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Journal articles on the topic 'Methoxyanillne'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Pankratov, Alexei, and Inna Uchaeva. "Protonation site for anilines in aqueous media." Journal of the Serbian Chemical Society 67, no. 2 (2002): 111–13. http://dx.doi.org/10.2298/jsc0202111p.

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By means of the PM3 method it has been shown that the protonation of 2-, 3 4-methoxyanilines, 4-methylthioaniline, 2-, 3-, 4-aminobenzoic acids, 2 3-, 4-nitroanilines in the gaseous phase proceeds via the amine nitrogen atom. The same result, attributed to the aqueous medium, was obtained for 4-methoxyaniline, 4-aminobenzoic acid and 4-nitroaniline.

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2

Manjunatha, M. S., and J. Sannappa. "Molecular Interaction Study of someorthoandparaSubstituted Anilines with 1-Octanol." E-Journal of Chemistry 7, no. 1 (2010): 308–10. http://dx.doi.org/10.1155/2010/686042.

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Interactions betweenorthoandparasubstituents of anilines such as chloroaniline, methylaniline and methoxyaniline with 1-octanol have been studied in carbon tetrachloride. The most likely association of complex between 1-octanol and substituents of anilines is 1:1 stoichiometric complex, through hydroxyl group of 1-octanol and amine group oforthoandparasubstituents of anilines. Interactions are studied on the bases of formation constant and free energy changes. Formation constant of the complex has been calculated using Nash method. The result shows that molecular interaction of 1-octanol as pr

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3

Modarresi-Alam, Ali Reza, and Ilnaz Shariati. "Silica-Supported Sulfuric Acid as Doping Agent in Synthesis of a New Composite of Poly(o-methoxyaniline) Under Solid-State Condition." Journal of Basic & Applied Sciences 17 (August 25, 2021): 115–26. http://dx.doi.org/10.29169/1927-5129.2021.17.13.

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The objective of this research is the synthesis and characterization of the novel composite of poly(o-methoxyaniline)/silica-supported sulfuric acid (POMA-SSSA). The synthesis is done by doping of poly (o-methoxyaniline) emeraldine base in the presence of silica-supported sulfuric acid (SiO2-H2SO4, SSSA) under solid-state (solvent-free) conditions. Herein, poly(o-methoxyaniline) emeraldine salt (POMA-SA) is prepared simply by mixing the base form with H2SO4 in solid-state. The doping process is verified by ultraviolet-visible, Fourier transform infrared spectroscopy and elemental analysis. It

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4

Shi, Yantao, Kaili Hou, Yanxiang Wang, et al. "Two methoxyaniline-substituted dibenzofuran derivatives as hole-transport materials for perovskite solar cells." Journal of Materials Chemistry A 4, no. 15 (2016): 5415–22. http://dx.doi.org/10.1039/c6ta00976j.

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5

Huo, Yingying, Junfeng Miao, Yaping Li, Yawei Shi, Heping Shi, and Wei Guo. "Aromatic primary monoamine-based fast-response and highly specific fluorescent probes for imaging the biological signaling molecule nitric oxide in living cells and organisms." Journal of Materials Chemistry B 5, no. 13 (2017): 2483–90. http://dx.doi.org/10.1039/c6tb03382b.

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6

Amaya, Toru, Ryosuke Sugihara, Dai Hata, and Toshikazu Hirao. "Self-doped polyaniline derived from poly(2-methoxyaniline-5-phosphonic acid) and didodecyldimethylammonium salt." RSC Advances 6, no. 27 (2016): 22447–52. http://dx.doi.org/10.1039/c5ra18468a.

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Salt formation of poly(2-methoxyaniline-5-phosphonic acid) (PMAP) with didodecyldimethylammonium bromide (DDDMABr) was performed to give the organic solvent soluble self-doped polyaniline, PMAP–DDDMA.

