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Journal articles on the topic 'Dimethyl-aniline'

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1

Sharma, V. K., Prem Paul Singh, Sanjeev Maken, and B. Singh. "Topological investigations of aniline and substituted anilines in binary solutions containing methylene bromide." Canadian Journal of Chemistry 71, no. 12 (1993): 2183–88. http://dx.doi.org/10.1139/v93-273.

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Molar excess volumes and molar excess enthalpies for various (i + j) binary methylene bromide (i) + aniline or N-methyl aniline and + N,N-dimethyl aniline (j) mixtures have been determined as a function of composition at 308.15 K. The data have been analysed in terms of the graph-theoretical approach and Sanchez and Lacombe theory. The graph-theoretical analyses of VE data suggest that aniline, N-methyl aniline, and N,N-dimethyl aniline exist as equilibrium mixtures of monomer and dimer and that these mixtures contain 1:1 molecular complexes. The IR studies lend further credence to the nature
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2

Journal, Baghdad Science. "spectroscopic stury of lewis bases coordinating to vanady." Baghdad Science Journal 3, no. 2 (2006): 344–47. http://dx.doi.org/10.21123/bsj.3.2.344-347.

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3

S. Srinivasan, S. Srinivasan, S. Chidambar Avinayagam, and B. S. Santhi B. S. Santhi. "Ultrasonic Studies on Molecular Interaction of Aniline, N-Methyl Aniline, N, N-Dimethyl Aniline and Cinnamaldehydein N-Hexane Solution at 303K." Global Journal For Research Analysis 3, no. 8 (2012): 15–17. http://dx.doi.org/10.15373/22778160/august2014/5.

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4

Chemical, Engineering: An International Journal (CEIJ). "Conversion of Dimethyl-Nitrobenzene to Dimethyl Aniline, Effect of Some Process Condition." Chemical Engineering: An International Journal (CEIJ) 1, no. 1 (2024): 13–23. https://doi.org/10.5281/zenodo.14043399.

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The catalytic transfer hydrogenation of dimethyl-nitrobenzene (DN) to Dimethyl-aniline (DA) was studiedin the temperature range 343–403 Ko, pressure range of 4–10 bar H2 and ethanol as solvent using Pd/Cas catalyst above agitation speed 800 rpm. The substrate feed concentration was varied in the range from0.124 to 0.745 kmol/m3 while catalyst loading was in the range 4–12% (w/w) of dimethyl-nitrobenzene.Dimethyl-aniline was the only reaction product, generated through the hydrogenation of the Nitro group ofdimethyl-nitrobenzene. The effects of hydrogen partial pressure,
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5

Kurup, Shilpa S., and Rakesh Kumar Jat. "Synthesis, Characterisation, Invitro anticancer activity of Diazo Derivatives of 1,3,4-oxadiazole." Journal of Drug Delivery and Therapeutics 13, no. 10 (2023): 94–99. http://dx.doi.org/10.22270/jddt.v13i10.5984.

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This study delves into the comprehensive evaluation of newly synthesized Diazo Derivatives of 1,3,4-oxadiazole compounds, including Aniline, Ortho nitro aniline, Meta nitro aniline, Ortho anisidine, Meta anisidine, 3-chloro aniline, 2,6-dimethyl aniline, 2,5- dicloro aniline, and 3,5- dichloro aniline, aiming to unravel their potential as antioxidants and anticancer agents. The assessment of antioxidant potential involved the utilization of the DPPH (2,2-diphenyl-1-picrylhydrazyl) assay. The cytotoxic activity of these compounds was assessed against MCF-7 breast cancer cells using the MTT assa
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6

Mansoor, Kazemimoghadam. "CONVERSION OF DIMETHYL-NITROBENZENE TO DIMETHY L ANILINE, EFFECT OF SOME PROCESS CONDITION." Chemical Engineering: An International Journal (CEIJ) 01, dec (2017): 01–11. https://doi.org/10.5281/zenodo.1319960.

