參考文獻 |
1. Freiser, M. J., Phys. Rev. Lett., 1970, 24, 1041-1043.
2. Lenmann, O., Crystals.Physikal. Chem., 1889, 4, 462-467.
3. Manisekaran, T.; Sarkar, A.; Bhagwat, L.; Talwar, S.; Prasad, J. S., Mol. Cryst. Liq. Cryst., 1995, 268, 55-59.
4. D. J. Wang, B. P. Xu, X. H. Wei and J. Zheng, J. Fluorine Chem., 2012, 140, 49–53.
5. K. Ono, K. Yoshikawa, Y. Tsuji, H. Yamaguchi, R. Uozumi, M. Tomura, K. Taga and K. Saito, Tetrahedron, 2007, 63, 9354–9358.
6. R. Yoshii, A. Nagai, K. Tanaka and Y. Chujo, Macromol. Rapid Commun., 2014, 35, 1315−1319.
7. R. S. Singh, M. Yadav, R. K. Gupta, R. Pandey and D. S. Pandey, Dalton Trans., 2013, 42, 1696–1707.
8. M. J. Kwak and Y. Kim, Bull. Korean Chem. Soc., 2009, 30, 2865–2866.
9. K. Benelhadj, J. Massue and G. Ulrich, New J. Chem., 2016, 40, 5877–5884.
10. Q. Liu, X. Wang, H. Yan, Y. Wu, Z. Li, S. Gong, P. Liu and Z. Liu, J. Mater. Chem. C, 2015, 3, 2953–2959.
11. T. M. H. Vuong, J. Weimmerskirch-Aubatin, J. F. Lohier, N. Bar, S. Boudin, C. Labbé, F. Gourbilleau, H. Nguyen, T. T. Dang and Didier Villemin, New J. Chem., 2016, 40, 6070–6076.
12. Y. Meesala, V. Kavala, H. C. Chang, T. S. Kuo, C. F. Yao and W. Z. Lee, Dalton Trans., 2015, 44, 1120–1129.
13. W. Li, W. Lin, J. Wang and X. Guan, Org. Lett., 2013, 15, 1768–1771.
14. X. Zhang, H. Yu and Y. Xiao, J. Org. Chem., 2012, 77, 669−673.
15. S. M. Barbon, J. T. Price, P. A. Reinkeluers and J. B. Gilroy, Inorg. Chem., 2014, 53, 10585−10593.
16. H. M. Ko, J. Korean Chem. Soc., 2016, 60, 21−27.
17. A. D′Aléo, A. Felouat, V. Heresanu, A. Ranguis, D. Chaudanson, A. Karapetyan, M. Giorgi and F. Fages, J. Mater. Chem. C, 2014, 2, 5208–5215.
18. E. Cogné-Laage, J. F. Allemand, O. Ruel, J. B. Baudin, V. Croquette, M. Blanchard-Desce, and Ludovic Jullien, Chem. Eur. J., 2004, 10, 1445–1455.
19. L. A. Padilha, S. Webster, O. V. Przhonska, H. Hu, D. Peceli, T. R. Ensley, M. V. Bondar, A. O. Gerasov, Y. P. Kovtun, M. P. Shandura, A. D. Kachkovski, D. J. Hagan and E. W. Van Stryland, J. Phys. Chem. A, 2010, 114, 6493–6501.
20. C. Ran, X. Xu, S. B. Raymond, B. J. Ferrara, K. Neal, B. J. Bacskai, Z. Medarova and A. Moore, J. Am. Chem. Soc., 2009, 131, 15257–15261.
