4.6 Article

Triazolium cations: from the click pool to multipurpose applications

期刊

NEW JOURNAL OF CHEMISTRY
卷 38, 期 2, 页码 474-480

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c3nj00667k

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  1. Ministerio de Economia y Competitividad (MINECO, Spain) [CTQ2010-21625-C02-01]
  2. Gobierno Vasco [ETORTEK-nanoIKER IE-11/304]
  3. Gobierno Vasco
  4. UPV/EHU

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Accessing 1,2,3-triazole compounds through the copper-catalysed azide-alkyne click cycloaddition reaction is now a routine synthetic tool which has resulted in a huge amount of novel molecules of varied complexity bearing such heterocycles. 3-N-Alkyl-1,2,3-triazolium salts constitute an example of post-click chemistry arising from the click pool. This Focus review outlines emerging fields of application for triazolium cations, including their use as functional ionic liquids, as precursors of mesoionic carbenes, or as components of supramolecular assemblies and molecular machines.

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