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The catalytic transfer hydrogenation of dimethyl-nitrobenzene (DN) to Dimethyl-aniline (DA) was studied in the temperature range 343–403 K o , pressure range of 4–10 bar H2 and ethanol as solvent using Pd/C as catalyst above agitation speed 800 rpm. The substrate feed concentration was varied in the range from 0.124 to 0.745 kmol/m3 while catalyst loading was in the range 4–12% (w/w) of dimethyl-nitrobenzene. Dimethyl-aniline was the only reaction product, generated through the hydrogenation of the Nitro group of dimethyl-nitrobenzene. The effects of hydrogen partial pressure
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7

Ge, Hui Lin, Shu Shen Liu, Peng Zhou, Yao Wan, Yan Ling Zhang, and Ling Yun Mo. "Assessment and Prediction of Mixture Effects of Four Different Types of Organic Pollutants on Photobacterium." Applied Mechanics and Materials 448-453 (October 2013): 277–80. http://dx.doi.org/10.4028/www.scientific.net/amm.448-453.277.

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The low-dose and combined effects of aniline, 2-methyl-aniline, 3-methyl-aniline, 4-methyl-aniline, nitrobenzene, 4-methyl-nitrobenzene, phenol, 2-methyl-phenol, 3-methyl-phenol, 4-methyl-phenol, dimethyl phthalate, and diethyl phthalate on photobacterium Vibrio qinghaiensis were predicted and evaluated by using concentration addition and independent action models. The mixture effects can be predicted by concentration addition and independent action models. Combined effect of environmental pollutants should be considered in risk assessment practice.
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8

Hasan, Nehad Tariq, and Azhar Kamil Rashid. "Synthesis, Characterization of New Polyamides Bearing Triarylamine for Lightemitting Diodes." Ibn AL- Haitham Journal For Pure and Applied Science 32, no. 1 (2019): 81. http://dx.doi.org/10.30526/32.1.1991.

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In this work, new di-acid monomers 4, 4’-di-carboxillic-4”-bromo-2”, 6”-dimethyl triphenylamine (Ma), 4, 4’- di-carboxylic -4”-chloro-2”, 6”-dimethyl triphenylamine (Mb) and 4, 4’- di-carboxylic -2”,4”-dichloro-6”-methyl triphenylamine (Mc) were synthesized by reaction of p-cyanobenzofluride with three different aromatic amines (4-bromo,2,6-dimethyl aniline, 4-chloro,2,6-dimethyl aniline and 2,4 dichloro, 6- methyl aniline ) via aromatic nucleophilc substitution method to form three di cyano intermediates 4, 4’-Dicyano-4”-bromo-2”, 6”-dimethyl triphenylamine (Da), 4, 4’-dicyano-4”-chloro-2”, 6
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9

Wang, Zhuan, Song Xu, Wan Peng Hu та Ya Jie Xie. "Green Process for the Production of 4-(β-sulfotaethylsulfone)-N-Ethyl-Aniline". Advanced Materials Research 718-720 (липень 2013): 141–45. http://dx.doi.org/10.4028/www.scientific.net/amr.718-720.141.

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4-(β-sulfatoethylsulfone)-N-ethyl-aniline was synthesized from 4-(β-hydroxyethyl-sulfonyl)-N-ethyl-aniline in the presence of sulfuric acid using toluene andN,N-dimethyl-dodecylamine as mix solvent. The product was efficiently precipitated from the reaction mixture by addition of a sufficient amount of acetone. Several influencing factors on the esterification were investigated, and the results show that, the optimal conditions were: the molar ratio of 4-(β-hydroxyethylsulfonyl)-N-ethyl-aniline,N,N-dimethyl-dodecylamine and sulfuric acid was 1:1:1.5, the dosage of toluene 800 mL per molar 4-(β
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10

Sun, Hong Juan, Ying Liu, Tong Jiang Peng, Hai Feng Liu, and Jin Mei Sun. "Synthesis and Electrical Conductivity Measurement of Polyaniline / Vermiculite Nanocomposites." Advanced Materials Research 96 (January 2010): 221–26. http://dx.doi.org/10.4028/www.scientific.net/amr.96.221.

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A series of polyaniline/vermiculite nanocomposites was synthesized. The interlayer space of vermiculite was initially increased by the insertion of dioctadecyl dimethyl ammonium bromide, and then the aniline monomers were inserted into the interlayer space of vermiculite replacing dioctadecyl dimethyl ammonium cations. The polyaniline/vermiculite nanocomposites materials were prepared via in situ polymerization of the aniline monomers in the interlayer space of vermiculite. The as-synthesized polyaniline/vermiculite nanocomposite materials were characterized by X-ray diffraction analysis, infr
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11

Fang, Xiaolong, Chunyan Zhang, Jin Chen, Hongping Zhu, and Youzhu Yuan. "Synthesis and catalytic performance of ruthenium complexes ligated with rigid o-(diphenylphosphino)aniline for chemoselective hydrogenation of dimethyl oxalate." RSC Advances 6, no. 51 (2016): 45512–18. http://dx.doi.org/10.1039/c6ra00320f.

