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DOI: 10.1055/s-2003-36811
Synthesis of 4′-Substituted-2,2′:6′,2′′-Terpyridines
Publication History
Publication Date:
22 January 2003 (online)
Abstract
The terdentate ligand 2,2′:6′,2′′-terpyridine (tpy) has increasingly become one of the most popular ligands in coordination chemistry. A variety of substituents are utilised to tailor the properties of its metal complexes. 2,2′:6′,2′′-Terpyridine was reacted with almost all transition metals to form complexes. Among a series of tpy ligand derivatives, those containing substituents at the C(4′) position are of especial interest. Metal-bonded tpy ligands with spacers at C(4′) provide a means of directionality, and thus a means of linear communication, it means that electronic communication can occur along the coordination axis. In addition, the insertion of a single substituent at the C(4′)-position of the tpy ligand results in no enantiomeric derivatives, as the derivative retains its plane of symmetry. The synthetic strategies used to prepare tpy ligands are reviewed comprehensively.
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1 Introduction
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2 The Configuration of 2,2′:6′,2′′-Terpyridine
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3 Methods for the Synthesis of tpy Ligands
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3.1 Condensation Methodology
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3.2 Pyrolysis of Hydrazonium Salt
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3.3 Tohda Methodology
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3.4 Metal-mediated Methodologies
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3.5 Sauer Methodology
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4. Synthesis of Ligands
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4.1 4′-Aromatic Substituted-2,2′:6′,2′′-terpyridines
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4.2 Synthesis of tpy Ligands Possessing Functional Groups Directly Attached to C(4′)
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4.2.1 Preparation of Trimethyl Derivatives of 2,2′:6′,2′′-Terpyridine
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4.2.2 Carbonyl Derivatives of tpy Ligands
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4.2.3 Synthesis of 4′-Carbaldehyde Oxime-2,2′:6′,2′′-terpyridine
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4.2.4 Carboxylate Derivatives of tpy Ligands
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4.2.5 Synthesis of 4′-Nitro-2,2′:6′,2′′-Terpyridines
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4.2.6 Synthesis of 4′-Hydroxy-2,2′:6′,2′′-terpyridines
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4.2.7 Synthesis of 4′,4′-Bis(2,2′:6′,2′′-terpyridyl)amine
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4.2.8 Synthesis of 4′-Thio-substituted 2,2′:6′,2′′-Terpyridines
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4.2.9 Synthesis of 2,2′:6′,2′′-Terpyridine-1′-oxides
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5 Conclusion
Key words
terpyridine - bipyrdine - oligopyridine oxide - coupling reaction - supramolecular chemistry
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Reactions
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References
Fallahpour R.-A. unpublished results.