An anthracene extended viologen-incorporated ionic porous organic polymer for efficient aerobic photocatalysis and antibacterial activity.

A new conjugated ionic porous organic polymer (AN-POP), incorporated with anthracene-extended viologen, has been rationally designed and prepared to explore its dual functions in photocatalytic oxidation and bacterial killing. Compared with its anthracene-free counterpart (BD-POP), AN-POP showed a superior photocatalytic oxidation performance and antibacterial activity demonstrating the critical role of an anthracene-extended viologen structure.

Supramolecular gel from self-assembly of a C3-symmetrical discotic molecular bearing pillar[5]arene.

A novel C3-symmetric benzene-1,3,5-tricarboxamide (BTAs) decorated with three identical pillar[5]arene tails was designed, synthesized and characterized. The compound can gelate acetonitrile at low concentration (0.2 wt%) upon sonication at room temperature, but a precipitate was obtained by a conventional heating-cooling process. Scanning electron microscopy revealed that the gel and precipitate were constructed by entangled, high-aspect-ratio flexible bundles of nanofibrils. UV-vis spectroscopy, circular dichroism, Fourier transform infrared microscopy and powder X-ray diffraction showed that the compound formed chiral, elongated, columnar aggregates with nanofiber morphology by a combination of intermolecular hydrogen bonding between the N-H and C[double bond, length as m-dash]O of amides, π-π stacking (H-aggregates) and hydrophobic interactions of peripheral groups.

Preassembly-driven ratiometric sensing of H2PO4(-) anions in organic and aqueous environments.

Gemini surfactant-like receptor is designed and synthesized. The special preassembly phenomenon of in a nonpolar solvent facilitates the novel ratiometric fluorescence sensing of H2PO4(-)via an anion-induced reassembly process in organic solvents and an anion-induced disassembly process in water.

Synthesis of porous hierarchical MgO and its superb adsorption properties.

The porous hierarchical MgO with superb adsorption properties has been synthesized by a facile and scaled-up method. The X-ray powder diffraction, electron microscopy, Fourier transformed infrared, and N2 adsorption-desorption were carried out to study the microstructure of the as-synthesized precursor and product. It has been demonstrated that the as-prepared MgO has a porous hierarchical structure and a high specific surface area (148 m(2) g(-1)). And the MgO sample exhibited super adsorption properties, with maximum adsorption capacity of 2409 mg g(-1) for Congo red, which is the highest reported value. Moreover, the adsorption process of Congo red on porous hierarchical MgO was systematically investigated, which was found to obey the pseudo-second-order rate equation and Langmuir adsorption model.

FRET-based ratiometric fluorescent probes for selective Fe3+ sensing and their applications in mitochondria.

Efficient ratiometric fluorescent Fe(3+) probes were designed and synthesized by linking a conjugated naphthalene chromophore to a rhodamine platform and a lipophilic triphenylphosphonium (TPP) cation. The probes could sensitively and selectively detect mitochondrial Fe(3+) in living cells.

Aggregation-induced emission of a novel conjugated phosphonium salt and its application in mitochondrial imaging.

A new conjugated phosphonium salt TPP was synthesized readily from phosphine-triggered ring-opening of 2,4,5-triphenylpyrylium salt. In aqueous solution, it exhibited interesting AIEE properties and self-assembled into fluorescent nanoparticles, which can be used as a fluorescence probe to image mitochondria in cells.

A new two-dimensional cadmium metal-organic framework: poly[bis(4,7-diphenyl-1,10-phenanthroline)(µ3-5-nitroisophthalato)cadmium(II)].

