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Journal articles on the topic 'Dithiooxamide'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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1

Mihsen, Hayder Haimed. "Synthesis, Characterization, and Biological Activitiy of Copper (II) Complexes Containing Bidentate Schiff Bases." University of Thi-Qar Journal of Science 4, no. 2 (2014): 59–65. http://dx.doi.org/10.32792/utq/utjsci/v4i2.595.

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Three ligands have been prepared by condensation of dithiooxamide with 2,4,5- trimethoxy benzaldehyde, 4- dimethylamino benzaldehyde and Vanailin. These ligands are named N,N- bis( 2,4,5 – trimethoxybenzalidene) dithiooxamide(LH1), N,N-bis(4-dimethylaminobenzalidene) dithiooxamide(LH2) and N,N-bis (vanaillidene) dithiooxamide(LH3), respectively. Complexes of LH1, LH2 and LH3 were prepared with 1:2 M:L molar ratio, with copper ion in the formulas [Cu(LH1)2(H2O)2] Cl2.H2O.0.5CH2Cl2, [Cu (LH2)2(H2O)Cl] Cl.H2O and [Cu (LH3)2(H2O)2] CL2.H2O. The ligands and their complexes have been characterized b

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2

Abdulghani, Ahlam J., and Nada M. Abbas. "Synthesis Characterization and Biological Activity Study of New Schiff and Mannich Bases and Some Metal Complexes Derived from Isatin and Dithiooxamide." Bioinorganic Chemistry and Applications 2011 (2011): 1–15. http://dx.doi.org/10.1155/2011/706262.

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Two new Schiff and Mannich bases, namely, 1-Morpholinomethyl-3(1′ -N-dithiooxamide)iminoisatin (LIH) and 1-diphenylaminomethyl-3-1′-N-dithiooxamide)iminoisatin (LIIH), were prepared from condensation reaction of new Schiff base 3-(1′-N-dithiooxamide)iminoisatin (SBH) with morpholine or diphenylamine respectively in presence of formaldehyde . The structures were characterized by IR,1HNMR, mass spectrometry, and CHN analyses. Metal complexes of the two ligands were synthesized, and their structures were characterized by elemental analyses, atomic absorption, IR and UV-visible spectra, molar cond

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3

NEGOIU, Maria, Tudor ROSU, Liliana STOICESCU, Viorel CARCU та Mihai CONTINEANU. "SOME COMPLEXES OF COPPER(II) WITH N,N-DISUBSTITUTED DITHIOOXAMIDES DERIVED FROM α-AMINOACIDS AND α-AMINOACID ESTERS". SOUTHERN BRAZILIAN JOURNAL OF CHEMISTRY 6, № 7 (1998): 17–25. http://dx.doi.org/10.48141/sbjchem.v6.n7.1998.19_1998_2.pdf.

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The binuclear copper(II) complexes Cu2(L-4H)(H2O)2 (L = N,N -bis (carboxymethyl) dithiooxamide -GlyDTO and N,N-bis(1-carboxyethyl) dithiooxamide -AlaDTO) and Cu2(L-2H)Cl2 (L =methyl or ethyl ester of L) were synthesized. The structure of the complexes was studied employing IR, electronic, and ESR spectroscopy and conductivity measurements. The IR data indicate that the ligands act as bistridentates, with N, S, 0 -coordination to the copper(II) ion.

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4

Atzei, Davide, Paola Deplano, Emanuele F. Trogu, Francesco Bigoli, Maria Angela Pellinghelli, and Alberto Vacca. "Interaction of diiodine with some tetra-substituted dithiooxamides. Crystal and molecular structure of bis(morpholinothiocarbonyl)bis(diiodine)." Canadian Journal of Chemistry 66, no. 6 (1988): 1483–89. http://dx.doi.org/10.1139/v88-239.

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The reaction of some tetra-substituted dithiooxamides R2NC(S)C(S)NR2 (R = CH3:Me4dto; R = C2H5:Et4dto; R2N = OC4H8N:Mo2dto) with diiodine has been investigated by spectrophotometric methods in CHCl3. The formation in solution of 1:1 and 1:2 charge-transfer (c.t.) complexes between the reagents has been observed. A new computer program, derived from "SUPERQUAD" (P. Gans, A. Sabatini, and A. Vacca. J. Chem. Soc. Dalton Trans. 1195 (1985)), has been applied to evaluate the formation constants. The 1:2 c.t. complexes have been isolated in the solid state, and an X-ray structure analysis of the [OC

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5

Abboudi, M., and A. Mosset. "A palladium–dithiooxamide complex." Acta Crystallographica Section C Crystal Structure Communications 50, no. 7 (1994): 1057–59. http://dx.doi.org/10.1107/s0108270193013216.

