To introduce a design strategy for improving optical properties, two silver-amino alkylpyridine nitrate complexes, AgCHNO and AgCHNO, were successfully synthesized using a recrystallization method. By employing polarizable π-conjugated [NO] ions, two types of pyridine ligands, and silver cations with a high affinity for pyridine, we obtained a one-dimensional chain structure with 4-aminomethylpyridine (AgCHNO) and a zero-dimensional molecular compound by introducing a relatively flexible aliphatic chain with 4-(2-aminoethyl)pyridine (AgCHNO). The compounds crystallize in the triclinic crystal system with the centrosymmetric -1 space group, exhibiting a change in orientation between the π-conjugated system and the silver ion.
View Article and Find Full Text PDFTwo positional isomers, 4-amino-3-methylpyridine and 3-amino-5-methylpyridine, produce 4-amino-3-methylpyridinium and 5-methylpyridin-3-aminium, respectively, under acidic conditions. The two protonated isomers create different hydrogen bonding networks, resulting in different coordination environments of the [MnX] unit embedded in molecular compounds such as 4-amino-3-methylpyridinium manganese bromide, [(CHN)MnBr] and 5-methylpyridin-3-aminium manganese bromide, [(CHN)MnBr(HO)·(MnBr)]. Both compounds can be prepared using the slow evaporation method or mechanochemical synthetic procedures.
View Article and Find Full Text PDFA series of Yb-substituted Zintl phases in the CaYbAlSb (0 ≤ ≤ 0.81(1)) system has been synthesized by initial arc melting and post-heat treatment, and their isotypic crystal structures were characterized by both powder and single crystal X-ray diffraction analysis. All four title compounds adopted the CaAlAs-type structure (space group , Pearson code 28, = 4).
View Article and Find Full Text PDFEstablishing high performance ultraviolet (UV) nonlinear optical (NLO) selenite crystals with well-balanced properties is very challenging attributable to their strong absorption for UV light. Here a rare-earth selenite, Sc(HSeO ) , with excellent UV NLO properties is introduced. Sc(HSeO ) crystallizing in the polar NCS space group, Cc, features a 3D archetiture built up by interconnected ScO octahedra and HSeO groups.
View Article and Find Full Text PDFRhodium nanoparticles are promising transition metal nanocatalysts for electrochemical and synthetic organic chemistry applications. However, notwithstanding their potential, to date, Rh nanoparticles have not been utilized for biological applications; there has been no cytotoxicity study of Rh reported in the literature. In this regard, the absence of a facile and controllable synthetic strategy of Rh nanostructures with various sizes and morphologies might be responsible for the lack of progress in this field.
View Article and Find Full Text PDFGold nanomaterials are commonly used in biomedical applications owing to their excellent biocompatibility and unique physicochemical and optical properties, whereas Pd nanomaterials are mainly used as catalysts. Here, we re-examined the possible applications of Pd nanomaterials. Reducing agent-assisted excessive galvanic replacement-mediated porous Au nanoplates, porous Pt nanoplates, and porous Pd nanoplate synthesis enabled us to compare the properties and efficiency of nanoplates composed of three metal elements (Au, Pt, and Pd).
View Article and Find Full Text PDFHerein, hybrid nanocomposite of praseodymium doped TiO2 nanocrystals and graphene oxide nanosheets are prepared by facile hydrothermal treatment. As-synthesized Pr-TiO2 /NGO hybrid nanocomposite exhibits enhanced photocatalytic activity under visible light irradiation by the intact graphene oxide and doped lanthanide mediated band gap narrowing compared to TiO2 . Moreover, high payload and controlled release of doxorubicin by charge reversal of hybrid nanocomposite at endosomal pH and near-infrared irradiation mediated efficient photothermal conversion provide highly favorable features in therapeutic applications.
View Article and Find Full Text PDFTwo different 3D porous metal-organic frameworks, [Zn4O(NTN)2]·10DMA·7H2O (SNU-150) and [Zn5(NTN)4(DEF)2][NH2(C2H5)2]2·8DEF·6H2O (SNU-151), are synthesized from the same metal and organic building blocks but in different solvent systems, specifically, in the absence and the presence of a small amount of acid. SNU-150 is a doubly interpenetrated neutral framework, whereas SNU-151 is a non-interpenetrated anionic framework containing diethylammonium cations in the pores. Comparisons of the N2, H2, CO2, and CH4 gas adsorption capacities as well as the CO2 adsorption selectivity over N2 and CH4 in desolvated SNU-150' (BET: 1852 m(2) g(-1)) and SNU-151' (BET: 1563 m(2) g(-1)) samples demonstrate that the charged framework is superior to the neutral framework for gas storage and gas separation, despite its smaller surface area and different framework structure.
View Article and Find Full Text PDFA new organically templated noncentrosymmetric polar zinc chloride, [N(CH(3))(4)]ZnCl(3), has been synthesized hydrothermally, and the structure was determined by single crystal X-ray diffraction. The reported material exhibits a unidimensional crystal structure consisting of chains of anionic ZnCl(4) tetrahedra that are separated by [N(CH(3))(4)](+) cations. Second-harmonic generation (SHG) measurement on the noncentrosymmetric [N(CH(3))(4)]ZnCl(3), using 1064 nm radiation, indicate the material has a SHG efficiency of approximately 15 x alpha-SiO(2).
View Article and Find Full Text PDF