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New Journal of Chemistry

Volumn 38, Issue 12, 2014, Pages 5686-5690

Colour-tunable aggregation-induced emission of trifunctional o-carborane dyes

(4) Tominaga, Masato a Naito, Hirofumi a Morisaki, Yasuhiro a Chujo, Yoshiki a

a KYOTO UNIVERSITY (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CARBORANE DERIVATIVE; DYE;

ABSORPTION; AGGREGATION INDUCED EMISSION; ARTICLE; CHEMICAL REACTION; DENSITY FUNCTIONAL THEORY; FLUORESCENCE; HYDROPHOBICITY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;

EID: 84910029101 PISSN: 11440546 EISSN: 13699261 Source Type: Journal
DOI: 10.1039/c4nj00955j Document Type: Article

Times cited : (59)

References (48)

1
- 0003714767
- Marcel Dekker, New York, 2nd edn
- T. A. Skotheim, R. L. Elsenbaumer and J. R. Reynolds, Handbook of Conducting Polymers, Marcel Dekker, New York, 2nd edn, 1997
- (1997) Handbook of Conducting Polymers
- Skotheim, T.A.¹ Elsenbaumer, R.L.² Reynolds, J.R.³

2
- 33846219497
- J. E. Anthony Chem. Rev. 2006 106 5028 5048
- (2006) Chem. Rev. , vol.106 , pp. 5028-5048
- Anthony, J.E.¹

3
- 34248339106
- J. Zaumseil H. Sirringhaus Chem. Rev. 2007 107 1296 1323
- (2007) Chem. Rev. , vol.107 , pp. 1296-1323
- Zaumseil, J.¹ Sirringhaus, H.²

4
- 73249138888
- Y.-J. Cheng S.-H. Yang C.-S. Hsu Chem. Rev. 2009 109 5868 5923
- (2009) Chem. Rev. , vol.109 , pp. 5868-5923
- Cheng, Y.-J.¹ Yang, S.-H.² Hsu, C.-S.³

5
- 20444411862
- Z. Li Y. Dong B. Mi Y. Tang M. Häussler H. Tong Y. Dong J. W. Y. Lam Y. Ren H. H. Sung K. S. Wong P. Gao I. D. Williams H. S. Kwok B. Z. Tang J. Phys. Chem. B 2005 109 10061 10066
- (2005) J. Phys. Chem. B , vol.109 , pp. 10061-10066
- Li, Z.¹ Dong, Y.² Mi, B.³ Tang, Y.⁴ Häussler, M.⁵ Tong, H.⁶ Dong, Y.⁷ Lam, J.W.Y.⁸ Ren, Y.⁹ Sung, H.H.¹⁰ Wong, K.S.¹¹ Gao, P.¹² Williams, I.D.¹³ Kwok, H.S.¹⁴ Tang, B.Z.¹⁵

6
- 41849129902
- L. Heng Y. Dong J. Zhai B. Z. Tang L. Jiang Langmuir 2008 24 2157 2161
- (2008) Langmuir , vol.24 , pp. 2157-2161
- Heng, L.¹ Dong, Y.² Zhai, J.³ Tang, B.Z.⁴ Jiang, L.⁵

7
- 74049101131
- W. Z. Yuan H. Zhao X. Y. Shen F. Mahtab J. W. Y. Lam J. Z. Sun B. Z. Tang Macromolecules 2009 42 9400 9411
- (2009) Macromolecules , vol.42 , pp. 9400-9411
- Yuan, W.Z.¹ Zhao, H.² Shen, X.Y.³ Mahtab, F.⁴ Lam, J.W.Y.⁵ Sun, J.Z.⁶ Tang, B.Z.⁷

8
- 77549084486
- S. Liu F. Li Q. Diao Y. Ma Org. Electron. 2010 11 613 617
- (2010) Org. Electron. , vol.11 , pp. 613-617
- Liu, S.¹ Li, F.² Diao, Q.³ Ma, Y.⁴

9
- 84860378382
- H. Lu F. Su Q. Mei Y. Tian W. Tian R. H. Johnson D. R. Meldrum J. Mater. Chem. 2012 22 9890 9900
- (2012) J. Mater. Chem. , vol.22 , pp. 9890-9900
- Lu, H.¹ Su, F.² Mei, Q.³ Tian, Y.⁴ Tian, W.⁵ Johnson, R.H.⁶ Meldrum, D.R.⁷

