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Journal articles on the topic 'Dinitrobenzoic acid'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Cao, Xiang Yu, Jian Li Liu, Xiu Li Lu, Tie Min Li, Wei Wang, and Qi Jiu Li. "Study on the Interaction between 3, 5-Dinitrobenzoic Acid and Bovine Serum Albumin by Fluorescence Spectroscopic Method." Advanced Materials Research 233-235 (May 2011): 113–16. http://dx.doi.org/10.4028/www.scientific.net/amr.233-235.113.

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The interaction between 3, 5-dinitrobenzoic acid and bovine serum albumin (BSA) was studied by the method of fluorescence spectroscopy. By the analysis of fluorescence spectra and fluorescence intensity, it was observed that the 3, 5-dinitrobenzoic acid had a strong ability to quench the intrinsic fluorescence of BSA through static quenching process. Based on fluorescence quenching results, the apparent binding constant (K) between 3, 5-dinitrobenzoic acid and BSA was 7.08×106 and the number of binding sites (n) was 1.5 at 298 K. The distance (r) between donor (BSA) and acceptor (3, 5-dinitrob

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2

Zhang, Xiang, Jian Chen, Jinzhong Hu, et al. "The solubilities of benzoic acid and its nitro-derivatives, 3-nitro and 3,5-dinitrobenzoic acids." Journal of Chemical Research 45, no. 11-12 (2021): 1100–1106. http://dx.doi.org/10.1177/17475198211058617.

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The solubilities of benzoic acid and its nitrated derivatives (3-nitrobenzoic acid and 3,5-dinitrobenzoic acid) in seven pure solvents—water, methanol, ethanol, acetonitrile, dichloromethane, toluene, and ethyl acetate—were determined experimentally over a temperature range from 273.15 K to 323.15 K under 101.3 kPa. The solubility of the above substances in these solvents increased with temperature. The solubility values of benzoic acid in these seven solvents follow the following order: ethanol > ethanol > acetonitrile > ethyl acetate > dichloromethane > toluene > water, whi

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3

Lynch, Daniel E., Graham Smith, Karl A. Byriel, and Colin H. L. Kennard. "Designing Linear Hydrogen-Bonded Arrays by Using Substituted Charge-Transfer Complexes. The Crystal Structure of the 1 : 1 Adduct of Indole-2-carboxylic Acid with 3,5-Dinitrobenzoic Acid." Australian Journal of Chemistry 51, no. 11 (1998): 1019. http://dx.doi.org/10.1071/c98119.

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Five adducts consisting of carboxylic acid-substituted indoles with nitro-substituted benzoic acids have been synthesized and tested for second-order non-linear optical properties. These were indole-2-carboxylic acid with 2,4-dinitrobenzoic acid (1), 3,5-dinitrobenzoic acid (2), and 2,4,6-trinitrobenzoic acid (3), and indole-3-acetic acid with 3,5-dinitrobenzoic acid (4), and 2,4,6-trinitrobenzoic acid (5). Compound (2) produced clear, yellow crystals (space group P -1 with a 6·8400(7), b 15·150(2), c 16·097(2) Å, α 84·911(9), β 87·088(10), γ 77·865(9)°, Z 4) which allowed the structure to be

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4

Marczak, Maria, Kinga Biereg, Beata Zadykowicz, and Artur Sikorski. "Structural characterization and theoretical calculations of the monohydrate of the 1:2 cocrystal salt formed from acriflavine and 3,5-dinitrobenzoic acid." Acta Crystallographica Section C Structural Chemistry 77, no. 2 (2021): 116–22. http://dx.doi.org/10.1107/s2053229621000681.

