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Solvatomorphism in a series of copper(II) complexes with the 5-phenylimidazole/perchlorate system as ligands.
Loukopoulos, Edward; Papatriantafyllopoulou, Constantina; Moushi, Eleni; Kitos, Alexandros A; Tasiopoulos, Anastasios J; Perlepes, Spyros P; Nastopoulos, Vassilios.
Afiliación
  • Loukopoulos E; Department of Chemistry, University of Patras, Patras, 26504, Greece.
  • Papatriantafyllopoulou C; Department of Chemistry, University of Cyprus, Nicosia, 1678, Cyprus.
  • Moushi E; Department of Chemistry, University of Cyprus, Nicosia, 1678, Cyprus.
  • Kitos AA; Department of Chemistry, University of Patras, Patras, 26504, Greece.
  • Tasiopoulos AJ; Department of Chemistry, University of Cyprus, Nicosia, 1678, Cyprus.
  • Perlepes SP; Department of Chemistry, University of Patras, Patras, 26504, Greece.
  • Nastopoulos V; Department of Chemistry, University of Patras, Patras, 26504, Greece.
Acta Crystallogr B Struct Sci Cryst Eng Mater ; 80(Pt 4): 347-359, 2024 Aug 01.
Article en En | MEDLINE | ID: mdl-39136540
ABSTRACT
In the course of an investigation of the supramolecular behaviour of copper(II) complexes with the 5-phenylimidazole/perchlorate ligand system (`blend') remarkable solvatomorphism has been observed. By employing a variety of crystallization solvents (polar protic, polar/non-polar aprotic), a series of 12 crystalline solvatomorphs with the general formula [Cu(ClO4)2(LH)4]·x(solvent) have been obtained [LH = 5-phenylimidazole, x(solvent) = 3.3(H2O) (1), 2(methanol) (2), 2(ethanol) (3), 2(1-propanol) (4), 2(2-propanol) (5), 2(2-butanol) (6), 2(dimethylformamide) (7), 2(acetone) (8), 2(tetrahydrofurane) (9), 2(1,4-dioxane) (10), 2(ethyl acetate) (11) and 1(diethyl ether) (12)]. The structures have been solved using single-crystal X-ray diffraction and the complexes were characterized by thermal analysis and infrared spectroscopy. The solvatomorphs are isostructural (triclinic, P1), with the exception of compound 9 (monoclinic, P21/n). The supramolecular structures and the role of the various solvents is discussed. All potential hydrogen-bond functionalities, both of the [Cu(ClO4)2(LH)4] units and of the solvents, are utilized in the course of the crystallization process. The supramolecular assembly in all structures is directed by strong recurring Nimidazole-H...Operchlorate motifs leading to robust scaffolds composed of the [Cu(ClO4)2(LH)4] host complexes. The solvents are located in channels and, with the exception of the disordered waters in 1 and the diethyl ether in 12, participate in hydrogen-bonding formation with the [Cu(ClO4)2(LH)4] complexes, serving as both hydrogen-bond acceptors and donors (for the polar protic solvents in 2-6), or solely as hydrogen-bond acceptors (for the polar/non-polar aprotic solvents in 7-11), linking the complexes and contributing to the stability of the crystalline compounds.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Acta Crystallogr B Struct Sci Cryst Eng Mater Año: 2024 Tipo del documento: Article País de afiliación: Grecia Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Acta Crystallogr B Struct Sci Cryst Eng Mater Año: 2024 Tipo del documento: Article País de afiliación: Grecia Pais de publicación: Reino Unido