Highly Thermostable One-Dimensional Lanthanide(III) Coordination Polymers Constructed from Benzimidazole-5,6-dicarboxylic Acid and 1,10-Phenanthroline: Synthesis, Structure, and Tunable White-Light Emission
Source abstract
Abstract
Three novel isostructural lanthanide(III) coordination polymers (LnCPs), {[Ln 3 (bidc) 4 (phen) 2 (NO 3 )]·2H 2 O} n (Ln = Gd ( 1 ), Eu ( 2 ), Tb ( 3 ); H 2 bidc = benzimidazole-5,6-dicarboxylic acid, and phen = 1,10-phenanthroline), were synthesized via hydrothermal reaction and characterized. The complexes crystallize in the chiral space group P 2 1 2 1 2 1 . They possess 1D structures based on lanthanide trinuclear clusters containing Ln(1)O 9, Ln(2)O 6 N 2, and Ln(3)O 6 N 2 polyhedra by bidc linkers, and phen and nitrate act as terminal ligands. The bidc and phen ligands provide efficient energy transfer for the sensitization of Eu(III) and Tb(III) complexes. The complexes 2 and 3 emit red and green light, respectively. Lifetimes and quantum yields of luminescence are 0.86 ms and 13.20% for 2 and 0.32 ms and 2.08% for 3 . Tuning of white-light emission by adjusting the doping concentration of Eu(III) and Tb(III) ions in the Gd(III) complex was achieved.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Lanthanide and Transition Metal Complexes · Magnetism in coordination complexes
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, Capital Normal University, Beijing 100048, People's Republic of China
Department of Chemistry, Beijing Normal University, Beijing 100875, People's Republic of China
References (62)
Show source-provided references
1. Schubert E. F. · Science · 2005 · 308 · 127410.1126/science.1108712 ↗
2. Feldmann C. · Adv. Funct. Mater. · 2003 · 13 · 51110.1002/adfm.200301005 ↗
3. Carlos L. D. · Chem. Soc. Rev. · 2011 · 40 · 53610.1039/C0CS00069H ↗
4. Bünzli J.-C. G. · Chem. Rev. · 2010 · 110 · 272910.1021/cr900362e ↗
5. DiMaio J. R. · Opt. Express · 2006 · 14 · 1141210.1364/OE.14.011412 ↗
6. Wang M.-S. · J. Am. Chem. Soc. · 2009 · 131 · 1357210.1021/ja903947b ↗
7. Liu J. · Adv. Mater. · 2008 · 20 · 135710.1002/adma.200701705 ↗
8. Coppo P. · Angew. Chem., Int. Ed. · 2005 · 44 · 180610.1002/anie.200461953 ↗
9. He J. · J. Am. Chem. Soc. · 2012 · 134 · 155310.1021/ja2073559 ↗
10. Shelton A. H. · Chem. Commun. · 2012 · 48 · 274910.1039/c2cc17182a ↗
11. Cui Y. J. · Chem. Rev. · 2012 · 112 · 112610.1021/cr200101d ↗
12. Liu K. · Cryst. Growth Des. · 2010 · 10 · 1610.1021/cg900990w ↗
13. Li S.-M. · Inorg. Chem. · 2012 · 51 · 120110.1021/ic201425v ↗
14. Rao X. T. · J. Mater. Chem · 2012 · 22 · 321010.1039/c2jm14127b ↗
15. Sava D. F. · J. Am. Chem. Soc. · 2012 · 314 · 398310.1021/ja211230p ↗
16. Guo N. · J. Phys. Chem. C · 2012 · 116 · 132910.1021/jp209891b ↗
17. Molla M. R. · Chem. Eur. J. · 2012 · 18 · 129010.1002/chem.201103600 ↗
18. Chung J. H. · J. Mater. Chem. · 2012 · 22 · 399710.1039/c2jm15332g ↗
19. Bünzli J.-C. G. · Chem. Rev. · 2010 · 110 · 272910.1021/cr900362e ↗
20. Allendorf M. D. · Chem. Soc. Rev. · 2009 · 38 · 133010.1039/b802352m ↗
