-
3
-
-
67650312019
-
-
For benzo[b]furans and indoles
-
For benzo[b]furans and indoles: a) M. Nakamura, L. Ilies, S. Otsubo, E. Nakamura, Angew. Chem. 2006, 118, 958 -961;
-
(2006)
Angew. Chem.
, vol.118
, pp. 958-961
-
-
Nakamura, M.1
Ilies, L.2
Otsubo, S.3
Nakamura, E.4
-
4
-
-
32044441685
-
-
Angew. Chem. Int. Ed. 2006, 45, 944 - 947;
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 944-947
-
-
-
5
-
-
33746144885
-
-
M. Nakamura, L. Ilies, S. Otsubo, E. Nakamura, Org. Lett. 2006, 8, 2803-2805.
-
(2006)
Org. Lett.
, vol.8
, pp. 2803-2805
-
-
Nakamura, M.1
Ilies, L.2
Otsubo, S.3
Nakamura, E.4
-
6
-
-
41549100591
-
-
For benzo[b] siloles
-
For benzo[b]siloles: L. Ilies, H. Tsuji, Y. Sato, E. Nakamura, J. Am. Chem. Soc. 2008, 130, 4240-4241.
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 4240-4241
-
-
Ilies, L.1
Tsuji, H.2
Sato, Y.3
Nakamura, E.4
-
7
-
-
52649112790
-
-
For benzo[b]phospholes
-
For benzo[b]phospholes: H. Tsuji, K. Sato, L. Ilies, Y. Itoh, Y. Sato, E. Nakamura, Org. Lett. 2008, 10, 2263-2265.
-
(2008)
Org. Lett.
, vol.10
, pp. 2263-2265
-
-
Tsuji, H.1
Sato, K.2
Ilies, L.3
Itoh, Y.4
Sato, Y.5
Nakamura, E.6
-
8
-
-
34848839222
-
-
For benzo[1,2-b:4,5-b']difurans
-
For benzo[1,2-b:4,5-b']difurans: H. Tsuji, C. Mitsui, L. Ilies, Y. Sato, E. Nakamura, J. Am. Chem. Soc. 2007, 129, 11902-11903.
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 11902-11903
-
-
Tsuji, H.1
Mitsui, C.2
Ilies, L.3
Sato, Y.4
Nakamura, E.5
-
9
-
-
0041589615
-
-
H. Z. Chen, Y. D. Jin, R. S. Xu, B. X. Peng, H. Desseyn, J. Janssens, P. Heremans, G. Borghs, H. J. Geise, Synth. Met. 2003, 139, 529-534.
-
(2003)
Synth. Met.
, vol.139
, pp. 529-534
-
-
Chen, H.Z.1
Jin, Y.D.2
Xu, R.S.3
Peng, B.X.4
Desseyn, H.5
Janssens, J.6
Heremans, P.7
Borghs, G.8
Geise, H.J.9
-
13
-
-
0025914845
-
-
G.K.B. Prasad, A. Burchat, G. Weeratunga, I. Watts, G. I. Dmitrienko, Tetrahedron Lett. 1991, 32, 5035-5038.
-
(1991)
Tetrahedron Lett.
, vol.32
, pp. 5035-5038
-
-
Prasad, G.K.B.1
Burchat, A.2
Weeratunga, G.3
Watts, I.4
Dmitrienko, G.I.5
-
14
-
-
0032132094
-
-
U. Salzner, J. B. Lagowski, P. G. Pickup, R. A. Poirier, Synth. Met. 1998, 96, 177-189.
-
(1998)
Synth. Met.
, vol.96
, pp. 177-189
-
-
Salzner, U.1
Lagowski, J.B.2
Pickup, P.G.3
Poirier, R.A.4
-
15
-
-
0030233020
-
-
For examples of polypyrrole HIMs
-
For examples of polypyrrole HIMs: a) J. Gao, A. J. Heeger, J. Y. Lee, C. Y. Kim, Synth. Met. 1996, 82, 221 - 223;
-
(1996)
Synth. Met.
, vol.82
, pp. 221-223
-
-
Gao, J.1
Heeger, A.J.2
Lee, J.Y.3
Kim, C.Y.4
-
16
-
-
33846569974
-
-
T. Hirao, Y. Otomaru, Y. Inoue, T. Moriuchi, T. Ogata, Y. Sato, Synth. Met. 2006, 156, 1378-1382.
-
(2006)
Synth. Met.
