Theoretical study of structural and electronic properties of conducting polymers
Polymer synthesis
ผลงานวิจัย
Suramitr, S., Kerdchareon, T., Srikhirin, T., and Hannongbua, S. Electronic properties of alkoxy derivatives of poly(para-phenylenevinylene), investigated by time dependent density functional theory calculations. Synthetic Metals 2005, 155: 27-34. (Impact Factor (2007) = 1.788)
Sriwichitkamol, K., Suramitr, S., Poolmaee P., and Hannongbua, S. Structures, absorption spectra, and electronic properties of polyfluorene and its derivatives: A theoretical study. J. Theor. Comp. Chem. 2006, 5, 595-608. (Impact Factor (2007) = 0.923)
Suramitr, S., Hannongbua, S. and Wolschann, P. Conformational analysis and electronic transition of carbazole-based oligomers as explained by density functional theory. J. Mol. Struct. (THEOCHEM) 2007, 807, 109-119. (Impact Factor (2007) = 1.112)
Meeto, W., Suramitr, S., Vannarat, S., and Hannongbua, S. Structural and electronic properties of poly(fluorene–vinylene) copolymer and its derivatives: Time-dependent density functional theory investigation. Chemical Physics 2008, 349, 1-8. (Impact Factor (2007) = 1.805)
Prajongtat, P., S. Suramitr, M.P.Gleeson, K.Mitsuke, S.Hannongbua.2013. “Enhancement of the Solubility, Thermal Stability, and Electronic Properties of Carbon Nanotubes Functionalized with MEH-PPV: A Combined Experimental and Computational Study”Monatsh. Chem. 144(7): 925-935.
Promkatkaew, M., S. Suramitr, T. Karpkird, S. Wanichwecharungruang, M. Ehara, S. Hannongbua.2014.“Photophysical Properties and Photochemistry of Substituted Cinnamates and Cinnamic Acids for UVB Blocking: Effect of Hydroxy, Nitro, and Fluoro Substitutions at ortho, meta, and para Positions”Photochem. Photobiol. Sci. 13: 583-594.
Piyasaengthong, A., N. Boonyalai, S. Suramitr, A. Songsasen.2015.“Synthesis, Characterization, and Pepsin Inhibition Study of Au(III)–3-(2′-thiazolylazo)-2,6-Diaminopyridine Complex” Inorg. Chem. Commun.59: 88-90.
Treesuwan, W., S. Suramitr, S. Hannongbua.2015.“Elucidation of Hydroxyl Groups-antioxidant Relationship in Mono- and Dihydroxyflavones Based on O-H Bond Dissociation Enthalpies”J. Mol. Model. 21(6): 137(1)-137(10).
