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Terpyridine-Based Materials (For Catalytic, Optoelectronic and Life Science Applications) || Synthesis, Properties, and Applications of Functionalized 2,2′:6′,2″-Terpyridines

✍ Scribed by Schubert, Ulrich S.; Winter, Andreas; Newkome, George R.

Book ID
120238635
Publisher
Wiley-VCH Verlag GmbH & Co. KGaA
Year
2011
Tongue
German
Weight
860 KB
Edition
1
Category
Article
ISBN
3527330380

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✦ Synopsis

In recent years, the utilization of terpyridines both in macromolecular structure assembly and device chemistry has exploded, enabling, for example, supramolecular polymer architectures with switchable chemical and physical properties as well as novel functional materials for optoelectronic applications such as light-emitting diodes and solar cells. Further applications include the usage of terpyridines and their metal complexes as catalysts for asymmetric organic reactions and, in a biological context, as anti-tumor agents or biolabels.

This book covers terpyridine-based materials topics ranging from syntheses, chemistry, and multinuclear metal complexes, right up to functionalized polymers, 3D-architectures, and surfaces.

The book is of interest for materials scientists, (in)organic chemists, polymer chemists, complex chemists, physical chemists, biochemists, and libraries.

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Terpyridine-Based Materials (For Catalyt
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✍ Schubert, Ulrich S.; Winter, Andreas; Newkome, George R. 📂 Article 📅 2011 🏛 Wiley-VCH Verlag GmbH & Co. KGaA 🌐 German ⚖ 109 KB

In recent years, the utilization of terpyridines both in macromolecular structure assembly and device chemistry has exploded, enabling, for example, supramolecular polymer architectures with switchable chemical and physical properties as well as novel functional materials for optoelectronic applicat

New 4′-Functionalized 2,2′:6′,2′′-Terpyr
New 4′-Functionalized 2,2′:6′,2′′-Terpyridines for Applications in Macromolecular Chemistry and Nanoscience
✍ Philip R. Andres; Ralph Lunkwitz; Gunther R. Pabst; Karlheinz Böhn; Daan Wouters 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 310 KB 👁 1 views

## Abstract The well‐known reaction of 4′‐chloro‐2,2′:6′,2′′‐terpyridine with alkoxide nucleophiles leads to 4′‐functionalized 2,2′:6′,2′′‐terpyridines. This reaction allows the easy introduction of different functional groups onto the terpyridine at the 4′‐position, i.e. opposite to the metal bind