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Citation
Tags
HERO ID
6932826
Reference Type
Journal Article
Title
28-Hetero-2,7-Naphthiporphyrins: Horizontal Expansion of the m-Benziporphyrin Macrocycle
Author(s)
Szyszko, B; Matviyishyn, M; Hirka, S; Pacholska-Dudziak, Ewa; Bialonska, A; Latos-Grazynski, L; ,
Year
2019
Is Peer Reviewed?
1
Journal
Organic Letters
ISSN:
1523-7060
EISSN:
1523-7052
Publisher
AMER CHEMICAL SOC
Location
WASHINGTON
Page Numbers
7009-7014
PMID
31423794
DOI
10.1021/acs.orglett.9b02587
Web of Science Id
WOS:000485089300085
Abstract
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 carbaporphyrinoids. This group retains some features of parent m-benziporphyrins, but due to larger size and different shape of the macrocyclic cavity, their coordination properties are different. Upon reduction and conformational rearrangement the 28-thia- and 28-selena-2,7-naphthiporphyrin form organophosphorus(V) complexes.
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