journal article·2013-06-05

Chiral Coordination Polymers with SHG-Active and Luminescence: An Unusual Homochiral 3D MOF Constructed from Achiral Components

Na Chen, Ming-Xing Li, Peng Yang, Xiang He, Min Shao, Shou-Rong Zhu

Crystal Growth & Design· Volume 13· Issue 6
Publisher page

Abstract

Six new coordination polymers, namely, [Cd(SO 4 )(4-abpt)(H 2 O)] n ·3 n H 2 O ( 1 ), [Cu 3 (CN) 3 (4-abpt) 2 ] n ( 2 ), [Cd(D-cam)(2-PyBIm)(H 2 O)] n ( 3 ), [Co(D-Hcam)(cptpy)] n ( 4 ), [Cd(D-cam)(btmb)] n ( 5 ), and [Cd 2 (D-cam)(L-cam)(btmbb)] n ( 6 ) (4-abpt = 4-amino-3,5-bis(4-pyridyl)-1,2,4-triazole, D-H 2 cam = d -camphoric acid, 2-PyBIm = 2-(2-pyridyl)benzimidazole, Hcptpy = 4′-(4-carboxyphenyl)-3,2′:6′,3″-terpyridine, btmb = 1,4-bis(1,2,4-triazol-1-ylmethyl)benzene, btmbb = 4,4′-bis(1,2,4-triazol-1-ylmethyl)-1,1′-biphenyl), have been synthesized under hydro(solvo)thermal conditions. Their structures were determined by single-crystal X-ray diffraction analysis and further characterized by elemental analysis, infrared spectra, powder X-ray diffraction, circular dichroism, and thermogravimetric analysis. Complex 1 features a 3D porous metal–organic framework, which is a rare example to obtain a homochiral compound from achiral components. Complex 2 exhibits a 2D polymeric network constructed from μ 2 -cyanide, μ 2 -4-abpt, and monodentate 4-abpt ligands. Complex 3 is a homochiral 1D helical chain polymer. Complex 4 displays a 1D ladder-like polymeric structure in which cptpy – is tetradentate and D-Hcam – acts as a side arm. Complex 5 displays a homochiral 2D network with (4,4) topology. Complex 6 shows a [Cd 2 (D-cam)(L-cam)] n (4,4)-connected network with a paddle-wheel Cd 2 (COO) 4 as node, which is further pillared by a btmbb spacer into a 3D metal–organic framework. d -Camphoric acid underwent racemization under hydrothermal conditions. Cd(II) complexes 1, 3, and 5 crystallize in chiral space groups, and their circular dichroism spectra exhibit obvious positive or negative Cotton effects. Moreover, 1, 3, and 5 are SHG-active, and the SHG efficiency, respectively, is 0.15, 0.4, and 0.4 times as much as that of KH 2 PO 4 . All the complexes exhibit relatively high thermal stability. 1, 3, 5, and 6 emit violet luminescence originating from ligand-centered emission.
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Research context

OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Magnetism in coordination complexes · X-ray Diffraction in Crystallography

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

Affiliations

Department of Chemistry, College of Sciences, Shanghai University, Shanghai 200444, People’s Republic of China

State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou 350002, People’s Republic of China

Laboratory for Microstructures, Shanghai University, Shanghai 200444, People’s Republic of China

References (65)

