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Journal articles on the topic 'Bromoaniline'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Waware, Umesh S., A. M. S. Hamouda, A. Shahul Hameed, and Gabriel J. Summers. "Tuning the electrical properties of polyaniline by copolymerization with o-bromoaniline." Functional Materials Letters 10, no. 04 (2017): 1750039. http://dx.doi.org/10.1142/s1793604717500394.

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Polyaniline, poly(o-bromoaniline) and poly(aniline-co-o-bromoaniline)s have been prepared by chemical oxidative polymerization methods. A series of poly(aniline-co-o-bromoaniline) derivatives has been prepared by the chemical oxidative copolymerization of aniline with different mole ratio of o-bromoaniline by varying the feed ratios of the monomers with the introduction of o-bromoaniline units along the polymer backbone. The morphology of each poly(aniline-co-o-bromoaniline) derivative is observed as a porous network of aggregated nanoparticles with each nanoparticle having smaller nanoflake s

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2

Stejskal, Jaroslav, Miroslava Trchová, and Jan Prokeš. "Poly(2-bromoaniline) and Its Colloidal Dispersions." Collection of Czechoslovak Chemical Communications 67, no. 3 (2002): 393–404. http://dx.doi.org/10.1135/cccc20020393.

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Poly(2-bromoaniline) was prepared by oxidation of 2-bromoaniline with ammonium peroxydisulfate in the presence of hydrochloric acid. The conductivity of the poly(2-bromoaniline) hydrochloride so produced was 10-6 S cm-1, its density at 20 °C 1.78 g cm-3 and weight-average molar mass 18 500 g mol-1. The degree of protonation was estimated as being a half of that of polyaniline. The structure of poly(2-bromoaniline) is discussed on the basis of FTIR spectra. Colloidal dispersions were produced when the polymerization had been carried out in the presence of a particulate or polymeric stabilizer,

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3

Khalaji, Aliakbar Dehno, Alexandra M. Z. Slawin, and J. Derek Woollins. "N-(2-Benzylidenepropylidene)-4-bromoaniline." Acta Crystallographica Section E Structure Reports Online 63, no. 11 (2007): o4257. http://dx.doi.org/10.1107/s1600536807048222.

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The title compound, C16H14BrN, at 93 (2) K crystallizes with two independent molecules in the asymmetric unit. The molecules are slightly non-planar with the substituents adopting an E configuration with respect to the imine C=N bond.

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4

Şahin, Yücel, Sabriye Peŗin, Mutlu Şahin, and Güleren Özkan. "Electrochemical preparation of poly(2-bromoaniline) and poly(aniline-co-2-bromoaniline) in acetonitrile." Journal of Applied Polymer Science 90, no. 9 (2003): 2460–68. http://dx.doi.org/10.1002/app.12994.

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5

Harikishna, V., and N. V. S. Naidu. "Facile and Sensitive Spectrophotometric Technique for the Determination of Carbofuran in its Formulations, Water and Grain Samples with Substituted Anilines." E-Journal of Chemistry 2, no. 4 (2005): 218–23. http://dx.doi.org/10.1155/2005/172909.

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Methods are described for the determination of carbofuran in its formulations, in water and grain samples by the diazotization coupling spectrophotometric technique, using substituted anilines such as 4-bromoaniline, 4-methylaniline and 4-aminobenzaldehyde as the coupling agents. The orange red colour formed with 4-bromoaniline shows maximum absorption at 478 nm, yellow colour obtained with 4-methylaniline have maximum absorption at 465 nm whereas a red colour derivative formed with 4-aminobenzaldehyde shows λmaxat 472 nm. The methods could be successfully applied for the determination of carb

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6

Ran, deep Kaur Sandhar, R. Sharma J., and R. Manrao M. "Synthesis and fungitoxicity of aldimines and 4-thiazolidinones derived from 4-bromoaniline." Journal of Indian Chemical Society Vol. 85, Feb 2008 (2008): 220–23. https://doi.org/10.5281/zenodo.5808967.

