journal article·2007-01-01

Syntheses, Structures, and Physical Properties of Three Novel Metal−Organic Frameworks Constructed from Aromatic Polycarboxylate Acids and Flexible Imidazole-Based Synthons

Lili Wen, Zhenda Lu, Jianguo Lin, Zhengfang Tian, Huizhen Zhu, Qingjin Meng

Crystal Growth & Design· Volume 7· Issue 1
Publisher page

Abstract

Three novel interesting coordination polymers, [Cd 3 (SIP) 2 (bbi) 5 ·3H 2 O] n ( 1 ), [Co 3 (SIP) 2 (bix) 4 (2H 2 O)·2H 2 O] n ( 2 ), and [Cd(2,5-pydc) 2 (bix) 1.5 ·H 2 O] n ( 3 ) (SIP = 5-sulfoisophthalic acid monosodium salt; bbi = 1,1‘-(1,4-butanediyl)bis(imidazole); bix = 1,4-bis(imidazol-1-ylmethyl)-benzene; 2,5-pydc = pyridine-2,5-dicarboxylic acid), have been isolated under hydrothermal conditions and structurally characterized. Polymer 1 has a 3D complicated framework comprised of an infinite 1D ladder-like chain and 2D layer structure. Polymer 2 features a 3D hydrated framework with uncoordinated water molecules trapped in the pores. Polymer 3 is a 2D infinite layer framework, which is further interconnected by hydrogen-bond interactions to lead to a 3D supramolecular architecture. Compounds 1 and 3 exhibit medium-strong fluorescent emissions in the solid state at room temperature and could be significant in the field of photoactive materials.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Magnetism in coordination complexes · Chemical Synthesis and Characterization

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

Affiliations

Coordination Chemistry Institute, State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093, P.R. China

References (45)

Show source-provided references
1. Khlobystov A. N. · Coord. Chem. Rev. · 2001 · 222 · 15510.1016/S0010-8545(01)00370-8 ↗
2. Inoue K. · Angew. Chem., Int. Ed. · 2001 · 40 · 424210.1002/1521-3773(20011119)40:22<4242::AID-ANIE4242>3.0.CO;2-H ↗
3. Perry J. J. · J. Chem. Commun. · 2004 · 253410.1039/B408973A ↗
4. Batten S. R. · Coord. Chem. Rev. · 2003 · 246 · 10310.1016/S0010-8545(03)00119-X ↗
5. Carlucci L. · Coord. Chem. Rev. · 2003 · 246 · 24710.1016/S0010-8545(03)00126-7 ↗
6. Masaoka S. · Angew. Chem., Int. Ed. · 2001 · 40 · 381710.1002/1521-3773(20011015)40:20<3817::AID-ANIE3817>3.0.CO;2-3 ↗
7. 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 ↗
8. Kitaura R. · Angew. Chem., Int. Ed. · 2002 · 41 · 13310.1002/1521-3773(20020104)41:1<133::AID-ANIE133>3.0.CO;2-R ↗
9. Kondo M. · Angew. Chem., Int. Ed. · 1999 · 38 · 14010.1002/(SICI)1521-3773(19990115)38:1/2<140::AID-ANIE140>3.0.CO;2-9 ↗
10. Shimizu G. K. H. · Chem. Commun. · 1999 · 46110.1039/a807991i ↗
11. Li H. · Nature · 1999 · 402 · 27610.1038/46248 ↗
12. Chui S. S. Y. · Science · 1999 · 283 · 114810.1126/science.283.5405.1148 ↗
13. Kim J. · J. Am. Chem. Soc. · 2001 · 123 · 823910.1021/ja010825o ↗
14. Rosi N. L. · Science · 2003 · 300 · 112710.1126/science.1083440 ↗
15. Wang Z. Q. · J. Angew. Chem., Int. Ed. · 2005 · 44 · 287710.1002/anie.200500156 ↗
16. Barthelet K. · Angew. Chem., Int. Ed. · 2002 · 41 · 28110.1002/1521-3773(20020118)41:2<281::AID-ANIE281>3.0.CO;2-Y ↗
17. Millange F. · Chem. Commun. · 2002 · 82210.1039/b201381a ↗
18. Dybtsev D. N. · Angew. Chem., Int. Ed. · 2004 · 43 · 503310.1002/anie.200460712 ↗
19. Wen L. L. · J. Inorg. Chem. · 2005 · 44 · 716110.1021/ic0509985 ↗
20. Wen L. L. · J. Cryst. Growth Des. · 2006 · 6 · 53010.1021/cg050458i ↗
21. Zang S. Q. · J. Inorg. Chem. · 2006 · 45 · 385510.1021/ic060286u ↗
22. Zang S. Q. · J. Inorg. Chem. · 2006 · 45 · 17410.1021/ic051502m ↗
23. Song J. L. · Inorg. Chem. · 2004 · 43 · 563010.1021/ic049376u ↗
24. Sun Z. M. · Inorg. Chem. · 2004 · 43 · 33610.1021/ic0343307 ↗
25. Qin C. · Inorg. Chem. · 2005 · 44 · 712210.1021/ic050906b ↗
26. Min D. · Inorg. Chim. Acta · 2001 · 324 · 29310.1016/S0020-1693(01)00621-1 ↗
27. Garcaí-Zarracino R. · Angew. Chem. Int. Ed. · 2004 · 43 · 150710.1002/anie.200352862 ↗
28. Humphrey S. M. · J. Am. Chem. Soc. · 2004 · 126 · 1323610.1021/ja046351l ↗
29. Liu Y. L. · J. Am. Chem. Soc. · 2005 · 127 · 726610.1021/ja051259q ↗
30. Wei Y. L. · Cryst. Growth Des. · 2005 · 5 · 140510.1021/cg049596i ↗
31. Hoskins B. F. · J. Am. Chem. Soc. · 1997 · 119 · 295210.1021/ja9642626 ↗
32. Ballester L. · J. Polyhedron · 1998 · 17 · 361310.1016/S0277-5387(98)00157-0 ↗
33. SAINT Software Reference Manual; Bruker AXS: Madison, WI, 1998.
34. Moulton B. · Chem. Rev. · 2001 · 101 · 162910.1021/cr9900432 ↗
35. Eddaoudi M. · Acc. Chem. Res. · 2001 · 34 · 31910.1021/ar000034b ↗
36. Batten S. R. · Angew. Chem., Int. Ed. · 1998 · 37 · 146110.1002/(SICI)1521-3773(19980619)37:11<1460::AID-ANIE1460>3.0.CO;2-Z ↗
37. Evans O. R. · Acc. Chem. Res. · 2002 · 35 · 51110.1021/ar0001012 ↗
38. Tao J. · J. Chem. Soc., Dalton Trans. · 2000 · 366910.1039/b005438k ↗
39. Fujita M. · Bull. Chem. Soc. Jpn. · 1998 · 71 · 179910.1246/bcsj.71.1799 ↗
40. Kulynych A. D. · CrystEngComm · 2002 · 4 · 10210.1039/b200503d ↗
41. Tao J. · Eur. J. Inorg. Chem. · 2004 · 12510.1002/ejic.200300355 ↗
42. Sun D. F. · Eur. J. Inorg. Chem. · 2003 · 9410.1002/ejic.200390018 ↗
43. Ye B. H. · Coord. Chem. Rev. · 2005 · 249 · 54510.1016/j.ccr.2004.07.006 ↗
44. Adamson A. W. · 1975
45. Photochemistry · 1987