178476-63-6

Upstream product

• 29162-73-0 5,10,15,20-tetrakis(p-bromophenyl)porphyrin 
• 6147-53-1 cobalt(II) diacetate tetrahydrate 
• 71-48-7 cobalt(II) acetate 

Relevant academic research and scientific papers

Synthesis, Spectral, and Coordination Properties of Halogen-Substituted Tetraarylporphyrins

2,3,7,8,12,13,17,18-Ocatbromo-5,10,15,20-tetra-(4-chloroprienyl)porphyrin and 2,3,7,8,12,13,17,18-octachloro-5,10,15,20-tetra-(4-bromophenyl)porphyrin have been synthesized. The obtained compounds have been identified by electronic absorption and 1/

Microporous cobaltporphyrin covalent polymer mediated Co3O4@PNC nanocomposites for efficient catalytic C-H bond activation

A Cobalt porphyrin conjugated porous polymer (Co/PCP) was obtained by hybrid polymerization of a mixture of Co(II)(5,10,15,20-tetrakis(4-bromophenyl)-21H,23H-porphyrin) (CoTBPP) and 5,10,15,20-tetrakis(4-bromophenyl)-21H,23H-porphyrin (TBPP) (3:7 M ratio) with the coupling reagent of p-phenyldiboric acid. This Co/PCP was carbonized at 400 °C and the obtained catalyst (denoted as Co3O4@PNC-400) was composed of Co3O4 nanoclusters wrapped in the nitrogen-carbon materials. This catalyst has an extremely high catalytic activity for the aerobic oxidation of C–H bonds. It can efficiently catalyze the oxidation of the C–H bonds in toluene and cyclohexane with high conversion and high selectivity of (alcohol + aldehyde), (alcohol + ketone) compounds, respectively. When heat-treated at 400 °C, the porous framework structure of the porphyrin polymer was partially retained, and the highly active Co3O4 nanoclusters were generated in situ. The reaction of C[dbnd]N to C–N and connection with the Co3O4 nanoclusters also occurred. Co3O4@PNC-400 has obvious synergistic catalytic effect between Co3O4 and nitrogen-carbon framework during the catalytic reaction. The defective structure caused by the migration of cobalt also greatly improved the catalytic activity. Co/PCPs with different cobalt contents were also synthesized and heat treated at different temperature. These catalysts were a new type of efficient C–H oxidation catalysts with excellent potential application value.

A Br-regulated transition metal active-site anchoring and exposure strategy in biomass-derived carbon nanosheets for obtaining robust ORR/HER electrocatalysts at all pH values

A novel Br-regulated "Transition Metal Active-site Anchoring and Exposure" (TMAAE) strategy is reported, for the first time, to fabricate a hierarchical porous Co/N-doped bio-carbon bifunctional electrocatalyst (CoTBrPP?bio-C) for an all-pH ORR and HER by using a simple one-pot co-pyrolysis over a mushroom (MR) template with adsorbed Br-substituted porphyrinato cobalt (CoTBrPP). Introduction of CoTBrPP onto the MR template not only leads to a larger specific area of 604 m2 g-1 in CoTBrPP?bio-C relative to that of CoTPP?bio-C (CoTPP = Br-free CoTBrPP), 98 m2 g-1, but more importantly also regulates the oriented distribution of pores precisely which promotes effective exposure of multiple active sites depending on the departure of Br-species attached to the Co-N4 macrocycle periphery. Impressively, CoTBrPP?bio-C with a Co loading down to 0.77 at% exhibits higher all-pH ORR and HER performance compared to CoTPP?bio-C with a Co loading of 3.5 at%. An efficient TMAAE makes CoTBrPP?bio-C possess higher onset and half-wave potentials of 0.93 and 0.85 V for the ORR, and a smaller Tafel slope of 80 mV dec-1 for the HER in an alkaline medium. CoTBrPP?bio-C also had a superior all-pH long-term stability and outstanding methanol tolerance, surpassing commercial Pt/C and most non-precious-metal catalysts reported to date. Furthermore, Zn-air batteries assembled with CoTBrPP?bio-C exhibited a higher peak power density of 100 mW cm-2 and excellent durability than Pt/C.

Synthesis and properties of bromine-substituted Co(II) tetraphenylporphyrinates

The interaction of bromine-substituted tetraphenylporphyrins with cobalt(II) acetate in a chloroform–methanol mixture yielding the corresponding cobalt(II) porphyrinates has been studied by means of spectrophotometry. Treatment of Co(II) porphyrinates wit

Super absorbent conjugated microporous polymers: A synergistic structural effect on the exceptional uptake of amines

Conjugated microporous polymers exhibit a synergistic structural effect on the exceptional uptake of amines, whereas the dense porphyrin units facilitate uptake, the high porosity offers a large interface and the swellability boosts capacity. They are efficient in the uptake of both vapor and liquid amines, are applicable to various types of amines, and are excellent for cycle use.