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Department of Biochemistry and Chemistry, Punjab Agricultural University, Ludhiana-141 004, Punjab, India <em>Manuscript received 26 October 2005, revised 1 August 2007, accepted 26 November 2007</em> Condensation of 4-bromoaniline with benzaldehyde and substituted benzaldehydes (1-8) in equimolar ratio resulted in the formation of benzal-4-bromoaniline and its C-phenyl derivatives (la-8a). Addition of thioglycolic acid to la-8a yielded the respective 4-thiazolidinone (lb-8b). The synthesized compounds were characterized on the basis of elemental analysis and spectral studies and were screened

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7

Delaporte, Nicolas, Karim Zaghib, and Daniel Bélanger. "In situ formation of bromobenzene diazonium ions and their spontaneous reaction with carbon-coated LiFePO4 in organic media." New Journal of Chemistry 40, no. 7 (2016): 6135–40. http://dx.doi.org/10.1039/c6nj00132g.

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8

Mishra, Manish Kumar, Pallavi Ghalsasi, M. N. Deo, et al. "In situhigh pressure study of an elastic crystal by FTIR spectroscopy." CrystEngComm 19, no. 47 (2017): 7083–87. http://dx.doi.org/10.1039/c7ce01664f.

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Anin situhigh pressure-FTIR study on a 2,3-dichlorobenzylidine-4-bromoaniline elastic crystal shows significant structural changes at high pressure which revert back to the ambient structure on decompression.

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9

Peixoto, Daniela, Abel Locati, Carolina S. Marques, Albertino Goth, J. P. Prates Ramalho, and Anthony J. Burke. "A catalytic route to dibenzodiazepines involving Buchwald–Hartwig coupling: reaction scope and mechanistic consideration." RSC Advances 5, no. 121 (2015): 99990–99. http://dx.doi.org/10.1039/c5ra19599c.

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10

KHALAJI, Aliakbar Dehno, та William T. A. HARRISON. "Crystal Structure of β-Phenylcinnamaldehyde-4-bromoaniline". Analytical Sciences: X-ray Structure Analysis Online 24 (2008): x3—x4. http://dx.doi.org/10.2116/analscix.24.x3.

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11

Aparicio, Enrique B., Stephen R. Isbel, and Alejandro Bugarin. "Four-Step Synthesis of 3-Allyl-2-(allyloxy)-5-bromoaniline from 2-Allylphenol." Molbank 2024, no. 1 (2024): M1773. http://dx.doi.org/10.3390/m1773.

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This communication reports a four-step protocol to produce 3-allyl-2-(allyloxy)-5-bromoaniline 5 from commercially available 2-allylphenol. The synthetic steps used were nitration, selective bromination, allylation, and reduction of the nitro group.

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12

Ojala, William. "A Crystallographic Search for Isomorphism among “Bridge-Flipped” 2,2′-Disubstituted Benzylideneanilines." Structural Dynamics 12, no. 2_Supplement (2025): A407. https://doi.org/10.1063/4.0000713.

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We have labelled as “bridge-flipped isomers” those pairs of molecules that differ only in the orientation of a bridge of atoms linking two larger parts of the molecules. Among the benzylideneanilines, this isomerism is R-CH=N-R′ vs. R-N=CH-R′. Pairs of these isomers that are isomorphous might be capable of forming solid solutions with tailorable properties. Although differences in molecular space-filling properties between bridge-flipped benzylideneanilines are minimal, isomorphous pairs are rare. Differences in crystal structure can result from differences in molecular conformation due to ste

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13

A., P. MISHRA, K. SRIVASTAVA S, and SRIVASTAVA VIBHUTI. "Synthesis, Characterisation and Antibacterial Activity of some 3d-Metal Complexes with Thiophene-2-aldehyde-4-chloro/bromoaniline." Journal of Indian Chemical Society Vol. 74, Jun 1997 (1997): 487–88. https://doi.org/10.5281/zenodo.5881710.

