An unusual 3D coordination polymer based on bridging interactions of the nucleobase adenine

Inorganic Chemistry

Volumn 43, Issue 15, 2004, Pages 4549-4551

  García Terán, Juan P ^a   Castillo, Oscar ^a   Luque, Antonio ^a   García Couceiro, Urko ^a   Román, Pascual ^a   Lezama, Luis ^a  

^a UNIVERSITY OF THE BASQUE COUNTRY UPV EHU   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

ADENINE DERIVATIVE; ANION; COPPER DERIVATIVE; LIGAND; NUCLEIC ACID BASE; OXALIC ACID; POLYMER; WATER;

ARTICLE; CHEMICAL STRUCTURE; COVALENT BOND; CRYSTAL STRUCTURE; CRYSTALLIZATION; MAGNETISM; MOLECULAR INTERACTION; MOLECULAR SIZE; NANOTUBE; REACTION ANALYSIS; STRUCTURE ANALYSIS; SYNTHESIS; X RAY ANALYSIS;

ADENINE; COPPER; CRYSTALLOGRAPHY, X-RAY; LIGANDS; MODELS, CHEMICAL; MOLECULAR CONFORMATION; ORGANOMETALLIC COMPOUNDS; POLYMERS; THERMODYNAMICS;

EID: 3242801445     PISSN: 00201669     EISSN: None     Source Type: Journal    
DOI: 10.1021/ic049512v     Document Type: Article

References (37)

1. (a) Moulton, B.; Zaworotko, M. J. Chem. Rev. 2001, 101, 1629.
2. (b) James, S. L. Chem. Soc. Rev. 2003, 32, 276.
3. Janiak, C. J. Chem. Soc., Dalton Trans. 2003, 2781.
4. Braga, D.; Desiraju, G. R.; Miller, J. S.; Orpen, A. G.; Price, S. L. CrystEng Comm 2002, 4, 500.
5. Beobide, G.; Castillo, O.; Luque, A.; García-Couceiro, U.; García-Terán, J. P.; Román, P.; Lezama, L. Inorg. Chem. Commun. 2003, 6, 1224.
6. (a) Beatty, A. M. CrystEng Comm 2001, 51, 1.
7. (b) Roesky, H. W.; Andruh, M. Coord. Chem. Rev. 2003, 236, 91.
8. Allen, F. H. Acta Crystallogr. 2002, B58, 380.
9. Abdus, M.; Aoki, K. Inorg. Chim. Acta 2000, 311, 15.
10. Lippert, B. Coord. Chem. Rev. 2000, 200-202, 487.
11. Berners-Price, S. J.; Sadler, P. J. Coord. Chem. Rev. 1996, 151, 1.
12. (a) Price, C.; Shipman, A.; Rees, N. H.; Elsegood, M. R. J.; Edwards, A. J.; Clegg, W.; Houlton, A. Chem. Eur. J. 2001, 7, 1194.
13. (b) Price, C.; Horrocks, B. R.; Mayeux, A.; Elsegood, M. R. J.; Clegg, W.; Houlton, A. Angew. Chem., Int. Ed. 2002, 41, 1047.
14. (a) Sheldrick, W. S. Acta Crystallogr. 1981, B37, 945.
15. (b) Sletten, E.; Sletten, J.; Froystein, N. A. Acta Chem. Scand. 1988, A42, 413.
16. Vestues, P. I.; Sletten, E. Inorg. Chim. Acta 1981, 52, 269.
17. 26: C, 22.33; H, 4.06; N, 21.70; Cu, 19.69. Found: C, 22.16; H, 4.00; N, 21.45; Cu, 19.33%.
18. -3.
19. de Meester, P.; Skapski, A. C. J. Chem. Soc. 1971, A13, 2167.
20. Terzis, A.; Beauchamp, A. L.; Rivest, R. Inorg. Chem. 1973, 12, 1166.
21. Sletten, E. Acta Crystallogr. 1969, B25, 1480.
22. (a) Hubert, J.; Beauchamp, A. L. Can. J. Chem. 1980, 58, 1439.
23. (b) Hubert, J.; Beauchamp, A. L. Acta Crystallogr. 1980, B36, 2613.
24. (c) Charland, J. P.; Britten, J. F.; Beauchamp, A. L. Inorg. Chim. Acta 1986, 124, 161.
25. (a) Zhu, F. C.; Schmalle, H. W.; Fischer, B.; Dubler, E. Inorg. Chem. 1998, 37, 1161.
26. (b) Chifotides, H. T.; Katsaros, N.; Pneumatikakis, G. J. Inorg. Biochem. 1994, 56, 249.
27. (c) Chifotides, H. T.; Dunbar, K. R.; Katsaros, N.; Pneumatikakis, G. J. Inorg. Biochem. 1994, 55, 203.
28. (a) Korn, S.; Sheldrick, W. S. Inorg. Chim. Acta 1997, 254, 85.
29. (b) Annen, P.; Schildberg, S.; Sheldrick, W. S. Inorg. Chim. Acta 2000, 307, 115.
30. (c) Fish, R. H.; Jaouen, G. Organometallics 2003, 22, 2166.
31. Rojas-González, P. X.; Castiñeiras, A.; González- Pérez, J. M.; Choquesillo-Lazarte, D.; Niclós-Gutiérrez, J. Inorg. Chem. 2002, 41, 6190.
32. Spek, A. L. PLATON, A Multipurpose Crystallographic Tool; Utrecht University: Utrecht, Holland, 1998.
33. -3) spreading out around the crystallographic 3-fold screw axis at the center of the voids. No satisfactory model for the disorder could be found, and for further refinements, the contribution of the missing solvent molecules was subtracted from the reflection data by the SQUEEZE method (Van der Sluis, P.; Spek, A. L. Acta Crystallogr. 1990, A46, 194) as implanted in PLATON. The final R1 [I > 2σ(I)] and wR2 values before SQUEEZE were 0.1148 and 0.2211, respectively. An accurate determination of the stoichiometric quantity of solvent was obtained from the TGA/DTA curves (see Supporting Information).
34. Curran, R. T.; Villa, J. F. Proc. 16th Int. Conf. Coord. Chem. 1974, 2.2Ia, 3.
35. Hanson, M. V.; Smith, C. B.; Simpson, G. D.; Carlisle, G. O. Inorg. Nucl. Chem. Lett. 1975, 11, 225.
36. Salam, M. A.; Aoki, K. Inorg. Chim. Acta 2001, 314, 71.
37. Bleaney, B.; Bowers, K. D. Proc. R. Soc. London, Ser. A 1952, 214, 451.