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12

Tariq, Muhammad Ilyas, Shahbaz Ahmad, M. Nawaz Tahir, Muhammad Sarfaraz, and Ishtiaq Hussain. "2,3-Dimethyl-N-[(E)-4-nitrobenzylidene]aniline." Acta Crystallographica Section E Structure Reports Online 66, no. 7 (2010): o1561. http://dx.doi.org/10.1107/s160053681001932x.

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13

Tahir, M. Nawaz, Muhammad Ilyas Tariq, Shahbaz Ahmad, Muhammad Sarfraz, and Abdul Qayyum Ather. "(E)-2,3-Dimethyl-N-(2-nitrobenzylidene)aniline." Acta Crystallographica Section E Structure Reports Online 66, no. 7 (2010): o1817. http://dx.doi.org/10.1107/s1600536810024165.

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14

Hussain, Abid, M. Nawaz Tahir, Muhammad Ilyas Tariq, Shahbaz Ahmad, and Abdullah M. Asiri. "2,3-Dimethyl-N-[(E)-2,4,5-trimethoxybenzylidene]aniline." Acta Crystallographica Section E Structure Reports Online 66, no. 8 (2010): o1953. http://dx.doi.org/10.1107/s1600536810025894.

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15

Zheng, Lei, Xiu-juan Yin, Cong-ling Yang, Ying Li, and Shu-fan Yin. "N,N-Dimethyl-4-[(E)-phenyliminomethyl]aniline." Acta Crystallographica Section E Structure Reports Online 65, no. 3 (2009): o506. http://dx.doi.org/10.1107/s1600536809003791.

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16

Delatouche, Régis, Aurélien Lesage, Floraine Collette, Valérie Héroguez, and Philippe Bertrand. "Investigations into Competitive Cycloaddition/Cyclization or Elimination from 1,1-Dimethyl-propargylcarbamates of Anilines." Australian Journal of Chemistry 64, no. 2 (2011): 166. http://dx.doi.org/10.1071/ch10344.

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The copper-catalyzed reaction of 1,1-dimethyl-O-propargyl aniline carbamates was studied and revealed the unexpected formation of oxazolidin-2-ones and alkylamines. An in-depth study of the reaction conditions showed that the formation of these products was highly dependent on the solvent, copper catalyst and aniline substituents. The reaction can be oriented towards oxazolidinones in pyridine and alkylamines in ethanol, whereas cycloaddition can be achieved in dry tetrahydrofuran.
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17

Hamadi, Adel S. "Selective Additives for Improvement of Gasoline Octane Number." Tikrit Journal of Engineering Sciences 17, no. 2 (2010): 22–35. http://dx.doi.org/10.25130/tjes.17.2.03.

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High octane blend base gasoline stocks are reformulated from 30% LSRN, 45% Reformate and 25% Powerformate on volume basis. ASTM standard and IROX 2000 analysis are performed to test blend stocks sample. Different additive types are used to improve octane number. These additives are tetraethyl lead, methylcyclopentadienyl manganese tricarbonyl; methyl alcohol, ethyl alcohol, iso-propanol, n-butanol, sec-butanol, tertiary butyl alcohol, tert-amyl alcohol, active amyl alcohol, iso-pentyl alcohol, isobutyl carbinol, benzol ,telone, xylene, amino benzene, N-N-dimethyl aniline, dimethyl ketone, and
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18

Akhtar, Yasmin. "ULTRASONIC INTERACTION STUDIES OF TERNARY MIXTURE SOLUTIONS AT 303 AND 313 TEMPERATURE." International Journal of Engineering Technologies and Management Research 7, no. 9 (2020): 10–13. http://dx.doi.org/10.29121/ijetmr.v7.i9.2020.750.