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Inorganic Research Laboratories, Department or Chemistry, Dr. H <em>S. </em>Gour University, Sagar-470 003 <em>Manuscript received 8 May 1995 revised 16 April 1996, accepted 2 May 1996</em> Synthesis, Characterisation and Antibacterial Activity of some 3d-Metal Complexes with Thiophene-2-aldehyde-4-chloro/bromoaniline

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14

Xie, Yu, Xiao-Wei Hong, and Ya Wei. "Crystal structure of N-diphenylphosphoryl-4-bromoaniline, C18H15BrNOP." Zeitschrift für Kristallographie - New Crystal Structures 225, no. 2 (2010): 349–50. http://dx.doi.org/10.1524/ncrs.2010.0152.

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15

Jothi, L., G. Anuradha, G. Vasuki, R. Ramesh Babu, and K. Ramamurthi. "Crystal structure of N-(p-methylbenzylidene)-p-bromoaniline." Journal of Structural Chemistry 58, no. 2 (2017): 370–72. http://dx.doi.org/10.1134/s0022476617020226.

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16

Johmoto, Kohei, Takashi Ishida, Akiko Sekine, Hidehiro Uekusa, and Yuji Ohashi. "Relation between photochromic properties and molecular structures in salicylideneaniline crystals." Acta Crystallographica Section B Structural Science 68, no. 3 (2012): 297–304. http://dx.doi.org/10.1107/s0108768112010993.

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The crystal structures of the salicylideneaniline derivatives N-salicylidene-4-tert-butyl-aniline (1), N-3,5-di-tert-butyl-salicylidene-3-methoxyaniline (2), N-3,5-di-tert-butyl-salicylidene-3-bromoaniline (3), N-3,5-di-tert-butyl-salicylidene-3-chloroaniline (4), N-3,5-di-tert-butyl-salicylidene-4-bromoaniline (5), N-3,5-di-tert-butyl-salicylidene-aniline (6), N-3,5-di-tert-butyl-salicylidene-4-carboxyaniline (7) and N-salicylidene-2-chloroaniline (8) were analyzed by X-ray diffraction analysis at ambient temperature to investigate the relationship between their photochromic properties and mo

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17

Roopashree, Rangaswamy, Toreshettahally R. Swaroop, Chalya M. Shivaprasad, Swamy Jagadish, and Kanchugarakoppal S. Rangappa. "Synthesis and Cytotoxic Studies of Pyrrolopyrimidine Derivatives." Asian Journal of Chemistry 33, no. 8 (2021): 1855–60. http://dx.doi.org/10.14233/ajchem.2021.23261.

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The synthesis and in vitro cytotoxicity of new pyrrolopyrimidine derivatives is reported in this work. All the compounds were characterized by IR, NMR and MS. They are examined for cytotoxic activity against HeLa. Pyrrolopyrimidine derivatives of benzyl amine (8g) and 4-bromoaniline (8k) showed a potent activity, which is comparable to that of standard Sorafenib.

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18

Bei, M. P., and A. P. Yuvchenko. "Synthesis of aromatic and heterocyclic fumaropimaric acid triamides." Журнал общей химии 93, no. 7 (2023): 1001–6. http://dx.doi.org/10.31857/s0044460x2307003x.

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A method was developed for the synthesis of previously unknown triamides of fumaropimaric acid by the reaction of anilide and 1-(piperidin-1-ylcarbonyl) derivative of fumaropimaric acid with aromatic and heterocyclic amines [4-toluidine, 4-pentylaniline, 4-biphenylamine, 4-methoxy-, ethoxy-, phenoxy-, bromoaniline, 2-picolylamine, 2-(aminomethyl)furan, 2-(aminomethyl)thiophene] under the action of propanephosphonic acid anhydride.

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19

Yamanaka, Hiroshi, Takao Sakamoto, and Yoshinori Kondo. "Facile Synthesis of 2-Substituted Indoles from o-Bromoaniline." HETEROCYCLES 24, no. 1 (1986): 31. http://dx.doi.org/10.3987/r-1986-01-0031.

