Exploring crystal structure, Hirshfeld surface and quantum mechanical attributes of symmetric thiophene Schiff base

Author:

Meral Seher,Agar Ayşen Alaman,Cinar Emine Berrin,Dege Necmi,Kanmazalp Sibel Demir,Vidya V. G.,Kumar V. G. VijuORCID

Publisher

Springer Science and Business Media LLC

Subject

General Chemistry

Reference39 articles.

1. P. Nitschke, B. Jarzabek, A. Bejan, M. Damaceanu, Effect of protonation on optical and electrochemical properties of thiophene−phenylene-based schiff bases with alkoxy side groups. J. Phys. Chem. B 125, 8588–8600 (2021)

2. K. Hadi, F. Mehdi, B. Reza, T. Vajiheh, S.M. Khurram, A. Muhamma, N.T. Muhammad, Sonication-assisted synthesis of new Schiff bases derived from 3-ethoxysalicylaldehyde: crystal structure determination, Hirshfeld surface analysis, theoretical calculations and spectroscopic studies. J. Mol. Str. 1243(5), 130782 (2021)

3. J. Arezoo, S. Mehdi, M. Valiollah, M. Majid, M. Iraj, T. Shahram, A.R. Hadi, K. Hadi, K. Reza, G. Sajjad, Studies on DNA binding properties of new Schiff base ligands using spectroscopic, electrochemical and computational methods: influence of substitutions on DNA-binding. J. Mol. Liq. 253, 61–71 (2018). https://doi.org/10.1016/j.molliq.2018.01.029

4. K. Hadi, B. Reza, F. Mehdi, T. Vajiheh, S.M. Khurram, A. Muhammad, N.T. Muhammad, Ultrasound-based synthesis, SC-XRD, NMR, DFT, HSA of new Schiff bases derived from 2-aminopyridine: experimental and theoretical studies. J. Mol. Struct. 1233(5), 130105 (2021)

5. A.A. Amir, K. Hadi, F. Nourollah, N.T. Muhammed, Synthesis, characterization, crystal structures and antibacterial activities of some Schiff bases with N2O2 donor sets. J. Iran. Chem. Soc. 15, 1495–1504 (2018). https://doi.org/10.1007/s13738-018-1347-6.2

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