-
1
-
-
82955163987
-
Highly efficient and stable deep-blue emitting anthracene-derived molecular glass for versatile types of non-doped OLED applications
-
I. Cho, S.H. Kim, J.H. Kim, S. Park, and S.Y. Park Highly efficient and stable deep-blue emitting anthracene-derived molecular glass for versatile types of non-doped OLED applications J Mater Chem 22 2012 123 129
-
(2012)
J Mater Chem
, vol.22
, pp. 123-129
-
-
Cho, I.1
Kim, S.H.2
Kim, J.H.3
Park, S.4
Park, S.Y.5
-
2
-
-
35948958950
-
A novel ambipolar spirobifluorene derivative that behaves as an efficient blue-light emitter in organic light-emitting diodes
-
Y.L. Liao, C.Y. Lin, K.T. Wong, T.H. Hou, and W.Y. Hung A novel ambipolar spirobifluorene derivative that behaves as an efficient blue-light emitter in organic light-emitting diodes Org Lett 9 2007 4511 4514
-
(2007)
Org Lett
, vol.9
, pp. 4511-4514
-
-
Liao, Y.L.1
Lin, C.Y.2
Wong, K.T.3
Hou, T.H.4
Hung, W.Y.5
-
3
-
-
80054945551
-
Density functional theory study of photophysical properties of Iridium(III) complexes with phenylisoquinoline and phenylpyridine ligands
-
X. Li, B. Minaev, H. Ågren, and H. Tian Density functional theory study of photophysical properties of Iridium(III) complexes with phenylisoquinoline and phenylpyridine ligands J Phys Chem C 115 2011 20724 20731
-
(2011)
J Phys Chem C
, vol.115
, pp. 20724-20731
-
-
Li, X.1
Minaev, B.2
Ågren, H.3
Tian, H.4
-
4
-
-
79951667838
-
Bipolar anthracene derivatives containing hole and electron-transporting moieties for highly efficient blue electroluminescence devices
-
J.H. Huang, J.H. Su, X. Li, M.K. Lam, K.M. Fung, and H.H. Fan Bipolar anthracene derivatives containing hole and electron-transporting moieties for highly efficient blue electroluminescence devices J Mater Chem 21 2011 2957 2964
-
(2011)
J Mater Chem
, vol.21
, pp. 2957-2964
-
-
Huang, J.H.1
Su, J.H.2
Li, X.3
Lam, M.K.4
Fung, K.M.5
Fan, H.H.6
-
5
-
-
21544459113
-
Organic electroluminescent diodes
-
C.W. Tang, and S.A. Vanslyke Organic electroluminescent diodes Appl Phys Lett 51 1987 913 915
-
(1987)
Appl Phys Lett
, vol.51
, pp. 913-915
-
-
Tang, C.W.1
Vanslyke, S.A.2
-
6
-
-
0030573843
-
Organic electroluminescent devices with improved stability
-
C.W. Tang, S.A. Vanslyke, and C.H. Chen Organic electroluminescent devices with improved stability Appl Phys Lett 69 1996 2160 2162
-
(1996)
Appl Phys Lett
, vol.69
, pp. 2160-2162
-
-
Tang, C.W.1
Vanslyke, S.A.2
Chen, C.H.3
-
7
-
-
79957455344
-
Considerable improvement in the stability of solution processed small molecule OLED by annealing
-
G.L. Mao, Z.X. Wua, Q. He, B. Jiao, G.J. Xu, and X. Hou Considerable improvement in the stability of solution processed small molecule OLED by annealing Appl Surf Sci 257 2011 7394 7398
-
(2011)
Appl Surf Sci
, vol.257
, pp. 7394-7398
-
-
Mao, G.L.1
Wua, Z.X.2
He, Q.3
Jiao, B.4
Xu, G.J.5
Hou, X.6
-
8
-
-
33646492835
-
