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(Ed.: H. Dürr, H. Bouas-Laurent), Elsevier, Amsterdam
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a) Photochromism - Molecules and Systems (Ed.: H. Dürr, H. Bouas-Laurent), Elsevier, Amsterdam, 2003;
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(Ed.: B. L. Feringa), Wiley-VCH, Weinheim
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b) Molecular Switches (Ed.: B. L. Feringa), Wiley-VCH, Weinheim, 2001;
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c) Special Issue: "Photochromism: Memories and Switches", Chem. Rev. 2000, 100, 1683-1890;
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(Eds.: J. C. Crano, R. J. Guglielmetti), Kluwer Academic/Plenum Publishers, New York
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d) Organic Photochromic and Thermochromic Compounds (Eds.: J. C. Crano, R. J. Guglielmetti), Kluwer Academic/Plenum Publishers, New York, 1999;
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Organic Photochromic and Thermochromic Compounds
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(Ed.: A. V. El'tsov), Consultants Bureau, New York
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e) Organic Photochromes (Ed.: A. V. El'tsov), Consultants Bureau, New York, 1990.
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Organic Photochromes
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14
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23744464557
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and references therein
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S. Hecht, Small 2005, 1, 26-29, and references therein.
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Small
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Hecht, S.1
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15
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0035155783
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For the side-chain approach, see: a) O. Pieroni, A. Fissi, N. Angelini, F. Lenci, Acc. Chem. Res. 2001, 34, 9-17;
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Pieroni, O.1
Fissi, A.2
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16
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22244487296
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for the tether approach, see: b) G. A. Woolley, Acc. Chem. Res. 2005, 38, 486-493;
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Woolley, G.A.1
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17
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0035576193
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for related polyisocyanates with azobenzene-containing side chains, see: c) S. Mayer, R. Zentel, Prog. Polym. Sci. 2001, 26, 1973-2013.
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Prog. Polym. Sci.
, vol.26
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Mayer, S.1
Zentel, R.2
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18
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0030823475
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a) J. C. Nelson, J. G. Saven, J. S. Moore, P. G. Wolynes, P. G. Science 1997, 277, 1793-1796;
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Science
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Nelson, J.C.1
Saven, J.G.2
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19
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0033531714
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b) R. B. Prince, J. G. Saven, P. G. Wolynes, J. S. Moore, J. Am. Chem. Soc. 1999, 121, 3114-3121;
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Prince, R.B.1
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21
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33746305452
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See the Supporting Information
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See the Supporting Information.
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22
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0000303206
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For the use of (S)-β-methyltri(ethyleneglycol) side chains, see: a) R. B. Prince, L. Brunsveld, E. W. Meijer, J. S. Moore, Angew. Chem. 2000, 112, 234-236;
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Prince, R.B.1
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24
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0035476560
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b) R. B. Prince, J. S. Moore, L. Brunsveld, E. W. Meijer, Chem. Eur. J. 2001, 7, 4150-4154.
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Chem. Eur. J.
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Prince, R.B.1
Moore, J.S.2
Brunsveld, L.3
Meijer, E.W.4
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25
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0034703708
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For related examples, see: a) S. Lahiri, J. L. Thompson, J. S. Moore, J. Am. Chem. Soc. 2000, 122, 11 315-11 319;
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J. Am. Chem. Soc.
, vol.122
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Lahiri, S.1
Thompson, J.L.2
Moore, J.S.3
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26
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1642487704
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b) H. Goto, J. M. Heemstra, D. J. Hill, J. S. Moore, Org. Lett. 2004, 6, 889-892.
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Org. Lett.
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Goto, H.1
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Hill, D.J.3
Moore, J.S.4
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27
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33746281559
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note
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Solutions in aqueous acetonitrile were used for the CD experiments to maximize the CD signal as a result of the increased hydrophobic driving force and therefore ensure more accurate kinetic data.
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28
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33746282916
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note
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cis mixture.
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29
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1242297021
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For example, see: L.-X. Liao, F. Stellacci, D. V. McGrath, J. Am. Chem. Soc. 2004, 126, 2181-2185.
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J. Am. Chem. Soc.
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Liao, L.-X.1
Stellacci, F.2
McGrath, D.V.3
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30
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0000593831
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For example, see: W. Y. Yang, R. B. Prince, J. Sabelko, J. S. Moore, M. Gruebele, J. Am. Chem. Soc. 2000, 122, 3248-3249.
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J. Am. Chem. Soc.
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Yang, W.Y.1
Prince, R.B.2
Sabelko, J.3
Moore, J.S.4
Gruebele, M.5
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31
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23044503853
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For an elegant example, see: a) A. Koçer, M. Walko, W. Meijberg, B. L. Feringa, Science 2005, 309, 755-758;
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(2005)
Science
, vol.309
, pp. 755-758
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Koçer, A.1
Walko, M.2
Meijberg, W.3
Feringa, B.L.4
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32
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17944373131
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for a recent review, see: b) K. Kinbara, T. Aida, Chem. Rev. 2005, 105, 1377-1400.
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Chem. Rev.
, vol.105
, pp. 1377-1400
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Kinbara, K.1
Aida, T.2
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0034728690
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R. B. Prince, S. A. Barnes, J. S. Moore, J. Am. Chem. Soc. 2000, 122, 2758-2762.
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(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 2758-2762
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Prince, R.B.1
Barnes, S.A.2
Moore, J.S.3
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