Multivalent hydrogen-bonded architectures directed by self-complementarity between [Cu(2,20-biimidazole)] and malonate building blocks
Abstract:
The synthesis and structural characterization of four novel supramolecular hydrogen-bonded arrangements based on self-assembly from molecular ‘[Cu(2,2<sup>0</sup>biimidazole)]’ modules and malonate anions are presented, namely, tetrakis-(2,2<sup>0</sup>-biimidazole)di-chlorido-dimalonatotricopper(II) pentahydrate, [Cu<inf>3</inf>(C<inf>3</inf>H<inf>2</inf>O<inf>4</inf>)<inf>2</inf>Cl<inf>2</inf>(C<inf>6</inf>H<inf>6</inf>N<inf>4</inf>)<inf>4</inf>]·5H<inf>2</inf>O or [Cu(H<inf>2</inf>biim)<inf>2</inf>(-Cl)Cu<inf>0.5</inf>(mal)]<inf>2</inf>·5H<inf>2</inf>O, aqua-(2,2<sup>0</sup>-biimidazole)malonatocopper(II) dihydrate, [Cu(C<inf>3</inf>H<inf>2</inf>O<inf>4</inf>)(C<inf>6</inf>H<inf>6</inf>N<inf>4</inf>)(H<inf>2</inf>O)]·-2H<inf>2</inf>O or [Cu(H<inf>2</inf>biim)(mal)(H<inf>2</inf>O)]·2H<inf>2</inf>O, bis[aquabis(2,2<sup>0</sup>-biimidazole)copper(II)] dimalonatodiperchloratocopper(II) 2.2-hydrate, [Cu(C<inf>6</inf>H<inf>6</inf>N<inf>4</inf>)<inf>2</inf>(H<inf>2</inf>O)]<inf>2</inf>[Cu(C<inf>3</inf>H<inf>2</inf>O<inf>4</inf>)(ClO<inf>4</inf>)<inf>2</inf>]·2.2H<inf>2</inf>O or [Cu(H<inf>2</inf>biim)<inf>2</inf>(H<inf>2</inf>O)]<inf>2</inf>[Cu(mal)<inf>2</inf>(ClO<inf>4</inf>)<inf>2</inf>]·2.2H<inf>2</inf>O, and bis(2,2<sup>0</sup>-biimidazole)copper(II) bis[bis(2,2<sup>0</sup>-biimidazole)(2-carboxyacetato)malonatocopper(II)] tridecahydrate, [Cu(C<inf>6</inf>H<inf>6</inf>N<inf>4</inf>)<inf>2</inf>][Cu(C<inf>3</inf>H<inf>2</inf>O<inf>4</inf>)(C<inf>3</inf>H<inf>3</inf>O<inf>4</inf>)(C<inf>6</inf>H<inf>6</inf>N<inf>4</inf>)<inf>2</inf>]·13H<inf>2</inf>O or [Cu(H<inf>2</inf>biim)<inf>2</inf>][Cu(H<inf>2</inf>biim)<inf>2</inf>(Hmal)(mal)]<inf>2</inf>·13H<inf>2</inf>O. These assemblies are characterized by self-complementary donor–acceptor molecular interactions, demonstrating a recurrent and distinctive pattern of hydrogen-bonding preferences among the carboxylate, carboxylic acid and N—H groups of the coordinated 2,2<sup>0</sup>-biimidazole and malonate ligands. Additionally, coordination of the carboxylate group with the metallic centre helps sustain remarkable supramolecular assemblies, such as layers, helices, double helix columns or 3D channeled architectures, including mixed-metal complexes, into a single structure.
Año de publicación:
2024
Keywords:
- 2,20-biimidazole
- copper(II)
- Crystal structure
- Hydrogen bonding
- malonate
- supramolecular
Fuente:
scopusTipo de documento:
Article
Estado:
Acceso restringido
Áreas de conocimiento:
- Química inorgánica
- Cristalografía de rayos X
- Química teórica
Áreas temáticas de Dewey:
- Química física
- Química inorgánica
- Química orgánica
Objetivos de Desarrollo Sostenible:
- ODS 2: Hambre cero
- ODS 12: Producción y consumo responsables
- ODS 9: Industria, innovación e infraestructura