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Analytical and Spectral Study of Furan Ring Containing Organic Ligands

Received: 12 December 2019    Accepted: 26 December 2019    Published: 30 January 2020
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Abstract

The reaction of Ethyl 5-(piperidin-1-yl-methyl)furan-2-carboxylate with 4-amino salicylic acid afford a 4-(5-((diphenylamino)methyl)furan-2-carboxamido)-2-hydroxybenzoic acid (PFSA). The transition metal complexes of Cu2+, Co2+, Ni2+, Mn2+ and Zn2+ of PFSA have been prepared. The objective of the research work is synthesis, characterization and chelating properties of furan ring containing organic ligands. To monitor its antimicrobial activity. PFSA and all the metal complexes were characterized by elemental analyses, spectral studies, magnetic moment determination, molar conductivity measurement. The free ligand and it’s complexes have been tested for their antibacterial activities against two types of human pathogenic bacteria the first group is gram positive while the second group is gram negative (by using agar well diffusion method). Finally, it was found that compounds show different activity of inhibition on growth of the bacteria. The conclusion is Ni (II) Cu (II), Co (II) and Mn (II) complexes possess octahedral geometry around the central metal ion.

Published in Chemical and Biomolecular Engineering (Volume 5, Issue 1)
DOI 10.11648/j.cbe.20200501.14
Page(s) 21-25
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

Ethyl 5-(Piperidin-1-yl-methyl) Furan-2-Carboxylate, 4-Amino Salicylic Acid, Metal Chelates, Complexes, Spectral Studies, Magnetic Moment, Antibacterial and Antifungal Activity

References
[1] Vagdevi HM, Vaidya VP. Ind J Heterocyclic Chem. 2001; 10, 253-260.
[2] DesaiNC, SatodiyaHM, Rajpara KM, Joshi VV, Vaghani HV, J. Saudi Chem. Soc.; 2014; doi: 10.1016; j. jscs. 2013; 12.005.
[3] PadmashaliB, VaidyaVP, VijayaKumarMLA, Ind. J. HeterocyclicChem. 2002; 12 (2), 89-94.
[4] Mahadevan KM, Vaidya VP, Vagdevi HM, Ind. J. Chem. 2003; 42B (8), 1931-1936.
[5] VarshneyMM, Husain A, Parcha V, Med. Chem. Res. 2014; 23 (9), 4034-4041.
[6] Ravindra KV, Vagdevi HM, Vaidya VP, Ind. J. Chem. 2008; 47B (8), 1271-1276.
[7] Mohanambal D, Antony S. A., 2014, Int. J. Pharma. Bio. Sci., 5 (3), 600-611.
[8] El-BindaryA. A., GhoneimMM, DiabMA, El-SonbatiA. Z., SeragLS, J. hermodyn. Catal., 2014; 5 (2), 135.
[9] Ukrainczyk M, GredicakM, Jeric I, Kralj D, Cryst. Growth Des. 2014; 14 (9), 4335-4346.
[10] Tilborg A, NorbergB, Wouters J, Eur. J. Chem. 2014; 74, 411-426.
[11] Hong S, Nebbioso A, CarafaV, ChenY, Yang B, Altucci L, You Q, Bioorg. Med. Chem., 2008; 17 (1), 7992-8002.
[12] Baily WR, Scott EG, Diagnostic Microbiology, The C. V. Moshy Co. St. Lovis, 1966; 257.
[13] Bhatt AK, Shah PK, Karadia HG, Patel HD, Orient. J. Chem., 2003; 19 (3), 704-706.
[14] Silverstein RM, Spectrometric Identification of organic compounds, 5th Ed., John Wiley, 1991.
[15] Kemp W, Organic Spectroscopy ELBS. Macmillan, UK, 1998.
[16] Nakamoto K, Infared Spectra of Inorganic and Co-Ordination Compound, Wiley, NY, 1970.
[17] Lever A. P, Inorganic Electronic Spectroscopy, Elsevier, NY, 1968.
[18] Figgis BN, Introduction to Ligands Field, Wiley Eastern Ltd. NY, 1976.
[19] Carlin RN, Dryneveldt AJV, Magnetic properties of Transition Metal Compound, Springe-Berlag, NY, 1997.
[20] Patel JC, Dholariya HR, PatelKS, Patel KD, Appl. Organomet. Chem., 2012; 26 (11), 604-613.
[21] Kettle FA, 1975, Coordination Compounds, Thomas Nelson & Sons.
[22] Patel J. C., Dholariya H. R., Patel K. S., Bhatt J., Patel K. D., 2014, Med. Chem. Res., 23 (8), 3714-3724.
[23] Patel Harshadkumar P., Patel Sefali S. and Patel Asha D. Journal 2015, of Chemical and Pharmaceutical Research, 7 (9): 690-694.
[24] Patel Harshadkumar P., 2018, International Journal of Current Advanced Research; Volume 7; Issue 2 (I); 10216-10219.
[25] Patel Harshadkumar P. and Patel Asha D., 2016, Der Pharma Chemica, 2016, 8 (1): 462-466.
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  • APA Style

