P. , Solovieva S. , Igor A.S.
Influence of Neutral Auxiliary Ligands on Crystal Structure and Magnetic Behaviour of New [MnII2MnIII2] Clusters Supported by p-Adamantylcalix[4]arene
New Journal of Chemistry. 2024. V.48. N1. P.203-215. DOI: 10.1039/d3nj04809h WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: WOS:001113403900001
Scopus: 2-s2.0-85179163598
OpenAlex: W4388844003
Цитирование в БД:
БД Цитирований
OpenAlex 9
Scopus 8
Web of science 8
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