Abstract
Schiff base ligand, (E)-methyl 2-(5-bromo-2-hydroxybenzylideneamino)-6-phenyl-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate (L) generated from condensation of 5-bromo-salicylaldehyde with methyl 2-amino-6-methyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylate and its Co(II) and Pd(II) metal complexes were prepared by using a molar ratio of ligand:metal as 1:1. The complex compounds were obtained by the coordination of donor atoms of the ligand according to the spectral data. The structures of the obtained complex compounds were determined by elemental analysis, fourier transform infrared, 1H and 13C nuclear magnetic resonance, ultraviolet–visible, mass spectrometry, thermogravimetry–differential thermal analysis and magnetic susceptibility techniques. The optical features of Schiff base ligand and its metal complex compounds were compared for different solvents and molarities.
Similar content being viewed by others
References
S.E.H. Etaiw, D.M. Abd El-Aziz, E.H. Abd El-Zaher, and E.A. Ali, Spectrochim. Acta A 79, 1331–1337 (2011).
Z. Travnicek, M.M. Matikova, and R.J. Novotna, Inorg. Biochem. 105, 937–948 (2011).
K.H. Kumar Naik, S. Selvaraj, and N. Nagaraja, Spectrochim. Acta A 131, 599–605 (2014).
G. Tomasello, G.G. Olaso, and P. Altoe, J. Am. Chem. Soc. 131, 5172–5186 (2009).
M.N. Chaur, D. Collado, and J.M. Lehn, Chem. Eur. J. 17, 248–258 (2011).
B. Mohan, A. Jana, N. Das, S. Bharti, M. Choudhary, S. Muhammad, S. Kumare, A.G. Al-Sehemid, and H. Algarnic, Inorg. Chim. Acta 484, 148–159 (2019).
F. Yakuphanoglu and M. Arslan, Opt. Mater. 27, 29–37 (2004).
H. Neumann, W. Horig, E. Reccius, H. Sobotta, B. Schumann, and G. Kuhn, Thin Solid Films 61, 13–22 (1979).
R. Adiguzel, N. Turan, K. Buldurun, and H. Körkoca, Int. J. Pharmacol. 14, 9–19 (2018).
M.M. Mashalay, Synth. React. Inorg. Met. Org. Chem. 32, 373–397 (2002).
M. Tümer, Synth. React. Inorg. Met. Org. Chem. 41, 211–223 (2011).
N. Turan, K. Buldurun, Y. Alan, A. Savci, N. Çolak, and A. Mantarcı, Res. Chem. Intermediat. 45, 3525–3540 (2019).
T. Mehmet, E. Duygu, T. Ferhan, and B. Akif, Spectrochim. Acta A 67, 916–929 (2007).
S. Ilhan, H. Temel, A. Kılıc, and E. Tas, Transit. Met. Chem. 32, 1012–1017 (2007).
G.G. Mohamed, M.M. Omar, and A.M. Hindy, Turk. J. Chem. 30, 361–382 (2006).
M.M. Moustafa, J. Therm. Anal. 50, 463–471 (1997).
E. Canpolat, A. Yazici, and M. Kaya, Transit. Met. Chem. 31, 653–667 (2006).
A.S. El-Tabl and S.A. El-Enein, J. Coord. Chem. 57, 281–294 (2004).
P.R. Chetana, B.S. Srinatha, M.N. Somashekar, and R.S. Policegoudra, J. Mol. Struct. 1106, 352–365 (2016).
A.S. El-Tabl, F.A. El-Saied, and A.N. Al-Hakimi, Trans. Met. Chem. 32, 689–701 (2007).
K. Shanker, R. Rohini, K. Shravankumar, P.M. Reddy, Y.P. Ho, and V. Ravinder, J. Ind. Chem. Soc. 86, 153–161 (2009).
G. Ceyhan, M. Köse, V. McKee, S. Uruş, A. Gölcü, and M. Tümer, Spectrochim. Acta A 95, 382–398 (2012).
B. Gündüz, Polym. Adv. Technol. 27, 144–155 (2016).
B. Gündüz, Polym. Bull. 72, 3241–3267 (2015).
J. Tauc, A. Menth, and J. Noncryst, Solids 8–10, 569–585 (1972).
B. Gündüz, Opt. Mater. 36, 425–436 (2013).
S.K. Tripathy, Opt. Mater. 46, 240–246 (2015).
C. Orek, B. Gündüz, O. Kaygılı, and N. Bulut, Chem. Phys. Lett. 678, 130–138 (2017).
Acknowledgments
I want to thank Associate Prof. Bayram GÜNDÜZ for his help.
Author information
Authors and Affiliations
Corresponding author
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Electronic supplementary material
Below is the link to the electronic supplementary material.
Rights and permissions
About this article
Cite this article
Turan, N. Synthesis, Spectroscopy, Optical Characteristics and Parameters of Co(II), Pd(II) Complexes and Schiff Base Ligand. J. Electron. Mater. 48, 7366–7371 (2019). https://doi.org/10.1007/s11664-019-07562-3
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11664-019-07562-3