29213-03-4

Transition metal doped cobalt ferrite (CoM0.2Fe1.8O4 (M = Co, Ni, Cu, Zn)) nanoparticles were fabricated using the sol-gel methodology. The obtained ferrite nanoparticles were annealed at 400 °C and characterized using Fourier transform infra-red spectroscopy (FT-IR), X-ray diffraction (XRD), high resolution transmission electron microscopy (HR-TEM), vibrating sample magnetometry (VSM) and energy dispersive X-ray (EDX) and scanning transmission electron microscopy (STEM). In the FT-IR spectra two bands in the range 1000-400 cm-1 were observed corresponding to the M-O bond in the tetrahedral and octahedral sites. XRD patterns confirmed the formation of a cubic spinel structure with a Fd3m space-group. HR-TEM analysis revealed a quasi-spherical shape with particle sizes in the range 20-30 nm for all the synthesized ferrite nanoparticles. The lattice inter-planar distances of 0.29, 0.25, 0.21 and 0.16 nm obtained from HR-TEM corresponding to the (2 2 0), (3 1 1), (4 0 0) and (5 1 1) lattice planes respectively were in complete agreement with the XRD data. The EDX-STEM confirmed the elemental composition as per the desired stoichiometric ratio. The catalytic efficiency of the synthesized ferrite samples was explored for the reduction of nitrophenols. Cu substituted cobalt ferrite nanoparticles (CoCu0.2Fe1.8O4) possessed excellent catalytic activity while CoM0.2Fe1.8O4 (M = Co, Ni and Zn) were inactive for the same. The substrate scope of the developed protocol was also evaluated for the reduction of various CH3-, NH2-, Br-, Cl- etc. substituted nitroaromatic compounds.

A Cu4L4 metal-organic cage (MOC) composed of amine-protected ligands forms supramolecular coordination polymers (SCPs) upon covalent post-assembly deprotection. The amorphous SCPs form by virtue of aniline-copper coordination and possess a tunable porosit

2-Nitrophenylboronic acids serve as interesting starting materials for the construction of biphenyl- and terphenyl-based amines if subjected to the Suzuki–Miyaura reaction. Unfortunately, these boronic acids suffer from low reactivity in Suzuki reactions, alongside their low stability in the presence of Pd. Herein, a general method for the construction of 2-nitro-substituted bi- and terphenyls is presented, with special emphasis on the synthesis of 2-amino-2'-nitrobi- and terphenyls. Comparisons are made with other boronic acids that have some of the aforementioned issues. Finally, the application of the obtained 2-amino-2'-nitrobi- and terphenyls as starting materials for the synthesis of bi- and terphenyl based di- and triamines is encountered for, with emphasis on the use of these amines as precursors for Schiff base ligands. In addition, the synthesis of some Zn complexes of these ligands is presented.

This paper emphasizes the preparation of nonlinear optical (NLO) responsive chromophores and their corresponding polymers. Initially, the carboxyl acid group-based precursors of the chromophores containing strong acceptors such as nitro-substituted thiazo

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The synthesis of 2,6-disubstituted N,N,N′,N′-tetramethyl-p-phenylenediamines (R = Cl, Br, I, CN, or C≡CSi(CH3)3), potential precursors/building blocks for molecular magnets, is presented. In addition to standard methods (1

Pyrimido[5,4-d]pyrimidines of the general formula [Figure] which have an inhibitory effect on signal transduction mediated by tyrosine kinases, their use for the treatment of oncoses, and their preparation. Exemplary compounds are: (a) 4-(5-indolylamino)-6-morpholinopyrimido[5,4-d]pyrimidine; (b) 4-(5-indolylamino)-6-[trans-(4-hydroxycyclohexyl)amino]pyrimido[5,4-d]pyrimidine; (c) 4-[(3-chloro-4-fluorophenyl)amino]-6-[4-(morpholinocarbonylmethyl)-1-piperazinyl]pyrimido[5,4-d]pyrimidine; (d) 4-[(3-chloro-4-fluorophenyl)amino]-6-[(4-morpholinyl)amino]pyrimido[5,4-d]pyrimidine; (e) 4-[(3-chloro-4-fluorophenyl)amino]-6-(4-picolylamino)pyrimido[5,4-d]pyrimidine; (f) 4-[(3-chloro-4-fluorophenyl)amino]-6-[1-trifluoroacetyl-4-piperidinylamino]pyrimido[5,4-d]pyrimidine; (g) 4-[(3-chloro-4-fluorophenyl)amino]-6-(endo-tropinylamino)pyrimido[5,4-d]pyrimidine; and, (h) 4-[(3-chloro-4-fluorophenyl)amino]-6-(exo-tropinylamino)pyrimido[5,4-d]pyrimidine.

Pyrimido[5,4-d]pyrimidines of the general formula [Figure] which have an inhibitory effect on signal transduction mediated by tyrosine kinases, their use for the treatment of disorders, in particular of oncoses, and their preparation. Exemplary compounds are: 4-[(3-Chloro-4-fluorophenyl)amino]-6-[1-methyl-4-piperidinylamino]pyrimido[5,4-d]pyrimidine, and 4-[(3-Chloro-4-fluorophenyl)amino]-6-[trans-4-dimethyl-aminocycohexylamino]pyrimido[5,4-d]pyrimidine.

The present invention relates to pyrimido?5,4-d!pyrimidines of the general formula STR1 in which Ra to Rc are as defined herein, their tautomers, their stereoisomers and their salts, in particular their physiologically tolerated salts with inorganic or organic acids or bases which have valuable pharmacological properties, in particular an inhibiting action on signal transduction mediated by tyrosine kinases, their use for the treatment of diseases, in particular tumor diseases.