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20

Gao, Wei. "Synthesis and Structure Analysis of N-diphenylphosphoryl-4-bromoaniline." Molecular Crystals and Liquid Crystals 609, no. 1 (2015): 155–60. http://dx.doi.org/10.1080/15421406.2014.950469.

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21

Barraza, Scott, and Scott Denmark. "Unexpected Rearrangement of 2-Bromoaniline under Biphasic Alkylation Conditions." Synlett 28, no. 20 (2017): 2891–95. http://dx.doi.org/10.1055/s-0036-1590882.

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Alkylation of 2-bromoaniline with benzyl bromide under ostensibly basic N-alkylation conditions resulted in migration of bromine from the 2- to the 4-aryl position. Herein we report our studies to elucidate the mechanism of this rearrangement with the objective of suppressing this unexpected outcome. We find that careful choice of reagents is critical, and that this behavior may be extrapolated to alkylation reactions of electron-rich bromo- and iodoanilines in general.

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22

Mahudeswaran, A., J. Vivekanandan, P. S. Vijayanand, T. Kojima, and S. Kato. "A facile synthesis of poly(aniline-co-o-bromoaniline) copolymer: Characterization and application as semiconducting material." International Journal of Modern Physics B 30, no. 05 (2016): 1650008. http://dx.doi.org/10.1142/s0217979216500089.

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Poly(aniline-co-o-bromoaniline) (p(an-co-o-BrAn)) copolymer has been synthesized using chemical oxidation method in the hydrochloric acid medium. Copolymerization of aniline with o-bromoaniline of different compositions, such as 1:1, 1:2, 2:1, 1:3 and 3:1 molar ratios were prepared. The synthesized copolymer is soluble in polar solvents like dimethyl sulphoxide (DMSO), dimethyl formamide (DMF), Tetrahydrofuran (THF) and 1-methyl 2-pyrrolidone (NMP). The copolymer is analyzed by various characterization techniques, such as FTIR, UV–Visible (UV–Vis) spectroscopy, X-ray diffraction (XRD), conduct

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23

Yang, Hao, Yifan Ouyang, Yutong Sun, et al. "Facile Synthesis of 1-(4-Bromophenyl)-1H-Tetrazol-5-Amine and Related Amide Derivatives." Journal of Chemical Research 41, no. 10 (2017): 581–85. http://dx.doi.org/10.3184/174751917x15064232103128.

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An efficient one-pot synthesis of 1-(4-bromophenyl)-1 H-tetrazol-5-amine was performed using 4-bromoaniline as the starting material. A novel and widely applicable amidation procedure was then employed, whereby 1-(4-bromophenyl)-1 H-tetrazol-5-amine was acylated with different acyl chlorides in the presence of lithium bis(trimethylsilyl)amide as catalyst, for the high-yield synthesis of [1-(4-bromophenyl)-1 H-tetrazol-5-yl]amide derivatives.

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24

Bunev, Alexander S., Maksim A. Vasiliev, Gennady I. Ostapenko, Alexander S. Peregudov, and Victor N. Khrustalev. "(Z)-N-[1-(Aziridin-1-yl)-2,2,2-trifluoroethylidene]-4-bromoaniline." Acta Crystallographica Section E Structure Reports Online 70, no. 5 (2014): o550. http://dx.doi.org/10.1107/s1600536814007867.

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The title compound, C10H8BrF3N2, crystallizes with two independent molecules in the asymmetric unit, which can be considered as being related by a pseudo-inversion center, so their conformations are different; the corresponding N=C—N—C torsion angles are 54.6 (5) and −50.5 (5)°. In the crystal, molecules related by translation in [001] interact through short intermolecular Br...F contacts [3.276 (2) and 3.284 (2) Å], thus forming two types of crystallographically independent chains.

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25

Kazak, D. V., Е. А. Dikusar, E. A. Akishina, R. S. Alexeev, N. A. Bumagin, and V. I. Potkin. "Synthesis and properties of esters and amides of pyridine- and 1,2-azolcarbonic acids." Proceedings of the National Academy of Sciences of Belarus, Chemical Series 57, no. 2 (2021): 185–94. http://dx.doi.org/10.29235/1561-8331-2021-57-2-185-194.

