Luong Xuan Dien, Nguyen Xuan Truong, Ngo Duc Quan, Ken-ichi Yamashita, Kenichi Sugiura

Main Article Content

Abstract

Abstract: The 1(Ni) and Ni(II) complex was synthesized based on the reaction between
N,O-bidentate ligand 2-((methylimino)methyl) pyrene-1-ol (1) and nickel acetate in a mixed solvent of toluene, ethanol and NaOAc. The characters of the complex, such as elemental analysis (EA), IR, NMR, MS spectroscopy and single crystal X-ray diffraction, were investigated. With respect to the nickel atom, 1(Ni) complex adopts a distorted square planar trans-coordination geometry. Concerning the ligand arrangement, 1(Ni) complex has a step configuration with an angle of 35.5o between the mean planes of the pyrene rings in the two independent molecules and step distance S = 1.93 Å, whereas the referent nickel(II) bis(salicylaldiminato) takes a much smaller step configuration with an angle of 17.6o and step distance S = 0.845 Å (Chart 1). 


Keywords: Coordination chemistry, Nickel, Pyrene, expanded ligand, salicylaldimine.


References
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Keywords: Coordination chemistry, Nickel, Pyrene, π-Expanded ligand, Salicylaldimine

References

References
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[2] H. Makio, N. Kashiwa, T. Fujita, Adv. Synth. Catal. 344 (2002) 477.
[3] V. C. Gibson, S. K. Spitzmesser, Chem. Rev. 103 (2003) 283.
[4] T. Matsugi, T. Fujita, Chem. Soc. Rev. 37 (2008) 1264.
[5] D. A. Bansleben, S. K. Freiedrich, T. R. Younkin, R. H. Grubbs, C. Wnag, R.T. Li (1998) WO98/03165.
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[7] T. R. Younkin, E. F. Connor, J. I. Henderson, S. K. Friedrich, R. H. Grubbs, D. A. Bansleben, Science, 287 (2000) 460.
[8] E. F. Connor, T. R. Younkin, J. I. Henderson, A. W. Waltman, R. H. Grubbs, Chem. Commun. (2003) 2272.
[9] W. H. Sun, H. Yang, Z. Li, Y. Li, Organometallics 22 (2003) 3678.
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[11] C. Carlini, M. Martinelli, A. M. R. Galletti, G. Sbrana, J. Polym. Sci. A 44 (2006) 1514.
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[16] Y. Chen, S. Mandal, A. Sen, Organometallics 29 (2010) 3160.
[17] M. Kang, A. Sen, Organometallics 24 (2005) 3508.
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[22] F. Y. Pong, S. Mandal, A. Sen, Organometallics 33 (2014) 7044.
[23] Y. Murata, H. Ohgi, T. Fujihara, J. Terao, Y. Tsuji, Inorg. Chim. Acta 368 (2011) 237.
[24] T. Wiedemann, G. Voit, A. Tchernook, P. Roesle, I. Goettker-Schnetmann, S. Mecking, J. Am. Chem. Soc. 136 (2014) 2078.
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[35] L. Sacconi, M. Ciampolini, J. Chem. Soc. (1964) 276.
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[37] L. Sacconi, M. Ciampolini, J. Am. Chem. Soc. 85 (1963) 1750.
[38] L. Sacconi, J. Chem. Soc. (1963) 4608.
[39] A. Chakravorty, R. H. Holm, Inorg. Chem. (1964) 3(7).
[40] S. Hara, H. Houjou, I. Yoshikawa, K. Araki, Cryst. Growth Des. 11 (2011) 5113.