10
- 0035929223
- J. Luo Z. Xie J. W. Y. Lam L. Cheng H. Chen C. Qiu H. S. Kwok X. Zhan Y. Liu D. Zhu B. Z. Tang Chem. Commun. 2001 1740 1741
- (2001) Chem. Commun. , pp. 1740-1741
- Luo, J.¹ Xie, Z.² Lam, J.W.Y.³ Cheng, L.⁴ Chen, H.⁵ Qiu, C.⁶ Kwok, H.S.⁷ Zhan, X.⁸ Liu, Y.⁹ Zhu, D.¹⁰ Tang, B.Z.¹¹

11
- 46149126423
- X. Fan J. Sun F. Wang Z. Chu P. Wang Y. Dong R. Hu B. Z. Tang D. Zou Chem. Commun. 2008 2989 2991
- (2008) Chem. Commun. , pp. 2989-2991
- Fan, X.¹ Sun, J.² Wang, F.³ Chu, Z.⁴ Wang, P.⁵ Dong, Y.⁶ Hu, R.⁷ Tang, B.Z.⁸ Zou, D.⁹

12
- 84863959374
- G.-F. F. Zhang M. P. Aldred W.-L. L. Gong C. Li M.-Q. Q. Zhu Chem. Commun. 2012 48 7711 7713
- (2012) Chem. Commun. , vol.48 , pp. 7711-7713
- Zhang, G.-F.F.¹ Aldred, M.P.² Gong, W.-L.L.³ Li, C.⁴ Zhu, M.-Q.Q.⁵

13
- 84878625521
- Z. Wang S. Chen J. W. Y. Lam W. Qin R. T. Kwok N. Xie Q. Hu B. Z. Tang J. Am. Chem. Soc. 2013 135 8238 8245
- (2013) J. Am. Chem. Soc. , vol.135 , pp. 8238-8245
- Wang, Z.¹ Chen, S.² Lam, J.W.Y.³ Qin, W.⁴ Kwok, R.T.⁵ Xie, N.⁶ Hu, Q.⁷ Tang, B.Z.⁸

14
- 84875305352
- R. Yoshii A. Nagai K. Tanaka Y. Chujo Chem.-Eur. J. 2013 19 4506 4512
- (2013) Chem.-Eur. J. , vol.19 , pp. 4506-4512
- Yoshii, R.¹ Nagai, A.² Tanaka, K.³ Chujo, Y.⁴

15
- 84886924777
- 12
- ch. 9, 301-540
- 12", Carboranes, ch. 9, pp. 301-540
- Carboranes
- Grimes, R.N.¹

16
- 80755183274
- ed. N. S. Hosmane, CRC Press, Boca Raton
- B. P. Dash, R. Satapathy, J. A. Maguireb and N. S. Hosmane, in Boron Science: New Technologies and Applications, ed., N. S. Hosmane, CRC Press, Boca Raton, 2011, pp. 675-699
- (2011) Boron Science: New Technologies and Applications , pp. 675-699
- Dash, B.P.¹ Satapathy, R.² Maguireb, J.A.³ Hosmane, N.S.⁴

17
- 0000338437
- V. I. Bregadze Chem. Rev. 1992 92 209 223
- (1992) Chem. Rev. , vol.92 , pp. 209-223
- Bregadze, V.I.¹

18
- 57349090378
- A. González-Campo E. J. Juárez-Pérez C. Viñas B. Boury R. Sillanpää R. Kivekäs R. Núñez Macromolecules 2008 41 8458 8466
- (2008) Macromolecules , vol.41 , pp. 8458-8466
- González-Campo, A.¹ Juárez-Pérez, E.J.² Viñas, C.³ Boury, B.⁴ Sillanpää, R.⁵ Kivekäs, R.⁶ Núñez, R.⁷

19
- 80052796110
- F. Issa M. Kassiou L. M. Rendina Chem. Rev. 2011 111 5701 5722
- (2011) Chem. Rev. , vol.111 , pp. 5701-5722
- Issa, F.¹ Kassiou, M.² Rendina, L.M.³