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Based on esters of nicotinic and isonicotinic acids with hydroxybenzaldehydes, a series of functionally substituted derivatives containing isoxazole and isothiazole heterocycles in the molecule have been synthesized. Azomethines were obtained by condensation of nicotinates and isonicotinates with p-bromoaniline and m-aminophenol, which have been reduced with sodium triacetoxyborohydride to give the corresponding amines. Acylation of amino derivatives of nicotinates and isonicotinates with 5-arylisoxazole- and 4,5-dichloroisothiazolecarbonyl chlorides leads to the esters and amides with isoxazo

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26

Longkumer, Naruti, Kikoleho Richa, Rituparna Karmaker, Basanta Singha, and Upasana Bora Sinha. "Facile Green Synthesis of Bromoaniline Molecules: An Experimental and Computational Insight into their Antifungal Behaviour." Asian Journal of Chemistry 34, no. 12 (2022): 3115–24. http://dx.doi.org/10.14233/ajchem.2022.23994.

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Through the bromination of organic substrates using cetyltrimethylammonium tribromide (CTMATB), a series of bromoanilines have been synthesized using a greener synthetic process. The synthesized bromoanilines were optimized by testing for antifungal activity against Fusarium oxysporum, Penicillium italicum, Candida albicans and Aspergillus niger. The ADMET profiling was studied to determine the drug likeliness of the compounds. In silico studies were done to understand the ligand-protein interaction of the compounds with a target protein. Density functional theory (DFT) studies have been carri

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27

Bouabida, N. El-hoda, A. Hachemaoui, A. Yahiaoui та ін. "Fabrication and Characterization of Poly(aniline-co-4-bromoaniline)/Сlay Nanocomposite". Polymer Science, Series B 62, № 2 (2020): 163–68. http://dx.doi.org/10.1134/s1560090420020013.

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28

Unver, H., A. Karakas, and A. Elmali. "Crystal structure and nonlinear optical properties ofN-(3-hydroxybenzalidene)4-bromoaniline." Acta Crystallographica Section A Foundations of Crystallography 64, a1 (2008): C458. http://dx.doi.org/10.1107/s0108767308085280.

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29

Gök, Ayşegül, Bekir Sari, and Muzaffer Talu. "Polymers, composites, and characterization of conducting polyfuran and poly(2-bromoaniline)." Journal of Applied Polymer Science 98, no. 5 (2005): 2048–57. http://dx.doi.org/10.1002/app.22404.

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30

Gök, Ayşegül, Bekir Sari, and Muzaffer Talu. "Polymers, composites, and characterization of conducting polyfuran and poly(2-bromoaniline)." Journal of Applied Polymer Science 98, no. 6 (2005): 2440–49. http://dx.doi.org/10.1002/app.22439.

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31

Gök, Ayşegül, Bekir Sari, and Muzaffer Talu. "Polymers, composites, and characterization of conducting polyfuran and poly(2-bromoaniline)." Journal of Applied Polymer Science 100, no. 5 (2006): 4270. http://dx.doi.org/10.1002/app.24291.

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32

Senra, Jaqueline D., Aires C. Silva, Raquel V. Santos, Luiz Fernando B. Malta, and Alessandro B. C. Simas. "Palladium on Layered Double Hydroxide: A Heterogeneous System for the Enol Phosphate Carbon-Oxygen Bond Activation in Aqueous Media." Journal of Chemistry 2017 (2017): 1–10. http://dx.doi.org/10.1155/2017/8418939.

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In this work, a new catalytic approach for the C-O activation of enol phosphates based on a palladium supported on layered double hydroxide was developed. In this case, two different ketene aminal phosphates were used as models to study the synthesis ofα-phenyl enecarbamates N-Boc/CBz under the Suzuki-Miyaura conditions. The use of an ortho-bromoaniline as precursor allowed the synthesis of the 2-phenyl indole through an arylation/Heck cyclization. Catalyst reusability enabled the synthesis of the heterocycle in moderate yields for four consecutive runs.

