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1

Yunnikova, Lidiya P., Yuliya E. Likhareva, and Svetlana Yu Balandina. "N-TROPYLATION OF ARYLAMINES." IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENII KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA 62, no. 2 (2019): 79–84. http://dx.doi.org/10.6060/ivkkt.20196202.5751.

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An efficient method for introduction of biogenic tropylium cycle into aromatic amines molecules is offered. Introduction is carried out in the presence of imidazole as a strong base. Interaction between tropylium salts (tetrafluoroborate or perchlorate) and aromatic amines with either nitro- or acetyl groups (meta-nitroaniline, para-nitroaniline, 2-methyl-4-nitroaniline and para-acetylaniline) as electron-acceptor substituents in the benzol ring results in stable products resulting from substitution of the hydrogen atom in the amino group of aromatic amines, namely: 4-nitro-N-(1'-cyclohepta-2'
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2

Chaithanya, U., Sabine Foro, and B. Thimme Gowda. "N-(2-Chlorophenyl)-2-nitrobenzenesulfonamide." Acta Crystallographica Section E Structure Reports Online 68, no. 8 (2012): o2575. http://dx.doi.org/10.1107/s1600536812033107.

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In the title compound, C12H9ClN2O4S, the N—H bond in the –SO2—NH– segment issynto both theortho-nitro group in the sulfonylbenzene ring and theortho-Cl atom in the aniline ring. The molecule is twisted at the S—N bond with a torsion angle of 75.0 (2)°. The dihedral angle between the sulfonylbenzene and aniline rings is 54.97 (11)°. The amide H atom shows bifurcated hydrogen bonding, generatingS(7) andC(4) motifs. In the crystal, N—H...O(S) hydrogen bonds link the molecules into chains.
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3

Sarwade, Vasudeo, and Sharad Funde. "Biotransformation of nitro aromatic amines in artificial alkaline habitat by pseudomonas DL17." Environmental Analysis Health and Toxicology 37, no. 1 (2022): e2022001. http://dx.doi.org/10.5620/eaht.2022001.

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Nitro-aromatics are listed in carcinogenic, teratogenic, and mutagenic compounds list. p- nitro-aniline is one of them used as a precursor of various chemical compounds in many industries like dyes, drugs, paints and several others. These are mostly given out as an effluent in rivers, lakes or open passage of land which exert several hazards to living creatures and environment. Some of the organic compounds are stable in alkaline condition and persist longer in environment. Very few reports are elaborating bio-remediation in alkaline condition using different hydrocarbons. This study was plann
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4

Journal, Baghdad Science. "Synthesis and Identification of Some New Derivative of Trimethoprim and Paracetemol Drugs." Baghdad Science Journal 10, no. 1 (2013): 182–88. http://dx.doi.org/10.21123/bsj.10.1.182-188.

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In this research two series of the new derivatives of Trimethoprim and paracetamol drugs have been prepared which known as a high medicinal effectiveness. Series (A) is including the interaction of diazonium salt of trimethoprim and coupling with some substituted phenol compounds (2-amino phenol, 3-ethyl phenol, 1-naphthol, 2-nitro phenol, Salbutamol). Series (B) is including the interaction coupling alkali solution of paracetamol with diazonium salt of some substituted aniline compounds (Benzedine, 2, 3-di chloro aniline, Trimethoprim, Anilinium chloride, 2-nitro- 4-chloro aniline).Chemical s
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5

Thamer, Hind F., Saadiyah A. Dhahir, Sanaa A. Al-Sahib, and Issra A. Kattom. "Synthesis and Identification of Some New Derivative of Trimethoprim and Paracetemol Drugs." Baghdad Science Journal 10, no. 1 (2013): 182–88. http://dx.doi.org/10.21123/bsj.2013.10.1.182-188.

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In this research two series of the new derivatives of Trimethoprim and paracetamol drugs have been prepared which known as a high medicinal effectiveness. Series (A) is including the interaction of diazonium salt of trimethoprim and coupling with some substituted phenol compounds (2-amino phenol, 3-ethyl phenol, 1-naphthol, 2-nitro phenol, Salbutamol). Series (B) is including the interaction coupling alkali solution of paracetamol with diazonium salt of some substituted aniline compounds (Benzedine, 2, 3-di chloro aniline, Trimethoprim, Anilinium chloride, 2-nitro- 4-chloro aniline).Chemical s
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6

Wade, Colin B., Dillip K. Mohanty, Philip J. Squattrito, Nicholas J. Amato, and Kristin Kirschbaum. "A series ofN-(2-phenylethyl)nitroaniline derivatives as precursors for slow and sustained nitric oxide release agents." Acta Crystallographica Section C Crystal Structure Communications 69, no. 11 (2013): 1383–89. http://dx.doi.org/10.1107/s0108270113025869.