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7

Singpanna, Kanokwan, Panupun Limpachayaporn, Monrudee Sukma, Anan Athipornchai, and Nopparat Nuntharatanapong. "Synthesis of Fluorinated <i>N</i>- Benzylaniline Derivatives and Evaluations on Anti-Tyrosinase and Anti-Melanogenic Activities." Key Engineering Materials 914 (March 21, 2022): 87–92. http://dx.doi.org/10.4028/p-92oxa7.

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Melasma, freckles, age spots, and acne scars are common aesthetic problems resulted from melanin overproduction. This study aimed to develop new skin depigmenting compounds and characterize on melanin inhibition activities. The fluorinated N-benzylaniline derivatives were synthesized and evaluated for their in vitro anti-tyrosinase activity. Derivatives with p-fluorine monosubstition, N-(4-fluorobenzyl)-3-fluoro-4-methoxyaniline (3d), was the most potent inhibitor against mushroom tyrosinase with 75.4 ± 0.34 % inhibition at 500 µM which was as potent as the positive control, kojic acid. Furthe

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8

Odabaşogˇlu, M., and O. Büyükgüngör. "3-(Methoxyanilino)phthalides." Acta Crystallographica Section A Foundations of Crystallography 63, a1 (2007): s200—s201. http://dx.doi.org/10.1107/s0108767307095463.

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9

Sarantou, Antonia, and George Varvounis. "1-[2-(1H-Pyrrole-2-carbonyl)phenyl]-3-(4-methoxyphenyl)urea." Molbank 2023, no. 1 (2022): M1531. http://dx.doi.org/10.3390/m1531.

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For the synthesis of 1-(2-(1H-pyrrole-2-carbonyl)phenyl)-3-(4-methoxyphenyl)urea, the final product, two different methods were used, in one or two steps, from (2-aminophenyl)(1H-pyrrol-2-yl)methanone. The one-step synthesis entailed a carbonylation reaction with 1/3 equivalent of triphosgene in the presence of two equivalents of trimethylamine, followed by the addition of 4-methoxyaniline to the in situ generated aryl isocyanate. The two-step synthesis required first the preparation of phenyl(2-(1H-pyrrole-2-carbonyl)phenyl)carbamate and then a substitution reaction by 4-methoxyaniline. The f

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10

Ren, Xiao-Yan, Yu-Feng Ding, and Fang-Fang Jian. "N-(4-Chlorobenzylidene)-4-methoxyaniline." Acta Crystallographica Section E Structure Reports Online 64, no. 9 (2008): o1793. http://dx.doi.org/10.1107/s1600536808026111.

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11

Gupta, Mool C., and Suresh S. Umare. "Studies on poly(o-methoxyaniline)." Macromolecules 25, no. 1 (1992): 138–42. http://dx.doi.org/10.1021/ma00027a023.

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12

Ma, Rui, Yubang Hou, Xuejian Yong, and Yunbin Cen. "N-(4-Bromobenzylidene)-4-methoxyaniline." Acta Crystallographica Section E Structure Reports Online 63, no. 10 (2007): o4188. http://dx.doi.org/10.1107/s1600536807046855.

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13

Xin, Chun-Wei, Tao Zeng, and Jiang-Sheng Li. "2,6-Di-tert-butyl-4-[(4-methoxyphenylimino)methyl]phenol." Acta Crystallographica Section E Structure Reports Online 62, no. 4 (2006): o1560—o1561. http://dx.doi.org/10.1107/s1600536806010130.

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The title compound, C22H29NO2, was prepared from 3,5-di-tert-butyl-4-hydroxybenzaldehyde and 4-methoxyaniline by an indirect reductive amination process. Intermolecular O—H...N hydrogen bonds seem to be effective in the stabilization of the crystal structure.

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14

Lin, Yuanqiong, Xiao Zhang, Jinchuan Lu, et al. "Improvement in Dibenzofuran-Based Hole Transport Materials for Flexible Perovskite Solar Cells." Molecules 29, no. 6 (2024): 1208. http://dx.doi.org/10.3390/molecules29061208.

