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Please use this identifier to cite or link to this item: https://oldena.lpnu.ua/handle/ntb/46427
Title: Synthesis and characterization of mixed ligand complexes of zirconium(IV) with sulphur, nitrogen and oxygen donоr ligands
Other Titles: Синтез і характеристика змішаних лігандних комплексів цирконію(IV) з сульфур-, нітроген- та оксиген-донор лігандами
Authors: Srivastava, Abhishek
Srivastava, Neetu
NathTripathi, Umesh
Siddiqui, Afshan
Affiliation: G.L.A. University
Deen Dayal Upadhyaya Gorakhpur University
Bibliographic description (Ukraine): Synthesis and characterization of mixed ligand complexes of zirconium(IV) with sulphur, nitrogen and oxygen donоr ligands / Abhishek Srivastava, Neetu Srivastava, Umesh NathTripathi, Afshan Siddiqui // Chemistry & Chemical Technology. — Lviv : Lviv Politechnic Publishing House, 2019. — Vol 13. — No 1. — P. 23–32.
Bibliographic description (International): Synthesis and characterization of mixed ligand complexes of zirconium(IV) with sulphur, nitrogen and oxygen donоr ligands / Abhishek Srivastava, Neetu Srivastava, Umesh NathTripathi, Afshan Siddiqui // Chemistry & Chemical Technology. — Lviv : Lviv Politechnic Publishing House, 2019. — Vol 13. — No 1. — P. 23–32.
Is part of: Chemistry & Chemical Technology, 1 (13), 2019
Issue: 1
Issue Date: 28-Feb-2019
Publisher: Видавництво Львівської політехніки
Lviv Politechnic Publishing House
Place of the edition/event: Львів
Lviv
Keywords: цирконій(IV)
дитіофосфат
піразолін
наночастинка
соль-гель
zirconium(IV)
dithiophosphate
pyrazoline
nanoparticle
sol-gel
Number of pages: 10
Page range: 23-32
Start page: 23
End page: 32
Abstract: Досліджено новий спосіб синтезу нано- мірних змішаних лігандних комплексів Zr(IV) за реакцією хлориду цирконію(IV) з 3(2'-гідроксифеніл)-5-(4-заміщеним феніл) піразолінами та солями дитіофосфату амонію, який після оброблення H2S діє як прекурсор для ZrS2. За допомогою рентгено-дифракційного аналізу досліджено кристалічну/аморфну природу синтезованих комплексів. Визначено, що всі комплекси є аморфними твердими речо- винами. При визначенні молекулярної маси та проведенні елементарного аналізу і спектроскопічних дослідженнь (ІЧ, 1H ЯМР, 31P ЯМР) доведена димерна природа комплексів, в яких дитіофосфат та піразолін є бідентатним лігандом. З використанням скануючої електронної мікроскопії пока- зано, що частинки знаходяться в нанодіапазоні. Запропо- новано координаційне число 6 для цирконію з восьмигранною геометрією.
A new route to synthesize new nanosized mixed ligand complexes of Zr(IV) have been investigated by the reaction of zirconium(IV) chloride with 3(2'-hydroxyphenyl)-5-(4-substituted phenyl)pyrazolines and ammonium salts of dithiophosphate, which after being treated with H2S gas acts as a precursor for ZrS2. These complexes have been examined for crystalline/amorphous nature through XRD. The morphology of the complexes was studied by employing XRD which shows that all the complexes are amorphous solid. Molecular weight measurements, elemental analysis in conjugation with spectroscopic (IR, 1H NMR, 31P NMR) studies reveal dimeric nature of the complexes, in which dithiophosphate and pyrazoline are bidentate. Scanning electron microscopic images indicate that the particles are in a nano range. Putting all the facts together, coordination number six is proposed for zirconium with octahedral geometry.