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2,4-Dinitro-N-(2-phenylethyl)aniline, C14H13N3O4, (I), crystallizes with one independent molecule in the asymmetric unit. The adjacent amine and nitro groups form an intramolecular N—H...O hydrogen bond. Theanticonformation about the ethyl C—C bond leads to the phenyl and aniline rings being essentially parallel. Molecules are linked into dimers by intermolecular N—H...O hydrogen bonds, such that each amine H atom participates in a three-centre interaction with two nitro O atoms. Though the dimers pack so that the arene rings of adjacent molecules are parallel, the rings are staggered and π–π
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7

Garden, Simon J., James L. Wardell, John N. Low, Janet M. S. Skakle, and Christopher Glidewell. "2-Iodo-4-nitro-N-(trifluoroacetyl)aniline: sheets built from iodo–nitro and nitro–nitro interactions." Acta Crystallographica Section E Structure Reports Online 62, no. 9 (2006): o3762—o3764. http://dx.doi.org/10.1107/s1600536806029072.

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8

Glidewell, Christopher, John N. Low, Janet M. S. Skakle, Solange M. S. V. Wardell та James L. Wardell. "Isomeric iodo-N-(nitrobenzyl)anilines: interplay of hard and soft hydrogen bonds, iodo...nitro interactions and aromatic π...π stacking interactions". Acta Crystallographica Section B Structural Science 60, № 4 (2004): 472–80. http://dx.doi.org/10.1107/s0108768104012017.

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Molecules of 2-iodo-N-(4-nitrobenzyl)aniline, 4-O2NC6H4CH2NHC6H4I-2′ (1) are linked into chains by C—H...O hydrogen bonds. In the isomeric compound 3-iodo-N-(4-nitrobenzyl)aniline (2) a combination of N—H...O and C—H...O hydrogen bonds and iodo...nitro and aromatic π...π stacking interactions links the molecules into a three-dimensional framework structure. The two-dimensional supramolecular structure of 4-iodo-N-(4-nitrobenzyl)aniline (6) is built from a combination of C—H...O and N—H...π(arene) hydrogen bonds and aromatic π...π stacking interactions. 2-Iodo-N-(2-nitrobenzyl)aniline (7) cryst
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9

Asiri, Abdullah M., Hassan M. Faidallah, Seik Weng Ng, and Edward R. T. Tiekink. "4-Nitro-N-[(E)-thiophen-2-ylmethylidene]aniline." Acta Crystallographica Section E Structure Reports Online 68, no. 7 (2012): o2288. http://dx.doi.org/10.1107/s1600536812028346.

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10

Piri, Farideh, Mina Behrouzi Fard Moghaddama, and Babak Karimi. "Palladium Catalyzed Reactions of 2-Nitroaniline with Vinylethers." E-Journal of Chemistry 4, no. 4 (2007): 519–22. http://dx.doi.org/10.1155/2007/962515.

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A new method for the synthesis of hemiaminal ether have been suggested. The reactions of 2-nitro aniline with vinyl ether in the presence of PdCl2(CH3CN)2produces hemiaminal ether compounds. The resulting products have been identified by spectral data.
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11

Prousek, Josef, and Viktor Hayden. "Preparation and electron transfer-induced cis-trans isomerization reactions of 1-(5-nitro-2-furyl)-, 1-(5-nitro-2-thienyl)-, and 1-(4-nitrophenyl)-2-R ethylenes." Collection of Czechoslovak Chemical Communications 54, no. 6 (1989): 1675–82. http://dx.doi.org/10.1135/cccc19891675.

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Mixtures of E- and Z-isomers of 1,2-bis(5-nitro-2-furyl)ethylene (I), 1-(5-nitro-2-furyl)-2-(4-nitrophenyl)ethylene (II), 1,2-bis(4-nitrophenyl)ethylene (III), 1-(5-methoxycarbonyl-2-furyl)-2-(4-nitrophenyl)ethylene (IV), 1-(5-methoxycarbonyl-2-furyl)-2-(5-nitro-2-furyl)ethylene (V) and 1-(5-methoxycarbonyl-2-furyl)-2-(5-nitro-2-thienyl)ethylene (VI) were prepared by the Wittig reaction. These derivatives were isomerized by electron transfer-induced reactions via the radical anion in the CT-complex using aniline as electron donor at 25 °C in the light or at 80 °C in the dark. The starting as w
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12

Mini, R., T. Joselin Beaula, P. Muthuraja та V. Bena Jothy. "Supramolecular Assembly Interceded by C-H···O Hydrogen Bonds and Nitro···π(arene) Interactions of Antibacterial 4-Methyl-(2-nitro benzylidene)aniline using DFT and its Spectral Studies". Asian Journal of Chemistry 32, № 5 (2020): 1048–58. http://dx.doi.org/10.14233/ajchem.2020.22517.

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4-Methyl-(2-nitrobenzylidene)aniline (MNBA) was grown and its structural as well as spectral analyses (FT-IR, FT-Raman, UV and NMR) using experimental and DFT computations were performed to understand its biological applications. Stability of molecule, charge delocalization, charge analysis and charge transfer interactions had been explored to examine the structural analysis. Docking studies also suggested that 4-methyl-(2-nitrobenzylidene)aniline exhibit antibacterial activity. Supramolecular assembly of 4-methyl-(2-nitrobenzylidene)aniline molecule was interceded by C-H···O hydrogen bonds an
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13

Islam, Md Zahidul, Anyarat Watthanaphanit, Sangwoo Chae, and Nagahiro Saito. "Li–air battery and ORR activity of nanocarbons produced with good synthesis rate by solution plasma process." Materials Advances 2, no. 8 (2021): 2636–41. http://dx.doi.org/10.1039/d0ma00926a.

