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Induction of an Enantiomeric Excess in a Calix[4]arene/Bipyridine-Based chiral copper(i) complex

✍ Scribed by Jean-Bernard Regnouf-de-Vains; Roger Lamartine; Bernard Fenet


Publisher
John Wiley and Sons
Year
1998
Tongue
German
Weight
491 KB
Volume
81
Category
Article
ISSN
0018-019X

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✦ Synopsis


Abstract

Introduction of the non‐complexing chiral (S)‐2‐methylbutoxy substituent close to the complexing site of a bis[(bipyridinyl)methoxy]calixarene podand resulted in the induction of an enantiomeric excess of ca. 30 % in the corresponding chiral Cu^I^ complex. Structural investigations by high‐resolution NMR studies led us to propose the left‐handed prohelical [Cu^I^(bpy)~2~] substructure for the major enantiomer.


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✍ Jean-Bernard Regnouf De Vains; Roger Lamartine; Bernard Fenet; Claude Bavoux; Al 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 German ⚖ 758 KB

The hetero-armedp-(tert -butyl)calix[4]arene 1 was synthesized by a stepwise procedure. This ligand presented a very strong complexing behavior towards Cu', giving the chiral complex 2 and parent species when reacted with Cu" salts. High-resolution NMR techniques were employed for the characterizati