Solvatochromism and Optoelectronic Properties of Thiosemicarbazone Derivatives Having π-Conjugated Systems
Author:
Funder
Bitlis Eren Üniversitesi
Publisher
Springer Science and Business Media LLC
Subject
Physical and Theoretical Chemistry,Molecular Biology,Biochemistry,Biophysics
Link
https://link.springer.com/content/pdf/10.1007/s10953-023-01248-5.pdf
Reference40 articles.
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2. Bingül, M.: Synthesis of indole-3-carboxyaldehyde thiosemicarbazone derivatives and investigation of antioxidant and anticholinesterase properties. Afyon Kocatepe Üniversitesi Fen ve Mühendislik Bilimleri Dergisi 19, 317–327 (2019). https://doi.org/10.35414/akufemubid.542712
3. Tom, L., Aiswarya, N., Sreejith, S.S., Kurup, M.P.: Self-organized three dimensional architectures based on non-covalent interactions in square planar Cu (II) thiosemicarbazone: solvent mediated crystallization and EPR based correlation study. Inorg. Chim. Acta 473, 223–235 (2018). https://doi.org/10.1016/j.ica.2018.01.005
4. İlhan-Ceylan, B., Bolukbasi, O., Yilmaz, A., Kaya, K., Kurt, Y., Ülküseven, B.: Synthesis, spectroscopic characterization and quantum chemical studies of a dioxomolybdenum (VI) complex with an N S-substituted pyridoxal thiosemicarbazone. Polyhedron 193, 114884 (2021). https://doi.org/10.1016/j.poly.2020.114884
5. Gülseven, Y., Taşal, E., Sıdır, İ, Güngör, T., Berber, H., Öğretir, C.: Solvatochromic effect studies on the absorption spectra of 4-((2-ethylphenyl)diazenyl)benzene-1,3-diol and 2-((2-ethylphenyl)diazenyl)benzene-1,3,5-triol molecules. Int. J. Hydrog. Energy 34(12), 5255–5259 (2009). https://doi.org/10.1016/j.ijhydene.2008.10.070
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