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1

Zhu, Yuner, and Philip D. Evans. "Surface Protection of Wood with Metal Acetylacetonates." Coatings 11, no. 8 (2021): 916. http://dx.doi.org/10.3390/coatings11080916.

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Metal acetylacetonates are coordination complexes of metal ions and the acetylacetonate anion with diverse uses including catalysts, cross-linking agents and adhesion promotors. Some metal acetylacetonates can photostabilize polymers whereas others are photocatalysts. We hypothesize that the ability of metal acetylacetonates to photostabilize wood will vary depending on the metal in the coordination complex. We test this hypothesis by treating yellow cedar veneers with different acetylacetonates (Co, Cr, Fe, Mn, Ni, and Ti), exposing veneers to natural weathering in Australia, and measuring ch
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2

Makarenko, Alexander M., Sergey V. Trubin, and Kseniya V. Zherikova. "Breaking through the Thermodynamics “Wilds” of Metal–Organic Chemical Vapor Deposition Precursors: Metal tris-Acetylacetonates." Coatings 13, no. 8 (2023): 1458. http://dx.doi.org/10.3390/coatings13081458.

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Metal acetylacetonates belong to the β-diketonate family and are considered as classics among precursors for metal–organic chemical vapor deposition (MOCVD). The success of film preparation is crucially dependent on the volatilization thermodynamics of the precursors used. Data on the volatilization thermodynamics of metal acetylacetonates are in huge disarray. We amassed and analyzed experimental data on the vapor pressures and on the enthalpies and entropies of fusion, vaporization, and sublimation of acetylacetonate tris-complexes of metals(III) (Al, Sc, Cr, Mn, Fe, Co, Ru, Rh, In, and Ir)
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3

David, Lawrence D., Ronald M. Anderson, Joseph M. Dynys, Charles C. Goldsmith, and Andrew Szule. "Synthesis and characterization of cordierite from acetylacetonate/alkoxide precursors." Journal of Materials Research 8, no. 7 (1993): 1697–702. http://dx.doi.org/10.1557/jmr.1993.1697.

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Syntheses of ultrafine glass powders in the MgO–Al2O3–SiO2 ternary oxide system were effected by drying and calcining sols derived from acetylacetonate-tetraethoxysilane ethanol solutions. A mixture of magnesium and aluminum acetylacetonates, dissolved with Si(OC2H5)4 in an ethanol solution in a 2:4:5 Mg: Al: Si mole ratio, was hydrolyzed, spray-dried, and calcined to yield a glass powder of 70 Å primary particle size, which sintered to densities ≥ 2.5 g/cm3 and which formed μ-cordierite as the only crystalline phase below 1000 °C. Incorporation of dopant quantities of boron and phosphorus, vi
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4

Зломанов, Владимир Павлович, Родион Сергеевич Эшмаков, and Игорь Владиславович Пролубщиков. "Formation of a solvate of manganese(III) acetylacetonate with chloroform." Kondensirovannye sredy i mezhfaznye granitsy = Condensed Matter and Interphases 24, no. 1 (2022): 29–32. http://dx.doi.org/10.17308/kcmf.2022.24/9052.

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Metal acetylacetonates are coordination compounds consisting of the acetylacetonate anion (CH3COCHCOCH3, indicated as acac) and metal ions. Typically, both oxygen atoms of the anion bind with the metal and form a six-membered chelate ring. The simplest complexes have the formulas M(acac)3 and M(acac)2. Many complexes are soluble in organic solvents, and such solutions are used for the synthesis of catalysts. The processes of formation of solvates of acetylacetonates of various metals have not been studied properly. It should be noted that the determination of the composition and properties of
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5

Dziemidkiewicz, Anna, Magdalena Maciejewska, and Martyna Pingot. "Thermal analysis of halogenated rubber cured with a new cross-linking system." Journal of Thermal Analysis and Calorimetry 138, no. 6 (2019): 4395–405. http://dx.doi.org/10.1007/s10973-019-08881-7.