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14

Geiger, David K., H. Cristina Geiger, and James S. Donohoe. "2-Amino-5-nitro-N-[(E)-thiophen-2-ylmethylidene]aniline." Acta Crystallographica Section E Structure Reports Online 68, no. 10 (2012): o2867. http://dx.doi.org/10.1107/s1600536812037464.

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15

Capobianco, Amedeo, Sara Meninno та Alessandra Lattanzi. "Unravelling the mechanism of the organocatalyzed aminolytic kinetic resolution of α-nitroepoxides: a theoretical study". Catalysis Science & Technology 10, № 5 (2020): 1422–30. http://dx.doi.org/10.1039/c9cy01800j.

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16

Mungmeechai, T., Suesat Jantip, and P. Suwanruji. "Study of the Relationships between the Chemical Structures of Azo Disperse Dyes and their Dyeing Properties on Polyester." Advanced Materials Research 93-94 (January 2010): 332–35. http://dx.doi.org/10.4028/www.scientific.net/amr.93-94.332.

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A series of azo disperse dyes was synthesized using 4-nitro aniline and 2-chloro-4-nitro aniline as diazo components. The coupling components were N,N-diethyl aniline, N,N-bis-β-hydroxyethyl aniline, N,N-bis-β-acetoxyethyl aniline, N,N-diethyl-m-toluidine, N,N-bis-β-hydroxyethyl-m-toluidine and N,N-bis-β-acetoxyethyl-m-toluidine. The structures of the synthesized dyes were confirmed by TLC, 1H NMR and elemental analysis. The spectroscopic properties of the dyes when dissolved in the organic solvents viz. ethyl acetate and methyl benzoate, were investigated. The absorption spectra of the dyes s
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17

Shaikh, Julekha A. "Synthesis, Spectral Characterization and X–Ray Diffraction Studies of some Pd(II) Complexes with Schiff Bases." International Letters of Chemistry, Physics and Astronomy 36 (July 2014): 272–80. http://dx.doi.org/10.18052/www.scipress.com/ilcpa.36.272.

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The synthesis, spectroscopic and X – Ray Diffraction studies of some Pd(II) complexes with bidentate Schiff bases are reported here. These Schiff bases were derived by condensing aldehydes like 2-hydroxy-1-naphthaldehyde, 5-chloro salicyladehyde with amines like 4-nitro aniline, 4-methyl aniline and 4-methoxy aniline. The complexes were characterized on the basis of elemental analysis, molar conductivity, spectral (IR, 1H and electronic) as well as thermal analysis. All the Pd (II) complexes exhibit square planar geometry with 1:2 (metal : ligand) stoichiometry. The X- ray diffraction studies
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18

Shaikh, Julekha A. "Synthesis, Spectral Characterization and X–Ray Diffraction Studies of some Pd(II) Complexes with Schiff Bases." International Letters of Chemistry, Physics and Astronomy 36 (July 15, 2014): 272–80. http://dx.doi.org/10.56431/p-6z40h5.

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The synthesis, spectroscopic and X – Ray Diffraction studies of some Pd(II) complexes with bidentate Schiff bases are reported here. These Schiff bases were derived by condensing aldehydes like 2-hydroxy-1-naphthaldehyde, 5-chloro salicyladehyde with amines like 4-nitro aniline, 4-methyl aniline and 4-methoxy aniline. The complexes were characterized on the basis of elemental analysis, molar conductivity, spectral (IR, 1H and electronic) as well as thermal analysis. All the Pd (II) complexes exhibit square planar geometry with 1:2 (metal : ligand) stoichiometry. The X- ray diffraction studies
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19

Kang, Gihaeng, Tae Ho Kim, Eui-Jae Lee, and Chang Ho Kang. "Crystal structure of 2-bromo-4,6-dinitroaniline." Acta Crystallographica Section E Crystallographic Communications 71, no. 11 (2015): o813. http://dx.doi.org/10.1107/s2056989015017946.

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In the title compound, C6H4BrN3O4, the dihedral angles between the nitro groups and the aniline ring are 2.04 (3) and 1.18 (4)°, respectively. In the crystal, N—H...O and C—H...O hydrogen bonds and weak side-on C—Br...π interactions [3.5024 (12) Å] link adjacent molecules, forming a three-dimensional network. A close O...Br contact [3.259 (2) Å] may also add additional stability.
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20

Scarborough, Timothy D., Collin J. McAcy, Joshua Beck, and Cornelis J. G. J. Uiterwaal. "Comparison of ultrafast intense-field photodynamics in aniline and nitrobenzene: stability under amino and nitro substitution." Physical Chemistry Chemical Physics 21, no. 12 (2019): 6553–58. http://dx.doi.org/10.1039/c8cp07866a.

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Intense-field stability of photoionization and fragmentation are compared for aniline (C<sub>6</sub>H<sub>5</sub>–NH<sub>2</sub>) and nitrobenzene (C<sub>6</sub>H<sub>5</sub>–NO<sub>2</sub>), with amine vs. nitro substitutions explored.
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21

Khalaj, Mehdi, Abolfazl Olyaei, Mahdieh Sadeghpour, Arash Lalegani, Janusz Lipkowski, and Alan J. Lough. "Platinum(II) complex with 4-nitro-N-(pyridin-2-ylmethylidene)aniline: synthesis, characterization, crystal structure and antioxidant activity." Acta Crystallographica Section C Structural Chemistry 76, no. 11 (2020): 1005–9. http://dx.doi.org/10.1107/s205322962001308x.

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A novel complex has been prepared using the (E)-4-nitro-N-(pyridin-2-ylmethylidene)aniline bidentate Schiff base ligand and PtCl2, namely, dichlorido[(E)-4-nitro-N-(pyridin-2-ylmethylidene)aniline-κ2 N,N′]platinum(II) acetonitrile hemisolvate, [PtCl2(C12H9N3O2)]·0.5CH3CN, 1. According to the X-ray measurements of the crystal structure, the PtII ion adopts a PtCl2N2 square-planar coordination. The coordination of the Schiff base ligand to the PtII ion occurs in a cyclic bidentate fashion, as a result of which a five-membered metallacycle is formed. Furthermore, in the structure of 1, the neutra
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22

Mahasneh, Ali S. "Synthesis of Some 2-Aminonitroethanes via Silica Gel-Catalyzed Nitro-Mannich Reaction." Zeitschrift für Naturforschung B 61, no. 9 (2006): 1162–65. http://dx.doi.org/10.1515/znb-2006-0918.

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Abstract A direct one pot, three-component nitro-Mannich reaction of a nonenolizable aldehyde, aniline or one of its ring-substituted derivatives and nitromethane was carried out on silica gel surface. The products of the reaction, 2-aminonitroethane, were obtained in high yields. IR, 1H NMR, 13C NMR spectra and elemental analysis confirmed the structures of the products.
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23

Gao, Yang, Yuanyou Mao, Biwei Zhang, Yingying Zhan, and Yanping Huo. "Regioselective nitration of anilines with Fe(NO3)3·9H2O as a promoter and a nitro source." Organic & Biomolecular Chemistry 16, no. 21 (2018): 3881–84. http://dx.doi.org/10.1039/c8ob00841h.

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A novel and efficient ortho-nitration reaction of aniline derivatives using the inexpensive and nontoxic Fe(NO<sub>3</sub>)<sub>3</sub>·9H<sub>2</sub>O as a promoter and a nitro source has been developed.
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24

Kapoor, Kamini, Vivek K. Gupta, Indresh Kumar, Nisar A. Mir, and Rajni Kant. "4-Methoxy-N-(4-nitrobenzyl)aniline." Acta Crystallographica Section E Structure Reports Online 68, no. 4 (2012): o988. http://dx.doi.org/10.1107/s160053681200846x.

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In the title compound, C14H14N2O3, the nitro group is nearly coplanar with the benzene ring to which it is bonded [dihedral angle = 1.70 (2)°], and this ring ispara-substituted by the aminomethylene group. The dihedral angle between the benzene rings is 57.8 (1)°. The crystal structure is stabilized by N—H...O and C—H...O hydrogen bonds and weak C—H...π interactions are also observed.
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25

B., THIMME GOWDA, and JAGAN MOHANA RAO P. "Kinetics of Chlorination of Aniline and Substituted -anilines by N,N-Dichlorotoluene-p-sulphonamide in Buffered Water- Methanol Medium." Journal of Indian Chemical Society Vol. 66, Mar 1989 (1989): 151–56. https://doi.org/10.5281/zenodo.5939890.

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Department of Post-Graduate Studies and Research in Chemistry, Mangalore University, Mangalagangothri-574 199 <em>Manuscript received 14 July 1988, revised 2 December 1988, accepted 14 December 1988</em> Kinetics of chlorination of aniline and substituted-aniline&amp; by <em>N</em>,<em>N</em> -dichlorotoluene-p-sulphonamide have been studied in acetate buffered 1 : 1 (v/v) water-methanol medium. The substituted-anilines studied were <em>p</em>-chloro, <em>p</em>-bromo, <em>p</em>-methyl, <em>p</em>-methoxy, <em>o</em>-chloro, <em>m</em>-chloro, <em>m</em>-nitro, 2,4- dichloro and <em>N</em>-me
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26

Rosenberg, Michal, Ernest Šturdík, Tibor Liptaj, et al. "Reactions of 1-(5-nitro-2-furyl)-2-nitroethylene with amino and hydroxy groups." Collection of Czechoslovak Chemical Communications 50, no. 2 (1985): 470–81. http://dx.doi.org/10.1135/cccc19850470.

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Reactions have been studied of l-(5-nitro-2-furyl)-2-nitroethylene with -NH, and -OH groups of low-molecular compounds (butylamine, aniline, glycine, taurine, glucosamine, tyramine, tryptamine, noradrenaline, histamine, ethanol, methanol, OH- ions) as well as biopolymers (ribonuclease, albumin DNA, RNA, Newcastle disease virus). With the low-molecular amines and alcohols it has been found that the reactions proceed as nucleophilic additions in aqueous medium, and the respective nucleophilic groups attack the more electrophilic C(1) atom of the exocyclic double bond of nitrofurylethylene. The m
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27

Pradip, P. Deohate, and N. Berad B. "The convenient microwave-assisted synthesis, characterization and structural study of substituted bis-[1,2,4]-dithiazolidines." Journal of Indian Chemical Society Vol. 91, Jul 2014 (2014): 1361–64. https://doi.org/10.5281/zenodo.5726594.