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Densities and ultrasonic velocities of Aniline in cyclohexane + Dimethyl ketone and Aniline in cyclohexane + ethyl methyl ketone of these ternary mixtures of different compositions have been determined experimentally at 303 and 313 K. The results obtained from density and ultrasonic velocity measurement have been used to calculate the acoustical parameters such as, adiabatic compressibility (Ks), free Length (Lf ) , and acoustic impedance (Z). The results are discussed in terms of the intermolecular hydrogen bonding and molecular association in these ternary systems.
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19

Su, Bi-Yun, Jia-Xiang Wang, Xiang Liu, and Qian-Ding Li. "3,4-Dimethyl-N-[1-(1H-pyrrol-2-yl)ethylidene]aniline and the 1-(1-thiophen-2-yl) analogue." Acta Crystallographica Section C Crystal Structure Communications 69, no. 9 (2013): 1073–76. http://dx.doi.org/10.1107/s0108270113022142.

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The title compounds, 3,4-dimethyl-N-[1-(1H-pyrrol-2-yl)ethylidene]aniline, C14H16N2, (I), and its analogue 3,4-dimethyl-N-[1-(1-thiophen-2-yl)ethylidene]aniline, C14H15NS, (II), both have basic heterocyclic imino structures showing a planar backbone with similar features, but differing in the heteroatoms of the five-membered heterocyclic rings,i.e.N in (I) and S in (II). The dihedral angles formed by the five-membered and benzene rings are 81.78 (8) and 75.89 (7)° for (I) and (II), respectively. In (I), centrosymmetric iminopyrrole dimers are assembled by means of two inverted N—H...N hydrogen
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20

Grego, Sandra, Fabio Aricò, and Pietro Tundo. "Phosgene-free carbamoylation of aniline via dimethyl carbonate." Pure and Applied Chemistry 84, no. 3 (2011): 695–705. http://dx.doi.org/10.1351/pac-con-11-07-17.

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The synthesis of N-phenylcarbamate from aniline and dimethyl carbonate (DMC) in the presence of homogeneous, supported heterogeneous, and heterogeneous catalysts was investigated in batch conditions. First, a selection of homogeneous catalysts was studied and their reactivity in the same reaction conditions was compared to zinc acetate, a catalyst extensively used for this reaction. Then the best homogeneous catalysts were supported on silica or alumina, and the resulting heterogeneous supported catalysts were tested for the carbamoylation of aniline. Finally, several heterogeneous catalysts w
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21

Thekku Veedu, Sreevidya, Mirko Scholz, Reza Kia, Carsten Paulmann, and Simone Techert. "N,N-Dimethyl-4-(pyren-1-yl)aniline." Acta Crystallographica Section E Structure Reports Online 70, no. 1 (2013): o16. http://dx.doi.org/10.1107/s1600536813032698.

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22

Snauwaert, Ph, R. Lazzaroni, J. Riga, and J. J. Verbist. "Electronic structure and properties of dimethyl-aniline polymers." Synthetic Metals 21, no. 1-3 (1987): 181–87. http://dx.doi.org/10.1016/0379-6779(87)90084-1.

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23

Yang, Xiu-Ying, Yu-Feng Li, Jian Zheng, and Fang-Fang Jian. "N-3,5-Dimethyl-[1-(4-nitrophenyl)ethylidene]aniline." Acta Crystallographica Section E Structure Reports Online 63, no. 4 (2007): o1611—o1612. http://dx.doi.org/10.1107/s1600536807001365.

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24

Leesakul, Nararak, Suthirat Yoopensuk, Chaveng Pakawatchai, Saowanit Saithong, and Kanidtha Hansongnern. "N,N-Dimethyl-4-[(2-pyridyl)diazenyl]aniline." Acta Crystallographica Section E Structure Reports Online 66, no. 8 (2010): o1923. http://dx.doi.org/10.1107/s1600536810025754.

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25

Gajecki, Leah, Brendan Twamley, and David J. Berg. "Synthesis and crystal structures of tetrameric [2-(4,4-dimethyl-2-oxazolin-2-yl)anilido]sodium and tris[2-(4,4-dimethyl-2-oxazolin-2-yl)anilido]ytterbium(III)." Acta Crystallographica Section E Crystallographic Communications 76, no. 5 (2020): 703–9. http://dx.doi.org/10.1107/s2056989020005034.

