Excited-State Conformational/Electronic Responses of Saddle-ShapedN,N′-Disubstituted-Dihydrodibenzo[a,c]phenazines: Wide-Tuning Emission from Red to Deep Blue and White Light Combination

Zhiyun Zhang; Kuo-Chun Tang; Chi-Lin Chen; Jr-Wei Ho; Jianhua Su; He Tian; Pi-Tai Chou

doi:10.1021/jacs.5b03491

journal article Jun 29, 2015

Excited-State Conformational/Electronic Responses of Saddle-ShapedN,N′-Disubstituted-Dihydrodibenzo[a,c]phenazines: Wide-Tuning Emission from Red to Deep Blue and White Light Combination

Zhiyun Zhang

Kuo-Chun Tang Chi-Lin Chen Jr-Wei Ho Jianhua Su He Tian

Pi-Tai Chou

Journal of the American Chemical Society Vol. 137 No. 26 pp. 8509-8520 · American Chemical Society (ACS)

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References

58

[1]

Doroshenko A. O. Theor. Exp. Chem. (2002) 10.1023/a:1019696700763

[2]

Vollmer F. J. Fluoresc. (1994) 10.1007/bf01876657

[3]

Chien Y.-Y. Chem. Commun. (2002) 10.1039/b208269a

[4]

Wong K.-T. J. Org. Chem. (2005) 10.1021/jo0512047

[5]

Terenziani F. J. Am. Chem. Soc. (2006) 10.1021/ja064521j

[6]

Marini A. J. Phys. Chem. B (2010) 10.1021/jp1097487

[7]

Liu C. J. Phys. Chem. A (2012) 10.1021/jp310711e

[8]

Sension R. J. J. Chem. Phys. (1993) 10.1063/1.464824

[9]

Gepshtein R. J. Phys. Chem. B (2006) 10.1021/jp065139w

[10]

Stavrov S. S. J. Am. Chem. Soc. (2006) 10.1021/ja0555421

[11]

Gil M. J. Am. Chem. Soc. (2007) 10.1021/ja066976e

[12]

Zhu L. J. Am. Chem. Soc. (2013) 10.1021/ja400456h

[13]

Pullen S. H. J. Chem. Phys. (1998) 10.1063/1.476366

[14]

Tang K.-C. J. Chem. Phys. (2011) 10.1063/1.3557054

[15]

Kim S. J. Am. Chem. Soc. (2012) 10.1021/ja3027295

[16]

Waluk J. (2000)

[17]

Tanner C. Science (2003) 10.1126/science.1091708

[18]

Huynh M. H. V. Chem. Rev. (2007) 10.1021/cr0500030

[19]

Fang C. Nature (2009) 10.1038/nature08527

[20]

Hsieh C.-C. Acc. Chem. Res. (2010) 10.1021/ar1000499

[21]

Hsieh C.-C. J. Am. Chem. Soc. (2011) 10.1021/ja107945m

[22]

Excited-state proton coupled charge transfer modulated by molecular structure and media polarization

Alexander P. Demchenko, Kuo-Chun Tang, Pi-Tai Chou

Chemical Society Reviews 2013 10.1039/c2cs35195a

[23]

Valat P. J. Am. Chem. Soc. (1992) 10.1021/ja00029a023

[24]

Demeter A. J. Phys. Chem. (1996) 10.1021/jp951133n

[25]

Grabner G. J. Phys. Chem. A (1998) 10.1021/jp9727815

[26]

Baumgarten M. J. Phys. Chem. A (2000) 10.1021/jp9932315

[27]

Inoue Y. J. Am. Chem. Soc. (2002) 10.1021/ja016858l

[28]

Keinan S. J. Phys. Chem. A (2006) 10.1021/jp0646168

[29]

Chen Y. J. Org. Chem. (2012) 10.1021/jo202215x

[30]

Shukla D. J. Am. Chem. Soc. (1993) 10.1021/ja00060a063

[31]

Yuan C. J. Am. Chem. Soc. (2013) 10.1021/ja404198h

[32]