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Abstract The aim of this work was to examine the influence of new curing agents proposed for brominated butyl rubber (BIIR) on the cross-linking process of rubber compounds and the thermal behavior of the vulcanizates. Rubber blends that were filled with carbon black and contained acetylacetonates of different transition metals in the presence of triethanolamine (TEOA) as new cross-linking agents were prepared. The performed studies showed that metal acetylacetonates (Me(acac)) are effective cross-linking agents for BIIR, which was confirmed by high values of the torque increment (∆M) and sign
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6

Halz, Jan Henrik, Christian Heiser, Christoph Wagner, and Kurt Merzweiler. "Syntheses and crystal structures of three [M(acac)2(TMEDA)] complexes (M = Mn, Fe and Zn)." Acta Crystallographica Section E Crystallographic Communications 76, no. 1 (2020): 66–71. http://dx.doi.org/10.1107/s2056989019016372.

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The complexes bis(acetylacetonato-κ2 O,O′)(N,N,N′,N′-tetramethylethylenediamine-κ2 N,N′)manganese(II), [Mn(C5H7O2)2(C6H16N2)], bis(acetylacetonato-κ2 O,O′)(N,N,N′,N′-tetramethylethylenediamine-κ2 N,N′)iron(II), [Fe(C5H7O2)2(C6H16N2)], and bis(acetylacetonato-κ2 O,O′)(N,N,N′,N′-tetramethylethylenediamine-κ2 N,N′)zinc(II), [Zn(C5H7O2)2(C6H16N2)], were synthesized from the reaction of the corresponding metal acetylacetonates [M(acac)2(H2O)2] with N,N,N′,N′-tetramethylethylenediamine (TMEDA) in toluene. Each of the complexes displays a central metal atom which is nearly octahedrally surrounded by
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7

Laode, A. Kadir, Azis Thamrin, . Imran, Ode Kadidae La, Usman Ida, and . Agusriyadin. "Synthesis and Characterization of Bis-Acetylacetonatozink (II) [(Zn(acac)2(H2o)]." International Journal of Current Science Research and Review 07, no. 06 (2024): 4315–19. https://doi.org/10.5281/zenodo.12577863.

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Abstract : The synthesis of the bis-acetylacetonate zink (II) monohydrate complex [Zn(acac)<sub>2</sub>(H<sub>2</sub>O)] has been conducted. FTIR analysis, TGA-DSC, and SEM micrographic analysis performed complex characterization. The yield of the complex compound [Zn(acac)<sub>2</sub>(H<sub>2</sub>O)] was 36.24% using NaOH as a pH regulator. Based on the FTIR characterization of the typical absorption complex [Zn(acac)<sub>2</sub>(H<sub>2</sub>O)] appears at 763.88 cm<sup>-1</sup>&nbsp;for Zn-O, C-H at 933.9 cm<sup>-1</sup>&nbsp;and 1020 cm<sup>-1</sup>, C=C and C=O at 1516 cm<sup>-1</sup>, 1
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8

Dziemidkiewicz, Anna, and Magdalena Maciejewska. "Manganese and Nickel Acetylacetonates as Curatives for Chloroprene Rubber Based on Heck’s Reaction." Materials 14, no. 4 (2021): 807. http://dx.doi.org/10.3390/ma14040807.

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The commonly used curing system for chloroprene rubber (CR) is a combination of two metal oxides, such as magnesium oxide (MgO) and zinc oxide (ZnO). Application of MgO and ZnO enables to obtain a good balance between processability of rubber compounds and mechanical properties of the vulcanizates. Despite high activity in crosslinking reactions, ZnO is classified as ecotoxic to aquatic organisms, thus environmental legislation requires its quantity in technology to be limited. In our studies more environmentally friendly curing systems were applied, which enabled eliminating ZnO from CR compo
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9

Panasenko, Alexander E., Lyudmila A. Zemnukhova, and Nicolay P. Shapkin. "Fabrication and extraction of silicon-containing products from rice husks." Butlerov Communications 61, no. 1 (2020): 133–39. http://dx.doi.org/10.37952/roi-jbc-01/20-61-1-133.

