1D Copper(I) Coordination Polymer [Cu2(μ-L)(μ-I)2]n : Synthesis, Crystal Structure, Spectral and Thermal Study

Document Type : Research Paper

Authors

1 Department of Chemistry, Shahrood University of Technology, Shahrood, Iran

2 Department of Chemistry, Faculty of Science, Golestan University, Gorgan, Iran

3 Department of Chemistry, Payame Noor University, Mashhad, Iran

4 Institute of Physic of the Czech Academy of Sciences, Na Slovance 2, 182 21 Prague, Czech Republic

Abstract

A new 1D copper(I) coordination polymer [Cu2(μ-L)(μ-I)2]n (1), where L is N,N'-bis(4-nitrobenzylidene)butane-1,4-diamine, was synthesized and characterized by CHN, FT-IR, 1H NMR, and single-crystal X-ray analyses. Based on X-ray results, this new compound crystallizes in a monoclinic system with space group P21/c. The asymmetric unit consists of one copper and one iodine atoms and half of the Schiff base ligand (L). The flexible Schiff base compound is coordinated to copper(I) ion as a bis-monodentate ligand. The coordination geometry around the copper(I) ions is distorted trigonal planar. The thermal behavior of 1 was studied using thermogravimetry analysis. Moreover, the nanoparticles of 1 were prepared via the ultrasonic-assisted method and characterized by XRD and SEM analyses.

Graphical Abstract

1D Copper(I) Coordination Polymer [Cu2(μ-L)(μ-I)2]n : Synthesis, Crystal Structure, Spectral and Thermal Study

