Citation: Ikhile Monisola I, Ngila J Catherine. Synthesis and Characterization of Some Ferrocenylphenylimine Compounds[J]. Chinese Journal of Inorganic Chemistry, ;2015, 31(10): 2079-2088. doi: 10.11862/CJIC.2015.272 shu

Synthesis and Characterization of Some Ferrocenylphenylimine Compounds

  • Corresponding author: Ikhile Monisola I,  Ngila J Catherine, 
  • Received Date: 23 June 2015
    Available Online: 31 August 2015

    Fund Project:

  • A novel series of ferrocenylimine compounds (5~12) were synthesized via the same route by refluxing a mixture of corresponding ferrocenylaniline with aromatic aldehyde. Compounds 5~12 were air stable without any decomposition when exposed to air. The compounds were all characterized by 1H and 13C NMR spectroscopy, mass spectrometry, IR, UV-Visible and elemental analysis. The single crystal structure of compound 10 was also reported, which revealed that compound 10 crystallized in monoclinic system with P21/c space group. CCDC: 1010246, 10.
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    1. [1]

      [1] Coleman K S, Turberville S, Pascu S I, et al. J. Organomet. Chem., 2005,690:653-658

    2. [2]

      [2] Ikhile M I, Bala M D, Nyamori V O, et al. Appl. Organometal. Chem., 2013,27:98-108

    3. [3]

      [3] Togni A, Hayashi T (Eds.) Ferrocenes:Homogeneous Catalysis, Organic Synthesis and Material Science. Weinheim:VCH, 1995.

    4. [4]

      [4] Diallo A K, Ornelas C, Salmon L, et al. Chem. Commun., 2007:4946-4948

    5. [5]

      [5] Nazarov A A, Hartinger C. G, Arion V B, et al. Tetrahedron, 2002,58:8489

    6. [6]

      [6] Gibson V C, Gregson C K A, Halliwell C M, et al. Organomet. Chem., 2004,690:6271-6283

    7. [7]

      [7] Andrieux C P, Blocman C, Dumas-Bouchiat J M, et al. J. Am. Chem. Soc., 1980,102:3806-3813

    8. [8]

      [8] Ferreira C L, Ewart C B, Barta C A, et al. Inorg. Chem., 2006,45:8414-8422

    9. [9]

      [9] Mishra L, Dubey S K. Spectrochim. Acta A, 2007,68:364-368

    10. [10]

      [10] Bildstein B, Malaun M, Kopacka H, et al. J. Organomet. Chem., 1999,572:177-187

    11. [11]

      [11] Thomas J L, Howarth J, Kennedy A M. Molecules, 2002,7:861-866

    12. [12]

      [12] Bai Y, Zhang B G, Duan C Y, et al. New J. Chem., 2006, 30:266-271

    13. [13]

      [13] Ling S, Xin Z, Yan H, et al. Chin. Chem. Lett., 2006,36:325-330

    14. [14]

      [14] Van Staveren D R, Metzler-Nolte N. Chem. Rev., 2004,104:5931-5985

    15. [15]

      [15] Allardyce C S, Dorcier A, Scolaro C, et al. Appl. Organomet. Chem., 2005,19:1-10

    16. [16]

      [16] Neuse E W J. Inorg. Organomet. Polym. Mater., 2005,15:3-32

    17. [17]

      [17] Fouda M F R, Abd-Elzaher M M, Abdelsamaia R A, et al. Appl. Organomet. Chem., 2007,21:613-625

    18. [18]

      [18] Ornelas C. New J. Chem., 2011,35:1973-1985

    19. [19]

      [19] Mathiyalagan K, Gopal S, Ramasamy E, et al. Int. J. ChemTech Res., 2012,4:1775-1781

    20. [20]

      [20] Kondapi A K, Satyanarayana N, Saikrishna A D. Arch. Biochem. Biophys., 2006,450:123-132

    21. [21]

      [21] Itoh T, Shirakami S, Ishida N, et al. Bioorg. Med. Chem. Lett., 2000,10:1657-1659

    22. [22]

      [22] Zhang J. Appl. Organomet. Chem., 2008,22:6-11

    23. [23]

      [23] Hillard E A, Vessieres A, Jaouen G. Top Organomet. Chem., 2010,32:81-117

    24. [24]

      [24] Mohammed I A, Subrahmanyam E V S. Acta Pharma. Sci., 2009,51:163-168

    25. [25]

      [25] Anand P, Patil V M, Sharma V K, et al. Int. J. Drug. Des. Discov., 2012,3:851-868

    26. [26]

      [26] Hranjec M, Starcevic K, Pavelic K S, et al. Eur. J. Med. Chem., 2011,46:2274-2279

    27. [27]

      [27] Chetan B, Bunha M, Jagrat M, et al. Bioorg. Med. Chem. Lett., 2010,20:3906-3910

    28. [28]

      [28] Kundariya D S, Bheshdadia B M, Joshi N K, et al. Int. J. Chem. Tech. Res., 2011,3:238-243

    29. [29]

      [29] Thomas A B, Nanda R K, Kothapalli L P, et al. Arabian J. Chem., 2011,55:960-968

    30. [30]

      [30] Sondhi S, Singh N, Kumar A, et al. Bioorg. Med. Chem., 2006,14:3758-3765

    31. [31]

      [31] Kumar K S, Ganguly S, Veerasamy R, et al. Eur. J. Med. Chem., 2010,45:5474-5479

    32. [32]

      [32] Shreenivas M T, Chetan B P, Bhat A R. J. Pharm. Sci. Tech., 2009,1:88-94

    33. [33]

      [33] Sashidhara K V, Rosaiah J N, Bhatia G, et al. Eur. J. Med. Chem., 2008,43:2592-2596

    34. [34]

      [34] Baluja S, Solanki A, Kachhadia N. J. Iranian Chem. Soc., 2006,3:312-317

    35. [35]

      [35] Khan K M, Khan M, Ali M, et al. Bioorg. Med. Chem., 2009,17:7795-7801

    36. [36]

      [36] Aly M M, Mohameda Y A, El-Bayouki K A M, et al. Eur. J. Med. Chem., 2010,45:3365-3373

    37. [37]

      [37] Bhat M A, Al-Omar M A. Acta Poloniae Pharmaceutica Drug Res., 2011,64:375-380

    38. [38]

      [38] Zaheer M, Shah A, Akhter Z, et al. Appl. Organometal. Chem., 2011,25:61-69

    39. [39]

      [39] Chen W O, Wang L, Hao Y, et al. Dalton Trans., 2013,42:15678-15686

    40. [40]

      [40] Abd-Elzaher M M. Chin. J. Chem. Soc., 2004,51:499-504

    41. [41]

      [41] Ping H, Zhao K Q, Xu H B. Molecules, 2001,6:M250 DOI:10.3390/M250

    42. [42]

      [42] Dolomanov O V, Bourhis L J, Gildea R J, et al. J. Appl. Cryst., 2009,42:339-341

    43. [43]

      [43] Sheldrick G M. Acta Cryst., 2008,A64:112-122

    44. [44]

      [44] Ping H, Zhao K Q, Xu H B. Molecules, 2001,6:M249 DOI:10.3390/M249

    45. [45]

      [45] Motswainyana W M, Onani M O, Madieke A M. Polyhedron, 2014,41:44-51

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