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pro vyhledávání: '"Maksym Matviyishyn"'
Autor:
Maksym Matviyishyn, Bartosz Szyszko
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 19, Iss 1, Pp 1630-1650 (2023)
Porphyrins and crown ether hybrids have emerged as a promising class of molecules composed of elements of a tetrapyrrole macrocycle and an oligo(ethylene glycol) segment. These hybrid systems constitute a broad group of compounds, including crowned p
Externí odkaz:
https://doaj.org/article/a71728d0566e461b9e1e90e47cd67e3b
Publikováno v:
Angewandte Chemie. 134
Publikováno v:
Angewandte Chemie International Edition. 61
Crownphyrins are hybrid macrocycles combining structural features of porphyrin and crown ethers. The molecular architecture renders them an intriguing class of hosts capable of binding neutral, and ionic guests. The presence of dynamic covalent imine
Publikováno v:
Angewandte Chemie International Edition. 59:20137-20146
Di-2,7-naphthihexaphyrin(1.1.1.1.1.1), a non-aromatic carba-analogue of the hexaphyrin(1.1.1.1.1.1), incorporating two built-in 2,7-naphthylene moieties was synthesized as two separate, conformationally locked stereoisomers. Both conformers followed
Autor:
Maksym Matviyishyn, Ewa Pacholska-Dudziak, Bartosz Szyszko, Agata Białońska, Serhii Hirka, Lechosław Latos-Grażyński
Publikováno v:
Organic Letters. 21:7009-7014
Replacement of the m-phenylene moiety of m-benziporphyrins with the 2,7-naphthalenyl subunit yielded 28-hetero-2,7-naphthiporphyrins—macrocycles that can be considered as expanded carbaporphyrinoid...
Autor:
Bartosz, Szyszko, Maksym, Matviyishyn, Serhii, Hirka, Ewa, Pacholska-Dudziak, Agata, Białońska, Lechosław, Latos-Grażyński
Publikováno v:
Organic letters. 21(17)
Replacement of the