2007
DOI: 10.1002/ejic.200700623
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Syntheses, Crystal Structures, Thermal Stabilities, and Magnetic and Luminescent Properties of 3D Heterometal Phosphonates: NaM[O3PCH(OH)CO2] (M = Mn, Fe, Co, Zn)

Abstract: Keywords:Crystal structure / Phosphorus / Luminescence / Magnetism / Thermal stability 3-groups into an interesting 3D heterometallic framework. Thermogravimetric and pow-

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Cited by 18 publications
(5 citation statements)
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“…The structure of NaFe[O 3 PCH(OH)CO 2 ] 21 formed by the phosphoryl organic and Fe 2+ ions is shown in 1b, the calculated XRD diffraction peaks of the purple line are highly consistent with the reported PXRD diffraction peaks of the black line 21,23 . The calculated three strongest diffraction peaks at 19.95°, 30.42° and 31.97° correspond to the crystal planes (021), (222), and (213), respectively, while the experimental PXRD showed these peaks shifted to 19.98°, 30.19°, and 31.62°.…”
Section: Resultssupporting
confidence: 70%
“…The structure of NaFe[O 3 PCH(OH)CO 2 ] 21 formed by the phosphoryl organic and Fe 2+ ions is shown in 1b, the calculated XRD diffraction peaks of the purple line are highly consistent with the reported PXRD diffraction peaks of the black line 21,23 . The calculated three strongest diffraction peaks at 19.95°, 30.42° and 31.97° correspond to the crystal planes (021), (222), and (213), respectively, while the experimental PXRD showed these peaks shifted to 19.98°, 30.19°, and 31.62°.…”
Section: Resultssupporting
confidence: 70%
“…The peak band of solid 1-300 shows a 86 nm bathochromic-shift compared to that of as-prepaed 1, which maybe due to slightly irreversible changes of H 2 L 42 anion after heating treatment at 300 uC under an air atmosphere. 13 This indicates that luminescent colors of solid 1 can be irreversibly transformed from purple into blue-green by simple heat-treatment at 300 uC under an air atmosphere.…”
mentioning
confidence: 98%
“…Compared to the free ligand, compound 1 gave a fluorescent emission at λ max =420 nm under the same experimental conditions. It demonstrated that the emission spectra of compound 1 was attributed to the ligand–centered π–π* transition because their fluorescent emission bands were very similar to that of the free ligand . While the compound 2 displayed a fluorescent emission band at λ max =420 nm upon excitation at 325 nm.…”
Section: Resultsmentioning
confidence: 93%