URI: https://ena.lpnu.ua/handle/ntb/46427
Copyright owner: © Національний університет „Львівська політехніка“, 2019
© Srivastava A., Srivastava N., Tripathi U., Siddiqui A., 2019
URL for reference material: https://doi.org/10.1021/ja4045289
https://doi.org/10.1007/s11814-013-0140-6
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2. Lee Y., Kim J., Ahm W., Korean J. Chem. Eng., 2013, 30, 1667. https://doi.org/10.1007/s11814-013-0140-6
3. Long J., Yaghi O., Chem. Soc. Rev., 2009, 38, 1213. https://doi.org/10.1039/b903811f
4. Sharma S., Jain A., Saxena S., J. Korean Chem. Soc., 2012, 56, 440. https://doi.org/10.5012/jkcs.2012.56.4.440
5. Bhatt S., Kumari R., Sharma N., Chaudhary S., Ind. J. Chem. A, 2004, 43, 778.
6. Grafov A., Mazurenko E., Battiston G. et al., J. Phys. IV France, 1995, 5, P.5-497. https://doi.org/10.1051/jphyscol:1995557
7. Thomas R., Milanov A., Bhakta R. et al., Chem.Vap. Deposition, 2006, 12, 295. https://doi.org/10.1002/cvde.200506481
8. Pasko S., Abrutis A., Hubert-Pfalzgraf L.:Mater. Lett., 2005, 59, 261. https://doi.org/10.1016/j.matlet.2004.07.061
9. Banerjee M., Seidel R., Winter M. et al., Dalton Trans., 2014, 43, 2384. https://doi.org/10.1039/P.3DT52335G
10. Fleeting K., O’Brien P., Jones A. et al., J. Chem. Soc., Dalton Trans., 1999, 2853. https://doi.org/10.1039/A901666J
11. Malghe Y., Prabhu R., Raut R., Acta. Pol. Pharm., 2009, 66, 45.
12. Tret’yakova I., Chernii V., Tomachinskaya L. et al., Theor. Exp. Chem., 2006, 42, 175. https://doi.org/10.1007/s11237-006-0034-3
13. Bajju G., Devi G., Kotcha S. et al., Bioinorg. Chem. Appl., 2013, 2013. https://doi.org/10.1155/2013/903616
14. Kostova I., Momekov G., Eur. J. Med. Chem., 2006, 41, 717. https://doi.org/10.1016/j.ejmech.2006.03.020
15. Liu K., Wu Q., Mu X. et al., Polyhedron, 2013, 52, 222. https://doi.org/10.1016/j.poly.2012.09.044
16. El- Zoghbi I., Whiyehorne T., Schaper F., Dalton Trans., 2013, 42, 9376. https://doi.org/10.1039/P.2DT31761C
17. Lenton T., Bercaw J., Panchenko V. et al., J. Am. Chem. Soc., 2013, 135, 10710. https://doi.org/10.1021/ja403170u
18. Saha T., Chakraborty D., Polym. Int., 2013, 62, 1507. https://doi.org/10.1002/pi.4450
19. Whitelaw E., Jones M., Mahon M., Kociok-Kohn G., Dalton Trans., 2009, 41, 9020. https://doi.org/10.1039/b911545e
20. Manicone P., Iommetti P., Raffaelli L., J. Dentistry, 2007, 35, 819. https://doi.org/10.1016/j.jdent.2007.07.008
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23. Saxena S., Chakravarty R., Kumar Y. et al., Separ. Sci. Technol., 2013, 48, 2108. https://doi.org/10.1080/01496395.2013.765472
24. Li W., Deng Q., Fang G. et al., J. Mater. Chem. B, 2013, 1, 1947. https://doi.org/10.1039/P.3tb20127a
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29. Li L., Wang H., Fang X. et al., Energ. Environ. Sci., 2011, 7, 2586. https://doi.org/10.1039/P.1ee01286j
30. Jang J., Jeong S., Seo J. et al., J. Am. Chem. Soc., 2011, 133, 7636. https://doi.org/10.1021/ja200400n
31. Srivastava T., J. Ind. Chem. Soc., 1981, 58, 710.
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34. Sharma T., Saxena V., Reddy N., Acta Chim., 1977, 93, 4.
35. Chauhan H., Chauhan B., Srivastava G., Mehrotra R., Phosphorus Sulphur, 1983, 15, 99. https://doi.org/10.1080/03086648308073283
Content type: Article
Appears in Collections:Chemistry & Chemical Technology. – 2019. – Vol. 13, No. 1

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