Marzieh Sohrabi

ORCID: 0000-0002-6045-0607
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About
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Research Areas
  • Metal complexes synthesis and properties
  • X-ray Diffraction in Crystallography
  • Crystallization and Solubility Studies
  • Molecular Sensors and Ion Detection
  • Advanced biosensing and bioanalysis techniques
  • Organophosphorus compounds synthesis
  • Synthesis and biological activity
  • Nanocluster Synthesis and Applications
  • Organometallic Compounds Synthesis and Characterization
  • Nanoplatforms for cancer theranostics
  • Advanced Glycation End Products research
  • Hydrogen Storage and Materials
  • Synthesis and Characterization of Heterocyclic Compounds
  • Ferrocene Chemistry and Applications
  • Luminescence and Fluorescent Materials
  • Organometallic Complex Synthesis and Catalysis
  • RNA Interference and Gene Delivery
  • Quinazolinone synthesis and applications
  • Enzyme function and inhibition
  • Quantum, superfluid, helium dynamics
  • Synthesis and Reactivity of Sulfur-Containing Compounds
  • Crystal structures of chemical compounds
  • Asymmetric Hydrogenation and Catalysis
  • MXene and MAX Phase Materials
  • Electrochemical Analysis and Applications

Tehran University of Medical Sciences
2021-2022

Isfahan University of Technology
2017-2022

University of Isfahan
2018

Islamic Azad University, Tehran
2015

Islamic Azad University Shahr-e-Rey
2012

A highly sensitive quinoline based “dual” chemosensor used for fluorometric detection of Zn<sup>2+</sup>, live-cell imaging, and colorimetric Co<sup>2+</sup>.

10.1039/c8nj01580e article EN New Journal of Chemistry 2018-01-01

The present article describes the design, synthesis, in vitro urease inhibition, and silico molecular docking studies of a novel series nitrothiazolacetamide conjugated to different thioquinazolinones. Fourteen bearing thioquinazolinones derivatives (8a-n) were synthesized through reaction isatoic anhydride with amine, followed by carbon disulfide KOH ethanol. intermediates then converted into final products treating them 2-chloro-N-(5-nitrothiazol-2-yl)acetamide DMF. All characterized...

10.1038/s41598-022-05736-4 article EN cc-by Scientific Reports 2022-02-07

Abstract A series of novel phosphoramidates with a general formula P(O) X 1 2 3 , where = 1H‐1,2,4‐triazol ( ); N ‐phenylhydrazine Br, ), dipropylamine 4 and 1,4‐dioxa‐8‐azaspiro[4.5]decane 5 ) as well [P(O)(NC H 8 NH‐CH + .3Cl ‐ ] 6 were synthesized characterized by H, 13 C, 31 P NMR, IR spectroscopy, elemental analysis. It is interesting that the atoms compounds are most upfielded (δ( P) −23.00, −21.65 ppm) among molecules 1–6 . This indicates Br atom acts strong electron donor to via...

10.1002/hc.21040 article EN Heteroatom Chemistry 2012-01-01

The dihydrogen bonding (DHB) interactions were studied theoretically between the hydrogen atoms of BeH2 (1) and MgH2 (2) with those HC≡CX where X = H (3), CH3 (4), F (5), Cl (6) to form complexes H-Be-H ... (7–10) H-Mg-H …HC≡CX (11–14), respectively. structures compounds 1–1 4 optimized at MP2 method using 6-311++G(d,p) basis set. most negative binding energy was measured for structure among isolated analogues 3–6. 9 14 indicated BSSE corrected ΔEdihydrogen values bonded compounds, A linear...

10.3233/mgc-150175 article EN Main Group Chemistry 2015-10-13

New organophosphorus compounds with formula C6 H5 C(O)NHP(O)(2,4-OCH3 -C6 H3 -NH)2 (1), CCl3 C(O)NHP(O)(Cl)[N(C2 )2 ] (2) and CF3 C(O)NHP(O)(C6 (3) were synthesized characterized by 1 H, 13 C, 31 P NMR, IR spectroscopy elemental anal

10.3233/mgc-2012-0065 article EN Main Group Chemistry 2012-01-01
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