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Journal articles on the topic 'Chlorotoluene'

Author: Grafiati

Published: 4 June 2021

Last updated: 27 July 2025

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1

Craik, DJ, RM Drew, I. Kyratzis, ID Rae, and JA Weigold. "Relaxation Processes in Aromatic Methyl-Groups. I. 2-Chloro-Toluene and 2,6-Dichloro-Toluene." Australian Journal of Chemistry 39, no. 12 (1986): 2049. http://dx.doi.org/10.1071/ch9862049.

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Three series of selectively deuterated toluenes, 2-chlorotoluenes and 2,6-dichlorotoluenes have been synthesized, and their methyl group 1H n.m.r. relaxation pathways have been determined by 1H, 2H and 13C n.m.r. spin-lattice relaxation time measurements. 1H spin-lattice relaxation in the methyl groups of these series occurs predominantly through an intramethyl H-H dipolar mechanism as well as through the spin-rotation mechanism. Dipolar spin-lattice relaxation rates for intramethyl H-H pairs are 0.012, 0.020 and 0.025 s-1 for toluene, 2,6-dichlorotoluene and 2-chlorotoluene respectively, sugg

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2

IFTIKHAR, A. KHAN, K. MANGLIK AJAY, and K. SANGAL S. "Nitration of p-Chlorotoluene and p-Chloroisopropylbenzene." Journal of Indian Chemical Society Vol. 65, Jun 1988 (1988): 415–16. https://doi.org/10.5281/zenodo.6298938.

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Department of Chemistry, Meerut College, Meerut-250 001 <em>Manuscript received  23 October 1987, accepted 12 April 1988</em> The nitrations of <em>p-</em>chlorotoluene and <em>p</em>-chloroisopropylbenzene with nitric acid in acetic anhydride have been studied. The product composition from the nitration of  <em>p</em>-chlorotoluene in acetic anhydride when examined alongwith the previously known product compositions obtained from the nitrations of <em>p</em>-chlorotoluene in varying percentages of sulphuric acid gave information of the degree of attack by the nitronium ion at variou

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3

ANSHU, MANJU RANI, and SANJEEV MAKEN. "Optical Studies of Binary Mixture of Chloro Substituted Benzene and n-Hexane or Cyclohexane or 1,4-Dioxane." Asian Journal of Chemistry 33, no. 2 (2021): 291–98. http://dx.doi.org/10.14233/ajchem.2021.22920.

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Thermophysical properties of binary liquid mixtures are highly beneficial for getting information about the intermolecular interactions and geometrical effects in the system. The chloro-substituted benzene compounds like 2-chlorotoluene, 4-chlorotoluene, 1,3-dichlorobenzene also have wide range of industrial and biomedical areas. In present work, the refractive indices (n) of haloarenes, hydrocarbons, ether, and respective possible binary mixtures were experimentally determined over the entire compositions at T= (298.15-318.15) K. The mixtures selected were 2-chlorotoluene or 4-chlorotoluene o

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4

Wang, Aili, Xiaoyan Zhu, Hengbo Yin, Yujun Fu, and Xiangxiang Hou. "Chlorination of Toluene to o-Chlorotoluene Catalyzed by Ionic Liquids." Catalysts 8, no. 11 (2018): 532. http://dx.doi.org/10.3390/catal8110532.

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Ionic liquids with [BMIM], [Et3NH], and [BPy] cations and AlnCl−3n+1, ZnnCl−2n+1, and CunCl−n+1 anions were used as the catalysts for the chlorination of toluene with Cl2. The ZnnCl−2n+1 containing ionic liquids with high Lewis acid strength had high catalytic activity for the selective chlorination of toluene to o-chlorotoluene via the electrophilic substitution reaction. Dichlorotoluenes were favorably formed when the AlnCl−3n+1 containing ionic liquids with both Lewis and Brönsted acid sites were used as the catalysts. When the CunCl−n+1 containing ionic liquids with weak Lewis acid strengt

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5

Melikova, I. H. "Oxidation of chlorotoluene, toluene and chlorobenzene in the presence of Ag/MnO2 catalyst." Azerbaijan Oil Industry, no. 10 (October 15, 2022): 47–52. http://dx.doi.org/10.37474/0365-8554/2022-10-47-52.