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6

Ogunyemi, Babatunde Temitope, and Sunday Gbenga Borisade. "THEORETICAL MODELING OF IMINOISATIN DERIVATIVES AS CORROSION INHIBITORS OF STEEL IN ACID SOLUTION." FUDMA JOURNAL OF SCIENCES 4, no. 3 (2020): 672–78. http://dx.doi.org/10.33003/fjs-2020-0403-372.

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The effect of two iminoisatin derivatives [1-morpholinomethyl-3(1-N-dithiooxamide) iminoisatin (molecule 1)] and 1-diphenylaminomethyl-3(1-N-dithiooxamide) iminoisatin (molecule 2) on corrosion inhibition were theoretically investigated using quantum mechanical method. Their electronic parameters and quantum chemical descriptors that predict their adsorption and hence their inhibition efficiency were estimated using the DFT//B3LYP/6-31G (d) method. The results established a relationship between the quantum descriptors and corrosion inhibition efficiency, and also confirmed molecule 2 to be a b

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7

Li, Jiabao, Jinliang Li, Taiqiang Chen, Ting Lu, Wenjie Mai, and Likun Pan. "Metal chelate induced in situ wrapping of Ni3S2 nanoparticles into N, S-codoped carbon networks for highly efficient sodium storage." Inorganic Chemistry Frontiers 6, no. 3 (2019): 694–704. http://dx.doi.org/10.1039/c8qi01326h.

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8

Singh, Manorama, Anjumala Sahu, Suhasini Mahata, Puneet K. Singh, Vijai K. Rai, and Ankita Rai. "Efficient electrochemical determination of p-aminophenol using a novel tricomponent graphene-based nanocomposite." New Journal of Chemistry 43, no. 37 (2019): 14972–78. http://dx.doi.org/10.1039/c9nj03680f.

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Design and synthesis of a gold nanoparticle@dithiooxamide functionalized graphene (AuNP@DFG) nanocomposite is reported herein, which is employed for the electrochemical determination of p-aminophenol successfully.

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9

Nizovtseva, T. V., T. N. Komarova, and A. S. Nahmanovich. "Reaction of dithiooxamide with benzoylacetylene." Russian Journal of General Chemistry 76, no. 4 (2006): 659–60. http://dx.doi.org/10.1134/s1070363206040281.

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10

Fun, Hoong-Kun, Wan-Sin Loh, Annada C. Maity, and Shyamaprosad Goswami. "1,10-Phenanthroline–dithiooxamide (2/1)." Acta Crystallographica Section E Structure Reports Online 66, no. 6 (2010): o1320. http://dx.doi.org/10.1107/s1600536810016405.

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11

Cui, Jian-Zhong, Dan Zhang, Fan-Li Lu, Hong-Ling Gao, and Hai-Tao Wang. "N,N′-Bis(3-dimethylaminopropyl)dithiooxamide." Acta Crystallographica Section E Structure Reports Online 61, no. 12 (2005): o4011—o4012. http://dx.doi.org/10.1107/s1600536805035828.

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12

Bermejo, E., R. Carballo, A. Castiñeiras, and C. Maichle-Mössmer. "N,N'-Bis(2-pyridylmethyl)dithiooxamide." Acta Crystallographica Section C Crystal Structure Communications 54, no. 8 (1998): 1130–31. http://dx.doi.org/10.1107/s0108270198002510.

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13

Jean, Y. C. "N,N'-Bis(2-hydroxypropyl)dithiooxamide." Acta Crystallographica Section C Crystal Structure Communications 50, no. 7 (1994): 1163–65. http://dx.doi.org/10.1107/s0108270193013393.

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14

Aversa, Maria Chiara, Paola Bonaccorsi, Duncan W. Bruce, et al. "Mesomorphic Dithiooxamide Complexes of Platinum(II)." Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 348, no. 1 (2000): 53–64. http://dx.doi.org/10.1080/10587250008024795.

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15

Cui, Jian-Zhong, Dan Zhang, Hong Zhang, et al. "N,N′-Bis[2-(dimethylamino)ethyl]dithiooxamide." Acta Crystallographica Section E Structure Reports Online 61, no. 5 (2005): o1496—o1497. http://dx.doi.org/10.1107/s1600536805012225.

