Acid-base and potassium disorders occur frequently in the setting of liver disease. As the liver's metabolic function worsens, particularly in the setting of renal dysfunction, hemodynamic compromise, and hepatic encephalopathy, acid-base disorders ensue. The most common acid-base disorder is respiratory alkalosis. Metabolic acidosis alone or in combination with respiratory alkalosis also is co...

How to develop a new, efficient photo catalyst is still a big challenge to us. A suitable band gap is the key for light absorption of semiconductor. Herein, an innovative anion intercalation strategy is, for the first time, developed to regulate the energy band of semiconductor. Typically, we introduce a layered sulfate compound (Bi2O(OH)2SO4) as a new photo catalyst, which has not been known b...

In the mononuclear title salt, [Ag(C3H8N2S)(C18H15P)3](CH3COO), the Ag(I) ion exhibits a distorted tetra-hedral coordination sphere defined by three P atoms from three tri-phenyl-phosphane ligands and one S atom from a 1,3-di--methyl-thio-urea ligand. In the crystal, the acetate anion is linked with the complex cation via duplex N-H⋯O hydrogen bonds [graph-set motif R (2) 2(8)].

In this study, for the first time, the anion dependency of Ag-deposition on self-assembled monolayers (SAMs) with alkyl chains long enough to meet the densely packed and well-organized surface is reported. Irrespective of pH, types of terminal groups of the SAMs, and the convective mass transfer condition, SAM structures show the "sieving behaviour" to the Ag deposition by the composition of th...

In the structure of the title compound, [Ag(C(2)H(3)O(2))(C(12)H(6)N(2)O(2))]·3H(2)O, the Ag(I) atom is coordinated by both 1,10-phenanthroline-5,6-dione N atoms and one O atom from the acetate anion. The three water mol-ecules are involved in extensive hydrogen bonding to each other and to the acetate O and 1,10-phenanthroline-5,6-dione O atoms. In addition, there are weak C-H⋯O inter-actions.

The asymmetric unit of the title mononuclear compound, [Ag(C(6)H(5)ClNO(3)S)(C(18)H(15)P)(2)], contains four independent mol-ecules. In each of the mol-ecules, the Ag(I) cation is three-coordinated by two triphenyl-phosphine ligands, and one N atom from a 2-amino-5-chloro-benzene-sulfonate anion. The mol-ecules are linked into a one-dimensional supra-molecular structure by N-H⋯O hydrogen bonds.

The title compound, [Ag(C(3)H(4)N(2))(2)](2)(C(10)H(6)O(6)S(2)), exists in the form of isolated cations and anions with electrostatic inter-action between them. The Ag atom is two-coordinated by the N atoms of two crystallographically independent imidazole mol-ecules. The naphthalene-1,5-disulfonate anion is located on a crystallographic center of symmetry. The cations and anions are connected ...

In this study, a full-potential density functional theory was used to investigate the effects of Ti substitution by different cations. In both rutile and anatase, Ti atom was replaced by Ce, Au, Sn, Ag, Mo, Nb, Zr, and Y. Phase stability, electronic structure and formation energy of oxygen vacancy were compared for rutile and anatase. The results indicated that substitution of Ce and Zr increas...

In the title compound, [Ag(C(14)H(10)N(4)O)(2)]CF(3)SO(3), two N atoms from two independent pyridyl rings of two N'-3-cyano-benzyl-ideneisonicotinohydrazide ligands coordinate to the unique Ag(I) ion, forming a nearly linear coordination geometry. Adjacent silver complexes are primarily linked together by Ag⋯N inter-actions, with Ag⋯N separations of 2.877 (2) and 3.314 (2) Å. On the other hand,...

A new synthetic strategy has been developed for the fabrication of Au-Ag bimetallic core-shell nanoparticles (NPs) using polyelectrolyte multilayers (PEMs) as unique nanoreactors. Bimetallic NPs composed of Au core and Ag shell were successively incorporated into PEMs by repeating anion/cation exchange/reduction cycle multiple times in a stepwise manner. The strategy described here allows for t...