-
8
-
-
33747694468
-
-
Lebel, O.; Maris, T.; Perron, M.-E.; Demers, E.; Wuest, J. D. J. Am. Chem. Soc. 2006, 128, 10372.
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 10372
-
-
Lebel, O.1
Maris, T.2
Perron, M.-E.3
Demers, E.4
Wuest, J.D.5
-
9
-
-
0034031562
-
-
For 1.3,5-triarylbenzene- and triarylamine-based systems, see: (a) Shirota, Y. I Mater. Chem. 2000, 10, 1.
-
For 1.3,5-triarylbenzene- and triarylamine-based systems, see: (a) Shirota, Y. I Mater. Chem. 2000, 10, 1.
-
-
-
-
12
-
-
34248326379
-
-
For spirobifluorene-based systems, see
-
(d) Forrest. S. R.: Thompson, M. E. Chem. Rev. 2007, 107, 923-1386. For spirobifluorene-based systems, see:
-
(2007)
Chem. Rev
, vol.107
, pp. 923-1386
-
-
Forrest, S.R.1
Thompson, M.E.2
-
13
-
-
0031381007
-
-
Salbeck, J.; Yu. N.; Bauer, J.: Weissörtel, F.: Bestgen,' H. Synth Met. 1997, 91, 209.
-
(e) Salbeck, J.; Yu. N.; Bauer, J.: Weissörtel, F.: Bestgen,' H. Synth Met. 1997, 91, 209.
-
-
-
-
14
-
-
0032184168
-
-
Johansson, N.: Salbeck, J.; Bauer, J.; Weissörtel. F.; Broms, P.; erson. A.; Salaneck. W. R. Adv. Mater. 1998, 10, 1136.
-
(f) Johansson, N.: Salbeck, J.; Bauer, J.; Weissörtel. F.; Broms, P.; erson. A.; Salaneck. W. R. Adv. Mater. 1998, 10, 1136.
-
-
-
-
15
-
-
0035900508
-
-
(g) Kim, Y.- H.: Shin, D.-C; Kim. S.-H.; Ko. C.-H.: Yu, H.-S.; Chae, Y.-S.: Kwon, S.-K. Adv. Mater. 2001, 13, 1690.
-
(2001)
Adv. Mater
, vol.13
, pp. 1690
-
-
Kim, Y.H.1
Shin, D.-C.2
Kim, S.-H.3
Ko, C.-H.4
Yu, H.-S.5
Chae, Y.-S.6
Kwon, S.-K.7
-
16
-
-
1542724644
-
-
For tetraarylmethane-based systems, see
-
(h) Shen. W.-J.; Dodda. R.; Wu, C.-C; Wu, F.-L; Liu, T.-H.; Chen. H.-H.; Chen, C. H.; Shu, C.-F. Chem. Mater. 2004, 16, 930. For tetraarylmethane-based systems, see:
-
(2004)
Chem. Mater
, vol.16
, pp. 930
-
-
Shen, W.-J.1
Dodda, R.2
Wu, C.-C.3
Wu, F.-L.4
Liu, T.-H.5
Chen, H.-H.6
Chen, C.H.7
Shu, C.-F.8
-
17
-
-
0034314775
-
-
(i) Robinson, M. R.; Wang, S.: Bazan, G. C; Cao, Y. Adv. Mater. 2000, 12, 1701.
-
(2000)
Adv. Mater
, vol.12
, pp. 1701
-
-
Robinson, M.R.1
Wang, S.2
Bazan, G.C.3
Cao, Y.4
-
18
-
-
0034697645
-
-
(j) Wang, S.; Oldham, W. J., Jr.; Hudack, R. A., Jr.; Bazan, G. C. J. Am. Chem. Soc. 2000, 122, 5695.
-
(2000)
J. Am. Chem. Soc
, vol.122
, pp. 5695
-
-
Wang, S.1
Oldham Jr., W.J.2
Hudack Jr., R.A.3
Bazan, G.C.4
-
19
-
-
0035657364
-
-
For hexaarvlbenzene-based systems, see
-
(k) Robinson, M. R.; Wang, S.; Heeger, A. J.; Bazan, G. C. Adv. Funct. Mater. 2001, 413. For hexaarvlbenzene-based systems, see:
-
(2001)
Adv. Funct. Mater
, pp. 413
-
-
Robinson, M.R.1
Wang, S.2
Heeger, A.J.3
Bazan, G.C.4
-
20
-
-
0033740678
-
-
Wu, I.-Y.; Lin, J. T.; Tao. Y.-T.: Balasubramaniam. E. Adv. Mater. 2000, 12, 668.
