- X-ray Diffraction in Crystallography
- Crystallization and Solubility Studies
- Metal complexes synthesis and properties
- Crystal structures of chemical compounds
- Magnetism in coordination complexes
- Metal-Organic Frameworks: Synthesis and Applications
- Crystallography and molecular interactions
- Lanthanide and Transition Metal Complexes
- Organometallic Compounds Synthesis and Characterization
- Synthesis and Characterization of Heterocyclic Compounds
- Metal-Catalyzed Oxygenation Mechanisms
- Organometallic Complex Synthesis and Catalysis
- Synthesis and biological activity
- Inorganic and Organometallic Chemistry
- Molecular Sensors and Ion Detection
- Electrochemical Analysis and Applications
- Analytical chemistry methods development
- Analytical Chemistry and Sensors
- Synthesis and Reactivity of Heterocycles
- Synthesis of Tetrazole Derivatives
- Ferrocene Chemistry and Applications
- Phenothiazines and Benzothiazines Synthesis and Activities
- Synthesis and Reactivity of Sulfur-Containing Compounds
- Synthesis of heterocyclic compounds
- Electrochemical sensors and biosensors
Farhangian University
2016-2025
Shahid Beheshti University
2007-2016
Islamic Azad University, Tehran
2007-2016
Kharazmi University
2016
Islamic Azad University Shahr-e-Rey
2007-2014
Semnan University
2014
Sharif University of Technology
2009-2013
Islamic Azad University North Tehran Branch
2011-2012
Urmia University
2011
Shahid Rajaee Teacher Training University
2005-2006
Bioreducible FA-PEG-<italic>b</italic>-P(α-Pt(<sc>ii</sc>)-SS-CL/CL) conjugates have been successfully developed in order to build redox-responsive micelles with targeting and site-specific drug releasing abilities.
Multi-walled carbon nanotubes (MWNTs) decorated with Fe3O4 nanoparticles have been prepared using a coprecipitation technique and were surface modified poly(citric acid) (PC) dendrimer. These PC-functionalized magnetic (MWCNT/MA@PC) used as novel support for Pt(II) complex immobilized nanocatalyst (MWCNT/MA@PC/Pt(II)). The morphology structural features of the characterized different microscopic spectroscopic techniques, including FT-IR, TEM, EDX, BET, XRD, TGA, ICP, VSM. nitro nitrile...
Mononuclear and coordination polymer compounds of 2,2′-dimethyl-4,4′-bithiazole (dm4bt) ligand have been prepared by metallation dm4bt with Cd(NO3)2 · 4H2O CdCl2 H2O. The were characterized IR, 1H NMR, UV–Vis spectroscopy, X-ray crystallography. structural study [Cd(dm4bt)2(NO3)2] H2O (1) shows that the complex is a monomeric seven-coordinate (CdN4O3) cadmium(II)-bithiazole system two bidentate mono nitrates. structure [Cd(dm4bt)Cl2] n (2) distorted octahedral environment around cadmium(II)...
The complexes [Fe(dm4bt)3][FeCl4]2 (1) and [Fe(dm4bt)3][FeBr4]2 (2) were prepared from the reaction of 2,2′-dimethyl-4,4′-bithiazole (dm4bt) with FeCl3·6H2O FeBr3, respectively, in methanol. Both characterized by IR, UV-Vis 1H NMR spectroscopy their structures studied single-crystal diffraction. methylated bithiazole led to high spin Fe(II) centers octahedral cation part 1 2 Fe–N distance 2.220 Å, spite low unsubstituted ligands. Crystal structure determination was performed at 90, 120 298...
Highly efficient magnetic organosilica‐supported gold nanoparticles were developed as an artificial metalloenzyme for the synthesis of propargylamines through C–H activation in water under ambient atmosphere. Herein, we present a very simple and method deposition Au on porous organosilica (Fe 3 O 4 @SiO 2 ‐Cl) thermal reduction organometallic III complex. As nucleophile, polypyridyl coordination complex could react with alkyl halides from Fe ‐Cl to form quaternary ammonium salt ionic liquid;...
[Fe(dmbipy)Cl4][dmbipyH], 1 (dmbipy is 4,4′-dimethyl-2,2′-bipyridine), was prepared from reaction of FeCl3 · 6H2O with 4,4′-dimethyl-2,2′-bipyridine in 0.1 molar aqueous HCl. Treatment dimethyl sulfoxide methanol produced [Fe(dmbipy)Cl3(DMSO)], 2 (DMSO sulfoxide). Both complexes were characterized by IR, UV-vis, and 1H-NMR spectroscopies their structures studied single crystal diffraction. Compounds are high-spin spin multiplicity six.