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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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.