Óscar Vázquez-Vera
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Óscar Vázquez-Vera has a total of 8 co-authors. Here are the top co-authors by number of shared publications:
- Alejandro Islas-Jácome
Departamento de Química Universidad Autónoma Metropolitana‐Iztapalapa Ciudad de Mexico Mexico
1 shared publication - Atilano Gutiérrez-Carrillo
Departamento de Química, Universidad Autónoma Metropolitana-Iztapalapa, Av. San Rafael, Atlixco 186, Leyes de Reforma 1ra Secc., Ciudad de México 09340, Mexico
1 shared publication - Eduardo González-Zamora
Departamento de Química, Universidad Autónoma Metropolitana-Iztapalapa, Av. Ferrocarril San Rafael Atlixco 186, Col. Leyes de Reforma 1A Sección, Iztapalapa, Ciudad de Mexico C.P. 09310, Mexico
1 shared publication - Galdina Vanessa Suárez-Moreno
Unidad Profesional Interdisciplinaria de Biotecnología, Instituto Politécnico Nacional, Av. Acueducto S/N, Ciudad de México 07340, Mexico
1 shared publication - Julio César Flores Reyes
Departamento de Química, Universidad Autónoma Metropolitana-Iztapalapa, Avenida Ferrocarril San Rafael Atlixco, Número 186, Colonia Leyes de Reforma 1A Sección, Alcaldía Iztapalapa, Ciudad de México 09310, Mexico
1 shared publication - Leticia Lomas-Romero
Departamento de Química, Universidad Autónoma Metropolitana-Iztapalapa, Av. San Rafael Atlixco No. 186, Ciudad de México, C.P. 09340, Mexico
1 shared publication
Latest Publications
- Open Access
- 14 November 2021
- Published by MDPI AG in Chemistry Proceedings
- Vol. 8 (1) , 25
Synthesis of a Symmetrical tris-Tetrazole as Isostere of a Tricarboxylic Acid: Behind New Tridentate Ligands for MOFs
The synthesis and characterization of three tridentate ligands for new MOFs are described. A triple aminolysis of the 1,3,5-tribenzoyl chloride with p-aminobenzoic acid gave the tricarboxylic acid 3 in 90% yield. Moreover, the same reaction, also from the 1,3,5-tribenzoyl chloride, but using p-aminobenzonitrile gave the new tris-benzonitrile 5 in 85% yield. Finally, this later one was treated with sodium azide and a Lewis acid to synthesize the new tris-tetrazole-based ligand 7 in 72% yield through a [3 + 2] azide-nitrile cycloaddition. It is noteworthy that the isosterism between carboxylic acids and tetrazoles may be considered to design and fabricate new MOFs with similar properties.
- 14 November 2021
- Published by MDPI AG in Chemistry Proceedings
- Vol. 8 (1) , 25
Open AccessSynthesis of a Symmetrical tris-Tetrazole as Isostere of a Tricarboxylic Acid: Behind New Tridentate Ligands for MOFs
The synthesis and characterization of three tridentate ligands for new MOFs are described. A triple aminolysis of the 1,3,5-tribenzoyl chloride with p-aminobenzoic acid gave the tricarboxylic acid 3 in 90% yield. Moreover, the same reaction, also from the 1,3,5-tribenzoyl chloride, but using p-aminobenzonitrile gave the new tris-benzonitrile 5 in 85% yield. Finally, this later one was treated with sodium azide and a Lewis acid to synthesize the new tris-tetrazole-based ligand 7 in 72% yield through a [3 + 2] azide-nitrile cycloaddition. It is noteworthy that the isosterism between carboxylic acids and tetrazoles may be considered to design and fabricate new MOFs with similar properties.