, vol.156
, pp. 1378-1382
-
-
Hirao, T.1
Otomaru, Y.2
Inoue, Y.3
Moriuchi, T.4
Ogata, T.5
Sato, Y.6
-
17
-
-
67650340637
-
-
For examples of small molecular HIMs, US Pat. 4720432
-
For examples of small molecular HIMs: a) S. A. VanSlyke, C. W. Tang, L. C. Roberts, US Pat. 4720432, 1988;
-
(1988)
-
-
VanSlyke, S.A.1
Tang, C.W.2
Roberts, L.C.3
-
18
-
-
0042520574
-
-
C. Hosokawa, H. Higashi, T. Kusumoto, Appl. Phys. Lett. 1993, 62, 3238 -3240;
-
(1993)
Appl. Phys. Lett.
, vol.62
, pp. 3238-3240
-
-
Hosokawa, C.1
Higashi, H.2
Kusumoto, T.3
-
19
-
-
0028491651
-
-
Y. Shirota, Y. Kuwabara, H. Inada, T. Wakimoto, H. Nakada, Y. Yonemoto, S. Kawami, K. Imai, Appl. Phys. Lett. 1994, 65, 807-809.
-
(1994)
Appl. Phys. Lett.
, vol.65
, pp. 807-809
-
-
Shirota, Y.1
Kuwabara, Y.2
Inada, H.3
Wakimoto, T.4
Nakada, H.5
Yonemoto, Y.6
Kawami, S.7
Imai, K.8
-
20
-
-
0028767281
-
-
For examples of polymeric HIMs
-
For examples of polymeric HIMs: a) Y. Yang, A. J. Heeger, Appl. Phys. Lett. 1994, 64, 1245 - 1247;
-
(1994)
Appl. Phys. Lett.
, vol.64
, pp. 1245-1247
-
-
Yang, Y.1
Heeger, A.J.2
-
21
-
-
0033898177
-
-
L. Groenendaal, F. Jonas, D. Freitag, H. Pielartzik, J. R. Reynolds, Adv. Mater. 2000, 12, 481 - 494;
-
(2000)
Adv. Mater.
, vol.12
, pp. 481-494
-
-
Groenendaal, L.1
Jonas, F.2
Freitag, D.3
Pielartzik, H.4
Reynolds, J.R.5
-
22
-
-
0036355927
-
-
K. Luan, T. Dao, J. Kido, J. Photopolym. Sci. Technol. 2002, 15, 261-264.
-
(2002)
J. Photopolym. Sci. Technol.
, vol.15
, pp. 261-264
-
-
Luan, K.1
Dao, T.2
Kido, J.3
-
23
-
-
67650337478
-
-
Formation of the dizincio intermediate was confirmed by a deuteration experiment by quenching the reaction mixture with D2O (98% yield, 93% D incorporation)
-
Formation of the dizincio intermediate was confirmed by a deuteration experiment by quenching the reaction mixture with D2O (98% yield, 93% D incorporation).
-
-
-
-
24
-
-
67650281114
-
-
Spectra and voltammograms are shown in Supporting Information
-
Spectra and voltammograms are shown in Supporting Information.
-
-
-
-
25
-
-
67650302506
-
-
We also measured photoluminescence of the BDPs (see Supporting Information). Details will be discussed elsewhere
-
We also measured photoluminescence of the BDPs (see Supporting Information). Details will be discussed elsewhere.
-
-
-
-
26
-
-
33747604897
-
-
M. Honda, K. Kanai, K. Komatsu, Y. Ouchi, H. Ishii, K. Seki, Mol. Cryst. Liq. Cryst. 2006, 455, 219-225.
-
(2006)
Mol. Cryst. Liq. Cryst.
, vol.455
, pp. 219-225
-
-
Honda, M.1
Kanai, K.2
Komatsu, K.3
Ouchi, Y.4
Ishii, H.5
Seki, K.6
-
27
-
-
67650324314
-
-
Partial aggregation occurred to form dark spots when the device B was fabricated, and the data were collected using a uniformly illuminating area. We also fabricated an OLED device including compound 3c (doped with PPB) as the HIL. However, significant aggregation occurred, and its OLED characteristics were exceptionally poor, probably because of the aggregation
-
Partial aggregation occurred to form dark spots when the device B was fabricated, and the data were collected using a uniformly illuminating area. We also fabricated an OLED device including compound 3c (doped with PPB) as the HIL. However, significant aggregation occurred, and its OLED characteristics were exceptionally poor, probably because of the aggregation.
-
-
-
|