Yong-Lin An

New framework iodoargentates: M(en)3Ag2I4 (M=Zn, Ni) with tridymite topology.

Two novel framework compounds, Zn(en) 3Ag2I4 (1) and Ni(en) 3Ag2I4 (2), have been synthesized by a self-assembly reaction. Both of them contain an unexpected framework, Ag2I4(2-) with tridymite topology, and the discrete M(en)3(2+) cations are located in the channels. Their thermal properties and circular dichroism spectra were investigated.

Copper-Rich Framework Sulfides: A4Cu8Ge3S12 (A = K, Rb) with Cubic Perovskite Structure

Two copper-rich open-framework sulfides, K(4)Cu(8)Ge(3)S(12) (1) and Rb(4)Cu(8)Ge(3)S(12) (2), have been synthesized under solvothermal conditions. Compounds 1 and 2 are isostructural and contain icosahedral [Cu(8)S(12)](16-) clusters as basic building blocks. These clusters are primitive cubic packed and connect to one another by discrete Ge(4+) ions to generate 3D copper-rich Cu-Ge-S framework and form 3D channels along 100 directions where the alkali metal cations reside. These two open-framework sulfides crystallize in cubic perovskite structure.

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 solvothermal synthesis of a novel 1D ladder-like (NH 3 CH 2 CH 2 NH 3 )AgAsS 4 containing N¿H ¿ S hydrogen bonding

Abstract A one-dimensional compound (NH3CH2CH2NH3)AgAsS4 with ladder-like chains was synthesized solvothermally. This compound crystallizes in the monoclinic system, space group C2/c, with a=13.5805(8) A, b=6.5331(3) A, c=22.7711(9) A, α=90°, β=106.42(3)°, γ=90°, Z=8. The rare type hydrogen bonding of N–H⋯S and electrostatic force hold the anionic chains together.

Mild solvothermal syntheses and characterization of layered copper thioantimonates(III) and thioarsenate(III).

The new copper thioantimonates(III) and thioarsenate(III) Rb2Cu2Sb2S5 (1), Cs2Cu2Sb2S5 (2), and Rb8Cu6As8S19 (3) have been synthesized solvothermally. Compound 1 contains a [Cu2SbS3] net to which [Sb2S4] chains adhere through Cu-S bonds and Sb-Cu interactions to give a layered structure. In compound 2, the layer is formed by edge-sharing tetrahedral CuS4 chains linked by dimeric [Sb2S5] units. The layered structure in compound 3 is constructed by helical chains built from [Cu3S7] moieties and dimeric [As2S5] units which are further connected by tetrameric [As4S9] groups. Their optical and thermal properties have been investigated.

Coordination-Induced Syntheses of Two Hybrid Framework Iodides: A Thermochromic Luminescent Thermometer

Two new 3D hybrid framework iodides, Hmta[(Hmta)Ag4I4] (1; Hmta = hexamethylenetetramine) and [(Hmta)2Ag8I6]I2 (2), have been synthesized under solvothermal conditions. Compound 1 consists of a neutral 3D framework built up from alternation of the tetrahedral Ag4I4 unit and Hmta with dia-b topology. Compound 2 features a 3D cationic framework with flu topology, constructed by cationic [Ag8I6](2+) units linked with Hmta. Tetrahedral Hmta plays crucial structure-directing roles in the formation of these 3D frameworks with high symmetry. The temperature-dependent photoluminescent measurement reveals luminescent thermochromism of the compounds, the emission maximum of which shows a gradual blue shift with increasing temperature. The results indicate that 1 is a promising wavelength- and intensity-dependent luminescent thermometer applicable in two different temperature ranges.

Mild Solvothermal Syntheses of Thioargentates A–Ag–S (A = K, Rb, Cs) and A–Ag–Ge–S (A = Na, Rb): Crucial Role of Excess Sulfur

A series sulfides of A-Ag-S (1-3; A = K, Rb, Cs), Na5AgGe2S7 (4), and Rb2Ag2GeS4 (5) have been prepared solvothermally in the presence of excess sulfur. Among these compounds, 4 is a new compound that has a novel layered structure; the others were obtained under mild conditions. The results showed that excess sulfur could increase the solubility of silver sulfide and lower the synthetic temperature effectively. The mineralizer effect of excess sulfur is discussed in detail.