English

• 

• 1. [1] J. Lisowski, Enantiomeric self-secognition in homo-and heterodinuclear macrocyclic lanthanide(Ⅲ) complexes, Inorg. Chem. 50 (2011) 5567-5576.[1] J. Lisowski, Enantiomeric self-secognition in homo-and heterodinuclear macrocyclic lanthanide(Ⅲ) complexes, Inorg. Chem. 50 (2011) 5567-5576.

  2. [2] C. Liu, M.R. Sawaya, P.N. Cheng, et al., Characteristics of amyloid-related oligomers revealed by crystal structures of macrocyclic b-sheet mimics, J. Am. Chem. Soc. 133 (2011) 6736-6744.[2] C. Liu, M.R. Sawaya, P.N. Cheng, et al., Characteristics of amyloid-related oligomers revealed by crystal structures of macrocyclic b-sheet mimics, J. Am. Chem. Soc. 133 (2011) 6736-6744.

  3. [3] S. Srimurugan, B. Viswanathan, T.K. Varadarajan, et al., Synthesis and crystal structure of [2+2] calixsalens, Org. Biomol. Chem. 4 (2006) 3044-3047.[3] S. Srimurugan, B. Viswanathan, T.K. Varadarajan, et al., Synthesis and crystal structure of [2+2] calixsalens, Org. Biomol. Chem. 4 (2006) 3044-3047.

  4. [4] I. Alfonso, M. Bolte, M. Bru, M.I. Burguete, et al., Supramolecular control for the modular synthesis of pseudopeptidic macrocycles through an anion-templated reaction, J. Am. Chem. Soc. 130 (2008) 6137-6144.[4] I. Alfonso, M. Bolte, M. Bru, M.I. Burguete, et al., Supramolecular control for the modular synthesis of pseudopeptidic macrocycles through an anion-templated reaction, J. Am. Chem. Soc. 130 (2008) 6137-6144.

  5. [5] S.O. Kang, J.M. Llinares, D. Powell, et al., New polyamide cryptand for anion binding, J. Am. Chem. Soc. 125 (2003) 10152-10153.[5] S.O. Kang, J.M. Llinares, D. Powell, et al., New polyamide cryptand for anion binding, J. Am. Chem. Soc. 125 (2003) 10152-10153.

  6. [6] (a) B. Zheng, F. Wang, S. Dong, et al., Supramolecular polymers constructed by crown ether-based molecular recognition, Chem. Soc. Rev. 41 (2012) 1621-1636;[6] (a) B. Zheng, F. Wang, S. Dong, et al., Supramolecular polymers constructed by crown ether-based molecular recognition, Chem. Soc. Rev. 41 (2012) 1621-1636;

  7. [7]

     (b) X. Yan, F. Wang, B. Zheng, et al., Stimuli-responsive supramolecular polymeric materials, Chem. Soc. Rev. 41 (2012) 6042-6065;(b) X. Yan, F. Wang, B. Zheng, et al., Stimuli-responsive supramolecular polymeric materials, Chem. Soc. Rev. 41 (2012) 6042-6065;

  8. [8]

     (c) M. Xue, Y. Yang, X. Chi, et al., Pillararenes, a new class of macrocycles for supramolecular chemistry, Acc. Chem. Res. 45 (2012) 1294-1308;(c) M. Xue, Y. Yang, X. Chi, et al., Pillararenes, a new class of macrocycles for supramolecular chemistry, Acc. Chem. Res. 45 (2012) 1294-1308;

  9. [9]

     (d) L.F. Lindoy, K.M. Park, S.S. Lee, Metals, macrocycles and molecular assemblies macrocyclic complexes in metallo supramolecular chemistry, Chem. Soc. Rev. 42 (2012) 1713-1727.(d) L.F. Lindoy, K.M. Park, S.S. Lee, Metals, macrocycles and molecular assemblies macrocyclic complexes in metallo supramolecular chemistry, Chem. Soc. Rev. 42 (2012) 1713-1727.

