Effect of Anions on the Self-Assembly of Cd(II)-Containing Coordination Polymers Based on a Novel Flexible Tetrakis(imidazole) Ligand
Source abstract
Abstract
Thirteen Cd(II)-containing coordination polymers based on the novel tetradentate ligand tetrakis(imidazol-1-ylmethyl)methane (L), namely, [Cd 2 (L) 2 (SO 4 ) 2 (H 2 O) 2 ]·4H 2 O ( 1 ), [Cd(L)(H 2 O) 2 ](NO 3 ) 2 ( 2 ), [Cd(L)(Br) 2 ]·H 2 O ( 3 ), [Cd(L) 0.5 (L 1 )] ( 4 ), [Cd 5 (L 2 ) 5 (H 2 O) 2 ]·6H 2 O ( 5 ), [CdL 3 (L) 0.5 ] ( 6 ), [CdL 4 (L) 0.5 (H 2 O)]·H 2 O ( 7 ), [Cd 2 (L 5 ) 2 (L)]·2H 2 O ( 8 ), [Cd 3 (L 6 ) 2 (L)]·4H 2 O ( 9 ), [Cd 3 (L 7 ) 2 (L)(H 2 O) 2 ]·2.5H 2 O ( 10 ), [Cd(HL 8 )(L)]·0.75H 2 O ( 11 ), [Cd 7 (L 9 ) 3 (μ 3 -OH) 2 (L) 2 ]·8H 2 O ( 12 ), [Cd 2 (L 10 )(L)(H 2 O) 2 ]·H 2 O ( 13 ), where H 2 L 1 = fumaric acid, H 2 L 2 = adipic acid, H 2 L 3 = 1,3-benzenedicarboxylic acid, H 2 L 4 = 1,4-benzenedicarboxylic acid, H 2 L 5 = 5-OH-1,3-benzenedicarboxylic acid, H 3 L 6 = 1,3,5-benzenetricarboxylic acid, H 3 L 7 = 1,2,3-benzenetricarboxylic acid, H 3 L 8 = 1,2,4-benzenetricarboxylic acid, H 4 L 9 = 1,2,4,5-benzenetetracarboxylic acid, and H 4 L 10 = 4,4′-oxidiphthalic acid, have been synthesized under hydrothermal conditions. Compound L·5H 2 O shows a novel three-dimensional (3D) (3,8)-connected supramolecular architecture with a unique (3·5 2 ) 2 (3 4 ·4 2 ·5 6 ·6 12 ·7 3 ·8) topology. Compounds 1 − 3 were isolated by the reactions of L with inorganic anions (SO 4 2−, NO 3 −, Br − ). Compound 1 displays a 4-connected PtS network. Compound 2 exhibits a 3D 4-connected zeolite ABW net, while compound 3 is a two-dimensional (2D) (4 4 )- sql net. Compounds 4 − 8 were isolated by the reactions of L with organic dicarboxylate ligands. 4 exhibits a 2-fold interpenetrating α-Po net, while 5 shows a noninterpenetrating 3D framework. 6 shows a 3D (6 5 ·8) CdSO 4 -type framework, whereas compound 7 has a different 3D framework with (4·6 2 ·7 2 ·8)(4 2 ·6 2 ·7·8) topology. 8 shows a 2D layer structure, which is further extended into a 3D supramolecular framework by the hydrogen bonds. Compounds 9 − 11 have been obtained by the reactions of L with organic tricarboxylate ligands. In 9, the Cd(II) atoms are bridged by L and L 6 ligands to form a 3D structure. In 10, the trinuclear Cd(II) clusters are linked by the L and L 7 ligands to generate a chiral 3D α-Po structure. In 11, the Cd(II) centers are connected by the L ligands and the partially deprotonated HL 8 ligand to yield a 2D layer structure. Compounds 12 and 13 were synthesized by the reactions of L with different organic tetracarboxylate ligands. In compound 12, the L 9 ligands link the Cd(II) centers to form a 3D Cd-L 9 framework, and the L ligands further stabilize the 3D structure. In compound 13, L 10 ligands coordinate to the Cd(II) atoms in tetradentate mode to generate a 2D layer, which is further linked by L ligands to form a 3D framework. The structural differences of compounds 1 − 13 indicate that the presence of the different anions play an important role in the resulting structures of the coordination polymers. The infrared spectra and luminescent properties were also investigated for the compounds.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Metal complexes synthesis and properties · Crystal structures of chemical compounds
