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77951190108
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Recent reviews and articles
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Recent reviews and articles
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64649106986
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Mishra, A.; Ma, C.-Q.; Baüerle, P. Chem. Rev 2009, 109, 1141
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Chem. Rev
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Mishra, A.1
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67749145468
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Banerjee, M.; Shukla, R.; Rathore, R. J. Am. Chem. Soc. 2009, 131, 1780
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Banerjee, M.1
Shukla, R.2
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4
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70349736092
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Lovett, J. E.; Hoffmann, M.; Cnossen, A.; Shutter, A. T. J.; Hogben, H. J.; Warren, J. E.; Pascu, S. I.; Kay, C. W. M.; Timmel, C. R.; Anderson, H. L. J. Am. Chem. Soc. 2009, 131, 13852
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Lovett, J.E.1
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Hogben, H.J.5
Warren, J.E.6
Pascu, S.I.7
Kay, C.W.M.8
Timmel, C.R.9
Anderson, H.L.10
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5
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65349127828
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Grimsdale, A. C.; Chan, K. L.; Rainer, E.; Martin, R. E.; Jokisz, P. G.; Holmes, A. B. Chem. Rev. 2009, 109, 897
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Chem. Rev.
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Grimsdale, A.C.1
Chan, K.L.2
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Martin, R.E.4
Jokisz, P.G.5
Holmes, A.B.6
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6
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68349128873
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Ikeda, T.; Aratani, N.; Osuka, A. Chem. Asian J. 2009, 4, 1248
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Chem. Asian J.
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Ikeda, T.1
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76449106438
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Liu, Y.; Di, C.- a.; Du, C.; Liu, Y.; Lu, K.; Qiu, W.; Yu, G. Chem. - Eur. J. 2010, 16, 2231
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Chem. - Eur. J.
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Liu, Y.1
Di, C.-A.2
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Lu, K.5
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Yu, G.7
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9
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0346434119
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Tsubaki, K.; Miura, M.; Morikawa, H.; Tanaka, H.; Kawabata, T.; Furuta, T.; Tanaka, K.; Fuji, K. J. Am. Chem. Soc. 2003, 125, 16200
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Tsubaki, K.1
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Kawabata, T.5
Furuta, T.6
Tanaka, K.7
Fuji, K.8
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33747392107
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Tsubaki, K.; Tanaka, H.; Takaishi, K.; Miura, M.; Morikawa, H.; Furuta, T.; Tanaka, K.; Fuji, K.; Sasamori, T.; Tokitoh, N.; Kawabata, T. J. Org. Chem. 2006, 71, 6579
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Tsubaki, K.1
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Miura, M.4
Morikawa, H.5
Furuta, T.6
Tanaka, K.7
Fuji, K.8
Sasamori, T.9
Tokitoh, N.10
Kawabata, T.11
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33745524498
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Tsubaki, K.; Takaishi, K.; Tanaka, H.; Miura, M.; Kawabata, T. Org. Lett. 2006, 8, 2587
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Org. Lett.
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Tsubaki, K.1
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Takaishi, K.; Tsubaki, K.; Tanaka, H.; Miura, M.; Kawabata, T. Yakugaku Zasshi 2006, 126, 779
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Yakugaku Zasshi
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Takaishi, K.1
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Tanaka, H.3
Miura, M.4
Kawabata, T.5
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34249827281
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Tsubaki, K.; Takaishi, K.; Sue, D.; Kawabata, T. J. Org. Chem. 2007, 72, 4238
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J. Org. Chem.
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Tsubaki, K.1
Takaishi, K.2
Sue, D.3
Kawabata, T.4
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Tsubaki, K.; Takaishi, K.; Sue, D.; Matsuda, K.; Kanemitsu, Y.; Kawabata, T. J. Org. Chem. 2008, 73, 4279
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J. Org. Chem.
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Tsubaki, K.1
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Kanemitsu, Y.5
Kawabata, T.6
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65949112025
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Sue, D.; Takaishi, K.; Harada, T.; Kuroda, R.; Kawabata, T.; Tsubaki, K. J. Org. Chem. 2009, 74, 3940
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Sue, D.1
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67649547743
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Takaishi, K.; Sue, D.; Kuwahara, S.; Harada, N.; Kawabata, T.; Tsubaki, K. Tetrahedron 2009, 65, 6135
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Tetrahedron
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77951175668
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For examples of 2,2′-bridged-1,1′-binaphthyls, see
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For examples of 2,2′-bridged-1,1′-binaphthyls, see
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19
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0013210188
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Ernesstimpson, J. E.; Daub, G.; Hayes, F. N. J. Org. Chem. 1973, 38, 1771
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8944259895
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24
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Tu, T.; Maris, T.; Wuest, J. D. J. Org. Chem. 2008, 73, 5255
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For examples of Geländer-type molecules, see
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For examples of Geländer-type molecules, see
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0032538784
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Kiupel, B.; Niederalt, C.; Nieger, M.; Grimme, S.; Vögtle, F. Angew. Chem., Int. Ed. 1998, 37, 3031
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0035542909
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Modjewski, M.; Lindeman, S. V.; Rathore, R. Org. Lett. 2009, 11, 4656
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77951148159
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Dihedral angles of the two naphthalene rings in the X-ray crystal structure of the bridged dimers are observed slightly above 50° see
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Dihedral angles of the two naphthalene rings in the X-ray crystal structure of the bridged dimers are observed slightly above 50° see
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31
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0031976716
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35
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0001926888
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Berova N. Nakanishi K. Harada N., Eds.; Wiley-VCH: New York
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Koslowski, A.; Sreerama, N.; Woody, R. W. In Circular Dichroism: Principles and Applications; Berova, N.; Nakanishi, K.; Harada, N., Eds.; Wiley-VCH: New York, 2000; pp 55-95.
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Circular Dichroism: Principles and Applications
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36
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0035835042
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† = 33 kcal/mol in decalin), see
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† = 33 kcal/mol in decalin), see: Park, J.-W.; Ediger, M. D.; Green, M. M. J. Am. Chem. Soc. 2001, 123, 49
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Rosini, C.1
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38
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33846044312
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Hydroxy groups of BINOL are involved in its fluorescence quenching, see
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Hydroxy groups of BINOL are involved in its fluorescence quenching, see: Wang, Q.; Chen, X.; Tao, L.; Wang, L.; Xiao, D.; Yu, X.-Q.; Pu, L. J. Org. Chem. 2007, 72, 97
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39
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77951149084
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1 state have been studied; see
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1 state have been studied; see
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40
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3242892199
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Fujiyoshi, S.; Takeuchi, S.; Tahara, T. J. Phys. Chem. A 2004, 108, 5938
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Fujiyoshi, S.1
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Tahara, T.3
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41
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77951161865
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Both the HOMO and LUMO of an open form octinaphthalene are localized on about three naphthalene rings (Figure S6, Supporting Information).
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Both the HOMO and LUMO of an open form octinaphthalene are localized on about three naphthalene rings (Figure S6, Supporting Information).
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