10.1002/asia.201701666
Chemistry - An Asian Journal
[23] O.B. Locos, C.C. Heindl, A. Corral, M.O. Senge, E.M. Scanlan, Eur. J. Org. Chem. 2010, 6, 1026-1028.
[24] M. Severac, L.L. Pleux, A. Scarpaci, E. Blart, F. Odobel, Tetrahedron Lett. 2007, 48, 6518-6522.
[25] T. Palacin, H.L. Khanh, B. Jousselme, P. Jegou, A. Filoramo, C. Ehli, D.M. Guldi, S. Campidelli, J. Am.
Chem. Soc. 2009, 131, 15394-15402.
[ 26 ] a) D. Mendoza-Espinosa, G.E. Negron-Silva, D. Angeles-Beltran, A. Alvarez-Hernandez, O.R.
Suarez-Castillo, R. Santillan, Dalton Trans. 2014, 43, 7069-7077; b) F. Saleem, G.K. Rao, A. Kumar, G.
Mukherjee, A.K. Singh, Organometallics 2013, 32, 3595-3603; c) H. Struthers, B. Spingler, T.L. Mindt, R.
Schibli, Chem. Eur. J. 2008, 14, 6173-6183; d) H.-F. Chow, C.-M. Lo, Y. Chen, Top. Heterocycl. Chem.
2012, 28, 137-162.
[27] M. Toganoh, H. Harada, Y, Ikawa, H. Furuta, Chem. Lett. 2010, 39, 252-253.
[28] X.P. Tan, L.Y. Kong, H. Dai, X.H. Cheng, F. Liu, C. Tschierske, Chem. Eur. J. 2013, 19, 16303-16313.
[29] S. Cecioni, S. Faure, U. Darbost, I. Bonnamour, H. Parrot-Lopez, O. Roy, C. Taillefumier, M. Wimmerová,
J.-P. Praly, A. Imbert, S. Vidal, Chem. Eur. J. 2011, 17, 2146-2159.
[30] C.A Hunter, J.K.M Sanders, J. Am. Chem. Soc. 1990, 112, 5525-5534.
[31] a) K. Ohta, N. Yamaguchi, I. Yamamoto, J. Mater. Chem. 1998, 8, 2637-2650; b) K. Ohta, S. Azumane, W.
Kawahara, N. Kobayashi, I. Yamamoto, J. Mater. Chem. 1999, 9, 2313-2320; c) K. Hatsusaka, K. Ohta, I.
Yamamoto, H. Shirai, J. Mater. Chem. 2001, 11, 423-433; d) T. Nakai, K. Ban, K. Ohta, M. Kimura, J. Mater.
Chem. 2002, 12, 844-850.
[32] T. Wöhrle, I. Wurzbach, J. Kirres, A. Kostidou, N. Kapernaum, J. Litterscheidt, J.C. Haenle, P. Staffeld, A.
Baro, F. Giesselmann, S. Laschat. Chem. Rev. 2016, 116, 1139-1241.
[33] CAChe 3.2, Oxford Molecular Ltd, Oxford, UK, 1999.
[34] a) M. Prehm, F. Liu, U. Baumeister, X Zeng, G. Ungar, C. Tschierske, Angew. Chem., Int. Ed. 2007, 46,
7972-7975; b) H.-J. Kim, F. Liu, J.-H. Ryu, S.-K. Kang, X. Zeng, G. Ungar, J.-K. Lee, W.-C. Zin, M. Lee, J.
Am. Chem. Soc. 2012, 134, 13871-13880.
[35] Another possible molecular self assembly model is shown in Fig. S5, in which the porphyrin molecule may
adopt a bowl shape, i.e. the branched triazole wedges most likely adopt a fan shape that wrap around the
stacked porphyrin core. Based on the length of the branched triazole wedges (L = 3.33 nm) and the length of
the projection of the branched triazole wedges (Lpro = 1.51 nm) (Fig. S5), the tilt angle θ of approximately 63°
with respect to the cross section of the column was estimated. Related hexagonal columnar phase was form
by bowl shaped petidic macrocycles: K. Sato, Y. Itoh, T. Aida. J. Am. Chem. Soc. 2011, 133, 13767-13769.
[36] M. Nappa, J.S. Valentine, J. Am. Chem. Soc. 1978, 100, 5075-5080.
[37] C. Tekuri, D.K. Singh, M. Nath, Dyes and Pigments 2016, 132, 194-203.
[38] T. Kishida, N. Fujita, K. Sada, S. Shinkai, Langmuir 2005, 21, 9432-9439.
[39] M. Hamaguchi, H. Sawada, J. Kyokane, K. Yoshino, Chem. Lett. 1996, 7, 527-528.
[40] K.L. Cunningham, K.M. McNett, R.A. Pierce, K.A. Davis, H.H. Harris, D.M. Falck, D.R. McMillin, Inorg.
Chem. 1997, 36, 608-613.
[41] X.P. He, Z. Song, Z.Z. Wang, X.X. Shi, K. Chen, G.R. Chen, Tetrahedron 2011, 67, 3343-3347.
[42] S. Cao, Z. Pei, Y. Xu, R. Zhang, Y. Pei, RSC Adv. 2015, 5, 45888-45896.
[43] D.-H. Xie, X.-J. Wang, C. Sun, J. Han, Tetrahedron Lett. 2016, 57, 5834-5836.
[44] D.T. Shi, B. Zhang, Y.X. Yang, C.-C. Guan, X.-P. He, Y.-C. Li, G.-R. Chen, K.X. Chen, Analyst 2013, 138,
2808-2811.
[45] R. Krȁmer, Angew. Chem. Int. Ed. 1998, 37, 772-773.
[46] A. Friggeri, B. L. Feringa, J. van Esch, J. Controlled Release 2004, 97, 241-248.
This article is protected by copyright. All rights reserved.