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Lab of Polyoxometalate Science, Department of Chemistry, Northeast Normal University, Changchun 130024, People’s Republic of China
References (87)
Show source-provided references
1. Zang B. · J. Am. Chem. Soc. · 1997 · 119 · 275110.1021/ja9634583 ↗
2. Li J.-R. · Chem. Soc. Rev. · 2009 · 38 · 147710.1039/b802426j ↗
3. Chae H. K. · Nature · 2004 · 427 · 52310.1038/nature02311 ↗
4. Wang Z. · Chem. Rev. · 2009 · 109 · 32210.1021/cr800406u ↗
5. Seo J. S. · Nature · 2000 · 404 · 98210.1038/35010088 ↗
6. Hagrman P. J. · Angew. Chem., Int. Ed. · 1999 · 38 · 2639
7. Halder G. J. · Science · 2002 · 298 · 176210.1126/science.1075948 ↗
8. Kahn O. · Acc. Chem. Res. · 2000 · 33 · 64710.1021/ar9703138 ↗
9. Cramb D. T. · Nat. Mater. · 2008 · 7 · 22910.1038/nmat2101 ↗
10. Batten S. R. · Angew. Chem., Int. Ed. · 1998 · 37 · 146010.1002/(SICI)1521-3773(19980619)37:11<1460::AID-ANIE1460>3.0.CO;2-Z ↗
11. Ockwig N. W. · Acc. Chem. Res. · 2005 · 38 · 17610.1021/ar020022l ↗
12. Venkataraman D. · Chem. Mater. · 1996 · 8 · 203010.1021/cm950594i ↗
13. Hagrman P. J. · Angew. Chem., Int. Ed. · 1999 · 38 · 263810.1002/(SICI)1521-3773(19990917)38:18<2638::AID-ANIE2638>3.0.CO;2-4 ↗
14. Barnett S. A. · Coord. Chem. Rev. · 2003 · 246 · 14510.1016/S0010-8545(03)00121-8 ↗
15. Zaworotko M. J. · Chem.Commun. · 2000 · 1
16. Roesky H. W. · Coord. Chem. Rev. · 2003 · 236 · 9110.1016/S0010-8545(02)00218-7 ↗
17. Yang J. · Cryst. Growth Des. · 2008 · 8 · 438310.1021/cg701119g ↗
18. Zhao W. · New J. Chem. · 2004 · 28 · 114210.1039/B317043H ↗
19. Liu H.-K. · Chem. Commun. · 2000 · 59110.1039/b000259n ↗
20. Sun W.-Y. · Chem.−Eur. J · 2001 · 7 · 255710.1002/1521-3765(20010618)7:12<2557::AID-CHEM25570>3.0.CO;2-U ↗
21. Fan J. · Inorg. Chem. · 2005 · 44 · 699810.1021/ic050314t ↗
22. Hoskins B. F. · Angew. Chem., Int. Ed. · 1997 · 36 · 275210.1002/anie.199727521 ↗
23. Cui G.-H. · Cryst. Growth Des. · 2005 · 5 · 177510.1021/cg050039l ↗
24. Wu L. P. · Inorg. Chim. Acta · 1997 · 256 · 15510.1016/S0020-1693(96)05424-2 ↗
25. Ma J.-F. · Inorg. Chem. · 2003 · 42 · 753110.1021/ic034846q ↗
26. Wen L.-L. · Inorg. Chem. · 2005 · 44 · 716110.1021/ic0509985 ↗
27. Zhang W.-L. · Polyhedron · 2008 · 27 · 335110.1016/j.poly.2008.07.026 ↗
28. Zhang W.-L. · Cryst. Growth Des. · 2008 · 8 · 125010.1021/cg7008978 ↗
29. Liu Y.-Y. · Inorg. Chem. · 2007 · 46 · 302710.1021/ic061575l ↗
30. Qi Y. · Cryst. Growth Des. · 2008 · 8 · 60610.1021/cg700758c ↗
31. Qi Y. · Cryst. Growth Des. · 2008 · 8 · 165410.1021/cg7011217 ↗
32. Wei G.-H. · Dalton Trans. · 2008 · 308010.1039/b716657e ↗
33. Zhang L.-P. · CrystEngComm · 2008 · 10 · 1405
34. Li F.-F. · Inorg. Chem. · 2005 · 44 · 937410.1021/ic050984z ↗
35. Yang J. · Cryst. Growth Des. · 2009 · 9 · 189410.1021/cg801085d ↗
36. Yang J. · Inorg. Chem. · 2007 · 46 · 654210.1021/ic700613c ↗
37. Xu Z. · Adv. Mater. · 2001 · 13 · 639
38. Choi H. J. · J. Am. Chem. Soc. · 1998 · 120 · 1062210.1021/ja980504l ↗
39. Zheng S. L. · Inorg. Chem. · 2001 · 40 · 356210.1021/ic001237z ↗
40. Shostakovskii M. F. · Zh. Obshch. Khim. · 1965 · 35 · 804
41. Sheldrick G. M. · 1997
42. Sheldrick G. M. · 1997
