Abstract
The different substituted group will have a substantial effect on the crystal structures of the resulting compounds. Tetrazole–carboxylate ligands are outstanding blocks for construction of novel coordination architectures. Three derivative ligands of tetrazole-2-acetic acid, H3-pytza, H4-pytza and H3tzpha, where H3-pytza = 5-(3-pyridyl)tetrazole-2-acetic acid, H4-pytza = 5-(4-pyridyl)tetrazole-2-acetic acid and H3tzpha = 1,3,5-tris(tetrazol-5-yl)benzene-N2,N2′,N2″-triacetic acid, have been chosen to be reacted with Mg(NO3)2·6H2O, resulting in the formation of three new compounds, [Mg(H2O)6](3-pytza)2·2H2O (1), [Mg(4-pytza)2(H2O)4] (2) and [Mg3(tzpha)2(H2O)12]·10H2O (3). These compounds were characterized by elemental analysis, IR spectroscopy and single-crystal X-ray diffraction. The X-ray diffraction reveals that compounds 1 and 2 are mononuclear structures, while compound 3 shows a one-dimensional chain. The structures of these compounds are controlled by not only the different 5-substituted group of the tetrazole-2-acetic acid, but also the complementary hydrogen bonds. Furthermore, the luminescence studies show that compounds 1–3 show stronger emission than the corresponding ligands.
Graphical Abstract
Three Mg(II) coordination compounds 5-substituted group derivative of tetrazole-2-acetic acid (H3-pytza, H4-pytza and H3tzpha) show different luminescence properties.
Similar content being viewed by others
References
G. Aromi, L.A. Barrios, O. Roubeau, P. Gamez, Coord. Chem. Rev. 255, 485–546 (2011)
M. Wriedt, A.A. Yakovenko, G.J. Halder, A.V. Prosvirin, K.R. MDunbar, H.C. Zhou, J. Am. Chem. Soc. 135, 4040–4050 (2013)
M. Wriedt, J.P. Sculley, A.A. Yakovenko, Y.G. Ma, G.J. Halder, P.B. Balbuena, H.C. Zhou, Angew. Chem. Int. Ed. 51, 9804–9808 (2012)
D.Y. Chen, J.H. Zou, W.X. Li, B. Xu, Q.Y. Li, G.W. Yang, J. Wang, Y.M. Ding, Y. Zhang, X.F. Shen, Inorg. Chem. Commun. 40, 35–38 (2014)
H.Y. Yang, L.K. Li, J. Wu, H.W. Hou, B. Xiao, Y.T. Fan, Chem. Eur. J. 15, 4049–4056 (2009)
M.F. Wu, Z.F. Liu, S.H. Wang, J. Chen, G. Xu, F.K. Zheng, G.C. Guo, J.S. Huang, CrystEngComm 13, 6386 (2011)
Q. Ye, Y.M. Song, W.X.G.K. Chen, D.W. Fu, P.W.H. Chan, J.S. Zhu, S.D. Huang, R.G. Xiong, J. Am. Chem. Soc. 128, 6554–6555 (2006)
D.W. Fu, J.Z. Ge, J. Dai, H.Y. Ye, Z.R. Qu, Inorg. Chem. Commun. 12, 994–997 (2009)
J.H. Zou, D.Y. Chen, G.W. Yang, Q.Y. Li, J. Yang, L. Shen, RSC Adv. 5, 27887–27890 (2015)
Q.Y. Li, H. Tian, X.Y. Li, J.H. Zou, G.D. Mei, L.J. Qiu, B. Wei, G.W. Yang, RSC Adv. 5, 43741–43749 (2015)
J.H. Zou, D.L. Zhu, F.F. Li, F.S. Li, H. Wu, Q.Y. Li, G.W. Yang, P. Zhang, Y.X. Miao, J. Xie, Z. Anorg, Allg. Chem. 640(11), 2226–2231 (2014)
G.W. Yang, F.F. Zhang, Q. Wu, M.J. Cao, Y. Bai, Q.Y. Li, B. Wei, J.H. Zou, RSC Adv. 5, 84439–84445 (2015)
L. Sun, L. Ma, J.B. Cai, L. Liang, H. Deng, CrystEngComm 14, 890 (2012)
A. Rodrıguez-Dieguez, A. Salinas-Castillo, A. Sironi, CrystEngComm 12, 876–1879 (2010)
M.F. Wu, M.S. Wang, S.P. Guo, Cryst. Growth Des. 11, 2 (2011)
J. Chen, S.H. Wang, Z.F. Liu, M.F. Wu, Y. Xiao, F.K. Zheng, G.C. Guo, J.S. Huang, N. J. Chem. 38, 269–276 (2014)
Y. Zhou, G.W. Yang, Q.Y. Li, K. Liu, G.Q. Gu, Y.S. Ma, R.X. Yuan, Inorg. Chim. Acta 362, 1723 (2009)
J.H. Zou, H.J. Cui, B. Xu, D.L. Zhu, Q.Y. Li, G.W. Yang, Y.C. Hua, Inorg. Chim. Acta 423, 430–434 (2014)
B.J. Wang, J.H. Zou, W.X. Li, Z. Wang, B. Xu, S. Li, Y.S. Zhai, D.L. Zhu, Q.Y. Li, G.W. Yang, J. Organomet. Chem. 749, 428–432 (2014)
Q.Y. Li, G.W. Yang, L. Shen, M.H. He, W. Shen, K. Gu, J.N. Jin, Z. Anorg. Allg. Chem. 638, 826–831 (2012)
J. Yang, Q.Y. Li, L. Shen, G.W. Yang, X.Y. Tang, C. Zhai, H.D. Ding, J.N. Jin, W. Shen, J Chem Crystallogr 41, 1483–1489 (2011)
C.C. Auriga, Rigaku corporation (Tokyo, Japan, 2005)
G.M. Sheldrick, SHELXS-97, Program for Solution of Crystal Structures (University of Gottingen, Gottingen, 1997)
J.H. Zou, H. Tian, Z. Wang, F.S. Li, F.F. Zhang, L.Y. Zhao, P. Zhang, D.L. Zhu, G.W. Yang, Q.Y. Li, Z. Anorg, Allg. Chem. 640(12–13), 2566–2570 (2014)
Acknowledgments
The authors acknowledge financial support from the Natural Science Foundation of Jiangsu Province (Grant No. BK2012210), the Natural Science Foundation of the Jiangsu Higher Education Institutions of China (Grant No. 10KJB430001) and the Opening Fund of Jiangsu Key Laboratory of Advanced Functional Materials (Grant No. 12KFJJ010).
Author information
Authors and Affiliations
Corresponding authors
Electronic supplementary material
Below is the link to the electronic supplementary material.
Rights and permissions
About this article
Cite this article
Wu, J., Bai, Y., Lu, Y.M. et al. Substituted group-directed magnesium(II) coordination compounds based on the derivatives of tetrazole-2-acetic acid. J IRAN CHEM SOC 13, 2155–2162 (2016). https://doi.org/10.1007/s13738-016-0933-8
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s13738-016-0933-8