journal article·2007-06-01

Three Novel Cd(II) Metal−Organic Frameworks Constructed from Mixed Ligands of Dipyrido[3,2-d:2‘,3‘-f]quinoxaline and Benzene-dicarboxylate: From a 1-D Ribbon, 2-D Layered Network, to a 3-D Architecture

Xiu-Li Wang, Yan-Feng Bi, Hong-Yan Lin, Guo-Cheng Liu

Crystal Growth & Design· Volume 7· Issue 6
Publisher page

Abstract

The use of dipyrido[3,2- d:2‘,3‘- f ]quinoxaline ( Dpq ) combined with three structurally related benzene-dicarboxylic acid ligands [benzene-1,3-dicarboxylic acid (H 2 L 1 ), benzene-1,2-dicarboxylic acid (H 2 L 2 ), and biphenyl-4,4‘-dicarboxylic acid (H 2 L 3 )] has allowed the rational design of three novel Cd(II) coordination polymers, [Cd 3 ( Dpq ) 3 ( L 1 ) 3 ]·4.5H 2 O ( 1 ), [Cd( Dpq )( L 2 )(H 2 O)] ( 2 ), and [Cd 2 ( Dpq ) 2 ( L 3 ) 2 ]·1.5H 2 O ( 3 ), which were hydrothermally synthesized and structurally determined by X-ray analysis. Compound 1 features a 1-D ribbonlike structure, compound 2 shows novel 2-D four-connected networks, and compound 3 possesses an interesting 6-connected 2-fold interpenetrated 3-D α-Po-related architecture. The Dpq ligand takes a chelating coordination mode while the other two nitrogen atoms did not coordinate to the Cd(II) ions. In these complexes, the three benzene−dicarboxylate ligands are able to link Cd(II) ions in various coordination modes, giving rise to 1-, 2-, and 3-dimensional Cd complexes, respectively. In addition, complexes 1 − 3 exhibit blue/green emission in the solid state at room temperature.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Metal complexes synthesis and properties · Chemical Synthesis and Characterization

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Faculty of Chemistry and Chemical Engineering, Bohai University, Jinzhou 121000, P. R. China

References (52)

