Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Kamil Kupietz"'
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
Autor:
Michał J. Białek, Bartosz Szyszko, Piotr J. Chmielewski, Monika Przewoźnik, Kamil Kupietz, Agata Białońska, Lechosław Latos-Grażyński
Publikováno v:
Journal of the American Chemical Society. 141:6060-6072
The analogue of octaphyrin(1.1.1.0.1.1.1.0) bearing two dimethoxyphenanthrene units was synthesized and characterized in solution and solid state. The macrocycle was demonstrated to exist as two locked conformers that can be easily separated and hand
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc1056b9e334f4c4f07821da49507b5d
https://doi.org/10.1021/jacs.9b01357
https://doi.org/10.1021/jacs.9b01357
Publikováno v:
Inorganic Chemistry. 58:1451-1461
5,6-Dimethoxyphenanthriporphyrin 1 and 5,6-dioxophenanthriporphyrin 2 act as suitable organometallic ligands for copper(III), adopting trianionic [CCNN] coordination cores. Under oxidizing conditions, in the presence of methanol, copper(III) phenanth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bf7b134f70c8a8c4e360e8ddc9da441
https://doi.org/10.1021/acs.inorgchem.8b02997
https://doi.org/10.1021/acs.inorgchem.8b02997
Autor:
Agnieszka Hassa, Lechosław Latos-Grażyński, Kamil Kupietz, Natasza Sprutta, Karolina Kodź-Wichowska, Michał J. Białek
Publikováno v:
Chemistry - A European Journal. 24:14686-14692
A porphyrinogen macrocycle incorporating two azulenes, phenylene and thiophene into the framework, joined by four C(sp3 ) atoms has been obtained as a mixture of six isomers. They were successfully separated and characterized spectroscopically. The i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cde5e4a4c132b56f8884756aa9b5d09a
https://doi.org/10.1002/chem.201802972
https://doi.org/10.1002/chem.201802972
Publikováno v:
Organic Chemistry Frontiers. 5:3068-3076
The incorporation of a 9,10-dimethoxyphenanthrene moiety into a porphyrin framework results in the formation of a hybrid macrocycle – 5,6-dimethoxyphenanthriporphyrin 1, fusing the structural features of polycyclic aromatic hydrocarbons and porphyr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9fcd7511dbfbfddb27ce150f2f3ce54c
https://doi.org/10.1039/c8qo00751a
https://doi.org/10.1039/c8qo00751a
Publikováno v:
Inorganic chemistry. 58(18)
Photooxidation of copper(III) 5,6-dimethoxyphenathriporphyrin and copper(III) 5,6-dioxophenanthriporphyrin, which contain phenanthrene or dioxophenathrene moieties built into the macrocyclic frameworks, resulted in the regioselective cleavage that af
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd9c33ec2eae3a47cee32807f62af2a6
https://pubmed.ncbi.nlm.nih.gov/31454233
https://pubmed.ncbi.nlm.nih.gov/31454233
Publikováno v:
Chemistry - A European Journal. 20:1376-1382
The reaction of p-benziporphyrin, sodium tetrachloroaurate(III) dihydrate, and potassium carbonate in dichloromethane yielded gold(III) 5,10,15,20-tetraaryl-21-carbaporphyrin owing to the contraction of p-phenylene to cyclopentadiene. This molecule i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::436aedff3fd7b15f47bd34f820af4961
https://doi.org/10.1002/chem.201304162
https://doi.org/10.1002/chem.201304162
Autor:
Agata Białońska, Anna Berlicka, Bartosz Szyszko, Michał J. Białek, Kamil Kupietz, Marcin Małecki, Ewa Pacholska-Dudziak, Lechosław Latos-Grażyński
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 22(22)
32-Hetero-5,6-dimethoxyphenanthrisapphyrins-macrocycles that link structural features of polycylic aromatic hydrocarbons and expanded porphyrins-were obtained in a straightforward [3+1] condensation reaction of dimethoxyphenanthritripyrrane and 2,5-b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4ec4b69734388d23b3324eed68408ff
https://pubmed.ncbi.nlm.nih.gov/27098207
https://pubmed.ncbi.nlm.nih.gov/27098207
Autor:
Natasza Sprutta, Lechosław Latos-Grażyński, Michał J. Białek, Karolina Kodź-Wichowska, Agnieszka Hassa, Kamil Kupietz
Publikováno v:
Chemistry - A European Journal. 24:14570-14570
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0baaa215f57ab5431cb10488b734585a
https://doi.org/10.1002/chem.201804477
https://doi.org/10.1002/chem.201804477
Publikováno v:
ECS Meeting Abstracts. :951-951
A replacement of a single pyrrole of meso-tetraarylporphyrin by cyclopentadiene moiety seems to be a notion of the very first choice for the creation of meso-substituted or β-substituted 21-carbaporphyrins which ideally conserve the fundamental fram
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11a650aa8e5a11b21df2340a7776310a
https://doi.org/10.1149/ma2015-01/11/951
https://doi.org/10.1149/ma2015-01/11/951