-
(2000)
Adv. Mater
, vol.12
, pp. 668
-
-
Wu, I.-Y.1
Lin, J.T.2
Tao, Y.-T.3
Balasubramaniam, E.4
-
21
-
-
27744492729
-
-
For benzocoronene-based hole-transporting systems, see
-
(m) Thomas, K. R. J.; Velusamy, M.; Lin, J. T.; Chuen, C. H.; Tao, Y.-T. J. Mater. Chem. 2005, 15, 4453. For benzocoronene-based hole-transporting systems, see:
-
(2005)
J. Mater. Chem
, vol.15
, pp. 4453
-
-
Thomas, K.R.J.1
Velusamy, M.2
Lin, J.T.3
Chuen, C.H.4
Tao, Y.-T.5
-
22
-
-
7244254381
-
-
For binaphthyl-based systems, see
-
(n) Wu, J.; Baumgarten, M.; Debije, M. G.; Warman, J. M.: Mullen, K. Angew. Chem., Int. Ed. 2004, 43, 5331. For binaphthyl-based systems, see:
-
(2004)
Angew. Chem., Int. Ed
, vol.43
, pp. 5331
-
-
Wu, J.1
Baumgarten, M.2
Debije, M.G.3
Warman, J.M.4
Mullen, K.5
-
23
-
-
0035887466
-
-
(o) Ostrowski, J. C; Hudack. R. A., Jr.; Robinson, M. R.; Wang, S.; Bazan, G. C. Chem.-Eur. J. 2001, 7, 4500.
-
(2001)
Chem.-Eur. J
, vol.7
, pp. 4500
-
-
Ostrowski, J.C.1
Hudack Jr., R.A.2
Robinson, M.R.3
Wang, S.4
Bazan, G.C.5
-
25
-
-
33745887771
-
-
For biphenyl-based systems, see
-
(q) He, Q.; Lin, H.; Weng, Y.; Zhang, B.; Wang, Z.; Lei, G.; Wang, L.; Qiu, Y.; Bai, F. Adp. Funct. Mater. 2006, 16, 1343. For biphenyl-based systems, see:
-
(2006)
Adp. Funct. Mater
, vol.16
, pp. 1343
-
-
He, Q.1
Lin, H.2
Weng, Y.3
Zhang, B.4
Wang, Z.5
Lei, G.6
Wang, L.7
Qiu, Y.8
Bai, F.9
-
26
-
-
0043236540
-
-
(r) He, F.; Cheng, G.; Zhang, H.; Zheng, Y.; Xte, Z.; Yang, B.; Ma, Y.; Liu, S.; Shen, J. Chem. Common. 2003, 2206.
-
(2003)
Chem. Common
, pp. 2206
-
-
He, F.1
Cheng, G.2
Zhang, H.3
Zheng, Y.4
Xte, Z.5
Yang, B.6
Ma, Y.7
Liu, S.8
Shen, J.9
-
27
-
-
5044221190
-
-
(s) He, F.; Xia, H.; Tang. S.; Duan, Y.; Zheng, M.; Liu, L.; Li, M.; Zhang, H.; Yang. B.; Ma, Y.; Liu, S.; Shen, J. J. Mater. Chem. 2004, 14, 2735.
-
(2004)
J. Mater. Chem
, vol.14
, pp. 2735
-
-
He, F.1
Xia, H.2
Tang, S.3
Duan, Y.4
Zheng, M.5
Liu, L.6
Li, M.7
Zhang, H.8
Yang, B.9
Ma, Y.10
Liu, S.11
Shen, J.12
-
28
-
-
27944496551
-
-
(t) He, F.; Xu, H.; Yang, B.; Duan, Y.; Tian, L.; Huang, K.; Ma, Y.; Liu, S.; Feng, S.; Shen. J. Adv. Mater. 2005, 17, 2710.
