[1] Cimerman, Z.; Miljanić, S.; Galić, N.J.C.C.A. Schiff bases derived from aminopyridines as spectrofluorimetric analytical reagents.
Journal of Catalysts 2000,
73, 81-95, DOI:
10.1155/2013/893512.
[3] Ahmed, A.A.; Al-mashhadani, M.H.; Hashim, H.; Ahmed, D.S.; Yousif, E. Morphological, Color Impact and Spectroscopic Studies of New Schiff Based Derived From 1,2,4-Triazole Ring. Progresss in Color, Colorants and Coatings 2021 14, 27-34.
[4] Sathe, B.S.; Jaychandran, E.V.; Jagtap, A.; Sreenivasa, G.M. Synthesis characterization and anti-inflammatory evaluation of new fluorobenzothiazole schiff's bases. International Journal of Pharmaceutical Research and Development 2011, 3, 164–169.
[5] Sondhi, S.M.; Singh, N.; Kumar, A.; Lozach, O.; Meijer, L. Synthesis, anti-inflammatory, analgesic and kinase (CDK-1, CDK-5 and GSK-3) inhibition activity evaluation of benzimidazole/benzoxazole derivatives and some Schiff's bases,”
Bioorganic and Medicinal Chemistry 2006,
14, 3758–3765, DOI:
10.1016/j.bmc.2006.01.054
[6] Pandey, A.; Dewangan, D.; Verma, S.; Mishra, A.; Dubey, R. Synthesis of Schiff bases of 2-amino-5-aryl-1, 3,4-thiadiazole And its Analgesic, Anti- Inflammatory,Anti-Bacterial and Anti- Tubercular Activity. International Journal of ChemTech Research 2011, 3, 178–184. ISSN : 0974-429
[7] Chandramouli; Shivanand, M.R.; Nayanbhai, T.B.; Bheemachari; Udupi, R.H. Synthesis and biological screening of certain new triazole schiff bases and their derivatives bearing substituted benzothiazole moiety. Journal of Chemical and Pharmaceutical Research 2012, 4, 1151-1159.
[8] Chinnasamy, R.P.; Sundararajan, R.; Govindaraj, S. Synthesis, characterization, and analgesic activity of novel Schiff base of isatin derivatives.
J Adv Pharm Technol Res 2010,
1, 342-347,
https://doi.org/10.4103/0110-5558.72428.
[9] Mounika, K.; Pragathi, A.; Gyanakumari, C. Synthesis¸ Characterization and Biological Activity of a Schiff Base Derived from 3-Ethoxy Salicylaldehyde and 2-Amino Benzoic acid and its Transition Metal Complexes.
Journal of Scientific Research 2010,
2, 513–524,
https://doi.org/10.3329/jsr.v2i3.4899.
[10] Venkatesh, P. Synthesis, characterization and antimicrobial activity of various schiff bases complexes of Zn(II) and Cu(II) ions.
Asian J Pharm Hea Sci 2011,
1, 8-11,
https://doi.org/10.1155/2013/47934
[11] Kumar, C.; Pandeya, S.N. Synthesis & anticonvulsant activity (Chemo Shock) of Schiff and Mannich bases of Isatin derivatives with 2-Amino pyridine (mechanism of action). International Journal of PharmTech Research 2012, 4, 590-598.
[12] Aboul-Fadl, T.; Mohammed, F.A.-H.; Hassan, E.A.-S. Synthesis, antitubercular activity and pharmacokinetic studies of some schiff bases derived from 1- alkylisatin and isonicotinic acid hydrazide (inh).
Archives of Pharmacal Research 2003,
26, 778-784,
https://doi.org/10.1007/BF02980020.
[13] Miri, R.; Razzaghi-asl, N.; Mohammadi, M.K. QM study and conformational analysis of an isatin Schiff base as a potential cytotoxic agent.
Journal of Molecular Modeling 2013,
19, 727-735,
https://doi.org/10.1007/s00894-012-1586-x.
[14] Ali, S.M.; Azad, M.A.; Jesmin, M.; Ahsan, S.; Rahman, M.M.; Khanam, J.A.; Islam, M.N.; Shahriar, S.M. In vivo anticancer activity of vanillin semicarbazone.
Asian Pac J Trop Biomed 2012,
2, 438-442,
https://doi.org/10.1016/s2221-1691(12)60072-0.
[15] Wei, D.; Li, N.; Lu, G.; Yao, K. Synthesis, catalytic and biological activity of novel dinuclear copper complex with Schiff base.
Science in China Series B 2006,
49, 225-229,
https://doi.org/10.1007/s11426-006-0225-8.
[16] Avaji, P.G.; Vinod Kumar, C.H.; Patil, S.A.; Shivananda, K.N.; Nagaraju, C. Synthesis, spectral characterization, in-vitro microbiological evaluation and cytotoxic activities of novel macrocyclic bis hydrazone.
European Journal of Medicinal Chemistry 2009,
44, 3552-3559,
https://doi.org/10.1016/j.ejmech.2009.03.032.
