ARCHIVES

1. R. G. Mohamed, F. M. Elantabli, N. H. Helal, S. M. El-Medani. New group 6 metal carbonyl complexes with 4,5-dimethyl-N,Nbis(
pyridine-2-yl-methylene)benzene-1,2-diimine Schiff base: Synthesis, spectral, cyclic voltammetry and biological activity studies.
Spectrochim. Acta Part A Mol. Biomol. Spectrosc. 141 (2015) 316–326. https://doi.org/10.1016/j.saa.2015.01.054.
2. M. A. O. Ali. Palladium(II) and zinc(II) complexes of neutral (N2O2) donor Schiff bases derived from furfuraldehyde: Synthesis,
characterization, fluorescence and corrosion inhibitors of ligands. Spectrochim. Acta Part A Mol. Biomol. Spectrosc. 132 (2014) 132, 52–
60. https://doi.org/10.1016/j.saa.2014.03.127.
3. D. Nasrin, M. A. Alam, M. N. Hossain, M. Nazimuddin. Synthesis, Characterization and Antimicrobial Activity of Metal Complexes of
Schiff ’ s Base Derived from S-benzyldithiocarbazate with 2-hydroxyacetophenone. J. Chem. 03(01) (2013) 13–19. ISSN 2049 – 954X.
4. L. H. Abdel-Rahman, M. S. S. Adam, N. Al-Zaqri, M. R. Shehata, H. E.–S. Ahmed, S. K. Mohamed. Synthesis, characterization,
biological and docking studies of ZrO (II), VO (II) and Zn (II) complexes of a halogenated tetra-dentate Schiff base. Arab. J. Chem. 159(5)
(2022) 103737. https://doi.org/10.1016/j.arabjc.2022.103737.
5. M. T. Basha, B. S. Al-Farhan, M. R. Shehata, S. K. Mohamed, Y. Ramli, L. H. Abdel-Rahman. [Cu (dipicolinoylamide)(NO3)(H2O)]
as anti-COVID-19 and antibacterial drug candidate: Design, synthesis, crystal structure, DFT and molecular docking. J. Mol. Struct. 1247
(2022) 131348. https://doi.org/10.1016/j.molstruc.2021.131348.
6. M. Ismael, L. H. Abdel-Rahman, M. T. Basha, B. S. Al-Farhan. Synthesis, biological assay, chemical descriptors, and molecular docking
calculations of novel copper (II) mixed-ligand complexes of n-benzoyl-dl-phenylalanine and n-heterocyclic nitrogen bases. J. Mol. Struct.
1250(20) (2022) 131854. https://www.researchgate.net/doi.10.1016/j.molstruc.2021.131854.
7. A. Abdelghani, N. Al-Zaqri, E. M. Abdalla, L. H. Abdel Rahman. Physicochemical, in vitro therapeutic activity, DNA-binding, and in
silico molecular docking studies of samarium (III) complexes bearing N, O-chelated Schiff base ligands. J. Coord. Chem. 75(7-8) (2022)
994–1018. https://doi.org/10.1080/008972.2022.2095267.
8. A. Wolf, J. B. Swift, H. L. Swinney, J. A. Vastano. Determining lyapunov exponents from a time series. Phys. D Nonlinear Phenom. 16
(1985) 285–317. https://doi.org/10.1016/0167-2789(85)90011-9.
9. S. P. Fricker. The therapeutic application of lanthanides. Chem. Soc. Rev. 35(6) (2006) 524–533.
https://pubmed.ncbi.nlm.nih.gov/doi.10.1039/b509608c.
10. M. Thankamony and K. Mohanan, “Synthesis, spectral studies, thermal decomposition kinetics, reactivity and antibacterial acti vity of
some lanthanide(III) nitrate complexes of 2- (N-indole-2-one)amino-3-carboxyethyl-4,5,6,7-tetrahydrobenzo[b]thiophene,”. NIScPR
Online Peridical Repository/NIScPR Publications/Research Journals/Indian Journal of Chemistry-Section A (IJC-A)/IJC-A. 46A[
2007]/IJC-A 46A(02) [February2007] 247–251. ISSN 0376-4710. http://nopr.nscpr.res-in.
11. N. Bharti, S. Sharma, F. Naqvi, and A. Azam, “New palladium( II) complexes of 5-nitrothiophene-2-carboxaldehyde thiosemicarbazones:
synthesis, spectral studies and in vitro anti-amoebic activity,” Bioorg. & Med. Chem. 11(13) (2003) 2923–2929.
https://doi.org/10.1016/30968-0896(03)00213-x.