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To isolate silicon-containing products from plant materials, the reaction of interaction of rice husks with triethanolamine and ethylene glycol have been investigated. The effect of pretreatment of raw materials and the reaction conditions on the yield of soluble products containing silicon has been studied. It has been shown that the highest enrichment of rice husks with silicon occurs upon its treatment with concentrated hydrochloric acid and the Schweitzer's reagent. The highest degree of silicon extraction (69%) was achieved at using native rice husks and vanadyl acetylacetonate as a catal
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10

Dziemidkiewicz, Anna, Martyna Pingot, and Magdalena Maciejewska. "METAL COMPLEXES AS NEW PRO-ECOLOGICAL CROSSLINKING AGENTS FOR CHLOROPRENE RUBBER BASED ON HECK COUPLING REACTION." Rubber Chemistry and Technology 92, no. 3 (2019): 589–97. http://dx.doi.org/10.5254/rct.19.81465.

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ABSTRACT The influence of new pro-ecological curing agents on the crosslinking process of chloroprene rubber (CR) was examined. The proposed curing system used a simpler recipe (no need to apply harmful products such as zinc oxide and ethylene thiourea) and cost less than standard metal oxides. It was expected that the mechanism of crosslinking would be similar to that of Heck-type reactions. Heck-type reactions are powerful tools for the creation of new C=C bonds. They provide the simplest and most efficient way to synthesize a variety of important compounds used in many areas, such as pharma
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11

Svistunova, Irina V., Nikolay P. Shapkin, Galina O. Tretyakova, and Dina V. Saigak. "Silicon-Containing metal Acetylacetonates." Phosphorus, Sulfur, and Silicon and the Related Elements 190, no. 10 (2015): 1632–45. http://dx.doi.org/10.1080/10426507.2015.1012666.

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12

Bulgakov, R. G., S. P. Kuleshov, A. N. Zuzlov, and R. R. Vafin. "Triboluminescence of lanthanide acetylacetonates." Russian Chemical Bulletin 53, no. 12 (2004): 2712–14. http://dx.doi.org/10.1007/s11172-005-0180-0.

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13

A., K. BANERJEE, K. GHOSH MONOJIT, K. SINHA SAILENDRA, and K. ROY S. "Alkali Metal Complexes. Binuclear Alkali Metal Complexes with Magnesium(II) and Zinc(II) Acetylacetonates." Journal of Indian Chemical Society Vol. 62, Apr 1985 (1985): 272–74. https://doi.org/10.5281/zenodo.6324541.

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Chemistry Department, Patna University, Patna-800 005 <em>Manuscript received 16 June 1983, accepted 30 April 1985</em> Heterobinuclear alkali metal complexes have been synthesised by treating metal chelates of magnesium and zinc acetylacetonates with alkali metal salts of 1-nitroso&shy;-2-naphthol and 8-hydroxyquinoline in ethanol/benzene-ethanol mixture. The general formula of the complex has been established as [M<sub>&alpha;&nbsp;</sub>(acac)<sub>2</sub>&nbsp;M<sub>b</sub>L], where M<sub>&alpha;</sub>&nbsp;-magnesium or zinc, acac<em>- </em>acetylacetonate, and M<sub>b</sub>L -Li, Na and K
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14

Pittkowski, Rebecca, та Thomas Strassner. "Enhanced quantum yields by sterically demanding aryl-substituted β-diketonate ancillary ligands". Beilstein Journal of Organic Chemistry 14 (21 березня 2018): 664–71. http://dx.doi.org/10.3762/bjoc.14.54.