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The π-conjugated system and the steric configuration of hole transport materials (HTMs) could greatly affect their various properties and the corresponding perovskite solar cells’ efficiencies. Here, a molecular engineering strategy of incorporating different amounts of p-methoxyaniline-substituted dibenzofurans as π bridge into HTMs was proposed to develop oligomer HTMs, named mDBF, bDBF, and tDBF. Upon extending the π-conjugation of HTMs, their HOMO energy levels were slightly deepened, significantly increasing the thermal stability and hole mobility. The incorporation of p-methoxyaniline br

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15

Zhu, Guoxun, Yan Lin, Wenxian Zhou, Huacan Song, and Zhengquan Li. "Study of the electronic effect and quantitative spectra predictions of o-methoxyaniline-terminated monoazonaphthols: a combined experimental and DFT study." RSC Advances 13, no. 48 (2023): 33736–42. http://dx.doi.org/10.1039/d3ra05518c.

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A combined experimental and DFT study on the UV-Vis spectra of o-methoxyaniline-terminated mono azo dyes was conducted. This revealed excitation mechanisms about the UV-Vis spectra formation, and explained how chemical structures influenced transition dipole moments, and spectra features.

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16

Lu, Lihua, and Liang He. "1-(2-Methoxyanilino)anthraquinone." Acta Crystallographica Section E Structure Reports Online 66, no. 5 (2010): o1117. http://dx.doi.org/10.1107/s1600536810013310.

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17

Nesterov, Vladimir N., Elena A. Viltchinskaia, and Svitlana V. Nesterova. "[(2-Methoxyanilino)methylene]malononitrile." Acta Crystallographica Section E Structure Reports Online 59, no. 5 (2003): o625—o627. http://dx.doi.org/10.1107/s1600536803007293.

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18

Murár, Miroslav, Gabriela Addová, and Andrej Boháč. "Synthesis of 5-(ethylsulfonyl)-2-methoxyaniline: An important pharmacological fragment of VEGFR2 and other inhibitors." Beilstein Journal of Organic Chemistry 9 (January 25, 2013): 173–79. http://dx.doi.org/10.3762/bjoc.9.20.

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Background: 5-(Ethylsulfonyl)-2-methoxyaniline (5) is part of the structure in 131 compounds possessing different biological activities. In most cases, they have antitumor properties (112 compounds). Other compounds are described as cardiovascular agents, ion-channel blockers, nervous-system blockers, anti-inflammatory agents, or antidiabetic, antiosteoporotic and hypolipemic species. Compound 5 is a precursor of different protein-kinase inhibitors or enzyme modulators (EGFR, PDGFR, ckit, CDK 2 and 4, MMPs 2, 3, 9 and 13, etc.). The structure of 5 represents a fragment for several powerful inh

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19

Aldabbagh, Asmaa Baker. "Tautomerism of para-Aminobenzylidene-para-methoxyaniline." International Journal of Chemistry Education Research 4, no. 1 (2020): 33–36. http://dx.doi.org/10.20885/ijcer.vol4.iss1.art5.

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ABSTRACT: In the early seventies received wide attention when Patai [1] published his book tagged the chemistry of the azomethane group and the aforementioned group is very important in the fields of chemistry, life sciences, chemical and pharmaceutical industries and medicine. The chemistry of imines includes two main groups is Schiff bases and oximes. as well as presence of double bonds in the imines facilitated the possibility of their presence in the form of two Geometrical Isomers. Curtin and Husser [2] are among the first to discover the presence of imines in two forms, syn and anti, and

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20

Rofouei, Mohammad Kazem, Zahra Ghalami, Jafar Attar Gharamaleki, Giuseppe Bruno, and Hadi Amiri Rudbari. "4-[(4-Chlorophenyl)diazenyl]-3-methoxyaniline." Acta Crystallographica Section E Structure Reports Online 67, no. 7 (2011): o1852. http://dx.doi.org/10.1107/s160053681102472x.

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21

Nogueira, J. S., L. H. c. Mattoso, Carlos M. Lepienski, and R. M. Faria. "AC conduction of poly(o-methoxyaniline)." Synthetic Metals 69, no. 1-3 (1995): 259–60. http://dx.doi.org/10.1016/0379-6779(94)02440-a.