[17] Venugopala, K.; Jayashree, B. Synthesis and characterization of carboxamides of 2'-amino-4'-(6-bromo-3-coumarinyl) thiazole for their analgesic and anti-inflammatory activity. Asian Journal of Chemistry 2003, 12, 307-310.
[18] Vashi, K.; Naik, H.B. Synthesis of Novel Schiff Base and Azetidinone Derivatives and their Antibacterial Activity.
E-Journal of Chemistry 2004,
1,
https://doi.org/10.1155/2004/158924.
[19] Ahmed, N.; S. Ahmed, D.; Mohammed, H.; Al-mashhadani, M.; Hussain, Z.; Salam, C.; Mohammed, A.; Rahimi, M.; Yusop, R.; Yousif, E. Inhibition of Corrosion: Mechanisms and Classifications an Overview.
Al-Qadisiyah Journal Of Pure Science 2020,
25, 1-9,
https://doi.org/10.29350/qjps.2020.25.2.1072.
[20] Li, S.; Chen, S.; Lei, S.; Ma, H.; Yu, R.; Liu, D.J.C.S. Investigation on some Schiff bases as HCl corrosioninhibitors for copper.
1999,
41, 1273-1287. DOI:
10.5402/2012/842836 Sep 17, 2014
[22] Patai, E.S. The chemistry of carbon-nitrogen double bond. John Wiley and Sons, New York, 1970; pp.61-146.
[23] Jarrahpour, A.A.; Zarei; M. Synthesis of 2-({[4-(4-{[(E)-1-(2-hydroxy-3-methoxyphenyl)methylidene amino}phenoxy)phenyl imino}methyl)- 6 -methoxy phenol.
Molbank 2010,
M352.
https://doi.org/10.3390/molecules15106850
[24] Kumar, S. Synthesis and antimicrobial study of some Schiff bases of sulfonamides. Journal of Current Pharmaceutical Research 2010, 01, 39-42.
[25] Havaldar, F.H.; Mishra, S.K.J.J.I.J.O.H.C. Synthesis of biologically active 1-(3'-bromo-4'-methoxybenzoyl)-4-formyl-3-(substituted phenyl) pyrazoles. Bioorganic & Medicinal Chem. 2003, 13, 165-166, https://doi.org/10.1016/s0968-0896(97)00111-9.
[26] Patil, S.; Jadhav, S.; Deshmukh, M.; Patil, U. Natural Acid Catalyzed Synthesis of Schiff under Solvent-Free Condition: As a Green Approach.
International Journal of Organic Chemistry 2012,
02, 166-171,
https://doi.org/10.4236/ijoc.2012.22025.
[27] Bendale, A.; Bhatt, R.; Nagar, D.; Narkhede, S.; Jadhav, A.; Vidyasagar, G. Schiff base synthesis by unconventional route: An innovative green approach. Der Pharma Chemica 2011, 3, 34-38.
[28] Kuehne, M.E. The applications of enamines to a new synthesis of b-ketonitriles. J. Am.Chem. Soc. 1959, 81. (b) Westheimer, F.; Taguchi, K.J.T.J.O.O.C. Catalysis by molecular sieves in the preparation of ketimines and enamines. 1971, 36, 1570-1572. https://doi.org/10.1021/ja01529a037
[29] Zhu, J.; Chen, L.; Wu, H.; Yang, J.J.C.J.o.C. Highly Efficient Procedure for the Synthesis of Schiff Bases Using Hydrotalcite‐like Materials as Catalyst.
2009,
27, 1868-1870.
https://doi.org/10.1155/2014/848543
[30] Abbaspour, A.; Esmaeilbeig, A.; Jarrahpour, A.; Khajeh, B.; Kia, R.J.T. Aluminium (III)-selective electrode based on a newly synthesized tetradentate Schiff base.
Talanta 2002,
58, 397-403. DOI:
10.1016/s0039-9140(02)00290-4 PMID: 18968765
[31] Mahajan, R.; Kaur, I.; Kumar, M.J.S.; Chemical, A.B. Silver ion-selective electrodes employing Schiff base p-tert-butyl calix [4] arene derivatives as neutral carriers.
Sens. Actuators 2003,
91, 26-31. http://dx.doi.org/
10.1016/S0925-4005(03)00062-5
[32] Jain, A.; Gupta, V.; Ganeshpure, P.; Raisoni, J.J.A.c.a. Ni (II)-selective ion sensors of salen type Schiff base chelates. 2005, 553, 177-184. doi: 10.1016/j.aca.2008.06.054. Epub 2008 Jul 9.
[33] Gupta, V.K.; Singh, A.K.; Mehtab, S.; Gupta, B.J.A.c.a. A cobalt (II)-selective PVC membrane based on a Schiff base complex of N, N′-bis (salicylidene)-3, 4-diaminotoluene.
2006,
566, 5-10. DOI
10.1016/j.aca.2006.02.038
[34] Li, S.; Chen, S.; Lei, S.; Ma, H.; Yu, R.; Liu, D.J.C.S. Investigation on some Schiff bases as HCl corrosioninhibitors for copper.
