Unique hemispherical coordination-drivened pesticide residue probes: Enhanced stability in linear recognition for trifluralin.

Trifluralin (TRL) is an effective and persistent herbicide, but its extensive and prolonged use has increasingly posed ecological and environmental health risks, making the development of convenient and rapid TRL detection methods essential for environmental protection and food safety. In the present research, a novel fluorescent probe was designed and developed, Zn-χ-L, for the rapid and selective detection of TRL in complex environments. The sensor demonstrates excellent sensitivity and stability, while also exhibiting significant resistance to interference from other pesticides and metal ions.

Preparation of a New Hexafluorobutanol-Farnesol Based Supramolecular Solvent and Its Application in Microextraction of Sudan Dyes From Beverage and Water Samples.

In this work, a new supramolecular solvent (SUPRAS) was prepared for the first time using hexafluorobutanol (HFB) and farnesol (FO). FO acts as an amphiphile and HFB as a coacervation inducer and density regulator. The method of dispersive liquid-liquid microextraction followed by high-performance liquid chromatography, supported by a vortex technique, was established using the prepared SUPRAS for the determination of Sudan dyes in aqueous samples.

Thorium Cluster Synthesized by a Solvent-Free Flux Approach: The Richest Coordination Diversity and Application Exploration.

The renaissance of research interests in actinide oxo clusters in the past decade arises from both the concerns of radioactive contamination and their potential utility as nanoscale materials. Compared to the uranium cluster, the thorium (Th) cluster shows less coordination variation. Herein, we presented a unique Th cluster () that exhibits the most diverse coordination chemistry found within a single Th cluster via a solvent-free flux synthesis approach.

Dithio-Fused Boron Dipyrromethenes: Synthesis and Impact of S-Heteroaromatic Annulation Mode.

Three dithio-fused boron dipyrromethenes (BODIPYs), , , and , in which symmetrically S-heteroaromatic ring units fused at [], zigzag, and [] bonds of the parent BODIPY core, respectively, were prepared from the facile and efficient post-functionalization of tetra-halogenated BODIPYs through Pd-catalyzed cyclization. Dithio-fusion at various positions of BODIPY effectively tunes their photophysical properties and single-crystal structural packing arrangements. The single-crystalline microribbons of exhibit commendable hole mobilities in air, reaching up to 0.

Effect of Tb and Ce Co-doping on the Structure and Photoluminescence Properties of Hexagonal Boron Nitride Phosphors.

In the paper, we have successfully prepared hexagonal boron nitride (h-BN:Tb, Ce) phosphors with melamine as the nitrogen source. The X-ray powder diffraction patterns confirm that the sample possesses a hexagonal crystal structure within the P m2 space group. It is interesting that the co-doping combination of Tb and Ce can markedly enhance the threshold concentration of doped activators within the limited solid solution of h-BN phosphors.

Two Purely Inorganic Cationic Tellurite Materials Based on Group IB Metal Tetrafluoroborates with Similar Lamellar Cationic Layers: [CuF(TeO)](BF) and [AgO(TeO)(TeO)(BF)]·2HBF.

Two new purely inorganic cationic tellurite networks of Group IB metal-based tetrafluoroborates, namely, [CuF(TeO)](BF), , and [AgO(TeO)(TeO)(BF)]·2HBF, , have been hydrothermally synthesized under mild conditions. The prepared materials have been characterized by single-crystal X-ray diffraction, powder X-ray diffraction, IR and Raman spectroscopy, SEM-energy-dispersive spectroscopy, UV-vis-NIR diffuse reflectance, magnetic study, and TG analyses. Single-crystal diffraction studies show that both materials have similar cationic Cu/Ag tellurite layers with tetrafluoroborates as interlamellar charge-balancing anions.

Mild Periodic Acid Flux and Hydrothermal Methods for the Synthesis of Crystalline f-Element-Bearing Iodate Compounds.

f-element-bearing iodate compounds are a large family mostly synthesized by hydrothermal reactions starting with actinide/lanthanide ions and iodic acid or iodate salt. In this work, we introduce melting periodic acid flux as a new reaction medium and provide a safe way for single-crystal growth of a series of new f-element iodate compounds including UO(IO)·HO (1), UO(IO)(HO)·HIO (2), α-Th(IO)(NO)(OH) (3), β-Th(IO)(NO)(OH) (4), and (HO)Nd(IO)·3HIO (5). The structures of these compounds deviate from those afforded from hydrothermal reactions.

Systematic Investigation of the in Situ Reduction Process from U(VI) to U(IV) in a Phosphonate System under Mild Solvothermal Conditions.

The oxidation state greatly affects the chemical behavior of uranium in the nuclear fuel cycle and in the environment. Phosphonate ligands, on the other hand, show strong complexation toward uranium at different oxidation states and are widely used in nuclear fuel reprocessing. Therefore, in this work, the reduction behavior of U(VI) with the presence of a phosphonate ligand is investigated under mild solvothermal conditions.