    Harshadkumar P. Patel. (2020). Analytical and Spectral Study of Furan Ring Containing Organic Ligands. Chemical and Biomolecular Engineering, 5(1), 21-25. https://doi.org/10.11648/j.cbe.20200501.14

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    ACS Style

    Harshadkumar P. Patel. Analytical and Spectral Study of Furan Ring Containing Organic Ligands. Chem. Biomol. Eng. 2020, 5(1), 21-25. doi: 10.11648/j.cbe.20200501.14

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    AMA Style

    Harshadkumar P. Patel. Analytical and Spectral Study of Furan Ring Containing Organic Ligands. Chem Biomol Eng. 2020;5(1):21-25. doi: 10.11648/j.cbe.20200501.14

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  • @article{10.11648/j.cbe.20200501.14,
      author = {Harshadkumar P. Patel},
      title = {Analytical and Spectral Study of Furan Ring Containing Organic Ligands},
      journal = {Chemical and Biomolecular Engineering},
      volume = {5},
      number = {1},
      pages = {21-25},
      doi = {10.11648/j.cbe.20200501.14},
      url = {https://doi.org/10.11648/j.cbe.20200501.14},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.cbe.20200501.14},
      abstract = {The reaction of Ethyl 5-(piperidin-1-yl-methyl)furan-2-carboxylate with 4-amino salicylic acid afford a 4-(5-((diphenylamino)methyl)furan-2-carboxamido)-2-hydroxybenzoic acid (PFSA). The transition metal complexes of Cu2+, Co2+, Ni2+, Mn2+ and Zn2+ of PFSA have been prepared. The objective of the research work is synthesis, characterization and chelating properties of furan ring containing organic ligands. To monitor its antimicrobial activity. PFSA and all the metal complexes were characterized by elemental analyses, spectral studies, magnetic moment determination, molar conductivity measurement. The free ligand and it’s complexes have been tested for their antibacterial activities against two types of human pathogenic bacteria the first group is gram positive while the second group is gram negative (by using agar well diffusion method). Finally, it was found that compounds show different activity of inhibition on growth of the bacteria. The conclusion is Ni (II) Cu (II), Co (II) and Mn (II) complexes possess octahedral geometry around the central metal ion.},
     year = {2020}
    }
    

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  • TY  - JOUR
    T1  - Analytical and Spectral Study of Furan Ring Containing Organic Ligands
    AU  - Harshadkumar P. Patel
    Y1  - 2020/01/30
    PY  - 2020
    N1  - https://doi.org/10.11648/j.cbe.20200501.14
    DO  - 10.11648/j.cbe.20200501.14
    T2  - Chemical and Biomolecular Engineering
    JF  - Chemical and Biomolecular Engineering
    JO  - Chemical and Biomolecular Engineering
    SP  - 21
    EP  - 25
    PB  - Science Publishing Group
    SN  - 2578-8884
    UR  - https://doi.org/10.11648/j.cbe.20200501.14
    AB  - The reaction of Ethyl 5-(piperidin-1-yl-methyl)furan-2-carboxylate with 4-amino salicylic acid afford a 4-(5-((diphenylamino)methyl)furan-2-carboxamido)-2-hydroxybenzoic acid (PFSA). The transition metal complexes of Cu2+, Co2+, Ni2+, Mn2+ and Zn2+ of PFSA have been prepared. The objective of the research work is synthesis, characterization and chelating properties of furan ring containing organic ligands. To monitor its antimicrobial activity. PFSA and all the metal complexes were characterized by elemental analyses, spectral studies, magnetic moment determination, molar conductivity measurement. The free ligand and it’s complexes have been tested for their antibacterial activities against two types of human pathogenic bacteria the first group is gram positive while the second group is gram negative (by using agar well diffusion method). Finally, it was found that compounds show different activity of inhibition on growth of the bacteria. The conclusion is Ni (II) Cu (II), Co (II) and Mn (II) complexes possess octahedral geometry around the central metal ion.
    VL  - 5
    IS  - 1
    ER  - 

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Author Information
  • Faculty of Chemistry, S. S. Polytechnic College, Visnagar, India

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