20
- 80052710326
- B. P. Dash R. Satapathy J. A. Maguireb N. S. Hosmane New J. Chem. 2011 35 1955 1972
- (2011) New J. Chem. , vol.35 , pp. 1955-1972
- Dash, B.P.¹ Satapathy, R.² Maguireb, J.A.³ Hosmane, N.S.⁴

21
- 71549133390
- J. J. Peterson M. Werre Y. C. Simon E. B. Coughlin K. R. Carter Macromolecules 2009 42 8594 8598
- (2009) Macromolecules , vol.42 , pp. 8594-8598
- Peterson, J.J.¹ Werre, M.² Simon, Y.C.³ Coughlin, E.B.⁴ Carter, K.R.⁵

22
- 80051727890
- F. Lerouge A. Ferrer-Ugalde C. Viñas F. Teixidor A. Abreu E. Xochitiotzi N. Farfán R. Santillan R. Sillanpää R. Núñez Dalton Trans. 2011 40 7541 7550
- (2011) Dalton Trans. , vol.40 , pp. 7541-7550
- Lerouge, F.¹ Ferrer-Ugalde, A.² Viñas, C.³ Teixidor, F.⁴ Abreu, A.⁵ Xochitiotzi, E.⁶ Farfán, N.⁷ Santillan, R.⁸ Sillanpää, R.⁹ Núñez, R.¹⁰

23
- 79958840756
- B. P. Dash R. Satapathy E. R. Gaillard K. M. Norton J. A. Maguire N. Chug N. S. Hosmane Inorg. Chem. 2011 50 5485 5493
- (2011) Inorg. Chem. , vol.50 , pp. 5485-5493
- Dash, B.P.¹ Satapathy, R.² Gaillard, E.R.³ Norton, K.M.⁴ Maguire, J.A.⁵ Chug, N.⁶ Hosmane, N.S.⁷

24
- 78650889436
- K. Kokado Y. Chujo J. Org. Chem. 2011 76 316 319
- (2011) J. Org. Chem. , vol.76 , pp. 316-319
- Kokado, K.¹ Chujo, Y.²

25
- 80053351016
- J. J. Peterson A. R. Davis M. Werre E. B. Coughlin K. R. Carter ACS Appl. Mater. Interfaces 2011 3 1796 1799
- (2011) ACS Appl. Mater. Interfaces , vol.3 , pp. 1796-1799
- Peterson, J.J.¹ Davis, A.R.² Werre, M.³ Coughlin, E.B.⁴ Carter, K.R.⁵

26
- 84855338091
- A. Ferrer-Ugalde E. J. Juárez-Pérez F. Teixidor C. Viñas E. Pérez-Inestrosa R. Sillanpää R. Núñez Chem.-Eur. J. 2012 18 544 553
- (2012) Chem.-Eur. J. , vol.18 , pp. 544-553
- Ferrer-Ugalde, A.¹ Juárez-Pérez, E.J.² Teixidor, F.³ Viñas, C.⁴ Pérez-Inestrosa, E.⁵ Sillanpää, R.⁶ Núñez, R.⁷

27
- 84865507769
- A. R. Davis J. J. Peterson K. R. Carter ACS Macro Lett. 2012 1 469 472
- (2012) ACS Macro Lett. , vol.1 , pp. 469-472
- Davis, A.R.¹ Peterson, J.J.² Carter, K.R.³

28
- 84858066267
- K.-R. Wee W.-S. Han D. W. Cho S. Kwon C. Pac S. O. Kang Angew. Chem., Int. Ed. 2012 51 2677 2680
- (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 2677-2680
- Wee, K.-R.¹ Han, W.-S.² Cho, D.W.³ Kwon, S.⁴ Pac, C.⁵ Kang, S.O.⁶

29
- 84868091776
- K.-R. Wee Y.-J. Cho S. Jeong S. Kwon J.-D. Lee I.-H. Suh S. O. Kang J. Am. Chem. Soc. 2012 134 17982 17990
- (2012) J. Am. Chem. Soc. , vol.134 , pp. 17982-17990
- Wee, K.-R.¹ Cho, Y.-J.² Jeong, S.³ Kwon, S.⁴ Lee, J.-D.⁵ Suh, I.-H.⁶ Kang, S.O.⁷

