-
5
-
-
11744270473
-
-
e) G. P. de Gaudemaris, B. Sillion, and J. Prévé, Bull. Soc. Chim., France, 1964, 1793 (1964).
-
(1964)
Bull. Soc. Chim., France
, vol.1964
, pp. 1793
-
-
De Gaudemaris, G.P.1
Sillion, B.2
Prévé, J.3
-
6
-
-
0001106859
-
-
f) J. K. Stille, J. R. Williamson, and F. Arnold, J. Polym. Sci. A, 3, 1013 (1965).
-
(1965)
J. Polym. Sci. A
, vol.3
, pp. 1013
-
-
Stille, J.K.1
Williamson, J.R.2
Arnold, F.3
-
9
-
-
0000423805
-
-
i) K. Niume, S. Kurosawa, F. Toda, M. Hasegawa, and Y. Iwakura, Bull. Chem. Soc. Jpn., 55, 2293 (1982).
-
(1982)
Bull. Chem. Soc. Jpn.
, vol.55
, pp. 2293
-
-
Niume, K.1
Kurosawa, S.2
Toda, F.3
Hasegawa, M.4
Iwakura, Y.5
-
11
-
-
0023768781
-
-
k) J. Harmenberg, B. Wahren, and J. Bergman, Antimicrob. Agents Chemother., 32, 1720 (1988).
-
(1988)
Antimicrob. Agents Chemother.
, vol.32
, pp. 1720
-
-
Harmenberg, J.1
Wahren, B.2
Bergman, J.3
-
14
-
-
0001791205
-
-
b) A. Rajesh, A. Chapla, and S. Charanjeet, Acta Pharm. Jugosl., 38, 11 (1988).
-
(1988)
Acta Pharm. Jugosl.
, vol.38
, pp. 11
-
-
Rajesh, A.1
Chapla, A.2
Charanjeet, S.3
-
15
-
-
0023768781
-
-
c) J. Harmenberg, B. Wahren, and J. Bergman, Antimicrob. Agents Chemother., 32, 1720 (1988).
-
(1988)
Antimicrob. Agents Chemother.
, vol.32
, pp. 1720
-
-
Harmenberg, J.1
Wahren, B.2
Bergman, J.3
-
16
-
-
0001727284
-
-
a) P. Chaudhuri, T. Weyhermüller, E. Bill, and K. Wieghardt, Inorg. Chim. Acta, 252, 195 (1996).
-
(1996)
Inorg. Chim. Acta
, vol.252
, pp. 195
-
-
Chaudhuri, P.1
Weyhermüller, T.2
Bill, E.3
Wieghardt, K.4
-
17
-
-
0000153854
-
-
b) C. J. Fahrni, A. Pfaltz, M. Neuburger, and M. Zehnder, Helv. Chim. Acta, 81, 507 (1998).
-
(1998)
Helv. Chim. Acta
, vol.81
, pp. 507
-
-
Fahrni, C.J.1
Pfaltz, A.2
Neuburger, M.3
Zehnder, M.4
-
18
-
-
0000318458
-
-
c) Y. Hosokawa, H. Yamane, Y. Nakao, K. Matsumoto, S. Takamizawa, W. Mori, S. Suzuki, and H. Kimoto, Inorg. Chim. Acta, 283, 118 (1998).
-
(1998)
Inorg. Chim. Acta
, vol.283
, pp. 118
-
-
Hosokawa, C.Y.1
Yamane, H.2
Nakao, Y.3
Matsumoto, K.4
Takamizawa, S.5
Mori, W.6
Suzuki, S.7
Kimoto, H.8
-
19
-
-
0001046574
-
-
d) T. Koga, H. Furutachi, T. Nakamura, N. Fukita, M. Ohba, K. Takahashi, and H. Okawa, Inorg. Chem., 37, 989 (1998).
-
(1998)
Inorg. Chem.
, vol.37
, pp. 989
-
-
Koga, T.1
Furutachi, H.2
Nakamura, T.3
Fukita, N.4
Ohba, M.5
Takahashi, K.6
Okawa, H.7
-
20
-
-
0032775245
-
-
e) B. Kersting, G. Steinfeld, and J. Hausmann, Eur. J. Inorg. Chem., 1999, 179.
-
Eur. J. Inorg. Chem.
