Synthesis and Characterization of Novel Triazine Schiff ’s Bases Complexes with Transition Metal(II) Ions
DOI:
https://doi.org/10.32628/IJSRST25126266Keywords:
1,3,5-triazine, TRIPOD, Tripodal Schiff’s Bases, TRIPOD-SBNA complexesAbstract
1,3,5-triazines are a very important class of six- membered aromatic heterocyclic compounds receiving much attention in scientific research. This study focuses mainly on synthesis of 1,3,5- triazine derivative (TRIPOD) and TRIPOD-Schiff’s Bases by using microwave irradiation and their metal complexes with transition metal (II) ions. Schiff’s Bases synthesized from TRIPOD with different substituted aniline and metal (II) complexes of copper (II), nickel(II) and cobalt(II) of Tripod-Schiff’s bases were obtained in good yield. The characterization of newly synthesized compounds has been carried out by using FTIR, UV, XRD. The absorption peaks of Schiff’s bases synthesized and their complexes shows absorption peaks at different frequencies. TRIPOD shows characterized peak at 1567 cm-1 due to- CHO whereas all compounds have a conjugate system of double bonds on their backbone. The x-ray diffraction Spectrum of TRIPOD shows characteristic of crystalline and amorphous phases of conventional semi-crystalline compounds. Spectrum of complexes indicates amorphous nature of TRIPOD-SBNA complexes. FTIR spectra of TRIPOD gives characterized peak at 1567 cm-1 due to -CHO. Whereas Tripod-Schiff’s bases and their complexes gives peak which are in good arrangement with Literature values.
Downloads
References
Benzoguanamine, J. K., Simons, and Saxton, M. R.; Organic synthesis Coll, 1953, 33, 13. DOI: https://doi.org/10.15227/orgsyn.033.0013
Comins, D. L., and Connor, O. “Advances in Heterocyclic Chemistry”;Katritzky, A. R., Ed.; Academic: New York, NY, 1988,44, 243.
Vida, J. A., Medicinal Chemistry Part-III, Wolf, M. W.; Burger, A., eds.John Wiley and Sons, New York, 1981, 787.
Karen, A.; Edward, M. and Goodman, L.; J. Org.Chem. 1962, 27, 1717-1722. DOI: https://doi.org/10.1021/jo01052a055
Agrawal, A.; Shrivastav, K.; Puri, S.K. and Chauhan, M.S.P.;Bioorg. Med. Chem. Lett.; 2005, 15, 531-533. DOI: https://doi.org/10.1016/j.bmcl.2004.11.052
Griven, A N. ;Pharm. Chem. J. 1973, 7, 269. DOI: https://doi.org/10.1007/BF00772307
Pankaj, B. K.; Kishor, H. C.; Shah, K. N. and Patel, D. P. Design, synthesisand antimicrobial evaluation of s-triazinyl urea and thiourea derivatives.Arkivoc. 2009 (xi) 326-335. DOI: https://doi.org/10.3998/ark.5550190.0010.b30
Meredith, S. S., and Jerry, W. K., Solubilities of Triazine pesticides in pureand modified subcritical water. Anal.Chem. 2001, 73(4), 740-745. DOI: https://doi.org/10.1021/ac000906n
Hasegawa, Y.; Yanagisawa, T.; Okui, Y.; Sato, T.; Hosaka, K.; Chin, M. S.and Mitsuhashi, H., Chem. Pharm. Bull. 1991 39(12), 3180-3182. DOI: https://doi.org/10.1248/cpb.39.3180
Stefan, A.; Tomcufeik and Sloboda A E, Ger Offen, 1979, 2, 914, 051;Chem. Abstr., 1980, 92, Antiarthritic agents. 94443.
Lukashov, O. I.; Sokolova, N. A. ; Morozov, A. V.; Kazakov, P. V. ,Mirzabekova, N. S. and Kuz’mina, N. E.; Pharm. Chem.J., 2012,46, (4), 46 – 49.
Mooibroek, T. J.; Gamez, P. Inorg. Chim. Acta 2007, 360, 381-404. 2. DOI: https://doi.org/10.1016/j.ica.2006.07.061
Therrien, B. J. Organomet. Chem. 2011, 696, 637-651. 3. DOI: https://doi.org/10.1364/BOE.2.000696
B.R. Manzano, M.C. Carrion, A. Guerrero, J. Am. Chem. Soc., 42(3), 885 (2003).
G. Forlani, C.B. Vicentine, S. Guccione, L. Giurato, J. Am. Chem. Soc., 53(10), 3848(2005). DOI: https://doi.org/10.1021/jf0500029
Z. Ye, M. Tan, G. Wang, J. Yuan, Anal. Chem., 76(3), 513 (2004). DOI: https://doi.org/10.1021/ac030177m
K. Srinivas, S. Sitha, V.J. Rao, K. Bhanuprakash, K. Ravikumar, S.P. Anthony, T.P.Radhakrishnan, J. Mater. Chem., 15, 965 (2005). DOI: https://doi.org/10.1039/B414311F
Z.H. Chohan, S.K.A. Sheazi, Synth. React. Inorg. Met. Org.Chem. 29, 105 (1999) .
