-
1
-
-
0003699562
-
-
VCH, Weinheim
-
For an overview of switchable molecular devices, see a) J.-M. Lehn, Supramolecular Chemistry, VCH, Weinheim, 1995, pp. 124-138;
-
(1995)
Supramolecular Chemistry
, pp. 124-138
-
-
Lehn, J.-M.1
-
2
-
-
0000499466
-
-
b) M. Ward, Chem. Ind. 1997, 16, 640-645;
-
(1997)
Chem. Ind.
, vol.16
, pp. 640-645
-
-
Ward, M.1
-
3
-
-
0542373936
-
-
c) V. Balzani, M. Gómez-López, J. F. Stoddart, Acc. Chem. Res. 1998, 31, 405-414.
-
(1998)
Acc. Chem. Res.
, vol.31
, pp. 405-414
-
-
Balzani, V.1
Gómez-López, M.2
Stoddart, J.F.3
-
4
-
-
0001720756
-
-
(Ed.: D. N. Reinhoudt), Pergamon-Elsevier, Oxford
-
a) V. Balzani, F. Scandola in Comprehensive Supramolecular Chemistry, Vol. 5 (Ed.: D. N. Reinhoudt), Pergamon-Elsevier, Oxford, 1996, pp. 687-746;
-
(1996)
Comprehensive Supramolecular Chemistry
, vol.5
, pp. 687-746
-
-
Balzani, V.1
Scandola, F.2
-
5
-
-
0027304533
-
-
b) B. L. Feringa, W. F. Jager, B. de Lange, Tetrahedron 1993, 49, 8267-8310;
-
(1993)
Tetrahedron
, vol.49
, pp. 8267-8310
-
-
Feringa, B.L.1
Jager, W.F.2
De Lange, B.3
-
6
-
-
0000400550
-
-
c) H. Dürr, Angew. Chem. 1989, 101, 427-445;
-
(1989)
Angew. Chem.
, vol.101
, pp. 427-445
-
-
Dürr, H.1
-
8
-
-
37049070846
-
-
For another example of such a system, see J. Achatz, C. Fischer, J. Salbeck, J. Daub, J. Chem. Soc. Chem. Commun. 1991, 504-507.
-
(1991)
J. Chem. Soc. Chem. Commun.
, pp. 504-507
-
-
Achatz, J.1
Fischer, C.2
Salbeck, J.3
Daub, J.4
-
10
-
-
0002476898
-
-
R. E. Martin, J. Bartek, F. Diederich, R. R. Tykwinski, E. C. Meister, A. Hilger, H. P. Lüthi, J. Chem. Soc. Perkin Trans. 2 1998, 233-241.
-
(1998)
J. Chem. Soc. Perkin Trans. 2
, pp. 233-241
-
-
Martin, R.E.1
Bartek, J.2
Diederich, F.3
Tykwinski, R.R.4
Meister, E.C.5
Hilger, A.6
Lüthi, H.P.7
-
11
-
-
0000639443
-
-
a) J. Daub, T. Knöchel, A. Mannschreck, Angew. Chem. 1984, 96, 980-981;
-
(1984)
Angew. Chem.
, vol.96
, pp. 980-981
-
-
Daub, J.1
Knöchel, T.2
Mannschreck, A.3
-
13
-
-
0001278008
-
-
b) J. Daub, S. Gierisch, U. Klement, T. Knöchel, G. Maas, U. Seitz, Chem. Ber. 1986, 119, 2631-2646;
-
(1986)
Chem. Ber.
, vol.119
, pp. 2631-2646
-
-
Daub, J.1
Gierisch, S.2
Klement, U.3
Knöchel, T.4
Maas, G.5
Seitz, U.6
-
15
-
-
0002769275
-
-
(Eds.: F. Diederich, P. J. Stang), WILEY-VCH, Weinheim
-
K. Sonogashira in Metal-catalyzed Cross-coupling Reactions (Eds.: F. Diederich, P. J. Stang), WILEY-VCH, Weinheim, 1998, pp. 203-269.
-
(1998)
Metal-catalyzed Cross-coupling Reactions
, pp. 203-269
-
-
Sonogashira, K.1
-
16
-
-
0001226638
-
-
R. R. Tykwinski, M. Schreiber, R. Pérez Carlón, F. Diederich, Helv. Chim. Acta 1996, 79, 2249-2281.
-
(1996)
Helv. Chim. Acta
, vol.79
, pp. 2249-2281
-
-
Tykwinski, R.R.1
Schreiber, M.2
Pérez Carlón, R.3
Diederich, F.4
-
17
-
-
33747541328
-
-
note
-
13C NMR spectroscopy, FAB-MS, and elemental analysis.
-
-
-
-
18
-
-
33747543403
-
-
note
-
2) = 0.16 for 566 parameters and 3377 reflections with I > 2σ(I) and θ < 50°. The disordered seven-membered ring, based on one set of atomic positions, is nearly planar. However, by refining partial atoms as mentioned above, two different conformations are obtained. The one shown in Figure 1 (based on a population parameter of 0.63) is approximately boat shaped, whereas the other (based on a population parameter of 0.37) is less clear. Crystallographic data (without structure factors) for the structure reported in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication no CCDC-102924. Copies of the data can be obtained free of charge on application to CCDC, 12 Union Road, Cambridge CB21EZ (fax: (+44)1223-336-033; e-mail: deposit@ccdc.cam.ac.uk).
-
-
-
-
19
-
-
33747561900
-
-
note
-
[13] An absolute error of about 10% is claimed for the quantum yields.
-
-
-
-
22
-
-
0004267504
-
-
Wiley, Chichester
-
b) A. M. Braun, M.-T. Maurette, E. Oliveros, Photochemical Technology, Wiley, Chichester, 1991, pp. 70-106.