, vol.1999
, pp. 179
-
-
Kersting, B.1
Steinfeld, G.2
Hausmann, J.3
-
22
-
-
0032803183
-
-
g) A. Aukauloo, X. Ottenwaelder, R. Ruiz, S. Poussereau, Y. Pei, Y. Journaux, P. Fleurat, F. Volatron, B. Cervera, and M. C. Muñoz, Eur. J. Inorg. Chem., 1999, 1067.
-
Eur. J. Inorg. Chem.
, vol.1999
, pp. 1067
-
-
Aukauloo, A.1
Ottenwaelder, X.2
Ruiz, R.3
Poussereau, S.4
Pei, Y.5
Journaux, Y.6
Fleurat, P.7
Volatron, F.8
Cervera, B.9
Muñoz, M.C.10
-
23
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0001785785
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-
note
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2) δ 7.41(1H, ddd, J = 7.5, 7.5, 1.0 Hz, H-9), 7.56(1H, ddd, J = 8.0, 1.0, 0.5 Hz, H-7), 7.69(1H, ddd, J = 8.0, 7.5, 1.0 Hz, H-8), 7.72(1H, ddd, J = 8.5, 7.0, 1.5 Hz, H-2), 7.78(1H, ddd, J = 8.0, 7.0, 1.5 Hz, H-3), 8.09(1H, ddd, J = 8.0, 1.5, 0.5 Hz, H-4), 8.28(1H, ddd, J = 8.5, 1.5, 0.5 Hz, H-1). 8.42(1H, ddd, J = 7.5, 1.0, 0.5 Hz, H-10), and 8.76(1H, brds, NH-6).
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-
-
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24
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0001807065
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-
note
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-, m/z 218.0718).
-
-
-
-
25
-
-
0000031880
-
-
a) H. J. Schlesinger, H. C. Broun, H. R. Hoekstra, and L. R. Papps, J. Am. Chem. Soc., 75, 199 (1953).
-
(1953)
J. Am. Chem. Soc.
, vol.75
, pp. 199
-
-
Schlesinger, H.J.1
Broun, H.C.2
Hoekstra, H.R.3
Papps, L.R.4
-
27
-
-
0034655863
-
-
c) S. Takekuma, H. Takekuma, T. Matsumoto, and Z. Yoshida, Tetrahedron Lett., 41, 2929 (2000).
-
(2000)
Tetrahedron Lett.
, vol.41
, pp. 2929
-
-
Takekuma, S.1
Takekuma, H.2
Matsumoto, T.3
Yoshida, Z.4
-
28
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0001963691
-
-
note
-
The yield of the product is based on the consumed starting material.
-
-
-
-
29
-
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0001791211
-
-
note
-
The parameters were confirmed by a computer-assisted simulation analysis.
-
-
-
-
30
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0001879254
-
-
note
-
a) The sample dried well in a vacuum desiccator was used for the thermal, elemental and spectroscopic analyses. b) The freshly recrystallized sample, which was not dried in a vacuum desiccator, was used for the X-ray crystallographic analysis.
-
-
-
-
31
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0001801288
-
-
note
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2 using the program SHELXL 97. All calculations were performed using the teXsan crystallographic software package.
-
-
-
-
32
-
-
4243703942
-
-
a) F. A. Cotton, M. Matusz, and R. Poli, Inorg. Chem., 26, 1474 (1987).
-
(1987)
Inorg. Chem.
, vol.26
, pp. 1474
-
-
Cotton, F.A.1
Matusz, M.2
Poli, R.3
-
33
-
-
0001415417
-
-
b) L. Sacconi, C. Mealli, and D. Gatteschi, Inorg. Chem., 13, 1985 (1974).
-
(1974)
Inorg. Chem.
, vol.13
, pp. 1985
-
-
Sacconi, L.1
Mealli, C.2
Gatteschi, D.3
-
34
-
-
0033550524
-
-
c) S-Y. Lai, T-W. Lin, Y-H. Chen, C-C. Wang, G-H. Lee, M-h. Yang, M-k. Leung, and S-M. Peng, J. Am. Chem. Soc., 121, 250 (1999).
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 250
-
-
Lai, S.-Y.1
Lin, T.-W.2
Chen, Y.-H.3
Wang, C.-C.4
Lee, G.-H.5
Yang, M.-H.6
Leung, M.-K.7
Peng, S.-M.8
-
35
-
-
0001708347
-
-
note
-
max 470 nm) of complex 3 is near to the maximum wavelength of the solar spectrum (ca. 500 nm). Thus, the basic studies on physical and chemical functions of complex 3 are of interest from a viewpoint of potential utility of functional delocalized electron system such as photosensitive dyes.
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