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Department of Chemistry, Shri Radhakisan Laxminarayan Toshniwal College of Science, Akola-444 001, Maharashtra, India Department of Chemistry, Rashtrasant Tukadoji Maharaj Nagpur University, Nagpur-440 033, Maharashtra, India <em>E-mail </em>: pradip222091@yahoo.co.in <em>Manuscript received online 05 December 2012, revised 21 February 2014, accepted 28 February 2014</em> A convenient synthesis of substituted bis-[1,2,4]-dithiazolidines has been developed by using the environmentfriendly technique of microwave irradiation. The microwave-assisted synthesis of several members of the titled class
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28

Smith, Graham, and Urs D. Wermuth. "4-Amino-N-(4,6-dimethylpyrimidin-2-yl)benzenesulfonamide–2-nitrobenzoic acid (1/1)." Acta Crystallographica Section E Structure Reports Online 69, no. 2 (2013): o234. http://dx.doi.org/10.1107/s1600536813000779.

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In the asymmetric unit of the title co-crystal, C12H14N4O2S·C7H5NO4, the sulfamethazine and 2-nitrobenzoic acid molecules form a heterodimer through intermolecular amide–carboxylic acid N—H...O and carboxylic acid–pyrimidine O—H...N hydrogen-bond pairs, giving a cyclic motif [graph setR22(8)]. The dihedral angle between the two aromatic ring systems in the sulfamethazine molecule is 88.96 (18)° and the nitro group of the acid is 50% rotationally disordered. Secondary aniline N—H...Osulfonehydrogen-bonding associations give a two-dimensional structure lying parallel to theabplane.
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Saphu, Watcharin, and Kittipong Chainok. "Crystal structure of 4-nitro-N-[(pyridin-2-yl)methylidene]aniline." Acta Crystallographica Section E Crystallographic Communications 71, no. 10 (2015): o760. http://dx.doi.org/10.1107/s2056989015016928.

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The title compound, C12H9N3O2, adopts anEconformation at the imine double bond. The pyridyl ring makes a dihedral angle of 47.78 (5)° with the benzene ring, indicating the molecule is twisted. In the crystal, molecules are π–π stacked into columns parallel to [100], with an interplanar separation of 3.8537 (8) Å, corresponding to the length of theaaxis. The chains are further linkedviaweak C—H...O and C—H...N hydrogen bonds, forming two-dimensional sheets parallel to (010). The sheets interact by van der Waals interactions.
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30

R, Idamalarselvi, Ragasudha G, Priscilla R, and Raja Ramachandra. "Fabrication of 5-Nitrosalicylaldehyde with Aniline as Sensitizer for Dye Sensitized Solar Cells." Indian Journal of Science and Technology 15, no. 37 (2022): 1884–91. https://doi.org/10.17485/IJST/v15i37.360.

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Abstract <strong>Objectives:</strong>&nbsp;To create a DSSC circuit, combine 5-Nitro Salicylaldehyde with Aniline (5NSA).&nbsp;<strong>Methods:</strong>&nbsp;Working and counter electrodes are made of TiO<sub>2</sub>&nbsp;and activated carbon film. Digital multimeters are used to test the conductive side of FTO glass prior to deposition. Graphite is used as the counter electrode. A functioning electrode was developed on conductive glass. FTO glass plate edges with Scotch tape (on the conductive side as determined by a multimeter). Distribute three drops of TiO<sub>2</sub>&nbsp;blade-coated ele
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31

Liu, Huihui, Gaik Khuan Chuah, and Stephan Jaenicke. "Alumina-entrapped Ag catalyzed nitro compounds coupled with alcohols using borrowing hydrogen methodology." Physical Chemistry Chemical Physics 17, no. 22 (2015): 15012–18. http://dx.doi.org/10.1039/c5cp00330j.

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Time-yield plots for the N-alkylation of nitroarenes with benzyl alcohol in the presence of Ag/Al<sub>2</sub>O<sub>3</sub>. (■) conversion; (⋄) N-phenylbenzylamine 3; (▲) N-benzylideneaniline 4; (□) azobenzene 5; and (+) aniline 6.
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32

Patel, H. S., and H. D. Desai. "Synthesis of Some New Azetidinone Derivatives Containing Aryl Sulfonyloxy Group." E-Journal of Chemistry 1, no. 4 (2004): 194–98. http://dx.doi.org/10.1155/2004/258752.