12. A. A. Soliman. Thermogravimetric and spectroscopic studies on Cadmium complexes with Two Salicylidene Thiophenol Schiff Bases.
Jou. Of Therm. Analy. And Calori. 63 (2001) 221 -231. https://doi.org/10.1023/A:1010109125051.
13. A. F. Petrovic, D. M. Petrovic, V. M. Leovac, and M. Budimir. Thermal Analysis of Fe(II) Complexes with Salicylaldehyde Semi-,
Thiosemi-and-S-methylisothiosemi-carbazones. J. of Thermal Analy.Calori. 58(3) (1999) 589-596.
https://doi.org/10.1023/a:1010100427217.
14. A. D. Garnovskii, I. S. Vasilchenko, D. A. Garnovskii& B. I. Kharisov. Molecular design of mononuclear complexes of acyclic Schiff-
base ligands. Jour. of Coord. Chem. 62(2) (2009) 151 – 204. https://doi.10.1080/00958970802398178.
15. Nayaz Ahmed, Riaz, Mohd., Altaf Ahmed and Bagat, Madhulika. Synthesis, Characterization, and Biological Evalution of Zn(II) Complex
with Tridentate (NNO Dono) Schiff Base ligand. Int. of Inorganic Chemistry. (2015). https://doi.10.1155/2015/607178.16. C. Boulechfar, H. Ferkous, A. Delimi, A. Djedouani, A. Kahlouche, A. Boublia, A. S. Darwish, T. Lemaoui, R. Verma and Y. Benguerba.
Schiff bases and their metal Complexes: A review on the history, synthesis, and applications. Inorg. Chem. Commun. 150 (2023) 110451.
https:doi.org/10.1016/j.inoche.2023.110451.
17. F. Sánchez-Férez, X. Solans-Monfort, L. Rodríguez-Santiago, T. Calvet, M. Font-Bardia and j. Pons. Structure directing factors and
photophysical properties of five Cu(I)-iodide materials with N-donor heteroaromatic ligands. J. Solid State Chem. 333 (2024) 124639.
https://doi.101016/j.jssc.2024.124639.
18. D. Royo, S. Moreno, M. Rodríguez-Castillo, M. Monge, M. E. Olmos, F. I. Zubkov, A. A. Pronina, G. Mahmoudi, and J. M. López-De-
Luzuriaga. Terpyridine isomerism as a tool for tuning red-to-NIR emissive properties in heteronuclear gold(I)-thallium(I) complexes.
Dalton Trans. 53 (2024) 4652–4661. https://doi.10.1039/D3DT04161A.
19. P. Li, L. Guo, J. Li, Z.Yang, H. Fu, K. Lai, H. Dong, C. Fan and Z. Liu. Mitochondria-targeted neutral and cationic iridium(iii) anticancer
complexes chelating simple hybrid sp2-N/sp3-N donor ligands. Dalton Trans. 53 (2024) 1977–1988.
https://doi.org/10.1039/D3DT03700B.
20. M.. Rathinam, A. SaravanaVadivu, P. Vijayan, S. Ramasamy, A. H. Hirad, & V. P. MuthaiahPillai. (2025). Evaluation of Co (II) Schiff
base complexes: Catalysis, theoretical and biomolecular interaction studies. Journal of Molecular Structure, 1321, 139842.
21. F. E. Ambaison, S. K. Ramasamy, S. Natarajan, G. Venkatesan, T. A. Alahmadi, P. Rohini, & A. Anderson. (2024). A carboethoxy
quinoline-Derived Schiff base chemosensor: Crystal structure, selective Hg2+ ion detection and its computational study. Environmental
Research, 252, 118983.
22. C. Kanagavalli, M. Kalanithi, M. Sankarganesh & T. J. K. Christopher Jeya. (2025). Novel azo-based benzimidazole Schiff base ligand
and its Co (II), Ni (II) Cu (II) complexes: computational and biological studies. Journal of Coordination Chemistry, 1-17.
23. L. Kótai. Metal Complexes with N-donor Ligands. Inorganics. 12 (2024) 130. https://doi.org/ 10.3390/inorganics12050130.
24. M. S. More, P. G. Joshi, Y. K. Mishra and P. K. Khanna. Metal complexes driven from Schiff bases and semicarbazones for biomedical
and allied applications: A review. Mater. Today Chem. 14 (2019) 100195. https://doi.org/10.1016/j.mtchem.2019.100195.
