Crystal engineering or crystal mysticism? A case study

CrystEngComm

Volumn 7, Issue , 2005, Pages 458-461

  Miller, Joel S ^a  

^a UNIVERSITY OF UTAH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 25844474408     PISSN: 14668033     EISSN: None     Source Type: Journal    
DOI: 10.1039/b507527k     Document Type: Article

References (17)

1. "The methyl, ethyl, butyl, futile syndrome," refers to "... restricting their studies to very simple organic systems lacking any serious functionality..." see for example, L. S. Hegedus, Angew. Chem. Int. Ed., 1988, 27, 1113;
2. P. Laszlo, HYLE - Int. J. Phil. Chem., 2001, 7, 125.
3. e.g. D. Braga, L. Brammer and M. R. Chamness, CrystEngComm, 2005, 7, 1;
4. D. Braga, G. R. Desiraju, J. S. Miller, A. G. Orpen and S. Price, CrystEngComm, 2002, 4, 500;
5. D. Braga, L. Maini, M. Polito and F. Grepioni, in Strength from Weakness: Structural Consequences of Weak Interactions in Molecules, Supermolecules, and Crystals, ed. A. Domenicano and I. Hargittai, Kluwer Academic Publishers, 2002, pp. 335-353;
6. D. Braga, Dalton Trans., 2000, 3705;
7. A. Nangia and G. R. Desiraju, in NATO ARW Supramolecular Engineering of Synthetic Metallic Materials: Conductors and Magnets, ed. J. Veciana, C. Rovira and D. Amabilino, 1999, C518, 1;
8. M. D. Hollingsworth, Science, 2002, 295, 2410;
9. P. Erk, H. Hengelsberg, M. F. Haddow and R. van Gelder, CrystEngComm, 2004, 6, 474.
10. O. M. Yaghi, M. O'Keeffe, M. W. Ockwig, H. K. Chae, M. Eddaoudi and J. Kim, Nature, 2003, 423, 705.
11. T. E. Vos, Y. Liao, W. W. Shum, J-H. Her, P. W. Stephens, W. M. Reiff and J. S. Miller, J. Am. Chem. Soc., 2002, 124, 9336.
12. Fooled perhaps is more appropriate.
13. T. F. Nagy, S. D. Mahanti and J. L. Dye, Zeolites, 1997, 19, 57.
14. D. Yoshioka, M. Mikuriya and M. Handa, Chem. Lett., 2002, 31, 1044.
15. T. E. Vos and J. S. Miller, Angew. Chem. Int. Ed., 2005, 44, 2416;
16. T. E. Vos and J. S. Miller, Angew. Chem., 2005, 117, 2468.
17. "There's ethyl and propyl, but butyl is futile." referring to "...4-position homologues of mescaline..." (i.e. Buscaline) are pharmacologically less active. http://leda.lycaeum.org/?ID=9436.