Organic light-emitting diode (OLED) technology: Materials, devices and display technologies
-
B. Geffroy, P. Roy, and C. Prat Organic light-emitting diode (OLED) technology: materials, devices and display technologies Polym Int 55 2006 572 582
-
(2006)
Polym Int
, vol.55
, pp. 572-582
-
-
Geffroy, B.1
Roy, P.2
Prat, C.3
-
9
-
-
80053383215
-
Synthesis and optoelectronic properties of symmetric thiophene based 2,5-disubstiuted 1,3,4-oxadiazoles: Highly fluorescent materials for OLED applications
-
S.I. Panchamukhi, N. Belavagi, M.H. Rabinal, and I.A. Khazi Synthesis and optoelectronic properties of symmetric thiophene based 2,5-disubstiuted 1,3,4-oxadiazoles: highly fluorescent materials for OLED applications J Fluoresc 21 2011 1515 1519
-
(2011)
J Fluoresc
, vol.21
, pp. 1515-1519
-
-
Panchamukhi, S.I.1
Belavagi, N.2
Rabinal, M.H.3
Khazi, I.A.4
-
10
-
-
65349127828
-
Synthesis of light-emitting conjugated polymers for applications in electroluminescent devices
-
A.C. Grimsdale, K.L. Chan, R.E. Martin, P.G. Jokisz, and A.B. Holmes Synthesis of light-emitting conjugated polymers for applications in electroluminescent devices Chem Rev 109 2009 897 1091
-
(2009)
Chem Rev
, vol.109
, pp. 897-1091
-
-
Grimsdale, A.C.1
Chan, K.L.2
Martin, R.E.3
Jokisz, P.G.4
Holmes, A.B.5
-
11
-
-
4243893235
-
Conjugated poly(thiophenes): Synthesis, functionalization, and applications
-
J. Roncali Conjugated poly(thiophenes): synthesis, functionalization, and applications Chem Rev 92 1992 711 738
-
(1992)
Chem Rev
, vol.92
, pp. 711-738
-
-
Roncali, J.1
-
12
-
-
33748766325
-
Photochromic thiophene oligomers based on bisthienylethene: Synthesis, photochromic and two-photon properties
-
Y.L. Feng, Y.L. Yan, S. Wang, W.H. Zhu, S.X. Qian, and H. Tian Photochromic thiophene oligomers based on bisthienylethene: synthesis, photochromic and two-photon properties J Mater Chem 16 2006 3685 3692
-
(2006)
J Mater Chem
, vol.16
, pp. 3685-3692
-
-
Feng, Y.L.1
Yan, Y.L.2
Wang, S.3
Zhu, W.H.4
Qian, S.X.5
Tian, H.6
-
13
-
-
33646527615
-
X-shaped electroactive molecular materials based on oligothiophene architectures: Facile synthesis and photophysical and electrochemical properties
-
X.B. Sun, Y.Q. Liu, S.Y. Chen, W.F. Qiu, G. Yu, and Y.Q. Ma X-shaped electroactive molecular materials based on oligothiophene architectures: facile synthesis and photophysical and electrochemical properties Adv Funct Mater 16 2006 917 925
-
(2006)
Adv Funct Mater
, vol.16
, pp. 917-925
-
-
Sun, X.B.1
Liu, Y.Q.2
Chen, S.Y.3
Qiu, W.F.4
Yu, G.5
Ma, Y.Q.6
-
14
-
-
64649106986
-
Functional oligothiophenes: Molecular design for multidimensional nanoarchitectures and their applications
-
A. Mishra, C.Q. Ma, and P. Bäuerle Functional oligothiophenes: molecular design for multidimensional nanoarchitectures and their applications Chem Rev 109 2009 1141 1276
-
(2009)
Chem Rev
, vol.109
, pp. 1141-1276
-
-
Mishra, A.1
Ma, C.Q.2
Bäuerle, P.3