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The synthesis and structural characterization of the monohydrated 1:2 cocrystal salt of acriflavine with 3,5-dinitrobenzoic acid [systematic name: 3,6-diamino-10-methylacridin-10-ium 3,5-dinitrobenzoate–3,5-dinitrobenzoic acid–water (1/1/1), C14H14N3 +·C7H3N2O6 −·C7H4N2O6·H2O] are reported. Single-crystal X-ray diffraction measurements show that the title solvated monohydrate salt crystalizes in the monoclinic space group P21 with one acriflavine cation, a 3,5-dinitrobenzoate anion, a 3,5-dinitrobenzoic acid molecule and a water molecule in the asymmetric unit. The neutral and anionic forms of

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5

Aziz-ur-Rehman, Madeleine Helliwell, Saqib Ali, and Saira Shahzadi. "4-Chloro-3,5-dinitrobenzoic acid." Acta Crystallographica Section E Structure Reports Online 63, no. 4 (2007): o1743—o1744. http://dx.doi.org/10.1107/s1600536807011221.

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6

Tahir, M. Nawaz, Abdul Rauf Raza, Aisha Saddiqa, Muhammad Danish, and Iram Saleem. "2-Methyl-3,5-dinitrobenzoic acid." Acta Crystallographica Section E Structure Reports Online 65, no. 11 (2009): o2819. http://dx.doi.org/10.1107/s1600536809042627.

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7

Smith, Graham, Daniel E. Lynch, and Raymond C. Bott. "Molecular Cocrystals of Carboxylic Acids. XXVIII. Nitro-Substituted Carboxylic Acids with Lewis Bases: the Crystal Structures of the Adducts of 3,5-Dinitrobenzoic Acid with N-Methylaniline (1 : 1), (4-Nitrophenyl)acetic Acid with Cyclohexane-1,4-diamine (2 : 1), and 5-Nitrosalicylic Acid with 2-Imidazolidone (2 : 1)." Australian Journal of Chemistry 51, no. 2 (1998): 159. http://dx.doi.org/10.1071/c97143.

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A number of molecular adducts of nitro-substituted aromatic acids with Lewis bases have been prepared and characterized by infrared spectroscopy and in three cases by X-ray diffraction methods. These three compounds are the adducts of: 3,5-dinitrobenzoic acid (dnba) with N-methylaniline (nma), [(dnba)-(nma)+] (1); (4-nitrophenyl)acetic acid (4-npa) with cyclohexane-1,4-diamine (dach), [(4-npa)22-(dach)2+] (4); 5-nitrosalicylic acid (5-nsa) with 2-imidazolidone (idaz), [(5-nsa)2(idaz)] (5). Other compounds are the adducts of 3,5-dinitrobenzoic acid with 2,6-dimethylpyridine (dmp), [(dnba)(dnba)

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8

Lynch, DE, G. Smith, KA Byriel, and CHL Kennard. "Molecular Cocrystals of Carboxylic Acids.II. The Crystal Structure of the 1 : 2 Adduct of Phenoxyacetic Acid With 3,5-Dinitrobenzoic Acid." Australian Journal of Chemistry 44, no. 7 (1991): 1017. http://dx.doi.org/10.1071/ch9911017.

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The 1 : 2 molecular adduct between phenoxyacetic acid and 3,5-dinitrobenzoic acid, with formula [(C6H5OCH2COOH)2{3,5-(NO2)2C6H3COOH}4(H2O)2], has been prepared and its structure determined by X-ray diffraction. Crystals are triclinic, space group Pī with two complex units in a cell with dimensions a 7.202(2), b 18.519(5), c 20.924(6)Ǻ, α 66.33(3),β 86.04(2),γ 89.32(2)°. The molecular repeating unit comprises two phenoxyacetic acid molecules [forming hydrogen-bonded cyclic dimers (O̷O, 2.71, 2.74 Ǻ)], four 3,5- dinitrobenzoic acid molecules [giving two unusual one-bond hydrogen bonds (O…O, 2.59

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9

Prince, P., F. R. Fronczek, and R. D. Gandour. "Two polymorphs of 3,5-dinitrobenzoic acid." Acta Crystallographica Section C Crystal Structure Communications 47, no. 4 (1991): 895–98. http://dx.doi.org/10.1107/s0108270190010198.

