Tunability in dimension, metal and ligand coordination modes and emission properties in Cd(II) and Zn(II) coordination networks based on 4,4’-(hydrazine-1,2-diyilidenebis(methanylylidene)) dibenzoic acid linker
Cd(II) and Zn(II) coordination polymers based on dicarboxylic azine chromophore, 4,4'-(hydrazine-1,2-diylidenebis(methanylylidene)) dibenzoic acid (H2(4-dbahz)), were obtained and include 1D coordination polymer {[Cd(4-dbahz)(dmso)2(H2O)]·(dmso)2}n (1, 2) in the forms of monoclinic and orthorho...
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Veröffentlicht in: | Journal of solid state chemistry 2022-06, Vol.310, p.123021, Article 123021 |
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Sprache: | eng |
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Zusammenfassung: | Cd(II) and Zn(II) coordination polymers based on dicarboxylic azine chromophore, 4,4'-(hydrazine-1,2-diylidenebis(methanylylidene)) dibenzoic acid (H2(4-dbahz)), were obtained and include 1D coordination polymer {[Cd(4-dbahz)(dmso)2(H2O)]·(dmso)2}n (1, 2) in the forms of monoclinic and orthorhombic polymorphs, 2D coordination grid {[Zn(4-dbahz)(dmso)]·0.5(dmso·dmf)}n (3), and 3D MOF {[Cd2(4-dbahz)2(dmso)2]·dmso}n (4). The coordination compounds and H2(4-dbahz) chromophore were studied using spectroscopic (FTIR, NMR, PL) and X-ray diffraction methods of analysis. The organic chromophore H2(4-dbahz) reveals dual emission indicated by the emission bands in the high and low energy regions of spectrum. The tuning of emission properties was followed for the as-synthesized coordination polymers 1, 3, 4 and their desolvated products and showed excellent sensing of solvated dmso. The significant enhancement of photoluminescence in the blue region in 1 is associated with elimination of π-π stacking interactions due to accommodation of dmso solvent.
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•Synthesis of dicarboxylic azine chromophore, 4,4'-(hydrazine-1,2-diylidenebis (methanylylidene)) dibenzoic acid.•Preparation of different coordination polymers on its base.•3D MOF with {Cd4(COO)8} metal cluster as building block.•Tuning luminescent properties for solvated and desolvated forms. |
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ISSN: | 0022-4596 1095-726X |
DOI: | 10.1016/j.jssc.2022.123021 |