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Heterobimetallic three-dimensional 4d-4f coordination polymers based on 5-methyl-1-(pyridyn-4-ylmethyl)-1H-1,2,3-triazole-3,4-dicarboxylate
Three novel 4f-4d heterometallic coordination polymers (CPs), [Ln(H2O)3CdL2(NO3)]·6H2O (L = ethyl 5-methyl-1-(pyridin-4-ylmethyl)-1H-1,2,3-triazole-3,4-dicarboxylate; Ln = Eu, Gd, Tb 1, 2 and 3, respectively) have been successfully synthesized by hydrothermal treatment and slow cooling-down crys...
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Published in: | Journal of solid state chemistry 2022-06, Vol.310, p.123027, Article 123027 |
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Main Authors: | , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Three novel 4f-4d heterometallic coordination polymers (CPs), [Ln(H2O)3CdL2(NO3)]·6H2O (L = ethyl 5-methyl-1-(pyridin-4-ylmethyl)-1H-1,2,3-triazole-3,4-dicarboxylate; Ln = Eu, Gd, Tb 1, 2 and 3, respectively) have been successfully synthesized by hydrothermal treatment and slow cooling-down crystallization. These CPs have been structurally characterized by single-crystal X-ray diffraction. 1–3 are isostructural and consist of a three-dimensional network showing channels. The networks are reinforced via hydrogen bonds and π-π stacking interactions. The crystal topology analysis shows an infinite 2D layer topology with net symbol {4,4} (sql). The magnetic behavior of these compounds is explained by the expected contribution of almost isolated Ln (III) ions. An energy gap of 375 cm−1 between the 7F0 ground state and the first excited state of compound 1 has been deduced from magnetic data showing an excellent agreement with the spectroscopic data.
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•3D molecular and crystal structure with tri-dimensional features was confirmed by single crystal X-ray diffraction and discussed.•Topologies Analyses were performed and discussed.•Thermal, luminescent, and magnetic properties reveal that this type of compound is a good candidate for solid-state luminescent material. |
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ISSN: | 0022-4596 1095-726X |
DOI: | 10.1016/j.jssc.2022.123027 |