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Reaction of 2-(4,4-dimethyl-2-oxazolin-2-yl)aniline (H2-L1) with one equivalent of Na[N(SiMe3)2] in toluene afforded pale-yellow crystals of tetrameric poly[bis[μ3-2-(4,4-dimethyl-2-oxazolin-2-yl)anilinido][μ2-2-(4,4-dimethyl-2-oxazolin-2-yl)aniline]tetrasodium(I)], [Na4(C11H13N2O)4] n or [Na4(H-L1)4] n (2), in excellent yield. Subsequent reaction of [Na4(H-L1)4] n (2) with 1.33 equivalents of anhydrous YbCl3 in a 50:50 mixture of toluene–THF afforded yellow crystals of tris[2-(4,4-dimethyl-2-oxazolin-2-yl)anilinido]ytterbium(III), [Yb(C11H13N2O)3] or Yb(H-L1)3 (3) in moderate yield. Direct re
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26

Dotsenko, Victor V., Alena A. Russkih, Nikolai A. Aksenov, and Inna V. Aksenova. "Synthesis of New 2-Oxo-1,2-Dihydropyridine-3-Carboxylic Acid Derivatives." Proceedings 41, no. 1 (2019): 24. http://dx.doi.org/10.3390/ecsoc-23-06523.

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2,2-Dimethyl-5-((phenylamino)methylene)-1,3-dioxane-4,6-dione, prepared by the reaction of Meldrum’s acid with triethyl orthoformate and aniline, reacts with active methylene nitriles to afford 2-oxo-1,2-dihydropyridine-3-carboxylic acid derivatives, which are useful as drug precursors or perspective ligands.
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27

Stephenson, W. Kirk, and Richard Fuchs. "Enthalpies of interaction of nitrogen base solutes with organic solvents." Canadian Journal of Chemistry 63, no. 9 (1985): 2540–44. http://dx.doi.org/10.1139/v85-420.

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Heats of solution of triethylamine, aniline, pyridine, and model compounds (3-ethylpentane, benzene) in 17 organic solvents (n-heptane, cyclohexane, carbon tetrachloride, 1,2-dichloroethane, α,α,α-trifluorotoluene, triethylamine, butyl ether, ethyl acetate, dimethylformamide, dimethyl sulfoxide, benzene, toluene, mesitylene, t-butyl alcohol, 1-octanol, methanol, 2,2,2-trifluoroethanol) have been combined with solute heats of vaporization to give enthalpies of transfer from vapor to solvent (ΔH(v → s)). Differences between solute and model values (ΔΔH(v → s) = ΔH(v → s) (solute) – ΔH(v → s) (mo
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28

ZHANG, Q., B. KANG, H. XU, and H. LIN. "Indirect Electrochemical Oxidation of 4-Amino-dimethyl-aniline Hydrochloride1." Chemical Research in Chinese Universities 22, no. 3 (2006): 360–63. http://dx.doi.org/10.1016/s1005-9040(06)60116-5.

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29

Crampton, Michael R., Lynsey C. Rabbitt, and François Terrier. "Electrophilic aromatic substitution in substituted anilines; kinetics of the reaction with 4,6-dinitrobenzofuroxan." Canadian Journal of Chemistry 77, no. 5-6 (1999): 639–46. http://dx.doi.org/10.1139/v99-033.

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Kinetic results are reported for reaction of aniline and six of its N- and ring-substituted derivatives with 4,6-dinitrobenzofuroxan (DNBF) in water - dimethyl sulfoxide mixtures. In acidic solution σ-adducts, the result of electrophilic substitution in the anilines, are formed with bonding between a ring-carbon atom of the anilines and the 7-position of DNBF. Reaction normally occurs at the 4-position of the aniline unless this carries a substituent, when reaction occurs at the 2-position. A value of 2.0 for kH/kD, the kinetic isotope effect, indicates that in the reaction with aniline bond f
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30

Deepa, H. R., J. Thipperudrappa, and H. M. Suresh Kumar. "A study on fluorescence quenching of a laser dye by aromatic amines in alcohols." Canadian Journal of Physics 93, no. 4 (2015): 469–74. http://dx.doi.org/10.1139/cjp-2014-0190.

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The fluorescence quenching of 1,2,3,8-tetrahydro-1,2,3,3,8-pentamethyl-5-(trifluoromethyl)-7H-pyrrolo[3,2-g]quinolin-7-one (LD-473) by aromatic amines, namely, aniline, dimethyl aniline, and diethyl aniline, in methanol, ethanol, propanol, and butanol has been studied at room temperature using steady-state and time-resolved methods. A positive deviation from linearity has been observed in Stern–Volmer (S–V) plots. Various quenching rate parameters have been determined using the extended S–V equation and are found to be dependent on the dielectric constant of alcohols. The quenching ability of
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31

Ge, Hui Lin, Shu Shen Liu, Bing Xia Su, Jian Guo Li, Gui Hao Yin, and Ling Yun Mo. "Mixture Effects of Five Different Types of Organic Pollutants on Photobacterium Q67." Advanced Materials Research 726-731 (August 2013): 768–71. http://dx.doi.org/10.4028/www.scientific.net/amr.726-731.768.