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16

Rosace, Giuseppe, Gaetano Giuffrida, Marcello Saitta, Giovanni Guglielmo, Sebastiano Campagna, and Santo Lanza. "Luminescence Properties of Platinum(II) Dithiooxamide Compounds." Inorganic Chemistry 35, no. 23 (1996): 6816–22. http://dx.doi.org/10.1021/ic9514004.

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17

Fujishima, M., Y. Nagao, R. Ikeda, S. Kanda, and H. Kitagawa. "Substituent effect on the magnetic properties of copper coordination polymers with dithiooxamide and N,N′-bis-(hydroxyethyl)dithiooxamide." Synthetic Metals 133-134 (March 2003): 433–35. http://dx.doi.org/10.1016/s0379-6779(02)00281-3.

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18

Giannetto, Antonino, Santo Lanza, Giuseppe Bruno, Francesco Nicoló, and Hadi Amiri Rudbari. "Crystal structure ofN,N′-bis(4-methylphenyl)dithiooxamide." Acta Crystallographica Section E Crystallographic Communications 71, no. 2 (2015): o67. http://dx.doi.org/10.1107/s2056989014027911.

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Two half molecules of the title compound, C16H16N2S2, are present in the asymmetric unit and both molecules are completed by crystallographic inversion centers at the mid-points of the central C—C bonds: the lengths of these bonds [1.538 (5) and 1.533 (5) Å] indicate negligible electronic delocalization. Thetrans-dithiooxamide fragment in each molecule is characterized by a pair of intramolecular N—H...S hydrogen bonds. In the crystal, molecules are linked by weak C—H..π interactions, generating a three-dimensional network.

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19

Cui, Jian-Zhong, Dan Zhang, Shuo-Wen Pan, Peng Cheng, Dai-Zheng Liao, and Geng-Lin Wang. "N,N′-Bis[2-(2-pyridyl)ethyl]dithiooxamide." Acta Crystallographica Section E Structure Reports Online 61, no. 6 (2005): o1913—o1915. http://dx.doi.org/10.1107/s1600536805016338.

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20

Poo̵ński, Tadeusz. "Optical activity of cis-oxamide and -dithiooxamide chromophores." Tetrahedron: Asymmetry 5, no. 2 (1994): 149–52. http://dx.doi.org/10.1016/s0957-4166(00)86159-5.

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21

Dommisse, R. A., A. J. Aarts, J. A. Lepoivre, and H. O. Desseyn. "13C-NMR spectra of Thio- and Dithiooxamide Derivatives." Bulletin des Sociétés Chimiques Belges 88, no. 4 (2010): 261–62. http://dx.doi.org/10.1002/bscb.19790880411.

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22

RABE, G., H. W. ROESKY, R. BOHRA, H. G. SCHMIDT, and M. NOLTEMEYER. "ChemInform Abstract: Reaction of Dithiooxamide with Dimeric Hexafluorothioacetone." ChemInform 23, no. 5 (2010): no. http://dx.doi.org/10.1002/chin.199205136.

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23

Gong, Young-Tae, Mi-Sook Won, Yoon-Bo Shim, and Su-Moon Park. "CuII-poly (dithiooxamide) film coated anion selective electrode." Electroanalysis 8, no. 4 (1996): 356–61. http://dx.doi.org/10.1002/elan.1140080411.

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24

Li, Yi-Zhi, Wei-Wei Liu, Yan-Jie Li, Guo-Jun Pan, and Hong-Wen Hu. "2,3-Bis(2-methylphenylimino)-1,4-dithiacyclohexane." Acta Crystallographica Section C Crystal Structure Communications 59, no. 11 (2003): o611—o612. http://dx.doi.org/10.1107/s0108270103021000.

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An N,N′-disubstituted dithiooxamide derivative reacts with 1,2-dibromoethane to produce the title compound, C18H18N2S2, a heterocycle with a double Schiff base. In the crystal structure, the molecule of the title compound lies on a twofold axis. Weak C—H...π interactions are the principal intermolecular forces, mediating the formation of layers parallel to the ab plane. Each molecule participates as donor and acceptor in two such contacts.

