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1

Banerjee, Samya, Ila Pant, Imran Khan, Puja Prasad, Akhtar Hussain, Paturu Kondaiah i Akhil R. Chakravarty. "Remarkable enhancement in photocytotoxicity and hydrolytic stability of curcumin on binding to an oxovanadium(iv) moiety". Dalton Transactions 44, nr 9 (2015): 4108–22. http://dx.doi.org/10.1039/c4dt02165g.

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2

Yuan, Caixia, Liping Lu, Yanbo Wu, Zhiwei Liu, Maolin Guo, Shu Xing, Xueqi Fu i Miaoli Zhu. "Synthesis, characterization, and protein tyrosine phosphatases inhibition activities of oxovanadium(IV) complexes with Schiff base and polypyridyl derivatives". Journal of Inorganic Biochemistry 104, nr 9 (wrzesień 2010): 978–86. http://dx.doi.org/10.1016/j.jinorgbio.2010.05.003.

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3

Lu, Liping, Jinjun Yue, Caixia Yuan, Miaoli Zhu, Hong Han, Zhiwei Liu i Maolin Guo. "Ternary oxovanadium(IV) complexes with amino acid-Schiff base and polypyridyl derivatives: Synthesis, characterization, and protein tyrosine phosphatase 1B inhibition". Journal of Inorganic Biochemistry 105, nr 10 (październik 2011): 1323–28. http://dx.doi.org/10.1016/j.jinorgbio.2011.07.008.

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4

Yuan, Caixia, Liping Lu, Xiaoli Gao, Yanbo Wu, Maolin Guo, Ying Li, Xueqi Fu i Miaoli Zhu. "Ternary oxovanadium(IV) complexes of ONO-donor Schiff base and polypyridyl derivatives as protein tyrosine phosphatase inhibitors: synthesis, characterization, and biological activities". JBIC Journal of Biological Inorganic Chemistry 14, nr 6 (17.03.2009): 841–51. http://dx.doi.org/10.1007/s00775-009-0496-6.

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5

Ohde, Christian, Christian Limberg, Reinhard Stösser i Serhiy Demeshko. "Oxovanadium(IV) Silsesquioxane Complexes". Inorganic Chemistry 49, nr 5 (marzec 2010): 2479–85. http://dx.doi.org/10.1021/ic902392y.

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6

Baran, Enrique J. "OXOVANADIUM(IV) COMPLEXES OF CARBOHYDRATES". Journal of Carbohydrate Chemistry 20, nr 9 (31.12.2001): 769–88. http://dx.doi.org/10.1081/car-100108656.

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7

Williams, Patricia A. M., Evelina G. Ferrer i Enrique J. Baran. "OXOVANADIUM(IV) COMPLEXES OF CAPTOPRIL". Journal of Coordination Chemistry 42, nr 4 (1.11.1997): 261–69. http://dx.doi.org/10.1080/00958979708022856.

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8

Pandya, Bhavna J., i Pabitra K. Bhattacharya. "Binary and ternary complexes of oxovanadium(IV) and homobinuclear double-bridged oxovanadium(IV) complexes". Transition Metal Chemistry 12, nr 5 (październik 1987): 398–400. http://dx.doi.org/10.1007/bf01171645.

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9

Mishra, Mahendra Kumar, Ruchita Tripathi, Pandeya Kb i Tripathi Ip. "α-AMYLASE INHIBITION AND ELECTROCHEMICAL BEHAVIOR OF SOME OXOVANADIUM (IV) COMPLEXES OF L-AMINO ACIDS". Asian Journal of Pharmaceutical and Clinical Research 11, nr 8 (7.08.2018): 218. http://dx.doi.org/10.22159/ajpcr.2018.v11i8.25800.

