Estimating the Individual Spectroscopic Properties of Three Unique Eu III Sites in a Coordination Polymer

• Published in: Inorganic chemistry 2018-12, Vol.57 (24), p.15421-15429
• Main Authors: Monteiro, Jorge H S K, Dutra, José D L, Freire, Ricardo O, Formiga, André L B, Mazali, Italo O, de Bettencourt-Dias, Ana, Sigoli, Fernando A
• Format: Article
• Language: English
• ISSN: 0020-1669; 1520-510X
• DOI: 10.1021/acs.inorgchem.8b02720

We isolated a coordination polymer with the formula [Eu (3,5-dcba) (H O)(dmf) ]·2dmf, with three unique Eu coordination sites in the asymmetric unit, with the Eu ions bridged by 3,5-dichlorobenzoato (3,5-dcba) ligands. The coordination polymer crystallized in the triclinic space group P1̅ with unit cell dimensions a = 12.4899(15), b = 16.326(2), and c = 25.059(3) Å, α = 84.271(3)°, β = 84.832(3)°, and γ = 68.585(3)° and V = 4725.2(10) Å . The characteristic D → F ( J = 0-4) Eu transitions were observed upon ligand-centered excitation. Emission lifetimes of 0.825 ± 0.085 and 1.586 ± 0.057 ms were observed and were attributed to the sites with coordination of water or dimethylformamide (dmf) molecules to each ion, respectively. Through a combination of spectroscopy and calculations, we determined the photophysical properties of each unique Eu site. Energy-transfer rates ligand → Eu were determined for each unique site using the overlapped polyhedra method. The rates depend on the coordinated water molecules and the different donor-acceptor distances. The two sites without coordinated water molecules and shortest donor-acceptor distance display the fastest energy-transfer rate ligand → Eu , whereas the site with coordinated water molecules and longest donor-acceptor distance displays the slowest energy-transfer rate. Donor-acceptor distances were estimated computationally and were confirmed by calculating the frontier orbitals in the asymmetric units of the polymer using density functional theory.