30
- 84862727242
- L. Weber J. Kahlert R. Brockhinke L. Böhling A. Brockhinke H.-G. Stammler B. Neumann R. A. Harder M. A. Fox Chem.-Eur. J. 2012 18 8347 8357
- (2012) Chem.-Eur. J. , vol.18 , pp. 8347-8357
- Weber, L.¹ Kahlert, J.² Brockhinke, R.³ Böhling, L.⁴ Brockhinke, A.⁵ Stammler, H.-G.⁶ Neumann, B.⁷ Harder, R.A.⁸ Fox, M.A.⁹

31
- 84872512981
- L. Weber J. Kahlert L. Böhling A. Brockhinke H.-G. Stammler B. Neumann R. A. Harder P. J. Low M. A. Fox Dalton Trans. 2013 42 2266 2281
- (2013) Dalton Trans. , vol.42 , pp. 2266-2281
- Weber, L.¹ Kahlert, J.² Böhling, L.³ Brockhinke, A.⁴ Stammler, H.-G.⁵ Neumann, B.⁶ Harder, R.A.⁷ Low, P.J.⁸ Fox, M.A.⁹

32
- 84889571121
- A. Ferrer-Ugalde E. J. Juárez-Pérez F. Teixidor C. Viñas R. Núñez Chem.-Eur. J. 2013 19 17021 17030
- (2013) Chem.-Eur. J. , vol.19 , pp. 17021-17030
- Ferrer-Ugalde, A.¹ Juárez-Pérez, E.J.² Teixidor, F.³ Viñas, C.⁴ Núñez, R.⁵

33
- 84883513527
- K.-R. Wee Y.-J. Cho J. K. Song S. O. Kang Angew. Chem., Int. Ed. 2013 52 9682 9685
- (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 9682-9685
- Wee, K.-R.¹ Cho, Y.-J.² Song, J.K.³ Kang, S.O.⁴

34
- 84905171706
- A. Ferrer-Ugalde A. González-Campo C. Viñas J. Rodríguez-Romero R. Santillan N. Farfán R. Sillanpää A. Sousa-Pedrares R. Núñez F. Teixidor Chem.-Eur. J. 2014 20 9940 9951
- (2014) Chem.-Eur. J. , vol.20 , pp. 9940-9951
- Ferrer-Ugalde, A.¹ González-Campo, A.² Viñas, C.³ Rodríguez-Romero, J.⁴ Santillan, R.⁵ Farfán, N.⁶ Sillanpää, R.⁷ Sousa-Pedrares, A.⁸ Núñez, R.⁹ Teixidor, F.¹⁰

35
- 0036741206
- J. Llop C. Viñas J. M. Oliva F. Teixidor M. A. Flores R. Kivekas R. Sillanpää J. Organomet. Chem. 2002 657 232 238
- (2002) J. Organomet. Chem. , vol.657 , pp. 232-238
- Llop, J.¹ Viñas, C.² Oliva, J.M.³ Teixidor, F.⁴ Flores, M.A.⁵ Kivekas, R.⁶ Sillanpää, R.⁷

36
- 25844501561
- J. M. Oliva N. L. Allan P. v. R. Schleyer C. Viñas F. Teixidor J. Am. Chem. Soc. 2005 127 13538 13547
- (2005) J. Am. Chem. Soc. , vol.127 , pp. 13538-13547
- Oliva, J.M.¹ Allan, N.L.² Schleyer, P.V.R.³ Viñas, C.⁴ Teixidor, F.⁵

37
- 66549111520
- K. Kokado Y. Chujo Macromolecules 2009 42 1418 1420
- (2009) Macromolecules , vol.42 , pp. 1418-1420
- Kokado, K.¹ Chujo, Y.²

38
- 84883487893
- The first synthesis of C1,B9- and C1,B12-bifunctional o-carboranes was reported in 2002
- M. Tominaga Y. Morisaki Y. Chujo Macromol. Rapid Commun. 2013 34 1357 1362
- (2013) Macromol. Rapid Commun. , vol.34 , pp. 1357-1362
- Tominaga, M.¹ Morisaki, Y.² Chujo, Y.³

39
- 0036097269
- Behaviours of B-functionalized o-carborane clusters were investigated. For example, see
- M. A. Fox K. Wade J. Mater. Chem. 2002 12 1301 1306
- (2002) J. Mater. Chem. , vol.12 , pp. 1301-1306
- Fox, M.A.¹ Wade, K.²