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Objective: Diabetes is complex metabolic disease having a symptom of hyperglycemia. Oxovanadium (IV) and l-amino acids are used to normalize the hyperglycemic condition. The aim of this study was to screen the α-amylase inhibitory activity of l-amino acids, their oxovanadium (IV) complexes, and electrochemical activity of oxovanadium (IV) complexes.Methods: All the oxovanadium (IV) complexes were synthesized according to the solubility of l-amino acids; the molar ratio of metal to l-amino acid was 1:2. The synthesized oxovanadium (IV) complexes were examined for their electrochemical behavior in 0.01 M sodium perchlorate solution. Further, the oxovanadium (IV) complexes of l-amino acids and l-amino acids were screened for their α-amylase inhibitory activity using spectrophotometric assay system.Results: The synthesized complexes were divided into four groups according to nature of amino acids. Entire complexes show simple irreversible wave for VO redox couples in −900–50 mV potential range and scan rate was 300 mV/S. All the complexes and l-amino acids were screened for their α-amylase inhibitory activity. L-Histidine and their oxovanadium (IV) complex show the minimum IC50 value, i.e. 4199.05 μM and 101.015 μM, respectively, in their respective groups.Conclusion: The data obtained from our study, it reveals that the entire oxovanadium (IV) complexes are an irreversible wave for VO redox system and the l-histidine and its oxovanadium (IV) complex is the most potent inhibitor for the α-amylase. Further, the complexes show minimum IC50 value on comparing their respective ligands due to the interaction of Vanadyl complex to the enzyme, at the sixth vacant position of Vanadyl complex.
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10

Hasan, M. F., A. M. Seyam i H. A. Hodali. "Oxovanadium(IV) Complexes with Azooxime Ligands". Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 26, nr 2 (1.02.1996): 181–89. http://dx.doi.org/10.1080/00945719608004257.

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11

Costa Pessoa, J., I. Cavaco, I. Correia, I. Tomaz, T. Duarte i P. M. Matias. "Oxovanadium(IV) complexes with aromatic aldehydes". Journal of Inorganic Biochemistry 80, nr 1-2 (maj 2000): 35–39. http://dx.doi.org/10.1016/s0162-0134(00)00037-4.

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12

Garribba, Eugenio, Giovanni Micera, Daniele Sanna i Elzbieta Lodyga-Chruscinska. "Oxovanadium(IV) complexes of quinoline derivatives". Inorganica Chimica Acta 348 (maj 2003): 97–106. http://dx.doi.org/10.1016/s0020-1693(02)01483-4.

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13

Patsalides, E., i K. Robards. "Configurational isomerism in oxovanadium(IV) complexes". Inorganica Chimica Acta 299, nr 2 (marzec 2000): 192–98. http://dx.doi.org/10.1016/s0020-1693(99)00496-x.

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14

Gonz�lez-Bar�, A. C., i E. J. Baran. "Oxovanadium(IV) complexes of halogenated oxines". Monatshefte f�r Chemie Chemical Monthly 128, nr 4 (kwiecień 1997): 323–35. http://dx.doi.org/10.1007/bf00810769.

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15

Kiss, Tamás, Péter Buglyó, Giovanni Micera, Alessandro Dessì i Daniele Sanna. "Oxovanadium(IV) complexes of mercaptocarboxylic acids". J. Chem. Soc., Dalton Trans., nr 12 (1993): 1849–55. http://dx.doi.org/10.1039/dt9930001849.

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16

Zamian, Jos� R., i Edward R. Dockal. "Tetradentate Schiff base oxovanadium(IV) complexes". Transition Metal Chemistry 21, nr 4 (sierpień 1996): 370–76. http://dx.doi.org/10.1007/bf00139036.

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17

Tasiopoulos, Anastasios J., Antonis T. Vlahos, Anastasios D. Keramidas, Themistoklis A. Kabanos, Yiannis G. Deligiannakis, Catherine P. Raptopoulou i Aris Terzis. "Models of Oxovanadium(IV)–Protein Interactions: The First Oxovanadium(IV) Complexes with Dipeptides". Angewandte Chemie International Edition in English 35, nr 21 (18.11.1996): 2531–33. http://dx.doi.org/10.1002/anie.199625311.

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18

Baran, Enrique J. "Oxovanadium(IV) and oxovanadium(V) complexes relevant to biological systems". Journal of Inorganic Biochemistry 80, nr 1-2 (maj 2000): 1–10. http://dx.doi.org/10.1016/s0162-0134(00)00032-5.