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25

Roesky, Herbert W., Hartmut Hofmann, Mathias Noltemeyer, and George M. Sheldrick. "Synthese und Kristallstruktur von 1,1,1,3,3,3-Hexafluor-2-propylamino-1-thiooxamid / Synthesis and Crystal Structure of 1,1,1,3,3,3-Hexafluoro-2-propylamino-1-thiooxamide." Zeitschrift für Naturforschung B 40, no. 1 (1985): 124–26. http://dx.doi.org/10.1515/znb-1985-0124.

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Dithiooxamide 1 reacts with hexafluoroacetone 2 at room temperature to yield 1,1,1,3,3,3-hexafluoro-2-propylamino-1-thiooxamide 3 and sulfur. The modes of formation of the bis(trifluoromethyl)-methyl group from hexafluoroacetone, the migration of oxygen and the elimination of sulfur are not clear. Crystals of 3 are monoclinic, space group Cc, with a = 2865.3(13), b = 924.4(9), c = 702.9(6) pm, β = 93.3(7)°. The structure was refined to R = 0.067 from 614 reflections

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26

Nguyễn, Thiên Thuý Trang, Jean-François Longevial, and Stéphanie Hesse. "Synthesis of Thiazolo[5,4-d]thiazoles in an Eco-Friendly L-Proline–Ethylene Glycol Mixture." Molecules 30, no. 4 (2025): 938. https://doi.org/10.3390/molecules30040938.

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The hazardousness of solvents used in synthetic organic chemistry is well established. In this context, it is relevant to search for safer and greener alternatives. Within the last decades, deep eutectic solvents have been considered as possible and promising alternatives. Consequently, this study aims at using deep eutectic solvents to synthesize an emerging class of heteroaromatic compounds named thiazolo[5,4-d]thiazoles, for which interest is growing in the field of organics, electronics, and biology. To address this challenge, we developed a straightforward synthetic protocol consisting of

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27

Barnard, Keith R., Anthony G. Wedd, and Edward R. T. Tiekink. "Molybdenum dithiooxamide complexes: is the ligand oxidized or reduced?" Inorganic Chemistry 29, no. 5 (1990): 891–92. http://dx.doi.org/10.1021/ic00330a001.

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28

Gurnule, W. B., and S. S. Katkamwar. "Non-isothermal Kinetic Study ofp-Cresol-Dithiooxamide-Formaldehyde Terpolymer." E-Journal of Chemistry 7, no. 4 (2010): 1380–90. http://dx.doi.org/10.1155/2010/858327.

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Terpolymer (p-CDF) has been prepared by using the monomerp-cresol, dithiooxanude and formaldehyde in 1:1:2 molar proportions. The structure ofp-CDF terpolymer has been elucidated on the basis of elemental analysis and various physicochemical technique like UV-visible, FTIR,1H NMR and TG analysis. Detailed thermal degradation curve is discussed which shows four steps decomposition. The activation energy (Ea) and thermal stability calculated by using the Sharp Wentworth, Frceman-Carroll methods. Thermodynamics parameters such as entropy change (ΔS), apparent entropy change (S*) and frequency fac

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29

Nuñez, L., L. Barral, and G. Pilcher. "Enthalpies of combustion of oxamic acid, oxamide, and dithiooxamide." Journal of Chemical Thermodynamics 20, no. 10 (1988): 1211–16. http://dx.doi.org/10.1016/0021-9614(88)90105-x.

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30

Hasegawa, Yoshitsugu, Midori Kamikawaji, and Kaname Sasaki. "Synthesis of Copper(II)–Dithiooxamide Complex in Zirconium Phosphate." Bulletin of the Chemical Society of Japan 59, no. 11 (1986): 3465–68. http://dx.doi.org/10.1246/bcsj.59.3465.

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31

Vogler, Arnd, and Michael Bodensteiner. "Synthesis, crystal structure and photoluminescence of [Rh(III)(phpy)2(dithiooxamide)]Cl (phpy = 2-(2-pyridyl)phenyl)." Zeitschrift für Naturforschung B 74, no. 5 (2019): 405–8. http://dx.doi.org/10.1515/znb-2018-0242.

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AbstractThe salt [Rh(III)(phpy)2(dtoxa)]Cl with phpy = 2-(2-pyridyl)phenyl anion and dtoxa = dithiooxamide has been characterized by its crystal structure and its electronic spectra. Since Rh(III) is rather redox-inert, the lowest-energy excited state of the complex cation is of the IL (dtoxa) type. In the solid state as well as in solution the complex is luminescent and displays a dtoxa IL phosphorescence at λmax = 607 nm with φϕ = 10−3 and τ = 3.7 ns in CH2Cl2.