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Luminescent organometallic platinum(II) compounds are of interest as phosphors for organic light emitting devices. Their emissive properties can be tuned by variation of the ligands or by specific electron-withdrawing or electron-donating substituents. Different ancillary ligands can have a profound impact on the emission color and emission efficiency of these complexes. We studied the influence of sterically hindered, aryl-substituted β-diketonates on the emission properties of C^C* cyclometalated complexes, employing the unsubstituted methyl-phenyl-imidazolium ligand. The quantum yield was s
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15

Svistunova, I. V., та E. V. Fedorenko. "α-substituted boron difluoride acetylacetonates". Russian Journal of General Chemistry 78, № 8 (2008): 1515–23. http://dx.doi.org/10.1134/s1070363208080094.

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16

Such, K. P., and G. Lehmann. "E.P.R. of Mn2+in acetylacetonates." Molecular Physics 60, no. 3 (1987): 553–60. http://dx.doi.org/10.1080/00268978700100361.

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17

Isakova, V. G., I. A. Baidina, N. B. Morozova та I. K. Igumenov. "γ-Halogenated iridium(III) acetylacetonates". Polyhedron 19, № 9 (2000): 1097–103. http://dx.doi.org/10.1016/s0277-5387(00)00358-2.

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18

Hansen, S., and G. Lehmann. "EPR of Fe3+ in acetylacetonates." Applied Magnetic Resonance 1, no. 1 (1990): 47–53. http://dx.doi.org/10.1007/bf03166008.

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19

Dikio, Charity W., Ikechukwu P. Ejidike, Fanyana M. Mtunzi, Michael J. Klink, and Ezekiel D. Dikio. "HYDRAZIDE SCHIFF BASES OF ACETYLACETONATE METAL COMPLEXES: SYNTHESIS, SPECTROSCOPIC AND BIOLOGICAL STUDIES." International Journal of Pharmacy and Pharmaceutical Sciences 9, no. 12 (2017): 257. http://dx.doi.org/10.22159/ijpps.2017v9i12.22225.

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Objective: The study was focused on the synthesis and spectroscopic studies of metal acetylacetonates and their complexes using bidentate Schiff-base ligands (NO), evaluation of their in-vitro antibacterial potentials against pathogenic microorganism.Methods: Acetylacetonate salts of Cobalt(II), Manganese(II) and Magnesium(II) were prepared by reacting their metal hydroxides with acetylacetone. The metal complexes of N'-{(E)-[4-(diethylamino)-2-hydroxyphenyl]methylidene}-4-nitrobenzohydrazide (HL1), N'-{(E)-[4-(diethylamino)-2-hydroxyphenyl]methylidene}-4-methoxybenzohydrazide (HL2) obtained f
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20

Ho, Sally Fae, Adriana Mendoza-Garcia, Shaojun Guo, et al. "A facile route to monodisperse MPd (M = Co or Cu) alloy nanoparticles and their catalysis for electrooxidation of formic acid." Nanoscale 6, no. 12 (2014): 6970–73. http://dx.doi.org/10.1039/c4nr01107d.

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21

Lamprey, H. "PROPERTIES AND APPLICATIONS OF METAL ACETYLACETONATES." Annals of the New York Academy of Sciences 88, no. 2 (2006): 519–25. http://dx.doi.org/10.1111/j.1749-6632.1960.tb20049.x.

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22

Kubo, M. K., Y. Sakai, T. Tominaga, K. Nishiyama, and K. Nagamine. "Diamagnetic muon yields of metal acetylacetonates." Journal of Radioanalytical and Nuclear Chemistry Letters 136, no. 1 (1989): 61–66. http://dx.doi.org/10.1007/bf02165087.

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23

Bulgakov, R. G., S. P. Kuleshov, R. R. Vafin, A. G. Ibragimov, and U. M. Dzhemilev. "Reactions of lanthanide acetylacetonates with triethylaluminum." Kinetics and Catalysis 49, no. 2 (2008): 299–304. http://dx.doi.org/10.1134/s0023158408020195.

