Importance of the Applicability of O-Vanillin Schiff Base Complexes: Review

سال انتشار: 1400
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 177

فایل این مقاله در 17 صفحه با فرمت PDF قابل دریافت می باشد

استخراج به نرم افزارهای پژوهشی:

لینک ثابت به این مقاله:

شناسه ملی سند علمی:

JR_AJCS-4-2_002

تاریخ نمایه سازی: 31 فروردین 1400

چکیده مقاله:

Ortho-vanillin Schiff baseare multipurpose ligands which are synthesized from the condensation of 2-Hydroxy-3-methoxybenzaldehyde with amines compounds to designing an infinite number of potential compounds. Ortho-vanillin Schiff base grow into very common in coordination chemistry for the reason that it can form compounds that have high stability with most metals, and this is due tonitrogen (N) of azomethine group beside two oxygen (O) atoms of hydroxyl and methoxy groups. Ortho-vanillin Schiff base and its metal complexes are very important as antibacterial, antifungal, antioxidant and anticancer, Also, many available pharmaceutical researches predict how these compounds can interaction with DNA. Many efforts are made in the possibility of using Ortho-vanillin Schiff baseas catalyst, polymers, dyes, Analogues and pharmaceutical fields.  This review will try to shed light on the most used applications by researchers of Ortho-vanillin Schiff base compounds to stimulate more and more efforts to achieve maximum benefit from potential infinite number of compounds.

نویسندگان

Ali Hassan

Chemistry Department, Faculty of Science, Al-Azhar University, Nasr City ۱۱۸۸۴, Egypt

Ahmed Said

Senior Researcher Chemist, Greater Cairo Water Company, Cairo, Egypt

مراجع و منابع این مقاله:

لیست زیر مراجع و منابع استفاده شده در این مقاله را نمایش می دهد. این مراجع به صورت کاملا ماشینی و بر اساس هوش مصنوعی استخراج شده اند و لذا ممکن است دارای اشکالاتی باشند که به مرور زمان دقت استخراج این محتوا افزایش می یابد. مراجعی که مقالات مربوط به آنها در سیویلیکا نمایه شده و پیدا شده اند، به خود مقاله لینک شده اند :
  • [1] S.A. Abdel-Latif, H.B. Hassib, Y.M. Issa, Spectrochim. Acta A, ...
  • [2] K.A. Maher, S.R. Mohammed, Int. J. Curr. Rev., 2015, ...
  • [3] J. Devi, M. Yadav, D. Kumar, L.S. Naik, D.K. ...
  • [4] S. Muche, K. Harms, A. Biernasiuk, A. Malm, Ł. ...
  • [5] M. Andruh, Dalton Trans., 2015, 44, 16633–16653.‏ ...
  • [6] V. Prakash, Int. J. Eng. Res. Sci., 2017, 3, ...
  • [7] Z. Wang, J. Gao, J. Wang, X. Jin, M. ...
  • [8] V.A. Joseph, J.J. Georrge, J.H. Pandya, R.N. Jadeja, J. ...
  • [9] N. Turan, K. Buldurun, B. Gündüz, J. Nanoelectron. Optoelectron., ...
  • [10] H. Cherif, D.G. Bisson, P. Jarzem, M. Weber, J.A. ...
  • [11] A. Thevenon, J.A. Garden, A.J. White, C.K. Williams, Inorg. ...
  • [12] Y. Anjaneyulu, R.P. Rao, Synth. React. Inorg. Met. Org. Chem., ...
  • [13] B.G. Tweedy, Phytopathology, 1964, 55, 910–914. ‏ ...
  • [14] J.H. Jorgensen, J.D. Turnidge, In Manual of Clinical Microbiology, ...
  • [15] R.N. Patel, N. Singh, K.K. Shukla, V.L.N. Gundla, U.K. ...
  • [16] S. Manju, K. Rani, K. Vijayalakshmi , P.N. Sudha, ...
  • [17] K.W. HenriL, J. Tagenine, B.M. Gupta , Indian J. ...
  • [18] M.A. Neelakantan, M. Esakkiammal, S.S. Mariappan, J. Dharmaraja, , ...
  • [19] K. Rathore, R.K. Singh, H.B. Singh, E- J. Chem., ...
  • [20] S. Norrihan, A. Md Abu, S. Md Abdus, B. ...
  • [21] A.O. Sobola, G.M. Watkins, J. Serbian Chem. Soc., 2018, ...
  • [22] A.O. Sobola, G.M. Watkins, B. Van Brecht, S. Afr. ...
  • [23] B. Rizwana, S.S. Lakshmi, Int. J. Chemtech. Res., 2012, ...
  • [24] G.Y. Nagesh, U.D. Mahadev, B.H. M. Mruthyunjayaswamy, Int. J. ...
  • [25] M.D. Udayagiri, N.G. Yernale, B.H. Mathada, Int. J. Pharm. ...
  • [26] A.M. Hassan, A. Osman Said, B.H. Heakal, A. Younis, ...
  • [27] A.M. Hassan, B.H. Heakal, A.O. Said, W.M. M. A. ...
  • [28] A. Malik, G. Goyat  , K. Vikas, K.K. Verma, ...
  • [29] X. Li, C.H. Li, J. H. Jiang, H.W. Gu, ...
  • [30] K. Das, C. Patra, C. Sen, A. Datta, C. ...
  • [31] R.K. Mohapatra, P.K. Das, M.M. El-ajaily, U. Mishra, D.C. ...
  • [32] B. Kavitha, M. Sravanthi, P.S. Reddy, J. Mol. Struct., ...
  • [33] M. Sivasankaran Nair, S. Suda Kumari, M.A. Neelakantan, J. ...
  • [34] C. Jayabalakrishnan, K. Natarajan, Synth. React. Inorg. Met-Org. Nano-Met. ...
  • [35] M.A. Shaheen, W. Xiao, M. Aziz, A. Karim, M. ...
  • [36] R.O. Shaibu, G.M. Watkins, Ife J. Sci., 2019, 21, ...
  • [37] N. Turan, K. Buldurun, Y. Alan, A. Savci, N. ...
  • [38] M. Zubair, M. Sirajuddin, K. Ullah, A. Haider, F. ...
  • [39] B. Anupama, M. Sunita, D.S. Leela, B. Ushaiah, C.G. ...
  • [40] S. Kumar, K.K. Aravindakshan, J. Pharm. Chem. Biol.  Sci., ...
  • [41] G.A. Al‐Hazmi, K.S. Abou‐Melha, N.M. El‐Metwaly, I. Althagafi, F. ...
  • [42] A. Marton, E. Kusz, C. Kolozsi, V. Tubak, G. ...
  • [43] M.R. Rodríguez, J. Del Plá, L.M. Balsa, I.E. León, ...
  • [44] M.R. Rodríguez, L.M. Balsa, J. Del Plá, J. García-Tojal, ...
  • [45] M.J. Niu, Z. Li, G.L. Chang, X.J. Kong, M. ...
  • [46] H. Bahron, S.S. Khaidir, A.M. Tajuddin, K. Ramasamy, B. ...
  • [47] Z. Faghih, A. Neshat, A. Wojtczak, Z. Faghih, Z. ...
  • [48] S.S. Khaidir, H. Bahron, A.M. Tajuddin, K. Ramasamy, S. ...
  • [49] L. Subha, C. Balakrishnan, S. Thalamuthu, M.A. Neelakantan, J. ...
  • [50] E.N. Md Yusof, M. A.M. Latif, M.I.M. Tahir, J.A. ...
  • [51] L. Zarei, Z. Asadi, M. Dusek, V. Eigner, J. ...
  • [52] D. Majumdar, D.K. Singh, D.K. Pandey, D. Parai, K. ...
  • [53] A. De, H.P. Ray, P. Jain, H. Kaur, N. ...
  • [54] B. Jing, J. Dong, Q. Wei, T. Xu, L. ...
  • [55] X.J. Chen, W.J. Hu, Y. Qin, G.L. Zhao, Asian ...
  • [56] X. Li, J. H. Jiang, S.X. Xiao, H.W. Gu, ...
  • [57] R.P. Singh, K.N. Chidambara Murthy, G.K. Jayaprakasha, J. Agric. ...
  • [58] H. Mitsuda,  Eiyo to shokuryo, 1966, 19, 210–221. ‏ ...
  • [59] M. Oyaizu, Jpn. J. Nutr. Diet., 1986, 44, 307–315. ...
  • [60] W. Wu, Y. Xuan, J.L. Yin, L. Shujie, Synth. ...
  • [61] E. Al-Abbad, F. Alakhras, I. Anastopoulos, D. Das, A. ...
  • [62] S. Gao, Z. Cheng, X. Zhou, Y. Liu, J. ...
  • [63] M. Nikoorazm, A. Ghorbani-Choghamarani, M. Khanmoradi. RSC Adv., 2016, ...
  • [64] V.A. Neacşu, C. Maxim, A.M. Mădălan, M. Hillebrand, C. ...
  • [65] Y. Zou, W.L. Liu, C.S. Lu, L.L. Wen, Q.J. ...
  • [66] N.P. Priya, S. Arunachalam, A. Manimaran, D. Muthupriya, C. ...
  • [67] S. Sashikala, S.S. Shafi, Pharm. Lett., 2014, 6, 90–97.‏ ...
  • [68] A.S. Amarasekara, A. Razzaq, Int. Sch. Res. Notices, 2012, ...
  • [69] I. Kaya, A. Bilici, M. Gül, Polym. Adv. Technol., ...
  • نمایش کامل مراجع