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Some novel azetidinone derivatives containing aryl sulfonyloxy group have been prepared. The 4-sulfonyloxy aniline derivative (2) has been prepared by reaction of 4-nitro phenol (sodium salt) with N-acetyl sulfanilyl chloride (ASC) followed by hydrolysis by ethanolic HCl. This compound (2) undergoes facile condensation reaction with aromatic aldehydes to yield different Schiff’s bases (3a-h). Cyclocondensation of compounds (3a-h) with chloro acetyl chloride yields different 2-azetidinone derivatives (4a-h).
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33

Pekdemir, Merve, Şamil Işık, Sümeyye Gümüş, Erbil Ağar, Sema Öztürk Yıldırım, and Ray J. Butcher. "2-Methyl-3-nitro-N-{(E)-[5-(4-nitrophenyl)furan-2-yl]methylidene}aniline." Acta Crystallographica Section E Structure Reports Online 68, no. 9 (2012): o2630. http://dx.doi.org/10.1107/s1600536812033818.

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34

Sarah Mohammed Abed and Hasan Thamer Ghanem. "Synthesis and characterization Some of heterocyclic compounds from Nitrogen derivative." International Journal of Research in Pharmaceutical Sciences 10, no. 4 (2019): 3186–96. http://dx.doi.org/10.26452/ijrps.v10i4.1621.

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This paper involves the synthesis of new oxazepine derivatives by multi-reaction steps. The first step synthesis azo derivative from 2-naphthol with 3-aminoacetophenone. The second step was the condensation reaction between ketone group of the azo compound and different primary aromatic amines (4-amino phenol, 3-nitro aniline and 4-methyl aniline) to yiled new azo Schiff base compounds (S1-S3) respectively. In the final step, Oxazepine compounds (L1-L3)and (L4-L6)were prepared from reaction imine compounds (S1-S3) with maleic and phthalic anhydride in toluene as solvent. All these derivatives
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35

Kumar, S. Anil, and B. L. Bhaskar. "Computational and Spectral Studies of Nimesulide Impurity D: 4-Nitro-2-phenoxy Aniline." Asian Journal of Chemistry 27, no. 10 (2015): 3907–12. http://dx.doi.org/10.14233/ajchem.2015.19068.

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36

Denisov, Mikhail S., Olga N. Gagarskikh, and Taisiya A. Utushkina. "Pyridylimine palladium(II) complexes: one-pot synthesis and monoamine oxidase inhibition." Вестник Пермского университета. Серия «Химия» = Bulletin of Perm University. CHEMISTRY 11, no. 1 (2021): 30–58. http://dx.doi.org/10.17072/2223-1838-2021-1-30-58.

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An efficient one-pot synthesis of the cis-pyridylimine palladium (II) complexes is reported. The compo- sition and structure were proved by NMR, IR, X-ray, and elemental analysis. The monoamine oxidase inhibition activity of synthesized complexes, including six complexes previously unknown, were inves- tigated on native mouse brains. Some of the synthesized compounds: cis-dichlorido-2,6-dimethyl-N- ((pyridin-2-yl)methylene)anilinepalladium(II), cis-dichlorido-4-nitro-N-((pyridin-2-yl)methylene)- anilinepalladium(II), and cis-dibromido-2,6-di(propan-2-yl)-N-((pyridin-2-yl)methylene)aniline- pal
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37

Figueroa, K., M. Campos-Vallette, and R. Contreras R. "A Theoretical Analysis of the Contributions to the Internal Rotation Barrier in N-Benzylideneanilines." Zeitschrift für Naturforschung A 45, no. 9-10 (1990): 1199–204. http://dx.doi.org/10.1515/zna-1990-9-1020.

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Abstract An analysis, using CNDO wave functions, has been carried out on the different contributions to the internal rotation barrier in N-benzylideneaniline (1) and p-dimethylaminobenzylidene-p-nitro-aniline (2) in several conformations. The stability of the different structures has been expressed in terms of a partition of the total energy into electronic, net charges and steric hindrance contributions. Based on the shape of the total energy surface it appears that the barrier composition may be reasonably well described without approaching the absolute minimum. Rotation of the aniline group
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38

McManus, Iain J., Helen Daly, Haresh G. Manyar, S. F. Rebecca Taylor, Jillian M. Thompson, and Christopher Hardacre. "Selective hydrogenation of halogenated arenes using porous manganese oxide (OMS-2) and platinum supported OMS-2 catalysts." Faraday Discussions 188 (2016): 451–66. http://dx.doi.org/10.1039/c5fd00227c.

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Porous manganese oxide (OMS-2) and platinum supported on OMS-2 catalysts have been shown to facilitate the hydrogenation of the nitro group in chloronitrobenzene to give chloroaniline with no dehalogenation. Complete conversion was obtained within 2 h at 25 °C and, although the rate of reaction increased with increasing temperature up to 100 °C, the selectivity to chloroaniline remained at 99.0%. Use of Pd/OMS-2 or Pt/Al<sub>2</sub>O<sub>3</sub> resulted in significant dechlorination even at 25 °C and 2 bar hydrogen pressure giving a selectivity to chloroaniline of 34.5% and 77.8%, respectivel
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39

Selvaraj, Revathy, J. Suresh, E. Vakees, and A. Arun. "Synthesis of Novel Organic Compounds from Cyanuric Chloride Containing 1-(4-(7-Chloroquinolin-4-ylamino)phenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one Chalcone for Biological Applications." Asian Journal of Chemistry 34, no. 5 (2022): 1139–44. http://dx.doi.org/10.14233/ajchem.2022.23662.