  10. [7] N.E. Borisova, M.D. Reshetova, Y.A. Ustynyuk, Metal-free methods in the synthesis of macrocyclic schiff bases, Chem. Rev. 107 (2007) 46-79.[7] N.E. Borisova, M.D. Reshetova, Y.A. Ustynyuk, Metal-free methods in the synthesis of macrocyclic schiff bases, Chem. Rev. 107 (2007) 46-79.

  11. [8] P.A. Vigato, S. Tamburini, The challenge of cyclic and acyclic schiff bases and related derivatives, Coord. Chem. Rev. 248 (2004) 1717-2128.[8] P.A. Vigato, S. Tamburini, The challenge of cyclic and acyclic schiff bases and related derivatives, Coord. Chem. Rev. 248 (2004) 1717-2128.

  12. [9] J.L. Sessler, E. Katayev, G.D. Pantos, et al., Fine tuning the anion binding properties of 2,6-diamidopyridine dipyrromethane hybrid macrocycles, J. Am. Chem. Soc. 44 (2005) 7386-7390.[9] J.L. Sessler, E. Katayev, G.D. Pantos, et al., Fine tuning the anion binding properties of 2,6-diamidopyridine dipyrromethane hybrid macrocycles, J. Am. Chem. Soc. 44 (2005) 7386-7390.

  13. [10] P.A. Vigato, S. Tamburini, L. Bertolo, The development of compartmental macrocyclic Schiff bases and related polyamine derivatives, Coord. Chem. Rev. 251 (2007) 1311-1492.[10] P.A. Vigato, S. Tamburini, L. Bertolo, The development of compartmental macrocyclic Schiff bases and related polyamine derivatives, Coord. Chem. Rev. 251 (2007) 1311-1492.

  14. [11] A. Easwaran, C.F. Christopher, C.N. Bruce, et al., Squaraine-derived rotaxanes: sterically protected fluorescent near-IR dyes, J. Am. Chem. Soc. 127 (2005) 3288-3289.[11] A. Easwaran, C.F. Christopher, C.N. Bruce, et al., Squaraine-derived rotaxanes: sterically protected fluorescent near-IR dyes, J. Am. Chem. Soc. 127 (2005) 3288-3289.

  15. [12] P. Hu, S.Y. Guo, Q.L. Zhang, et al., Synthesis, characterization of novel [1+1] schiff base macrocyclic compounds, Chin. J. Org. Chem. 33 (2013) 325-331.[12] P. Hu, S.Y. Guo, Q.L. Zhang, et al., Synthesis, characterization of novel [1+1] schiff base macrocyclic compounds, Chin. J. Org. Chem. 33 (2013) 325-331.

  16. [13] A.A. Khandar, A.H.Y. Seyed, Synthesis, X-ray crystal structure, and solution properties of nickel(Ⅱ) complexes of new 16-membered mixed-donor macrocyclic Schiff base ligand incorporating a pendant alcohol function, Polyhedron 22 (2003) 1481-1487.[13] A.A. Khandar, A.H.Y. Seyed, Synthesis, X-ray crystal structure, and solution properties of nickel(Ⅱ) complexes of new 16-membered mixed-donor macrocyclic Schiff base ligand incorporating a pendant alcohol function, Polyhedron 22 (2003) 1481-1487.

  17. [14] D.M. Liu, Study on the synthesis and characterization of new macrocyclic Schiff base and macrocyclic amide, Master's thesis of Jilin University, 2009, 22-24.[14] D.M. Liu, Study on the synthesis and characterization of new macrocyclic Schiff base and macrocyclic amide, Master's thesis of Jilin University, 2009, 22-24.

  18. [15] S. Özkar, D. Ülkü, L.T. Yíldírím, et al., Crystal and molecular structure of bis(acetylacetone) ethylenediimine: intramolecular ionic hydrogen bonding in solid state, J. Mol. Struct. 688 (2004) 207-211.[15] S. Özkar, D. Ülkü, L.T. Yíldírím, et al., Crystal and molecular structure of bis(acetylacetone) ethylenediimine: intramolecular ionic hydrogen bonding in solid state, J. Mol. Struct. 688 (2004) 207-211.

•