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Effect of Chirality on the Binding of Viologen Guests in Porphyrin Macrocycles
Author(s) -
Varghese Shaji,
Spierenburg Bram,
Bruekers Jeroen P. J.,
Swartjes Anne,
White Paul B.,
Elemans Johannes A. A. W.,
Nolte Roeland J. M.
Publication year - 2019
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.201900221
Subject(s) - viologen , chemistry , porphyrin , chirality (physics) , selectivity , calixarene , molecule , combinatorial chemistry , enantioselective synthesis , fluorescence , photochemistry , stereochemistry , catalysis , organic chemistry , chiral symmetry breaking , physics , quantum mechanics , nambu–jona lasinio model , quark
As part of a project aimed at the development of chiral processive catalysts that can write information on a polymer chain we describe the synthesis of two optically active porphyrin macrocycles, which are prepared in 3 steps from an achiral precursor compound. Fluorescence and 1 H‐NMR studies show that one of the macrocycles displays selectivity in the binding of chiral viologen guest molecules.

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