C. Jayabalakrishnan, K. Natarajan, Synth. React. Inorg. Met. Org. Chem. 31, 983 (2001) DOI: https://doi.org/10.1081/SIM-100105255
T. Jeeworth, H.L.K. Wah, M.G. Bhowon, D. Ghoorhoo, K. Babooram, Synth. React. Inorg. Met. Org. Chem. 30, 1023 (2000). DOI: https://doi.org/10.1080/00945710009351817
Thomas, A. Angew. Chem. Int. Ed. 2010, 49, 8328-8344. DOI: https://doi.org/10.1002/anie.201000167
Y. Ding, F. Wang, Z.J. Ku, L.S. Wang, Q.R. Wang, Russ. J. Coord. Chem. 35, 360 (2009). DOI: https://doi.org/10.1134/S107032840905008X
Z.E. Koc, S. Uysal, Helv. Chim. Acta 93, 910 (2010). DOI: https://doi.org/10.1002/hlca.200900294
I. Kaya, M. Yıldırım, Synth. Met. 159, 1572 (2009). DOI: https://doi.org/10.1016/j.synthmet.2009.04.019
S. Karabocek, S. Guner, N.J. Karabocek, Inorg. Biochem. 66, 57 (1997).
Anastas, P. T.; Warner, J. C. Green chemistry: Theory and Practice, Oxford University Press, New York 1998, 29-56.
De la Hoz, A.; Dı́ az -Ortiz, A.; Elguero, J.; Martı́ nez, L. J.; Moreno, A.; Sánchez- Migallón, A.Tetrahedron 2001, 57, 4397-4403. DOI: https://doi.org/10.1016/S0040-4020(01)00340-4
De la Hoz, A.; Blasco, H.; Diaz-Ortiz, A.; Elguero, J.; Foces-Foces, C.; Moreno, A.; SanchezMigallon,A.; Valiente, G. New J. Chem. 2002, 26, 926-932. DOI: https://doi.org/10.1039/b200169c
Diaz-Ortiz, A.; de la Hoz, A.; Moreno, A.; Sanchez-Migallon, A.; Valiente, G. Green Chem. 2002, 4,339-343. DOI: https://doi.org/10.1039/B202014A
Diaz-Ortiz, A.; Elguero, J.; Foces-Foces, C.; de la Hoz, A.; Moreno, A.; del Carmen Mateo, M.;Sanchez-Migallon, A.; Valiente, G. New J. Chem. 2004, 28, 952-958. DOI: https://doi.org/10.1039/B315956F
Gamez, P.; Reedijk, J. Eur. J. Inorg. Chem. 2006, 2006, 29-42. 4. DOI: https://doi.org/10.1002/ejic.200500672
I. M. El‐Anwar, S. M. Saad, Bull. NRC Egypt 1983, 8, 151.
A.I. Vogel, Text Book of Quantitative Chemical Analysis, 5th Edn., Longmann (1989).
R.J. Angellici, Synthesis and Techniques in Inorganic Chemistry, W.B. Saunders Company (1969).
J. Bassett, R.C. Denney, G.H. Jeffery, J. Mendham, Vogel’s Textbook of Quantitative Inorganic Analysis, Longman scientific & technical, London, UK, 4th edition (1986).
Yawale S.P. and Pakade S.V.; J. Mater. Sci., 20,(1993), 5451. DOI: https://doi.org/10.1007/BF00367814
Hassib H., Razik A.; Solid State Commun., 147, (2008), 346.
R.N. Figgis, R.S.J. Nyholm, Chem. Soc., 4, 190 (1958).
A. Earnshaw, Introduction to Magnetochemistry, Acad. Press, New York, (1968). DOI: https://doi.org/10.1016/B978-1-4832-3198-3.50005-9
R. Cruickshank, Medical Microbiology, 11th Edn. The ELBS Livingstone Ltd., Great Britain, 652, 901 (1970).
R. Adams, J.E. Bullock,W.C. Wilson, J. Am. Chem. Soc 45 (1923) 521. DOI: https://doi.org/10.1021/ja01655a032
M. Grigoras, C.O. Catanescu, C.I. Simionescu, Rev. Roum. Chim. 46 (2001) 927.
M. Grigoras, C.O. Catanescu, J. Macromol. Sci. Part C: Polym. Rev. 44 (2004) 131. DOI: https://doi.org/10.1081/MC-120034152
L. Marin, V. Cozan, M. Bruma, V.C. Grigoras, Eur. Polym. J. 42 (2006) 1173. DOI: https://doi.org/10.1016/j.eurpolymj.2005.11.010
H. Tanaka, Y. Shibahara, T. Sato, T. Ota, Eur. Polym. J. 2 (1993) 1525. DOI: https://doi.org/10.1016/0014-3057(93)90241-7
Downloads
Published
Issue
Section
License
Copyright (c) 2025 International Journal of Scientific Research in Science and Technology

This work is licensed under a Creative Commons Attribution 4.0 International License.
https://creativecommons.org/licenses/by/4.0