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The process of oxidation of toluene, chlorotoluene and chlorobenzene is studied and the optimum parameters for successful implementation of the synthesis modeling industrial processes selected as well. The results obtained in catalytic oxidation of toluene, chlorotoluene and chlorobenzene justify that Ag/MnO2 based catalytic systems have high activeness. Mentioned hydrothermal synthesized catalyst keeps its activeness and properties during the reaction of transition of compounds of toluene, chlorotoluene and chlorobenzene. In the presence of catalysts with Ag/MnO2 nanoparticles, the reaction r

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6

Pollmann, Katrin, Victor Wray, and Dietmar H. Pieper. "Chloromethylmuconolactones as Critical Metabolites in the Degradation of Chloromethylcatechols: Recalcitrance of 2-Chlorotoluene." Journal of Bacteriology 187, no. 7 (2005): 2332–40. http://dx.doi.org/10.1128/jb.187.7.2332-2340.2005.

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ABSTRACT To elucidate possible reasons for the recalcitrance of 2-chlorotoluene, the metabolism of chloromethylcatechols, formed after dioxygenation and dehydrogenation by Ralstonia sp. strain PS12 tetrachlorobenzene dioxygenase and chlorobenzene dihydrodiol dehydrogenase, was monitored using chlorocatechol dioxygenases and chloromuconate cycloisomerases partly purified from Ralstonia sp. strain PS12 and Wautersia eutropha JMP134. Two chloromethylcatechols, 3-chloro-4-methylcatechol and 4-chloro-3-methylcatechol, were formed from 2-chlorotoluene. 3-Chloro-4-methylcatechol was transformed into

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7

Pollmann, Katrin, Stefan Beil, and Dietmar H. Pieper. "Transformation of Chlorinated Benzenes and Toluenes byRalstonia sp. Strain PS12 tecA(Tetrachlorobenzene Dioxygenase) and tecB (Chlorobenzene Dihydrodiol Dehydrogenase) Gene Products." Applied and Environmental Microbiology 67, no. 9 (2001): 4057–63. http://dx.doi.org/10.1128/aem.67.9.4057-4063.2001.

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ABSTRACT The tecB gene, located downstream of tecAand encoding tetrachlorobenzene dioxygenase, inRalstonia sp. strain PS12 was cloned into Escherichia coli DH5α together with the tecA gene. The identity of the tecB gene product as a chlorobenzene dihydrodiol dehydrogenase was verified by transformation into the respective catechols of chlorobenzene, the three isomeric dichlorobenzenes, as well as 1,2,3- and 1,2,4-trichlorobenzenes, all of which are transformed by TecA into the respective dihydrodihydroxy derivatives. Di- and trichlorotoluenes were either subject to TecA-mediated dioxygenation

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8

Feldgus, Steven H., Matthew J. Schroeder, Robert A. Walker, Wing-Keung Woo, and James C. Weisshaar. "Hindered internal rotation in S1 meta-chlorotoluene and D0 meta-chlorotoluene+." International Journal of Mass Spectrometry and Ion Processes 159, no. 1-3 (1996): 231–44. http://dx.doi.org/10.1016/s0168-1176(96)04453-9.

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9

Goud, B. Busa, P. Venkatesu, and M. V. Prabhakara Rao. "Excess Volumes of 1,1,2,2-Tetrachloroethane or Tetrachloroethene + 2-Chlorotoluene, + 3-Chlorotoluene, and + 4-Chlorotoluene at 303.15 and 313.15 K." Journal of Chemical & Engineering Data 40, no. 6 (1995): 1211–13. http://dx.doi.org/10.1021/je00022a013.