-
15
-
-
84862946751
-
Replacing phenyl ring with thiophene: An approach to longer wavelength aza-dipyrromethene boron difluoride (aza-BODIPY) dyes
-
X.F. Zhang, H.B. Yu, and Y. Xiao Replacing phenyl ring with thiophene: an approach to longer wavelength aza-dipyrromethene boron difluoride (aza-BODIPY) dyes J Org Chem 77 2012 669 673
-
(2012)
J Org Chem
, vol.77
, pp. 669-673
-
-
Zhang, X.F.1
Yu, H.B.2
Xiao, Y.3
-
16
-
-
84855334382
-
Thiophene-containing Pechmann dyes and related compounds: Synthesis and experimental and DFT characterisation
-
E.A.B. Kantchev, T.B. Norsten, M.L.Y. Tan, J.J.Y. Ng, and M.B. Sullivan Thiophene-containing Pechmann dyes and related compounds: synthesis and experimental and DFT characterisation Chem Eur J 18 2012 695 708
-
(2012)
Chem Eur J
, vol.18
, pp. 695-708
-
-
Kantchev, E.A.B.1
Norsten, T.B.2
Tan, M.L.Y.3
Ng, J.J.Y.4
Sullivan, M.B.5
-
17
-
-
61449218879
-
A red doped OLEDS with a good device performance at high doping concentration
-
G.Y. Ryu, J.H. Seo, J.H. Park, S.G. Lee, S.H. Lim, and D.M. Shin A red doped OLEDS with a good device performance at high doping concentration Mol Cryst Liq Cryst 499 2009 397 406
-
(2009)
Mol Cryst Liq Cryst
, vol.499
, pp. 397-406
-
-
Ryu, G.Y.1
Seo, J.H.2
Park, J.H.3
Lee, S.G.4
Lim, S.H.5
Shin, D.M.6
-
18
-
-
0027678070
-
Efficient light-emitting diodes based on polymers with high electron affinities
-
N.C. Greenham, S.C. Moratti, D.D.C. Bradley, R.H. Friend, and A.B. Holmes Efficient light-emitting diodes based on polymers with high electron affinities Nature 365 1993 628 630
-
(1993)
Nature
, vol.365
, pp. 628-630
-
-
Greenham, N.C.1
Moratti, S.C.2
Bradley, D.D.C.3
Friend, R.H.4
Holmes, A.B.5
-
19
-
-
33750507480
-
Fabrication of photoluminescent dyes/poly(acrylonitrile) coaxial nanotubes using vapor deposition polymerization
-
J.L. Kyung, H.O. Joon, K. Younggeun, and J. Jyongsik Fabrication of photoluminescent dyes/poly(acrylonitrile) coaxial nanotubes using vapor deposition polymerization Chem Mater 18 2006 5002 5008
-
(2006)
Chem Mater
, vol.18
, pp. 5002-5008
-
-
Kyung, J.L.1
Joon, H.O.2
Younggeun, K.3
Jyongsik, J.4
-
20
-
-
0027930603
-
Condensation reactions in water of active methylene compounds with arylaldehydes: One-pot synthesis of flavonols
-
F. Ringuelli, G. Pani, O. Piermatti, and F. Pizzo Condensation reactions in water of active methylene compounds with arylaldehydes: one-pot synthesis of flavonols Tetrahedron 50 1994 11499 11508
-
(1994)
Tetrahedron
, vol.50
, pp. 11499-11508
-
-
Ringuelli, F.1
Pani, G.2
Piermatti, O.3
Pizzo, F.4
-
21
-
-
0001246451
-
Direct synthesis of alpha, beta-unsaturated nitriles catalyzed by nonionic superbases
-
B.A. D'Sa, P. Kisanga, and J.G. Verkade Direct synthesis of alpha, beta-unsaturated nitriles catalyzed by nonionic superbases J Org Chem 63 1998 3961 3967
-
(1998)
J Org Chem
, vol.63
, pp. 3961-3967
-
-
D'Sa, B.A.1
Kisanga, P.2
