Supramolecular interactions in Cobalt(II)–nucleobases complexes: A methyl matter

  • Khaled Hassanein
  • , Félix Zamora
  • , Oscar Castillo*
  • , Pilar Amo-Ochoa
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

Direct reactions between cobalt(II) acetate and the corresponding modified nucleobase lead to the mononuclear complexes [Co(TAcO)2(H2O)4] (1) and [Co(UAcO)2(H2O)4] (2), (TAcO = thymine-1-acetate, UAcO = uracil-1-acetate). Additionally the reactions between the Co(II) salt with equimolar amount of 2,6-diaminopurine (HDap) and either TAcOH or UAcOH give rise to {[Co(HDap)2(H2O)4]·(TAcO)2·3H2O} (3) and {[Co(HDap)2(H2O)4]·(UAcO)2·3H2O} (4), respectively. The X-ray analysis of all of these complexes show a common feature, the presence of four water molecules in the basal plane coordinated to the Co(II) center. In case of complexes 1 and 2 the coordination environment around the Co(II) is a CoO2Ow4with two modified nucleobases coordinated in a monodentate way through one oxygen of the carboxylate group, whereas for 3 and 4 the coordination environment is CoN2Ow4as a consequence of the coordination to the nitrogen atoms of two HDap ligands. The extended inter-H-bond interactions between water molecules and nucleobase moieties, play crucial role in the crystal packing of complexes.

Original languageEnglish
Pages (from-to)251-257
Number of pages7
JournalInorganica Chimica Acta
Volume452
DOIs
StatePublished - 2016
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2016 Elsevier B.V.

Keywords

  • H-bonding
  • Metal–nucleobase complexes
  • Molecular recognition

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Inorganic Chemistry
  • Materials Chemistry

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