Citation: PENG Yu-Xin, GAN Yi-Tao, Tao TAO, QIAN Hui-Fen, HUANG Wei. 5, 6-Alkoxyl Protected and 3-/3, 8-Triphenylamine Extended 1, 10-Phenanthroline Derivatives and Their Selective Silver Ion Recognition[J]. Chinese Journal of Inorganic Chemistry, ;2017, 33(11): 2075-2082. doi: 10.11862/CJIC.2017.252 shu

5, 6-Alkoxyl Protected and 3-/3, 8-Triphenylamine Extended 1, 10-Phenanthroline Derivatives and Their Selective Silver Ion Recognition

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  • The introduction of alkoxyl groups to 5, 6-positions of 1, 10-phenanthroline can not only lead to the enhancement of the reaction activity, but also increase the solubility of the targeted compounds. Crystal structure analyses reveal that the two alkoxyl groups at 5, 6-positions of 1, 10-phenanthroline adopt double six-membered ethylenedioxy cyclic conformation. Both TPA1 and TPA2 show selective recognition toward the silver ion. No obvious fluorescence quenching is found after the treatment of TPA1 and Ag+, in which a red shift of 47 nm in the fluorescence emission spectrum is observed. On the other hand, the two emission peaks at 415 and 542 nm in the fluorescence emission spectra are quenched when TPA2 is reacted with Ag+. However, the fluorescence quenching effect for Ag+ is not obvious in the case of TPA3, which makes it not a good candidate for the metal-ion recognition.
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    1. [1]

      Daniel C, Gourlaouen C. Coord. Chem. Rev., 2017, 344:131-149  doi: 10.1016/j.ccr.2016.10.010

    2. [2]

      (a) Han H B, Cui R Z, Jing Y M, et al. J. Mater. Chem. C, 2017, 5:8150-8159
      (b)Wei X F, Tan W Y, Zou J H, et al. J. Mater. Chem. C, 2017, 5:2329-2336

    3. [3]

      Wu Y Y, Wang P, Wang Y H, et al. J. Mater. Chem. A, 2013, 1:9862-9868  doi: 10.1039/c3ta11571b

    4. [4]

      (a) Jiang L, Chen W C, Zheng J W, et al. ACS Appl. Mat. Interfaces, 2017, 9:26958-26964
      (b)Gavriluta A, Fix T, Nonat A, et al. J. Mater. Chem. A, 2017, 5:14031-14040

    5. [5]

      Bai Z P, Gao Y N, Zhu P H, et al. Inorg. Chem., 2010, 49: 9005-9011  doi: 10.1021/ic101362y

    6. [6]

      (a) Shi S, Liu J, Yao T M, et al. Inorg. Chem., 2008, 47:2910-2912
      (b)Ren P P, Wang R J, Pu S Z, et al. J. Phys. Org. Chem., 2014, 27:183-190
      (c)Batista R M F, Costa S P G, Belsley M, et al. Dyes Pigm., 2009, 80:329-336

    7. [7]

      (a) Collin J P, Kayhanian R, Sauvage J P, et al. Chem. Commun., 1997:775-776
      (b)Yang P J, Yang X J, Wu B. Eur. J. Inorg. Chem., 2009: 2951-2958
      (c)Peng Y X, Wang N, Dai Y, et al. RSC Adv., 2015, 5:6395-6406
      (d)Batista R M F, Costa S P G, Lodeiro C, et al. Tetrahedron, 2008, 64:9230-9238
      (e)Kassio P S Z, Neyde Y M I. Dalton Trans., 2017, 46:9951-9958

    8. [8]

      Wang X Xu, Tao T, Geng J, et al. Chem. Asian J., 2014, 9: 514-525  doi: 10.1002/asia.201301284

    9. [9]

      (a) Tao Y T, Wang Q, Ao L, et al. J. Phys. Chem. C, 2010, 114:601-609
      (b)Usta H, Sheets W S, Denti M, et al. Chem. Mater., 2014, 26:6542-6556

    10. [10]

      Peng Y X, Xu D, Wang N, et al. Tetrahedron, 2016, 72:3443-3453  doi: 10.1016/j.tet.2016.04.061

    11. [11]

      (a) Bodige S, MacDonnell F M. Tetrahedron Lett., 1997, 38: 8159-8160
      (b)Liu X Q, Zhou X, Shu X, et al. Macromolecules, 2009, 42:7634-7637
      (c)Liu Y, Wang Y F, Guo H P, et al. J. Phys. Chem. C, 2011, 115:4209-4216

    12. [12]

      (a) SAINT Ver. 4, Software Reference Manual. Madison: Siemens Analytical X-Ray Systems, 2000.
      (b)Sheldrick G M. SADABS, Program for Empirical Absorp-tion Correction of Area Detector Data, University of Göttingen, Germany, 2000.
      (c)SHELXTL Ver. 6.10, Reference Manual. Madison: Siemens Analytical X-Ray Systems, 2000.

    13. [13]

      Ritter K, Pehlken C, Sorsche D, et al. Dalton Trans., 2015, 44:8889-8905  doi: 10.1039/C5DT00214A

    14. [14]

      (a) Estrada L A, Neckers D C. Org. Lett., 2011, 13:3304-3307
      (b)Shirai Y, Osgood A J, Zhao Y, et al. J. Am. Chem. Soc., 2006, 128:4854-4864

    15. [15]

      (a) Roquet S, Cravino A, Leriche P O, et al. J. Am. Chem. Soc., 2006, 128:3459-3466
      (b)Mikroyannidis J A, Kabanakis A N, Sharma S S, et al. Org. Electron., 2011, 12:774-784
      (c)Shen P, Sang G Y, Lu J J, et al. Macromolecules, 2008, 41:5716-5722

    16. [16]

      (a) Batey H D, Whitwood A C, Duhme-Klair A K, et al. Inorg. Chem., 2007, 46:6516-6528
      (b)Shin D H. Ind. Eng. Chem. Res., 2006, 45:656-662
      (c)Engel Y, Dahan A, Rozenshine-Kemelmakher E, et al. J. Org. Chem., 2007, 72:2318-2328

    17. [17]

      (a) Mandal S, Ghosh S, Banerjee C, et al. J. Phys. Chem. B, 2013, 117:12212-12223
      (b)Elmes R B P, Turner P, Jolliffe K A. Org. Lett., 2013, 15: 5638-5641
      (c)Wang J F, Chu Q H, Liu X M, et al. J. Phys. Chem. B, 2013, 117:4127-4133

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