Your browser doesn't support javascript.
loading
Assembly of Polyiodide Networks with Cu(II) Complexes of Pyridinol-Based Tetraaza Macrocycles.
Martínez-Camarena, Álvaro; Savastano, Matteo; Blasco, Salvador; Delgado-Pinar, Estefanía; Giorgi, Claudia; Bianchi, Antonio; García-España, Enrique; Bazzicalupi, Carla.
Afiliación
  • Martínez-Camarena Á; ICMol, Department of Inorganic Chemistry, University of Valencia, C/Catedrático José Beltrán 2, 46980 Paterna, Spain.
  • Savastano M; Department of Chemistry "Ugo Schiff", University of Florence, Via della Lastruccia 3-13, 50019 Sesto Fiorentino, Italy.
  • Blasco S; ICMol, Department of Inorganic Chemistry, University of Valencia, C/Catedrático José Beltrán 2, 46980 Paterna, Spain.
  • Delgado-Pinar E; ICMol, Department of Inorganic Chemistry, University of Valencia, C/Catedrático José Beltrán 2, 46980 Paterna, Spain.
  • Giorgi C; Department of Chemistry, CQC, University of Coimbra, P3004-535 Coimbra, Portugal.
  • Bianchi A; Department of Chemistry "Ugo Schiff", University of Florence, Via della Lastruccia 3-13, 50019 Sesto Fiorentino, Italy.
  • García-España E; Department of Chemistry "Ugo Schiff", University of Florence, Via della Lastruccia 3-13, 50019 Sesto Fiorentino, Italy.
  • Bazzicalupi C; ICMol, Department of Inorganic Chemistry, University of Valencia, C/Catedrático José Beltrán 2, 46980 Paterna, Spain.
Inorg Chem ; 61(1): 368-383, 2022 Jan 10.
Article en En | MEDLINE | ID: mdl-34933551
Polyiodide networks are currently of great practical interest for the preparation of new electronic materials. The participation of metals in the formation of these networks is believed to improve their mechanical performance and thermal stability. Here we report the results on the construction of polyiodide networks obtained using Cu(II) complexes of a series of pyridinol-based tetraazacyclophanes as countercations. The assembly of these crystalline polyiodides takes place from aqueous solutions on the basis of similar structural elements, the [CuL]2+ and [Cu(H-1L)]+ (L = L2, L2-Me, L2-Me3) complex cations, so that the peculiarities induced by the increase of N-methylation of ligands, the structural variable of ligands, can be highlighted. First, solution equilibria involving ligands and complexes were analyzed (potentiometry, NMR, UV-vis, ITC). Then, the appropriate conditions could be selected to prepare polyiodides based on the above complex cations. Single-crystal XRD analysis showed that the coordination of pyridinol units to two metal ions is a prime feature of these ligands, leading to polymeric coordination chains of general formula {[Cu(H-1L)]}nn+ (L = L2-Me, L2-Me3). In the presence of the I-/I2 couple, the polymerization tendency stops with the formation of [(CuL)(CuH-1L)]3+ (L = L2-Me, L2-Me3) dimers which are surrounded by polyiodide networks. Moreover, coordination of the pyridinol group to two metal ions transforms the surface charge of the ring from negative to markedly positive, generating a suitable environment for the assembly of polyiodide anions, while N-methylation shifts the directional control of the assembly from H-bonds to I···I interactions. In fact, an extended concatenation of iodine atoms occurs around the complex dimeric cations, the supramolecular I···I interactions become shorter and shorter, fading into stronger forces dominated by the orbital overlap, which is promising for effective electronic materials.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Inorg Chem Año: 2022 Tipo del documento: Article País de afiliación: España Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Inorg Chem Año: 2022 Tipo del documento: Article País de afiliación: España Pais de publicación: Estados Unidos