不对称二亚胺席夫碱的合成、表征和抗菌活性

Nartop Dilek Gürkan Perihan

引用本文: Nartop Dilek, Gürkan Perihan. 不对称二亚胺席夫碱的合成、表征和抗菌活性[J]. 无机化学学报, 2013, 29(6): 1227-1234. doi: 10.3969/j.issn.1001-4861.2013.00.227 shu
Citation:  Nartop Dilek, Gürkan Perihan. Synthesis, Characterization and Antibacterial Activities of Unsymmetric Diimine Schiff Bases and Their Fe(Ⅲ) and Ni(Ⅱ) Complexes[J]. Chinese Journal of Inorganic Chemistry, 2013, 29(6): 1227-1234. doi: 10.3969/j.issn.1001-4861.2013.00.227 shu

不对称二亚胺席夫碱的合成、表征和抗菌活性

  • 基金项目:

    Gazi Universtiy Research foundations资助项目(Supported by Gazi Universtiy Research foundations(FEF 05/2003-64) (Supported by Gazi Universtiy Research foundations(FEF 05/2003-64)

    (FEF 05/2005-37))。 (FEF 05/2005-37))

摘要: 用两步法合成了3种不对称二亚胺L,LMe和LCl。起始原料席夫碱2-羟基-N-(5-硝基糠叉)苯胺(SB-NO2)用5-硝基糠醛和2-羟基苯胺反应制得。SB-NO2然后在溶液中被还原为其氨基衍生物SB-NH2。在SB-NH2溶液中分别加入2-羟基苯甲醛,2-羟基-5-甲基苯甲醛和2-羟基-5-氯苯甲醛制得二亚胺化合物L,LMe and LCl。同时还合成了这些配体的Fe(Ⅲ) and Ni(Ⅱ)的二聚和双核配合物。用元素分析、LC-MS、IR、UV-Vis、1H and 13C-NMR、TGA、电导率和磁性测量等对二亚胺及其配合物进行了表征,还研究了席夫碱配体及其配合物对5种细菌的抗菌活性。所有化合物对大肠埃布氏菌、枯草芽孢杆菌、小肠结肠炎耶尔森氏菌均有中等强度的活性。Fe(Ⅲ)配合物对绿脓假单胞菌(绿脓杆菌)具有最高活性。

English

  • 
    1. [1] Schiff H. Justus Liebigs Ann. Chem., 1864,131:118-119[1] Schiff H. Justus Liebigs Ann. Chem., 1864,131:118-119

    2. [2] Behpour M, Ghoreishi S M, Salavati-Niasari M, et al. Corros. Sci., 2009,51(5):1073-1082[2] Behpour M, Ghoreishi S M, Salavati-Niasari M, et al. Corros. Sci., 2009,51(5):1073-1082

    3. [3] Stanly Jacob K, Parameswaran G. Corros. Sci., 2010,52:224- 228[3] Stanly Jacob K, Parameswaran G. Corros. Sci., 2010,52:224- 228

    4. [4] Kı lı ç A, Kayan C, Baysal A, et al. Appl. Organomet. Chem., 2011,25(5):390-394[4] Kı lı ç A, Kayan C, Baysal A, et al. Appl. Organomet. Chem., 2011,25(5):390-394

    5. [5] Zhou M D, Zhao J, Kühn F E, et al. Chem. Eur. J., 2007,13 (1):158-166[5] Zhou M D, Zhao J, Kühn F E, et al. Chem. Eur. J., 2007,13 (1):158-166

    6. [6] Yue S, Li J, Gu X P, et al. Russ. J. Coord. Chem., 2010,36: 547-551[6] Yue S, Li J, Gu X P, et al. Russ. J. Coord. Chem., 2010,36: 547-551

    7. [7] Derinkuyu S, Ertekin K, Çetinkaya E, et al. Dyes and Pigm., 2008,76:133-141[7] Derinkuyu S, Ertekin K, Çetinkaya E, et al. Dyes and Pigm., 2008,76:133-141

    8. [8] Aksuner N, Henden E, Cukurovali A, et al. Dyes and Pigm., 2009,83(2):211-217[8] Aksuner N, Henden E, Cukurovali A, et al. Dyes and Pigm., 2009,83(2):211-217

    9. [9] Shi L, Ge H M, Tan S H, et al. Eur. J. Med. Chem., 2007,42 (4):558-564[9] Shi L, Ge H M, Tan S H, et al. Eur. J. Med. Chem., 2007,42 (4):558-564

    10. [10] Pandeya S N, Sriram D, De Clercq, E. et al. Il Farmaco, 1999,54(9):624-628[10] Pandeya S N, Sriram D, De Clercq, E. et al. Il Farmaco, 1999,54(9):624-628