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22

Raposo, M., L. H. C. Mattoso, and O. N. Oliveira. "Adsorption isotherms of poly(o-methoxyaniline)." Thin Solid Films 327-329 (August 1998): 739–42. http://dx.doi.org/10.1016/s0040-6090(98)00754-8.

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23

Pandey, Shyam S., Wataru Takashima, and Keiichi Kaneto. "Photocarrier mobility in poly(2-methoxyaniline)." Journal of Applied Polymer Science 79, no. 8 (2000): 1506–12. http://dx.doi.org/10.1002/1097-4628(20010222)79:8<1506::aid-app180>3.0.co;2-b.

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24

Lunagariya, V. D., R. M. Desai, and V. H. Shah. "Studies on bioactive bis-1,3,5-triazinyl dithiocarbamates." Journal of the Serbian Chemical Society 72, no. 7 (2007): 635–41. http://dx.doi.org/10.2298/jsc0707635l.

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The compounds bis(4,6-dichloro/bis[(p-methoxyphenyl)amino]-1,3,5- -triazin-2-yl)1,2-hydrazine-1,2-dicarbodithioate/1,4-phenylenebis(carbamodithioate)/( 1,1?-biphenyl)-4,4?-diylbis(carbamodithioate)/(sulphonyldi-4,1-phenylene)- bis(carbamodithioate/1,2-ethanediylbis(carbamothioate) 4a-j were synthesized by two different methods. In the first method (A) for the preparation of 4a-e, 2,4,6- trichloro-1,3,5-triazine 1 was condensed with diammonium 1,2-hydrazine-1,2-dicarbodithioate/ 1,4-phenylenebis(carbamodithioate)/(1,1?-biphenyl)-4,4?diylbis(carbamodithioate)/( sulphonyl-di-4,1-phenylene)-bis(ca

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25

Mezhuev, Ya O., Yu V. Korshak, M. I. Shtil'man, et al. "The Competition between Processes of Oxidative Polymerisation of 2-Methoxyaniline and Oxidative Degradation of Poly-(2-Methoxyaniline)." International Polymer Science and Technology 42, no. 11 (2015): 21–24. http://dx.doi.org/10.1177/0307174x1504201104.

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26

Shu, Hong, Ning-Shu Yu, Guo-Lan Xie, and Li-Zhuang Chen. "2-[(4-Methoxyanilino)methyl]phenol." Acta Crystallographica Section E Structure Reports Online 67, no. 9 (2011): o2304. http://dx.doi.org/10.1107/s1600536811031679.

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27

Meehan, P. R., E. C. Alyea, and G. Ferguson. "2,6-Diacetylpyridinebis(p-methoxyaniline), a TerdentateNNNDonor Ligand." Acta Crystallographica Section C Crystal Structure Communications 53, no. 7 (1997): 888–90. http://dx.doi.org/10.1107/s0108270197002035.

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28

Bon, Volodimir, Svitlana Orysyk та Vasyl Pekhnyo. "trans-Dichloridobis(4-methoxyaniline-κN)palladium(II)". Acta Crystallographica Section E Structure Reports Online 65, № 6 (2009): m673. http://dx.doi.org/10.1107/s1600536809018509.

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In the title compound, [PdCl2(C7H9NO)2], the Pd atom is situated on a crystallographic centre of inversion. The coordination environment of the Pd atom shows a slightly distorted square-planar geometry. The crystal structure exhibits weak intermolecular Pd...Cl interactions, with Pd...Cl distances of 3.6912 (6) Å. A chain-like arrangement of molecules realized by intermolecular N—H...Cl hydrogen bonds is observed along [010].

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29

Armada, Walter, Guillermo Contrafatti, Leonardo Lizarraga, Estela María Andrade, and Fernando Victor Molina. "Electrochemomechanical properties of aniline/2-methoxyaniline copolymers." Journal of Electroanalytical Chemistry 625, no. 1 (2009): 75–81. http://dx.doi.org/10.1016/j.jelechem.2008.10.004.

