Producción Científica Profesorado

Copper(II) complexes supported by click generated mixed NN, NO, and NS 1,2,3-triazole based ligands and their catalytic activity in azide?alkyne cycloaddition



Mendoza Espinosa, Daniel

2014

Daniel Mendoza-Espinosa, Alejandro Álvarez-Hernández, Guillermo Enrique Negrón-Silva, Oscar R. Suárez-Castillo, Deyanira Ángeles-Beltrán and Rosa Santillán. Copper(II) complexes supported by click generated mixed NN, NO, and NS 1,2,3-triazole based ligands and their catalytic activity in azide?alkyne cycloaddition. Dalton Trans. 2014, 43, 7069-7077.


Abstract


The preparation and characterization of four new copper(II) complexes supported by click generated mixed NN, NO, and NS 1,2,3-triazoles are reported. The four complexes display a 1 : 2 copper/ligand ratio and give monomeric units in the solid state. Crystal structures demonstrate that depending on the flexibility of the ligand NX (X = O, N, S) pendant arm, the coordination environment around the metal center can feature square planar or octahedral geometries. All four complexes are catalytically active at room temperature in a copper-catalyzed alkyne?azide cycloaddition (CuAAC) reaction using sodium ascorbate as a reducing agent and water?ethanol as a solvent mixture. Complex 8 supported by the NS ligand displayed the best catalytic performance of the series allowing for the easy and high yielding preparation of a variety of mono-, bis- and tris-1,2,3-triazoles under low catalyst loadings.






Artículos relacionados

Total Syntheses of Five Indole Alkaloids from the Marine Bryozoan Flustra foliacea

Aromatic Bromination versus Oxidation of Indolylmalonates by Bromine

Absolute configuration determination of 2-(2-oxo-3-indolyl)acetamide derivatives

Regioselective Synthesis of 3-Indolyl(alkoxy)acetates

The absoluteconfiguration of cuauhtemone and related compounds

Reactivity of TpMe2Ir(C2H4)(DMAD) with carboxylic acids. A DFT study on geometrical isomers and stru...

Configuration, stereodynamics and crystal structure of 3-substituted-2-oxofuro[2,3-b]indoles

Synthesis of Indolylindolines Mediated by tert-BuNH2

Unimolecular rearrangements of ketene-O,O-acetals and fragmentations occurring in the gas phase

13C NMR and crystallographic evidence of push-pull effects in furoindolic ?-enamino esters