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10

Reddy, G. Om, and K. S. Ravikumar. "Thermal studies on the decomposition of 3,5-dinitrobenzoic acid and lead salts of 3,5-dinitrobenzoic acid." Thermochimica Acta 198, no. 1 (1992): 147–65. http://dx.doi.org/10.1016/0040-6031(92)85069-8.

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11

Hartshorn, MP, JM Readman, WT Robinson, CW Sies, and GJ Wright. "The Nitration of 3,4,5,6-Tetramethylbenzene-1,2-Dicarbonitrile, 2,3,5,6-Tetramethylbenzonitrile, 1,2,3-Trimethyl-4,6-Dinitrobenzene and 1,2,4,5-Tetramethyl-3,6-Dinitrobenzene. Methyl Migrations Following ipso-Substitution." Australian Journal of Chemistry 41, no. 3 (1988): 373. http://dx.doi.org/10.1071/ch9880373.

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Nitration of 3,4,5,6-tetramethylbenzene-1,2-dicarbonitrile (1a) gives epimeric pairs of dinitro ketones (6a) and (7a), and hydroxy ketones (9) and (10), in addition to the benzyl nitrate (4) and phthalide (5). Nitration of 2,3,5,6-tetramethylbenzonitrile (11) gives the epimeric dinitro ketones (15) and (16), in addition to the nitrobenzonitrile (12) and the nitrophthalide (13). Nitration of 1,2,3-trimethyl-4,6- dinitrobenzene (17) gives dimethylpropanedioic acid (23), the dinitrobenzoic acid (24), and the hydroxy dienone (25). Nitration of 1,2,4,5-tetramethyl-3,6-dinitrobenzene (18) gives dime

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12

Lynch, DE, G. Smith, KA Byriel, and CHL Kennard. "Molecular Cocrystals of Carboxylic Acids. I. The Crystal Structures of the Adducts of Indole-3-acetic-Acid With Pyridin-2(1H)-one, 3,5-Dinitrobenzoic Acid and 1,3,5-Trinitrobenzene." Australian Journal of Chemistry 44, no. 6 (1991): 809. http://dx.doi.org/10.1071/ch9910809.

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Three molecular cocrystal adducts of the plant hormone indole-3-acetic acid ( iaa ) have been prepared and their structures determined by X-ray diffraction. They are indole-3-acetic acid-bis [pyridin-2(1H)-one] (1), indole-3-acetic acid-3,5-dinitrobenzoic acid (2) and indole-3-acetic acid-1,3,5-trinitrobenzene (3). Complexes (2) and (3), which may be prepared in a solid-state reaction, are orange and are structurally similar, having significant π-π indole -benzene ring interactions. However, the colourless complex (1) shows no π-π ring interactions. In complex (2), the 3,5-dinitrobenzoic acid

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13

Lebedev, B. A., V. Yu Dolmatov, P. S. Zubarev, N. V. Latynov, M. M. Aleksandrov, and R. I. Ponamareva. "Preparation of 3,5-dinitrobenzoic acid from meta-nitrobenzoic acid." Pharmaceutical Chemistry Journal 22, no. 5 (1988): 399–401. http://dx.doi.org/10.1007/bf00769656.

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14

Toy, Patrick, Tracy But, and Jinni Lu. "Organocatalytic Mitsunobu Reactions with 3,5-Dinitrobenzoic Acid." Synlett 2010, no. 07 (2010): 1115–17. http://dx.doi.org/10.1055/s-0029-1219795.

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15

Ding, Xuehua, Shi Wang, Wenrui He, and Wei Huang. "3-Aminobenzonitrile–3,5-dinitrobenzoic acid (1/1)." Acta Crystallographica Section E Structure Reports Online 67, no. 11 (2011): o2833. http://dx.doi.org/10.1107/s1600536811039870.

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16

Abthorpe, M., A. V. Trask, and W. Jones. "3,5-Dinitrobenzoic acid–dimethyl sulfoxide (1/1)." Acta Crystallographica Section E Structure Reports Online 61, no. 3 (2005): o609—o611. http://dx.doi.org/10.1107/s1600536805003818.

