Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Bartosz Szyszko"'
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:
Nature Communications, Vol 8, Iss 1, Pp 1-6 (2017)
One of the challenges of synthetic self-assembled capsules is achieving selective recognition of specific cargoes. Here, authors synthesize a self-assembled porphyrin cubic cage that is capable of sequestering imidazole and thiazole-containing small
Externí odkaz:
https://doaj.org/article/aa6b5f198c7d4869a569764651de33d1
Autor:
Kamil Kupietz, Michał J. Białek, Bartosz Szyszko, Aleksandra Sarwa, Lechosław Latos-Grażyński
Publikováno v:
Organic Chemistry Frontiers. 9:2968-2976
The unique [Fe(CO)5]-induced cyclocarbonylation of the phenanthriporphyrin core is an intriguing example of a post-synthetic modification of the macrocyclic cavity.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::321a3900476836111201184ac353f02d
https://doi.org/10.1039/d2qo00437b
https://doi.org/10.1039/d2qo00437b
Publikováno v:
Chemistry – A European Journal. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8a44d71beb80cb7bb512fd2ae96fce0
https://doi.org/10.1002/chem.202300343
https://doi.org/10.1002/chem.202300343
Publikováno v:
Chemistry – A European Journal. 29
The self-assembly of 2,5-diformylpyrrole, tris(2-aminoethyl)amine, and silver(I) yielded, depending on the size and basicity of the anion, new cascade complexes or plenates, i.e., cryptates incorporating Agnn+ clusters. The nature of the product was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1628a6f8c9afa2c3090b5a083e28e723
https://doi.org/10.1002/chem.202203850
https://doi.org/10.1002/chem.202203850
Publikováno v:
Angewandte Chemie. 134
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a412ad67adc6484022b87cc3defb1f53
https://doi.org/10.1002/ange.202216583
https://doi.org/10.1002/ange.202216583
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1180e407bad3d0204a842c4f4548324
https://doi.org/10.1002/anie.202211671
https://doi.org/10.1002/anie.202211671
Autor:
Bartosz Szyszko
Publikováno v:
European Journal of Organic Chemistry. 2022
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::694d4ac1f1a1ee1556ec1541a33bfab3
https://doi.org/10.1002/ejoc.202200714
https://doi.org/10.1002/ejoc.202200714
Autor:
Emma Robbins, Radosław Deska, Katarzyna Ślusarek, Marta Dudek, Marek Samoć, Lechosław Latos-Grażyński, Bartosz Szyszko, Katarzyna Matczyszyn
Publikováno v:
RSC advances. 12(30)
The one- and two-photon absorption (1PA and 2PA) properties of three expanded aceneporphyrinoids, 28-thia-, 28-selena- and 28-tellura-2,7-naphthiporphyrin, have been studied. The open-aperture Z-scan technique was used to determine two-photon absorpt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d366c3941b1da463871836ce9867e5a
https://pubmed.ncbi.nlm.nih.gov/35865606
https://pubmed.ncbi.nlm.nih.gov/35865606
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7055c30c7c23aaf7d5a2df873f23334
https://doi.org/10.1002/anie.202008518
https://doi.org/10.1002/anie.202008518