Verkade, J.G.3
-
22
-
-
60349115857
-
Crystal structure and synthesis of benzimidazole substituted acrylonitriles and benzimidazo[1, 2-a]quinolines
-
M. Hranjec, G. Pavlovic, and G.K. Zamola Crystal structure and synthesis of benzimidazole substituted acrylonitriles and benzimidazo[1, 2-a]quinolines Struct Chem 20 2009 91 99
-
(2009)
Struct Chem
, vol.20
, pp. 91-99
-
-
Hranjec, M.1
Pavlovic, G.2
Zamola, G.K.3
-
23
-
-
2542511764
-
Novel synthesis of a new class of strongly fluorescent phenanthridine analogues
-
G.E.H. Elgemeie, A.M.E. Attiab, and N.M. Fathyc Novel synthesis of a new class of strongly fluorescent phenanthridine analogues J Chem Res 1997 112 113
-
(1997)
J Chem Res
, pp. 112-113
-
-
Elgemeie, G.E.H.1
Attiab, A.M.E.2
Fathyc, N.M.3
-
24
-
-
33847050909
-
Luminescence properties of aminobenzanthrones and their application as host emitters in organic light-emitting devices
-
M.X. Yu, L.C. Chang, C.H. Lin, J.P. Duan, F.I. Wu, and I.C. Chen Luminescence properties of aminobenzanthrones and their application as host emitters in organic light-emitting devices Adv Funct Mater 17 2007 369 378
-
(2007)
Adv Funct Mater
, vol.17
, pp. 369-378
-
-
Yu, M.X.1
Chang, L.C.2
Lin, C.H.3
Duan, J.P.4
Wu, F.I.5
Chen, I.C.6
-
25
-
-
67349108080
-
The synthesis and photophysical properties of novel triphenylamine derivatives containing α, β-diarylacrylonitrile
-
Y.F. Yue, J.H. Kang, and M.X. Yu The synthesis and photophysical properties of novel triphenylamine derivatives containing α, β-diarylacrylonitrile Dyes Pigments 83 2009 72 80
-
(2009)
Dyes Pigments
, vol.83
, pp. 72-80
-
-
Yue, Y.F.1
Kang, J.H.2
Yu, M.X.3
-
26
-
-
16244386901
-
Study on synthesis of organic light emitting diode materials of aminoanthrancenes and their light emitting property
-
M.X. Yu, X.H. Chen, and C.H. Cheng Study on synthesis of organic light emitting diode materials of aminoanthrancenes and their light emitting property Chin J Org Chem 25 2005 218 221
-
(2005)
Chin J Org Chem
, vol.25
, pp. 218-221
-
-
Yu, M.X.1
Chen, X.H.2
Cheng, C.H.3
-
27
-
-
77957850261
-
The synthesis and photoluminescence characteristics of novel α,β-diarylacrylonitrile derivatives containing both a biphenyl group and a triphenylamine unit
-
B. Li, Q. Li, B. Liu, Y.F. Yue, and M.X. Yu The synthesis and photoluminescence characteristics of novel α,β-diarylacrylonitrile derivatives containing both a biphenyl group and a triphenylamine unit Dyes Pigments 88 2011 301 306
-
(2011)
Dyes Pigments
, vol.88
, pp. 301-306
-
-
Li, B.1
Li, Q.2
Liu, B.3
Yue, Y.F.4
Yu, M.X.5
-
28
-
-
33846376761
-
Synthesis and properties of multi-triarylamine-substituted carbazole-based dendrimers with an oligothiophene core for potential applications in organic solar cells and light-emitting diodes
-
