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    Academic Journal

    Πηγή: Alternative Energy and Ecology (ISJAEE); № 6 (2022); 12-19 ; Альтернативная энергетика и экология (ISJAEE); № 6 (2022); 12-19 ; 1608-8298

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    Relation: https://www.isjaee.com/jour/article/view/2568/2085; Segura A., Geusdon J.P., Besson J.M., Chevy A. Fotovoltaic effect in InSe. Application to solar energy conversion. “Rev.Phys. appl.” 1979, t.14, N1, p.253.; Segura A. Geusdon J.P.,Besson J.M., Chevy A. Photoconductivity and fotovoltaic effect in in indium selenide. J.”Appl. Phys.” 1983,t.54,N2,p.876.; Детекторы оптического излучения на основе слоистых кристаллах GaSe и InSe. ЖТФ, 77(2007), с.80-85.; Нагиев К.Х., Салманов В.М. Оптические модуляторы на основе кристаллов GaSe и InSe. Республиканская научная конференция «Актуальные проблемы физики», посвященная 90-летию БГУ. Баку, 16 мая 2009 г., стр.18.; Гусейнов Г.Д., Искендеров Г.И., Керимова Е.М. Взаимодействие мягкого рентгеновского излучения с монокристаллами InSe.; Мустафаева С.Н., Асадов М.М., Исмаилов А.А. Перенос заряда по локализованным состояниям в монокристалле InSe и InSeSn//Физика Низких Температур, 2010, т.36, №4, с.394-397.; Мустафаева С.Н, Асадов М.М., Исмаилов А.А. Влияние -облучения на параметры локализованных состояний в монокристаллах p-InSe и n-InSeSn//Физика Низких Температур 2010, т.36, №7, с.805-808.; Исмаилов А.А., Гасымов Ш.Г., Мамедов Т.С., Аллахвердиев К.Р. Влияние давления на электропроводность и эффект холла селенида индия ФТП, 1992, т.26, в.11, с.1994-1996.; Рустамов П.Г., Халилов А.О., Алиджанов М.А., Алиев О.М. Исследование твердых растворов моноселенида самария а InSe. Неорганические материалы, 1978,т.14, №7, с.1261- 1264.; Kerimova E.M., Gasanov N.Z., Ismailov A.A. Electrical and photoelectric properties of solid solutions In1-xErxSe Electrical and photoelectric properties of solid solutions In1-xErxSe GESJ׃ Physics,2019 ,№1(21),рр.53-59.; https://www.isjaee.com/jour/article/view/2568

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    Academic Journal

    Πηγή: Fine Chemical Technologies; Vol 20, No 1 (2025); 47-54 ; Тонкие химические технологии; Vol 20, No 1 (2025); 47-54 ; 2686-7575 ; 2410-6593

