https://www.selleckchem.com/products/MLN8054.html Herein, we report the synthesis of a monocationic μ-nitrido-bridged iron porphycene dimer, a structural analogue of a monocationic μ-nitrido-bridged iron phthalocyanine dimer, which is known to be one of the most potent molecule-based catalysts for methane oxidation. 1H-NMR and single-crystal X-ray structural analyses showed that the porphycene complex includes two Fe(IV) ions, and the structure around the Fe-NFe core is quite similar to that of the monocationic μ-nitrido-bridged iron phthalocyanine dimer. Although methane was oxidized into MeOH, HCHO, and HCOOH in the presence of a silica-supported catalyst of this monocationic μ-nitrido-bridged iron porphycene dimer in an acidic aqueous solution containing excess H2O2, its reactive intermediate was not a high-valence iron-oxo species, as in the case of a monocationic μ-nitrido-bridged iron phthalocyanine dimer, but ˙OH. It is suggested that the high-valent iron-oxo species of the μ-nitrido-bridged iron porphycene dimer was gradually decomposed under these reaction conditions, and the decomposed compound catalyzed a Fenton-type reaction. This result indicates that the stability of the oxo-species is indispensable for achieving high catalytic methane oxidation activity using a μ-nitrido-bridged iron porphyrinoid dimer with an Fe-NFe core as a catalyst.Enhancement of the emission quantum yield and expansion of the emission tunability spectrum are the key aspects of an emitter, which direct the evolution of future generation light harvesting materials. In this regard, small molecular ligand-protected Cu nanoclusters (SLCuNCs) have emerged as prospective candidates. Herein, we report the broadband emission tunability in a SLCuNC system, mediated by in situ ligand replacement. 1,6-Hexanedithiol-protected blue emissive discrete Cu nanoclusters (CuNCs) and red emissive CuNC assemblies have been synthesized in one pot. The red emissive CuNC assemblies were characterized a