40
- 22944449746
- F. Teixidor G. Barberá a. Vaca R. Kiveäs R. Sillanpää J. Oliva C. Viñas J. Am. Chem. Soc. 2005 127 10158 10159
- (2005) J. Am. Chem. Soc. , vol.127 , pp. 10158-10159
- Teixidor, F.¹ Barberá, G.² Vaca, A.³ Kiveäs, R.⁴ Sillanpää, R.⁵ Oliva, J.⁶ Viñas, C.⁷

41
- 79960673881
- A. M. Spokoyny C. W. Machan D. J. Clingerman M. S. Rosen M. J. Wiester R. D. Kennedy C. L. Stern A. A. Sarjeant C. A. Mirkin Nat. Chem. 2011 3 590 596
- (2011) Nat. Chem. , vol.3 , pp. 590-596
- Spokoyny, A.M.¹ Machan, C.W.² Clingerman, D.J.³ Rosen, M.S.⁴ Wiester, M.J.⁵ Kennedy, R.D.⁶ Stern, C.L.⁷ Sarjeant, A.A.⁸ Mirkin, C.A.⁹

42
- 28244494548
- K. Ohta T. Goto Y. Endo Inorg. Chem. 2005 44 8569 8573
- (2005) Inorg. Chem. , vol.44 , pp. 8569-8573
- Ohta, K.¹ Goto, T.² Endo, Y.³

43
- 9644285669
- Y. Tohda K. Sonogashira N. Hagihara Tetrahedron Lett. 1975 16 4467 4470
- (1975) Tetrahedron Lett. , vol.16 , pp. 4467-4470
- Tohda, Y.¹ Sonogashira, K.² Hagihara, N.³

44
- 0038675906
- ed. E. Negishi, Wiley-Interscience, New York, Fluorescence spectra of, without normalization, are shown in Fig. S17 in the ESI For example, see
- K. Sonogashira, in Handbook of Organopalladium Chemistry for Organic Synthesis, ed., E. Negishi, Wiley-Interscience, New York, 2002, pp. 493-529
- (2002) Handbook of Organopalladium Chemistry for Organic Synthesis , vol.5 , pp. 493-529
- Sonogashira, K.¹

45
- 0035929223
- J. Luo Z. Xie J. W. Y. Lam L. Cheng H. Chen C. Qiu H. S. Kwok X. Zhan Y. Liu D. Zhu B. Z. Tang Chem. Commun. 2001 1740 1741
- (2001) Chem. Commun. , pp. 1740-1741
- Luo, J.¹ Xie, Z.² Lam, J.W.Y.³ Cheng, L.⁴ Chen, H.⁵ Qiu, C.⁶ Kwok, H.S.⁷ Zhan, X.⁸ Liu, Y.⁹ Zhu, D.¹⁰ Tang, B.Z.¹¹

46
- 69449083097
- J. Liu J. W. Y. Lam B. Z. Tang J. Inorg. Organomet. Polym. 2009 19 249 285
- (2009) J. Inorg. Organomet. Polym. , vol.19 , pp. 249-285
- Liu, J.¹ Lam, J.W.Y.² Tang, B.Z.³

47
- 84863959374
- G.-F. F. Zhang M. P. Aldred W.-L. L. Gong C. Li M.-Q. Q. Zhu Chem. Commun. 2012 48 7711 7713
- (2012) Chem. Commun. , vol.48 , pp. 7711-7713
- Zhang, G.-F.F.¹ Aldred, M.P.² Gong, W.-L.L.³ Li, C.⁴ Zhu, M.-Q.Q.⁵

48
- 84878625521
- 2O are shown in Fig. S18 in the ESI Recently, a multiple emission system using 1,2-dinaphtyl-o-carborane was achieved, in which the orbital overlap between the aromatic units and the C1-C2 orbital was controlled to form a new type of CT state; see ref. 7m
- Z. Wang S. Chen J. W. Y. Lam W. Qin R. T. Kwok N. Xie Q. Hu B. Z. Tang J. Am. Chem. Soc. 2013 135 8238 8245
- (2013) J. Am. Chem. Soc. , vol.135 , pp. 8238-8245
- Wang, Z.¹ Chen, S.² Lam, J.W.Y.³ Qin, W.⁴ Kwok, R.T.⁵ Xie, N.⁶ Hu, Q.⁷ Tang, B.Z.⁸

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