A porous coordination architecture assembled by silver triflate and 9,10-bis(3,5-dicyano-1-phenyl)anthracene and its gas adsorption profile

Tetrahedron Letters

Volumn 49, Issue 52, 2008, Pages 7361-7363

  Akimoto, Kazuhiko ^a,b   Kondo, Yoshihiko ^a   Endo, Ken ^a   Yamada, Manabu ^a   Aoyama, Yasuhiro ^c   Hamada, Fumio ^a  

^a AKITA UNIVERSITY   (Japan)

^b NISSAN CHEMICAL INDUSTRIES LTD   (Japan)

^c KYOTO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ACETONE; ANTHRACENE DERIVATIVE; BENZENE; POLYMER; SILVER DERIVATIVE;

ADSORPTION; ARTICLE; CRYSTAL STRUCTURE; GAS; MEASUREMENT; SAMPLE;

EID: 55549113141     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.10.044     Document Type: Article

References (25)

1. Wei K.-J., Ni J., Gao J., Liu Y., and Liu Q.-L. Eur. J. Inorg. Chem. (2007) 3868
2. Moussa J., and Amouri H. Angew. Chem., Int. Ed. 47 (2008) 1372
3. D'Souza F., El-Khouly M.E., Gadde S., Zandler M.E., McCarty A.L., Araki Y., and Ito O. Tetrahedron 62 (2006) 1967
4. Park Y.K., Choi S.B., Kim H., Kim K., Won B.-H., Choi K., Choi J.-S., Ahn W.-S., Won N., Kim S., Jung D.H., Choi S.-H., Kim G.-H., Cha S.-S., Jhon Y.H., Yang J.K., and Kim J. Angew. Chem., Int. Ed. 46 (2007) 8230
5. Zhang J.-J., Zhou H.-J., and Lachgar A. Angew. Chem., Int. Ed. 46 (2007) 4995
6. Dong Y.-B., Ma J.-P., Huang R.-Q., Smith M.D., and zur Loye H.-C. Inorg. Chem. 42 (2003) 294
7. Dong Y.-B., Cheng J.-Y., Huang R.-Q., Smith M.D., and zur Loye H.-C. Inorg. Chem. 42 (2003) 5699
8. Wei K.-J., Ni J., Gao J., Liu Y., and Liu Q.-L. Eur. J. Inorg. Chem. (2007) 3868
9. Hirsch K.A., Wilson S.R., and Moore J.S. Chem. Commun. (1998) 13
10. Raehm L., Mimassi L., Guyard-Duhayon C., and Amouri H. Inorg. Chem. 42 (2003) 5654
11. Moussa J., Guyard-Duhayon C., Boubekeur K., Amouri H., Yip S.-K., and Yam V.W.W. Cryst. Growth Des. 7 (2007) 962
12. Moussa J., Boubekeur K., and Amouri H. Eur. J. Inorg. Chem. (2005) 3808
13. Mimassi L., Guyard-Duhayon C., Raehm L., and Amouri H. Eur. J. Inorg. Chem. (2002) 2453
14. Kobayashi K., Endo K., Aoyama Y., and Masuda H. Tetrahedron Lett. 34 (1993) 7929
15. Kobayashi K., Koyanagi M., Endo K., Masuda H., and Aoyama Y. Chem. Eur. J. 4 (1998) 417
16. Endo K., Sawaki T., Koyanagi M., Kobayashi K., Masuda H., and Aoyama Y. J. Am. Chem. Soc. 117 (1995) 8341
17. Tanaka T., Endo K., and Aoyama Y. Chem. Lett. (2000) 1424
18. Sawaki T., and Aoyama Y. J. Am. Chem. Soc. 121 (1999) 4769
19. Tanaka T., Endo K., and Aoyama Y. Bull. Chem. Soc. Jpn. 74 (2001) 907
20. Endo K., Koike T., Sawaki T., Hayashida O., Masuda H., and Aoyama Y. J. Am. Chem. Soc. 119 (1997) 4117
21. Akimoto K., Suzuki H., Kondo Y., Endo K., Akiba U., Aoyama Y., and Hamada H. Tetrahedron 63 (2007) 6887
22. Ezuhara T., Endo K., and Aoyama Y. J. Am. Chem. Soc. 121 (1999) 3279
23. 3): δ 8.260 (s, 2H, phenyl-H), 7.825-7.833 (d, 4H, phenyl-H), 7.519 (m, 8H, antharcene-H).
24. -1 (-CN).
25. int = 0.059), 4950 observed reflections (I > 2.00σ (I)), 522 parameters, R = 0.0809, wR = 0.1623, refined against |F|, GOF = 1.6947. All crystallographic data of these crystals have been deposited at the Cambridge Crystallographic Data Center in CIF format CCDC No. 690241. Copies of the data can be obtained free of charge on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK (e-mail: deposit@ccdc.cam.ac.uk).