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    Relation: https://www.finechem-mirea.ru/jour/article/view/2218/2097; https://www.finechem-mirea.ru/jour/article/view/2218/2105; https://www.finechem-mirea.ru/jour/article/downloadSuppFile/2218/1597; Golcu A., Tumer M., Demirelli H., Wheatley R.A. Cd(II) and Cu(II) complexes of polydentate Schiff base ligands: synthesis, characterization, properties and biological activity. Inorg. Chim. Acta. 2005;358(6):1785–1797. https://doi.org/10.1016/j.ica.2004.11.026; Sinha D., Tiwari A.K., Singh S., Shukla G., Mishra P., Chandra H., Mishra A.K. Synthesis, characterization and biological activity of Schiff base analogues of indole-3-carboxaldehyde. Eur. J. Med. Chem. 2008;43(1): 160–165. https://doi.org/10.1016/j.ejmech.2007.03.022; Abbasova G.D., Pashajanov A.M., Ganbarova M.I., Gasanova S.M., Mammadova Z.A., Nasibova A.M. Synthesis and characterization of new metal complexes with tridentate hydrazone ligand. Azerbaijan Chemical Journal. 2023;4: 84–90. https://doi.org/10.32737/0005-2531-2023-4-84-90; Mohamed G.G. Synthesis, characterization and biological activity of bis(phenylimine) Schiff base ligands and their metal complexes. Spectrochim. Acta A. 2006;64(1):188–195. https://doi.org/10.1016/j.saa.2005.05.044; Tofazzal M., Tarafder H., Ali M.A., Saravanan N., Weng W.Y., Kumar S., Tsafe N.U., Crouse K.A. Coordination chemistry and biological activity of two tridentate ONS and NNS Schiff bases derived from S-benzyldithiocarbazate. Trans. Met. Chem. 2000;25:295–298. https://doi.org/10.1023/A:1007044910814; Chandra S., Jain D., Sharma A.K., Sharma P. Coordination Modes of a Schiff Base Pentadentate Derivative of 4-Aminoantipyrine with Cobalt(II), Nickel(II) and Copper(II) Metal Ions: Synthesis, Spectroscopic and Antimicrobial Studies. Molecules. 2009;14(1):174–190. https://doi.org/10.3390/molecules14010174; Karmakar M., Chattopadhyay S. A comprehensive overview of the orientation of tetradentate N2O2 donor Schiff base ligands in octahedral complexes of trivalent 3d metals. J. Molec. Struct. 2019;1186:155–186. https://doi.org/10.1016/j.molstruc.2019.02.091; Abu-Dief A.M., Mohamed I.M.A. A review on versatile applications of transition metal complexes incorporating Schiff bases. Beni-Suef Univ. J. Basic Appl. Sci. 2015;4(2):119–133. https://doi.org/10.1016/j.bjbas.2015.05.004; More M.S., Joshi P.G., Mishra Y.K., Khanna P.K. Metal complexes driven from Schiff bases and semicarbazones for biomedical and allied applications: a review. Mater. Today. Chem. 2019;14:100195. https://doi.org/10.1016/j.mtchem.2019.100195; Khalil M.M.H., Ismail E.H., Mohamed G.G., Zayed E.M., Badr A. Synthesis and characterization of a novel Schiff base metal complexes and their application in determination of iron in different types of natural water. Open J. Inorg. Chem. 2012;2(2):13–21. http://dx.doi.org/10.4236/ojic.2012.22003; Kajal A., Bala S., Kamboj S., Sharma N., Saini V. Schiff Bases: A Versatile Pharmacophore. J. Catalysts. 2013;2013:893512. https://doi.org/10.1155/2013/893512; Alsaygh A., Al-Humaidi J., Al-Najjar I. Synthesis of Some New Pyridine-2-yl-Benzylidene-Imines. Int. J. Org. Chem. 2014;4(2). http://doi.org/10.4236/ijoc.2014.42013; Utreja D., Vibha B.S.P., Singh S., Kaur M. Schiff Bases and their Metal Complexes as Anti-Cancer Agents: A Review. Current Bioactive Compounds. 2015;11(4):215–230. http://doi.org/10.2174/1573407212666151214221219; Chaudhary N.K. Synthesis and medicinal use of Metal complexes of Schiff Bases. Bibechana. 2013;9:75–80. https://doi.org/10.3126/bibechana.v9i0.7178; Sheikhshoaie I., Ebrahimipour S.Y., Sheikhshoaie M., Rudbari H.A., Khaleghi M., Bruno G. Combined experimental and theoretical studies on the X-ray crystal structure, FT-IR, 1HNMR, 13CNMR, UV–Vis spectra, NLO behavior andantimicrobial activity of 2-hydroxyacetophenone benzoylhydrazone. Spectrochim. Acta A. 2014;124:548–555. https://doi.org/10.1016/j.saa.2014.01.043; Krishnamoorthy P., Sathyadevi P., Butorac R.R.,.Cowley A.H, Bhuvanesh N.S., Dharmaraj N. Copper(I) and nickel(II) complexes with 1 : 1 vs. 1 : 2 coordination of ferrocenyl hydrazone ligands: Do the geometry and composition of complexes affect DNA binding/cleavage, protein binding, antioxidant and cytotoxic activities? Dalton Trans. 2012;41:4423–4436. https://doi.org/10.1039/C2DT11938B; Sharma M., Chauhan K., Srivastava R.K., Singh S.V., Srivastava K., Saxena J.K., Puri S.K., Chauhan P. Design and Synthesis of a New Class of 4-Aminoquinolinyl- and 9-Anilinoacridinyl Schiff Base Hydrazones as Potent Antimalarial Agents. Chem. Biol. Drug Des. 2014;84(2): 175–181. https://doi.org/10.1111/cbdd.12289; Vyas K.M., Jadeja R., Patel D., Devkar R., Gupta V.K. A new pyrazolone based ternary Cu(II) complex: Synthesis, characterization, crystal structure, DNA binding, protein binding and anti-cancer activity towards A549 human lung carcinoma cells with a minimum cytotoxicity to non-cancerous cells. Polyhedron. 