PL EN


Preferences help
enabled [disable] Abstract
Number of results
2019 | 126 | 222-247
Article title

Synthesis and bioactivity study of 2-((E)-(((E)-2,6-dichlorobenzylidene)hydrazono)methyl) phenol have N,O-Bidentate ligand site and it’s metal complex

Content
Title variants
Languages of publication
EN
Abstracts
EN
N,O-Bi-dentate ligands were prepared by the condensation of (E)-(2,6-dichlorobenzylidene) hydrazine with substituted Salicylaldehyde and different aromatic aldehydes. New synthesized metal complex are thermally stable and neither air- nor moisture sensitive at RT. Successive ligand and their metal complex are synthesized and characterized using IR, NMR, Elemental, Mass, Physical property. With Bioactivity study of ligand and there metal complexes.
Year
Volume
126
Pages
222-247
Physical description
Contributors
  • Chemical Research Laboratory, Department of Chemistry Saurashtra University, Rajkot - 360005, India
  • Chemical Research Laboratory, Department of Chemistry Saurashtra University, Rajkot - 360005, India
  • Chemical Research Laboratory, Department of Chemistry Saurashtra University, Rajkot - 360005, India
author
  • Chemical Research Laboratory, Department of Chemistry Saurashtra University, Rajkot - 360005, India
References
  • [1] Wail Al Zoubi, Biological Activities of Schiff Bases and Their Complexes: A Review of Recent Works. International Journal of Organic Chemistry, 2013, 3, 73-95
  • [2] Anant Prakash, Devjani Adhikari, Application of Schiff bases and their metal complexes - A Review. Int. J. ChemTech Res. 2011, 3(4)
  • [3] Sunita Bhagat, Nutan Sharma, and Tejpal Singh Chundawat, Synthesis of Some Salicylaldehyde-Based Schiff Bases in Aqueous Media. Journal of Chemistry Volume 2013, Article ID 909217
  • [4] A. Xavier, N. Srividhya. Synthesis and Study of Schiff base Ligands. IOSR Journal of Applied Chemistry Volume 7, Issue 11 Ver. I (Nov. 2014) 06-15
  • [5] Anu Kajal, Suman Bala, Sunil Kamboj, Neha Sharma, and Vipin Saini, Schiff Bases: A Versatile Pharmacophore. Journal of Catalysts Volume 2013, Article ID 893512
  • [6] Cleiton M. da Silva, Daniel L. da Silva, Luzia V. Modolo, Rosemeire B. Alves, Maria A. de Resende, Cleide V.B. Martins, Angelo de Fatima, Schiff bases: A short review of their antimicrobial activities. Journal of Advanced Research (2011) 2, 1–8
  • [7] Suzan A. Matar, Wamidh H. Talib, Mohammad S. Mustafa, Mohammad S. Mubarak Murad A. AlDamen, Synthesis, characterization, and antimicrobial activity of Schiff bases derived from benzaldehydes and 3,30-diaminodipropylamine. Arabian Journal of Chemistry (2015) 8, 850–857
  • [8] Emad Yousif, Ahmed Majeed, Khulood Al-Sammarrae, Nadia Salih, Jumat Salimon Bashar Abdullah, Metal complexes of Schiff base: Preparation, characterization and antibacterial activity. Arabian Journal of Chemistry (2017) 10, S1639–S1644
  • [9] Md. Saddam Hossain, C M Zakaria, Md. Kudrat-E-Zahan and B Zaman. Synthesis, Spectral and Thermal Characterization of Cu(II) Complexes with Two New Schiff Base Ligand towards Potential Biological Application, Der Chemica Sinica, 2017, 8(3): 380-392
  • [10] Ahmed M. Abu-Dief, Ibrahim M.A. Mohamed, A review on versatile applications of transition metal complexes incorporating Schiff bases. Beni-Suef University Journal of Basic and Applied Sciences 4 (2015) 11 9e133
  • [11] Kidwai, M. and Kumar, P. Microwave-induced syntheses of 6-(substituted aryl)-3-[(5-methyl-1,3,4-thiadiazol-2-ylsulfanyl)methyl]-1,2,4-triazolo[3,4b][1,3,4] thiadiazoles. ChemInform 27(41), October 2010. DOI:10.1002/chin.199641134
  • [12] A. Kamal, M. N. A. Khan, K. S. Reddy, K. Rohini, Bioorg. Med. Chem. 2007, 15, 1004-1013
  • [13] Ilknur Babahan, Esin Poyrazoglu Coban and Halil Biyik, Synthesis, characterisation and antimicrobial activities of vicdioxime derivatives containing heteroaromatic hydrazone groups and their metal complexes. Maejo Int. J. Sci. Technol. 2013, 7(01), 26-41
  • [14] Nora H. Al-Shaalan, Synthesis, Characterization and Biological Activities of Cu(II), Co(II), Mn(II), Fe(II), and UO2(VI) Complexes with a New Schiff Base Hydrazone: O-Hydroxyacetophenone-7-chloro-4-quinoline hydrazone, Molecules 2011, 16, 8629-8645
  • [15] Khalil K. Abid Bayader F. Abbas,Synthesis and characterization of some transition metal complexes with a coumarin derivative. Res Chem Intermed (2013) 39: 3991-3999
  • [16] Fazal Rahim, Waseeq-ur-rehamn, Muhammad Shehzad, Ajmal khan, Muhammad Taha,Synthesis and Antiurease & Antioxidant Activities of Bis-Schiff Bases of Isophthalaldehyde, Asian Journal of Chemistry Vol. 28, No. 1 (2016), 39-42.
