Construction of highly-stable covalent organic framework with combined enol-imine and keto-enamine linkages.

A novel covalent organic framework (COF) (Tp-BI-COF) with combined ketimine-type enol-imine and keto-enamine linkages was prepared through a cascade of ketimine condensation followed by aldimine condensation and characterized by XRD, solid state C NMR, IR, TGA and BET. Tp-BI-COF showed high stability toward acid, organic solvent, and boiling water. The 2D COF exhibited photochromic properties after being irradiated with a xenon lamp.

Metal-organic framework bearing new viologen ligand for ammonia and CrO sensing.

Three anionic metal-organic frameworks (MOFs) {[Zn(BTEC)(HO)(4-BCBPY)]·(HO)} (1-3) (BTEC = 1,2,4,5-benzenetetracarboxylic acid anion, 4-BCBPY = 1,1'-bis(4-cyanobenzyl)-4,4'-bipyridinium dication) were synthesized in the reaction of 1,2,4,5-benzenetetracarboxylic acid with different metal salts such as ZnNO, ZnCl, and ZnSO, under solvothermal conditions in the presence of 1,1'-bis(4-cyanobenzyl)-4,4'-bipyridinium chloride. Single crystal X-ray diffraction analysis shows that compounds 1, 2 and 3 have MOF structures based on binuclear metal building units, which are connected by two protonated BTEC ligands and three zinc ions, and the viologen cation 4-BCBPY is located in the channel to achieve charge balance. Compounds 1, 2 and 3 have good photosensitivity, respond to sunlight, UV light and blue ray, and turn blue.

Photocatalytic Degradation of Deoxynivalenol Using Cerium Doped Titanium Dioxide under Ultraviolet Light Irradiation.

Deoxynivalenol (DON) is a major mycotoxin with high toxicity that often contaminates grains, foods and feeds. The traditional approaches for DON removal are difficult to meet industry and agriculture demands due to the high stability of the DON molecule. Therefore, there is an urgent need to develop green and effective strategies for DON degradation.

Visible Light-Induced Decarboxylative Alkylation of Heterocyclic Aromatics with Carboxylic Acids via Anthocyanin as a Photocatalyst.

A visible light-induced decarboxylative alkylation of heterocyclic aromatics with aliphatic carboxylic acids was developed by using anthocyanins as a photocatalyst under mild conditions. A series of alkylated heterocyclic compounds were obtained in moderate to good yields by using the metal-free decarboxylative coupling reaction under blue light. This strategy uses cheap and readily available carboxylic acids as alkylation reagents with good functional group tolerance and environmental friendliness.

Using α-Pinene-Modified Triethoxysilane as the New Cross-Linking Agent To Improve the Silicone Rubber Properties.

α-Pinene-modified triethoxysilane (α-PTES) was synthesized by hydrosilylation in the presence of Karstedt's catalyst. The structure of α-PTES was determined by Fourier transform infrared spectroscopy and nuclear magnetic resonance. Under the catalysis of an organotin catalyst, α-PTES, which was the cross-linking agent, and the hydroxy-terminated poly(dimethylsiloxane) matrix were utilized to prepare the room-temperature vulcanized silicone rubber.

A visible-light-induced cascade reaction of etherification/C-C cyclization: efficient synthesis of dibenzo[b,d]oxepin-7(6H)-ones.

A visible-light-induced palladium-catalyzed cascade reaction was developed by etherification/C-C coupling cyclization of α-bromoacetophenones with phenols. A series of dibenzo[b,d]oxepin-7(6H)-one derivatives were efficiently synthesized by using this method in good yields. Furthermore, this method was applied to the synthesis of protosappanin A.

Crystal structure of poly[(2,2'-bi-pyridine-κ(2) N,N')tetra-kis-(μ-cyanido-κ(2) N:C)dinickel(II)].

The polymeric title complex, [Ni2(CN)4(C10H8N2)] n , was obtained serendipitously under hydro-thermal conditions. The asymmetric unit consists of one half of an [Ni(CN)4](2-) anion with the Ni(2+) cation situated on an inversion centre, and one half of an [Ni(2,2'-bpy)](2+) cation (2,2'-bpy is 2,2'-bi-pyridine), with the second Ni(2+) cation situated on a twofold rotation axis. The two Ni(2+) cations exhibit different coordination spheres.

catena-Poly[[(5-phenyl-2,2'-bipyridine-κN,N')copper(I)]-μ-thio-cyanido-κN:S].

The title compound, [Cu(NCS)(C(16)H(12)N(2))](n), was synthesised under hydro-thermal conditions. The Cu(I) ion shows distorted tetra-hedral geometry being coordinated by two N atoms from a 5-phenyl-2,2'-bipyridine ligand and by the N and S atoms from two different thio-cyanate anions. The Cu(I) ions are bridged by thio-cyanide groups, forming a one-dimensional coordination polymer along the b axis.

Poly[penta-kis-(μ-cyanido-κN:C)tris-(5-phenyl-2,2'-bipyridine-κN,N')penta-copper(I)].

The hydro-thermal reaction of Cu(acetate)(2) and K(3)[Fe(CN)(6)] with 5-phenyl-2,2'-bipyridine (5-ph-2,2'-bpy) in water yields the polymeric title complex, [Cu(5)(CN)(5)(C(16)H(12)N(2))(3)](n), which consists of ribbons along the a axis, constructed from 26-membered {Cu(10)(CN)(8)} rings. In these rings, the metal atoms are bridged by cyanide groups, except for one close Cu⋯Cu contact [2.7535 (12) Å], which can be considered as ligand-unsupported.

[Density functional theory calculation of SERS spectra of trans-1,2-bis(4-pyridyl)-ethylene on silver].

It has been found that trans-1, 2-bis(4-pyridyl)-ethylene has the best SERS signal and can be employed as a kind of self-assembly ? Im for the exploration of the SERS-active on the silver foil substrate. The shifts in the experiment surface enhanced Raman scattering of trans-1,2-bis(4-pyridyl)-ethylene were simulated by density functional theory calculation with the BP86, BPw91, B3LYP method. The basis set of 6-31++G(d,p) and Lan12dz was used by H, C, N atoms and Ag atom for the t-BPE-Ag complex.

Surface-enhanced Raman scattering of trans-1,2-bis (4-pyridyl)-ethylene on silver by theory calculations.

Surface-enhanced Raman spectra of trans-1,2-bis (4-pyridyl)-ethylene (t-BPE) on silver foil were detected at laser line of 514.5, 633, 785 and 1064 nm, respectively. The structure of Ag-t-BPE, Ag4-t-BPE, Ag6-t-BPE, Ag10-t-BPE and Ag20-t-BPE complexes has been calculated using a local version of the Amsterdam density functional program package.

Rare gas atomic number dependence of the hyperpolarizability for rare gas inserted fluorohydrides, HRgF (Rg = He, Ar, and Kr).

The three structures of rare gas inserted fluorohydrides HRgF (Rg = He, Ar, and Kr) with all real frequencies are obtained at the QCISD(T)/aug-cc-pVTZ level. The static first hyperpolarizabilities (beta(0)) at the QCISD/aug-cc-pVQZ level are 8 a.u.