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10

Wang, Jidong, Mingmin Ren, Shui Wang, and Yixin Qu. "Molecular structure and vibrational spectra of o-chlorotoluene, m-chlorotoluene, and p-chlorotoluene by ab initio HF and DFT calculations." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 78, no. 3 (2011): 1126–32. http://dx.doi.org/10.1016/j.saa.2010.12.064.

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11

He, Guang Yu, Hai Qun Chen, Jian Shi, Feng Li Bei, Xiao Qiang Sun та Xin Wang. "Theoretical Study on σ-Complexes in Ring-Chlorination of Toluene". Advanced Materials Research 335-336 (вересень 2011): 1047–50. http://dx.doi.org/10.4028/www.scientific.net/amr.335-336.1047.

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Theoretical studies on mechanism of mutual conversion between σ-complexes and the solvent effect in ring-chlorination of toluene were performed with density functional theory (DFT). All geometry optimizations, intrinsic reaction coordinate calculations and frequency analyses were carried out at B3LYP/6-311G** level. Calculation results indicate that ortho-, meta- and para-complexes can convert mutually by overcoming a π-complex structured transition state. It was also confirmed that the mutual conversion between ortho- and para- complexes can occur directly which give answer to the experimenta

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12

Liu, Bowen, Yumei Zhu, Xue Qin, and Fang Li. "Electrochemically facilitated synthesis of chlorotoluene." Tetrahedron Letters 165-166 (July 2025): 155643. https://doi.org/10.1016/j.tetlet.2025.155643.

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13

Chand, G. Praveen, M. Gowri Sankar, D. Ramachandran, and C. Rambabu. "Densities, Viscosities and Speeds of Sound of Binary Mixtures of 2-Chloroaniline with o-Chlorotoluene, m-Chlorotoluene and p-Chlorotoluene at Different Temperatures." Journal of Solution Chemistry 45, no. 2 (2016): 153–87. http://dx.doi.org/10.1007/s10953-016-0439-0.

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14

Zhou, Wei-Fang, Lang Chen, Jun Xie, Chak-Tong Au, and Shuang-Feng Yin. "Efficient synthesis of p-chlorobenzaldehyde through liquid-phase oxidation of p-chlorotoluene using manganese-containing ZSM-5 as catalyst." RSC Advances 5, no. 91 (2015): 74162–69. http://dx.doi.org/10.1039/c5ra16206h.

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15

Singh, Prem P., and Krishan K. Sharma. "On the role of partition and surface reactions in the adsorption of binary liquid mixtures on silica gel." Canadian Journal of Chemistry 66, no. 6 (1988): 1371–78. http://dx.doi.org/10.1139/v88-222.

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The adsorption behaviour of benzene (A), toluene (A), p-xylene (A), and o-xylene (A) in their binary mixtures with o-chlorotoluene (B) on silica gel has been studied at 308.15 K. The data have been analysed in terms of a model that assumes that partition and surface reactions play an important role in the adsorption process, and have revealed that while both partition and surface reactions dictate the adsorption (U-shaped isotherms) of o-chlorotoluene (OCTE) (B) from benzene (A) or toluene (A) + OCTE (B) mixtures, the adsorption of A and B entities of p-xylene (A) or o-xylene (A) + OCTE (B) mi

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16

Richard, Erik C., Robert A. Walker, and James C. Weisshaar. "Hindered internal rotation and torsion–vibrational coupling in ortho‐chlorotoluene (S1) and ortho‐chlorotoluene+ (D0)." Journal of Chemical Physics 104, no. 12 (1996): 4451–69. http://dx.doi.org/10.1063/1.471198.

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17

Wright, Luka A., Eric G. Hope, Gregory A. Solan, Warren B. Cross, and Kuldip Singh. "O,N,N-Pincer ligand effects on oxidatively induced carbon–chlorine coupling reactions at palladium." Dalton Transactions 44, no. 13 (2015): 6040–51. http://dx.doi.org/10.1039/c5dt00062a.