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30

Dawn, Arnab, and Arun K. Nandi. "Slow Doping Rate in DNA−Poly(o-methoxyaniline) Hybrid: Uncoiling of Poly(o-methoxyaniline) Chain on DNA Template." Macromolecules 38, no. 24 (2005): 10067–73. http://dx.doi.org/10.1021/ma051474r.

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31

UMESH, C. PANT, CHUGH MANJU, C. K. SHARMA (MRS.), and PANT SEEMA. "Syntheses of 1,5-Benzothiazepines. Part-IX. Syntheses of 8-Substituted-4-(p-methoxyanilino)-2-methyl-1,5- benzothiazepines." Journal of Indian Chemical Society Vol. 71, Oct 1994 (1994): 637–39. https://doi.org/10.5281/zenodo.5896721.

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Department of Chemistry, University of Rajasthan, Jaipur-302 004 <em>Manuscript received 17 July 1991, revised 28 July 1993, accepted 3 August 1993</em> Syntheses of 1,5-Benzothiazepines. Part-IX. Syntheses of 8-Substituted-4-(<em>p</em>-methoxyanilino)-2-methyl-1,5-benzothiazepines.

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32

Nishimura, Takahiro, Ryota Yabe, and Yusuke Ebe. "Iridium-Catalyzed Direct C–H Allylation of Ketimines." Synthesis 53, no. 17 (2021): 3051–56. http://dx.doi.org/10.1055/a-1477-7059.

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AbstractAromatic C–H allylation of N-sulfonyl ketimines with allyl alcohol or allyl phenyl ether as an allyl source is catalyzed by a cationic iridium complex. The presence of a catalytic amount of a pyridine derivative was found to be essential for the reaction. In contrast, direct C–H allylation of ketimines derived from benzophenone derivatives and p-methoxyaniline with allyl phenyl ether proceeded in the absence of pyridine derivatives.

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33

Yousif Al-labban, Hutham mahmood, Adil ibadi Al-luhaiby, Nuha salman salih, Widad ibrahem Yahya, and Ahmed Abdul jabbar Jaloob Aljanaby. "STUDY OF AZO COMPOUNDS DERIVED FROM P-CRESOL LIGAND: SYNTHESIS, CHARACTERIZATION AND BIOLOGICAL ACTIVITY." Journal of Experimental Biology and Agricultural Sciences 9, no. 3 (2021): 401–6. http://dx.doi.org/10.18006/2021.9(3).401.406.

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Azo compounds contain two aromatic rings separated by an azo (-N=N-) link. These are versatile molecules that have garnered a lot of interest in both basic and applied research. In this work, synthesis of some Azo dyes derivatives by coupling P-cresol with diazonium salts obtained from p-chloroaniline and p-methoxyaniline. The structure of the synthesized compound has been characterized by using techniques like UV-Vis Spectroscopy, and Fourier-transform infrared spectroscopy (FTIR). In addition, the antimicrobial activity of these synthesized dyes compounds was examined by using the disc diffu

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34

Gaffer, H. E., S. Shaaban, N. A. Abed, and E. Abdel-latif. "Synthesis of some new symmetrical diselenide dyestuffs for dyeing polyester fabrics." Pigment & Resin Technology 45, no. 6 (2016): 431–38. http://dx.doi.org/10.1108/prt-06-2015-0053.

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Purpose This paper aimed to synthesise some new selenium-containing pyrazole, thiazole and thiophene dyestuffs and investigate their application in dyeing polyester fabrics. Design/methodology/approach 4,4′-Diselanediyl-bis-(2-methoxyaniline) was diazotized by acetic acid/sodium nitrite and coupled with active methylene components such as malononitrile, ethyl cyanoacetate and ethyl acetoacetate, and their corresponding hydrazono products were cyclised with hydrazine or phenyl hydrazine to obtain a series of arylazo-pyrazole dyestuffs. Furthermore, diazo-coupling reactions of the diazotized 4,4

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35

Kolyamshin, O. A., Yu N. Mitrasov, V. A. Danilov, and Yu Yu Pylchikova. "Synthesis of New 1-(4-Anilinophenyl)-1H-pyrrole-2,5-diones." Russian Journal of Organic Chemistry 60, no. 10 (2024): 2036–39. https://doi.org/10.1134/s107042802410021x.

