Halogen Bonds in Two Silver(I) Mixed-ligand Supramolecular Frameworks: Synthesis, Structure and Photoluminescence

Two silver(I) tetrachlorophthalates incorporating aminopyrimidyl ligands, namely [Ag 4 (apym) 4 (tcpta) 2 ] n (1) and [Ag 2 (dmapym)(tcpta)] n (2), (apym = 2-aminopyrimidine, dmapym = 2-amino-4,6-dimethylpyrimidine, H 2 tcpta = tetrachlorophthalic acid), were synthesized and characterized by elemental analysis, IR spectroscopy and single-crystal X-ray diffraction. Both 1 and 2 form sheets which are assembled into 3D supramolecular frameworks via halogen bonds, hydrogen bonds and π ···π interactions. Even adding two more methyl groups to the pyrimidyl ring does not change the dimensions of 1 and 2, but it influences the arrangement of the N-and O-donors in the solid state which in turn results in different types of halogen bonds. The photoluminescence properties of 1 and 2 were investigated in the solid state at room temperature

Tetra­aqua­tetra­kis{μ3-3,3′-[(E,E)-ethane-1,2-diylbis(nitrilo­methyl­idyne)]benzene-1,2-diolato}octa­zinc(II) N,N-dimethyl­formamide hexa­solvate

The asymmetric unit of the title compound [Zn8(C16H12N2O4)4(H2O)4]·6C3H7NO, consists of eight ZnII cations, four tetra­valent anionic ligands, L 4− (L 4− = 3,3′-(1E,1′E)-(ethane-1,2-diylbis(azan-1-yl-1-yl­idene))bis­(methan-1-yl-1-yl­idene)dibenzene-1,2-bis­(olate), four coordinated water mol­ecules and six N,N-dimethyl­formamide solvate mol­ecules. The coordination complex comprises an octa­nuclear ZnII unit with its ZnII centers coordinated in two discrete distorted square-pyramidal geometries. Four ZnII atoms each coordinate to two nitro­gen atoms and two phenolate oxygen atoms from an individual L 4− ligand and one coordinated water mol­ecule. The other four ZnII atoms each bind to five phenolate oxygen atoms from three different L 4− ligands. In the crystal structure, the ZnII complex unit, coordinated water mol­ecules and dimethyl­formamide solvate mol­ecules are linked via O—H⋯O and C—H⋯O hydrogen bonds. Mol­ecules are connected by additional inter­molecular O—H⋯O and C—H⋯O hydrogen bonds, forming an extensive three dimensional framework

4-(4-Nitro­benz­yl)morpholine

In the title compound, C11H14N2O3, an inter­molecular inter­action between a nitro group O atom and a neighboring benzene ring helps to stabilize the crystal structure [N⋯centroid = 3.933 (2) Å]. No classical hydrogen bonds are observed in the crystal packing

Benzo[a]fluoren-11-one

The mol­ecule of the title compound, C17H10O, is nearly planar, the largest deviation from the mean plane being 0.06 Å. The crystal structure is governed by π–π inter­actions, with centroid–centroid distances ranging from .559 to 3.730 Å

Simultaneous Formation of CH₃NH₃PbI₃ and electron transport layers using antisolvent method for efficient perovskite solar cells

A new antisolvent method was developed to prepare CH₃NH₃PbI₃ and electron transport layers for making efficient hybrid perovskite solar cells. By directly using [6,6]-phenyl-C61-butyric acid methyl ester in chlorobenzene solution as antisolvent, CH₃NH₃PbI₃ and electron transport layers were simultaneously formed in the films. This method not only simplifies the fabrication process of devices, but also produces uniform perovskite films and improves the interfacial structures between CH₃NH₃PbI₃ and electron transport layers. Large perovskite grains were observed in these films, with the average grain size of >1 μm. The so-formed CH₃NH₃PbI₃/electron transport layers demonstrated good optical and charge transport properties. And perovskite solar cells fabricated using these simultaneously-formed layers achieved a higher power conversion efficiency of 16.58% compared to conventional antisolvent method (14.92%). This method reduces nearly 80% usage of chlorobenzene during the fabrication, offering a more facile and environment-friendly approach to fabricate efficient perovskite solar cells than the conventional antisolvent method

A Thiazole Orange Derivative Targeting the Bacterial Protein FtsZ Shows Potent Antibacterial Activity.

The prevalence of multidrug resistance among clinically significant bacteria calls for the urgent development of new antibiotics with novel mechanisms of action. In this study, a new small molecule exhibiting excellent inhibition of bacterial cell division with potent antibacterial activity was discovered through cell-based screening. The compound exhibits a broad spectrum of bactericidal activity, including the methicillin-resistant Staphylococcus aureus, vancomycin-resistant Enterococcus and NDM-1 Escherichia coli. The in vitro and in vivo results suggested that this compound disrupts the dynamic assembly of FtsZ protein and Z-ring formation through stimulating FtsZ polymerization. Moreover, this compound exhibits no activity on mammalian tubulin polymerization and shows low cytotoxicity on mammalian cells. Taken together, these findings could provide a new chemotype for development of antibacterials with FtsZ as the target

Capturing a Metastable Silver(I) Compound of Pyrazine-2,3-dicarboxylic Acid

A metastable 3D supramolecular compound [Ag(NH3)(2)]-[Ag-3(pzdca)(2)(NH3)(4)] (H(2)pzdca = pyrazine-2,3-dicarboxylic acid) (1) has been synthesized and characterized crystallographically. This study offers important information to in-depth understanding of the self-assembly process involving Ag-1 under ammoniacal conditions and conforms that [Ag(NH3)(2)](+)-containing compounds are the intermediates during synthesis of some Ag-1 coordination polymers.National Natural Science Foundation of China [20721001]; MSTC [2007CB815301]; National Science Fund of China for Fostering Talents in Basic Science [J0630429

3-Chloro-4-hydroxy­furan-2(5H)-one

In the title compound, C4H3ClO3, mol­ecules are linked via O—H⋯O hydrogen bonds into an infinite chain with graph-set motif C(6) along the c axis