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24

Ismail, Hamdy M. "A thermoanalytic study of metal acetylacetonates." Journal of Analytical and Applied Pyrolysis 21, no. 3 (1991): 315–26. http://dx.doi.org/10.1016/0165-2370(91)80006-t.

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25

Youssef, Tamer Ezzat, Sean O’Flaherty, Werner Blau, and Michael Hanack. "Phthalocyaninatoindium(III) Acetylacetonates for Nonlinear Optics." European Journal of Organic Chemistry 2004, no. 1 (2004): 101–8. http://dx.doi.org/10.1002/ejoc.200300463.

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26

Arod, Pallavi, and S. A. Shivashankar. "Synthesis of unique metal oxide/carbon composites via sealed-tube pyrolysis of metal acetylacetonates and the mechanism of their formation." RSC Advances 6, no. 70 (2016): 65366–72. http://dx.doi.org/10.1039/c6ra08455a.

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27

McNeill, I. C., and J. J. Liggat. "The effect of metal acetylacetonates on the thermal degradation of poly(methyl methacrylate)—I. Cobalt (III) acetylacetonate." Polymer Degradation and Stability 29, no. 1 (1990): 93–108. http://dx.doi.org/10.1016/0141-3910(90)90024-2.

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28

Long, S. R., S. R. Browning, and J. J. Lagowski. "The Electrochemical Synthesis of Transition-Metal Acetylacetonates." Journal of Chemical Education 85, no. 10 (2008): 1429. http://dx.doi.org/10.1021/ed085p1429.

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29

Samoilenkov, S. V., M. A. Stefan, and G. Wahl. "MOCVD of thick YSZ coatings using acetylacetonates." Surface and Coatings Technology 192, no. 1 (2005): 117–23. http://dx.doi.org/10.1016/j.surfcoat.2004.03.019.

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30

Masℝwska, J., and S. Starzyński. "Capillary gas chromatography of some metal acetylacetonates." Chromatographia 25, no. 8 (1988): 691–93. http://dx.doi.org/10.1007/bf02290472.

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31

Pasynkiewicz, S., and J. Lewiński. "Reactions of dialkylaluminium acetylacetonates with Lewis bases." Journal of Organometallic Chemistry 290, no. 1 (1985): 15–23. http://dx.doi.org/10.1016/0022-328x(85)80144-3.

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32

Zaitzeva, Irina G., Nataliya P. Kuzmina, and Larissa I. Martynenko. "The volatile rare earth element tetrakis-acetylacetonates." Journal of Alloys and Compounds 225, no. 1-2 (1995): 393–95. http://dx.doi.org/10.1016/0925-8388(94)07126-8.

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33

Kulevsky, Norman, and Kabuika Ngoy Butamina. "Molecular complexes of iodine with metal acetylacetonates." Spectrochimica Acta Part A: Molecular Spectroscopy 46, no. 1 (1990): 79–83. http://dx.doi.org/10.1016/0584-8539(93)80014-2.

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34

Boschmann, Erwin, and R. N. Keller. "Bonding in alkali and alkaline earth acetylacetonates." Journal of Molecular Structure 1195 (November 2019): 762–68. http://dx.doi.org/10.1016/j.molstruc.2019.05.131.

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35

McNeill, I. C., and J. J. Liggat. "The effect of metal acetylacetonates on the thermal degradation of poly(methyl methacrylate): Part II—Manganese (III) acetylacetonate." Polymer Degradation and Stability 37, no. 1 (1992): 25–32. http://dx.doi.org/10.1016/0141-3910(92)90088-m.

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36

Radlik, Monika, Wojciech Juszczyk, Krzysztof Matus, Wioletta Raróg-Pilecka, and Zbigniew Karpiński. "Hydrodechlorination of CHClF2 (HCFC-22) over Pd–Pt Catalysts Supported on Thermally Modified Activated Carbon." Catalysts 10, no. 11 (2020): 1291. http://dx.doi.org/10.3390/catal10111291.

