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Transition Metal Coordination Polymers with Trans-1,4-Cyclohexanedicarboxylate: Acidity-Controlled Synthesis, Structures and Properties Научная публикация

Журнал Materials
ISSN: 1996-1944
Вых. Данные Год: 2020, Том: 13, Номер: 2, Номер статьи : 486, Страниц : 16 DOI: 10.3390/ma13020486
Авторы Demakov Pavel A. 1,2 , Bogomyakov Artem S. 2,3 , Urlukov Artem S. 1,2 , Andreeva Aleksandra Yu. 1 , Samsonenko Denis G. 1,2 , Dybtsev Danil N. 1,2 , Fedin Vladimir P. 1,2
Организации
1 Nikolaev Institute of Inorganic Chemistry SB RAS, Novosibirsk 630090, Russia
2 Department of Natural Sciences, Novosibirsk State University, Novosibirsk 630090, Russia
3 International Tomography Center SB RAS, Novosibirsk 630090, Russia

Реферат: Five trans-1,4-cyclohexanedicarboxylate (chdc2−) metal–organic frameworks of transition metals were synthesized in aqueous systems. A careful control of pH, reaction temperature and solvent composition were shown to direct the crystallization of a particular compound. Isostructural [Co(H2O)4(chdc)]n (1) and [Fe(H2O)4(chdc)]n (2) consist of one-dimensional hydrogen-bonded chains. Compounds [Cd(H2O)(chdc)]n∙0.5nCH3CN (3), [Mn4(H2O)3(chdc)4]n (4) and [Mn2(Hchdc)2(chdc)]n (5) possess three-dimensional framework structures. The compounds 1, 4 and 5 were further characterized by magnetochemical analysis, which reveals paramagnetic nature of these compounds. A presence of antiferromagnetic exchange at low temperatures is observed for 5 while the antiferromagnetic coupling in 4 is rather strong, even at ambient conditions. The thermal decompositions of 1, 4 and 5 were investigated and the obtained metal oxide (cubic Co3O4 and MnO) samples were analyzed by X-ray diffraction and scanning electron microscopy.
Библиографическая ссылка: Demakov P.A. , Bogomyakov A.S. , Urlukov A.S. , Andreeva A.Y. , Samsonenko D.G. , Dybtsev D.N. , Fedin V.P.
Transition Metal Coordination Polymers with Trans-1,4-Cyclohexanedicarboxylate: Acidity-Controlled Synthesis, Structures and Properties
Materials. 2020. V.13. N2. 486 :1-16. DOI: 10.3390/ma13020486 WOS Scopus РИНЦ OpenAlex
Даты:
Поступила в редакцию: 26 дек. 2019 г.
Опубликована в печати: 19 янв. 2021 г.
Идентификаторы БД:
Web of science: WOS:000515499900232
Scopus: 2-s2.0-85079805625
РИНЦ: 43249315
OpenAlex: W2999662398
Цитирование в БД:
БД Цитирований
Web of science 10
Scopus 10
РИНЦ 11
OpenAlex 11
Альметрики: