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Syntheses, structures and properties of chiral dinuclear zinc complexes with Schiff-base ligands
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Two couples of enantiomerically chiral dinuclear zinc complexes with Schiff-base ligands, [Zn2(R-L1)3](ClO4)¡¤H2O (class=""boldFont"">1) and [Zn2(S-L1)3](ClO4)¡¤H2O (class=""boldFont"">2), [Zn2(R-L2)3](ClO4) (class=""boldFont"">3) and [Zn2(S-L2)3](ClO4) (class=""boldFont"">4) (R-L1 or S-L1 = R- or S-3-methoxy-6-(((methyl-2-pyridinylmethyl) imino)methyl)-Phenol, R-L2 or S-L2 = R- or S-1-((1-(pyridin-2-yl)ethylimino)methyl) naphthalen-2-ol), were synthesized and characterized. The strong solid-state fluorescence emissions were observed at around 490 nm for class=""boldFont"">1 and class=""boldFont"">2 and 580 nm for class=""boldFont"">3 and class=""boldFont"">4 at room temperature, respectively, which are attributed to the intraligand charge-transfer excite state. The fluorescence emissions of class=""boldFont"">3 and class=""boldFont"">4 exhibit obvious red-shift relative to class=""boldFont"">1 and class=""boldFont"">2.

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