Relevant bibliographies by topics / Dinitrobenzoic acid

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers
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Academic literature on the topic 'Dinitrobenzoic acid'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Dinitrobenzoic acid"

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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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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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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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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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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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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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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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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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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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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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Dissertations / Theses on the topic "Dinitrobenzoic acid"

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Boardman, N. D., Tasnim Munshi, Ian J. Scowen, and Colin C. Seaton. "Creation of a ternary complex between a crown ether, 4-aminobenzoic acid and 3,5-dinitrobenzoic acid." 2014. http://hdl.handle.net/10454/10192.

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Yes<br>The creation of ternary multi-component crystals through the introduction of 18-crown-6 to direct the hydrogen-bonding motifs of the other molecular components was investigated for 3,5-dinitrobenzoic acid (3,5-dnba) with 4-aminobenzoic acid (4-aba). The creation of a binary complex between 18-crown-6 and 4-aba (C12H24O6·2C7H7NO2)2 and a ternary salt between 3,5-dnba, 18-crown-6 and 4-aba (C12H24O6·C7H8NO2+·C7H3N2O6−·C7H4N2O6) were confirmed by single-crystal structure determination. In both structures, the amino molecules bind to the crown ether through N—H...O hydrogen bonds, leaving a
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Seaton, Colin C., Ian J. Scowen, and Nicholas Blagden. "Formation of a hybrid coordination-molecular complex." 2009. http://hdl.handle.net/10454/6174.

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Thomas, L. H., Nicholas Blagden, M. J. Gutmann, et al. "Tuning proton behavior in a ternary molecular complex." 2010. http://hdl.handle.net/10454/4855.

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no<br>The multicomponent ternary complex of 4-dimethylaminobenzoic acid (4-DABA), 3,5-dinitrobenzoic acid (3,5-DNBA), and 4,40-bipyridine (BIPY) has been studied by variable temperature X-ray and neutron diffraction. Proton disorder is observed within the 4-DABA homodimers present and quantitatively evaluated from neutron data. The effect of the crystal environment and in particular the pyramidalization of the nitrogen atom within the 4-DABA molecule and the consequential effect on the presence of hydrogen atom disorder are discussed with reference to the previously determined pure 4-DABA
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Book chapters on the topic "Dinitrobenzoic acid"

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand cobalt(II) complex with 3,5-dinitrobenzoic acid and 4,4′-bipyridine." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 6. Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-65056-1_179.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand nickel(II) complex with 3,5-dinitrobenzoic acid and 4,4′-bipyridine." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 6. Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-65056-1_237.

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Mitra, S., S. R. Gurrala, and R. S. Coleman. "Synthesis of the --Butyl--(3,5-dinitrobenzoyl)nitroxyl Radical." In Three Carbon-Heteroatom Bonds: Acid Halides; Carboxylic Acids and Acid Salts. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-020-01453.

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Lambert, Tristan H. "Construction of Single Stereocenters." In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0037.

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James L. Leighton at Columbia University reported (Nature 2012, 487, 86) that the commercially available allylsilane 2 allylated acetoacetone (1) to furnish the enantioenriched tertiary carbinol 3. Alexander T. Radosevich demonstrated (Angew. Chem. Int. Ed. 2012, 51, 10605) that diazaphospholidine 5 induced the formal reductive insertion of 3,5-dinitrobenzoic acid to α-ketoester 4 to generate adduct 6 enantioselectively. Tehshik P. Yoon at the University of Wisconsin at Madison found (J. Am Chem. Soc. 2012, 134, 12370) that aminoalcohol derivative 9 could be prepared via an asymmetric iron-cat
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Conference papers on the topic "Dinitrobenzoic acid"

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Afroz, Ziya, Mohd Faizan, Mohammad Jane Alam, Shabbir Ahmad, and Afaq Ahmad. "Theoretical studies of charge transfer and proton transfer complex formation between 3,5-dinitrobenzic acid and 1,2-dimethylimidazole." In 2ND INTERNATIONAL CONFERENCE ON CONDENSED MATTER AND APPLIED PHYSICS (ICC 2017). Author(s), 2018. http://dx.doi.org/10.1063/1.5033256.

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Reports on the topic "Dinitrobenzoic acid"

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Frankenbach, G. M., M. C. Etter, A. J. Schultz, and J. M. Williams. Analyzing carboxylic acid and amine-nitro hydrogen-bond geometry in the cocrystal of 4-aminobenzoic acid and 3,5-dinitrobenzoic acid by use of 298 K X-ray and 15 K neutron diffraction. Office of Scientific and Technical Information (OSTI), 1993. http://dx.doi.org/10.2172/10184515.

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Journal articles
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