43. Ludwing R. · Angew. Chem., Int. Ed. · 2001 · 40 · 180810.1002/1521-3773(20010518)40:10<1808::AID-ANIE1808>3.0.CO;2-1 ↗
44. Liu K. · Science · 1996 · 271 · 92910.1126/science.271.5251.929 ↗
45. Ye B.-H. · Inorg. Chem. · 2004 · 43 · 686610.1021/ic049232f ↗
46. Desiraju G. R. · Acc. Chem. Res. · 1996 · 29 · 44110.1021/ar950135n ↗
47. Custelcean R. · Angew. Chem., Int. Ed. · 2000 · 39 · 309410.1002/1521-3773(20000901)39:17<3094::AID-ANIE3094>3.0.CO;2-P ↗
48. Infantes L. · CrystEngComm · 2002 · 4 · 45410.1039/b204934a ↗
49. Infantes L. · CrystEngComm · 2003 · 5 · 48010.1039/b312846f ↗
50. Xu G.-J. · CrystEngComm · 2009 · 11 · 184210.1039/b904000e ↗
51. Choi S. B. · Cryst. Growth Des. · 2007 · 7 · 229010.1021/cg070640e ↗
52. Luo F. · Cryst. Growth Des. · 2008 · 8 · 200610.1021/cg8001898 ↗
53. Xie L. · Inorg. Chem. · 2007 · 46 · 778210.1021/ic062273m ↗
54. Dincă M. · J. Am. Chem. Soc. · 2006 · 128 · 1687610.1021/ja0656853 ↗
55. Ocwig N. W. · Acc. Chem. Res. · 2005 · 38 · 17610.1021/ar020022l ↗
56. Blatov V. A. · CrystEngComm · 2004 · 6 · 37710.1039/B409722J ↗
57. Lü X. Q. · Cryst. Growth Des. · 2006 · 6 · 191010.1021/cg060240b ↗
58. Robinson F. · Chem. Commun. · 1995 · 241310.1039/C39950002413 ↗
59. Withersby M. A. · Angew. Chem., Int. Ed. · 1997 · 36 · 232710.1002/anie.199723271 ↗
60. Green B. S. · Acc. Chem. Res. · 1979 · 12 · 19110.1021/ar50138a001 ↗
61. Koshima H. · Synth. Org. Chem. Jpn · 1998 · 56 · 26810.5059/yukigoseikyokaishi.56.268 ↗
62. Yi L. · Cryst. Growth Des. · 2005 · 5 · 121510.1021/cg049587+ ↗
63. Tian G. · Chem. Commun. · 2005 · 139610.1039/b417184e ↗
64. Wu Q. · Chem. Mater. · 2000 · 12 · 7910.1021/cm990372a ↗
65. McGarrah J. E. · Inorg. Chem. · 2001 · 40 · 451010.1021/ic015559u ↗
66. Santis G. D. · Angew. Chem., Int. Ed. · 1996 · 35 · 20210.1002/anie.199602021 ↗
67. Shi X. · Eur. J. Inorg. Chem. · 2004 · 18510.1002/ejic.200300390 ↗
68. Zhang X. M. · Eur. J. Inorg. Chem. · 2003 · 13810.1002/ejic.200390014 ↗
69. Tian G. · J. Mol. Struct. · 2006 · 787 · 4510.1016/j.molstruc.2005.10.036 ↗
70. Wen L. · Cryst. Growth Des. · 2006 · 6 · 53010.1021/cg050458i ↗
71. Wen L. · Cryst. Growth Des. · 2007 · 7 · 9310.1021/cg0604982 ↗
72. Lin J.-G. · CrystEngComm · 2007 · 9 · 91510.1039/b708389k ↗
73. Shi X. · Cryst. Growth Des. · 2005 · 5 · 20710.1021/cg049932v ↗
74. Shu M. · Cryst. Growth Des. · 2006 · 6 · 189010.1021/cg0602111 ↗
75. Mahata P. · Eur. J. Inorg. Chem. · 2005 · 215610.1002/ejic.200400937 ↗
76. Ikeda S. · J. Phys. Chem. · 1996 · 100 · 1052810.1021/jp960068u ↗
77. Chen W.-T. · Cryst. Growth Des. · 2006 · 6 · 228910.1021/cg060146v ↗
78. Chen W. · Inorg. Chem. · 2002 · 42 · 94410.1021/ic025871j ↗
79. Yang J. · Inorg. Chem. · 2006 · 45 · 285710.1021/ic051557o ↗
80. Thirumurugan A. · J. Chem. Soc., Dalton Trans. · 2004 · 292310.1039/b408403a ↗
81. Zheng X.-J. · New J. Chem. · 2005 · 29 · 79810.1039/b415337e ↗
82. Zhang X.-J. · Inorg. Chem. · 2004 · 43 · 160010.1021/ic0352699 ↗
83. Yang E.-C. · Cryst. Growth Des. · 2007 · 7 · 200910.1021/cg070356n ↗
84. Chen W. · Inorg. Chem. · 2003 · 42 · 94410.1021/ic025871j ↗
85. Ma J.-F. · Cryst. Growth Des. · 2005 · 5 · 80710.1021/cg049723a ↗
86. Fu Z. Y. · Eur. J. Inorg. Chem. · 2002 · 2730
87. Wen L.-L. · Inorg. Chem. · 2005 · 44 · 716110.1021/ic0509985 ↗