Surprising coordination for low-valent actinides resembling uranyl(vi) in thorium(iv) organic hybrid layered and framework structures based on a graphene-like (6,3) sheet topology.

Three thorium(iv)-based metal-organic hybrid compounds with 2D layered and 3D framework structures exhibiting graphene-like (6,3) sheet topologies were prepared with linkers with threefold symmetry. These compounds contain rare and relatively anisotropic coordination environments for low-valent actinides that are similar to those often observed for high-valent actinide ions.

Centrosymmetric and chiral porous thorium organic frameworks exhibiting uncommon thorium coordination environments.

The solvothermal reaction of thorium nitrate and tris-(4-carboxylphenyl)phosphine oxide in DMF affords a centrosymmetric porous thorium organic framework compound [Th(TPO)(OH)(H2O)]·8H2O (1). In contrast, the ionothermal reaction of the same reagents in the ionic liquid 1-butyl-2,3-dimethylimidazolium chloride results in the formation of a rare example of a chiral and porous thorium organic framework compound, [C9H17N2][Th(TPO)Cl2]·18H2O (2), which is derived solely from achiral starting materials. The geometries of the Th(iv) centers in compounds 1 and 2 are both atypical for low valent actinides, which can be best described as a ten-coordinate spherical sphenocorona and an irregular muffin, respectively.

Hybrid uranium-transition-metal oxide cage clusters.

Transition-metal based polyoxometalate clusters have been known for decades, whereas those built from uranyl peroxide polyhedra have more recently emerged as a family of complex clusters. Here we report the synthesis and structures of six nanoscale uranyl peroxide cage clusters that contain either tungstate or molybdate polyhedra as part of the cage, as well as phosphate tetrahedra. These transition-metal-uranium hybrid clusters exhibit unique polyhedral connectivities and topologies that include 6-, 7-, 8-, 10-, and 12-membered rings of uranyl polyhedra and uranyl ions coordinated by bidentate peroxide in both trans and cis configurations.

Copper(I) and copper(II) uranyl heterometallic hybrid materials.

Two copper-uranium heterometallic compounds, [(UO2)3Cu(II)O2(C6NO2)5] (1) and [(UO2)Cu(I)(C6NO2)3] (2), have been synthesized by the reaction of uranyl acetate with copper salts in the presence of isonicotinic acid. Both compounds have been characterized by single-crystal X-ray diffraction, IR, Raman, and UV-vis spectroscopy. In compound 1, interactions between copper and uranium centers occur and result in a three-dimensional pillar layered structure.

Synthesis of a uranyl persulfide complex and quantum chemical studies of formation and topologies of hypothetical uranyl persulfide cage clusters.

The compound Na(4)[(UO(2))(S(2))(3)](CH(3)OH)(8) was synthesized at room temperature in an oxygen-free environment. It contains a rare example of the [(UO(2))(S(2))(3)](4-) complex in which a uranyl ion is coordinated by three bidentate persulfide groups. We examined the possible linkage of these units to form nanoscale cage clusters analogous to those formed from uranyl peroxide polyhedra.

(UO2)2[UO4(trz)2](OH)2: a U(VI) coordination intermediate between a tetraoxido core and a uranyl ion with cation-cation interactions.

A uranyl triazole (UO(2))(2)[UO(4)(trz)(2)](OH)(2) (1) (trz = 1,2,4-triazole) was prepared using a mild solvothermal reaction of uranyl acetate with 1,2,4-triazole. Single-crystal X-ray diffraction analysis of 1 revealed it contains sheets of uranium-oxygen polyhedra and that one of the U(VI) cations is in an unusual coordination polyhedron that is intermediate between a tetraoxido core and a uranyl ion. This U(VI) cation also forms cation-cation interactions (CCIs).

Glycine-templated manganese sulfate with new topology and canted antiferromagnetism.

A new glycine-templated manganese(II) sulfate, (C(2)NO(2)H(5))MnSO(4) (1), has been solvothermally synthesized and characterized crystallographically and magnetically. Crystal data for 1: monoclinic, space group P2(1)/m, a = 4.8884(10) A, b = 7.

A novel three-dimensional coordination polymer: poly[di-mu3-acetato-di-mu2-acetato-di-mu3-hydroxido-octa-mu3-triazolato-heptamanganese(II)].

The title compound, [Mn7(C2H2N3)8(C2H3O2)4(OH)2]n, is composed of centrosymmetric heptanuclear building units with the central Mn atom on an inversion center. In the building block, three Mn(II) ions are held together by one mu3-hydroxide group, two mu2-triazolate (trz) ligands and two mu2-acetate groups, forming an Mn3 cluster. Two Mn3 clusters are bridged by an Mn atom via two mu2-trz ligands and two mu2-O atoms from two acetate ions to construct a heptanuclear building block.