Water tape assembled in 1,10-bis(2-pyrazinylcarbonyl)-1,4,7,10- tetraazadecane via H-bonding and π-π stacking

Crystal Growth and Design

Volumn 7, Issue 4, 2007, Pages 595-597

  Shi, Xue Fang ^a,b   Zhang, Wen Qin ^a  

^a TIANJIN UNIVERSITY   (China)

^b TIANJIN NORMAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 34247478636     PISSN: 15287483     EISSN: None     Source Type: Journal    
DOI: 10.1021/cg0606390     Document Type: Article

References (34)

1. Saito, S. Acc. Chem. Res. 1999, 32, 741-749.
2. Ludwig, R. Angew. Chem., Int. Ed. 2001, 40, 1809-1827.
3. Cheruzel, L. E.: Pometun, M. S.; Cecil, M. R.; Mark S. M: Wittebort, R. J.; Buchanan, R. M. Angew. Chem., Int. Ed. 2003, 42, 5452-5455.
4. Cukierman, S. Biophys. J. 2000, 78, 1825-1834.
5. Lanyi, J. K. Biochim. Biophys. Acta 2000, 1460, 1-3.
6. Kandori, H. Biochim. Biophys. Acta 2000, 1460, 177-191.
7. Kandori, H.; Shichida, Y. J. Am. Chem. Soc. 2000, 122, 11745-11746.
8. Mishima, O.; Stanley H. E. Nature 1998, 396, 329-335.
9. Eisenberg, D.; Kauzmann, W. The Structure and Properties of Water; Oxford University Press: New York, 1969.
10. Lobban, C.; Finney, J. L.; Kuhs, W. F. Nature 1998, 391, 268-270.
11. Koza, M.; Schober. H.; Tölle, A.: Fujara, F. Nature 1999, 397, 660-661.
12. Raghuraman, K.; Katti, K. K.; Barbour, L. J.: Pillarsetty, N.; Barnes, C. L.; Katti, K. V. J. Am. Chem. Soc. 2003, 125, 6955-6961.
13. Zuhayra, M.; Kampen, W. U.; Henze, E.; Soti, Z.; Zsolnai, L.; Huttner, G.; Oberdorfer, F. J. Am. Chem. Soc. 2006, 128, 424-425.
14. Atwood, J. L.; Barbour, L. J.; Ness, T. J.; Raston, C. L.; Raston, P. L. J. Am. Chem. Soc. 2001, 123, 7192-7193.
15. Janiak, C.; Scharmann, T. G.; Mason, S. A. J. Am. Chem. Soc. 2002, 124, 14010-14011.
16. Pal, S.; Sankaran, N. B.; Samanta, A. Angew. Chem., Int. Ed. 2003, 42, 1741-1743.
17. Moorthy, J. N.; Natarajan, R.; Venugopalan, P. Angew. Chem., Int. Ed. 2002, 41, 3417-3420.
18. Custelcean, R.; Afloroaei, C.; Vlassa, M.; Polverejan, M. Angew. Chem., Int. Ed. 2000, 39, 3094-3096.
19. Ma, B.-Q.; Sun, H.-L.; Gao, S. Angew. Chem., Int. Ed. 2004, 43, 1374-1376.
20. Lakshminarayanan, P. S.; Suresh, E.; Ghosh P. J. Am. Chem. Soc. 2005, 127, 13132-13133.
21. Infantes, L.; Motherwell, S. CrystEngComm 2002, 4, 454-461.
22. Infantes, L.; Chisholm, J.; Motherwell, S. CrystEngComm 2003, 5, 480-486.
23. Mascal, M.; Infantes L.; Chisholm, J. Angew. Chem., Int. Ed. 2006, 45, 32-36.
24. Sherfinski, J. S.; Marsh, R. E.; Chwang, A. K.; Sundaralingam, M. Acta Crystallogr., Sect. B 1979, 35, 2141-2144.
25. Seela, F.; Wiglenda, T.; Rosemeyer, H.; Eickmeier, H.; Reuter, H. Angew. Chem., Int. Ed. 2002, 41, 603-605.
26. Nardin, G.; Randaccio, L.; Bonomo, R.P.; Rizzarelli, E. J. Chem. Soc., Dalton Trans. 1980, 369-375
27. Bonomo, R. P.; Rizzarelli, E.; Bresciani-Pahor, N.; Nardin, G. J. Chem. Soc., Dalton Trans. 1982, 681-685.
28. MacLeod, A. M.; Grimwood, S.; Barton, C.; Bristow, L.; Saywell, K. L.; Marshall, G.R.; Ball, R.G. J. Med. Chem. 1995, 38, 2239-2243.
29. Delbaere, L. T. J. Biochem. J. 1974, 143, 197-205.
30. Michaelides, A.; Skoulika, S.; Bakalbassis, E. G.; Mrozinski, J. Cryst. Growth Des. 2003, 3, 487-492.
31. Blake, A. J.; Consterdine, V.; Dove, M. F. A.; Lammas, S.; Thompson, L. H. J. Chem. Soc., Dalton Trans. 1998, 3-4.
32. Cook, W. J.; Bugg, C. E. J. Pharm. Sci. 1975, 64, 221-225.
33. w = 1:1) to give white crystals (yield 47%).
34. Crystal data: X-ray single-crystal diffraction data for the compound were collected on a Bruker Smart 1000 CCD area-detector diffractometer at 294(2) K with Mo Ko. radiation (λ = 0.71073 A) in the ω-Φ scan mode in the range of 1.07 < θ < 26.33°. The SAINT program (Bruker AXS, SAINT Software Reference Manual; Bruker: Madison, WI, 2000) was used for integration of the diffraction profiles. All the structures were solved by direct methods using the SHELXS program of the SHELXTL package and refined by full-matrix least-squares methods with SHELXL (semiempirical absorption corrections were applied using the SADABS program) (Sheldrick, G. M. SHELXTL NT Program for Solution and Refinement of Crystal Structures, version 5.1: University of Göttingen: Göttingen, Germany, 1997). The maximum and minimum transmission factors were 0.990 and 0.962, respectively. In all cases, non-hydrogen atoms are refined anisotropically. Whenever possible, the hydrogen atoms were located on a difference Fourier map.