J.P. Lu, P.F. Xia, P.K. Lo, Y. Tao, and M.S. Wong Synthesis and properties of multi-triarylamine-substituted carbazole-based dendrimers with an oligothiophene core for potential applications in organic solar cells and light-emitting diodes Chem Mater 18 2006 6194 6203
-
(2006)
Chem Mater
, vol.18
, pp. 6194-6203
-
-
Lu, J.P.1
Xia, P.F.2
Lo, P.K.3
Tao, Y.4
Wong, M.S.5
-
29
-
-
34547092700
-
Synthesis and characterization of N-carbazole end-capped oligfluorene-thiophenes
-
V. Promarak, A. Punkvuang, T. Sudyoadsuk, S. Jungsuttiwong, A. Saengsuwan, and T. Keawin Synthesis and characterization of N-carbazole end-capped oligfluorene-thiophenes Tetrahedron 63 2007 8881 8890
-
(2007)
Tetrahedron
, vol.63
, pp. 8881-8890
-
-
Promarak, V.1
Punkvuang, A.2
Sudyoadsuk, T.3
Jungsuttiwong, S.4
Saengsuwan, A.5
Keawin, T.6
-
30
-
-
48849103085
-
Vapor-phase processable novel nonplanar donor acceptor quateraryls for blue OLEDs
-
A. Goel, M. Dixit, S. Chaurasia, A. Kumar, R. Raghunandan, and P.R. Maulik Vapor-phase processable novel nonplanar donor acceptor quateraryls for blue OLEDs Org Lett 10 2008 2553 2556
-
(2008)
Org Lett
, vol.10
, pp. 2553-2556
-
-
Goel, A.1
Dixit, M.2
Chaurasia, S.3
Kumar, A.4
Raghunandan, R.5
Maulik, P.R.6
-
31
-
-
2042507954
-
Palladium-catalyzed cross-coupling reactions of organoboron compounds
-
N. Miyaura, and A. Suzuki Palladium-catalyzed cross-coupling reactions of organoboron compounds Chem Rev 95 1995 2457 2483
-
(1995)
Chem Rev
, vol.95
, pp. 2457-2483
-
-
Miyaura, N.1
Suzuki, A.2
-
32
-
-
0345802559
-
A general method for the Suzuki-Miyaura cross-coupling of sterically hindered aryl chlorides: Synthesis of di-and triortho-substituted biaryls in 2-propanol at room temperature
-
O. Navarro, R.A. Kelly III, and S.P. Nolan A general method for the Suzuki-Miyaura cross-coupling of sterically hindered aryl chlorides: synthesis of di-and triortho-substituted biaryls in 2-propanol at room temperature J Am Chem Soc 125 2003 16194 16195
-
(2003)
J Am Chem Soc
, vol.125
, pp. 16194-16195
-
-
Navarro, O.1
Kelly Iii, R.A.2
Nolan, S.P.3
-
33
-
-
67650472189
-
Suzuki cross-coupling at the chiral groove of 1,1′-binaphthyl: Stereoconservation versus deracemization pathway
-
H. Brath, M. Mesková, and M. Putala Suzuki cross-coupling at the chiral groove of 1,1′-binaphthyl: stereoconservation versus deracemization pathway Eur J Org Chem 20 2009 3315 3318
-
(2009)
Eur J Org Chem
, vol.20
, pp. 3315-3318
-
-
Brath, H.1
Mesková, M.2
Putala, M.3
-
34
-
-
82255179109
-
Synthesis of 4-aryl-, 2,4-diaryl- and 2,4,7-triarylpyrrolo[2,3-d] pyrimidines by a combination of the Suzuki cross-coupling and N-arylation reactions
-
J. Dodonova, L. Skardziute, K. Kazlauskas, J. Saulius, and S. Tumkevicius Synthesis of 4-aryl-, 2,4-diaryl- and 2,4,7-triarylpyrrolo[2,3-d] pyrimidines by a combination of the Suzuki cross-coupling and N-arylation reactions Tetrahedron 68 2012 329 339
-
(2012)
Tetrahedron
, vol.68
, pp. 329-339
-
-
Dodonova, J.1
Skardziute, L.2
Kazlauskas, K.3
Saulius, J.4
Tumkevicius, S.5
|