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Commercial activated carbon, pretreated in helium at 1600 °C and largely free of micropores, was used as a support for two series of 2 wt.% Pd–Pt catalysts, prepared by impregnating the support with metal acetylacetonates or metal chlorides. The catalysts were characterized by temperature-programmed methods, H2 chemisorption, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and scanning transmission electron microscopy (STEM) with energy dispersive spectroscopy (EDS). Overall, the results confirmed the existence of well-dispersed Pd–Pt nanoparticles in the bimetallic catalysts,
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37

A., K. BANERJEE, PRASAD DHARAMBIR, and K. ROY S. "Metal Complexes as Ligands. Trinudear Alkali Metal Complexes with Copper(II) and Nickel(II) Acetylacetonates." Journal of Indian Chemical Society Vol. 64, Jan 1987 (1987): 9–11. https://doi.org/10.5281/zenodo.6159029.

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Chemistry Department, Patna University, Patna-800 005 <em>Manuscript received 20 May 1982, revised 10 February 1986, accepted 26 November 1986</em> The copper(II) and nickel(II) acetylacetonates [M<sub>&alpha;</sub>(acac)<sub>2</sub>] have been used as double-faced ligands (complex ligand) in the synthesis of novel trinuclear alkali metal complexes of the general formula [M<sub>&alpha;</sub>(acac)<sub>2</sub>&nbsp;(M<sub>b</sub>L)<sub>2</sub>]&nbsp;where M<sub>&alpha;</sub>&nbsp;&mdash; Cu<em><sup>ll</sup></em> and Ni<em><sup>ll</sup> </em>; M<sub>b</sub>L&nbsp;&mdash; Li, Na or K salt of the
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38

Long, S. R., and J. J. Lagowski. "The Direct Electrochemical Synthesis of Transition Metal Acetylacetonates." Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry 37, no. 10 (2007): 813–15. http://dx.doi.org/10.1080/15533170701748548.

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39

Takeichi, Tsutomu, Hiroaki Okumura, Yoshihiro Sakurada, and Yuzi Takayama. "Reactions of Metal Benzoylacetonates and Acetylacetonates with Formaldehyde." Bulletin of the Chemical Society of Japan 62, no. 5 (1989): 1679–81. http://dx.doi.org/10.1246/bcsj.62.1679.

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40

Tikhonov, Sergey A., Irina V. Svistunova, Ilya S. Samoilov, Ivan S. Osmushko, Aleksandr V. Borisenko, and Vitaliy I. Vovna. "Electronic structure of binuclear acetylacetonates of boron difluoride." Journal of Molecular Structure 1160 (May 2018): 92–100. http://dx.doi.org/10.1016/j.molstruc.2018.02.005.

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41

Gavrilenko, Mikhail A., Tatyana A. Kasymova, and Natalya A. Gavrilenko. "Solid Phase Sorption of Phenols on Metals Acetylacetonates." Procedia Chemistry 10 (2014): 103–7. http://dx.doi.org/10.1016/j.proche.2014.10.019.

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42

Stabnikov, P. A., G. I. Zharkova, L. A. Komissarova, A. I. Smolentsev, and S. V. Borisov. "Packing of chiral molecules of metal TRIS-acetylacetonates." Journal of Structural Chemistry 51, no. 3 (2010): 558–69. http://dx.doi.org/10.1007/s10947-010-0081-4.

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43

Koksharova, T. V. "COORDINATION COMPOUNDS OF 3D-METALS ACETYLACETONATES WITH THIOSEMICARBAZIDE." Odesa National University Herald. Chemistry 19, no. 2(50) (2015): 27. http://dx.doi.org/10.18524/2304-0947.2014.2(50).38957.

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44

Jasim, Fadhil, and Insaf Hamid. "Thermoanalysis and catalytic study of transition metals acetylacetonates." Thermochimica Acta 93 (September 1985): 65–68. http://dx.doi.org/10.1016/0040-6031(85)85017-6.

