Synthesis, characterization and spectral studies of mononuclear and binuclear Fe(II), Co (II), Ni (II), Zn(II) complexes with 2,4-dinitrophenylhydrazine dithiocarbamate

New complexes of dithiocarbamate of the general formula [M(2,4-dinitrphenhydra - dtc)2], [MM’(2,4-dinithrphenhydra-dtc)4] where: M=Fe (II), Co(II), Ni(II), M’=Zn(II), 2,4- dinitrphenhydra-dtc=2,4- di nitro phenyl hydrazine dithiocarbamate and [M(l,10-phen)3][M’(2,4 – dinitrphenhydra-dtc)4], [M(1,10- phen)3][M’2(2,4-dinitrphenhydra - dtc)6] Where: M=Co(II), Ni(II), M’=Zn(II), (1,10-phen)= 1,10-phenanthroline monohydrate. Have been prepared and characterized by atomic absorption spectroscopy infrared, conductance measurements, electronic absorption spectra, nuclear magnetic resonance and magnetic susceptibility measurements. Magnetic moments and electronic spectra indicate that the complexes of the type [M(2,-dinitrphenhydra-dtc)2], [MM’(2,4-dinitrphenhydra - dtc)4] are of square planner geometry while the complexes of the type [M(1,10-phen)3][M’(2,4-dinitrphenhydra-dtc)4] and [M(1,10 phen)3][M’2(2,4-dinitrphenhydra-dtc)6] have octahedral geometry.

Synthesis of efficient Co and N co-doped carbon catalysts with high surface areas for selective oxidation of ethylbenzene

In this manuscript, Co and N co-doped carbon catalysts with high surface areas were prepared via the pyrolysis of cobalt nitrate and 1,10-phenanthroline monohydrate, using Mg(OH)2 as a pore former, followed by acid etching.

Copper-Catalyzed Cleavage of Unstrained C–C Bonds for the Synthesis of 1-Acyloxy-2,2,6,6-tetramethylpiperidines from Cyclic or Acyclic Ketones

A copper-catalyzed approach for the synthesis of 1-acyloxy-2,2,6,6-tetramethylpiperidines through the C–C bond cleavage of cyclic or acyclic ketones was developed. In this chemistry, a combination of CuCl2·2H2O, 1,10-phenanthroline monohydrate, and aniline was crucial for the formation of the desired products by the reaction of ketones with TEMPO. This research provides a new strategy for the further transformation of α-aryl cyclic or acyclic ketones.

Enhanced Fluorescence Emission of Bonding Type Rare Earth Complexes Eu(MAA)3Phen

Rare earth fluorescent complexes monomer with activated double bonds was synthesized by using Eu as the central atom, Methacrylic acid and 1, 10-Phenanthroline monohydrate as ligand. The structure of resultant Eu (MAA)3Phen was determined by infrared spectrum, ultraviolet spectrum and element analysis, and the fluorescence property of the complexes was tested by fluorescence spectra and fluorescence microscopy. Compared with conventional luminescent materials, this resultant complexes show greater fluorescence intensity. The analysis has revealed that with the increase of rare earth ion concentration from 4×10-5mol·L-1 to 4×10-3mol·L-1, the fluorescence quenching phenomenon appeared in the complexes solution.

Understanding the role of water in 1,10-phenanthroline monohydrate

This study unravels why 1,10-phenanthroline forms a very stable stoichiometric channel hydrate withZ′ > 1.