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1
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Sato, O.1
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2
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0000996707
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Gu, Z.-Z.1
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Nagai, K.1
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4
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33748878612
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Cf. P. Gütlich, A. Hauser, and H. Spiering, Angew. Chem., Int. Ed. Engl., 33, 2024 (1994).
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5
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Hamachi, K.1
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Iwamura, H.4
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8
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10444274735
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in press
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a) S. Natatsuji, S. Takeuchi, T. Ojima, Y. Ogawa, H. Akutsu, and J. Yamada, Mol. Cryst. Liq. Cryst., in press.
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Mol. Cryst. Liq. Cryst.
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Natatsuji, S.1
Takeuchi, S.2
Ojima, T.3
Ogawa, Y.4
Akutsu, H.5
Yamada, J.6
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9
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10444274735
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accepted
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b) S. Takeuchi, Y. Ogawa, A. Naito, K. Sudo, Y. Yasuoka, H. Akutsu, J. Yamada, and S. Nakatsuji, Mol. Cryst. Liq. Cryst., accepted.
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Mol. Cryst. Liq. Cryst.
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Takeuchi, S.1
Ogawa, Y.2
Naito, A.3
Sudo, K.4
Yasuoka, Y.5
Akutsu, H.6
Yamada, J.7
Nakatsuji, S.8
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11
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0040336134
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note
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The progress of the photo-reaction was monitored by electronic spectral change of the vibronic absorptions in 320-390 nm in benzene and an apparent photo-stationary state was attained after 6 h (50% consumption of 1a: ca. 4.5 h). The gradual dissociation was observed for the backward reaction to reach a stationary state after 12 h (50% consumption of 1b: ca. 4 h). No clear isosbestic point was observed due partially to the solvent system used.
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12
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0039744250
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note
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-3. R = 0.053, wR = 0.041 [3034 observed reflections and 328 parameters, I > 3σ(I)].
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13
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0029255952
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Cf. a) J. Veciana, J. Cirujeda, C. Rovira, and J. Vidal-Gancedo, Adv. Mater., 7, 221 (1995).
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Veciana, J.1
Cirujeda, J.2
Rovira, C.3
Vidal-Gancedo, J.4
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14
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0000608059
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b) K. Togashi, R. Imachi, K. Tomioka, H. Tsuboi, T. Ishida, T. Nogami, N. Takeda, and M. Ishikawa, Bull. Chem. Soc. Jpn., 69, 2821 (1996).
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Bull. Chem. Soc. Jpn.
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Togashi, K.1
Imachi, R.2
Tomioka, K.3
Tsuboi, H.4
Ishida, T.5
Nogami, T.6
Takeda, N.7
Ishikawa, M.8
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15
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0030908878
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c) M. M. Matsushita, A. Izuoka, T. Sugawara, T. Kobayashi, N. Wada, N. Takeda, and M. Ishikawa, J. Am. Chem. Soc., 119, 4369 (1997).
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(1997)
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Matsushita, M.M.1
Izuoka, A.2
Sugawara, T.3
Kobayashi, T.4
Wada, N.5
Takeda, N.6
Ishikawa, M.7
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16
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0039744249
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note
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1b with benzene: orange rods, mp 225-228 °C (decomp.); 1b with dichloromethane: orange powder, mp 213-215 °C (decomp); 1b with chloroform: orange cubes, m.p. 221-223 °C (decomp). From the elemental analyses, their compositions have been estimated as 1b·2 benzene, 1b·1.5 dichloromethane and 1b·2 chloroform, respectively.
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17
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0039151780
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note
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-3. R = 0.069, wR = 0.058 [2707 observed reflections and 736 parameters, 1 > 3σ(I)].
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