Enayatollah Moradi Rufchahi | Chemistry | Best Researcher Award

Assoc. Prof. Dr. Enayatollah Moradi Rufchahi | Chemistry | Best Researcher Award

Assoc. Prof. Dr. Enayatollah Moradi Rufchahi, Islamic Azad University, Iran

Assoc. Prof. Dr. Enayatollah Moradi Rufchahi is an expert in Organic Chemistry at the Islamic Azad University, Lahijan Branch, Iran. He holds a Ph.D. in Organic Chemistry from Guilan University (2009), where he researched azo dyes’ synthesis and spectroscopic properties. His research interests include the design, synthesis, and structural characterization of azo dyes and pigments, synthetic organic chemistry, and organic medicinal chemistry. He has a strong academic background with an MSc from the University of Tehran and a BSc from Guilan University. Dr. Moradi Rufchahi is also active in scholarly platforms such as Google Scholar and Scopus. ๐Ÿ“š๐Ÿ”ฌ๐Ÿงช

 

Academic Background

Assoc. Prof. Dr. Enayatollah Moradi Rufchahi is a distinguished scholar in Organic Chemistry with a Ph.D. from Guilan University (2009). His doctoral research focused on the Synthesis and Spectroscopic Properties of Some New Azo Dyes under the guidance of Prof. M.R. Yazdanbakhsh. He completed his MSc in Organic Chemistry at the University of Tehran in 1998, exploring Hydroxylation of Alkenes with KMnO4 in the presence of quaternary ammonium salts as phase transfer catalysts. Dr. Moradi Rufchahi also holds a BSc in Pure Chemistry from Guilan University, earned in 1995. ๐ŸŽ“๐Ÿ”ฌ๐Ÿ“˜

 

Research Interests

Assoc. Prof. Dr. Enayatollah Moradi Rufchahiโ€™s research focuses on the design and synthesis of azo dyes and pigments, exploring their spectroscopic properties and structural characterization. His work delves into synthetic organic chemistry, where he develops novel chemical compounds and reaction methodologies. Additionally, Dr. Moradi Rufchahi is interested in organic medicinal chemistry, working to identify and synthesize compounds with potential therapeutic applications. His research contributes to advancements in both the chemical and medicinal fields. ๐Ÿ”ฌ๐Ÿ’ก๐ŸŽจ๐Ÿ’Š

Research Focus

The research of MR Yazdanbakhsh, H Yousefi, and their collaborators primarily focuses on the synthesis, characterization, and biological activity of azo dyes and heterocyclic compounds. Their studies cover a range of chemical properties, including solvatochromism, tautomerism, and spectroscopic characteristics. These researchers are also investigating antimicrobial activity and the application of these dyes in various fields, such as textile dyeing and material science. Their work contributes to organic chemistry, medicinal chemistry, and chemical applications with an emphasis on sustainable materials. ๐ŸŒˆ๐Ÿงช๐Ÿ”ฌ๐Ÿงฌ

 

Publication Top Notes

  • Synthesis, spectral characterization and antimicrobial activity of some new azo dyes derived from 4, 6-dihydroxypyrimidine โ€“ Cited by 84 (2012) ๐Ÿงช๐Ÿ”ฌ
  • Synthesis of some new azo dyes derived from 4-hydroxy coumarin and spectrometric determination of their acidic dissociation constants โ€“ Cited by 80 (2007) ๐Ÿงซ
  • Tautomerism, solvatochromism, preferential solvation, and density functional study of some heteroarylazo dyes โ€“ Cited by 66 (2019) ๐Ÿ’ป๐Ÿง‘โ€๐Ÿ”ฌ
  • Synthesis, characterization and spectroscopic properties of some new azo disperse dyes derived from 4-hydroxybenzo [h] quinolin-2-(1H)-one โ€“ Cited by 56 (2012) ๐ŸŽจ๐Ÿ’ก
  • Synthesis, spectral properties, biological activity and application of new 4-(benzyloxy) phenol derived azo dyes for polyester fiber dyeing โ€“ Cited by 52 (2013) ๐Ÿงต๐Ÿ’ง
  • Solvatochromism, tautomerism and dichroism of some azoquinoline dyes in liquids and liquid crystals โ€“ Cited by 52 (2012) ๐Ÿ”ฌ๐ŸŒˆ
  • Photo-physical and structural studies of some synthesized arylazoquinoline dyes โ€“ Cited by 36 (2017) ๐ŸŒž๐Ÿ”ฌ
  • Solvatochromism and dichroism of fluorinated azoquinolin-8-ol dyes in liquid and liquid crystalline solutions โ€“ Cited by 36 (2008) ๐ŸŒ๐Ÿ“˜
  • Novel azo dyes derived from 8-methyl-4-hydroxyl-2-quinolone: Synthesis, UVโ€“vis studies and biological activity โ€“ Cited by 34 (2013) ๐Ÿงช๐Ÿ’ก
  • Synthesis of 6-chloro and 6-fluoro-4-hydroxyl-2-quinolone and their azo disperse dyes โ€“ Cited by 30 (2010) ๐ŸŒŸ๐Ÿ”ฌ