1999,
41, 1273-1287. DOI:
10.5402/2012/842836 Sep 17, 2014
[35] Agata, B. Synthesis, thermal behavior and some properties of CuII complexes with N,O-donor Schiff bases. J Therm Anal Calorim 2018, 131, 1221–36.
[36] Al-Zaidi, BH.; Ahmed, HI.; Ali, NN. Preparation, characterization and biological activity of new tridentate imine-oxime ligand (H2L) and its metal complexes. Asian J Chem. 2018, 30,1157–64, DOI: 10.7324/JAPS.2019.90406
[37] AV. Synthesis, characterization antimicrobial and antioxidant activities of 2,4-dihydroxybenzaldehyde-4-phenyl-3- thiosemicarbazone (DHBPTSC) and its Pd(II), Ni(II)dppm mixed ligand and Cu(II) complex having heterocyclic bases. J Appl Pharm Sci, 2018, 8, 071-8. DOI: 10.7324/JAPS.2018.8410
[38] Peng-Peng, L.; Li Z, Ji-Xing, Z.; Zhao-Bin, Z. Crystal structure of (E)-1-(4-(((E)-4-(diethylamino)-2-hydroxybenzylidene)amino)phenyl) ethan-1-oneoxime, C19H23N3O2.
Z Kristallogr NCS,
2018, 233, 13–5. DOI:
https://doi.org/10.1515/ncrs-2017-0071 Published online:15 Nov 2017
[39] Senbagam, R.; Vijayakumar, R.; Rajarajan, M.; Balaji, S.; Manikandan, V.; Vanangamudi, G.; Thirunarayanan, G. Synthesis, assessment of substituent effect and antimicrobial activities of (4E)-4-(benzylideneamino)-1,2- dihydro-2,3-dimethyl- 1-phenylpyrazol-5-one compounds. Karbala Int J Mod Sci 2016, 2, 56–62. DOI: 10.1016/j.kijoms.2016.01.004
[40] Swati, B.; Uma, V. A new approach for extraction of heavy metal ion from industrial effluents by silver nanoparticles coated with N-(2- Hydroxybenzylidene)-2-Amino pyridine Schiff B. Asian J Sci Technol 2017, 6, 15945–55. DOI: 10.7324/JAPS.2019.90406
[41] Ratiram, GC.; Parvej, A.; Nilesh, VG.; Jay, AT.; Harjeet, DJ. Thermal decomposition kinetics of some transition metal coordination polymers of fumaroyl bis (paramethoxyphenylcarbamide) using DTG/DTA techniques.
Arab J Chem 2019,
12, 1070-1082.
https://doi.org/10.1016/j.arabjc.2016.03.008
[42] Ommenya, F.; Nyawade, F.K.; Andala, E.A; Kinyua, J.;Synthesis, Characterization and Antibacterial Activity of Schiff Base, 4-Chloro-2-{(E)-[(4-Fluorophenyl)imino]methyl}phenol Metal (II) Complexes. J. of Chem. 2020, 2020, Article ID 1745236, 8, https://doi.org/10.1155/2020/1745236
[43] Hui, Y.; Wei, Z.; Qing, Y.; Fu-Ping, H.; He-Dong, B.; Hong, L. Ni(II) complexes with Schiff base ligands: preparation, characterization, DNA/ protein interaction and cytotoxicity studies.
Molecules 2017,
22, 1772, doi:
10.3390/molecules22101772.
[44] Hao-Ran, J.; Jing, L.; Yin-Xia, S.; Jian-Qiang, G.; Bin. Y.; Na, W.; Li, X. Two supramolecular cobalt(II) complexes: syntheses, crystal structures, spectroscopic behaviors, and counter anion effects. Crystals, 2017, 7, 1–15. DOI: 10.3390/cryst7080247.
[45] Franz, AM.; Roland, CF.; Mark, S.; Andres, RA.; Diana, HT.; Salah, SM. Metal(II) complexes of compartmental poly nuclear Schiff bases containing phenolate and alkoxy groups. Crystals, 2016, 6, 1–17. https://doi.org/10.3390/cryst6080091
[46] Erdal, C.; Ayşe, A.; Hakan, Ş.; Mehmet, K. Some transition metal complexes of NO type Schiff base: preparation and characterization. Sci J (CSJ) 2016, 37, 65–73. DOI: 10.7324/JAPS.2019.90406.
[47] Kailas, K.H.; Sheeta, J. P.; Anita, P.P; Apoorva, H.P; Four synthesis methods of Schiff base ligands and preparation “of their metal complex with Ir and antimicrobial investigation,
World Journal of Pharmacy and Pharmaceutical Sciences 2016,
5, 1055–1063, DOI:
10.2323/jgam.51.133
[48] Juan, A.; Yaricruz, P.; Alina, B.; Juan, C. Synthesis, Characterization and Antibacterial Activity of a Tridentate Schiff Base Derived from Cephalexin and 1,6-Hexanediamine and its Transition Metal Complexes. Med chem. 2016, 6, 467-473. http://dx.doi.org/10.4172/2161-0444.1000385