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18

Syvitski, Raymond T., and E. Elliott Burnell. "NMR and molecular structure of partially oriented mono and para methyl- and chlorobenzenes dissolved in nematic liquid crystals." Canadian Journal of Chemistry 77, no. 11 (1999): 1761–74. http://dx.doi.org/10.1139/v99-144.

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Spectral parameters, order parameters, and structural parameters, including the vibrationally corrected ralpha structure of the partially oriented solutes p-xylene, p-chlorotoluene, p-dichlorobenzene, toluene, and chlorobenzene dissolved in three liquid crystal mixtures, are reported. For samples containing the three solutes p-xylene, p-dichlorobenzene, and 1,3,5-trichlorobenzene, multiple quantum (MQ) nuclear magnetic resonance was used to aid in the analysis of the complex high-resolution spectra of the p-xylene. The high-resolution spectra of 1,3,5-trichlorobenzene and p-dichlorobenzene wer

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19

Deng, Weiqiao, Jiping Zhan, Keli Han, Guozhong He, and Nanquan Lou. "Theo-chlorotoluene photodissociation at 266 nm." Science in China Series B: Chemistry 41, no. 5 (1998): 471–78. http://dx.doi.org/10.1007/bf02882800.

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20

Palaiologou, Maria M., and Ioanna E. Molinou. "Excess Volumes of Ethyl Acetate + Toluene, + o-Chlorotoluene, and + p-Chlorotoluene from 283.15 to 303.15 K." Journal of Chemical & Engineering Data 40, no. 4 (1995): 880–82. http://dx.doi.org/10.1021/je00020a031.

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21

B., Hari Babu, Venkateswara Rao K. T., Suh Y. W., Sai Prasad P. S., and Lingaiah N. "One-step selective synthesis of 2-chlorobenzonitrile from 2-chlorotoluene via ammoxidation." New Journal of Chemistry 42, no. 3 (2018): 1892–901. http://dx.doi.org/10.1039/c7nj03728g.

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Isolated and polymeric vanadia formulate V<sub>2</sub>O<sub>5</sub>/Al<sub>2</sub>O<sub>3</sub> catalysts selective for the synthesis of 2-chlorobenzonitrile from 2-chlorotoluene in a single step through ammoxidation.

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22

Kojima, Hiroshi, Kosaku Sakeda, Tadashi Suzuki, and Teijiro Ichimura. "Methyl Internal Rotation of Photoexcited Chlorotoluene Molecules." Journal of Physical Chemistry A 102, no. 45 (1998): 8727–33. http://dx.doi.org/10.1021/jp9814350.

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23

Ichimura, T., A. Kawana, T. Suzuki, T. Ebata, and N. Mikami. "Photophysics and photochemical dynamics of chlorotoluene molecule." Journal of Photochemistry and Photobiology A: Chemistry 80, no. 1-3 (1994): 145–50. http://dx.doi.org/10.1016/1010-6030(94)01042-0.

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24

Lee, Da Young, Jae Ho Cho, Woon Ki Lim, and Hae Ja Shin. "Detection of Chlorotoluene and Nitrotoluene Compounds by Recombinant Microbial Biosensors." Journal of Life Science 24, no. 1 (2014): 54–60. http://dx.doi.org/10.5352/jls.2014.24.1.54.

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25

Gromkov, A. S., N. M. Ignatenko, G. A. Melnikov, V. V. Suchilkin, and O. A. Manzhos. "Density, thermal expansion, dynamic viscosity of halogenated arenes." Proceedings of the Southwest State University. Series: Engineering and Technology 14, no. 3 (2024): 87–104. http://dx.doi.org/10.21869/2223-1528-2024-14-3-87-104.