25. C. Boulechfar, H. Ferkous, A. Delimi, A. Djedouani, A. Kahlouche, A. Boublia, A. S. Darwish, T. Lemaoui, R. Verma and Y. Benguerba.
Schiff bases and their metal complexes: A review on the history, synthesis, and applications. Inorg. Chem. Commun. 150 (2023) 110451.
https://doi.org/10.1016/j.inoche.2023.110451.
26. A. Catalano. Schiff bases: A short survey on a promising scaffold in drug discovery. Curr. Med. Chem. 30(37) (2023) 4170–4180.
https://doi.org./10.2174/0929867330666230201121432.
27. M. S. More, P. G. Joshi, Y. K. Mishra and P. K. Khanna. Metal complexes driven from Schiff bases and semicarbazones for biomedical
and allied applications: A review. Mater. Today Chem. 14 (2019) 100195. https://doi.org/10.1016/j.mtchem.2019.100195.
28. C. Boulechfar, H. Ferkous, A. Delimi, A. Djedouani, A. Kahlouche, A. Boublia, A. S. Darwish, T. Lemaoui, R. Verma and Y. Benguerba.
Schiff bases and their metal complexes: A review on the history, synthesis, and applications. Inorg. Chem. Commun. 150 (2023) 110451.
https://doi.org/10.1016/j.inoche.2023.110451.
29. A. Catalano. Schiff bases: A short survey on a promising scaffold in drug discovery. Curr. Med. Chem. 30(37) (2023) 4170–4180.
https://doi.org./10.2174/0929867330666230201121432.
30. R. Meena, P. Meena, A. Kumari, N. Sharma and N. Fahmi. Schiff Bases and Their Metal Complexes: Synthesis, Structural Characteristics
and Applications. In Schiff Base in Organic, Inorganic and Physical Chemistry; IntechOpen: London, UK. (2023) ISBN 978-1-80355-
679-6. https://doi.10.5772/intechopen.108396.
31. K. Mondal and S. Mistri. Schiff base based metal complexes: A review of their catalytic activity on aldol and henry reaction. Comments
Inorg. Chem. 43 (2023) 77–105. https://doi.10.1080/02603594.2022.2094919.
32. B. Nazirkar, M. Mandewale & Ramesh. Synthesis, characterization and antibacterial activity of Cu (II) and Zn (II) complexes of 5-
aminobenzofuran-2-carboxylate Schiff base ligands. Journ. of Taibah Uni. for Sci. 13 (1) (2019) 440-449.
https://doi.org/10.1080/16583655.2019.1592316.
33. A.Reiss, T. Caproiu and N. Stanica. Synthesis, Characterization and Antibacterial Studies of Transition Metal Complexes with 2-
Thiophenecarboxaldehyde Derived Schiff Base. Asian Journ. of Chem. 21( 7) (2009) 5305-5309. ISSN: 0975-427X (Online) | ISSN:
0970-7077 (Print).
34. H. Z. Chohan, M. Arif Mod, A. Akhtar and T. Supuran. Metal-Based Antibacterial and Antifungal Agents: Synthesis, Characterization,
and In Vitro Biological Evaluation of Co(II), Cu(II), Ni(II), and Zn(II) Complexes With Amino Acid-Derived Compounds. Hindawi
Publishing Corpora. Bioinorg. Chem. and Applis. (2006) Article ID 83131, 1–13. https://doi./10.1155/BCA/2006/83131.
35. A. Saadat, A. B. P. Mcardle and R. Jafari. Spectral, Structural, and Antibacterial Study of Copper(II) Complex with N2O2 Donor Schiff
Base Ligand and Its Usage in Preparation of CuO Nanoparticles. Journ. Of chem. (2022) Art. ID 8913874.
https://doi.org/10.1155/2022/8913874.
36. Mohd S. Khursheed, A. N. Khan, R. H. khan. An antibiotic (sulfamethoxazole) stabilizes polypeptide (human serum albumin) even under
extreme condition (elevated temperature). Int J Biol Macromol 135 (2019) 337-343. https://doi: 10.1016/j.ijbiomac.2019.05.152. Epub
2019 May 22, PMID: 31128176.
37. M. Biancalana, S. Koide, Molecular mechanism of thioflavin-T binding to amyloid fibrils,Biochim. Biophys. Acta, Proteins Proteomics.