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The low-dose and combined effects of aniline, nitrobenzene, phenol, dimethyl phthalate, and dichlorvos on photobacteriumVibrio qinghaiensiswere predicted and evaluated by using concentration addition and independent action models. The mixtures effects were greater than single components effects, which implied that combined effect of environmental pollutants should be considered in risk assessment practice.
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32

Nguyen, Hai Truong, and Phuong Hoang Tran. "Synthesis of pyrroles catalyzed by MIL-53(Al) via Paal-Knorr reaction under mild condition." Science and Technology Development Journal - Natural Sciences 1, T5 (2018): 116–25. http://dx.doi.org/10.32508/stdjns.v1it5.543.

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Metal-organic framework MIL-53(Al) was synthesized by a solvothermal method using aluminium nitrate as the aluminium source and 1,4- benzenedicarboxylic acid (H2BDC) as the organic ligand. The structure of MIL-53(Al) was characterized by X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FT-IR). The catalytic activity and recyclability of MIL-53(Al) catalyst were evaluated based on the Paal-Knorr reaction between aniline and acetonylacetone. The reaction conditions were optimized and the results showed that the MIL-53(Al) catalyst exhibited good catalytic activity and recycla
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33

Pant, B., D. Prakash та P. Sagar. "Microwave Assisted Solvent Free Catalytic Amino-Carbonylation of Aryl Bromide by Using μ-Dichloro-bis(benzylidene aniline)palladium(II) Complex as Catalyst". Asian Journal of Chemistry 35, № 2 (2023): 361–65. http://dx.doi.org/10.14233/ajchem.2023.26882.

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Solvent-free aminocarbonylation (Heck carbonylation) of aryl halide, catalyzed by μ-dichloro-bis(benzylidene aniline)palladium(II) complex yields dimethyl benzamide and their substitutes, has several useful industrial applications. In present work, dimethylformamide (DMF) serves as an effective in situ supplier of dimethyl amine and carbon monoxide. Bromobenzene along with more electron-rich aryl bromide generally undergo these reactions very smoothly, but the yield of respective products is less. To increase the yields of aryl amide, it is needed to be add amines from the external sources to
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34

Tahir, M. Nawaz, Muhammad Ilyas Tariq, Shahbaz Ahmad, Muhammad Sarfraz, and Riaz H. Tariq. "2,3-Dimethyl-N-[(E)-(1H-pyrrol-2-yl)methylidene]aniline." Acta Crystallographica Section E Structure Reports Online 66, no. 9 (2010): o2295. http://dx.doi.org/10.1107/s1600536810031867.

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35

Su, Bi-Yun, Wen-Long Qin, and Jia-Xiang Wang. "2,5-Dimethyl-N-[1-(1H-pyrrol-2-yl)ethylidene]aniline." Acta Crystallographica Section E Structure Reports Online 68, no. 11 (2012): o3088. http://dx.doi.org/10.1107/s1600536812040858.

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36

Athawale, Anjali A., Bhavana A. Deore, and Milind V. Kulkarni. "Spectroscopic and electrochemical properties of poly(2,5 dimethyl aniline) films." Materials Chemistry and Physics 60, no. 3 (1999): 262–67. http://dx.doi.org/10.1016/s0254-0584(99)00091-7.

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37

Stewart, Katherine M. E., Wei Ting Chen, Raafat R. Mansour, and Alexander Penlidis. "Doped poly (2,5-dimethyl aniline) for the detection of ethanol." Journal of Applied Polymer Science 132, no. 28 (2015): n/a. http://dx.doi.org/10.1002/app.42259.

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38

Bhattacharya, Suman, Binay K. Dutta, Manoranjan Shyamal, and Ranjan K. Basu. "Absorption of sulfur dioxide in aqueous dispersions of dimethyl aniline." Canadian Journal of Chemical Engineering 74, no. 3 (1996): 339–46. http://dx.doi.org/10.1002/cjce.5450740304.