In the title cadmium metal-organic framework complex, [Cd(C(8)H(3)NO(6))(C(24)H(16)N(2))](n) or [Cd(NIPH)(dpphen)] (NIPH is nitroisophthalate and dpphen is 4,7-diphenyl-1,10-phenanthroline), the unique Cd(II) cation in a general position is coordinated by four carboxy O atoms from three symmetry-related NIPH anions and two N atoms from a dpphen ligand. The Cd(II) cations are bridged by pairs of NIPH anions to generate a dinuclear molecular building block, [Cd(2)N(4)(CO(2)R)(4)], with a Cd···Cd separation of 4.0936 (10) Å. Each such building block is connected to four adjacent dinuclear building blocks by NIPH anions, resulting in a two-dimensional layer framework in the bc plane. The dpphen ligands occupy the space between these layers and are linked by π-π interactions, with a separation of 3.4541 (6) Å between the central aromatic rings of inversion-related dpphen ligands. The thermogravimetric and photoluminescent properties of the complex have also been investigated.

Syntheses and characterization of a series of silver-thioantimonates(III) and thioarsenates(III) containing two types of silver-sulfur chains.

Three framework silver-thioantimonates, K(3)Ag(9)Sb(4)S(12)(1), Rb(3)Ag(9)Sb(4)S(12)(2), and Cs(3)Ag(9)Sb(4)S(12)(3), and one layered silver-thioarsenate, CsAg(2)AsS(3)(4), have been synthesized solvothermally in the presence of thiophenol as a mineralizer. Compounds 1, 2, and 3 are isostructural and contain infinite silver-sulfur chains [Ag(9)S(12)](15-). These chains are connected to one another by the antimony atoms to generate wide channels along the [001] direction where the alkali metal cations reside. The structure of 4 consists of helical chains [Ag(2)S(3)](4-) linked by the arsenic atoms to form layers with potassium ions between the layers.

A facile oxidation and oxygen insertion of the cyclopentadiene ring by molecular oxygen in solution.

[reaction: see text] Oxidation of substituted cyclopentadienes by molecular oxygen afforded the corresponding pyrylium cations in acidic solution, whereby an oxygen atom was inserted into the cyclopentadiene ring. This novel one-step reaction proceeds in a different yield depending on substitution patterns of the cyclopentadiene. A possible reaction pathway and formation mechanism of the pyrylium cation are proposed and discussed.

Spectroscopic studies on 2,3,4,5-tetraphenylpyrylium salts with and without silver (I)-bridged structures.

Two novel phenylated pyrylium compounds, silver (I)-bridged 2,3,4,5-tetraphenylpyrylium perchlorate (P1) and its silver (I)-free pyrylium ligand (P2) were prepared from 1,2,3,4-tetraphenylcyclopentadiene to examine their spectroscopic behaviors. The UV/vis absorption and fluorescent emission spectra of P1 and P2, measured in three solvents (acetonitrile, dichloromethane and toluene), reveal that the photophysical behaviors are closely related to silver (I) fragment, and strongly dependent on solvent polarity. In polar acetonitrile, P1 displays longer absorption wavelength and much lower fluorescent emission intensity than P2, although they exhibit much similarity in shape. In contrast, in nonpolar toluene, while P2 shows an apparent absorption band at 338 nm, P1 displays a tail-like line without absorption band observed. All the spectra obtained indicate a better coplanarity and a stronger intra-molecular charge transfer in P1 due to the effect of silver (I) fragment. Additionally, the 1H NMR spectra of P1 and P2, which were recorded under the same conditions, indicate that the silver (I) fragment reinforces pyrylium ring's capacity to localize the formal positive charge within the heterocyclic ring.

(mu-2,11-Dithia[3.3]paracyclophane-kappa2S:S')bis[(6-carboxypyridine-2-carboxylato-kappa2N,O6silver(I)]: a mixed-ligand silver-based dinuclear compound.

