Abstract
Calixarenes are cavity-shaped cyclic molecules made up of phenol units linked via alkylidene groups (meta-cyclophanes). In spite of their attractive architecture, studies of host—guest chemistry related to calixarenes have been very limited [1–3]. In fact, Gutsche stated in his 1985 review article that there are no published data in support of solution complexes of calixarenes [2]. This is in sharp contrast to cyclodextrins which can form a variety of host—guest-type solution complexes. We considered that this difference is related to solubility: the host—guest chemistry of cyclodextrins has been studied in aqueous systems where the hydrophobic force is broadly operative for the stabilization of the host—guest complexes, whereas the efforts to seek evidence for solution complexes of calixarenes have been made in organic solvents where the host molecule must compete with solvent molecules for the guest [1–3]. We thus concluded that in order to find evidence for solution complexes, the primary experimental effort should be directed towards solubilization of calixarenes in water: this was the starting point of our calixarene studies [4, 5]. We have synthesized anionic, cationic, and neutral water-soluble calixarenes and obtained unequivocal evidence for the formation of solution complexes in aqueous systems [4, 5]. In this article we review the past development of functionalized calixarenes and discuss how calixarenes can be used as catalysts, ligands, and host molecules and the essential characteristics of calixarenes in comparison to cyclodextrins and crown ethers.
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References
C.D. Gutsche: Acc. Chem. Res. 16, 161 (1983).
C.D. Gutsche: Top. Curr. Chem. 123, 1 (1984)
C.D. GutscheHost-Guest Complex Chemistry/Macrocycles, Springer-Verlag, Berlin (1985), p. 375.
L. J. Bauer and C D. Gutsche: J. Am. Chem. Soc. 107, 6063 (1985).
S. Shinkai: Pure Appl. Chem. 58, 1523 (1986).
S. Shinkai and O. Manabe: Nippon Kagaku Kaishi 1917 (1988).
S. Shinkai, S. Mori, T. Tsubaki, T. Sone, and O. Manabe: Tetrahedron Lett. 25, 5315 (1984).
S. Shinkai, S. Mori, H. Koreishi, T. Tsubaki, and O. Manabe: J. Am. Chem. Soc. 108, 2409 (1986).
T. Arimura, T. Nagasaki, S. Shinkai, and T. Matsuda: J. Org. Chem. 54, 3766 (1989).
S. Shinkai, H. Kawabata, T. Arimura, T. Matsuda, H. Satoh, and O. Manabe: J. Chem. Soc. Perkin Trans. 1 1073 (1989).
S. Shinkai, T. Arimura, K. Araki, H. Kawabata, H. Satoh, T. Tsubaki, O. Manabe, and J. Sunamoto: J. Chem. Soc. Perkin Trans. 1 2039 (1989).
S. Shinkai, Y. Shirahama, T. Tsukabi, and O. Manabe: J. Chem. Soc. Perkin Trans. 1859 (1989).
S. Shinkai, Y. Shirahama, T. Tsubaki, and O. Manabe: J. Am. Chem. Soc. 111, 5477 (1989).
S. Shinkai, H. Kawabata, T. Matsuda, H. Kawaguchi, and O. Manabe: Bull. Chem. Soc. Jpn. 63, 1272 (1990).
S. Shinkai, K. Araki, J. Shibata, and O. Manabe: J. Chem. Soc., Perkin Trans. 1 195 (1989).
S. Shinkai, K. Araki, J. Shibata, D. Tsugawa, and O. Manabe: Chem. Lett. 931 (1989).
C. D. Gutsche and L. J. Bauer: J. Am. Chem. Soc. 107, 6052 (1985).
C. D. Gutsche and L. J. Bauer: Tetrahedron Lett. 22, 4763 (1981).
G. Happel, B. Mathiasch, and H. Kämmerer: Makromol. Chem. 176, 3317 (1975).
K. Araki, S. Shinkai, and T. Matsuda: Chem. Lett. 581 (1989).
Similar studies have already been reported on the basis of 60 MHz 1H NMR spectra: H. Kämmerer, G. Happel, and B. Mathiasch. Makromol. Chem. 182, 1685 (1981); see also [18].