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32

Vidal, M. C. F., I. Lens, A. Castiñeiras, A. Matilla Hernández, J. M. Tercero Moreno та J. Niclós–Gutiérrez. "N,N′-substituted dithiooxamides derived from alkyl-α-amino acids or from glycylglycine: acid dissociation properties in aqueous solution and crystal and molecular structures of N,N′-bis(carboxymethyl) dithiooxamide (GLYDTO) and N,N′-bis(1-carboxyethyl) dithiooxamide (ALADTO)". Polyhedron 18, № 25 (1999): 3313–19. http://dx.doi.org/10.1016/s0277-5387(99)00269-7.

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33

Lekstrom, Julie A., and Robert D. Koons. "Copper and Nickel Detection on Gunshot Targets by Dithiooxamide Test." Journal of Forensic Sciences 31, no. 4 (1986): 11907J. http://dx.doi.org/10.1520/jfs11907j.

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34

Kitagawa, Hiroshi, Yuki Nagao, Musashi Fujishima, Ryuichi Ikeda, and Seiichi Kanda. "Highly proton-conductive copper coordination polymer, H2dtoaCu (H2dtoa=dithiooxamide anion)." Inorganic Chemistry Communications 6, no. 4 (2003): 346–48. http://dx.doi.org/10.1016/s1387-7003(02)00749-9.

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35

Ferrari, Marisa Belicchi, Giovanna Gasparri Fava, Corrado Pelizzi, and Pieralberto Tarasconi. "Synthesis and structural characterization of chlorobis(triphenylphosphine)(dithiooxamide)copper(I)." Inorganica Chimica Acta 98, no. 3 (1985): L49—L52. http://dx.doi.org/10.1016/s0020-1693(00)87588-x.

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36

Whitcomb, David R., Nusrallah Jubran, and Daryle H. Busch. "The thermal behavior of dithiooxamide ligands and their nickel complexes." Thermochimica Acta 167, no. 1 (1990): 111–21. http://dx.doi.org/10.1016/0040-6031(90)80470-j.

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37

Abboudi, M., and A. Mosset. "Synthesis of d Transition Metal Sulfides from Amorphous Dithiooxamide Complexes." Journal of Solid State Chemistry 109, no. 1 (1994): 70–73. http://dx.doi.org/10.1006/jssc.1994.1073.

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38

Christensen, A., H. J. Geise, and B. J. van Der Veken. "The Crystal and Molecular Structure of N,N-Dimethyl-Dithiooxamide." Bulletin des Sociétés Chimiques Belges 84, no. 12 (2010): 1173–78. http://dx.doi.org/10.1002/bscb.19750841204.

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39

Xu, Jingsan, Jixin Zhu, Xiaofei Yang, et al. "Synthesis of Organized Layered Carbon by Self-Templating of Dithiooxamide." Advanced Materials 28, no. 31 (2016): 6727–33. http://dx.doi.org/10.1002/adma.201600707.

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40

Majles Ara, M. H., E. Koushki, S. H. Mousavi, S. Salmani, M. Rafizadeh, and A. Gharibi. "Nonlinear optical properties of a dithiooxamide determined by single beam techniques." Materials Chemistry and Physics 109, no. 2-3 (2008): 320–24. http://dx.doi.org/10.1016/j.matchemphys.2007.11.036.

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41

Khandwe, M., A. Bajpai, and U. D. N. Bajpai. "Coordination polymers of Zn(II) and N,N'-bis (carboxymethyl) dithiooxamide." Polymer Bulletin 23, no. 1 (1990): 51–56. http://dx.doi.org/10.1007/bf00983963.

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42

Slootmaekers, B., R. Keuleers, J. Janssens, and H. O. Desseyn. "Thermal analysis of some Au(III) and Cu(I) dithiooxamide complexes." Thermochimica Acta 311, no. 1-2 (1998): 141–47. http://dx.doi.org/10.1016/s0040-6031(97)00448-6.

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43

Nagao, Y., R. Ikeda, K. Iijima, T. Kubo, K. Nakasuji, and H. Kitagawa. "A new proton-conductive copper coordination polymer, (HOC3H6)2dtoaCu (dtoa = dithiooxamide)." Synthetic Metals 135-136 (April 2003): 283–84. http://dx.doi.org/10.1016/s0379-6779(02)00914-1.

