Books
in black and white
Main menu
Share a book About us Home
Books
Biology Business Chemistry Computers Culture Economics Fiction Games Guide History Management Mathematical Medicine Mental Fitnes Physics Psychology Scince Sport Technics
Ads

The porphyrin handbook - Kadish K.M.

Kadish K.M. The porphyrin handbook - Academic press, 2000. - 368 p.
Download (direct link): kadishsmishgulilard2000.djvu
Previous << 1 .. 178 179 180 181 182 183 < 184 > 185 186 187 188 189 190 .. 240 >> Next

data from the Cambridge Crystallographic Database.
B. AZOLOPHANES
Very recently Alcalde and coworkers described the synthesis of a series
of [14]azolophanes via a "3 + ' convergent stepwise synthesis (Scheme
4).92-93
Single crystals of 34a were grown from 96% ethanol. The structure
reveals the very nonplanar nature of this particular heterocalixarene
analogue (Figure 31). It also established that a hydrogen-bonding array
(not shown) is formed between the macrocycle and four water molecules
(also omitted from Figure 31).9?
XI. Conclusion
The goal of this chapter has been to summarize the state-of-the-art
chemistry of calixpyrroles and other nitrogen-containing calixarene
analogues. If nothing else, this brief review should serve to make clear
that the substrate-binding properties of these macrocycles are both rich
and underexplored and that this class of receptors is endowed with a
seemingly limitless number of synthetic possibilities. On this basis, we
predict that the calixpyrroles will continue to emerge as important
precursors to the generalized areas of polypyrrole and molecular
recognition chemistry.
Note Added in Proof
The discovery of new calixpyrrole chemistry continues apace. Since this
chapter was written, Eichen and coworkers have reported the synthesis of
a calix[6]pyrrole94 and Aida
45/Calixpyrroles: Novel Anion and Neutral Substrate Receptors
277
and coworkers have produced /V-substituted calix[4]pyrrole
derivatives.93

REFERENCES
1. Baeyer. A. Ber. Dtsch. Chem. Ges. 1886, 19, 2184.
2. Jacoby, L).; Floriani, C.; Chiesi-Villa. A.; Rizzoli, C.,/. Chem.
Soc., Chem. Commun. 1991, 220.
3. Jubb, J.; Jacoby, D.; Floriani, C.; Chiesi-Villa, A.; Rizzoli, C.
Inorg. Chem. 1992, 31, 1306.
4. Jubb, J.; Floriani, C.; Chiesi-Villa, A.; Rizzoli, C. J. Am. Chem.
Soc.
1992, 114, 6571.
5. Jacoby, D.; Floriani, C.: Chiesi-Villa, A.; Rizzoli, C. J. Am.
Chem. Soc. 1993, 115, 3595.
6. Jacoby, D.; Floriani, C.; Chiesi-Villa, A.; Rizzoli, C. J. Am.
Chem. Soc. 1993, 115, 7025.
7. Rosa, A.; Ricciardi, G.; Rosa, .; Sgamellotti, A.; Floriani, C.
J. Chem. Soc.. Dalton Trans. 1993, 3759.
8. Piarulli, U.; Floriani, C.; Chiesi-Villa, A.; Rizzoli. C. J. Chem.
Soc., Chem. Commun. 1994, 895.
9. DeAngelis, S.: Solari, E.; Floriani, C.; Chiesi-Villa, A.;
Rizzoli, C. J. Am. Chem. Soc. 1994, 116, 5691.
10. DeAngelis. S.; Solari, E.: Floriani, C.; Chiesi-Villa, A.:
Rizzoli, C. J. Am. Chem. Soc. 1994, 116. 5702.
11. Solari, E.: Musso, F.; Floriani, C.; Chiesi-Villa, A.; Rizzoli. C.
J. Chem. Soc., Dalton Trans. 1994, 2015.
12. DeAngelis, S.; Solari, E.; Floriani. C.; Chiesi-Villa, A.;
Rizzoli, C.
J. Chem. Soc., Dalton Trans. 1994, 2467.
13. Kretz, . .; Gallo, E.; Solari, E.; Floriani, C.; Chiesi-
Villa, A.;
Rizzoli, C. J. Am. Chem. Soc. 1994, 116, 10775.
14. Jacoby, D.; Isoz, S.; Floriani, C.; Chiesi-Villa, A.; Rizzoli, C.
J. Am. Chem. Soc. 1995. 117, 2805.
15. DeAngelis, S.; Solari, E.; Floriani. C.; Chiesi-Villa, A.;
Rizzoli, C.
Angew. Chem., Int. Ed. Engl. 1995, 34, 1092.
16. DeAngelis, S.; Solari, E.: Floriani, C.; Chiesi-Villa, A.;
Rizzoli, C.
Organometallics 1995, 14, 4505.
17. Jacoby. D.; Isoz, S.; Floriani, C.; Schenk, K.; Chiesi-Villa, A.;
Rizzoli, C. Organometallics 1995, 14. 4816.
18. Floriani, C. Chem. Commun. 1996, 1257.
19. Solari, G.; Solari, E.; Lemercier, G.; Floriani, C.; Chiesi-Villa,
A.; Rizzoli, C. Inorg. Chem. 1997, 36, 2691.
20. Solari, G.: Solari, E.; Floriani, C.; Chiesi-Villa, A.; Rizzoli,
C. Organometallics 1997, 16, 508.
21. Fan. E.; van Arman, S. A.; Kincaid, S.; Hamilton, A. D. Angew.
Chem. Int. Ed. Engl. 1993, 115, 369.
22. Kelley-Rowley, A. .; Lynch. V.M.; Anslyn, E. V../. Am. Chem. Soc.
1995. 117, 3438.
23. Bisson, A. P.; Lynch, V. .; Monahan. . . C.; Anslyn. E. V.
Angew. Chem. Int. Ed. Engl. 1997, 36, 2340.
24. Sessler, J. L.; Cyr, M. J.; Lynch, V.; McGhee. E.; lbers, J. A. J.
Am. Chem. Soc. 1990, 112, 2810.
25. Schmidtchen. F. P. Tetrahedron Lett. 1989, 30, 4493.
26. Metzger, A.; Anslyn, E. V. Angew. Chem. Int. Ed. Engl. 1998, 37,
649.
27. Sessler, J. L.; Burrell, A. K. Top. Curr. Chem. 1991, 161, 177.
28. Shionoya, .; Fumta, H.; Lynch, V.; Harriman, A.; Sessler, J. L.
J. Am. Chem. Soc. 1992. 114, 5714.
29. Sessler, J. L.; Weghorn. S. J.; Morishima, .; Rosingana, .;
Lynch, V.; Lee, V. J. Am. Chem. Soc. 1992. 114, 8306.
30. Sessler, J. L.; Mody, T. D.; Ford, D. A.; Lynch, V. Angew. Chem.,
Int. Ed. Engl. 1992, 31, 452.
31. Sessler, J. L.: Cyr, .; Furuta, H.; Krai, V.; Mody, .:
Previous << 1 .. 178 179 180 181 182 183 < 184 > 185 186 187 188 189 190 .. 240 >> Next