ReviewBeilstein journal of organic chemistry2019
1,2,3-Triazolium macrocycles in supramolecular chemistry.
Review in Beilstein journal of organic chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed.
- Synthesis, Physical and Ion-Conducting Properties of 1,2,3-Triazolium Ionic Liquids.Molecules (Basel, Switzerland) · 2026Article
- Core-Twisted, Cationic Perylene Diimides; Homochiral Dimerization and Chiroptical Anion Sensing.Chemistry (Weinheim an der Bergstrasse, Germany) · 2025Article
- Carbazole Framework as Functional Scaffold for the Design of Synthetic Receptors.Chemistry (Weinheim an der Bergstrasse, Germany) · 2025Review
- Selective sensing of adenosine monophosphate (AMP) by a calix[6]triazolium-based colorimetric sensing ensemble.RSC advances · 2022Article
- A Review of Crystalline Multibridged Cyclophane Cages: Synthesis, Their Conformational Behavior, and Properties.Molecules (Basel, Switzerland) · 2022Review
- The Heck reaction of allylic alcohols catalysed by an N-heterocyclic carbene-Pd(ii) complex and toxicity of the ligand precursor for the marine benthic copepodRSC advances · 2021Article
- Synthesis and Guest-Binding Properties of pH/Reduction Dual-Responsive Cyclophane Dimer.Molecules (Basel, Switzerland) · 2021Article
- Design and Synthesis of New 5-aryl-4-Arylethynyl-1Molecules (Basel, Switzerland) · 2021Article
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Authors and funding
3 authors.
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Abstract
In this short review, we describe different pathways for synthesizing 1,2,3-triazolium macrocycles and focus on their application in different areas of supramolecular chemistry. The synthesis is mostly relying on the well-known "click reaction" (CuAAC) leading to 1,4-disubstituted 1,2,3-triazoles that then can be quaternized. Applications of triazolium macrocycles thus prepared include receptors for molecular recognition of anionic species, pH sensors, mechanically interlocked molecules, molecular machines, and molecular reactors.
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