  • [17] Kuruba Siddappa and Nabiya Sultana Mayana, Synthesis, Spectroscopic Characterization, and Biological Evaluation Studies of 5-Bromo-3-(((hydroxy-2-methylquinolin-7-yl)methylene) hydrazono)indolin-2-one and Its Metal (II) Complexes, Bioinorganic Chemistry and Applications Volume 2014, Article ID 483282
  • [18] C.-N. Zhang and Y.-F. Zheng, 1,2-Bis(2-chlorobenzylidene)hydrazine, Acta Cryst. (2008), E64, o36
  • [19] Hayam M. Ashour Marwa H. El-Wakil Mounir A. Khalil Khadiga A. Ismail Ibrahim M. Labouta, Synthesis of some (E)-6-[2-(furan-2-yl)ethenyl]-1,2,4-triazin-5-ones and their biological evaluation as antitumor agents, Med Chem Res (2013) 22: 1909-1924
  • [20] Hamdi M. Hassaneen, Zakaria Ahmed Gomaa,Utility of Styrylpyrazoloformimidate in the Synthesis of Fused Heterocyclic Compounds. International Journal of Organic Chemistry, 2015, 5, 213-222
  • [21] Atef M. Amer, Ali Deeb, Wafaa I. El-Eraky, Sally A. El Awdan and Sebaey Mahgoub, Synthesis, Characterization and Evaluation of Anti-Inflammatory and Analgesic Activity of Some Novel Quinoline Based Thiazolidinone Heterocycles. Egypt. J. Chem. Special Issue (2018)
  • [22] Pravin Tatyaram Tryambake, One Pot Two Step Synthesis of 2-Arylidenehydrazinyl-4-arylthiazole, Orient. J. Chem. Vol. 34(3), 1646-1652 (2018)
  • [23] Narasimhan Balasubramanian, Kumar Pradeep, Sharma Deepika, Bio-logical activities of hydrazide derivatives in the new millennium, Acta Pharmaceutica Sciencia, 52 (2010) 169-180
  • [24] Rosa Purgatorio, Modesto de Candia, Annalisa De Palma, Francesco De Santis, Insights into Structure-Activity Relationships of 3-Arylhydrazonoindolin-2-One Derivatives for Their Multitarget Activity on -Amyloid Aggregation and Neurotoxicity, Molecules 2018, 23, 1544
  • [25] Manju Kumari and Rakesh Narang, Structure Activity Relationship and Mechanism of Action of Hydrazide Derivatives as Antimicrobial Molecule, J. Chem. Pharm. Res. 2016, 8(7): 823-836
  • [26] Raghunath B Toche, Prashant Nikam, Synthesis and evaluation of antimicrobial and antitubercular activity of arylidene hydrazines of indenothieno[2,3-d]pyrimidine, Chemistry & Biology Interface, 2015, 5, 4, 246-257
  • [27] Peng-Wu Zheng, Qiao-Mei Qiu, Yu-Yan Linc and Ke-Fan Liud, N,N00-Bis(2,6-dichlorobenzylidene)hydrazine,Acta Cryst. (2006). E62, o1913-o1914.
