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Synthesis, Characterization and DFT Studies of Some Co(II) and Cu(II) Complexes of 12-Membered Tetradentate [N4] Macrocyclic Schiff Base Derived from 9,10-Phenanthrenequinone
Asian Journal of Chemistry,
Vol. 31 No. 4 (2019): Vol 31 Issue 4
Abstract
The structures of some coordination compounds of cobalt(II) and copper(II) with macrocyclic Schiff bases obtained by the reaction of 9,10-phenanthrenequinone with diamines synthesized in 1:1 molar ratio(s) have been elucidated by various physico-chemical methods viz. elemental analysis, IR, UV-visible, mass, ESR. The surface morphology was determined by SEM analysis. Infrared spectra suggested that ligand was coordinated to the metal ion in a tetradentate manner through azomethine nitrogen atom by the change in its stretching frequency. ESR spectra of copper(II) complexes indicates the presence of unpaired electron in the dx2–y2 by calculating the g values. The optimized geometries which were calculated using the DFT/B3LYP method were compared with the molecular geometries obtained experimentally.
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References
M. del Carmen Fernández-Fernández, R. Bastida, A. Macías, L. Valencia and P. Pérez-Lourido, Polyhedron, 25, 783 (2006); https://doi.org/10.1016/j.poly.2005.07.045.
P.G. Edwards and F.E. Hahn, Dalton Transc., 40, 10278 (2011); https://doi.org/10.1039/C1DT10864F.
C. Jing and S.Y. Qiu, Transition Met. Chem., 32, 528 (2007); https://doi.org/10.1007/s11243-007-0210-x.
S. Brooker, Coord. Chem. Rev., 222, 33 (2001); https://doi.org/10.1016/S0010-8545(01)00300-9.
S. Chandra and S. Sharma, Transition Met. Chem., 32, 150 (2007); https://doi.org/10.1007/s11243-006-0117-y.
N.A. Rey, A. Neves, A.J. Bortoluzzi, C.T. Pich and H. Terenzi, Inorg. Chem., 46, 348 (2007); https://doi.org/10.1021/ic0613107.
A.J. Bradbury, S.F. Lincoln and K.P. Wainwright, New J. Chem., 32, 1500 (2008); https://doi.org/10.1039/b719183a.
A. Laviecambot, M. Cantuel, Y. Leydet, G. Jonusauskas, D. Bassani and N. McClenaghan, Coord. Chem. Rev., 252, 2572 (2008); https://doi.org/10.1016/j.ccr.2008.03.013.
K.C. Gupta and A.K. Sutar, Coord. Chem. Rev., 252, 1420 (2008); https://doi.org/10.1016/j.ccr.2007.09.005.
Y. He and C. Cai, Catal. Commun., 12, 678 (2011); https://doi.org/10.1016/j.catcom.2010.12.017.
R.H. Satpute, A.O. Dhokte, M.A. Sakhare and B.R. Arbad, Der Chem. Sinica, 6, 36 (2015).
H. Keypour, M. Mahmoudabadi, A. Shooshtari, L. Hosseinzadeh, F. Mohsenzadeh and R.W. Gable, Polyhedron, 127, 345 (2017); https://doi.org/10.1016/j.poly.2017.02.008.
C.M. da Silva, D.L. da Silva, L.V. Modolo, R.B. Alves, M.A. de Resende, C.V.B. Martins and A. de Fatima, J. Adv. Res., 2, 1 (2011); https://doi.org/10.1016/j.jare.2010.05.004.
V.E. Kuzmin, A.G. Artemenko, R.N. Lozytska, A.S. Fedtchouk, V.P. Lozitsky, E.N. Muratov and A.K. Mescheriakov, SAR QSAR Environ. Res., 16, 219 (2005); https://doi.org/10.1080/10659360500037206.
A.G. Bharathi Dileepan, T. Daniel Prakash, A. Ganesh Kumar, P. Shameela Rajam, V. Violet Dhayabaran and R. Rajaram, J. Photochem. Photobiol. B, 183, 191 (2018); https://doi.org/10.1016/j.jphotobiol.2018.04.029.
E.M. Zayed, M.A. Zayed, A.M. Fahim and F.A. El-Samahy, Appl. Organomet. Chem., 31, e3694 (2017); https://doi.org/10.1002/aoc.3694.
M. Shakir, Y. Azim, H.-T.-N. Chishti and S. Parveen, Spectrochim. Acta A Mol. Biomol. Spectrosc., 65, 490 (2006); https://doi.org/10.1016/j.saa.2005.11.029.
S. Roy, B. Sarkar, D. Bubrin, M. Niemeyer, S. Zalis, G.K. Lahiri and W. Kaim, J. Am. Chem. Soc., 130, 15230 (2008); https://doi.org/10.1021/ja804429v.
M. Kumar, A. Anjum, N. Jaiswal and R.K. Dubey, Asian J. Chem., 30, 1679 (2018); https://doi.org/10.14233/ajchem.2018.21363.
U. Kumar and S. Chandra, J. Indian Chem. Soc., 88, 853 (2011).
K. Singh, R. Thakur and V. Kumar, Beni- Suef University J. Basic Appl. Sci., 5, 21 (2016); https://doi.org/10.1016/j.bjbas.2016.02.001.
M. Shakir, Y. Azim, H.T.N. Chishti, N. Begum, P. Chingsubam and M.Y. Siddiqi, J. Braz. Chem. Soc., 17, 272 (2006); https://doi.org/10.1590/S0103-50532006000200009.
S. Akcha, S. Gómez-Ruiz, S. Kellou-Tairi, L. Lezama, F.B. Pérez and O. Benali-Baitich, Inorg. Chim. Acta, 482, 738 (2018); https://doi.org/10.1016/j.ica.2018.06.051.
M.Y. Nassar, H.M. Aly, M.E. Moustafa and E.A. Abdelrahman, J. Inorg. Organomet. Polym., 27, 1220 (2017); https://doi.org/10.1007/s10904-017-0569-x.
N.A.M. Barakat, M. El-Newehy, S.S. Al-Deyab and H.Y. Kim, Nanoscale Res. Lett., 9, 2 (2014); https://doi.org/10.1186/1556-276X-9-2.
J.A. Fernandes, O. Abosede and S. Galli, Powder Diffract., 33, 55 (2018); https://doi.org/10.1017/S0885715618000143.
K. Dhahagani, M.P. Kesavan, K. Gujuluva Gangatharan Vinoth, L. Ravi, G. Rajagopal and J. Rajesh, Mater. Sci. Eng. C, 90, 119 (2018); https://doi.org/10.1016/j.msec.2018.04.032.
G. Grivani, S.H. Baghan, M. Vakili, A.D. Khalaji, V. Tahmasebi, V. Eigner and M. Dusek, J. Mol. Struct., 1082, 91 (2015); https://doi.org/10.1016/j.molstruc.2014.10.058.
M. Enamullah, B.A. Joy and M.K. Islam, J. Mol. Struct., 1175, 56 (2019); https://doi.org/10.1016/j.molstruc.2018.07.068.
A.K. El-Sawaf, M.A. Azzam, A.M. Abdou and E.H. Anouar, Inorg. Chim. Acta, 483, 116 (2018); https://doi.org/10.1016/j.ica.2018.08.013.