Abstract

Four new metallophosphonates M(H2O)(PO3C10H6OH)·(H2O)0.5 (M = Mn, Co, Cu, Zn) were obtained as single crystal and polycrystalline powders by hydrothermal synthesis from the precursors 6-hydroxy-2-naphthylphosphonic acid and the corresponding metal salts. These analogous hybrids crystalized in the space group P121/c1 in a lamellar structure. Their layered structures consisted of inorganic [M(H2O)(PO3C)] layers stacked with organic bilayers of 6-hydroxy-2-naphthyl moieties "HO-C10H6" and free water molecules. Their structures were determined by single crystal X-ray diffraction and confirmed by powder X-ray diffraction and Le Bail refinement for the powder sample. The removal of water upon heating at 250 °C was studied by thermogravimetric analysis and temperature-dependent powder X-ray diffraction. Their magnetic properties were studied by SQUID magnetometry and show antiferromagnetic behavior for the Co analogue and the occurrence of a canted antiferromagnetic order at TN = 12.2 K for the Mn analogue. The Cu compound displayed an unprecedented ferromagnetic behavior. Their absorption and luminescence properties were investigated and revealed that the ligand and the compounds displayed a common behavior below a wavelength of 400 nm. Specific absorption bands were found in the compounds with Co2+ and Cu2+ at 539 nm and 849 nm, respectively. Moreover, particular luminescence bands were found for the compounds with Mn2+, Co2+ and Zn2+ at 598 nm, 551 nm and 530 and 611 nm, respectively.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.