H. Goldmann, W. Vogt, E. Paulus, and V. Böhmer: J. Am. Chem. Soc. 110, 6811 (1988).
S. W. Keller, G. M. Schuster, and F. L. Tobiason: Polym. Mater. Sci. Eng. 57, 906 (1987).
V. Böhmer, E. Schade, and W. Vogt: Makromol. Chem., Rapid Commun. 5, 221 (1984).
S. Shinkai, K. Araki, H. Koreishi, T. Tsubaki, and O. Manabe: Chem. Lett. 1351 (1986).
K. Araki, H. Kawaguchi, O. Manabe, and S. Shinkai: to be submitted.
G. D. Andreetti, R. Ungaro, and A. Pochini: J. Chem. Soc., Chem. Commun. 1005 (1979).
M. Coruzzi, G. D. Andreetti, V. Bocchi, A. Pochini, and R. Ungaro: J. Chem. Soc. Perkin Trans. 2 1133 (1982).
R. Ungaro, A. Pochini, G. D. Andreetti, and P. Domiano: J. Chem. Soc. Perkin Trans. 2 197 (1985).
S. G. Bott, A. W. Coleman, and J. L. Atwood: J. Am. Chem. Soc. 108, 1709 (1986)
S. G. Bott, A. W. Coleman, and J. L. Atwood: J. Am. Chem. Soc. 110, 610 (1988).
M. A. McKervey, E. M. Seward, G. Ferguson, and B. L. Ruhl: J. Org. Chem. 51, 3581 (1986).
A. W. Coleman, S. Bott, and J. L. Atwood: J. Incl. Phenom. 4, 247 (1986).
A water-soluble calixarene (p-tert-butylcalix[4]arene tetracarboxylic acid) was also reported by the Italian group, but the water solubility is not high, especially, in the presence of salts: A. Arduini, S. Reverberi, and R. Ungaro: J. Chem. Soc., Chem. Commun. 981 (1984). More recently, Poh et al. synthesized a new water-soluble macrocycle by condensation of formaldehyde and 1,8-dihydroxynaphthalene-3,5-disulfonate: B.-L. Poh, C. S. Lim, and K. S. Khoo: Tetrahedron Lett. 30, 1005 (1989).