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Abstract The reaction of N1-phenyl- and N1-(4-methoxyphenyl)benzene-1,4-diamines with maleic anhydride gave the corresponding maleic acid monoamides whose cyclization in the presence of p-toluenesulfonic acid afforded 1-[4-anilino- and 4-(4-methoxyanilino)phenyl]-1H-pyrrole-2,5-diones.

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36

K., R. DESAI, and H. DESAI P. "Synthesis of 2-(2'-Methoxyanilino )-4-(benzamldo-2'-yloxy)-6-(substituted-phenylureido)-s-triazine Derivatives and Study of their Antibacterial Activity." Journal of Indian Chemical Society Vol. 64, Dec 1987 (1987): 73–74. https://doi.org/10.5281/zenodo.6235951.

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Department of Chemistry, South Gujarat University, Surat-395 007 <em>Manuscript received 16 April 1987, accepted 3 November 1987</em> Synthesis of 2-(2'-Methoxyanilino )-4-(benzamldo-2'-yloxy)-6-(substituted-phenylureido)-s-triazine Derivatives and Study of their Antibacterial Activity  

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37

Nadkarni, N. G., and K. V. Mangaonkar. "Stability Studies of Transition Metal Chelates of 5-Bromosalicylidene-4-methoxyaniline andSalicylidene-2,3-dimethylaniline as Ligands." E-Journal of Chemistry 8, no. 4 (2011): 1911–15. http://dx.doi.org/10.1155/2011/924167.

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Binary and ternary complexes of the type M-Y and M-X-Y [M = Mn(II), Ni(II), Cu(II) and Zn(II); X = 5-bromosalicylidene-4-methoxyaniline and Y = salicylidene-2,3-dimethylaniline] have been examined pH-metrically at 27±0.5°C and at constant ionic strength, μ = 0.1 M (KCl) in 75 : 25(v/v) 1,4-dioxne-water medium. The stability constants for binary (M-Y) and ternary (M-X-Y) systems were calculated.

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38

Guo, Yan Feng, Dong Hao Sun, and Ying Wang. "Synthesis and Characterization of Poly(o-Methoxyaniline) Microsheets with pH-Sensitive Fluorescence Properties." Key Engineering Materials 703 (August 2016): 237–41. http://dx.doi.org/10.4028/www.scientific.net/kem.703.237.

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Functional poly(o-methoxyaniline) (POMA) microsheets are successfully synthesized in the presence of (NH4)3[CoMo6O24H6]·7H2O (CoMo6) under acidic conditions. It is proposed that the light-green CoMo6 precipitates formed in the initial reaction systerm serve as a polymerization reaction template for the formation of POMA microsheets. Moreover, POMA microsheets show pH-dependent fluorescence and exhibit enhanced fluorescence properties in comparision with POMA synthesized by conventional method in the absence of CoMo6.

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39

Gorokhov, Valery Yu, and Tatiana V. Makhova. "Para-(aza,thio)xanthenylated anilines in the pereaminination reaction." Butlerov Communications 60, no. 10 (2019): 32–35. http://dx.doi.org/10.37952/roi-jbc-01/19-60-10-32.

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It is known that the biochemical enzymatic reaction of the reversible transfer of an amino group from an amino-acid to a keto-acid is called a transamination reaction. However, the transamination reaction is applicable not only for biochemical enzymatic reactions, but is also often used in organic synthesis to produce aromatic azomethines. As objects of study in the transamination reaction, we selected substituted N-benzylidenanilines (imines, Schiff bases) and anilines, containing a biologically active heterocyclic fragment in the para-position of the aniline ring. We have shown the feasibili

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40

Jurášek, Adolf, Jarmila Štetinová, Jaroslav Kováč, et al. "Reactions of aromatic amines with 5-nitro-3-furoyl and 5-nitro-2-furoyl isothiocyanates." Collection of Czechoslovak Chemical Communications 54, no. 3 (1989): 699–705. http://dx.doi.org/10.1135/cccc19890699.

