o-Di-(pyrrole-2-carboxamides)-phenylene: Pseudopolymorphs and anions recognition

Tetrahedron Letters

Volumn 45, Issue 36, 2004, Pages 6803-6806

  Yin, Zhenming ^a   Li, Zucheng ^a   Yu, Ao ^a   He, Jiaqi ^a   Cheng, Jin Pei ^a  

^a NANKAI UNIVERSITY   (China)

Author keywords

Anion recognition; o Di (pyrrole 2 carboxamides) phenylene; Pseudopolymorphs

Indexed keywords

AMIDE; PYRROLE DERIVATIVE;

ANALYTIC METHOD; ARTICLE; CATALYSIS; CATALYST; CHEMICAL STRUCTURE; HYDROGEN BOND; MOLECULAR RECOGNITION; PROTON NUCLEAR MAGNETIC RESONANCE; STOICHIOMETRY; STRUCTURE ANALYSIS; SYNTHESIS;

EID: 4344560211     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.06.137     Document Type: Article

References (26)

1. A. Nangia, and G.R. Desiraju Chem. Commun. 1999 605 606
2. J. Bernstein, R.J. Davey, and J.-O. Henck Angew. Chem., Int. Ed. 38 1999 3440 3461
3. C. Bilton, J.A.K. Howard, N.N.L. Madhavi, A. Nangia, G.R. Desiraju, F.H. Allen, and C.C. Wilson Chem. Commun. 1999 1675 1676
4. V.R. Pedireddi, and J. PrakashaReddy Tetrahedron Lett. 44 2003 6679 6681
5. N. Tanifuji, and K. Kobayashi CrystEngComm. 3 2001 1 3
6. S.B. Raj, P.T. Muthiah, U. Rychlewska, and B. Warzajtis CrystEngComm. 5 2003 48 53
7. C. Schmuck, and W. Wienand J. Am. Chem. Soc. 125 2003 452 459
8. C. Schmuck, and M. Heil Org. Lett. 3 2001 1253 1256
9. C. Schmuck Tetrahedron 57 2001 3063 3067
10. C. Schmuck J. Org. Chem. 65 2000 2432 2437
11. C. Schmuck Eur. J. Org. Chem. 1999 2397 2403
12. S. Camiolo, P.A. Gale, M.B. Hursthouse, M.E. Light, and A. Shi J. Chem. Commun. 2002 758 759
13. P.A. Gale, K. Navakhun, S. Camiolo, M.E. Light, and M.B. Hursthouse J. Am. Chem. Soc. 124 2002 11228 11229
14. H. Adams, C.A. Hunter, K.R. Lawson, J. Perkins, S.E. Spey, C.J. Urch, and J.M. Sanderson Chem. Eur. J. 7 2001 4863 4878
15. P.A. Gale, S. Camiolo, G.J. Tizzard, C.P. Chapman, M.E. Light, S.J. Coles, and M.B. Hursthouse J. Org. Chem. 66 2001 7849 7853
16. P.A. Gale, S. Camiolo, C.P. Chapman, M.E. Light, and M.B. Hursthouse Tetrahedron Lett. 42 2001 5095 5097;
17. S.J. Coles, G. Denuault, P.A. Gale, P.N. Horton, M.B. Hursthouse, M.E. Light, and C.N. Warriner Polyhedron 22 2003 699 709;
18. C. Schmuck, and J. Lex Eur. J. Org. Chem. 2001 1519 1523
19. 3OH: Calcd: C, 62.57; H, 5.56; N, 17.17. Found: C, 62.76; H, 5.36; N, 16.96
20. 2 = 0.1088, CCDC 205664
21. 2 = 0.1170, CCDC 220440
22. G. Blay, I. Fernandez, J.R. Pedro, R. Ruiz-Garcia, M.C. Munoz, J. Cano, and R. Carrasco Eur. J. Org. Chem. 2003 1627 1630
23. R 3 3 (12) hydrogen bond motif represent the 12 member hydrogen bond ring with three donors and three acceptors. is the 10 member hydrogen bond ring with two donors and two acceptors. R 2 2 (10) is the 10 member hydrogen bond ring with two donors and two acceptors. See: M.C. Etter Acc. Chem. Res. 23 1990 120 126
24. S. Camiolo, P.A. Gale, M.B. Hursthouse, and M.E. Light Org. Biomol. Chem. 1 2003 741 744
25. A.T. Dubis, and S.J. Grabowshi New. J. Chem. 26 2002 165 169
26. K.A. Connors Binding Constants: The Measurement of Molecular Complex Stability 1987 Wiley-VCH New York