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39

Herberhold, Max, Volker Tröbs, Hong Zhou, and Bernd Wrackmeyer. "Reactivity and NMR Spectroscopic Properties of Tri(tert-butyl)plumbyl-amine." Zeitschrift für Naturforschung B 52, no. 10 (1997): 1181–84. http://dx.doi.org/10.1515/znb-1997-1005.

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Tri(tert-butyl)plumbyl-amine 1 was prepared and studied by one- (1D) and two-dimensional (2D) 1H, 13C, 15N and 207Pb NMR which allowed determination of the coupling signs 1J(207Pb,13C) (> 0), 2J(207Pb,13C) (> 0), 1J(207Pb,15N) (> 0; reduced coupling constant 1K(207Pb,I5N) < 0) and 2J(207Pb-N-1H) (< 0). Transamination of 1 with aniline and pyrazole afforded the corresponding aniline (2) and pyrazole derivatives (3), respectively. N-Lithiation of 1, followed by treatment with Me3SiCl gave the tri(tert-butyl)plumbyl-trimethylsilyl-amine 5. The multinuclear magnetic resonance data o
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40

Mikhailovskii, A. G., and D. A. Peretyagin. "Synthesis and properties for enaminoketoamides of 2,2-dimethyl-2,3-dihydrobenzo[<i>f</i>]isoquinoline series." Журнал органической химии 59, no. 7 (2023): 946–51. http://dx.doi.org/10.31857/s051474922307008x.

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The reaction of 1-R-6,6-dimethyl-5,6-dihydrobenzo[ f ]pyrrolo[2,1- a ]isoquinoline-8,9-diones (R = H, morpholinocarbonyl) with ammonia, morpholine, aniline and 1-naphtylamine proceeds with opening of dioxopyrroline cycle and forming enaminoketoamides. The conditions of reaction depends on the nature of nucleophile: ammonia and morpholine readily react at 20°C, the reaction with aromatic amines requires reflux in glacial acetic acid.
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41

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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42

Maleki, Ali, and Kobra Valadi. "Synthesis of Small Organic Molecule Based on Malononitrile Group toward Green Energy Performance in Organic Photovoltaic Solar Cells." Proceedings 9, no. 1 (2018): 16. http://dx.doi.org/10.3390/ecsoc-22-05653.

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In this study, a small organic compound containing cyano and N,N-dimethyl aniline as acceptor and donor groups, respectively linked through the conjugate system, were synthesized. Then, its structure was confirmed by FT-IR spectroscopy. Next, in order to investigate the photovoltaic properties of these organic molecules, it was tested in the fabrication of organic photovoltaic solar cells (OPVSCs). The organic solar cell with FTO/TiO2/dye molecules/electrolyte/Pt electrode configuration was constructed.
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43

Esakkidurai, Thirugnanasamy, and Kasi Pitchumani. "Zeolite-promoted selective mono-N-methylation of aniline with dimethyl carbonate." Journal of Molecular Catalysis A: Chemical 218, no. 2 (2004): 196–201. http://dx.doi.org/10.1016/j.molcata.2004.03.047.

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44

Boonrattanakij, Nonglak, Ming-Chun Lu, and Jin Anotai. "Kinetics and mechanism of 2,6-dimethyl-aniline degradation by hydroxyl radicals." Journal of Hazardous Materials 172, no. 2-3 (2009): 952–57. http://dx.doi.org/10.1016/j.jhazmat.2009.07.079.

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45

Fu, Zi-hua, and Yoshio Ono. "Selective N-monomethylation of aniline with dimethyl carbonate over Y-zeolites." Catalysis Letters 18, no. 1-2 (1993): 59–63. http://dx.doi.org/10.1007/bf00769498.

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46

Crampton, Michael R., та Ian A. Robotham. "Kinetic studies of bold σ -adduct formation and nucleophilic substitution in the reactions of ethyl 2,4,6-trinitrophenyl ether, some phenyl 2,4,6-trinitrophenyl ethers, and phenyl 2,4-dinitronaphthyl ether with aniline in dimethyl sulfoxide". Canadian Journal of Chemistry 76, № 6 (1998): 627–34. http://dx.doi.org/10.1139/v97-225.

