Crystal structures, red-shifted luminescence and iodide-anion recognition properties of four novel D-A type Zn(ii) complexes.

Four D-A type Zn(ii) coordination complexes, [Zn(C29H29N3O2)·(CH3OH)]·(CH3OH) (1), Zn2(C74H90N6O4)·(CH3OH) (2), [Zn(C30H28N4O2)·(CH3OH)]·(CH3OH) (3) and [Zn(C38H44N4O2)·(C2H5OH)]·(C2H5OH) (4), were designed, synthesized, and studied. Their fluorescence properties in the solid state and in THF solution were comprehensively analysed based on their single-crystal structures. The results showed that the red-shift of fluorescence emission from complexes 1 to 4 was successfully achieved via the strategy of enhancing intramolecular charge transfer (ICT) effects by increasing the number of electron-pulling and pushing groups gradually.

Two novel MOF-74 analogs exhibiting unique luminescent selectivity.

Two MOF-74 analogs with OH groups on 1D channel surfaces have been synthesized through multi-component self-assembly at room temperature. Their guest-free forms demonstrate a potential luminescent probe or sensor for small molecules, and OH-MOF-74 (2a) also showed exceptional fluorescence quenching and enhancement behavior for different types of aromatic molecules.

In situ ligand and complex transformation of an iron(III) Schiff base complex: structural evidence and theoretical calculations.

A C-C coupling reaction has been achieved at room temperature by in situ ligand transformation. The iron(III) complexes before and after the in situ transformation, [FeNaL(1)(2)(H(2)O)(4)](2)·2H(2)O (1) (H(2)L(1) = (Z)-2-(2-hydroxyl)benzylideneamino) and [FeL(2)](2)·7.5H(2)O (2) (H(3)L(2) = (E)-2-(2-hydroxyl-benzylideneamino)-3-hydroxyl-3-(2-hydroxyphenyl), have been studied by elemental analyses, FT-IR, UV-vis, TGA and X-ray single crystal diffraction analysis.