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19

Borah, Rakhimoni, Surabhi Lahkar, Naranarayan Deori i Sanfaori Brahma. "Synthesis, characterization and application of oxovanadium(iv) complexes with [NNO] donor ligands: X-ray structures of their corresponding dioxovanadium(v) complexes". RSC Advances 12, nr 22 (2022): 13740–48. http://dx.doi.org/10.1039/d2ra01448c.

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Oxovanadium(iv) complexes catalysed CO2 cycloaddition resulting up to 100% conversion of epoxides to cyclic carbonates under relatively benign condition. Transformation of oxovanadium(iv) to dioxovanadium(v) in the process of crystallization.
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20

Saha, Tapan K., Yutaka Yoshikawa, Hirouki Yasui i Hiromu Sakurai. "In vitro insulin-mimetic activity and in vivo metallokinetic feature of oxovanadium(IV)porphyrin complexes in healthy rats". Journal of Porphyrins and Phthalocyanines 16, nr 01 (styczeń 2012): 114–21. http://dx.doi.org/10.1142/s1088424612004458.

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We prepared [meso-tetrakis(4-carboxylatophenyl)porphyrinato]oxovanadium(IV) tetrasodium, ([VO(tcpp)]Na4), and investigated its in vitro insulin-mimetic activity and in vivo metallokinetic feature in healthy rats. The results were compared with those of previously proposed insulin-mimetic oxovanadium(IV)porphyrin complexes and oxovanadium(IV) sulphate. The in vitro insulin-mimetic activity and bioavailability of [VO(tcpp)]Na4 were considerably better than those of [meso-tetrakis (1-methylpyridinium-4-yl)porphyrinato]oxovanadium(IV)(4+) tetraperchlorate ([VO(tmpyp)](ClO4)4) and oxovanadium(IV) sulphate. On the other hand, [VO(tcpp)]Na4 and [meso-tetrakis(4-sulfonatophenyl) porphyrinato]oxidovanadate(IV)(4-)([VO(tpps)]) showed very similar in vitro insulin-mimetic activity and in vivo metallokinetic feature in healthy rats. In particular, the order of in vitro insulin-mimetic activity of the complexes was determined to be: [VO(tcpp)]Na4 ≈ [VO(tpps)] > ([VO(tmpyp)](ClO4)4 > oxovanadium(IV) sulphate.
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21

Rosenthal, Esther C. E. "From vanadium(V) to vanadium(IV) - and backwards". Pure and Applied Chemistry 81, nr 7 (30.06.2009): 1197–204. http://dx.doi.org/10.1351/pac-con-08-08-32.

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With bidentate alkoxy alkoxide and alkoxy alcohol ligands, respectively, a series of oxovanadium complexes in the oxidation state +4 is synthesized starting from oxovanadium(V) compounds. The reaction of two or more equivalents of 2-methoxyethanol with VOCl3 in n-hexane yields a mixture of the monomeric oxovanadium(IV) complex cis-[VOCl2(HOCH2CH2OMe-κ2O)(HOCH2CH2OMe-κO1)] and the alkoxide-bridged oxovanadium(IV) dimer syn-[VOCl(µ-OCH2CH2OMe-κ2O)]2, which are separated by fractionated crystallization. The same reaction with 2-ethoxy- and 2-iso-propoxyethanol gives only the alkoxide-bridged oxovanadium(IV) dimers anti-[VOCl(µ-OCH2CH2OR-κ2O)]2 (R = Et, iPr). All alkoxide bridged oxovanadium(IV) dimers are furthermore obtained as decomposition products of the chloride-bridged oxovanadium(V) complexes [VO(µ-Cl)Cl(OCH2CH2OR-κ2O)]2 (R = Me, Et, iPr) by Cl2 elimination and react inversely with Cl2 to the vanadium(V) compounds.
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22

Buglyó, Peter, Tamás Kiss, Elisabetta Alberico, Giovanni Micera i Dorothee Dewaele. "OXOVANADIUM(IV) COMPLEXES OF DI- AND TRIPHOSPHATE". Journal of Coordination Chemistry 36, nr 2 (październik 1995): 105–16. http://dx.doi.org/10.1080/00958979508022551.