-
(2005)
Adv. Mater
, vol.17
, pp. 2710
-
-
He, F.1
Xu, H.2
Yang, B.3
Duan, Y.4
Tian, L.5
Huang, K.6
Ma, Y.7
Liu, S.8
Feng, S.9
Shen, J.10
-
29
-
-
26844546343
-
-
Xie, /.: Yang, B.; Li, F.; Cheng. G.; Liu, L.; Yang, G.; Xu, H.; Ye, L.; Hanif, M.; Liu, S.; Ma, D.; Ma, Y. J. Am. Chem. Soc. 2005, 127, 14152.
-
(u) Xie, /.: Yang, B.; Li, F.; Cheng. G.; Liu, L.; Yang, G.; Xu, H.; Ye, L.; Hanif, M.; Liu, S.; Ma, D.; Ma, Y. J. Am. Chem. Soc. 2005, 127, 14152.
-
-
-
-
30
-
-
12844281636
-
-
(a) Natarajan, R.; Savitha, G.; Moorthy, J. N. Cryst. Growth Des. 2005, 5, 69.
-
(2005)
Cryst. Growth Des
, vol.5
, pp. 69
-
-
Natarajan, R.1
Savitha, G.2
Moorthy, J.N.3
-
31
-
-
17044380939
-
-
(b) Natarajan, R.; Savitha, G.; Dominiak, P.; Wozniak, K.; Moorthy. J. N. Angew. Chem., Int. Ed 2005, 44, 2115.
-
(2005)
Angew. Chem., Int. Ed
, vol.44
, pp. 2115
-
-
Natarajan, R.1
Savitha, G.2
Dominiak, P.3
Wozniak, K.4
Moorthy, J.N.5
-
32
-
-
26844432217
-
-
(c) Moorthy, J. N.; Natarajan, R.; Venugopalan, P. J. Org. Chem. 2005, 70, 8568.
-
(2005)
J. Org. Chem
, vol.70
, pp. 8568
-
-
Moorthy, J.N.1
Natarajan, R.2
Venugopalan, P.3
-
33
-
-
33646355429
-
-
(d) Moorthy, J. N.; Natarajan, R.; Savitha, G.; Venugopalan, P. Cryst. Growth Des. 2006, 6, 919.
-
(2006)
Cryst. Growth Des
, vol.6
, pp. 919
-
-
Moorthy, J.N.1
Natarajan, R.2
Savitha, G.3
Venugopalan, P.4
-
34
-
-
42649118125
-
-
In our recent preliminary investigations, we have shown that diary-laminobiphenyl-functionalized bimesityls serve as blue light emitting materials; see: (a) Moorthy, J. N, Venkatakrishanan, P, Huang, D, F, Chow, T. J. Chem. Comntun. 2008, 2146
-
In our recent preliminary investigations, we have shown that diary-laminobiphenyl-functionalized bimesityls serve as blue light emitting materials; see: (a) Moorthy, J. N.; Venkatakrishanan, P.; Huang, D.- F.; Chow, T. J. Chem. Comntun. 2008, 2146.
-
-
-
-
35
-
-
68549116889
-
-
Kafafi, Z. Ft, Ed, Optical Engineering 94; Taylor and Francis: Boca Raton, FL
-
(a) Organic Electroluminescence: Kafafi, Z. Ft., Ed.; Optical Engineering Vol. 94; Taylor and Francis: Boca Raton, FL, 2005.
-
(2005)
Organic Electroluminescence
-
-
-
36
-
-
67849132581
-
-
Shirota, Y. In Organic Electroluminescence: Kafafi, Z. H., Ed.; Optical Engineering, 94; Taylor and Francis: Boca Raton, FL, 2005; Chapter 4, p 147.
-
(b) Shirota, Y. In Organic Electroluminescence: Kafafi, Z. H., Ed.; Optical Engineering, Vol. 94; Taylor and Francis: Boca Raton, FL, 2005; Chapter 4, p 147.
-
-
-
-
37
-
-
84913521777
-
-
(a) Kasha, M.; Rawls, H. R.; Bayoumi, M. A. Pure Appl. Chem. 1965, 11, 371.
-
(1965)
Pure Appl. Chem
, vol.11
, pp. 371
-
-
Kasha, M.1
Rawls, H.R.2
Bayoumi, M.A.3
-
39
-
-
0033154109
-
-
(c) Moffitt, M.; Farmha, J. P. S.; Winnik, M. A.; Rohr, U.; Mullen, K. Macromolecules 1999, 32, 4895.