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33

Gonzalez-Pradas, E., A. Valverde-Garcia, M. Villaranca-Sanchez, F. Del, and Rey Bueno. "Adsorption of Para Substituted Anilines from Cyclohexane Solution on Sepiolite." Adsorption Science & Technology 4, no. 1-2 (1987): 79–85. http://dx.doi.org/10.1177/0263617487004001-207.

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The adsorption processes of different para-substituted anilines from cyclohexane solution on natural sepiolite have been studied. The adsorption isotherms may be classified as type L-2 of the Giles classification in the p-bromoaniline and p-toluidine cases, and as type H-2 in the p-acetylaniline case. The experimental data points have been fitted to the Langmuir equation and the adsorption capacities, surface areas available to the amine molecules and apparent equilibrium constants have been calculated. The apparent thermodynamic magnitudes corresponding to the adsorption processes have also b

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34

Maridevarmath, C. V., and G. H. Malimath. "Studies on dielectric relaxation in relation to viscosity of some anilines, phenol, and their binary mixtures at microwave frequencies." Canadian Journal of Physics 97, no. 2 (2019): 210–15. http://dx.doi.org/10.1139/cjp-2018-0136.

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In the present work, the study of variation of relaxation time (τ) with viscosity of the medium (η) is carried out on four polar samples: 2-Nitroaniline, 4-Bromoaniline, 4-Chloroaniline, 4-Chlorophenol, and also on the binary mixture of 2-Nitroaniline + 4-Bromoaniline at room temperature by using microwave bench operating at a frequency of 9.59 GHz. In this regard, the different parameters like dielectric constant ([Formula: see text]), dielectric loss ([Formula: see text]), relaxation time (τs), macroscopic steady state viscosity (ηs), dynamic viscosity (ηd), and viscoelastic relaxation time

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35

Patel, Yogesh S. "Studies on Oligomer Metal Complexes Derived from Bisamic Acid of Pyromellitic Dianhydride and 4-Bromoaniline." International Scholarly Research Notices 2014 (October 30, 2014): 1–7. http://dx.doi.org/10.1155/2014/516274.

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Novel oligomer metal complexes (2a–f) of the ligand 2,5-bis((4-bromophenyl)carbamoyl) terephthalic acid (1) were prepared using transition metal salts and characterized by various spectroscopic techniques. The geometry of oligomer metal complexes was carried out by electronic spectral analysis and magnetic measurement studies. Polymeric properties have also been carried out. Ligand was synthesized using pyromellitic dianhydride and 4-bromoaniline. It was duly characterized. All novel synthesized compounds 1 and 2a–f were evaluated for their antibacterial and antifungal activity. The results sh

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36

Serkan, Elçin. "Synthesis and structural characterization of mono acid-type partial cone conformation azocalix[4]arene." Journal of Ongoing Chemical Research 6, no. 1 (2022): 24–28. https://doi.org/10.5281/zenodo.6526076.

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This study describes the synthesis of chromogenic mono acid-type azocalix[4]arene derivatives. Four azocalix[4]arenes (<strong>3a-d</strong>) were prepared by linking 4-methoxy, 4-ethyl, 4-chloro, 4-bromoaniline to 25,26,27,28-<em>tetra</em>hydroxycalix[4]arene through a diazo-coupling reaction. Their mono ester units were carried out with ethyl bromoacetate and hydrolyzed in a basic medium to obtain <em>partial cone </em>conformation acid derivatives (<strong>5a-d</strong>). The synthesized molecules were characterized using FT-IR and <sup>1</sup>H-NMR spectroscopic m

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37

Waware, Umesh S., A. M. S. Hamouda, A. Shahul Hameed, and G. J. Summers. "Synthesis and characterization of electrically conductive poly(aniline-co-3-bromoaniline) nanocomposites." Journal of Materials Science: Materials in Electronics 28, no. 14 (2017): 10693–99. http://dx.doi.org/10.1007/s10854-017-6844-3.

