Repozytorium

Reversible reduction of oxatriphyrin(3.1.1)—adjusting the coordination abilities to the central ion.

Autorzy

Miłosz Pawlicki

Aneta Kędzia

Dominik Bykowski

Lechosław Latos-Grażyński

Rok wydania

2014

Czasopismo

Chemistry-A European Journal

Numer woluminu

20

Strony

17500-17506

DOI

10.1002/chem.201404570

Kolekcja

Naukowa

Język

Angielski

Typ publikacji

Artykuł

Streszczenie

Furan-fused oxatriphyrin(3.1.1) acts as a ligand towards boron(III), phosphorous(III), and phosphorous(V) ions. The coordination abilities are adjusted by changes of the oxidation state. Two coordination modes are possible, depending on the central-ion entrapped in the oxatriphyrin(3.1.1) environment. A free base, structurally similar to the complexes, can be easily obtained by regioselective reduction. The resulting molecules are highly emissive after conversion into a phlorin-like oxatriphyrin(3.1.1) frame (NON donors), and show chiral activity caused by the presence of a tetrahedral carbon.

Słowa kluczowe

boron, fluorescence, phosphorous, subporphyrin, triphyrin

Adres publiczny

http://dx.doi.org/10.1002/chem.201404570

Strona internetowa wydawcy

onlinelibrary.wiley.com

Podobne publikacje
2019

Organoboron complexes in edge-sharing macrocycles: the triphyrin(2.1.1)-tetraphyrin(1.1.1.1) hybrid.

Stawski Wojciech, Hurej Karolina, Skonieczny Janusz, Pawlicki Miłosz

2016

A mixed-valence bis-phosphorus complex entrapped in a oxatriphyrin (3.1.1) surrounding.

Idec Aneta, Skonieczny Janusz, Latos-Grażyński Lechosław, Pawlicki Miłosz

2020

Multi‐cation coordination in porphyrinoids.

Stawski Wojciech, Kijewska Monika, Pawlicki Miłosz