1804 (2010) 1405–1412, https:// doi.org/10.1016/j.bbapap.2010.04.001.
38. Baine, D. S. Georgie, E. Z. Shiferraw, T. P. T. Nguyen, L. A. Nogaj, D. A. Moffet. Inhibition of Aβ42 aggregation using peptides selected
from combinatorial libraries, J. Pept. Sci. (15) (2009) 499–503, https://doi.org/10.1002/psc.1150.
39. A. Qadeer, M. Zaman, R. H. Khan. Inhibitory effect of post-micellar SDS concentration on thermal aggregation and activity of papain,
Biochem. 79 (2014) 785–796, https:// doi.org/10.1134/S0006297914080069.
40. A. Rizvi, M. T. Alam, A. Naeem, Peroxidase improves the activity of catalase by preventing aggregation during TFE-induced denaturation.
J. Biomol. Struct. Dyn. 36 (2018) 551–560, https://doi.org/10.1080/07391102.2017.1287007.
41. S. Moh. Zakariya. Mohd F., M. Zaman, T. Ilm Chandel, S. M. Ali, Vladimir N. Uversky, R. H. Khan. An in-vitro elucidation of inhibitory
potential of carminic acid: Possible therapeutic approach for neurodegenerative diseases. Journal of Molecular Liquids. 303 (2020)
112692. https://doi,org/10.1016/j.molliq.2020.112692
42. Mohd. F., A. Rizvi, M.T. Alam, A. Naeem. Peroxidase improves the activity of catalase by preventing aggregation during TFE-induced
denaturation, J. Biomol. Struct. Dyn. 36 (2018) 551–560, https://doi.org/10.1080/07391102.2017.1287007.43. Christine Xue, T. Y. Lin, Dennis Chang, Zhefeng Guo. Thioflavin T as an amyloid dye: fibril quantification, optimal concentration and
effect on aggregation. R. Soc. Open Sci. 4(1) (2017) 160696. https;//doi.10.1098/rsos.160696. eCollection 2017 Jan. PMID: 28280572,
PMCID: PMC5319338.
44. K. Ibrahim, R. Zaky, E. Gomaa, L. Yasin. Computational simulation and biological studies on 3-(2-(2-hydroxybenzoyl)hydrazono)- N-
(pyridine-2-yl)butanamide complexes. J. Mol. Struct. 1101 (2015) 124–138. [CrossRef]
45. S. Slassi, M. Aarjane, A. Amine. New bidentate Schiff base ligands derived from histidine and their metal complexes: Synthesis, structural
analysis, antibacterial and antioxidant evaluation. J. Iran. Chem. Soc. 19 (2022) 19 3117–3125. [CrossRef]
46. S. Patil, S. D. Jadhav, and S. K. Shinde. CES as an Efficient Natural Catalyst for Synthesis of Schiff Bases under Solvent-Free Conditions:
An Innovative Green Approach. Hindawi Publishing Corpor. Org.anic chem.. Intern. (2012) Artricle ID 153159.
https://doi.10.1155/2012/153159.
47. R. Abdel, L.H., Abdelghani, A.A., AlObaid, A.A., El-ezz, D.A., Warad, I., Shehata,M.R. Novel Bromo and methoxy substituted Schiff
base complexes of Mn(II), Fe(III), and Cr(III) for anticancer, antimicrobial, docking, and ADMET studies. Sci Rep. 2023, 13, 3199.
[CrossRef].
48. N. N. Greenwood and A. Earnshaw, “Coordination compounds,” in Chemistry of the Elements. (1997) 1290–1326. Butterworth-
Heinemann, Oxford, UK, 2nd edition.
49. A. B. P. Lever, Inorganic Electronic Spectroscopy, vol. 481, Elsevier, London, UK, (1986).
50. G. L. Miessler and D. A. Tarr, “Coordination compounds,” in Inorganic Chemistry. (642) (1999) 315–316. Pearson Prentice Hall, New
York, NY, USA.
51. Abdel-Rahman, L.H., Abdelghani, A.A., AlObaid, A.A., El-ezz, D.A., Warad, I., Shehata, M.R. Novel Bromo and methoxy substituted
Schiff base complexes of Mn(II), Fe(III), and Cr(III) for anticancer, antimicrobial, docking, and ADMET studies. Sci Rep. 13 (2023)
3199. [CrossRef]
52. G. L. Miessler and D. A. Tarr. Inorganic Chemistry. Pearson Prentice Hall, New York. (1999) 315-316.
53. X. Han, Y. Zhong-Lu, X. Yong-Ting and W. Xiao-Min. Synthesis, characterization and crystal structure of a mononuclear zinc(II) complex
derived from 2-methoxy-6-[(3- cyclohexylaminopropylimino)methyl]phenol. J. Chem. Crystall. 36 (11) (2006) 743-746.
https://doi.10.1007/s10870-006-9131-3.