  • [28] Emerson T. da Silva, Adriele da Silva Araújo, Adriana M. Moraes, Leidiane A. de Souza,Maria Cristina Silva Lourenço, Marcus V. N. de Souza, James L. Wardell and Solange M. S. V. Wardell,Synthesis and Biological Activities of Camphor Hydrazone and Imine Derivatives. Sci. Pharm. 2016, 84, 467-483
  • [29] Sobhi M. Gomha, Magda A. Abdallah, Salim S. Al-Showiman, Mahmoud A. Morad, Yahia N.Mabkhot, Synthesis of new pyridopyrimidinone-based thiadiazoles and pyrazolines aspotential anti-breast cancer agents. Biomedical Research 2017; 28 (22): 9903-9909
  • [30] Nasry Jassim Hussien, Siti Fairus M. Yusoff, Mohamad J. Al-Jeboori, Yang Farina, Hamza M. Abosadiya, Enaam I. Yousif and Riyadh M. Ahmed,Crystal structure of N-phenyl-2-(propan-2-ylidene)hydrazine-1-carbothioamide, Z. Kristallogr. NCS 2019; 234(1): 31-32
  • [31] Osama M. Sayed, Ahmed E.M. Mekky, Ahmad M. Farag and Ahmad H.M. Elwahy, 3,4-Dimethyl-2,5-functionalized thieno[2,3-b]thiophenes: versatile precursors for novel bis-thiazoles. Journal of Sulfur Chemistry, 2015 Vol. 36, No. 2, 124-134
  • [32] Mohanambal D, Sridevi G, Arul antony S Angayarkani R review: a recent review in applications of heterocyclic compounds as antimicrobial agent. Asian J Pharm Clin Res Vol 11, Issue 12, 2018, 66-74
  • [33] Nabila M. Ibrahim,a Hisham A. A. Yosef,a Ewies F. Ewies,a Mohamed R. H. Mahran, Mamdouh M. Alib and Abeer E. Mahmoudb,Synthesis and Antitumor Evaluation of New Heterocycles Derived from 3-Methyl-2-benzothiazolinone Hydrazone. J. Braz. Chem. Soc. Vol. 26, No. 6, 1086-1097, 2015
  • [34] Dalia Hussein Soliman, Wagdy Mohamed Eldehn, Hazem Ahmed Ghabbour,Maha Mamdouh Kabil, Marwa Mostafa Abdel-Aziz, and Hatem Abdel-Kader Abdel-Azizh, Novel 6-Phenylnicotinohydrazide Derivatives: Design, Synthesis and Biological Evaluation as a Novel Class of Antitubercular and Antimicrobial Agents. Biol. Pharm. Bull. 40, 1883–1893 (2017)
  • [35] N. M. Goudgaon and Y. Rohini Reddy, Goudgaon and Reddy, Design, synthesis and antimicrobial evaluation of novel 1-(2-(4-fluoro benzylthio)pyrimidin-4-yl-amino)-4-(substituted phenyl)azetidin-2-ones. IJPSR 2015; Vol. 6(3): 1060-1065
  • [36] N. Shashidhar Reddy, B. S. Shankara, P. Murali Krishana, C. Basavaraj, and B.Mahesh ,Synthesis, Characterization, and Antibacterial Activity of Co(II), Ni(II), Cu(II), Zn(II), Cd(II), and Hg(II) Complexes of Schiff’s Base Type Ligands Containing Benzofuran Moiety. International Journal of Inorganic Chemistry Volume 2013, Article ID-614628
  • [37] Xianyou Wang, Hua Wang Peiyun Chen, Yanping Pang, Zhilei Zhao, and Guangchen Wu, Synthesis and Biological Activities of Some Novel (E)-Alpha-(methoxyimino)benzeneacetate Derivatives with Modified 1,2,4-Triazole Moiety. Journal of Chemistry Volume 2014, Article ID 681364
  • [38] Hessa H. Al-Rasheed, Monirah Al Alshaikh, Jamal M. Khaled, Naiyf S. Alharbi, and Ayman El-Faham, Ultrasonic Irradiation: Synthesis, Characterization, and Preliminary Antimicrobial Activity of Novel Series of 4,6-Disubstituted-1,3,5-triazine Containing Hydrazone Derivatives, Journal of Chemistry Volume 2016, Article ID 3464758
  • [39] Shital L. Nawale and Avinash S. Dhake, Synthesis and evaluation of novel thiazolidinedione derivatives for antibacterial activity. Der Pharma Chemica, 2012, 4(6): 2270-2277
Document Type
article
Publication order reference
Identifiers
YADDA identifier
bwmeta1.element.psjd-3e1c116c-5db4-4da7-a338-01d52fc78c25
JavaScript is turned off in your web browser. Turn it on to take full advantage of this site, then refresh the page.