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Synthesis of “V-Shaped” syn-Bidentate Ligands Based on Mesitylene-Derived [1.1.1.1]Metacyclophane Blocked in a 1,3-Alternate Conformation

✍ Scribed by Cédric Klein; Ernest Graf; Mir W. Hosseini; André De Cian; Nathalie Kyritsakas-Gruber


Book ID
102172674
Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
110 KB
Volume
2003
Category
Article
ISSN
1434-193X

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✦ Synopsis


Abstract

A series of five new syn‐bidentate ligands 14−18 based on the [1.1.1.1]metacyclophane backbone blocked in a 1,3‐alternate conformation was achieved. The common building block for the preparation of ligands bearing two interaction sites located in a syn fashion (CN, SMe, p‐pyridyl, p‐methoxyphenyl and p‐methylthiophenyl) is the dibromo derivative 12. All reported ligands were fully characterised by classical analytical methods and their 1,3‐alternate conformation demonstrated. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)


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✍ Cédric Klein; Ernest Graf; Mir Wais Hosseini; Gilles Mislin; André De Cian 📂 Article 📅 2000 🏛 Elsevier Science 🌐 French ⚖ 84 KB

The synthesis and structural analysis of two new exoligands 1 and 2 based on a [1.1.1.1]-metacyclophane backbone bearing either 2,2%-bipyridine or bisquinoline chelating units have been achieved.