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38

Li, Jun, Xuefeng Hu, and Jichang Wang. "Electrochemical Recognition of Chiral Molecules with Poly(4-bromoaniline) Modified Gold Electrode." Electroanalysis 25, no. 8 (2013): 1975–80. http://dx.doi.org/10.1002/elan.201300182.

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39

Jones, Charlotte, Chick Wilson, and Lynne Thomas. "Tuning colour in multi-component complexes: Molecular disorder as a design tool." Acta Crystallographica Section A Foundations and Advances 70, a1 (2014): C1007. http://dx.doi.org/10.1107/s205327331408992x.

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The key aim of multi-component crystallisation is modification of the physicochemical properties for a specific task.[1] Tuning colour using molecular components is a relatively unexplored area, which is surprising given the possible advantages in pigment development. In crystalline materials, the optical characteristics are not solely dependent on the molecules but also on the crystal packing;[2] it follows that the optical properties could be modified using crystal engineering techniques. We have systematically investigated co-crystallising haloanilines with dinitrobenzoic acids to build an

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40

Delgado, G., and A. J. Mora. "Crystal Structure Determination of p-Bromoaniline Using Laboratory X-Ray Powder Diffraction Data." Materials Science Forum 378-381 (October 2001): 795–97. http://dx.doi.org/10.4028/www.scientific.net/msf.378-381.795.

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41

Osman, Faridah, Guan-Yeow Yeap, and Daisuke Takeuchi. "Synthesis and mesomorphic behaviour of new disulphide bridge 4-n-alkoxybenzylidine-4′-bromoaniline." Liquid Crystals 41, no. 1 (2013): 106–12. http://dx.doi.org/10.1080/02678292.2013.839833.

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42

Waware, Umesh S., Mohd Rashid, and Gabriel J. Summers. "Studies of Chemical Oxidative Copolymerization of Functionalized Conducting Poly(aniline-co-2-bromoaniline)." Journal of Advanced Physics 3, no. 1 (2014): 45–50. http://dx.doi.org/10.1166/jap.2014.1107.

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43

Prakash, S., C. Sivakumar, T. Vasudevanand, A. Gopalan, and Ten-Chin Wen. "Growth Behavior and Characterizationof Poly(o-toluidine-co-m-bromoaniline)by Cyclic Voltammetry." International Journal of Polymer Analysis and Characterization 8, no. 1 (2003): 1–27. http://dx.doi.org/10.1080/10236660304885.

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Waware, Umesh S., A. M. S. Hamouda, Mohd Rashid, and Peter Kasak. "Towards the higher solubility and thermal stability of poly(aniline-co-m-bromoaniline)." Ionics 24, no. 12 (2018): 3837–44. http://dx.doi.org/10.1007/s11581-018-2561-z.

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Topaloglu-Sozuer, Isil, Seckiner Dulger Irdem, John J. Jeffery, Hayrullah Hamidov та Ozan Sanlı Senturk. "Oxo-Bridged (Haloarylimido)[tris(3,5-dimethylpyrazolyl)borato]- molybdenum(V) Complexes: Crystal Structures of Geometric Isomers of [MoTp*(O)Cl](μ-O)[MoTp*(Cl)(≡NC6H4Br)]". Zeitschrift für Naturforschung B 60, № 1 (2005): 15–21. http://dx.doi.org/10.1515/znb-2005-0103.

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The reaction between [MoTp∗(O)Cl2], [Tp* = hydrotris(3,5-dimetylpyrazol-1-yl)borate] and 4-bromoaniline in refluxing toluene gave geometric isomers of [MoTp*(O)Cl](μ-O)[MoTp*(Cl) (≡NC6H4Br)] (1a, cis; 1b, trans), but a similar reaction between [MoTp*(O)Cl2] and 4-chloroaniline yielded only one product, [MoTp*(O)Cl](μ-O)[MoTp∗(Cl)(≡NC6H4Cl)] (2) as a red crystalline solid. The new compounds were characterized by microanalytical data, mass, IR and 1H NMR spectroscopy. The X-ray structure analysis of 1a and 1b revealed that the complexes are geometric isomers, the two chloro ligands being cis in

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Shabeeb, Ghufran Mohammad, and Haider Abdulelah. "SYNTHESIS OF POLY ORTHO BROMO ANILINE AND STUDY ITS APPLICATION." International Journal Multidisciplinary (IJMI) 1, no. 2 (2024): 95–102. https://doi.org/10.61796/ijmi.v1i2.158.

