RhB-Embedded Mn-MOF with Cyclotriphosphazene Skeleton as Dual-Emission Sensor for Putrescine as well as Smart Fluorescent Response of Aromatic Diamines and Nitrophenol.

Luminescent metal-organic framework composites with multiple luminescence emissions have been efficient sensing platforms. Herein, a fluorescent sensor (RhB@1-0.4) with dual-emission fluorescence properties was prepared by introducing rhodamine B (RhB) into the framework of complex , [Mn(HCPCP)(HO)]·(CHCN) [HCPCP = hexa-(4-carboxyl-phenoxy)-cyclotriphosphazene and CHCN = acetonitrile), which is a novel crystalline two-dimensional (2D) coordinated organic framework material.

A Highly Stable 3D Luminescent Indium-Polycarboxylic Framework for the Turn-off Detection of UO, Ru, and Biomolecule Thiamines.

Hydrothermal reaction of the multidentate organic ligand (HTTHA) with indium chloride (InCl) produced a highly stable 3D luminescent indium-organic framework [In(OH)(HTTHA)(HO)] (1). Complex 1 exhibits remarkable luminescent properties, especially the multifunction sensitivity and selectivity for detecting Ru, UO; as well as small biomolecules thiamines (TPP, TMP, and TCl) based on a "turn-off" manner. In particular, the pyrophosphate groups of TPP and the phosphate groups of TMP could further affect the quenching rate, leading to different luminescent responds.

Syntheses, crystal structures and photophysical properties of Ag(I) coordination complexes.

Three Ag(I) coordination complexes, [Ag(pyzca)]n (1) (Hpyzca=pyrazine-2-carboxylic acid), Ag[(HNA)(NA)(H2O)4] (2) (HNA=nicotinic acid) and [Ag1Ag2-(2,3-pydc)]n (3) (H2pydc=pyridine-2, 3-dicarboxylic acid) have been synthesized by the hydrothermal method. Their structures are determined by single-crystal X-ray diffractometer. Complex 1 possesses the 3D infinite structure.

A series of Ti(IV)/Ti(III) coordination polymers: structures and surface photoelectric properties.

Three titanium coordination polymers, {[Ti(SO(4))(2)(H(2)O)]·0.5bipy·2H(2)O}(n)1, {[Ti1(SO(4))(2)(H(2)O)]·[Ti2(SO(4))(2)(H(2)O)]·bipy·5H(2)O}(n)2 and [Ti(tea)](n)3 (bipy=4,4'-bipyridine, H(3)tea=triethanolamine) were synthesized and characterized by IR, UV-Vis absorption spectra, TG analysis, X-ray single crystal diffraction and surface photovoltage spectroscopy (SPS). The surface photoelectric properties of titanium coordination polymers were discussed emphatically by the SPS.

Syntheses, structures and photophysical properties of tetranuclear Cd-Ln coordination complexes.

Four novel hetero-tetranuclear d-f coordination complexes, [Ln2Cd2(p-toluylate)10(phen)2] (Nd, 1; Pr, 2; Sm, 3) and [Ho2Cd2(p-chloro-benzoate)10(phen)2](4) (phen = 1, 10-phenanthroline), are synthesized by the hydrothermal method, and their structures are studied by single-crystal X-ray diffraction. Structures 1-3 are isomorphous and structure 4 has a similar molecular structure. In the near-infrared (NIR) region or in the visible region, complexes 1-4 show the characteristic emission bands of Ln(III) ions, which are attributed to the sensitization from the ligands and d-block (cadmium-ligand section) to f-block (lanthanide-ligand section).

[Crystal structures and luminescence property of d10 transition metal complexes].

Five Zn( [II)) and Cd(II) coordination complexes, [Zn(NA)2 (H2O)4](1), [Zn(INA)2 (H2O)4](2), [Zn(2,2'-bi-py)2 (SCN)2](3), [Cd(INA)2 (H2O)4](4) and [Cd(phen)2(NO3)](5) (HNA=nicotinic acid, HINA=isonicotinic acid, 2, 2'-bipy=2,2'-bipyridine, phen=1,10-phenanthroline), were synthesized through constant temperature magnetic stirrer or hydrothermal method, and their single-crystal structures were determined by X-ray diffraction. The authors measured the IR, UV-Vis-NIR and fluorescence spectra of the complexes and analyzed their photophysical properties. At room temperature in the solid state the five complexes can show strong fluorescence, i.