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The reaction of ethyl 2,4,6-trinitrophenyl ether with aniline in dimethyl sulfoxide containing Dabco occurs in two stages. The first gives 5, the σ -adduct intermediate on the substitution pathway, which has been identified spectroscopically. The second yields 2,4,6-trinitrodiphenylamine, the substitution product. Kinetic studies show that proton transfer is rate limiting both in the formation of the intermediate and in its subsequent acid-catalysed decomposition. Phenoxide is a considerably better leaving group than ethoxide and the substitution reactions of phenyl 2,4,6-trinitrophenyl ethers
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47

Keerthi Kumar, Chinnagiri T., Jathi Keshavayya, Tantry N. Rajesh, Sanehalli K. Peethambar, and Angadi R. Shoukat Ali. "Synthesis, Characterization, and Biological Activity of 5-Phenyl-1,3,4-thiadiazole-2-amine Incorporated Azo Dye Derivatives." Organic Chemistry International 2013 (August 18, 2013): 1–7. http://dx.doi.org/10.1155/2013/370626.

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5-Phenyl-1,3,4-thiadiazole-2-amine has been synthesized by single step reaction. A series of heterocyclic azodyes were synthesized by diazotisation of 5-phenyl-1,3,4-thiadiazole-2-amine by nitrosyl sulphuric acid followed by coupling with different coupling compounds such as 8-hydroxyquinoline, 2,6-diaminopyridine, 2-naphthol, N,N-dimethyl aniline, resorcinol, and 4,6-dihydroxypyrimidine. The dyes were characterized by UV-Vis, IR, 1H-NMR, 13C NMR, and elemental analysis. The synthesized compounds were also screened for biological activity.
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48

Asheri, Osman, Sayyed Mostafa Habibi-Khorassani, and Mehdi Shahraki. "A Study on the Kinetics and Mechanism of the One-Pot Formation of 3,4,5-Substituted Furan-2(5H)-Ones in the Presence of Lactic Acid: Effect of Different Substituents." Progress in Reaction Kinetics and Mechanism 43, no. 3-4 (2018): 286–99. http://dx.doi.org/10.3184/146867818x15319903829218.

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The kinetics of the reaction between para-substituted anilines and dimethyl acetylenedicarboxylate (DMAD) with derivatives of benzaldehyde for the one-pot formation of 3,4,5-substituted furan-2(5 H)-ones in the presence of lactic acid as a catalyst have been studied spectrophotometrically at different temperatures. A mechanism involving four steps was proposed for the reactions, all of which followed second-order kinetics. The partial orders with respect to substituted aniline and DMAD were one and one and the reactions revealed zero-order kinetics for benzaldehyde and its derivatives. Changin
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AL - Hamdani, Ahood J., and Nezar L. S. AL Dain and Ahmed Majeed. "Synthesis of Liquid crystals with terminal polar groups and study their mesomorphic and spectroscopic properties." Journal of the faculty of Education 1, no. 9 (2023): 18–35. http://dx.doi.org/10.60037/edu.v1i9.1213.

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Synthesis new Schiffs bases substituted with polar groups CI . Br , F , N02, CH3 , OCH3 , COCH3 in para position or aniline moiety, and derived Cu ( II ) complex from the Schiff base which substituted with COCH3. The Schiffs bases substituent with CH3 , OCH3 exhibited Nematic phase but the other Schiff bases and Cu ( II ) complex exhibited Smectic phase ( Sc ) only. Molecular complexes of Cu (II) complex&#x0D; with various nitrogen bases were studied spectrophotometrically in benzene solvent at&#x0D; different temperatures. These entire complex show a new broad charge transfer band in the visi
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Denisov, M. S., and Yu A. Beloglazova. "Nitro-Substituted Pyridinimine Complexes of Pd(II): Synthesis and Inhibition of MAO-B ex vivo." Координационная химия 49, no. 9 (2023): 553–64. http://dx.doi.org/10.31857/s0132344x23600066.

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The first ever synthesis of complexes [PdLCl2] (I) and [PdLBr2] (II) was successfully achieved,where L = 2,6-dimethyl-4-nitro-N-(pyridin-2-ylmethylildene)aniline, a ligand with a purported ability toinhibit monoamine oxidase B (MAO-B). To gain insight into the molecular structure of complexes Iand II, as well as the ligand precursor 2,6-dimethyl-4-nitroaniline L4 (CIF files CCDC nos. 2255106 (I),2255105 (II), 2255103 (L), 2255104 (L4)), X-ray diffraction analysis was utilized. Complex I underwent furthercharacterization to determine its stability, solubility, and lipophilicity. Cytotoxicity st
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