A mini review of the synthesis of poly-1,2,3-triazole-based functional materials

Abstract

Most recent advances of the synthesis of poly-1,2,3-triazole-based functional materials.

Retracted Article: Facile preparation of bithiazole-based material for inkjet printed light-emitting electrochemical cell

“…[30][31][32][33] Therefore, these have aroused interest in the syntheses of bithiazoles. [34][35][36] Based on our previous research, [37][38][39][40][41] the use of bithiazole ligands already explored by our group for photocatalytic technology has the advantage of an easy transformation of neutral complexes into charged ones by substitution on the N-atom of the thiazole moiety. 42,43 Furthermore, we demonstrate the fabrication of LEC devices by a combination of inkjet printing and spin coating, on A4 paper substrates for low cost, disposable and exible conductive pattern.…”

Polyvinylpolypyrrolidone‐Stabilized Copper Nanoparticles as an Efficient and Recyclable Heterogeneous Catalyst for the Click of 1,2,3‐Triazoles in Water

“…Since its discovery by Huisgen, the 1,3‐dipolar cycloaddition reaction between azide and alkyne has been applied for the syntheses of 1,4‐ and 1,5‐disubstituted‐1,2,3‐triazoles, which in turn have been served as important and key structural motifs in several applications ranging from biology to material sciences . However, the Huisgen reaction was characterized by being carried out at high temperatures, with a low rate and providing a mixture of both 1,4‐ and 1,5‐disubstituted‐1,2,3‐triazoles as regioisomers .…”

A Brief Minireview of poly-triazole: Alkyne and Azide Substrate Selective, Metal-catalyst Design

“…25 In this review, we will mostly focus on recent developments in the effects of different substrates containing azide and alkyne. Based on our research, [26][27][28][29][30][31] usage of the term click reaction is not only including the substrate classes of monoalkyne, diyne, triyne, fourfold-yne, mono-azide, diazide, triazide and fourfold-yne, but extended to structurally related compounds with selective, reactivity and productive yield, etc. Moreover, marco-molecular click reactions will be mentioned as well if they are necessary for the discussion or might act as springboard for future research.…”