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After producing poly orthobromo aniline, FT-IR spectroscopy was used to investigate its structure. We examined the optical and electrical characteristics of poly-o-bromo aniline (o-BrAn) in this work. O-bromoaniline/Ag, an original polymer, has been combined. Several techniques, including FT-IR spectroscopy and UV-visible spectra, have been employed for analyzing the mixer. The nonlinear changes in voltage and current are demonstrated by the I-V characteristics.The conductivity values ranged from o-BrAnp is 5.6×10-8 S/cm , but at o-BrAn/Ag0.25 is 3.1×10-7 S/cm. Since the conductivity value of

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Macháček, Vladimír, Makky M. M. Hassanien, Vojeslav Štěrba, and Antonín Lyčka. "Formation of the Meisenheimer spiro adduct of N-(2,4,6-trinitrophenyl)alanine methylamide and its rearrangement to 2-amino-N-methyl-N-(2,4,6-trinitrophenyl)propanamide." Collection of Czechoslovak Chemical Communications 51, no. 9 (1986): 1972–85. http://dx.doi.org/10.1135/cccc19861972.

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N-(2,4,6-trinitrophenyl)alanine methylamide (I) undergoes base-catalyzed cyclization in methanol to give the spiro adduct II. In aniline-anilinium chloride buffers, the spiro adduct is protonated at the oxygen atom of 2-nitro group to give the neutral compound III. In 4-bromoaniline buffers or by action of methanolic hydrogen chloride, the compound III is opened to E and Z isomers of 2-amino-N-methyl-N-(2,4,6-trinitrophenyl)propanamide hydrochloride (IV). The rate-limiting step of cyclization of compound Z-IV to compound III consists in the isomerization Z-IV → E-IV. At higher pH values (aceta

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Et al., Tamathir. "Spectrophotometric Assay of Salbutamol Sulphate in Pharmaceutical Preparations by Coupling with Diazotized ρ-bromoaniline". Baghdad Science Journal 16, № 3 (2019): 0610. http://dx.doi.org/10.21123/bsj.2019.16.3.0610.

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In this research, salbutamol sulphate (SAS) has been determined by a simple, rapid and sensitive spectrophotometric method. Salbutamol sulphate in this method is based on the coupling of SAS with diazotized ρ- bromoaniline reagent in alkaline medium of Triton X-100 (Tx) to form an orange azo dye which is stable and water-soluble. The azo dye is exhibiting maximum absorption at 441 nm. A 10 - 800 µg of SAS is obeyed of Beer's law in a final volume of 20 ml, i.e., 0.5- 40 ppm with ε, the molar absorptivity of 48558 L.mol-1.cm-1 and Sandell's sensitivity index of 0.01188 µg.cm-2. This new method

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Kaushik, R. D., Jaspal Singh, Malvika Chawla, and Kavita Rawat. "NANOGRAM DETERMINATION OF MNII CATALYST IN THE DEGRADATION OF P-BROMOANILINE BY PERIODATE ION." Rasayan Journal of chemistry 13, no. 01 (2020): 541–47. http://dx.doi.org/10.31788/rjc.2020.1315578.

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Li, Yuzhu, Jiajun Yang, Lai Xie, et al. "4-Bromoaniline Passivation for Efficient and Stable All-Inorganic CsPbI2Br Planar Perovskite Solar Cells." ACS Applied Energy Materials 4, no. 6 (2021): 5415–23. http://dx.doi.org/10.1021/acsaem.0c03034.

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