Show source-provided references
1. Eddaoudi M. · Science · 2002 · 295 · 46910.1126/science.1067208 ↗
2. Seo J. S. · Nature · 2000 · 404 · 98210.1038/35010088 ↗
3. Pan L. · Angew. Chem., Int. Ed. · 2003 · 42 · 54210.1002/anie.200390156 ↗
4. Chun H. · Angew. Chem., Int. Ed. · 2004 · 43 · 97110.1002/anie.200353139 ↗
5. Eddaoudi M. · Acc. Chem. Res. · 2001 · 34 · 31910.1021/ar000034b ↗
6. Moulton B. · Chem. Rev. · 2001 · 101 · 162910.1021/cr9900432 ↗
7. Evans O. R. · Acc. Chem. Res. · 2002 · 35 · 51110.1021/ar0001012 ↗
8. Yaghi O. M. · Nature · 2003 · 423 · 70510.1038/nature01650 ↗
9. James S. L. · Chem. Soc. Rev. · 2003 · 32 · 27610.1039/b200393g ↗
10. Rodíguez-Martín Y. · CrystEngComm · 2002 · 4 · 52210.1039/B202166H ↗
11. Go Y. B. · J. Inorg. Chem. · 2004 · 43 · 536010.1021/ic049341u ↗
12. Go Y. B. · J. Inorg. Chem. · 2005 · 44 · 826510.1021/ic050644d ↗
13. Ye B. H. · Coord. Chem. Rev. · 2005 · 249 · 54510.1016/j.ccr.2004.07.006 ↗
14. Hu T. L. · Cryst. Growth Des. · 2006 · 45 · 162
15. Wang X. L. · Chem. Commun. · 2005 · 478910.1039/b506398a ↗
16. Sun D. F. · J. Chem. Soc., Dalton Trans. · 2001 · 233510.1039/b102888j ↗
17. Wan Y. H. · Inorg. Chem. · 2003 · 42 · 498510.1021/ic034258c ↗
18. Wan Y. H. · J. Mol. Struct. · 2003 · 658 · 25310.1016/S0022-2860(03)00498-8 ↗
19. Liu G. F. · New J. Chem. · 2002 · 26 · 79110.1039/b109869a ↗
20. Ye B. H. · Cryst. Growth Des. · 2005 · 5 · 80110.1021/cg049742k ↗
21. Bunz U. H. F. · Chem. Rev. · 2000 · 100 · 160510.1021/cr990257j ↗
22. Seward C. · Angew. Chem., Int. Ed. · 2004 · 43 · 293310.1002/anie.200353126 ↗
23. Wu S. Z. · J. Am. Chem. Soc. · 2005 · 127 · 204810.1021/ja045356f ↗
24. Han Z. B. · Cryst. Growth Des. · 2005 · 5 · 69510.1021/cg049834+ ↗
25. Wang X. L. · J. Mol. Struct. · 2006 · 798 · 3410.1016/j.molstruc.2006.03.057 ↗
26. Collins J. G. · Inorg. Chem. · 1998 · 37 · 313310.1021/ic971194v ↗
27. Sheldrick G. M. · 1997
28. Sheldrick G. M. · 1997
29. Shi X. · Cryst. Growth Des. · 2005 · 5 · 20710.1021/cg049932v ↗
30. Shi X. · Cryst. Growth Des. · 2005 · 5 · 34110.1021/cg049884e ↗
31. Shi X. · Eur. J. Inorg. Chem. · 2004 · 18510.1002/ejic.200300390 ↗
32. Wu J. · Chem. Eur. J. · 2006 · 12 · 582310.1002/chem.200500905 ↗
33. Wei Y. L. · Cryst. Growth Des. · 2005 · 5 · 140510.1021/cg049596i ↗
34. Meng X. R. · J. Organomet. Chem. · 2004 · 689 · 121810.1016/j.jorganchem.2004.01.015 ↗
35. Chen W. · Inorg. Chem. Commun. · 2003 · 42 · 94410.1021/ic025871j ↗
36. Guo X. D. · Inorg. Chem. · 2005 · 44 · 385010.1021/ic0500457 ↗
37. Thirumurugan A. · Dalton Trans. · 2004 · 292310.1039/b408403a ↗
38. Ouyang X. M. · J. Chem. Soc., Dalton Trans. · 2003 · 183610.1039/b300479a ↗
39. Tao J. · Chem. Commun. · 2000 · 204310.1039/b005753n ↗
40. Tian Y. P. · New. J. Chem. · 2002 · 26 · 146810.1039/b203334h ↗
41. Photochemistry · 1987
42. Zhang X. M. · Eur. J. Inorg. Chem. · 2003 · 13810.1002/ejic.200390014 ↗
43. Zhang L. Y. · Eur. J. Inorg. Chem. · 2003 · 296510.1002/ejic.200300061 ↗
44. Guo X. D. · Inorg. Chem. · 2006 · 45 · 258110.1021/ic0518881 ↗
45. Guo X. D. · Inorg. Chem. · 2006 · 45 · 406510.1021/ic060116h ↗
46. Ciurtin D. M. · Chem. Mater. · 2001 · 13 · 274310.1021/cm0103545 ↗
47. Cariati E. · Chem. Mater. · 2000 · 12 · 338510.1021/cm0010708 ↗
48. Würthner F. · Chem. Commun. · 2000 · 44510.1039/a909892e ↗
49. Wu S. Z. · J. Am. Chem. Soc. · 2005 · 127 · 204810.1021/ja045356f ↗
50. Yuan R. X. · Inorg. Chem. Commun. · 2001 · 4 · 38410.1016/S1387-7003(01)00221-0 ↗
51. Fu Z. Y. · Eur. J. Inorg. Chem. · 2002 · 2730
52. Yaghi O. M. · J. Am. Chem. Soc. · 1995 · 117 · 1040110.1021/ja00146a033 ↗