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Poly[[tetra-aqua-(μ3-4-hy-droxy-pyridine-2,6-di-carboxyl-ato)di-μ2-oxalato-dipraseodymium(III)] 4.29-hydrate]
Aaqib Khurshid1, Apinpus Rujiwatra1,2, Thammanoon Chuasaard1,3
1Department of Chemistry Faculty of Science Chiang Mai University,Chiang Mai 50200 Thailand.
Abstract:
The coordination polymer of crystal formula [PrIII 2(C7H2NO5)(C2O4)2(H2O)4]·4.29H2O or [PrIII 2(HCAM)(ox)2(H2O)4]·4.29H2O was synthesized from praseodymium(III) nitrate in water using chelidamic acid (H3CAM) and oxalic acid (H2ox). There are two PrIII atoms in the asymmetric unit. One metal ion has nine-fold coordination from one pyridyl nitro-gen and eight oxygen atoms from one HCAM2-, two ox2-, and two coordinating water mol-ecules leading to the formation of a tricapped trigonal {PrIIINO8} prism. The other metal ion is coordinated by ten oxygen atoms from two HCAM2-, two ox2-, and two coordinating water mol-ecules, forming a bicapped square {PrIIIO10} unit. The HCAM2- linker has a μ2-κ2:κ1 chelating coordination mode via its carboxyl-ates and N-pyridyl donors, linking the {PrIIINO8} and {PrIIIO10} units into infinite chains. The μ2-κ1:κ1:κ1:κ1 bridging carboxyl-ates of the ox2- linkers connect adjacent chains into sheets in the ac plane. Adjacent layers further aggregate through inter-molecular hydrogen bonding, most of which involves the water mol-ecules of crystallization, and π-π inter-actions to form a tri-periodic supra-molecular framework. Some of the co-crystallizing water mol-ecules as well as one of the metal-coordinating water mol-ecules are disordered.
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