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17

Issa, Y. M., W. F. El-Hawary, and A. Talat. "Spectrophotometric Determination of Diazepam in Pure form, Tablets and Ampoules." International Journal of Biomedical Science 3, no. 1 (2007): 50–55. http://dx.doi.org/10.59566/ijbs.2007.3050.

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The interaction of diazepam with picric acid (I), 3, 5-dinitrobenzoic acid (II) and 2, 4-dinitrobenzoic acid (III) was found to be useful for its spectrophotometric determination. the quantitation was carried out at 475, 500, and 500 nm for the reaction with (I), (II) and (III), respectively. the effect of several variables on the coloring process was studied. the proposed methods have been applied successfully for the determination of diazepam in pure samples and in its pharmaceutical preparations with good accuracy and precision. the results were compared to those obtained by the pharmacopoe

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18

Liu, Xiangyu, Qi Yang, Zhiyong Su, et al. "3D high-energy-density and low sensitivity materials: synthesis, structure and physicochemical properties of an azide–Cu(ii) complex with 3,5-dinitrobenzoic acid." RSC Adv. 4, no. 31 (2014): 16087–93. http://dx.doi.org/10.1039/c4ra00635f.

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A novel 3D energetic coordination polymer of azide–Cu(ii), Cu(3,5-DNBA)(N<sub>3</sub>), was synthesized and structurally characterized by single crystal X-ray diffraction, where 3,5-DNBA represents 3,5-dinitrobenzoic acid.

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19

Zhong, H., X. M. Yang, H. L. Xie, and C. J. Luo. "2-Fluoro-3,5-dinitrobenzoic acid–ammonia (1/1)." Acta Crystallographica Section E Structure Reports Online 63, no. 9 (2007): o3831. http://dx.doi.org/10.1107/s1600536807039724.

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20

Liu, T., and J. Y. Zhu. "2-Amino-3,5-dinitrobenzoic acid–ammonia (1/1)." Acta Crystallographica Section E Structure Reports Online 63, no. 9 (2007): o3829. http://dx.doi.org/10.1107/s1600536807040068.

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21

Andreev, P. Yu, E. V. Potapenko, I. P. Pogorelova, S. N. Krasil’nikov, and A. N. Band. "A new procedure for preparing 3,4-dinitrobenzoic acid." Russian Journal of Applied Chemistry 81, no. 3 (2008): 503–5. http://dx.doi.org/10.1134/s1070427208030348.

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22

Yu, Hongmei, Li Zhang, Meiju Liu, et al. "Enhancing Solubility and Dissolution Rate of Antifungal Drug Ketoconazole through Crystal Engineering." Pharmaceuticals 16, no. 10 (2023): 1349. http://dx.doi.org/10.3390/ph16101349.

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To improve the solubility and dissolution rate of the BCS class II drug ketoconazole, five novel solid forms in 1:1 stoichiometry were obtained upon liquid-assisted grinding, slurry, and slow evaporation methods in the presence of coformers, namely, glutaric, vanillic, 2,6-dihydroxybenzoic, protocatechuic, and 3,5-dinitrobenzoic acids. Single-crystal X-ray diffraction analysis revealed that the hydroxyl/carboxylic acid. . .N-imidazole motif acts as the dominant supramolecular interaction in the obtained solid forms. The solubility of ketoconazole in distilled water significantly increased from

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23

Pavlyukova, Yuliya N., Natalya D. Shashurina, and Vladimir А. Ostrovskii. "KINETICS OF NITRATION OF M-NITROBENZOIC ACID IN AQUEOUS SOLUTIONS OF SULFURIC ACID." Bulletin of the Saint Petersburg State Institute of Technology (Technical University) 61 (2022): 57–61. http://dx.doi.org/10.36807/1998-9849-2022-61-87-57-61.