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44

Al-Hasani, Thana Jaafar, Hayder Hamied Mihsen, Kasim Mohammed Hello, and Farook Adam. "Catalytic esterification via silica immobilized p -phenylenediamine and dithiooxamide solid catalysts." Arabian Journal of Chemistry 10 (February 2017): S1492—S1500. http://dx.doi.org/10.1016/j.arabjc.2013.04.030.

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45

Grasseschi, Daniel, Vitor M. Zamarion, and Henrique E. Toma. "Probing the dynamics of dithiooxamide coordinated to gold nanoparticles using SERS." Journal of Raman Spectroscopy 49, no. 9 (2018): 1478–86. http://dx.doi.org/10.1002/jrs.5398.

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46

Green, Michael R., Nusrallah Jubran, Bruce E. Bursten, and Daryle H. Busch. "Transition-metal complexes of dithiooxamide ligands. Vibrational fine structure in the electronic spectra of symmetrically N,N'-disubstituted dithiooxamides and their divalent nickel ion complexes." Inorganic Chemistry 26, no. 14 (1987): 2326–32. http://dx.doi.org/10.1021/ic00261a032.

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47

Madhu, Sharma, Singh Upendra, K. Sharma Anil, K. Mudgal Punit, and S. Gupta K. "Kinetics of the peroxomonosulfate oxidation of sulfur(-II) compounds : thioacetamide, dithiooxamide and thiourea." Journal of Indian Chemical Society Vol. 87, Jan 2010 (2010): 53–63. https://doi.org/10.5281/zenodo.5775418.

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Department of Chemistry, University of Rajasthan, Jaipur-302 004, Rajasthan, India <em>E-mail :</em> guptaks14@rediffmail.com 11 Government G. D. Girls College, Alwar-301 001, Rajasthan, India R. R. College, Alwar-301 001, Rajasthan, India <em>Manuscript received 5 October 2009, accepted 9 October 2009</em> Kinetics of relatively faster oxidation of thioacetamide (TA), dithiooxamide (DTO) and thiourea (TA) by peroxomonosulfate (PMS) has been studied spectrophotometrically under pseudo order condition by keeping oxidant In excess. Under these conditions, the sulfur(-ll) compounds are oxidized t

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48

Zarei, Seyed Amir, Mohammad Piltan, Asmar Mashhun, Hadi Amiri Rudbari, and Giuseppe Bruno. "2,2′-[(Disulfanediyl)bis{5-[(1E)-(2-hydroxybenzylidene)amino]-1,3-thiazole-4,2-diyl}]diphenol: synthesis, crystal structure and calculation of molecular hyperpolarizability." Acta Crystallographica Section C Structural Chemistry 73, no. 8 (2017): 609–12. http://dx.doi.org/10.1107/s2053229617008257.

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The title Schiff base compound {systematic name: 2-[5-[(E)-(2-hydroxybenzylidene)amino]-4-(2-{5-[(E)-(2-hydroxybenzylidene)amino]-2-(2-hydroxyphenyl)-1,3-thiazol-4-yl}disulfanyl)-1,3-thiazol-2-yl]phenol}, C32H22N4O4S4, incorporating a disulfanediyl (dithio) linkage, was obtained from the condensation reaction between two equivalents of salicylaldehyde and one equivalent of dithiooxamide in dimethylformamide, and was characterized by elemental analysis, IR spectroscopic analysis and single-crystal X-ray diffraction. A one-dimensional chain is formed along the b axis via double intermolecular C—

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49

Mikhailov, O. V. "New Method for Preparation of Samples for Measurement of Electronic Absorption Spectra of Difficult Soluble Inorganic and Metallorganic Compounds." Applied Spectroscopy 46, no. 8 (1992): 1240–44. http://dx.doi.org/10.1366/0003702924124051.

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A new method has been developed for the preparation of test samples for the registration of standard electronic absorption spectra of insoluble inorganic and metallorganic compounds in which—unlike traditional spectroscopic methods—the analyzed substances are synthesized by a series of specific chemical processes in thin gelatin layers of various silver halogenide photographic materials. Some advantages of these test samples, in comparison with standard solutions of analyzed compounds and mechanical mixtures of ones with various fillers, have been demonstrated. In addition, examples of the pre

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Werkman, P. J., A. Schasfoort, R. H. Wieringa, and A. J. Schouten. "Langmuir–Blodgett films of a polymerisable N,N′-disubstituted dithiooxamide coordination compound." Thin Solid Films 323, no. 1-2 (1998): 243–50. http://dx.doi.org/10.1016/s0040-6090(98)01041-4.

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