    11. [11] Rathelot P, Vanelle P, Maldonado J, et al. Eur. J. Med. Chem., 1995,30:503-508[11] Rathelot P, Vanelle P, Maldonado J, et al. Eur. J. Med. Chem., 1995,30:503-508

    12. [12] Martins C V B, da Silva D L, de Resende M A, et al. J. Antimicrob. Chemother., 2009,63(2):337-339[12] Martins C V B, da Silva D L, de Resende M A, et al. J. Antimicrob. Chemother., 2009,63(2):337-339

    13. [13] Sriram D, Yogeeswari P, Saraswat V, et al. Bioorg. Med. Chem. Lett., 2006,16:2127-2129[13] Sriram D, Yogeeswari P, Saraswat V, et al. Bioorg. Med. Chem. Lett., 2006,16:2127-2129

    14. [14] Humphrey L C F, Rodolphe C, Sally B. Polyhedron, 2010, 29(4):1353-1357[14] Humphrey L C F, Rodolphe C, Sally B. Polyhedron, 2010, 29(4):1353-1357

    15. [15] Potgieter K, Mayer P, Booysen I N, et al. Polyhedron, 2009, 28(13):2808-2812[15] Potgieter K, Mayer P, Booysen I N, et al. Polyhedron, 2009, 28(13):2808-2812

    16. [16] Shadrick I M P, Ünige A L, Shengwen L. Inorg. Chim. Acta, 2010,363(13):3390-3398[16] Shadrick I M P, Ünige A L, Shengwen L. Inorg. Chim. Acta, 2010,363(13):3390-3398

    17. [17] Nartop D, Gürkan P, Çete S, et al. J. Coord. Chem., 2008, 61(21):3516-3524[17] Nartop D, Gürkan P, Çete S, et al. J. Coord. Chem., 2008, 61(21):3516-3524

    18. [18] Güngör O, Gürkan P, Spectrochim. Acta Part A: Mol. Biomol. Spect., 2010,77(1):304-311[18] Güngör O, Gürkan P, Spectrochim. Acta Part A: Mol. Biomol. Spect., 2010,77(1):304-311

    19. [19] Csaszar J. Acta Chim. Hung., 1987,124:245-257[19] Csaszar J. Acta Chim. Hung., 1987,124:245-257

    20. [20] Zhelyazkov L, Zikolova S, Farmatsia (Sofia, Bulgaria), 1964, 10(25):16-21[20] Zhelyazkov L, Zikolova S, Farmatsia (Sofia, Bulgaria), 1964, 10(25):16-21

    21. [21] Kandil S S, Ali G Y, El-Dissouky A. Trans. Met. Chem., 2002,27:398-406[21] Kandil S S, Ali G Y, El-Dissouky A. Trans. Met. Chem., 2002,27:398-406

    22. [22] Nakamoto K. Infrared and Raman Spectra of Inorganic and Coordination Compounds. New York: Wiley, 1986.[22] Nakamoto K. Infrared and Raman Spectra of Inorganic and Coordination Compounds. New York: Wiley, 1986.

    23. [23] Sar N, Gürkan P. Trans. Met. Chem., 2003,28:687-693[23] Sar N, Gürkan P. Trans. Met. Chem., 2003,28:687-693

    24. [24] Lever A B P. Inorganic Electronic Spectroscopy. New York: Elsevier, 1984.[24] Lever A B P. Inorganic Electronic Spectroscopy. New York: Elsevier, 1984.

    25. [25] Dubey R K, Dubey U K, Mishra C M. Trans. Met. Chem., 2006,31(7):849-855[25] Dubey R K, Dubey U K, Mishra C M. Trans. Met. Chem., 2006,31(7):849-855

    26. [26] Nag J K, Pal S, Sinha C. Trans. Met. Chem., 2005,30:523- 526[26] Nag J K, Pal S, Sinha C. Trans. Met. Chem., 2005,30:523- 526

    27. [27] Adediji J F, Obaleye J A, Akinremi C A, et al. J. Chem. Pharm. Res., 2012,4(8):4073-4078[27] Adediji J F, Obaleye J A, Akinremi C A, et al. J. Chem. Pharm. Res., 2012,4(8):4073-4078

    28. [28] Joshua A O, Johnson F A, Mattehew A A. Molecules, 2011, 16:5861-5874[28] Joshua A O, Johnson F A, Mattehew A A. Molecules, 2011, 16:5861-5874

  • 加载中
计量
  • PDF下载量:  488
  • 文章访问数:  790
  • HTML全文浏览量:  73
文章相关
  • 收稿日期:  2013-02-15
  • 网络出版日期:  2013-04-20
通讯作者: 陈斌, bchen63@163.com
  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

  1. 本站搜索
  2. 百度学术搜索
  3. 万方数据库搜索
  4. CNKI搜索

/

返回文章