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The kinetics of the nitration reaction of m-nitrobenzoic acid with nitric acid in a sulfuric acid medium of various concentrations was studied by UV spectroscopy. The observed differences in the rate of nitration of m-nitrobenzoic acid from the nitration of alkylbenzenes are associated with the electron-withdrawing nature of the carboxyl group, as well as with its protonation. During the reaction, not only 3,5-dinitrobenzoic acid is formed, but also products with significantly higher molar absorption coefficients

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24

Jones, Charlotte L., Chick C. Wilson, and Lynne H. Thomas. "Turning colour on and off using molecular disorder and proton transfer in multi-component molecular complexes." CrystEngComm 16, no. 26 (2014): 5849–58. http://dx.doi.org/10.1039/c4ce00229f.

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Three pairs of molecular complexes based around 4-iodoaniline and 3,5-dinitrobenzoic acid are reported. Within each pair, one complex is colourless and one red; the influences on the colour are discussed including the role of molecular disorder and proton transfer.

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25

Trask, A. V., M. Abthorpe, and W. Jones. "4-Methyl-3,5-dinitrobenzoic acid–dimethyl sulfoxide (1/1)." Acta Crystallographica Section E Structure Reports Online 61, no. 4 (2005): o1100—o1102. http://dx.doi.org/10.1107/s1600536805008779.

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26

Zeller, Matthias, Jake L. Stouffer, Virgil C. Solomon, and Larry S. Curtin. "High-Z′ and twinning behavior in 3,4-dinitrobenzoic acid." Acta Crystallographica Section C Crystal Structure Communications 67, no. 10 (2011): o397—o404. http://dx.doi.org/10.1107/s0108270111035797.

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27

Miao, Yanqing, та Tao Fan. "Poly[(μ-3,5-dinitrobenzoato)(μ-3,5-dinitrobenzoic acid)rubidium]". Acta Crystallographica Section E Structure Reports Online 67, № 8 (2011): m1040. http://dx.doi.org/10.1107/s160053681102513x.

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28

Ito, Yoshikatsu, and Satoru Arimoto. "Exothermic thermal reaction of dopamine with 3,5-dinitrobenzoic acid." Journal of Physical Organic Chemistry 16, no. 11 (2003): 849–57. http://dx.doi.org/10.1002/poc.669.

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29

But, Tracy Yuen Sze, Jinni Lu, and Patrick H. Toy. "ChemInform Abstract: Organocatalytic Mitsunobu Reactions with 3,5-Dinitrobenzoic Acid." ChemInform 41, no. 35 (2010): no. http://dx.doi.org/10.1002/chin.201035087.

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30

Lynch, Daniel E., Graham Smith, Karl A. Byriel, and Colin H. L. Kennard. "Molecular Cocrystals of Carboxylic Acids. XXXII The Crystal Structures of the Adducts of 2-Aminobenzothiazole with 3,5-Dinitrobenzoic Acid (Adduct Hydrate) and 3-Aminobenzoic Acid, and 2-Amino-2-thiazoline with 2-Aminobenzoic Acid." Australian Journal of Chemistry 51, no. 7 (1998): 587. http://dx.doi.org/10.1071/c97204.

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Two adducts of 2-aminobenzothiazole and one of 2-amino-2-thiazoline with aromatic carboxylic acids have been synthesized and their X-ray crystal structures determined. These are 2-aminobenzothiazole with 3,5-dinitrobenzoic acid (the 1 : 1 adduct hydrate) (1), and 3-aminobenzoic acid (1 : 1) (2), and 2-amino-2-thiazoline with 2-aminobenzoic acid (1 : 1) (3). Compound (1) is a non-centrosymmetric proton-transfer complex and gave a signal of 0·30 relative to urea when tested for second-order non-linear optical properties. Compound (3) is also a proton-transfer complex but (2) is not.

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31

Gündüz, Turgut, Esma Kiliç, Güleren Özkan, Muhammed F. Awaad, and Mustafa Tastekin. "Conductimetric and potentiometric investigation of effect of acidity on formation of homoconjugates in acetonitrile solvent." Canadian Journal of Chemistry 68, no. 5 (1990): 674–78. http://dx.doi.org/10.1139/v90-103.