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This article reported the synthesis of triazine having quinoline chalcone moiety and its derivatives. Cyanuric chloride, 1-(4-(7-chloroquinolin-4-ylamino)phenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one (KKC), aniline, 4-nitro aniline and 1-naphthol used for the synthesis. Triazine having chlorine atom was periodically replaced by the above materials to synthesize the desired product. Synthesized triazine based organic molecules were characterized using elemental analysis, FT-IR, 1H NMR and UV-visible spectroscopic techniques. Antibacterial activity of synthesized compounds was found on Gram-positiv
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40

Wink, Christoph, Dieter Schollmeyer, and Heiner Detert. "(E)-N,N-Diethyl-2,6-diisopropyl-4-[2-(4-nitrophenyl)ethenyl]aniline." Acta Crystallographica Section E Structure Reports Online 69, no. 12 (2013): o1785—o1786. http://dx.doi.org/10.1107/s1600536813030948.

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The title compound, C24H32N2O2, was prepared by Horner olefination of 4-diethylamino-3,5-diisopropylbenzaldehyde and diethylp-nitrobenzylphosphonate. There are two independent molecules (AandB) in the asymmetric unit. Their main axes, defined by the line connecting the N atoms of the nitro and amino groups, open an angle of 79.42 (3)°. Steric hindrance around the amino group is reflected in a long aryl C—N bond [1.434 (3) Å for moleculeAand 1.440 (3) Å for moleculeB], a pyramidal geometry [angle sum = 350.0 (2)° for moleculeAand 349.6 (2)° for moleculeB], and dihedral angles between the phenyl
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41

Badour, Alec R., John A. Wisniewski, Dillip K. Mohanty, and Philip J. Squattrito. "TwoN-(2-phenylethyl)nitroaniline derivatives as precursors for slow and sustained nitric oxide release agents." Acta Crystallographica Section C Structural Chemistry 72, no. 5 (2016): 405–10. http://dx.doi.org/10.1107/s2053229616005763.

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Notwithstanding its simple structure, the chemistry of nitric oxide (NO) is complex. As a radical, NO is highly reactive. NO also has profound effects on the cardiovascular system. In order to regulate NO levels, direct therapeutic interventions include the development of numerous NO donors. Most of these donors release NO in a single high-concentration burst, which is deleterious.N-Nitrosated secondary amines release NO in a slow, sustained, and rate-tunable manner. Two new precursors to sustained NO-releasing materials have been characterized.N-[2-(3,4-Dimethoxyphenyl)ethyl]-2,4-dinitroanili
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42

Sharma, Bandana, and Munish Kumar Yadav. "COMPUTATIONAL, EXPERIMENTAL SPECTRAL ANALYSIS AND STRUCTURAL PARAMETERS OF 4, 5-DIMETHYL-2- NITRO ANILINE." RASAYAN Journal of Chemistry 17, no. 03 (2024): 752–66. http://dx.doi.org/10.31788/rjc.2024.1738865.

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The infrared and laser Raman spectra of 4, 5-dimethyl-2-nitroaniline were measured and used for experimental spectrum analysis for current work. On a computational level, Hartree-Fock and density functional theory were employed to perform geometry and vibrational spectral analysis. Here, scaled frequencies are displayed in addition to IR, Raman intensities, and decreased masses. Utilizing HF/6-31+G (d, p), HF/6-311++G (d, p), and B3LYP/6-31+G (d, p) approaches, the various thermodynamical parameters are tabulated. These include entropy, enthalpy, and specific heat. The geometrical footprints,
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43

Sachdeva, Harshita, Rekha Saroj, Sarita Khaturia, and Diksha Dwivedi. "Environ-Economic Synthesis and Characterization of Some New 1,2,4-Triazole Derivatives as Organic Fluorescent Materials and Potent Fungicidal Agents." Organic Chemistry International 2013 (May 12, 2013): 1–19. http://dx.doi.org/10.1155/2013/659107.

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A multicomponent one-pot clean cyclocondensation reaction of 4-chloro-2-nitro aniline/amino acids and aromatic aldehydes/indole-2,3-diones with thiosemicarbazide in water yielding triazole/spiro indole-triazole derivatives in high yields and shorter reaction time and displaying excellent florescent property is reported. The developed MCR may provide a valuable practical tool for the synthesis of new drugs containing the title core fragment. All the newly synthesized compounds have been characterized by IR, 1HNMR, 13CNMR, and fluorescence study and also been screened for antimicrobial activity.
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44

Curtis, NJ. "N-Alkylations and O-Alkylations of Nitro-Substituted 1,3-Diphenylureas: Preparations of Propellant Stabilizer Derivatives." Australian Journal of Chemistry 41, no. 4 (1988): 585. http://dx.doi.org/10.1071/ch9880585.