-
(1999)
Macromolecules
, vol.32
, pp. 4895
-
-
Moffitt, M.1
Farmha, J.P.S.2
Winnik, M.A.3
Rohr, U.4
Mullen, K.5
-
40
-
-
0035906799
-
-
(d) Wurthner, F.; Thalacker, C; Dieke, S.; Tschierske, C. Chem.-Eur. J. 2001, 7, 2245.
-
(2001)
Chem.-Eur. J
, vol.7
, pp. 2245
-
-
Wurthner, F.1
Thalacker, C.2
Dieke, S.3
Tschierske, C.4
-
41
-
-
0035908561
-
-
(a) Cornil. J.; Beljonne, D.; Calbert, J. P.; Bréd as. J. L. Adv. Mater. 2001, 13, 1053.
-
(2001)
Adv. Mater
, vol.13
, pp. 1053
-
-
Cornil, J.1
Beljonne, D.2
Calbert, J.P.3
Bréd as, J.L.4
-
42
-
-
3843120891
-
-
Hallenx, V. de.; Calbert. J. P.; Brocorens, P.; Cornil, J.; Delercq, J. P.; Brédas, J. L. Adv. Fund. Mater. 2004, 14, 649.
-
(b) Hallenx, V. de.; Calbert. J. P.; Brocorens, P.; Cornil, J.; Delercq, J. P.; Brédas, J. L. Adv. Fund. Mater. 2004, 14, 649.
-
-
-
-
43
-
-
0032542579
-
-
(c) Cornil, J.; dos Santos, D. A.; Crispin, X.; Silbey. R.; Brédas, J. L. J. Am. Chem. Soc. 1998, 120, 1289.
-
(1998)
J. Am. Chem. Soc
, vol.120
, pp. 1289
-
-
Cornil, J.1
dos Santos, D.A.2
Crispin, X.3
Silbey, R.4
Brédas, J.L.5
-
44
-
-
26844546343
-
-
(d) Xie, Z.; Yang, B.; Li, F.; Cheng, G.; Liu. L.; Yang, G.; Xu. H.; Ye, L.; Hanif, M.; Liu, S.; Ma, D.; Ma, Y. J. Am. Chem. Soc. 2005, 127, 14152.
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 14152
-
-
Xie, Z.1
Yang, B.2
Li, F.3
Cheng, G.4
Liu, L.5
Yang, G.6
Xu, H.7
Ye, L.8
Hanif, M.9
Liu, S.10
Ma, D.11
Ma, Y.12
-
45
-
-
28444474554
-
-
Thompson. A. L.; Ahn. T. S.; Thomas. K. R. J.; Thayumanavan, S.; Martinez. T. J.: Bardeen, C. J. J. Am. Chem. Soc. 2005, 127. 16348.
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 16348
-
-
Thompson, A.L.1
Ahn, T.S.2
Thomas, K.R.J.3
Thayumanavan, S.4
Martinez, T.J.5
Bardeen, C.J.6
-
47
-
-
0010831076
-
Cross-Coupling Reactions: A Practical Guide
-
Miyaura, N, Ed, Springer Verlag: New York
-
(b) Miyaura, N., Ed. Cross-Coupling Reactions: A Practical Guide; Topics in Current Chemistry Series 219; Springer Verlag: New York, 2002.
-
(2002)
Topics in Current Chemistry Series
, vol.219
-
-
-
48
-
-
0035900508
-
-
For example, see: (a) Kim, Y. H.; Shin, D. C; Kim, S, H.: Ko, C. H.; Yu, H. S.; Chae, Y. S.; Kwon. S. K. Adv. Mater. 2001, 13, 1690.
-
For example, see: (a) Kim, Y. H.; Shin, D. C; Kim, S, H.: Ko, C. H.; Yu, H. S.; Chae, Y. S.; Kwon. S. K. Adv. Mater. 2001, 13, 1690.
-
-
-
-
49
-
-
27744507755
-
-
(b) Kim, Y. H.; Jeong, H. C; Kim, S. H.: Yang, K.; Kwon. S. K. Adv. Funct. Mater. 2005, 15, 1799.
-
(2005)
Adv. Funct. Mater
, vol.15
, pp. 1799
-
-
Kim, Y.H.1
Jeong, H.C.2
Kim, S.H.3
Yang, K.4
Kwon, S.K.5
-
51
-
-
0032163035
-
-
(d) Klärner, G.; Davey. M. H.: Chen. W. D.; Scott. J. C; Miller. R. D. Adv. Mater. 1998, 10, 993.