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In the present work, 11 aromatic and nine aliphatic carboxylic acids, namely benzoic, 2-nitrobenzoic, 3-nitrobenzoic, 4-nitrobenzoic, 2,4-dinitrobenzoic, 3,5-dinitrobenzoic, 2-aminobenzoic, 3-aminobenzoic, 4-aminobenzoic, o-phthalic, salicylic, formic, acetic, monochloroacetic, dichloroacetic, trichloroacetic, propionic, n-butyric, caprylic, and myristic acids, were titrated conductimetrically and potentiometrically with triethylamine in acetonitrile solvent, under a nitrogen atmosphere, at 25 °C. Closer investigation of the conductimetric titration curves of these acids showed that the acidit

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32

Smith, Graham, and Urs D. Wermuth. "4-[(4-Aminophenyl)sulfonyl]aniline–3,5-dinitrobenzoic acid (1/1)." Acta Crystallographica Section E Structure Reports Online 68, no. 3 (2012): o669. http://dx.doi.org/10.1107/s1600536812004709.

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33

Rosli, Mohd Mustaqim, Hoong-Kun Fun, Ibrahim Abdul Razak, Tanin Panawarangkul, and Suchada Chantrapromma. "The 1:1 adduct of 3,5-dinitrobenzoic acid and quinoline." Acta Crystallographica Section E Structure Reports Online 62, no. 2 (2006): o726—o728. http://dx.doi.org/10.1107/s1600536806002145.

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34

Hartl, Monika, Luke Daemen, Hans Hartl, Irene Brüdgam, and Jürgen Eckert. "Short hydrogen bonds in 2,4-dinitrobenzoic acid complexed with pyridine." Chemical Physics 427 (December 2013): 87–94. http://dx.doi.org/10.1016/j.chemphys.2013.10.016.

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35

Lynch, DE, G. Smith, NJ Calos, et al. "Molecular Cocrystals of Carboxylic Acids. XIII. Spectral Characterization of the Adducts of Triphenylphosphine Oxide With Substituted Benzoic Acids and the Crystal Structures of the 1 : 1 Adducts With 2,4,6-Trinitrobenzoic Acid and 3,5-Dinitrobenzoic Acid." Australian Journal of Chemistry 46, no. 10 (1993): 1535. http://dx.doi.org/10.1071/ch9931535.

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The 1:1 adducts of triphenylphosphine oxide with the 2-, 3- and 4-nitro-, 3,5-dinitro-, and 2,4,6-trinitro-substituted benzoic acids have been prepared, and characterized by infrared and 31P n.m.r. spectroscopy. The crystal structures of two of these adducts, (triphenylphosphine oxide-3,5-dinitrobenzoic acid) and ( triphenylphosphine oxide-2,4,6-trinitrobenzoic acid), have been determined by X-ray diffraction. In all examples, the presence of single directed hydrogen bonds between the phosphoryl oxygen and the carboxylic acid proton is confirmed. For the X-ray structures, the O…O distances are

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36

Lynch, DE, G. Smith, KA Byriel, and CHL Kennard. "Molecular Cocrystals of Carboxylic Acids. XIX. The Crystal Structures of Two Adducts of 3-Aminobenzoic Acid With 3,5-Dinitrobenzoic Acid: the 1:1 and the 2:2 Hydrate Cocrystals." Australian Journal of Chemistry 47, no. 9 (1994): 1789. http://dx.doi.org/10.1071/ch9941789.

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Two cocrystalline molecular adducts of 3-aminobenzoic acid (3-aba) with the aromatic carboxylic acid 3,5-dinitrobenzoic acid (dnba), [(3-aba)(dnba)](1) and [(3-aba)2(dnba)2(H2O)] (2), have been prepared and their hydrogen-bonding associations determined by means of single-crystal X-ray diffraction. Complex (1) is similar to known 1:1 complexes of 4-aminobenzoic acid with other aromatic acids, with protonation of the amine group and carboxylic acid-carboxylate hydrogen-bonding associations. However, the 2:2 hydrate complex (2) has only one hetero-pair involved in proton transfer, the other rema

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37

Muñiz, Francisco, Luis Simón, Silvia Sáez, César Raposo, Victoria Alcázar, and Joaquín Morán. "A Fluorescent Sensor for Dinitrobenzoic Acid Based on a Cyanuric Acid and Xanthene Skeleton." Sensors 8, no. 3 (2008): 1637–44. http://dx.doi.org/10.3390/s8031637.