In the title complex, [Ag2(C7H4NO4)2(C16H16S2)], each Ag(I) atom is trigonally coordinated by one S atom of a 2,11-dithia[3.3]paracyclophane (dtpcp) ligand, and by one N and one O atom of a 6-carboxypyridine-2-carboxylate ligand. Dtpcp acts as a bidentate ligand, bridging two inversion-related AgI atoms to give a dinuclear silver(I) compound. The dinuclear moieties are interconnected via O-H...O hydrogen bonds to form a two-dimensional zigzag sheet. Two such sheets are interwoven via pi-pi interactions between pyridine rings, affording an interwoven bilayer network.

Silver(I) coordination polymers of fluorescent oligo(phenylenevinylene) with pi-pi stackings: luminescence and conductivity.

Three luminescent silver(I)-oligo(phenylenevinylene) complexes, [Ag2(bmsb)(ClO4)2] (1), [Ag2(bmsb)(H2O)4](BF4)2 (2), and [Ag2(bdb)(CF3SO3)2] (3) (bmsb = 1, 4-bis(methylstyryl)benzene, bdb = 4,4'-bis(2, 5-dimethylstryryl)biphenyl), have been synthesized and structurally characterized. Complexes 1 and 2 are 2D networks with unique metallocyclophane motifs. Complex 3 affords a 2D zigzag sheet, in which silver triflates form tubelike double chains and bdb molecules act as linkages. Complex 2 exhibits high electric conductivity because of columnar aromatic stackings formed through intra- and intermolecular pi-pi interactions. Complexes 1-3 in the solid state exhibit luminescence, of which excitation and emission maxima are shifted to longer wavelength as compared to those of the corresponding metal-free ligands.

Conversion of phenyl-substituted cyclopentadienes to pyrylium cations.

Phenyl-substituted cyclopentadienes are proved to form phenylated pyrylium cations in the presence of silver(I) perchlorate by insertion of an oxygen atom into the cyclopentadiene-ring. Three phenylated pyrylium compounds, [(Ph(5)C(5)O(+))(ClO(4)(-))](2)(CH(2)Cl(2)) (1), Ag(ClO(4))(H(2)O)(Ph(4)HC(5)O(+)) (ClO(4)(-)) (2), and (Ph(3)H(2)C(5)O(+))(ClO(4)(-)) (3) have been synthesized and characterized. A possible reaction pathway and formation mechanism of the pyrylium cation are proposed and discussed.

Construction of Copper(I) Coordination Polymers of 1,2,4,5-Tetracyanobenzene with Zigzag Sheet and Porous Frameworks.

This paper describes two copper(I) supramolecules with the same anion and cation but quite different topologies and properties. The reaction of [Cu(CH(3)CN)(4)]PF(6) and 1,2,4,5-tetracyanobenzene (TCNB) leads to two novel polymeric coordination compounds, [Cu(2)(TCNB)(3)](PF(6))(2)(Me(2)CO)(4)( )()(1) and [Cu(2)(TCNB)(3)](PF(6))(2) (2), depending on the solvents used. The crystal structures have been determined by single-crystal X-ray diffraction. Crystal data are as follows. 1: C(21)H(15)N(6)O(2)CuPF(6), monoclinic, P2(1)/a, a = 11.553(4) Å, b = 16.135(7) Å, c = 15.046(3) Å, beta = 108.08(2) degrees, Z = 4. 2: C(15)H(3)N(6)CuPF(6), orthorhombic, Cmcm, a = 28.282(3) Å, b = 10.337(3) Å, c = 16.285(4) Å, Z = 16. In both polymers, copper(I) ions have similar pseudotetrahedral environments and the four coordination sites are fully occupied by the four bridging ligands, two &mgr;(2)-TCNB and two &mgr;(4)-TCNB groups. Polymer 1, obtained in acetone, revealed a two-dimensional zigzag sheet network between copper(I) ions, whereas 2, synthesized in methylethyl ketone, displayed a three-dimensional porous framework with different functional groups (or atom) in different cavities. The redox, magnetic, and conductive behaviors of both complexes are discussed. It is demonstrated that the two complexes give different physicochemical properties.