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23

Pandey, O. P. "Oxovanadium(IV) complexes of carbohydrazones and thiocarbohydrazones". Polyhedron 5, nr 10 (styczeń 1986): 1587–91. http://dx.doi.org/10.1016/s0277-5387(00)84562-3.

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24

Yadav, Sharda, Om Prakash Pandey i Soumitra Kumar Sengupta. "OXOVANADIUM(IV) COMPLEXES WITH JÄGER-TYPE LIGANDS". Journal of Coordination Chemistry 38, nr 1-2 (1.04.1996): 107–12. http://dx.doi.org/10.1080/00958979608022695.

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25

Fern�ndez, Eva, Ar�nzazu L�pez de la Calle i Mar�a J. Gonz�lez Garmendia. "Oxovanadium(IV) complexes with polydentate nitrogen ligands". Transition Metal Chemistry 12, nr 6 (grudzień 1987): 536–38. http://dx.doi.org/10.1007/bf01023843.

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26

Sharma, Neeraj, Meena Kumari i Reena Sharma. "Thermoanalytical studies of oxovanadium(IV)hydroxamate complexes". Journal of Thermal Analysis and Calorimetry 107, nr 1 (4.10.2011): 225–29. http://dx.doi.org/10.1007/s10973-011-1930-x.

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27

Arion, Vladimir B., Victor Ch Kravtsov, Richard Goddard, Eckhard Bill, Julieta I. Gradinaru, Nicolai V. Gerbeleu, Veaceslav Levitschi i in. "Oxovanadium(IV) and oxovanadium(IV)-barium(II) complexes with heterotopic macrocyclic ligands based on isothiosemicarbazide". Inorganica Chimica Acta 317, nr 1-2 (maj 2001): 33–44. http://dx.doi.org/10.1016/s0164-1212(00)00107-2.

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28

Ghosh, Tapas, Sharmila Bhattacharya, Chandrakanta Bandyopadhyay i Gurunath Mukherjee. "Ligand controlled synthesis of mixed-ligand oxovanadium(V) and oxovanadium(IV) complexes". Journal of Chemical Research 2004, nr 5 (1.05.2004): 350–52. http://dx.doi.org/10.3184/0308234041639773.

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29

Baran, Enrique J. "ChemInform Abstract: Oxovanadium(IV) and Oxovanadium(V) Complexes Relevant to Biological Systems". ChemInform 31, nr 47 (21.11.2000): no. http://dx.doi.org/10.1002/chin.200047288.

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30

Schumann, Hans. "Zur Redoxchemie und Struktur von Oxovanadium(IV,V)-KompIexen mit substituierten Dibenzotetraaza[14]annulen Liganden / Redox Chemistry and Structure of Oxovanadium(IV.V) Complexes Containing Substituted Dibenzotetraaza[14]annulene Ligands". Zeitschrift für Naturforschung B 50, nr 10 (1.10.1995): 1494–504. http://dx.doi.org/10.1515/znb-1995-1010.

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The oxovanadium(IV) complexes LVO and L′VO (L = dianion of 5,14-dihydro-6,8,15.17- tetramethyldibenzo[b.i][1,4.8,11]tetraazacyclotetradecine. H2L, and L′ = dianion of 5,14-dihydro-6,15-dimethyl-8,17-diphenyldibenzo[b,i][1,4,8,11]tetraazacyclotetradecine, H2L′) are redox active as indicated by cyclovoltammetric measurements and confirmed by preparative methods: Reversible oxidation to the corresponding oxovanadium (V) cations is observed at ca. 0.35 V vs. SCE in CH2Cl2, and these cations are prepared in high yield by oxidation of the oxovanadium(IV) precursors with [(C5H5)2Fe]SbF6 (reversible by addition of cobaltocene). Irreversible reduction waves are observed for both complexes in the range -1 .9 to 2.1 V vs. SCE in CH2Cl2. Preparative reduction of LVO with Na/K alloy affords very unstable anionic oxovanadium(IV) complexes containing a deprotonated or reduced ligand, while with Li[B(C2H5)3H] in THF the Lewis acid/Lewis base adduct LVOxB(C2H3)3 is isolated. Spectroscopic data including ESR [vanadium(IV)] and 51V NMR [vanadium(V)] are given and discussed. The complexes LVO and [LVO]SbF6 have been characterized by single crystal Xray structure determinations.
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31

Ikekwere, P. O., i A. A. Adeniyi. "Oxovanadium(IV) Complexes of Some Aromatic Carboxylic Acids". Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 19, nr 1 (styczeń 1989): 87–100. http://dx.doi.org/10.1080/00945718908048053.

