Synthesis and Crystal Structure of a Cadmium(II) Complex with 2-(4΄-Chlorine-Benzoyl)-Benzoic Acid and 1,10-Phenanthroline

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A new metal-organic complex Cd2(cbba)4(phen)2 (Hcbba = 2-(4΄-chlorine-benzoyl)- benzoic acid, phen = 1,10-phenanthroline) 1 has been hydrothermally synthesized and structurally characterized by elemental analysis, IR, fluorescence spectrum and single-crystal X-ray diffraction. The compound crystallizes in orthorhombic, space group Pbcn with a = 12.0976(4), b = 18.0925(6), c = 31.6829(10) Å, V = 6934.6(4) Å3, C80H48Cd2Cl4N4O12, Mr = 1623.82, Dc = 1.555 g/cm3, μ(MoKα) = 0.8365 mm1, F(000) = 3264, Z = 4, the final R = 0.0396 and wR = 0.0960 for 5372 observed reflections (I > 2(I)). It exhibits a 3D supramolecular network through π-π interactions and shows green luminescent property at room temperature.

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313-316

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September 2011

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© 2011 Trans Tech Publications Ltd. All Rights Reserved

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[1] J. M. Lehn, Supramolecular Chemistry, Concepts and Perspectives. VCH, New York 1995.

Google Scholar

[2] J. W. Steed, J. L. Atwood, Supramolecular Chemistry, Wiley and Sons, New York, 2000.

Google Scholar

[3] B. J. Holliday, C. A. Mirkin, Angew. Chem., Int. Ed. 40(2001) 2022-2043.

Google Scholar

[4] B. Moulton, M. J. Zaworotko, Chem. Rev. 101(2001) 1629-1658.

Google Scholar

[5] S. Leininger, B. Olenyuk, P. J. Stang, Chem. Rev. 100(2000) 853-908.

Google Scholar

[6] P. J. Hagrman, D. Hagrman, J. Zubieta,Angew. Chem., Int. Ed. 38(1999) 2638-2684.

DOI: 10.1002/(sici)1521-3773(19990917)38:18<2638::aid-anie2638>3.0.co;2-4

Google Scholar

[7] Q. W. Wang, X. M. Li, Q. L. Meng, B. Liu, G.. G. Gao, Chinese J. Struct. Chem. 28(2009), 335-337.

Google Scholar

[8] X. M. Li, Q. W. Wang, B. Liu, Z. T. Wang, Chinese J. Inorg. Chem. 26(2010) 1904-1907.

Google Scholar

[9] X. M. Li, Q. W. Wang, Z. T. Wang, B. Liu, Chinese J. Struct. Chem. 30(2011) 176-179.

Google Scholar

[10] G. M. Sheldrick, SHELXS 97, Program for the Solution of Crystal Structure, University of Göttingen, Germany 1997.

Google Scholar

[11] G. M. Sheldrick, SHELXS 97, Program for the Refinement of Crystal Structure, University of Göttingen, Germany 1997.

Google Scholar

[12] M. Devereux, D. O. Shea, A. Kellett, M. McCann, M. Walsh, D. Egan, C. Deegan, K. Kedziora, G. Rosair, H. J. Müller-Bunz, Inorg. Biochem. 101(2007) 881-892.

DOI: 10.1016/j.jinorgbio.2007.02.002

Google Scholar

[13] L. J. Farrugia, X. A. Wing, Windows Program for Crystal Structure Analysis, University of Glasgow, Glasgow, UK 1988.

Google Scholar

[14] D. Rendell, Fluorescence and Phosphorescence, John Willey & Sons, New York, 1987.

Google Scholar

[15] S. L. Zheng, X. M. Chen, Aust. J. Chem. 57(2004) 703-712. Table 1. Selected Bond Lengths (Å) and Bond Angles (°) Bond Dist. Bond Dist. Bond Dist. Cd(1)–O(1) 2.424(3) Cd(1)–O(2) 2.341(3) Cd(1)–N(1) 2.334(3) Cd(1)–O(4A) 2.224(2) Cd(1)–O(5) 2.257(2) Cd(1)–N(2) 2.372(3) Angle (°) Angle (°) Angle (°) O(4A)–Cd(1)–O(5) 107.20(10) N(1)–Cd(1)–O(2) 159.15(11) O(4A)–Cd(1)–O(1) 146.83(9) O(4A)–Cd(1)–N(1) 88.60(10) O(4A)–Cd(1)–N(2) 91.08(10) O(5)–Cd(1)–O(1) 81.79(9) O(5)–Cd(1)–N(1) 84.26(9) O(5)–Cd(1)–N(2) 148.85(10) N(1)–Cd(1)–O(1) 124.41(10) O(4A)–Cd(1)–O(2) 93.57(10) N(1)–Cd(1)–N(2) 70.90(10) O(2)–Cd(1)–O(1) 54.69(9) O(5)–Cd(1)–O(2) 114.68(11) O(2)–Cd(1)–N(2) 88.31(11) N(2)–Cd(1)–O(1) 96.70(10) Symmetry transformations used to generate the equivalent atoms: A: –x+1, –y, –z+1 Fig. 1. Molecular structure of the title coordination polymer Fig. 2. 3-D Supramolecular network viewed along the c axis in 1 Fig. 3. Solid-state emission spectrum of 1 at room temperature

Google Scholar