Yuan C. Chem.—Eur. J. (2014) 10.1002/chem.201303955

[33]

Holzapfel M. J. Chem. Soc., Perkin Trans. 2 (2002) 10.1039/b204392k

[34]

Miao Q. J. Am. Chem. Soc. (2003) 10.1021/ja036466+

[35]

Okamoto T. Org. Lett. (2003) 10.1021/ol0274458

[36]

Terada E. J. Org. Chem. (2005) 10.1021/jo051791w

[37]

Suzuki S. Org. Lett. (2009) 10.1021/ol9009927

[38]

Semiconducting π-Conjugated Systems in Field-Effect Transistors: A Material Odyssey of Organic Electronics

Chengliang Wang, Huanli Dong, Wenping Hu et al.

Chemical Reviews 2011 10.1021/cr100380z

[39]

Zheng Z. J. Mater. Chem. C (2014) 10.1039/c4tc01965b

[40]

Huang W. Chem. Commun. (2015) 10.1039/c4cc09613d

[41]

Hiraoka S. J. Am. Chem. Soc. (2004) 10.1021/ja0367748

[42]

Masuda Y. J. Am. Chem. Soc. (2009) 10.1021/ja808093z

[43]

Masuda Y. Pure Appl. Chem. (2010) 10.1351/pac-con-09-10-04

[44]

Arimori S. Org. Lett. (2002) 10.1021/ol026802b

[45]

Boden B. N. Org. Lett. (2006) 10.1021/ol060433s

[46]

Feng X. Pure Appl. Chem. (2009) 10.1351/pac-con-09-07-07

[47]

Morris J. Ber. Bunsen. Phys. Chem. (1974) 10.1002/bbpc.19740781211

[48]

Schuster G. B. J. Phys. Chem. (1980) 10.1021/j100451a020

[49]

Smith J. G. J. Organomet. Chem. (1972) 10.1016/s0022-328x(00)80668-3

[50]

Schmidt S. P. J. Am. Chem. Soc. (1980) 10.1021/ja00521a049

Showing 50 of 58 references

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Citations

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References

Details

Published: Jun 29, 2015
Vol/Issue: 137(26)
Pages: 8509-8520

Authors

Z

Zhiyun Zhang

Key Laboratory for Advanced Materials and Institute of Fine Chemicals, East China University of Science & Technology, Shanghai 200237, P. R. China; Department of Chemistry, National Taiwan University, Taipei, 10617 Taiwan, R.O.C.

K

Kuo-Chun Tang

Department of Chemistry, National Taiwan University, Taipei, 10617 Taiwan, R.O.C.

C

Chi-Lin Chen

Department of Chemistry, National Taiwan University, Taipei, 10617 Taiwan, R.O.C.

J

Jr-Wei Ho

Department of Chemistry, National Taiwan University, Taipei, 10617 Taiwan, R.O.C.

J

Jianhua Su

Key Laboratory for Advanced Materials and Institute of Fine Chemicals, East China University of Science & Technology, Shanghai 200237, P. R. China

H

He Tian

Key Laboratory for Advanced Materials and Institute of Fine Chemicals, East China University of Science & Technology, Shanghai 200237, P. R. China

P

Pi-Tai Chou

Department of Chemistry, National Taiwan University, Taipei, 10617 Taiwan, R.O.C.

Funding

National Natural Science Foundation of China

Ministry of Science and Technology of the People's Republic of China Award: 2013CB733700

Cite This Article

Zhiyun Zhang, Kuo-Chun Tang, Chi-Lin Chen, et al. (2015). Excited-State Conformational/Electronic Responses of Saddle-ShapedN,N′-Disubstituted-Dihydrodibenzo[a,c]phenazines: Wide-Tuning Emission from Red to Deep Blue and White Light Combination. Journal of the American Chemical Society, 137(26), 8509-8520. https://doi.org/10.1021/jacs.5b03491

Excited-State Conformational/Electronic Responses of Saddle-ShapedN,N′-Disubstituted-Dihydrodibenzo[a,c]phenazines: Wide-Tuning Emission from Red to Deep Blue and White Light Combination

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