54. X. Han, Z. L. You, Y. T. Xu, and X. M. Wang, “Synthesis, characterization and crystal structure of a mononuclear zinc(II) complex
derived from 2-methoxy- 6-[(3-cyclohexylaminopropylimino)methyl]phenol,” Journal of Chemical Crystallography. 36 (11) (2006) 743–
746.
55. A. Samir, Abdallatif, Yousry M. Issa. Spectroscopic, Thermal and magnetic Properties os some transition metal complexes derived from
1-Phenyl-3 substituted-4-nitr-Pyrazones. Journ. Of Natrural science. 2 (9) (2010). https://doi.10.4236/ns.2010.29127.
56. W.W. Simmons. The Sadtler Handbook of Proton NMR Spectra. Philadelphia, Pa: Sadtler Research Laboratories. (1978). ISBN:
0845600354.
57. D. J. Pasto. Organic Structure Determination. London,UK: Prentice Hall. (1969). ISBN-10: 0136408540, ISBN-13: 978-0136408543.
58. Mohd F., N. Ahmad Fazili, Mohd Afsar, A. Naeem. Analysing cytochrome C Aggregation and Fibrillation upon Interaction with
Acetonitrle: an in Vitro Study. 26 (6) (2016) 1959-1966. https://doi.org/10.1007/s10895-016-1889-x.
59. A. Rizvi, I. Naseem. Physiological serum copper concentrations found in malignancies cause unfolding induced aggregation of human
serum albumin in vitro. Archives of Biochemistry and Biophysics. 636 (2017) 71-78. www.elsevier.com/locate/yabbi.
60. R. Khurana, C. Coleman, Cristian Ionescu-Zanetti, Sue A Carter, Vinary Krishna, Rajesh K Grover, Raja Roy, Shashi Singh.Mechanism
of thioflavin T binding to amyloid fibrils. J. Struct. Biol. 151 (3) (2005) 229-38. https://doi.101016/j.jsb.2005.06.006. PMID: 16125973.
61. D. Matulis, R. Lovrien. 1-Anilino-8-naphthalene sulfonate anion-protein binding depends primarily on ion pair formation. J. Biophys.
74(1) (1998) 422-429. https://doi.org/10.1016/S0006-3495(98)77799-9
62. S. Nusrat,M. Zaman, A.Masroor,M.K. Siddqi, N. Zaidi, K. Neelofar, A.S. Abdelhameed, R.H. Khan, Deciphering the enhanced inhibitory,
disaggregating and cytoprotective potential of promethazine towards amyloid fibrillation, Int. J. Biol. Macromol. 106 (2018) 851–863.
https://doi.org/10.1016/j.ijbiomac.2017.08.081.
63. J. M. Khan, A. Qadeer, S. K. Chaturvedi, E. Ahmad, S. A. A. Rehman, S. Gourinath, R. H. Khan, SDS can be utilized as an amyloid
inducer: a case study on diverseproteins. PLoS One 7(1) (2012) e29694. https://doi.10.1371/journal.pone.0029694.
64. S. K. Chaturvedi, N. Zaidi, P. Alam, J.M. Khan, A. Qadeer, I.A. Siddique, S. Asmat, Y. Zaidi, R.H. Khan, Unraveling comparative anti-
amyloidogenic behavior ofpyrazinamide and D-cycloserine: a mechanistic biophysical insight. PLoS One 10 (8) (2015) e0136528.
https://doi,org/10.1371/journal.pone.0136528.
65. Mohd Khursheed Siddiqi, S. Mohammad Zakariya, Faez Iqbal Khan, Md. Imtaiyaz Hassan, Rizwan Hasan Khan. An In Vitro elucidation
of the antiaggregatory potential of Diosminover thermally induced unfolding of hen egg white lysozyme; A preventive quest for lysozyme
amyloidosis. Int. J. of Biol. Macromolecu. 129 (2-3) (2019) 1015–1023. https://doi.10.1016/j.ijbiomac.2019.02.107.