-
(1998)
Adv. Mater
, vol.10
, pp. 993
-
-
Klärner, G.1
Davey, M.H.2
Chen, W.D.3
Scott, J.C.4
Miller, R.D.5
-
57
-
-
42149136146
-
-
Only strong electrostatic interaction between electrochemically generated di-ions of opposite charges leads to excimer emission with a characteristic broad and red-shifted emission in sterically hindered phenylanthracene- functionalized spirobifluorenes; see: Sartin, M, Shu. C; Bard, A. J. J. Am. Chem. Soc. 2008, 130, 5354
-
Only strong electrostatic interaction between electrochemically generated di-ions of opposite charges leads to excimer emission with a characteristic broad and red-shifted emission in sterically hindered phenylanthracene- functionalized spirobifluorenes; see: Sartin, M.; Shu. C; Bard, A. J. J. Am. Chem. Soc. 2008, 130, 5354.
-
-
-
-
58
-
-
67849089802
-
-
The differences in the emission spectra for spin-coated and vacuum-deposited films point to differences in the molecular arrangements in the two films
-
The differences in the emission spectra for spin-coated and vacuum-deposited films point to differences in the molecular arrangements in the two films.
-
-
-
-
59
-
-
0031381007
-
-
Salbeck. J.; Yu, N.; Bauer. J.; Weissortel, F.; Bestgen. H. Synth. Met. 1997, 91, 209.
-
(1997)
Synth. Met
, vol.91
, pp. 209
-
-
Salbeck, J.1
Yu, N.2
Bauer, J.3
Weissortel, F.4
Bestgen, H.5
-
61
-
-
67849131840
-
-
When the films were subjected to heat treatment (annealing) under vacuum, the emission intensity of the films was found to decrease considerably by 2-3-fold with a broadening in their spectral profiles. Presumably, the annealing leads to some kind of reorganization of the molecules within the amorphous film in a way that the emission is suppressed. That the thermal heating does not lead to recrystallization was established from powder XRD of the bimesitylenes 1 and 5 before and after annealing; cf. the SI.
-
When the films were subjected to heat treatment (annealing) under vacuum, the emission intensity of the films was found to decrease considerably by 2-3-fold with a broadening in their spectral profiles. Presumably, the annealing leads to some kind of reorganization of the molecules within the amorphous film in a way that the emission is suppressed. That the thermal heating does not lead to recrystallization was established from powder XRD of the bimesitylenes 1 and 5 before and after annealing; cf. the SI.
-
-
-
-
62
-
-
8644265990
-
-
For use of MADN as a dopant, see: a
-
For use of MADN as a dopant, see: (a) Lee. M. T.; Chen, H. H.; Liao, C. H.; Tsai, C. H.; Chen, C. H. Appl. Phys. Lett. 2004, 85, 3301.
-
(2004)
Appl. Phys. Lett
, vol.85
, pp. 3301
-
-
Lee, M.T.1
Chen, H.H.2
Liao, C.H.3
Tsai, C.H.4
Chen, C.H.5
-
63
-
-
27144463154
-
-
(b) Lee, M. T.; Liao, C. H.; Tsai, C. H.; Chen. C. H. Adv. Mater. 2005, 17, 2493.
-
(2005)
Adv. Mater
, vol.17
, pp. 2493
-
-
Lee, M.T.1
Liao, C.H.2
Tsai, C.H.3
Chen, C.H.4
-
64
-
-
0034314775
-
-
For use of PVK as a host, see
-
For use of PVK as a host, see: Robinson, M. R.; Wang, S.; Bazan, G. C; Cao, Y. Adv. Mater. 2000, 12, 1701.
-
(2000)
Adv. Mater
, vol.12
, pp. 1701
-
-
Robinson, M.R.1
Wang, S.2
Bazan, G.C.3
Cao, Y.4
-
65
-
-
0001376595
-
-
(a) Kim, Y. H.; Kwon, S. K.; Yoo, D. S.; Rubner, M. F.; Wrighton, M. S. Chem. Mater. 1997, 9, 2699.
-
(1997)
Chem. Mater
, vol.9
, pp. 2699
-
-
Kim, Y.H.1
Kwon, S.K.2
Yoo, D.S.3
Rubner, M.F.4
Wrighton, M.S.5
-
69
-
-
0037010139
-
-
(e) Shih, H. T.; Lin, C. H.; Shih. H. H.; Cheng, C. H. Adv. Mater. 2002, 14, 1409.