-
(1991)
Photochemical Technology
, pp. 70-106
-
-
Braun, A.M.1
Maurette, M.-T.2
Oliveros, E.3
-
23
-
-
0001267164
-
-
a) M. Irie, O. Miyatake, K. Uchida, J. Am. Chem. Soc. 1992, 114, 8715-8716;
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 8715-8716
-
-
Irie, M.1
Miyatake, O.2
Uchida, K.3
-
24
-
-
37049068246
-
-
b) M. Hanazawa, R. Sumiya, Y. Horikawa, M. Irie, J. Chem. Soc. Chem. Commun. 1992, 206-207;
-
(1992)
J. Chem. Soc. Chem. Commun.
, pp. 206-207
-
-
Hanazawa, M.1
Sumiya, R.2
Horikawa, Y.3
Irie, M.4
-
25
-
-
84989537270
-
-
c) S. L. Gilat, S. H. Kwai, J.-M. Lehn, Chem. Eur. J. 1995, 1, 275-284;
-
(1995)
Chem. Eur. J.
, vol.1
, pp. 275-284
-
-
Gilat, S.L.1
Kwai, S.H.2
Lehn, J.-M.3
-
26
-
-
84989523797
-
-
d) S. W. Kwai, S. L. Gilat, R. P. Ponsinet, J.-M. Lehn, Chem. Eur. J. 1995, 1, 285-293.
-
(1995)
Chem. Eur. J.
, vol.1
, pp. 285-293
-
-
Kwai, S.W.1
Gilat, S.L.2
Ponsinet, R.P.3
Lehn, J.-M.4
-
27
-
-
33747568571
-
-
note
-
The rate constant for the thermal electrocyclization was determined by an exponential fit of the data obtained by following the decrease in intensity of the absorption band at 500 nm (trans-1c) and at 481 nm (4b) at 25°C in the dark.
-
-
-
-
28
-
-
0000480652
-
-
For donor-acceptor substituted TEEs and their nonlinear optical properties, see R. R. Tykwinski, U. Gubler, R. E. Martin, F. Diederich, C. Bosshard, P. Günter, J. Phys. Chem. B. 1998, 102, 4451-4465.
-
(1998)
J. Phys. Chem. B
, vol.102
, pp. 4451-4465
-
-
Tykwinski, R.R.1
Gubler, U.2
Martin, R.E.3
Diederich, F.4
Bosshard, C.5
Günter, P.6
-
29
-
-
0031191655
-
-
a) A. P. de Silva, H. Q. N. Gunaratne, T. Gunnlaugsson, A. J. M. Huxley, C. P. McCoy, J. T. Rademacher, T. E. Rice, Chem. Rev. 1997, 97, 1515-1566;
-
(1997)
Chem. Rev.
, vol.97
, pp. 1515-1566
-
-
De Silva, A.P.1
Gunaratne, H.Q.N.2
Gunnlaugsson, T.3
Huxley, A.J.M.4
McCoy, C.P.5
Rademacher, J.T.6
Rice, T.E.7
-
30
-
-
0009587780
-
-
b) A. P. de Silva, H. Q. N. Gunaratne, C. P. McCoy, Nature (London) 1993, 364, 42-44;
-
(1993)
Nature (London)
, vol.364
, pp. 42-44
-
-
De Silva, A.P.1
Gunaratne, H.Q.N.2
McCoy, C.P.3
-
31
-
-
11944261083
-
-
c) R. A. Bissell, A. P. de Silva, H. Q. N. Gunaratne, P. L. M. Lynch, G. E. M. Maguire, K. R. A. S. Sandanayake, Chem. Soc. Rev. 1992, 21, 187-195;
-
(1992)
Chem. Soc. Rev.
, vol.21
, pp. 187-195
-
-
Bissell, R.A.1
De Silva, A.P.2
Gunaratne, H.Q.N.3
Lynch, P.L.M.4
Maguire, G.E.M.5
Sandanayake, K.R.A.S.6
-
32
-
-
0000806855
-
-
d) L. Fabrizzi, M. Licchelli, P. Pallavicini, L. Parodi, Angew. Chem. 1998, 110, 838-841;
-
(1998)
Angew. Chem.
, vol.110
, pp. 838-841
-
-
Fabrizzi, L.1
Licchelli, M.2
Pallavicini, P.3
Parodi, L.4
-
37
-
-
0001409456
-
-
For systems with large fluorescence enhancement factors, see a) M. E. Huston, K. W. Heider, A. W. Czarnik, J. Am. Chem. Soc. 1988, 110, 4460-4462;
-
(1988)
J. Am. Chem. Soc.
, vol.110
, pp. 4460-4462
-
-
Huston, M.E.1
Heider, K.W.2
Czarnik, A.W.3
-
38
-
-
37049066860
-
-
b) R. A. Bissell, E. Calle, A. P. de Silva, H. Q. N. Gunaratne, J.-L. Habib-Jiwan, S. L. A. Peiris, R. A. D. D. Rupasinghe, T. K. S. D. Samarasinghe, K. R. A. S. Sandanayake, J.-P. Soumillion, J. Chem. Soc. Perkin Trans. 2 1992, 1559-1564.
-
(1992)
J. Chem. Soc. Perkin Trans. 2
, pp. 1559-1564
-
-
Bissell, R.A.1
Calle, E.2
De Silva, A.P.3
Gunaratne, H.Q.N.4
Habib-Jiwan, J.-L.5
Peiris, S.L.A.6
Rupasinghe, R.A.D.D.7
Samarasinghe, T.K.S.D.8
Sandanayake, K.R.A.S.9
Soumillion, J.-P.10
|