21. Armelao L. · Coord. Chem. Rev. · 2010 · 254 · 48710.1016/j.ccr.2009.07.025 ↗
22. Coppo P. · Angew. Chem., Int. Ed. · 2005 · 44 · 180610.1002/anie.200461953 ↗
23. Xu H.-B. · Chem. Commun. · 2009 · 731810.1039/b912474h ↗
24. Chen F.-F. · Coord. Chem. Rev. · 2010 · 254 · 99110.1016/j.ccr.2009.12.028 ↗
25. Ma Y. · Coord. Chem. Rev. · 2010 · 254 · 97210.1016/j.ccr.2010.02.013 ↗
26. Rocha J. · Chem. Soc. Rev. · 2011 · 40 · 92610.1039/C0CS00130A ↗
27. Zhou J. · Chem. Soc. Rev. · 2012 · 41 · 132310.1039/C1CS15187H ↗
28. Soares-Santos P. C. R. · Inorg. Chem. · 2010 · 49 · 342810.1021/ic902522j ↗
29. Shyni R. · Inorg. Chem. · 2007 · 46 · 1102510.1021/ic701075u ↗
30. Viswanathan S. · Inorg. Chem. · 2006 · 45 · 1013810.1021/ic061272r ↗
31. Guo H. L. · Adv. Mater. · 2010 · 22 · 419010.1002/adma.201000844 ↗
32. Matthes P. R. · J. Mater. Chem. · 2012 · 22 · 1017910.1039/c2jm15571k ↗
33. Liu K. · J. Mater. Chem. · 2010 · 20 · 327210.1039/b927465k ↗
34. Dang S. · J. Mater. Chem. · 2012 · 22 · 886810.1039/c2jm30389b ↗
35. Wang Z.-X. · CrystEngComm · 2010 · 12 · 113910.1039/B910701K ↗
36. Sun Y.-G. · Dalton Trans. · 2010 · 39 · 1138310.1039/c0dt00579g ↗
37. Wei Y. Q. · CrystEngComm · 2009 · 11 · 105410.1039/b815464c ↗
38. Liu Y.-R. · CrystEngComm · 2009 · 11 · 271210.1039/b909772d ↗
39. Li Z.-Y. · Cryst. Growth Des. · 2010 · 10 · 274610.1021/cg100245a ↗
40. Wei Y. Q. · Cryst. Growth Des. · 2008 · 8 · 208710.1021/cg800333g ↗
41. Yao Y. L. · Cryst. Growth Des. · 2008 · 8 · 229910.1021/cg7010106 ↗
42. Gurunatha K. L. · Inorg. Chem. · 2008 · 47 · 657810.1021/ic8007377 ↗
43. Sun Y.-G. · Inorg. Chem. Commun. · 2010 · 13 · 47910.1016/j.inoche.2010.01.013 ↗
44. Zhou Z.-Y. · Inorg. Chem. Commun. · 2010 · 13 · 158010.1016/j.inoche.2010.09.019 ↗
45. Zhang L.-X. · Inorg. Chem. Commun. · 2010 · 13 · 91410.1016/j.inoche.2010.04.024 ↗
46. Smith T. · Trans Opt. Soc. · 1931 · 33 · 7310.1088/1475-4878/33/3/301 ↗
47. aSheldrick, G. M.SHELXTL, version 5.1; Bruker Analytical X-ray Instruments Inc.: Madison, WI, 1998.
48. bSheldrick, G. M.SHELX-97, PC Version; University of Göttingen: Göttingen, Germany, 1997.
49. Hu M. · Inorg. Chem. Commun. · 2007 · 10 · 117710.1016/j.inoche.2007.04.011 ↗
50. Gańdara F. · Inorg. Chem. · 2007 · 46 · 347510.1021/ic0617689 ↗
51. Weng D. F. · Eur. J. Inorg. Chem. · 2006 · 418410.1002/ejic.200600491 ↗
52. Zheng X.-J. · Inorg. Chem. · 2004 · 43 · 160010.1021/ic0352699 ↗
53. Wang R. Y. · Inorg. Chem. · 2001 · 40 · 274310.1021/ic001469y ↗
54. Ferrira R. A. S. · ChemPhysChem · 2006 · 7 · 221510.1002/cphc.200600317 ↗
55. Gustafsson M. · Chem. Mater. · 2010 · 22 · 331610.1021/cm100503q ↗
56. Xu J. · Cryst. Growth Des. · 2011 · 11 · 33710.1021/cg101343k ↗
57. Weng D. F. · Eur. J. Inorg. Chem. · 2006 · 418410.1002/ejic.200600491 ↗
58. Zhu Q. L. · Cryst. Growth Des. · 2009 · 9 · 512810.1021/cg900518s ↗
59. Zhang H. · Cryst. Growth Des. · 2012 · 12 · 67010.1021/cg2008655 ↗
60. Yang A.-H. · Cryst. Growth Des. · 2010 · 10 · 21810.1021/cg9008575 ↗
61. Lin Z.-J. · Inorg. Chem. · 2012 · 51 · 181310.1021/ic202082w ↗
62. Ma S. Q. · Inorg. Chem. · 2009 · 48 · 207210.1021/ic801948z ↗