Cross-Linking CdSO-Type Nets with Hexafluorosilicate Anions to Form an Ultramicroporous Material for Efficient CH/CO and CH/CH Separation.

A 4.6.8 topology hybrid ultramicroporous material (HUM), {[CuF(SiF)(L)]·G}, (L = 4,4'-bisimidazolylbiphenyl, G = guest molecules), 1, formed by cross-linking interpenetrated 3D four-connected CdSO-type nets with hexafluorosilicate anions is synthesized and evaluated in the context of gas sorption and separation herein.

Efficient and Reversible Separation of Chloroform from Chlorinated Hydrocarbons and Water Utilizing a Two-Dimensional Coordination Network.

Chloroform is a volatile organic solvent and a contaminant that is slightly soluble in water, making the reversible separation of chloroform from water a critical and challenging task within the chemical and environmental industries. In this study, we present a newly developed coordination framework, [Zn(4-pmntd)(opa)] [4-pmntd, ,'-bis(4-pyridylmethyl)naphthalene diimide; opa, -phthalic acid], which demonstrates a high adsorption capacity for chloroform (2.5 mmol/g) and an excellent ability to separate chloroform from water.

Weighted gene correlation network analysis identifies the critical long non-coding RNAs participate in the progression of osteosarcoma.

This study aimed to identify more biomarkers associated with osteosarcoma progression via lncRNA-mRNA co-expression network. Dataset GSE99671 was downloaded from GEO database. The mRNAs and lncRNAs that were differentially expressed between tumor and normal samples were screened out.

Anions effect construction of 1D naphthalene diimide supramolecular chains by π interactions and fluorescence detect iodide anion.

Five diverse 1D supramolecular chains, {[4-pmntd]}(1), {H[4-pmntd]•2Br}(2), {H[4-pmntd]•2NO}(3), {H[4-pmntd]•2ClO}(4), {H[4-pmntd]•2BF}(5), (where 4-pmntd was N,N'-bis (4-pyridylmethyl)naphthalene diimide) were synthesized and characterized by X-ray single-crystal structure analysis, IR spectroscopy, elemental analyses, thermogravimetric analyses, fluorescence detection. The anions effect construction of their 1D chain structural diversity through different π interactions. Compound 1 through the adjacent pyridine rings parallel π∙∙∙π interactions formed 1D linear chain structure.

Diverse 1D chains supramolecular structures of N,N'-bis(3-pyridylmethyl)pyromellitic diimide and fluorescence iodide sensing.

Three diverse supramolecular compounds, {[3-pmpmd]}(1), {H[3-pmpmd]·2NO}(2), {H[3-pmpmd]·2tbb}(3), (where 3-pmpmd was N,N'-bis(3-pyridylmethyl)pyromellitic diimide; tbb was tertiary butyl benzoic acid) were synthesized and characterized by elemental analyses, IR spectroscopy, thermogravimetric analyses, and X-ray single-crystal structure analysis. The co-crystal anions affect their structural diversity. Compound 1 is a 1D stairway chain structure by perpendicular π⋯π interactions of pyromellitic diimide and the neighboring pyridine rings.

Selective Adsorption of Water, Methanol, and Ethanol by Naphthalene Diimide-Based Coordination Polymers with Constructed Open Cu Metal Sites and Separation of Ethanol/Acetonitrile.

The selective separation of ethanol/acetonitrile by porous materials has rarely been observed owing to their similar physicochemical properties. In this work, we report a new coordination network, [Cu(4-pmntd)(opd)](4-pmntd = ,'-bis(4-pyridymethy)naphthalene diimide, opd = disodium 1,2-benzenedicarboxylate), which exhibits selective separation of ethanol over acetonitrile. The weak coordination bonds formed by unsaturated Cu sites and hydroxyl groups are the key to such performance.

Synthesis, crystal structure, fluorescence properties of 1D chain Manganese (II) and Cadmium (II) complexes.

Two complexes, {[Mn(3-pmpmd)(Cl)]·2HO}(1), {[Cd(3-pmpmd) (I)]·CHCl·HO}(2), (3-pmpmd, N,N'-bis(3-pyridylmethyl)pyromellitic diimide) were synthesized and characterized by elemental analyses, IR spectroscopy, thermogravimetric analyses, and X-ray single-crystal structure analysis. The conformations of 3-pmpmd ligand affect their structural diversity. Complex 1 is a 1D double chain structure in edge-to-edge arrangement by π⋯π interactions.

Structural disorder and transformation in crystal growth: direct observation of ring-opening isomerization in a metal-organic solid solution.

A rare example is reported in which discrete Ag2 L 2 ring and (AgL)∞ chain motifs [L = N,N'-bis(3-imidazol-1-yl-propyl)-pyromellitic diimide] co-crystallize in the same crystal lattice with varying ratios and degrees of disorder. Crystal structures obtained from representative crystals reveal compatible packing arrangements of the cyclic and polymeric isomers within the crystal lattice, which enables them to co-exist within a crystalline solid solution. A feasible pathway for transformation between the isomers is suggested via facile rotation of the coordinating imidazolyl groups.

Construction of 0D to 3D cadmium complexes from different pyridyl diimide ligands.

Four semirigid ditopic ligands, N,N'-bis(3-pyridylmethyl)-pyromellitic diimide (L(1)), N,N'-bis(4-pyridylmethyl)-pyromellitic diimide (L(2)), N,N'-bis(3-pyridylmethyl)-naphthalene diimide (L(3)), and N,N'-bis(4-pyridylmethyl)-naphthalene diimide (L(4)), reacted with Cd(NO(3))(2) to result in four cadmium(II) complexes, namely, {[Cd(2)(L(1))(2)(NO(3))(4)(CH(3)OH)(4)]·H(2)O} (1), [Cd(L(2))(NO(3))(2)(CH(3)OH)(2)·Cd(2)(L(2))(3)(NO(3))(4)]·{4(HCCl(3))·2H(2)O}(n) (2), {[Cd(L(3))(2)(NO(3))(2)]}(n) (3), and {[Cd(L(4))(2)(NO(3))(2)]·2(CHCl(3))}(n) (4). These complexes have been characterized by elemental analyses, powder X-ray diffraction, thermogravimetric (TG) analyses, IR spectroscopy, and single-crystal X-ray diffraction. Structural analyses show that four types of structures are formed: (1) a discrete M(2)L(2) ring with two Cd ions and two cis-L(1) ligands comprising a zero-dimensional molecular rectangle (0D), (2) an unusual zigzag linear chain and a one-dimensional ladder existing simultaneously in the crystal lattice (1D), (3) a two-dimensional network of the (4,4) net structure (2D), and (4) an unusual chiral three-dimensional framework with 5-fold interpenetrating diamond (dia) topology (3D).

Construction of a novel Zn-Ni trinuclear Schiff base and a Ni2+ chemosensor.

A novel Zn-Ni heterotrinuclear Schiff base compound bearing acacen(2-) moieties was constructed through the selective assembly of a chemosensor Schiff base zinc compound with a Ni(2+) ion. Its crystal structure not only clearly explains the binding mode between the chemosensor molecule and the detected metal ion but also represents the first trinuclear complex based on a symmetric acacen(2-) base Schiff base.

Assembly of a 1D coordination polymer through in situ formation of a new ligand by double C-C coupling on CHCl3 under solvothermal conditions.

A rare in situ metal/ligand reaction has been observed during the assembly of a manganese-coordination polymer under solvothermal conditions, which leads to double C-C coupling on CHCl(3) involving cleavage of three C-Cl bonds and the formation of two new C-C bonds at the same carbon center.