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3
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0001382638
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Plenum, New York
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(a) M. Irie, in Organic Photochromic and Thermochromic Compounds, ed. J. C. Crano and R. J. Gugliemetti, Plenum, New York, 1999, vol. 1, p. 207;
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Organic Photochromic and Thermochromic Compounds
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Irie, M.1
Crano, J.C.2
Gugliemetti, R.J.3
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(b) M. Irie, Chem. Rev., 2000, 100, 1685;
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Irie, M.1
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ed. B. L. Feringa, Wiley-VCH, Weinheim, Germany
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(c) M. Irie, in Molecular Switches, ed. B. L. Feringa, Wiley-VCH, Weinheim, Germany, 2001, p. 37.
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Molecular Switches
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Irie, M.1
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0032853749
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(a) For an example where the acidity of a phenol -OH increases due to the creation of linear π-conjugation between the phenol and a pyridinium across a DTE backbone, see: S. H. Kawai, S. L. Gilat and J.-M. Lehn, Eur. J. Org. Chem., 1999, 2359;
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Eur. J. Org. Chem.
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Kawai, S.H.1
Gilat, S.L.2
Lehn, J.-M.3
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8
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1642568094
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(b) For an example where the coordination geometry around a copper(II) ion is photoregulated using the bis(pyridine) version of the DTE, see: K. Matsuda, K. Takayama and M. Irie, Inorg. Chem., 2004, 43, 482. Although this study demonstrates that there is a difference in the π-acceptor character of the pyridyl ligand in the two forms of the DTE, the authors only suggest it is due to variations in electronics in the pyridine of the closed form and do not attribute it to electronic communication between the free pyridine and the one that is electron poor owing to the coordination. In fact they later state that the distance between the two metal centres is too far for them to be effectively coupled.
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Inorg. Chem.
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Matsuda, K.1
Takayama, K.2
Irie, M.3
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(b) R. Cacciapaglia, S. Di Stefano and L. Mandolini, J. Am. Chem. Soc., 2003, 125, 2224;
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J. Am. Chem. Soc.
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Cacciapaglia, R.1
Di Stefano, S.2
Mandolini, L.3
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(c) F. Würthner and J. Rebek, Jr., Angew. Chem., Int. Ed. Engl., 1995, 34, 446;
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Angew. Chem., Int. Ed. Engl.
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Würthner, F.1
Rebek Jr., J.2
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16844368309
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For an example where DTE has been used to regulate reactivity based on geometric changes, see: D. Sud, T. B. Norsten and N. R. Branda, Angew. Chem., Int. Ed., 2005, 44, 2019.
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(2005)
Angew. Chem., Int. Ed.
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Sud, D.1
Norsten, T.B.2
Branda, N.R.3
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0001541127
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(b) J. W. Faller, C. C. Chen and C. J. Malerich, J. Inorg. Biochem., 1979, 11, 151;
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J. Inorg. Biochem.
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Faller, J.W.1
Chen, C.C.2
Malerich, C.J.3
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35349009957
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S. L. Gilat, S. H. Kawai and J.-M. Lehn, J. Chem. Soc., Chem. Commun., 1993, 1439.
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(1993)
J. Chem. Soc., Chem. Commun.
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Gilat, S.L.1
Kawai, S.H.2
Lehn, J.-M.3
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19
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0033590989
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M. Irie, T. Lifka, K. Uchida, S. Kobatake and Y. Shindo, Chem. Commun., 1999, 747.
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(1999)
Chem. Commun.
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Irie, M.1
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0034316119
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A. Peters, R. McDonald and N. R. Branda, Adv. Mater. Opt. Electron., 2000, 10, 245.
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Peters, A.1
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21
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0030887405
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For an example where photochemical fragmentation of a malachite green dye leads to complete decomplexation of a cation/aza-crown ether, see: K. Kimura, R. Mizutani, M. Yokoyama, M. Okamoto and H. Doe, J. Am. Chem. Soc., 1997, 119, 2062.
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J. Am. Chem. Soc.
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Kimura, K.1
Mizutani, R.2
Yokoyama, M.3
Okamoto, M.4
Doe, H.5
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0142138827
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A. Takata, M. Saito, A. Murakami, S. Nakamura, M. Irie and K. Uchida, Adv. Funct. Mater., 2003, 13, 755.
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(2003)
Adv. Funct. Mater.
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Takata, A.1
Saito, M.2
Murakami, A.3
Nakamura, S.4
Irie, M.5
Uchida, K.6
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