C. D. Gutsche and I. Alam: Tetrahedron 44, 4689 (1988).
F. M. Menger and C. E. Portnoy: J. Am. Chem. Soc. 90, 1875 (1968).
Y. Murakami, Y. Aoyama, and M. Kida: J. Chem. Soc. Perkin Trans. 2 1947 (1977).
F. M. Menger and U. V. Venkataram: J. Am. Chem. Soc. 108, 2980 (1986).
S. Shinkai, Y. Shirahama, T. Tsubaki, and O. Manabe: J. Am. Chem. Soc. 111, 5477 (1989).
S. Shinkai, Y. Shirahama, T. Tsubaki, and O. Manabe: J. Chem. Soc. Perkin Trans. 1 1859 (1989).
S. Shinkai, K. Araki, and O. Manabe: J. Am. Chem. Soc. 110, 7214 (1988).
S. Shinkai, K. Araki, T. Matsuda, and O. Manabe: Bull Chem. Soc. Jpn. 62, 3856 (1989).
T. Arimura, M. Kubota, K. Araki, S. Shinkai, and T. Matsuda: Tetrahedron Lett. 30, 2563 (1989).
R. Breslow: Acc. Chem. Res. 13, 170 (1980).
I. Tabushi: Acc. Chem. Res. 15, 66 (1982).
V. Böhmer, F. Marschollek, and L. Zetta: J. Org. Chem. 52, 3200 (1987).
H. Casabianca, J. Royer, A. Satrallah, A. Taty-C, and J. Vicens: Tetrahedron Lett. 28, 6595 (1987).
S. Shinkai, T. Arimura, H. Satoh, and O. Manabe: J. Chem. Soc., Chem. Commun. 1495 (1987).
T. Arimura, S. Edamitsu, S. Shinkai, O. Manabe, T. Muramatsu, and M. Tashiro: Chem. Lett. 2269 (1987).
S. Shinkai, T. Arimura, H. Kawabata, Y. Hirata, K. Fujio, O. Manabe, and T. Muramatsu: J. Org. Chem. in press.
R. Ungaro, A. Pochini, and G. D. Andreetti: J. Incl. Phenom. 2, 199 (1984).
A. Arduini, A. Pochini, S. Reverberi, R. Ungaro, G. D. Andreetti, and F. Ugozzoli: Tetrahedron 42, 2089 (1986).
S.-K. Chang and I. Cho: Chem. Lett. 474 (1984); S.-K. Chang and I. Cho: J. Chem. Soc. Perkin Trans. 1 211 (1986).
M. A. McKervey, E. M. Seward, G. Ferguson, B. Ruhl, and S. Harris: J. Chem. Soc., Chem. Commun. 388 (1985).
K. Kimura, M. Matsuo, and T. Shono: Chem. Lett. 615 (1988).
Y. Inoue, C. Fujiwara, K. Wada, A. Tai, and T. Hakushi: J. Chem. Soc., Chem. Commun. 393 (1987).
T. Arimura, M. Kubota, T. Matsuda, O. Manabe, and S. Shinkai: Bull. Chem. Soc. Jpn. 62, 1674 (1989).
G. W. Gokel and D. J. Cram: J. Chem. Soc., Chem. Commun. 482 (1973).
R. A. Bartsch, H. F. Haddock, and P. N. Juri: J. Am. Chem. Soc. 98, 6753 (1976).
H. Nakazumi, I. Szele, K. Yoshida, and H. Zollinger: Helv. Chim. Acta 66, 1721 (1983).
S. Shinkai, S. Edamitsu, T. Arimura, and O. Manabe: J. Chem. Soc., Chem. Commun. 1622 (1988).
S. Shinkai, T. Otsuka, K. Araki, and T. Matsuda: Bull Chem. Soc. Jpn. 62, 4055 (1989).
Calix[4]arenes with pyridine pendant groups were also reported by F. Bottino, L. Giunta, and S. Pappalardo: J. Org. Chem. 54, 5407 (1989).
M. A. Markowitz, R. Bielski, and S. L. Regen: J. Am. Chem. Soc. 110, 7545 (1988).
Y. Ishikawa, T. Kunitake, T. Matsuda, T. Otsuka, and S. Shinkai: J. Chem. Soc., Chem. Commun. 736 (1989).
A. H. Alberts and D. J. Cram: J. Am. Chem. Soc. 99, 3380 (1977).
I. Tabushi, Y. Kobuke, K. Ando, M. Kishimoto, and E. Ohara: J. Am. Chem. Soc. 102, 5948 (1980).
I. Tabushi, Y. Kobuke, and A. Yoshizawa: J. Am. Chem. Soc. 106, 2481 (1984).
S. Shinkai, H. Koreishi, K. Ueda, and O. Manabe: J. Chem. Soc., Chem. Commun. 233 (1986).
S. Shinkai, H. Koreishi, K. Ueda, T. Arimura, and O. Manabe: J. Am. Chem. Soc. 109, 6371 (1987).
T. Nagasaki, T. Arimura, and S. Shinkai: to be submitted.
S. Shinkai, Y. Shirahama, H. Satoh, and O. Manabe: J. Chem. Soc. Perkin Trans. 2 1167 (1989).
S. Shinkai, K. Kawano, K. Araki, and T. Matsuda: to be submitted.
A. Collet: Tetrahedron 43, 5725 (1987).
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Shinkai, S. (1991). Functionalized Calixarenes: New Applications as Catalysts, Ligands, and Host Molecules. In: Vicens, J., Böhmer, V. (eds) Calixarenes: A Versatile Class of Macrocyclic Compounds. Topics in Inclusion Science, vol 3. Springer, Dordrecht. https://doi.org/10.1007/978-94-009-2013-2_7
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DOI: https://doi.org/10.1007/978-94-009-2013-2_7
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