-
2
-
-
33845556264
-
-
M. Yoshifuji, I. Shima, N. Inamoto, K. Hirotsu, and T. Higuchi, J. Am. Chem. Soc., 103, 4587 (1981).
-
(1981)
J. Am. Chem. Soc.
, vol.103
, pp. 4587
-
-
Yoshifuji, M.1
Shima, I.2
Inamoto, N.3
Hirotsu, K.4
Higuchi, T.5
-
3
-
-
84960014905
-
-
N. Tokitoh, H. Suzuki, T. Matsumoto, Y. Matsuhashi, and R. Okazaki, J. Am. Chem. Soc., 113, 7047 (1991).
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 7047
-
-
Tokitoh, N.1
Suzuki, H.2
Matsumoto, T.3
Matsuhashi, Y.4
Okazaki, R.5
-
4
-
-
0033599299
-
-
K. Goto, T. Kubo, K. Yamamoto, K. Nakasuji, K. Sato, D. Shiomi, T. Takui, M. Kubota, T. Kobayashi, K. Yakushi, and J. Ouyang, J. Am. Chem. Soc., 121, 1619 (1999).
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 1619
-
-
Goto, K.1
Kubo, T.2
Yamamoto, K.3
Nakasuji, K.4
Sato, K.5
Shiomi, D.6
Takui, T.7
Kubota, M.8
Kobayashi, T.9
Yakushi, K.10
Ouyang, J.11
-
6
-
-
0000119625
-
-
N. Tokitoh, H. Suzuki, and R. Okazaki, J. Am. Chem. Soc., 115, 10428 (1993).
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 10428
-
-
Tokitoh, N.1
Suzuki, H.2
Okazaki, R.3
-
7
-
-
0001179655
-
-
There is a report that a radical center is stabilized by DtBuP groups in tris(3,5-di-tert-butylphenyl)methyl; B. Kahr, D. V. Engen, and K. Mislow, J. Am. Chem. Soc., 108, 8305 (1986).
-
(1986)
J. Am. Chem. Soc.
, vol.108
, pp. 8305
-
-
Kahr, B.1
Engen, D.V.2
Mislow, K.3
-
10
-
-
0000194685
-
-
K.-H. Menting, W. Eichel, K. Riemenschneider, H. L. K. Schmand, and P. Boldt, J. Org. Chem., 48, 2814 (1983).
-
(1983)
J. Org. Chem.
, vol.48
, pp. 2814
-
-
Menting, K.-H.1
Eichel, W.2
Riemenschneider, K.3
Schmand, H.L.K.4
Boldt, P.5
-
11
-
-
0008979780
-
-
V. P. Makovetskii, V. P. Grubyi, and A. M. Nesterenko, Theor. Exp. Chem., 25, 327, (1989); Teor. Eksp. Khim., 25 , 352 (1989).
-
(1989)
Theor. Exp. Chem.
, vol.25
, pp. 327
-
-
Makovetskii, V.P.1
Grubyi, V.P.2
Nesterenko, A.M.3
-
12
-
-
0008979780
-
-
V. P. Makovetskii, V. P. Grubyi, and A. M. Nesterenko, Theor. Exp. Chem., 25, 327, (1989); Teor. Eksp. Khim., 25 , 352 (1989).
-
(1989)
Teor. Eksp. Khim.
, vol.25
, pp. 352
-
-
-
13
-
-
0000756257
-
-
L. T. Scott, M. D. Rozeboom, K. N. Houk, T. Fukunaga, H. J. Lindner, and K. Hafner, J. Am. Chem. Soc., 102, 5169 (1980).
-
(1980)
J. Am. Chem. Soc.
, vol.102
, pp. 5169
-
-
Scott, L.T.1
Rozeboom, M.D.2
Houk, K.N.3
Fukunaga, T.4
Lindner, H.J.5
Hafner, K.6
-
14
-
-
0001528347
-
-
The corresponding dicyanomethylene derivatives, 11,11,12,12-tetracyano-2,6-naphthoquinodimethane (TNAP), is known as a stable molecule and used as an important component molecule for molecule-based conductor. The crystal structure of charge transfer complexes based on TNAP were reported. a) P. A. Berger, D. J. Dahm, G. R. Johnson, M. G. Miles, and J. D. Wilson, Phys. Rev., B12, 4085 (1975).
-
(1975)
Phys. Rev.
, vol.B12
, pp. 4085
-
-
Berger, P.A.1
Dahm, D.J.2
Johnson, G.R.3
Miles, M.G.4
Wilson, J.D.5
-
15
-
-
0009068201
-
-
b) J. Toyoda, A. Oda, I. Murata, A. Kawamoto, J. Tanaka, and K. Nakasuji, Bull. Chem. Soc. Jpn., 66, 2115 (1993).
-
(1993)
Bull. Chem. Soc. Jpn.
, vol.66
, pp. 2115
-
-
Toyoda, J.1
Oda, A.2
Murata, I.3
Kawamoto, A.4
Tanaka, J.5
Nakasuji, K.6
-
17
-
-
84979379265
-
-
note
-
RED2 = -0.81.
-
-
-
-
18
-
-
0003322015
-
-
ed by S. Patai, John Wiley & Sons, London Chap. 4
-
St. Berger and A. Rieker, in "The Chemistry of the Quinonoid Compounds," ed by S. Patai, John Wiley & Sons, London (1974), Part 1, Chap. 4, pp 195-204.
-
(1974)
The Chemistry of the Quinonoid Compounds
, Issue.PART 1
, pp. 195-204
-
-
Berger, St.1
Rieker, A.2
-
19
-
-
0000698485
-
-
The crystal structures of charge transfer complexes of quinhydrone type based on substituted 2,6-NQ were reported: K. Nakasuji, K.-i. Sugiura, T. Kitagawa, J. Toyoda, H. Okamoto, K. Okaniwa, T. Mitani, H. Yamamoto, I. Murata, A. Kawamoto, and J. Tanaka, J. Am. Chem. Soc., 113, 1862 (1991).
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 1862
-
-
Nakasuji, K.1
Sugiura, K.-I.2
Kitagawa, T.3
Toyoda, J.4
Okamoto, H.5
Okaniwa, K.6
Mitani, T.7
Yamamoto, H.8
Murata, I.9
Kawamoto, A.10
Tanaka, J.11
-
20
-
-
0009064173
-
-
note
-
2)) = 0.058 (0.073), Goodness-of-Fit = 2.02, reflection-parameter ratio = 11.15 based on 2955 observed reflections (I>2.00 σ(I)) and 265 parameters (all aromatic hydrogen atoms were refined isotropically).
-
-
-
|