Keywords


[1] S. Meghdadi, M. Amirnasr, E. Yavari, K. Mereiter,
M. Bagheri, Compt. Rend. Chim. 20 (2017) 730.
[2] N. Navon, H. Cohen, P. Paoletti, B. Valtancoli, A.
Bencini, D. Meyerstein, Ind. Eng. Chem. Res. 39
(2000) 3536.
[3] J.C. Castillo, N.F. Bravo, L.V. Tamayo, P.D. Mestizo,
J. Hurtado, M. Macias, J. Porttila, ACS Omega 5
(2020) 30148.
[4] D. Khalili, R. Evazi, A. Neshat, J. Aboonajmi, F.
Osanlou, Inorg. Chim. Acta 506 (2020) 119470.
[5] K. Ramakrishna C. Sivasankar, J. Org. Chem. 81
(2016) 6609.
[6] L. Meng, K.Y. Ngai, X. Chang, Z. Lin, J. Wang, Org.
Lett. 22 (2020) 1155.
[7] R. Yuan Z. Lin, ACS Catal. 4 (2014) 4466.
[8] A. N. Gupta, V. Singh, V. Kumar, L.B. Prasad, M.G.
B. Drew, N. Singh, Polyhedron 79 (2014) 324.
[9] X. Liu, Y. Shan, J. Xu, X. Zhang, S. Shang, X.L. Li,
Polyhedron 164 (2019) 152.
[10] J. Xiang, S.-C. Cheng, X.-X. Jin, Q.-Q. Su, X. Zhou,
W.-K. Chu, C.-F. Leung, C.-C. Ko, Dalt. Trans. 48
(2019) 741.
[11] A.P. Borges, Z.A. Carneiro, F.S. Ptado, J.R. Souza,
L.H. Furlan, Silva, C.G. Oliveira, V.M. Deflon, S.
Albuquerque, N.B. Leite, A.E.H. Machado, A.O.T.
Patrocinio, P.I.S. Maia, Polyhedron 155 (2018) 170.
[12] S. Chen, J. Gao, J. Chang, Y. Li, C. Huangfu, H.
Meng, Y. Wang, G. Xia, L. Feng, ACS Appl. Mater.
Interfaces 11 (2019) 17513.
[13] C. Li, W. Li, A.F. Henwood, D. Hall, D.B. Cordes,
A.M.Z. Slawin, V. Lemaur, T. Olivier, I.F.W. Samuel,
E. Zysman-Colman, Inorg. Chem. 59 (2020) 14772.
[14] A. Schinabeck, M.J. Leitl, H. Yersin, J. Phys. Chem.
Lett. 9 (2018) 2848.
[15] M.J. Leitl, F.R. Küchle, H.A. Mayer, L. Wesemann,
H. Yersin, J. Phys. Chem. A 117 (2013) 11823.
[16] D.M. Zink, D. Volz, T. Baumann, M. Mydlak, H.
Flugge, J. Friedrichs, M. Nieger, S. Brase, Chem.
Mater. 25 (2013) 4471.
[17] H. Ohara, A. Kobayashi, M. Kato, Dalt. Trans. 43
(2014) 17317.
[18] A.V. Artem’Ev, M.P. Davydova, A.S. Berezin, M.R.
Ryzhikov, D.G. Samsonenko, Inorg. Chem. 59 (2020)
10699.
[19] M. Morshedi, M. Amirnasr, A.M.Z. Slawin, J.D.
Woollins, A.D. Khalaji, Polyhedron 28 (2009) 167.
[20] S.M. Kuang, D.G. Cuttell, D.R. McMillin, P.E.
Fanwick, R.A. Walton, Inorg. Chem. 41 (2002) 3313.
[21] C.C. Chou, C.C. Su, A. Yeh, Inorg. Chem. 44 (2005)
6122.
[22] H.V.R. Dias, H.V.K. Diyabalanage, M.A.
Rawashdeh-Omary, M.A. Franzman, M.A. Omary, J.
Am. Chem. Soc. 125 (2003) 12072.
[23] H. Wang, M.X. Li, M. Shao, X. He, Polyhedron 26
(2007) 5171.
[24] E. Baladi, V. Nobakht, A. Tarassoli, D.M. Proserpio,
L. Carlucci, Cryst. Growth Des. 18 (2018) 7207.
[25] J. Troyano, E. Zapata, J. Perles, P. Amo-Ochoa, V.
Fernandezz-Moreira, J.I. Martinez, F. Zamora, SDelgado, Inorg. Chem. 58 (2019) 3290.
[26] A. Kobayashi, M. Fujii, Y. Shigeta, M. Yoshida, M.
Kato, Inorg. Chem. 58 (2019) 4456.
[27] A. Tarassoli, V. Nobakht, E. Baladi, L. Carlucci, D.
M. Proserpio, Cryst. Eng. Comm. 19 (2017) 6116.
[28] A. Beheshti, W. Clegg, V. Nobakht, R.W. Harrington,
Polyhedron 81 (2014) 256.
[29] A.D. Khalaji, S.J. Peyghoun, A. Akbari, N. Feizi, M.
Dusek, V. Eigner, Polyhedron 119 (2016) 429.
[30] Y. Li, Z.X. Zhang, T. Li, K.C. Li, Russ. J. Coord.
Chem. 36 (2010) 48.
[31] M. Morshedi, M. Amirnasr, S. Triki, A.D. Khalaji,
Inorg. Chim. Acta 362 (2009) 1637.
[32] A. Beheshti, V. Nobakht, L. Carlucci, D.M. Proserpio,
C. Abrahams, J. Mol. Struct. 1037 (2013) 236.
[33] A.D. Khalaji, S. Triki, D. Das, J. Therm. Anal.
Calorim. 103 (2011) 779.
[34] A.D. Khalaji, J. Rohlicek, P. Machek, D. Das, J.
Clust. Sci. 25 (2014) 1425.
[35] A.D. Khalaji, S.J. Peyghoun, A. Akbari, N. Feizi, M.
Dusek, V. Eigner, J. Mol. Struct. 1127 (2017) 511.
[36] A.D. Khalaji, S.J. Peyghoun, M. Dusek, V. Eigner, J.
Struct. Chem. 60 (2019) 1983.
[37] A.D. Khalaji S.J. Peyghoun, M. Dusek, M.
Kocerakova, V. Eigner, A. Akbari, N. Feizi, Maced.
J. Chem. Chem. Eng. 38 (2019) 207.
[38] A.D. Khalaji, K. Jafari, B. Bahramian, K. Fejfarova,
M. Dusek, Monats. Chem. 144 (2013) 1621.
[39] H. Naeimi, F.A.M. Malayeri, Z. Rashid, K. Rabiei,
Polycycl. Arom. Compd. 35 (2015) 457.
[40] C. Glidewell, J.N. Low, J.M.S. Skakle, J.L. Wardell,
Acta Crystallogr. Sect. C Cryst. Struct. Commun. 62
(2006) 2.
[41] L. Palatinus G. Chapuis, J. Appl. Crystallogr. 40
(2007) 786.
[42] V. Petrícek, M. Dušek, L. Palatinus, Z. Krist. 229
(2014) 345.
[43] A.D. Khalaji, M. Amirnasr, J.C. Daran, Acta
Crystallogr. Sect. E Struct. Rep. 62 (2006) 2200.
[44] K. Marjani, M. Mousavi, E. Ahmadi, D.L. Hughes,
Inorg. Chim. Acta 376 (2011) 408.
Volume 5, Issue 1
Spring and Summer
2021
Pages 10-18
  • Receive Date: 14 October 2020
  • Revise Date: 20 December 2020
  • Accept Date: 20 December 2020