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A procedure has been developed for the N- ethylation and methylation of 1,3-diphenylureas, ArNRCONHAr′ (R = H, Me or Et), through treatment with sodium hydride and iodoalkane in dimethylformamide. The reaction was general, provided that the aniline to be alkylated was substituted with no more than one nitro group. ArRNCONR′Ar′ derivatives prepared were: R = R′ = Et (and Me); Ar = phenyl, Ar′ = 2-nitrophenyl and 4- nitrophenyl ; Ar = 2-nitrophenyl, Ar′ = 2-nitrophenyl and 4-nitrophenyl; Ar = Ar′ = 4-nitrophenyl. Two mixed derivatives were also prepared: R = Et, R′ = Me, Ar = phenyl, Ar′ = 2-nit
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45

Bhimireddi, Rajasekhar, and Ramanand Rai. "Modification in Hygroscopic Nature of Urea via Formation of Solid Solution, and its Particle Size and Second Harmonic Generation Study." Advanced Materials Research 584 (October 2012): 107–11. http://dx.doi.org/10.4028/www.scientific.net/amr.584.107.

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Solid solution of m-dinitrobenzene (DNB) and 4-bromo-2-nitro aniline (BNA) in urea (U) were prepared based on the prior study of phase diagram. The formation of solid solution was studied using the powder X-ray diffraction techniques. The powder X-ray data were also used for the study of particle size and strain in solid solution. The vapor sorption and desorption studies revealed that the hygroscopic character of urea was modified in solid solution. The study for the second harmonic generation efficiency of urea, DNB, BNA and the solid solution was done with fundamental of Nd:YAG laser (1064
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46

N â€“ A . Omar, Tagreed. "Synthesis and Preliminary Pharmacological Evaluation of Esters and Amides Derivatives of Naproxen as Potential Anti-Inflammatory Agents." Iraqi Journal of Pharmaceutical Sciences ( P-ISSN 1683 - 3597 E-ISSN 2521 - 3512) 22, no. 1 (2017): 120–27. http://dx.doi.org/10.31351/vol22iss1pp120-127.

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4-chloro and 4- nitro substituted phenol and aniline incorporated to a carboxylic group of naproxen a well-known non-steroidal anti-inflammatory drug (NSAID) to increase bulkiness were synthesized for evaluation as a potential anti-inflammatory agents with expected COX-2 selectivity. In vivo acute anti-inflammatory activity of these compounds (I-IV) was evaluated in rats using egg-white induced edema model of inflammation in a dose equivalent to (2.5 mg/Kg) of naproxen. All tested compounds produced a significant reduction in paw edema with respect to the effect of propylene glycol 50% v/v (co
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47

Wu, Shouting, Xi Liang, Fang Luo, et al. "Synthesis, Crystal Structure and Bioactivity of Phenazine-1-carboxylic Acylhydrazone Derivatives." Molecules 26, no. 17 (2021): 5320. http://dx.doi.org/10.3390/molecules26175320.

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A phenazine-1-carboxylic acid intermediate was synthesized from the reaction of aniline and 2-bromo-3-nitro-benzoic acid. It was then esterified and reacted with hydrazine hydrate to afford phenazine-1-carboxylic hydrazine. Finally, 10 new hydrazone compounds 3a–3j were obtained by the condensation reaction of phenazine-1-carboxylic acid hydrazide and the respective aldehyde-containing compound. The structures were characterized by 1H and 13C NMR spectroscopy, MS and single crystal X-ray diffraction. The antitumor activity of the target compounds in vitro (HeLa and A549) was determined by thia
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48

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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49

Bouaoud, Yasmina, Graham Smith, Hocine Merazig, and Zouaoui Setifi. "Crystal structure ofN,N-diethylbenzene-1,4-diaminium dinitrate." Acta Crystallographica Section E Structure Reports Online 70, no. 11 (2014): o1191—o1192. http://dx.doi.org/10.1107/s1600536814022946.

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In the structure of the title molecular salt, C10H18N22+·2NO3−, the dinitrate salt of 4-(N,N-diethylamino)aniline, the two ethyl groups lie almost perpendicular to the plane of the benzene ring [the ring-to-ethyl C—C—N—C torsion angles are −59.5 (2) and 67.5 (3)°]. The aminium groups of the cation form inter-species N—H...O hydrogen bonds with the nitro O-atom acceptors of both anions, giving rise to chain substructures lying alongc. The chains are linkedviafurther N—H...O hydrogen bonds, forming two-dimensional networks lying parallel to (010). These sheets are linked by C—H...O hydrogen bond
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50

Abdulkarim, Aminu Zarewa, Umar Sani, and Safiyanu Lame Adamu. "SYNTHESIS, CHARACTERIZATION, CYTOTOXICITY AND ANTIMICROBIAL STUDIES OF SCHIFF BASE DERIVED FROM 2-BENZOYLBENZOIC ACID AND 4-NITRO ANILINE AND ITS METAL(II) COMPLEXES." FUDMA JOURNAL OF SCIENCES 7, no. 6 (2024): 200–205. http://dx.doi.org/10.33003/fjs-2023-0706-2104.

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Schiff base derived from 4-nitro aniline and 2-benzoylbenzoic acid, and its Mn(II), Co(II) and Ni(II) complexes have been synthesized and characterized based on their melting/decomposition temperature, solubility, magnetic and infrared analysis. Gravimetric analysis and Job’s method of continuous variation reveal that all metal complexes are in 1:2 metal-ligand ratios. All complexes have low conductance value (13.6-20.6 ohm-1cm-1mol-1), indicating that they are non-electrolyte. However the cytotoxic analysis indicates that Co(II) complex was more toxic with the LC50 value of 181.72 ug/ml than
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