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38

Ahmed, M. Y, Kumosani, A. T, Sabir, and S. M. J. "Bioremediation of 3,5-dinitrobenzoic acid and aniline by a Corynebacterium sp." African Journal of Microbiology Research 7, no. 37 (2013): 4582–89. http://dx.doi.org/10.5897/12.2334.

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39

Kaur, Manpreet, Hemmige S. Yathirajan, K. Byrappa, Eric Hosten, and Richard Betz. "Crystal structure of desvenlafaxinium 3,5-dinitrobenzoate 3,5-dinitrobenzoic acid monohydrate, C30H35N5O15." Zeitschrift für Kristallographie - New Crystal Structures 229, no. 4 (2014): 488–90. http://dx.doi.org/10.1515/ncrs-2014-0131.

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40

Chandrasekaran, J., B. Babu, S. Balaprabhakaran, P. Ilayabarathi, P. Maadeswaran, and K. Sathishkumar. "Growth, optical and mechanical studies of 3,5-dinitrobenzoic acid single crystals." Optik 124, no. 12 (2013): 1250–53. http://dx.doi.org/10.1016/j.ijleo.2012.03.005.

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41

La Rotta, Lina Katherine, Daniela Fonseca, John Hurtado, and María Teresa Cortés Montañez. "Electrochemical Characterization of Cobalt Complexes with Benzoate and Azole-Pyridine Ligands As Potential Electrolytes in Batteries." ECS Meeting Abstracts MA2025-01, no. 62 (2025): 2960. https://doi.org/10.1149/ma2025-01622960mtgabs.

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The study of electroactive species with multiple redox events is of interest due to their applications as electrolytes in Redox Flow Batteries (RFBs). This multi-electron behavior can be observed in organic molecules and coordination compounds containing ligands with heteroatoms such as O and N in π-extended systems. In this context, a study of 3,5-dinitrobenzoic acid, its respective cobalt complexes (1), and azole-pyridine co-ligands (2) was conducted. Electrochemical characterization of the cobalt complexes was performed using cyclic voltammetry. Measurements were conducted in a three-electr

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Lynch, Daniel E., Pardeep Sandhu, and Simon Parsons. "1 : 1 Molecular Complexes of 4-Amino-N-(4,6-dimethylpyrimidin-2-yl)benzene-sulfonamide (Sulfamethazine) with Indole-2-carboxylic Acid and 2,4-Dinitrobenzoic Acid." Australian Journal of Chemistry 53, no. 5 (2000): 383. http://dx.doi.org/10.1071/ch00021.

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The 1 : 1 molecular adducts of 4-amino-N-(4,6-dimethylpyrimidin-2-yl)benzenesulfonamide (Sulfamethazine) with respectively indole-2-carboxylic acid (1) and 2,4-dinitrobenzoic acid (2) have been prepared and their X-ray crystal structures determined. The acid groups in both structures form associative R22 (8) graph set hydrogen-bonding interactions across the N(11)–H/N(17) site of Sulfamethazine. Acomparison of the two distances between relevant non-hydrogen atoms in this configuration reveals that this association is not symmetrical. An average difference of 0.144 Å is observed for seven liste

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Motati, Ramya, Trisha Kandi, Jilawan Francis, et al. "Abraham General Solvation Parameter Model: Predictive Expressions for Solute Transfer into Isobutyl Acetate." Liquids 4, no. 3 (2024): 470–84. http://dx.doi.org/10.3390/liquids4030026.