-
(2002)
Adv. Mater
, vol.14
, pp. 1409
-
-
Shih, H.T.1
Lin, C.H.2
Shih, H.H.3
Cheng, C.H.4
-
70
-
-
0036734716
-
-
(f) Danel. K.; Hwang, T. H.; Lin, J. T.; Tao, Y. T.; Chen, C. H. Chem. Mater. 2002, 14, 3860.
-
(2002)
Chem. Mater
, vol.14
, pp. 3860
-
-
Danel, K.1
Hwang, T.H.2
Lin, J.T.3
Tao, Y.T.4
Chen, C.H.5
-
71
-
-
67849086129
-
-
(g) Yu, M. X.; Duan, J. P.; Lin, C. H.; Chung, C. H.; Tao, Y. T. Chem. Mater. 2002, 14, 3948.
-
(2002)
Chem. Mater
, vol.14
, pp. 3948
-
-
Yu, M.X.1
Duan, J.P.2
Lin, C.H.3
Chung, C.H.4
Tao, Y.T.5
-
73
-
-
24044514322
-
-
7, 3717. For a very recent synthesis and electroluminescence study on 2-fold anthracene-functionalized tetraarylsilicon, see
-
(a) Chiang, C. L.; Shu, C. R; Chen, C. T. Org. Lett. 2005, 7, 3717. For a very recent synthesis and electroluminescence study on 2-fold anthracene-functionalized tetraarylsilicon, see:
-
(2005)
Org. Lett
-
-
Chiang, C.L.1
Shu, C.R.2
Chen, C.T.3
-
74
-
-
54949149871
-
-
(b) Lyu, Y-Y.; Kwak, J.; Lee, S.-H.; Kim, D.; Lee, C; Char, K. adv. Mater. 2008, 20, 2720.
-
(2008)
adv. Mater
, vol.20
, pp. 2720
-
-
Lyu, Y.-Y.1
Kwak, J.2
Lee, S.-H.3
Kim, D.4
Lee, C.5
Char, K.6
-
75
-
-
0031123727
-
-
Toktto, S.; Tanaka, H.; Noda, K.; Okada, A.; Taga, T. Appl. Phys. Lett. 1997, 70, 1929.
-
(1997)
Appl. Phys. Lett
, vol.70
, pp. 1929
-
-
Toktto, S.1
Tanaka, H.2
Noda, K.3
Okada, A.4
Taga, T.5
-
77
-
-
1542724644
-
-
(a) Shen, W.-J.; Dodda, R.; Wu, C.-C; Wu, F.-I; Liu, T.-H.; Chen, H.-H.; Chen, C. H.; Shu, C.-F. Chem, Mater. 2004, 16, 930.
-
(2004)
Chem, Mater
, vol.16
, pp. 930
-
-
Shen, W.-J.1
Dodda, R.2
Wu, C.-C.3
Wu, F.-I.4
Liu, T.-H.5
Chen, H.-H.6
Chen, C.H.7
Shu, C.-F.8
-
78
-
-
0035900508
-
-
b
-
(b) Kim. Y.-H.; Shin, D.-C; Kim, S.-H.; Ko, C.-H.; Yu. H.-S.; Chae. Y.-S.; Kwon. S.-K. Adv. Mater. 2001, 13, 1690.
-
(2001)
Adv. Mater
, vol.13
, pp. 1690
-
-
Kim, Y.-H.1
Shin, D.-C.2
Kim, S.-H.3
Ko, C.-H.4
Yu, H.-S.5
Chae, Y.-S.6
Kwon, S.-K.7
-
79
-
-
0344445374
-
-
(c) Benmansour, H.; Shioya, T.; Sato, Y.; Bazan, G. C. Adv. Funct. Mater. 2003, 13, 883.
-
(2003)
Adv. Funct. Mater
, vol.13
, pp. 883
-
-
Benmansour, H.1
Shioya, T.2
Sato, Y.3
Bazan, G.C.4
-
80
-
-
36049044211
-
-
(d) Shih, P.-L; Chuang, C.-Y.; Chien, C.-H.; Diau, E. W.-G.; Shu. C.-F. Adv. Funct. Mater. 2007, 17, 3141.
