An Unprecedented Tridentate-Bridging Coordination Mode of Permanganate Ions: The Synthesis of an Anionic Coordination Polymer-[Co(NH)][(K(κ-Cl)(μ-(κ-O,O',O″-MnO))]-Containing Potassium Central Ion and Chlorido and Permanganato Ligands.

A unique compound (compound ) with structural features including an unprecedented tridentate-bridging coordination mode of permanganate ions and an eight-coordinated (rhombohedral) κ-chlorido and tridentate permanganato ligand in a potassium complex containing coordination polymer (Co(NH)][(K(κ-Cl)(μ-(κ-O,O',O″-MnO))) with isolated regular octahedral hexamminecobalt(III) cation was synthesized with a yield of >90%. The structure was found to be stabilized by mono and bifurcated N-H∙∙∙Cl and N-H∙∙∙O (bridging and non-bridging) hydrogen bonds. Detailed spectroscopic (IR, far-IR, and Raman) studies and correlation analysis were performed to assign all vibrational modes.

Hexakis(urea-O)iron Complex Salts as a Versatile Material Family: Overview of Their Properties and Applications.

Due to their Fe- and N-containing reactive urea ligand content, the hexakis(urea-O)iron(II) and hexakis(urea-O)iron(III) complexes were found to be versatile materials in various application fields of industry and environmental protection. In our present work, we have comprehensively reviewed the synthesis, structural and spectroscopic details, and thermal properties of hexakis(urea-O)iron(II) and hexakis(urea-O)iron(III) salts with different anions (NO, Cl, Br I, I, ClO, MnO, SO, CrO, and SO). We compared and evaluated the structural, spectroscopic (IR, Raman, UV-vis, Mössbauer, EPR, and X-ray), and thermogravimetric data.

Reaction of Partially Methylated Polygalacturonic Acid with Iron(III) Chloride and Characterization of a New Mixed Chloride-Polygalacturonate Complex.

We have described a new route for the preparation of partially methylated polygalacturonic acid containing hydrolyzed (acidic) and unhydrolyzed (methyl esterified) carboxylate groups in a ratio of 1:1 (PGA, compound ), and one of its basic Fe-salts (compound ) with a ~1:2 Fe:GA stoichiometry (GA means galacturonic acid and methylated galacturonic acid units). The partially hydrolyzed pectin was transformed into compound with the use of double ion exchange with a strongly acidic macroreticular sulfonated styrene-divinylbenzene copolymer as a hydrogen ion source. The reaction of compound with FeCl resulted in compound .

Thermally Induced Solid-Phase Quasi-Intramolecular Redox Reactions of [Hexakis(urea-)iron(III)] Permanganate: An Easy Reaction Route to Prepare Potential (Fe,Mn)O Catalysts for CO Hydrogenation.

Research on new reaction routes and precursors to prepare catalysts for CO hydrogenation has enormous importance. Here, we report on the preparation of the permanganate salt of the urea-coordinated iron(III), [hexakis(urea-)iron(III)]permanganate ([Fe(urea-O)](MnO)) via an affordable synthesis route and preliminarily demonstrate the catalytic activity of its (Fe,Mn)O thermal decomposition products in CO hydrogenation. [Fe(urea-O)](MnO) contains O-coordinated urea ligands in octahedral propeller-like arrangement around the Fe cation.

Carbon Microsphere-Supported Metallic Nickel Nanoparticles as Novel Heterogeneous Catalysts and Their Application for the Reduction of Nitrophenol.

Nickel nanoparticles are gaining increasing attention in catalysis due to their versatile catalytic action. A novel, low-cost and facile method was developed in this work to synthesize carbon microsphere-supported metallic nickel nanoparticles (Ni-NP/C) for heterogeneous catalysis. The synthesis was based on carbonizing a polystyrene-based cation exchange resin loaded with nickel ions at temperatures between 500 and 1000 °C.