Show source-provided references
1. Long J. R. · Chem. Soc. Rev. · 2009 · 38 · 121310.1039/b903811f ↗
2. Rowsell J. L. C. · Science · 2005 · 309 · 135010.1126/science.1113247 ↗
3. Cook T. R. · Chem. Rev. · 2013 · 113 · 73410.1021/cr3002824 ↗
4. Férey G. · Chem. Soc. Rev. · 2008 · 37 · 19110.1039/B618320B ↗
5. Zaworotko M. J. · Cryst. Growth Des. · 2007 · 7 · 410.1021/cg0680172 ↗
6. Hong M. · Cryst. Growth Des. · 2006 · 7 · 1010.1021/cg068015h ↗
7. Morris R. E. · Angew. Chem., Int. Ed. · 2008 · 47 · 496610.1002/anie.200703934 ↗
8. Kitagawa S. · Angew. Chem., Int. Ed. · 2004 · 43 · 233410.1002/anie.200300610 ↗
9. Ockwig N. W. · Acc. Chem. Res. · 2005 · 38 · 17610.1021/ar020022l ↗
10. Robin A. Y. · Coord. Chem. Rev. · 2006 · 250 · 212710.1016/j.ccr.2006.02.013 ↗
11. Zhang J. P. · Chem. Rev. · 2012 · 112 · 100110.1021/cr200139g ↗
12. Zhao H. · Chem. Soc. Rev. · 2008 · 37 · 8410.1039/B616738C ↗
13. Wang C. · Chem. Rev. · 2012 · 112 · 108410.1021/cr200252n ↗
14. Zhang W. · Chem. Rev. · 2012 · 112 · 116310.1021/cr200174w ↗
15. Crassous J. · Chem. Soc. Rev. · 2009 · 38 · 83010.1039/b806203j ↗
16. Hang T. · Cryst. Growth Des. · 2009 · 9 · 202610.1021/cg800618v ↗
17. Jiang X. M. · J. Am. Chem. Soc. · 2011 · 133 · 341010.1021/ja107921a ↗
18. Lin W. · Angew. Chem., Int. Ed. · 2009 · 48 · 65010.1002/anie.200803387 ↗
19. Rieter W. J. · J. Am. Chem. Soc. · 2008 · 130 · 1158410.1021/ja803383k ↗
20. Wu P. · J. Am. Chem. Soc. · 2012 · 134 · 1499110.1021/ja305367j ↗
21. Kesanli B. · Coord. Chem. Rev. · 2003 · 246 · 30510.1016/j.cct.2003.08.004 ↗
22. Ma L. · Chem. Soc. Rev. · 2009 · 38 · 124810.1039/b807083k ↗
23. Tong X. L. · Chem. Commun. · 2010 · 46 · 854310.1039/c0cc03111a ↗
24. Zhang J. · J. Am. Chem. Soc. · 2008 · 130 · 1288210.1021/ja805272j ↗
25. Wu S. T. · Angew. Chem., Int. Ed. · 2007 · 46 · 847510.1002/anie.200703443 ↗
26. Zang S. · Inorg. Chem. · 2006 · 45 · 297210.1021/ic0520418 ↗
27. Li Y. W. · RSC Adv. · 2012 · 2 · 434810.1039/c2ra00046f ↗
28. Bradshaw D. · J. Am. Chem. Soc. · 2004 · 126 · 610610.1021/ja0316420 ↗
29. Kepert C. · J. Am. Chem. Soc. · 2000 · 122 · 515810.1021/ja993814s ↗
30. Zhang J. · J. Am. Chem. Soc. · 2007 · 129 · 1416810.1021/ja076532y ↗
31. Zhang J. · J. Am. Chem. Soc. · 2008 · 130 · 1724610.1021/ja8075692 ↗
32. Zhang J. · Angew. Chem., Int. Ed. · 2007 · 46 · 611510.1002/anie.200701374 ↗
33. Liang X. Q. · Cryst. Growth Des. · 2009 · 9 · 487210.1021/cg900676x ↗
34. Yang P. · J. Mater. Chem. · 2012 · 22 · 239810.1039/c2jm14961c ↗
35. Klingele M. · Coord. Chem. Rev. · 2003 · 241 · 11910.1016/S0010-8545(03)00049-3 ↗
36. Cheng L. · Inorg. Chem. · 2007 · 46 · 113510.1021/ic061303i ↗
37. Meng X. · Inorg. Chem. · 2004 · 43 · 352810.1021/ic0354670 ↗
38. Li N. · Polyhedron · 2013 · 49 · 20710.1016/j.poly.2012.10.005 ↗
39. Schiffmann R. · J. Med. Chem. · 2006 · 49 · 51110.1021/jm050476z ↗
40. Sheldrick G. M. · 2000
41. He X. · Eur. J. Inorg. Chem. · 2006 · 249110.1002/ejic.200500978 ↗
42. Liang S. W. · Inorg. Chem. Commun. · 2006 · 9 · 131210.1016/j.inoche.2006.08.012 ↗
43. Deacon G. B. · Coord. Chem. Rev. · 1980 · 33 · 22710.1016/S0010-8545(00)80455-5 ↗
44. Meng Z. S. · Dalton Trans. · 2009 · 1028410.1039/b914702k ↗
45. Dupouy G. · Inorg. Chem. · 2008 · 47 · 892110.1021/ic800955r ↗
46. Guo H. M. · Polyhedron · 2011 · 30 · 198210.1016/j.poly.2011.05.006 ↗
47. Xu Z. · Chem. Commun. · 2012 · 48 · 573610.1039/c2cc31590d ↗
48. Xu J. · CrystEngComm · 2011 · 13 · 399810.1039/c0ce00800a ↗
49. Li M. X. · Inorg. Chem. · 2008 · 47 · 448110.1021/ic701346x ↗
50. Chen X. M. · Chem.—Eur. J. · 2002 · 8 · 481110.1002/1521-3765(20021018)8:20<4811::AID-CHEM4811>3.0.CO;2-R ↗
51. Moulton B. · Chem. Rev. · 2001 · 101 · 162910.1021/cr9900432 ↗
52. Wang Y. T. · Dalton Trans. · 2005 · 42410.1039/b416412a ↗
53. Liang X. Q. · Cryst. Growth Des. · 2010 · 10 · 259610.1021/cg1000107 ↗
54. Luo F. · CrystEngComm · 2010 · 12 · 276910.1039/c000734j ↗
55. Zhang J. · Chem. Mater. · 2007 · 19 · 508310.1021/cm071689a ↗
56. Colacio E. · Inorg. Chem. · 2002 · 41 · 514110.1021/ic025743v ↗
57. Phillips D. L. · Coord. Chem. Rev. · 2005 · 249 · 147610.1016/j.ccr.2004.09.015 ↗
58. Li M. X. · Cryst. Growth Des. · 2009 · 9 · 462610.1021/cg900079p ↗
59. Kurtz S. K. · J. Appl. Phys. · 1968 · 39 · 379810.1063/1.1656857 ↗
60. Liang L. L. · Dalton Trans. · 2010 · 39 · 772310.1039/c0dt00255k ↗
61. Liu C. M. · CrystEngComm · 2008 · 10 · 167410.1039/b811524a ↗
62. Zheng Y. Q. · CrystEngComm · 2010 · 12 · 274010.1039/b927448k ↗
63. Wong K. L. · Angew. Chem., Int. Ed. · 2005 · 44 · 343610.1002/anie.200500031 ↗
64. Liang L. L. · Cryst. Growth Des. · 2010 · 10 · 130710.1021/cg901353e ↗
65. Wang L. · Inorg. Chem. · 2009 · 48 · 429510.1021/ic802445q ↗