-
(2007)
Adv. Funct. Mater
, vol.17
, pp. 3141
-
-
Shih, P.-L.1
Chuang, C.-Y.2
Chien, C.-H.3
Diau, E.W.-G.4
Shu, C.-F.5
-
81
-
-
27744507755
-
-
(e) Kim, Y.-H.; Jeong, H.-C; Kim, S.-H.; Yang. K.; Kwon, S.-K. Adv. Funct. Mater. 2005, 15, 1799.
-
(2005)
Adv. Funct. Mater
, vol.15
, pp. 1799
-
-
Kim, Y.-H.1
Jeong, H.-C.2
Kim, S.-H.3
Yang, K.4
Kwon, S.-K.5
-
82
-
-
27144463154
-
-
(f) Lee. M.-T.; Liao, C.-H.; Tsai, C.-H.; Chen, C. H. Adv. Mater. 2005, 17, 2493.
-
(2005)
Adv. Mater
, vol.17
, pp. 2493
-
-
Lee, M.-T.1
Liao, C.-H.2
Tsai, C.-H.3
Chen, C.H.4
-
83
-
-
0037450558
-
-
(g) Zhang, X. H.; Liu, M. W.; Wong, O. Y.; Lee, C. S.; Kwong, H. L.; Lee, S. T.; Wu, S. K. Chem. Phys. Lett. 2003, 369, 478.
-
(2003)
Chem. Phys. Lett
, vol.369
, pp. 478
-
-
Zhang, X.H.1
Liu, M.W.2
Wong, O.Y.3
Lee, C.S.4
Kwong, H.L.5
Lee, S.T.6
Wu, S.K.7
-
84
-
-
7444259701
-
-
(h) Tao, S. L.; Hong, Z. R.; Peng, Z. K.; Ju, W. G.; Zhang, X. H.; Wang. P. F.; Wu, S. K.; Lee. S. T. Chem. Phys. Lett. 2004, 397, 1.
-
(2004)
Chem. Phys. Lett
, vol.397
, pp. 1
-
-
Tao, S.L.1
Hong, Z.R.2
Peng, Z.K.3
Ju, W.G.4
Zhang, X.H.5
Wang, P.F.6
Wu, S.K.7
Lee, S.T.8
-
86
-
-
1642604055
-
-
(j) Kan. Y.; Wang, L.; Duan, L.; Hu. Y.; Wu, G.; Qiu, Y. Appl. Phys. Lett. 2004, 84, 1513.
-
(2004)
Appl. Phys. Lett
, vol.84
, pp. 1513
-
-
Kan, Y.1
Wang, L.2
Duan, L.3
Hu, Y.4
Wu, G.5
Qiu, Y.6
-
87
-
-
33947262435
-
-
(k) Li. H.-C; Lin. Y.-P.; Chou. P.-T.; Cheng, Y.-M.; Liu. R.-S. Adv. Funct. Mater. 2007, 17, 520.
-
(2007)
Adv. Funct. Mater
, vol.17
, pp. 520
-
-
Li, H.-C.1
Lin, Y.-P.2
Chou, P.-T.3
Cheng, Y.-M.4
Liu, R.-S.5
-
88
-
-
0037450558
-
-
(a) Zhang. X. H.; Liu. M. W.; Wong. O. Y.; Lee. C. S.; Kwong, H. L.; Lee, S. T.; Wu, S. K. Chem. Phys. Lett. 2003, 369, 478.
-
(2003)
Chem. Phys. Lett
, vol.369
, pp. 478
-
-
Zhang, X.H.1
Liu, M.W.2
Wong, O.Y.3
Lee, C.S.4
Kwong, H.L.5
Lee, S.T.6
Wu, S.K.7
-
89
-
-
79956034847
-
-
Cheon, K. O.; Shinar, J. A^pl. Phys. Lett. 2002, 81, 1738.
-
(b) Cheon, K. O.; Shinar, J. A^pl. Phys. Lett. 2002, 81, 1738.
-
-
-
-
90
-
-
84985330460
-
-
For example, see
-
For example, see: Kido. J.; Hongawa. K.; Nagai, K. Macromol. Symp. 1994, 84, 81.
-
(1994)
Macromol. Symp
, vol.84
, pp. 81
-
-
Kido, J.1
Hongawa, K.2
Nagai, K.3
|