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5-Nitro-3-furoyl isothiocyanate reacts with 4-X-anilines (X = H, CH3, OH, N(C2H5)2, NHCOCH3, Cl, Br) to give the corresponding N-(5-nitro-3-furoyl)-N'-(4-X-phenyl)thioureas, in contrast to 4-methoxyaniline and 4-nitroaniline, which afford 5-nitro-3-furancarboxylic acid amides in a rather anomalous way. Formation of these amides is discussed and some properties of 2- and 3-substituted thioureas related to 5-nitrofuran are compared.

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41

Charles, A., R. Krishnaveni, and K. Sivara. "Synthesis, Characterization of Metal Complexes of Schiff Base derived from Pyrrole-2-carbaldehyde and 4-Methoxy Aniline and their Biological Studies." Asian Journal of Chemistry 32, no. 12 (2020): 3012–18. http://dx.doi.org/10.14233/ajchem.2020.22874.

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The metal complexes of Fe(II), Co(II) and Ni(II) have been synthesized from N-((1H-pyrrol-2- yl)methylene)-4-methoxyaniline. The synthesized Schiff base and its metal complexes were structurally characterized based on IR, NMR, UV-vis spectroscopic techniques. The presence of coordinated water molecules were confirmed by thermal studies. All the synthesized compounds were screened for their antibacterial (Escherichia coli, Bacillus substilis, Salmonella typhi, Staphylococcus epidermis) and antifungal (Aspergillus flavus) and DNA cleavage activity.

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42

Nogueira, J. S., L. H. C. Mattoso, and R. M. Faria. "Nomadic polarization in doped poly(o-methoxyaniline) films." Synthetic Metals 84, no. 1-3 (1997): 813–14. http://dx.doi.org/10.1016/s0379-6779(96)04159-8.

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Shrestha, R. P., D. Yang, and E. A. Irene. "Ellipsometry study of poly(o-methoxyaniline) thin films." Thin Solid Films 500, no. 1-2 (2006): 252–58. http://dx.doi.org/10.1016/j.tsf.2005.11.084.

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Macinnes, David, and B. Lionel Funt. "Poly-o-methoxyaniline: A new soluble conducting polymer." Synthetic Metals 25, no. 3 (1988): 235–42. http://dx.doi.org/10.1016/0379-6779(88)90248-2.

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Guo, R., J. N. Barisci, P. C. Innis, C. O. Too, G. G. Wallace, and D. Zhou. "Electrohydrodynamic polymerization of 2-methoxyaniline-5-sulfonic acid." Synthetic Metals 114, no. 3 (2000): 267–72. http://dx.doi.org/10.1016/s0379-6779(00)00242-3.

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Zhang, Lijuan, Hui Peng, Jing Sui, Christian Soeller, Paul A. Kilmartin, and Jadranka Travas-Sejdic. "Self-Assembly of Poly(o-methoxyaniline) Hollow Microspheres." Journal of Physical Chemistry C 113, no. 21 (2009): 9128–34. http://dx.doi.org/10.1021/jp900267t.

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Tsocheva, Dimitrinka, Pavlina Mokreva, and Levon Terlemezyan. "Copolymers of aniline ando-methoxyaniline. II. Thermoanalytical studies." Journal of Applied Polymer Science 104, no. 4 (2007): 2729–34. http://dx.doi.org/10.1002/app.25712.

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Mokreva, Pavlina, Dimitrinka Tsocheva, Galya Ivanova, and Levon Terlemezyan. "Copolymers of aniline ando-methoxyaniline: Synthesis and characterization." Journal of Applied Polymer Science 99, no. 1 (2005): 75–81. http://dx.doi.org/10.1002/app.22221.

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Patil, Sharmila, M. A. More, and P. P. Patil. "Poly(O-methoxyaniline) thin films: Cyclic voltammetry study." Journal of Applied Polymer Science 74, no. 13 (1999): 3009–15. http://dx.doi.org/10.1002/(sici)1097-4628(19991220)74:13<3009::aid-app1>3.0.co;2-b.

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