2013;65:262–274. https://doi.org/10.1016/j.poly.2013.08.051; Kratz F., Beyer U., Roth T., Tarasova N., Collery P., Lechenault F., Cazabat A., Schumcher P., Unger C., Falken U. Transferrin Conjugates of Doxorubicin: Synthesis, Characterization, Cellular Uptake, and in Vitro Efficacy. J. Pharm. Sci. 1998;87(3): 338–346. https://doi.org/10.1021/js970246a; Jaividhya P., Dhivya R., Akbarsha M.A., Palaniandavar M. Efficient DNA cleavage mediated by mononuclear mixed ligand copper(II) phenolate complexes: The role of co-ligand planarity on DNA binding and cleavage and anticancer activity. J. Inorg. Biochem. 2012;114:94–105. https://doi.org/10.1016/j.jinorgbio.2012.04.018; Apelgot S., Coppey J., Fromentin A., Guille E., Poupon M., Roussel A. Altered distribution of copper (64Cu) in tumorbearing mice and rats. Anticancer Res. 1986;6(2):159–164. https://europepmc.org/article/med/3707051#impact; Hasinoff B.B., Yadav A.A., Patel D., Wu X. The cytotoxicity of the anticancer drug elesclomol is due to oxidative stress indirectly mediated through its complex with Cu(II). J. Inorg. Biochem. 2014;137:22–30. https://doi.org/10.1016/j.jinorgbio.2014.04.004; Ebrahimipour S.Y., Sheikhshoaie I., Crochet A., Khaleghi M., Fromm K.M. A new mixed-ligand copper(II) complex of (E)-N′-(2-hydroxybenzylidene) acetohydrazide: Synthesis, characterization, NLO behavior, DFT calculation and biological activities. J. Mol. Struct. 2014;1072:267–276. https://doi.org/10.1016/j.molstruc.2014.05.024; Marzano C., Pellei M., Tisato F., Santini C. Copper complexes as anticancer agents. Anticancer Agents Med. Chem. 2009;9(2): 185–211. https://doi.org/10.2174/187152009787313837; Garbutcheon-Singh K.B., Grant M.P., Harper B.W., Krause-Heuer A.M., Manohar M., Orkey N., AldrichWright J.R. Transition Metal Based Anticancer Drugs. Curr. Top. Med. Chem. 2011;11(5):521–542. https://doi.org/10.2174/156802611794785226; Vogel H.G. (Ed.). Drug Discovery and Evaluation: Pharmacological Assays. Berlin: Springer; 2008. 2068 p. http://dx.doi.org/10.1007/978-3-540-70995-4; Ebrahimipour S.Y., Sheikhshoaie I., Castro J., Haase W., Mohamadi M., Foro S., Sheikhshoaie M., Mahani S.E. A novel cationic copper(II) Schiff base complex: Synthesis, characterization, crystal structure, electrochemical evaluation, anti-cancer activity, and preparation of its metal oxide nanoparticles. Inorganica Chimica Acta. 2015;430:245–252. https://doi.org/10.1016/j.ica.2015.03.016; Sheikhshoaie I., Ebrahimipour S.Y., Sheikhshoaie M., Mohamadi M., Abbasnejad M., Rudbari H.A., Bruno G. Synthesis, characterization, X-ray crystal structure, electrochemical evaluation and anti-cancer studies of a mixed ligand Cu(II) complex of (E)-N′-((2-hydroxynaphthalen-1yl)methylene)acetohydrazide J. Chem. Sci. 2015;127(12): 2193–2200. https://doi.org/10.1007/s12039-015-0978-8; Guliyeva E.A., Fatullayeva P.A., Hagverdiyeva T.M. Synthesis and studies of Cu(II), Ni(II), Co(II) complexes with bis(saliciliden)hydrazon. Azerbaijan Chemical Journal. 2023;2:116–122. https://doi.org/10.32737/0005-2531-2023-2-116-122; Abbasova G., Medjidov A. One-pot Synthesis of a New Hydroxamic Acid and its Complexes with Metals. Letters in Organic Chemistry. 2022;19(10):837–841. http://doi.org/10.2174/1570178619666220111121743; Sarwar A., Shamsuddin M.B., Lingtang H. Synthesis, Characterization and Luminescence Studies of Metal-Diimine Complexes. Mod. Chem. Appl. 2018;6(3):1000262. http://doi.org/10.4172/2329-6798.1000262; Naemi H., Moradian M. Synthesis and characterization of nitro-Schiff bases derived from 5-nitro-salicylaldehyde and various diamines and their complexes of Co(II). J. Coord. Chem. 2010;63(1):156–162. http://doi.org/10.1080/00958970903225866; Nakamoto K. Infrared and Raman spectra of Inorganic and Coordination Compounds. Wiley; 1991. 410 p.; Calinescu M., Manea L., Pavelescu G. Synthesys and spectroscopic properties of new complex compounds of europium(III) and terbium(III) with 2-hydroxy-1naphthaldehyde acetylhydrazone and heterocyclic bases. Rev. Roum.Chim. 2011;56(3):231–237. http://web.icf.ro/rrch/; Tarasevich B.N. IK spektry osnovnykh klassov organicheskikh soedinenii (IR Spectra of the Main Classes of Organic Compounds). Moscow; MSU; 2012. 54 p. (in Russ.).

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    Academic Journal

    Πηγή: Vestnik of Brest State Technical University; No. 1(133) (2024): Vestnik of Brest State Technical University; 10-13
    Вестник Брестского государственного технического университета; № 1(133) (2024): Вестник Брестского государственного технического университета; 10-13

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