journal article·2006-02-01

Polythreading of Infinite 1D Chains into Different Structural Motifs: Two Poly(pseudo-rotaxane) Architectures Constructed by Concomitant Coordinative and Hydrogen Bonds

Xin-Long Wang, Chao Qin, En-Bo Wang

Crystal Growth & Design· Volume 6· Issue 2
Publisher page

Abstract

Two new compounds, [Co(4,4‘-bipy)(H 2 O) 4 ]·(H 2 bptc)·2H 2 O ( 1 ) and [Ni(4,4‘-bipy)(H 2 O) 4 ]·0.5(btc)·H 2 O ( 2 ) (4,4‘-bipy = 4,4‘-bipyridine, H 4 bptc = 3,3‘,4,4‘-biphenyltetracarboxylate acid, H 4 btc = 1,2,4,5-benzenetetracarboxylate acid), have been synthesized under hydrothermal conditions and characterized by elemental analysis, IR, TG analysis, and single-crystal X-ray diffraction. X-ray structural analysis revealed that two different structural motifs (1D covalent zigzag chain and 1D hydrogen-bonded ladder for 1 and 1D linear chain and 2D hydrogen-bonded sheet for 2 ) can be found within their crystal structures, and most intriguingly, they coexist in such a way that 1D covalently bonded chains of composition [M(4,4‘-bipy)(H 2 O) 4 ] 2+ (M = Co or Ni) thread into the hydrogen-bonded 1D ladders or 2D sheets formed by uncoordinated carboxylate anions and lattice water molecules, giving rise to overall entangled architectures with unusual poly(pseudo-rotaxane)-type arrangements. Thermal stability of the two compounds was also studied in this paper.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Supramolecular Chemistry and Complexes · Metal-Organic Frameworks: Synthesis and Applications · Covalent Organic Framework Applications

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

Affiliations

Institute of Polyoxometalate Chemistry, Department of Chemistry, Northeast Normal University, Changchun 130024, P. R. China

References (49)

Show source-provided references
1. (a) Robson, R.; Abrahams, B. F.; Batten, S. R.; Gable, R. W.; Hoskins, B. F.; Liu, J.Supramolecular Architecture; American Chemical Society: Washington, DC, 1992; p 256.10.1021/bk-1992-0499.ch019 ↗
2. (b) Lehn, J. M.Supramolecular Chemstry: Concepts and Perspectives; VCH: Weinheim, Germany, 1995; Chapter 9.10.1002/3527607439 ↗
3. Batten S. R. · Angew. Chem., Int. Ed · 1998 · 37 · 149410.1002/(SICI)1521-3773(19980619)37:11<1460::AID-ANIE1460>3.0.CO;2-Z ↗
4. Hagrman P. J. · J. Angew. Chem., Int. Ed · 1999 · 38 · 2684
5. Steed J. W. · 2000
6. Subramanian S. · Coord. Chem. Rev · 1994 · 127 · 401
7. Fredericks J. R. · 1996 · 9
8. Holliday B. J. · Angew. Chem., Int. Ed · 2001 · 40 · 2043
9. Chen Z. N. · J. Chem. Soc., Dalton Trans · 1998 · 7 · 1136
10. Tong M. L. · New J. Chem · 2001 · 12 · 1485
11. Vujovic D. · J. Chem. Soc., Dalton Trans · 2003 · 4 · 637
12. Ghoshal D. · Cryst. Growth Des · 2003 · 3 · 1110.1021/cg025574p ↗
13. Yin P. · Chem. Mater · 2003 · 15 · 3236
14. Carlucci L. · J. Chem. Soc., Dalton Trans · 1997 · 1801 · 1803
15. Dong Y. B. · J. Chem. Soc., Dalton Trans · 2000 · 5 · 780
16. Wang Y. H. · Inorg. Chem · 2002 · 41 · 6357
17. Yang E. · Inorg. Chem · 2004 · 43 · 6527
18. Wang R. · Cryst. Growth Des · 2005 · 5 · 256
19. Wang X. L. · Chem. Commun · 2004 · 378 · 379
20. Sun D. F. · Chem. Commun · 2003 · 1528 · 1529
21. Shi Z. · Cryst. Grwoth Des · 2004 · 4 · 27
22. Maspoch D. · J. Chem. Commun · 2004 · 1164 · 1165
23. Samuel M. F. · J. Am. Chem. Soc · 2000 · 122 · 6294
24. Yan Y. · Cryst. Growth Des · 2005 · 5 · 827
25. Qin C. · Chem. Commun · 2004 · 1876 · 1877
26. Ghosh S. K. · Cryst. Growth Des · 2005 · 5 · 62910.1021/cg049838e ↗
27. Wu C. D. · Acta Crystallogr · 2002 · 58 · m198
28. Sun D. F. · Inorg. Chem · 2003 · 42 · 7518
29. Sheldrick G. M. · 1997
30. Sheldrick G. M. · 1997
31. Bellamy L. J. · 1958
32. Withersby M. A. · Angew. Chem., Int. Ed. Engl · 1997 · 36 · 232910.1002/anie.199723271 ↗
33. Carlucci L. · Chem.Eur. J · 1999 · 5 · 24310.1002/(SICI)1521-3765(19990104)5:1<237::AID-CHEM237>3.0.CO;2-T ↗
34. Ayyappa P. · Inorg. Chem · 2002 · 41 · 3330
35. Wang X. L. · Angew. Chem., Int. Ed · 2004 · 43 · 504010.1002/anie.200460382 ↗
36. Carlucci L. · Angew. Chem., Int. Ed · 2000 · 39 · 151010.1002/(SICI)1521-3773(20000417)39:8<1506::AID-ANIE1506>3.0.CO;2-U ↗
37. Hoskins B. F. · Angew. Chem., Int. Ed. Engl · 1997 · 36 · 275510.1002/anie.199727551 ↗
38. Ciurtin D. M. · Chem. Commun · 2002 · 74 · 75
39. Carlucci L. · Chem. Commun · 2004 · 380 · 381
40. Lu J. Y. · Chem. Commun · 2001 · 821 · 822
41. Li B. L. · Chem. Commun · 2005 · 2333 · 2335
42. Hagrman D. · J. Chem. Mater · 1998 · 10 · 2100
43. Sharma C. V. K. · Chem. Commun · 1999 · 83 · 84
44. Tong M. L. · Inorg. Chem · 2002 · 41 · 4848
45. Zaman M. B. · Chem. Commun · 2001 · 2256 · 2257
46. Biradha K. · Chem. Commun · 2002 · 1866 · 1867
47. Carlucci L. · Coord. Chem. Rev · 2003 · 246 · 28910.1016/S0010-8545(03)00126-7 ↗
48. Pan L. · J. Am. Chem. Soc · 2003 · 125 · 3067
49. Ren Y. P. · Angew. Chem., Int. Ed · 2003 · 42 · 53510.1002/anie.200390154 ↗