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Mole fraction of solubilities are reported for the: o-acetoacetanisidide, anthracene, benzoin, 4-tert-butylbenzoic acid, 3-chlorobenzoic acid, 3-chlorobenzoic acid, 2-chloro-5-nitrobenzoic acid, 4-chloro-3-nitrobenzoic acid, 3,4-dichlorobenzoic acid, 2,3-dimethoxybenzoic acid, 3,4-dimethoxybenzoic acid, 3,5-dimethoxybenzoic acid, 3,5-dinitrobenzoic acid, diphenyl sulfone, 2-ethylanthraquinone, 2-methoxybenzoic acid, 4-methoxybenzoic acid, 2-methylbenzoic acid, 3-methylbenzoic acid, 2-methyl-3-nitrobenzoic acid, 3-methyl-4-nitrobenzoic acid, 4-methyl-3-nitrobenzoic acid, 2-naphthoxyacetic acid,

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Abbas, Zahra Mohammed, and Rasmia Mahmood Rumez. "SYNTHESIS, CHARACTERIZATION AND SCREENING OF ANTIMICROBIAL ACTIVITY FOR SOME NEW SCHIFF BASES AND THIAZOLIDINONE DERIVATIVES DERIVED FROM AROMATIC CARBOXYLIC ACID." ChemChemTech 68, no. 7 (2025): 27–34. https://doi.org/10.6060/ivkkt.20256807.7189.

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In this study, the antimicrobial properties of newly synthesized Schiff bases (4a-4e) and thiazolidinone compounds (5a-5e) generated from 3,5-dinitrobenzoic acid were assessed. These compounds were obtained by reacting 3,5-dinitrobenzoic acid (1) with ethanol in a few drops of concentrated H2SO4 to produce the ester (2). The acid hydrazide (3), which was produced by treating the ester with hydrazine hydrate, reacted with the proper aldehydes, including 4-bromobenzaldehyde, 4-chlorobenzaldehyde, 4-hydroxybenzaldehyde, 4-methoxybenzaldehyde, and 4-hydroxy-3-methoxybenzaldehyde, respectively, to

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JI, Baoming, Fangfang JIAN, Hailian XIAO, and Chenxia DU. "Synthesis and Structure of Tris(2-benzimidazylmethyl)amine with 3,5-Dinitrobenzoic Acid." Analytical Sciences: X-ray Structure Analysis Online 20 (2004): x101—x102. http://dx.doi.org/10.2116/analscix.20.x101.

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Moreno-Fuquen, Rodolfo, Martha Lucía Zambrano, Mario Grajales-Tamayo, Julio Zukerman-Schpector, and Alan R. Kennedy. "The 1:1 complex of 3,5-dinitrobenzoic acid and 4-methylpyridineN-oxide." Acta Crystallographica Section E Structure Reports Online 58, no. 1 (2001): o50—o52. http://dx.doi.org/10.1107/s160053680102089x.

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Jones, Helen P., Amy L. Gillon, and Roger J. Davey. "A co-crystal of ethylenediammonium bis(3,5-dinitrobenzoate) and 3,5-dinitrobenzoic acid." Acta Crystallographica Section E Structure Reports Online 61, no. 6 (2005): o1823—o1825. http://dx.doi.org/10.1107/s1600536805015333.

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Ito, Yoshikatsu, Sadayuki Asaoka, Koji Kokubo Shigeru Ohba, and Shigeru Fukushima. "Photoreactivities of Donor-Acceptor Crystals between 3,5-Dinitrobenzoic Acid and N-Alkylcarbazoles." Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 313, no. 1 (1998): 125–34. http://dx.doi.org/10.1080/10587259808044266.

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Amalanathan, M., V. K. Rastogi, I. Hubert Joe, M. A. Palafox, and Rashmi Tomar. "Density functional theory calculations and vibrational spectral analysis of 3,5-(dinitrobenzoic acid)." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 78, no. 5 (2011): 1437–44. http://dx.doi.org/10.1016/j.saa.2011.01.023.

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Raj, Asha, Y. Sheena Mary, C. Yohannan Panicker, Hema Tresa Varghese, and K. Raju. "IR, Raman, SERS and computational study of 2-(benzylsulfanyl)-3,5-dinitrobenzoic acid." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 113 (September 2013): 28–36. http://dx.doi.org/10.1016/j.saa.2013.04.096.

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