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45

Zhang, Z., Y. Tanigami, and R. Terai. "Catalytic effect of acetylacetonates on gel formation of." Journal of Non-Crystalline Solids 191, no. 3 (1995): 304–10. http://dx.doi.org/10.1016/0022-3093(95)00316-9.

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46

Gómez-Sal, Pilar, Avelino Martín, Miguel Mena, Pascual Royo, and Ricardo Serrano. "Monopentamethylcyclopentadienyltitanium(IV) halo-alkoxides, alkyl-alkoxides and acetylacetonates." Journal of Organometallic Chemistry 419, no. 1-2 (1991): 77–84. http://dx.doi.org/10.1016/0022-328x(91)86165-m.

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47

Fdil, Naima, Abderrahmane Romane, Smail Allaoud, Abdallah Karim, Yves Castanet, and André Mortreux. "Terpenic olefin epoxidation using metals acetylacetonates as catalysts." Journal of Molecular Catalysis A: Chemical 108, no. 1 (1996): 15–21. http://dx.doi.org/10.1016/1381-1169(95)00284-7.

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48

Kiose, O. O., S. M. Savin, and E. V. Afanasenko. "Salts and double tartratogermanates/stannates of 3d-metals as modifiers of unsaturated oligoesters." Voprosy Khimii i Khimicheskoi Tekhnologii, no. 2 (May 2023): 67–74. http://dx.doi.org/10.32434/0321-4095-2023-147-2-67-74.

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The paper presents the results of the systematic research into effects of 3d-metals acetates, acetylacetonates and double tartrategermanates/stannates on the modification of polyglycol maleine phthalate. The copolymerization parameters of the prepared modified oligoesters with methyl methacrylate monomer and threeethyleneglycoldimethacrylate oligomer were determined. Modifiers were added to the reaction mixture before the start of polycondensation of maleic and phthalic anhydrides with ethylene glycol at the temperature of 1750C. The kinetics of copolymerization at the initial stages was deter
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Gazieva, Elizaveta A., Nataliya A. Gavrilenko, Tatiana A. Kasymova, and Mikhail A. Gavrilenko. "Sensor Based on Metals Acetylacetonates for Determination of Organic Substances Vapour in the Atmosphere." Key Engineering Materials 670 (October 2015): 241–45. http://dx.doi.org/10.4028/www.scientific.net/kem.670.241.

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There has been designed a sensor with detectors based on adsorption layers of metals acetylacetonates to measure air pollution components concentration. The electrical conductivity of the obtained sensor was studied under various synthesis conditions, temperature and detected substances kinds. The sensor was tested on model gaseous mixture and applied to detect organic substances in the environment.
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50

Zheleznova, Lidia, Lyudmila Sliusarchuk, Nadiia Ivakha, Serhii Kuleshov, and Olena Trunova. "SYNTHESIS AND STUDY OF THE HETERONUCLEAR ACETYLACETONATE Nd(III) AND Ni(II) COMPLEX AS A PRECURSOR FOR OBTAINING COMPLEX-OXIDE STRUCTURES." Ukrainian Chemistry Journal 85, no. 8 (2019): 83–93. http://dx.doi.org/10.33609/0041-6045.85.8.2019.83-93.

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The heterometallic acetylacetonate complex NdNi(АА)5·6Н2О has been synthesized to obtain nickel-neodymium-containing complex oxide materials. The properties of the complex have been investigated by physico-chemical methods of analysis (elemental analysis, differential thermal analysis, IR spectroscopy, X-ray powder diffraction).&#x0D; The data of X-ray powder diffraction and IR spectroscopy of NdNi(АА)5·6Н2О confirmed the formation of a new heterometallic single-phase compound. In the IR spectrum of NdNi(АА)5·6Н2О, a change is observed in the amount and position of the bands in the region of s
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