Pure and Applied Chemistry, 2010, Volume 82, No. 11, pp. 1993-2003, References

Pure Appl. Chem., 2010, Vol. 82, No. 11, pp. 1993-2003

http://dx.doi.org/10.1351/PAC-CON-09-12-17

Published online 2010-08-27

Homeotropic alignment through charge-transfer-induced columnar mesophase formation in an unsymmetrically substituted triphenylene derivative

Juanjuan Li¹, Zhiqun He¹*, Huan Zhao¹, Hemant Gopee², Xiangfei Kong¹, Min Xu¹, Xinxin An³, Xiping Jing³ and Andrew N. Cammidge²*

¹ Key Laboratory of Luminescence and Optical Information, Ministry of Education, Institute of Optoelectronic Technology, Beijing Jiaotong University, Beijing 100044, China
² School of Chemistry, University of East Anglia, Norwich NR4 7TJ, UK
³ College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China

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62. ¹H NMR (CDCl₃, TMS, 400 MHz): δ_H 7.91(2H, s, ArH-5,12), 7.83 (4H, d, J = 3.1 Hz, ArH-1,4,8,9), 4.42 (4H, t, J = 4.5 Hz, ArOCH₂CH₂OCH₂CH₂Cl), 4.21–4.25 (12H, m, OCH₂(CH₂)₄CH₃), 4.02 (4H, t, J = 4.7 Hz, ArOCH₂CH₂OCH₂CH₂Cl), 3.92 (4H, t, J = 5.8 Hz, ArO(CH₂)₂OCH₂CH₂Cl), 3.71 (4H, t, J = 5.8 Hz, ArOCH₂CH₂OCH₂CH₂Cl), 1.98-1.91 (8H, m, OCH₂CH₂), 1.39–1.59 (24H, m, O(CH₂)₂(CH₂)₃CH₃), 0.94 (12H, t, J = 7.1 Hz, CH₃); ¹³C NMR (CDCl₃; 75.45 MHz): δ_C 149.3, 148.6, 124.4, 123.8, 123.6, 108.7, 107.5, 107.3,70.5, 71.8, 70.2, 69.9, 69.8, 69.5, 43.1, 31.9, 29.6, 26.0, 22.9, 14.3; elemental analysis for C₅₀H₇₄O₈Cl: required C 68.71, H 8.53; found C 68.45, H 8.49; mass spectrum (m/z, ES) measured 895.5 ([M + Na]⁺, 100 %).
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Homeotropic alignment through charge-transfer-induced columnar mesophase formation in an unsymmetrically substituted triphenylene derivative

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Homeotropic alignment through charge-transfer-induced columnar mesophase formation in an unsymmetrically substituted triphenylene derivative

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