21. M. J. Mayoral, P. Ovejero, M. Cano and G. Orellana, Dalton Trans., 2011, 40, 377–383.
22. A. Sakai, M. Tanaka, E. Ohta, Y. Yoshimoto, K. Mizuno and H. Ikeda, Tetrahedron Lett., 2012, 53, 4138–4141.
23. G. Zhang, J. Chen, S. J. Payne, S. E. Kooi, J. N. Demas and C. L. Fraser, J. Am. Chem. Soc., 2007, 129, 8942–8943.
24. Y. Sun, D. Rohde, Y. Liu, L. Wan, Y. Wang, W. Wu, C. Di, G. Yu and D. Zhu, J. Mater. Chem., 2006, 16, 4499–4503.
25. C. A. DeRosa, J. Samonina-Kosicka, Z. Fan, H. C. Hendargo, D. H. Weitzel, G. M. Palmer and C. L. Fraser, Macromolecules, 2015, 48, 2967−2977.
26. R. Yoshii, A. Nagai, K. Tanaka and Y. Chujo, Chem. Eur. J., 2013, 19, 4506–4512.
27. R. Tan, Q. Lin, Y. Wen, S. Xiao, S. Wang, R. Zhang and T. Yi, CrystEngComm, 2015, 17, 66746680.
28. A. Loudet and K. Burgess, Chem. Rev., 2007, 107, 4891−4932.
29. N. Boens, V. Leen and W. Dehaen, Chem. Soc. Rev., 2012, 41, 1130–1172.
30. J. Bañuelos, F. L. Arbeloa, T. Arbeloa, V. Martinez and I. L. Arbeloa, Applied Science Innovations Pvt. Ltd. 2012.
31. J.-H. Olivier, F. Camerel, G. Ulrich, J. Barberá and R. Ziessel, Chem. Eur. J., 2010, 16, 7134–7142.
32. F. Camerel, L. Bonardi, G. Ulrich, L. Charbonnière, B. Donnio, C. Bourgogne, D. Guillon, P. Retailleau and R. Ziessel, Chem. Mater., 2006, 18, 5009–5021.
33. F. Camerel, L. Bonardi, M. Schmutz and R. Ziessel, J. Am. Chem. Soc., 2006, 128, 4548–4549.
34. S. M. Barbon, V. N. Staroverov, P. D. Boyle and J. B. Gilroy, Dalton Trans., 2014, 43, 240–250.
35. M. C. Chang, A. Chantzis, D. Jacquemin and E. Otten, Dalton Trans., 2016, 45, 9477–9484.
36. S. M. Barbon, J. T. Price, U. Yogarajah and J. B. Gilroy, RSC Adv., 2015, 5, 56316–56324.
37. M. C. Chang and E. Otten, Chem. Commun., 2014, 50, 7431–7433.
38. S. M. Barbon, V. N. Staroverov and J. B. Gilroy, J. Org. Chem., 2015, 80, 5226−5235.
39. A. Kamal, A. B. Shaik, B. B. Rao, I. Khan, G. B. Kumara and N. Jain, Org. Biomol. Chem., 2015, 13, 10162–10178.
40. H. Chuang, L. C. S. Huang, M. Kapoor, Y. J. Liao, C. L. Yang, C. C. Chang, C. Y. Wu, J. R. Hwu, T. J. Huang and M. H. Hsu, Med. Chem. Commun., 2016, 7, 832–836.
41. L. Yan, J. Wu, H. Chen, S. Zhang, Z. Wang, H. Wang and F. Wu, RSC Adv., 2015, 5, 73660–73669.
42. T. S. Kamatchi, P. Kalaivani, F. R. Fronczek, K. Natarajan and R. Prabhakaran, RSC Adv., 2016, 6, 46531–46547.
43. H. Andleeb, Y. Tehseen, S. J. A. Shah, I. Khan, J. Iqbal and S. Hameed, RSC Adv., 2016, 6, 77688–77700.
44. B. A. Chalyk, I. Y. Kandaurova, K. V. Hrebeniuk, O. V. Manoilenko, I. B. Kulik, R. T. Iminov, V. Kubyshkin, A. V. Tverdokhlebov, O. K. Ablialimov and P. K. Mykhailiuk, RSC Adv., 2016, 6, 25713–2572.
45. J. Fernández, J. Chicharro, J. M. Bueno and M. Lorenzo, Chem. Commun., 2016, 52, 10190–10192. |