30234-71-0Relevant academic research and scientific papers
Cyclometalated iridium(III) complexes based on phenyl-imidazole ligand
Baranoff, Etienne,Fantacci, Simona,De Angelis, Filippo,Zhang, Xianxi,Scopelliti, Rosario,Graetzel, Michael,Nazeeruddin, Md. Khaja
, p. 451 - 462 (2011/03/16)
Phenyl-imidazole-based ligands with various substitution patterns have been used as the main ligand for heteroleptic bis-cyclometalated iridium complexes. Two series of complexes have been prepared and their photophysical and electrochemical properties we
Synthesis and photophysics of some novel imidazole derivatives used as sensitive fluorescent chemisensors
Saravanan, Kanagarathinam,Srinivasan, Natesan,Thanikachalam, Venugopal,Jayabharathi, Jayaraman
body text, p. 65 - 80 (2012/04/23)
Some novel imidazole derivatives were developed for highly sensitive chemisensors for transition metal ions. Since these compounds are sensitive to different external stimulations such as UV irradiation, heat, increasing pressure and changing the environm
Iridium(III) complexes with orthometalated phenylimidazole ligands subtle turning of emission to the saturated green colour
Jayabharathi, Jayaraman,Thanikachalam, Venugopal,Saravanan, Kanagarathinam,Srinivasan, Natesan
experimental part, p. 507 - 519 (2012/05/05)
A series of novel six iridium complexes (1-6) bearing two substituted phenylimidazole and an additional acetylacetone as the third co-auxilary ligand are reported. The lowest absorption band for all iridium complexes consist of a mixture of heavy atom Ir(
Catalyst-free one-pot four component synthesis of polysubstituted imidazoles in neutral ionic liquid 1-butyl-3-methylimidazolium bromide
Hasaninejad, Alireza,Zare, Abdolkarim,Shekouhy, Mohsen,Ameri Rad, Javad
experimental part, p. 844 - 849 (2011/01/13)
A catalyst-free one-pot four component methodology for the synthesis of 1,2,4,5-substituted imidazoles under conventional heating and microwave irradiation using 1-butyl-3-methylimidazolium bromide, [Bmim]Br, as a neutral reaction media is described. A broad range of structurally diverse aldehydes (aromatic aldehydes bearing electron withdrawing and/or electron releasing groups as well as heteroaromatic aldehydes) and primary amines (aromatic and aliphatic) were applied successfully, and corresponding products were obtained in good to excellent yields without any byproduct.