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32

Nwabueze, J. N. "Oxovanadium(IV) Complexes of Cyclopropylcarbo- and Cyclohexylacetohydroxamic Acids". Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 27, nr 5 (maj 1997): 685–93. http://dx.doi.org/10.1080/00945719708000219.

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33

Maqsood, Zahida T., Khalid M. Khan, Uzma Ashiq, Rifat A. Jamal, Zahid H. Chohan, Mohammad Mahroof-Tahir i Claudiu T. Supuran. "Oxovanadium(IV) complexes of hydrazides: Potential antifungal agents". Journal of Enzyme Inhibition and Medicinal Chemistry 21, nr 1 (styczeń 2006): 37–42. http://dx.doi.org/10.1080/14756360500277459.

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34

Kumar, Reetesh, Puja Singh, Umesh Kumar, S. Suman Singh, A. K. Saha i Shivadhar Sharma. "Spectroscopic Characterization of Some Oxovanadium(IV, V) Complexes". Asian Journal of Chemistry 26, nr 16 (2014): 5298–300. http://dx.doi.org/10.14233/ajchem.2014.17755.

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35

Fujiwara, Kei, i Takayuki Ishida. "Ferromagnetic oxovanadium(IV) complexes chelated with tetrahalosalen ligands". Polyhedron 30, nr 18 (listopad 2011): 3073–78. http://dx.doi.org/10.1016/j.poly.2011.02.035.

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36

Williams, Patricia A. M., Susana B. Etcheverry i Enrique J. Baran. "Characterization of new oxovanadium(IV) complexes of saccharides". Carbohydrate Research 329, nr 1 (październik 2000): 41–47. http://dx.doi.org/10.1016/s0008-6215(00)00171-3.

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37

Baran, Enrique J. "Oxovanadium(IV) complexes of carbohydrates: A brief overview". Journal of Inorganic Biochemistry 103, nr 4 (kwiecień 2009): 547–53. http://dx.doi.org/10.1016/j.jinorgbio.2008.10.008.

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38

Nath, P. K., N. C. Misra, V. Chakravortty i K. C. Dash. "Oxovanadium(IV) complexes with 2-(2′-pyridyl)benzimidazole". Polyhedron 6, nr 3 (styczeń 1987): 455–59. http://dx.doi.org/10.1016/s0277-5387(00)81007-4.

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39

Das, Ramprasad, Kausik K. Nanda, Alok K. Mukherjee, Monika Mukherjee, Madeleine Helliwell i Kamalaksha Nag. "Macrocyclic oxovanadium(IV) complexes: structure, magnetochemistry and electrochemistry". Journal of the Chemical Society, Dalton Transactions, nr 14 (1993): 2241. http://dx.doi.org/10.1039/dt9930002241.

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40

Gyurcsik, Béla, Tamás Jakusch i Tamás Kiss. "Oxovanadium(IV) complexes of N-D-gluconylamino acids". Journal of the Chemical Society, Dalton Transactions, nr 7 (2001): 1053–57. http://dx.doi.org/10.1039/b009852n.

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41

Srivastava, Seema, Om P. Pandey i Soumitra K. Sengupta. "Binuclear oxovanadium(IV) complexes of phthalazine hydrazone ligands". Transition Metal Chemistry 21, nr 3 (czerwiec 1996): 262–65. http://dx.doi.org/10.1007/bf00165980.

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42

Pandya, Bhavna J., i Pabitra K. Bhattacharya. "Mixed-ligand and binuclear complexes of oxovanadium(IV)". Transition Metal Chemistry 12, nr 4 (sierpień 1987): 347–49. http://dx.doi.org/10.1007/bf01024031.

