Published 2021 | Version v1
Journal article

Complexes with furyl-substituted 3-hydroxychromone: synthesis, characterization and fluorescence studies

  • 1. Universidade Federal da Grande Dourados (UFGD), MS (Brazil)
  • 2. Institute of Chemistry and Biochemistry, Freie Universität Berlin, Berlin (Germany)

Description

2-(2-Furyl)-3-hydroxychromone (HL) reacts with MII ions in the formation of quadratic [Cu(L)2] (3), octahedral [M(L)2(OH2)2] (M = Co (1), Ni (2), Zn (4), Mn (5)) and seesaw [M(L)2] (M = Sn (6), Pb (7)) complexes. Recrystallization of complexes 1-3 in presence of pyridine lead to [M(L)2(py)2] (1a-3a) adducts. All compounds were characterized by Fourier transform infrared spectroscopy (FTIR). Complexes 1-7 were analyzed by UV-Vis and diffuse reflectance spectroscopies. The estimated band gap energies range from 2.90-3.15 eV. The crystal structure of complexes 6 and 7 revealed the influence of the stereochemically active lone pair due to their electronic configuration ns2 . An intense fluorescence emission band centered at approximately 600 nm (λexc centered at 340 nm) has been observed for complex 6 in the solid state. In N,N-dimethylformamide (DMF) solution, complex 6 showed two emission bands (468 and 538 nm) when excited from 300 to 380 nm, and only one emission band (468 nm) when excited from 385 to 420 nm. (author)

Additional details

Publishing Information

Journal Title
Journal of the Brazilian Chemical Society (Online)
Journal Volume
32
Journal Issue
8
Journal Page Range
p. 1519-1530
ISSN
1678-4790