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43

Salem, Mohamed A., i Saiid A. Amer. "The deoxygenation kinetics of new oxovanadium(IV) complexes". Transition Metal Chemistry 16, nr 3 (czerwiec 1991): 317–18. http://dx.doi.org/10.1007/bf01024072.

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44

Yadava, A. K., H. S. Yadav, Sanjay Singh, U. S. Yadav i D. P. Rao. "Synthesis and Characterization of Some Novel Schiff Base Complexes of Oxovanadium(IV) Cation". Journal of Chemistry 2013 (2013): 1–5. http://dx.doi.org/10.1155/2013/689518.

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A series of oxovanadium(IV) complexes of the type [VO(mac)]SO4(where mac = tetraazamacrocyclic ligands derived from condensation of 4,4,4-trifluro-1-(2-furyl)-1,3-butanedione or 4,4,4-trifluro-1-(2-thenyl)-1,3-butanedione withp-phenylenediamine and their reaction withβ-diketones) have been prepared using oxometal ion of vanadium as kinetic template. These complexes have been ascertained by electrical conductance, magnetic moment, elemental analyses, infrared, e.s.r. and electronic spectral data. All the oxovanadium(IV) complexes are five-coordinate ones.
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45

Yadava, Ashok Kumar, Hardeo Singh Yadav, Uma Shanker Yadav i Devendra Pratap Rao. "New Insights into the Chemistry of Oxovanadium(IV) Complexes with N4 Coordinating Ligands". ISRN Inorganic Chemistry 2013 (5.11.2013): 1–5. http://dx.doi.org/10.1155/2013/871640.

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The syntheses of new oxovanadium(IV) complexes having general formula [VO(mac)]SO4 have been carried out by using in situ method of preparation where vanadyl ion acts as kinetic template for the ligands derived by condensation of 2,2′-pyridil with 1,2-diaminopropane and 1,3-diaminopropane. The complexes were characterized by elemental analyses, molar conductance, magnetic moments, and spectral (infrared, electronic, and electron spin resonance) data. All the oxovanadium(IV) complexes are five coordinate wherein derived ligands act as tetradentate chelating agents.
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46

Singh, Sanjay, Hardeo S. Yadav, Ashok Kumar Yadava i Devendra Pratap Rao. "Synthesis of Oxovanadium(IV) Complexes with Tetraaza Coordinating Ligands". Journal of Chemistry 2013 (2013): 1–5. http://dx.doi.org/10.1155/2013/947325.

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Oxovanadium(IV) complexes of the type [VO(mac)]SO4(where mac = tetraaza macrocyclic ligands derived by condensation of thenil with 1,4-diaminobenzene or 3,4-diaminopyridine and their reaction withβ-diketones) have been prepared using vanadyl ion as kinetic template. The prepared macrocyclic complexes were characterized by elemental analyses, molar conductance, magnetic moments, and infrared, electronic, and electron spin resonance data. From the spectroscopic studies, five-coordinate square-pyramidal geometry for the VO2+complexes have been proposed wherein derived ligands act as tetradentate chelating agents.
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47

Sastry, Mandalika S., Udai P. Singh, Ranjana Ghose i Animesh K. Ghose. "Oxovanadium(IV) and Dioxouranium(VI) Complexes of Azo Dyes". Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 21, nr 1 (styczeń 1991): 73–88. http://dx.doi.org/10.1080/15533179108020166.

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Athar, Mohammad, i Naseer Ahmad. "Studies on the Schiff Base Complexes of Oxovanadium(IV)". Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 17, nr 7 (lipiec 1987): 723–45. http://dx.doi.org/10.1080/00945718708059469.

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Sanna, Daniele, Giovanni Micera, Peter Buglyó i Tamas Kiss. "Oxovanadium(IV) complexes of ligands containing phosphonic acid moieties". J. Chem. Soc., Dalton Trans., nr 1 (1996): 87–92. http://dx.doi.org/10.1039/dt9960000087.

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Wasson, John R. "Interpretation of electronic spectra of oxovanadium(IV), VO2+ complexes". Journal of Chemical Education 64, nr 3 (marzec 1987): 288. http://dx.doi.org/10.1021/ed064p288.2.

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