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Purpose. Experimental study of the density, thermal expansion and dynamic viscosity of halogenated arenes at temperatures from 293.15 to 343.15 K and atmospheric pressure 97.992 kPa.Methods. Density was determined by the pycnometric method, viscosity by the capillary method. A quartz pycnometer type PZh2 with a nominal capacity of 10 ml and a glass capillary viscometer type VPZh-2 with a nominal capillary diameter of 0.34 mm were used. The mass of liquids was measured using an electronic scale VSL-200/0.1A with a division value of 0.0001 g. Numerical methods were used to process the experiment

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26

Singh, A. P., S. Sharma, and S. M. Kale. "Selective chlorination of 4-chlorotoluene using zeolite catalysts." Journal of Molecular Catalysis A: Chemical 127, no. 1-3 (1997): 101–11. http://dx.doi.org/10.1016/s1381-1169(97)00114-3.

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27

Kojima, H., T. Suzuki, T. Ichimura, A. Fujii, T. Ebata, and N. Mikami. "Laser-induced fluorescence of jet-cooled chlorotoluene molecules." Journal of Photochemistry and Photobiology A: Chemistry 92, no. 1-2 (1995): 1–5. http://dx.doi.org/10.1016/1010-6030(95)04163-3.

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28

Sharma, V. K., A. Rohilla, J. S. Yadav, S. Solanki, and D. Sharma. "Excess Heat Capacities for Lactam + Chlorotoluene Binary Mixtures." Journal of Chemical & Engineering Data 58, no. 11 (2013): 2979–90. http://dx.doi.org/10.1021/je400408w.

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29

Yang, Sheng Chun, and Jia Qiang Wang. "Catalytic Oxidation of o-chlorotoluene to o-chlorobenzaldehyde by Vanadium Doped Anatase Mesoporous TiO₂." Advanced Materials Research 781-784 (September 2013): 182–85. http://dx.doi.org/10.4028/www.scientific.net/amr.781-784.182.

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A novel method for the catalytic oxidation of o-chlorotoluene (OCT) to o-chlorobenzaldehyde (CBD) was proposed using vanadium doped anatase mesoporous TiO2 (V/MTiO2), the catalytic reaction conditions were investigated. Under the optimum catalytic reaction conditions: 10 mL of acetic acid 100 °C of reaction temperature, 10 h of reaction time and 100 mg of catalyst, the conversion rate of OCT could reach to 95.3%, with a selectivity of 63.5%.

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30

Pavan Kumar, G., Ch Praveen Babu, and K. Samatha. "Thermodynamic Interactions of P-Chlorotoluene with P-Xylene at 303.15 K, 308.15 K, 313.15 K and 318.15 K." International Letters of Chemistry, Physics and Astronomy 52 (June 2015): 53–62. http://dx.doi.org/10.18052/www.scipress.com/ilcpa.52.53.

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Ultrasonic velocity, density and viscosity of the binary liquid mixtures of P-Chlorotoluene with p-xylene over the whole composition range at 303.15, 308.15, 313.15 and 315.15 K at frequency 2 MHz have been measured. Acoustical parameters such as adiabatic compressibility, intermolecular free length, impedance, molar volume, internal pressure, free volume, Rao constant and Wada constant. The acoustical parameters can be used to assess the strength of induced dipole-dipole interactions in this system studied.

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31

Pavan Kumar, G., Ch Praveen Babu, and K. Samatha. "Thermodynamic Interactions of P-Chlorotoluene with P-Xylene at 303.15 K, 308.15 K, 313.15 K and 318.15 K." International Letters of Chemistry, Physics and Astronomy 52 (June 2, 2015): 53–62. http://dx.doi.org/10.56431/p-vq45p3.

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Ultrasonic velocity, density and viscosity of the binary liquid mixtures of P-Chlorotoluene with p-xylene over the whole composition range at 303.15, 308.15, 313.15 and 315.15 K at frequency 2 MHz have been measured. Acoustical parameters such as adiabatic compressibility, intermolecular free length, impedance, molar volume, internal pressure, free volume, Rao constant and Wada constant. The acoustical parameters can be used to assess the strength of induced dipole-dipole interactions in this system studied.

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32

Melnikov, G. A., N. M. Ignatenko, L. P. Petrova, A. S. Gromkov, and O. A. Manzhos. "Study of Raman Scattering of Light in Liquid Arenes and Their Halogen-Substituted ones in the Low-Frequency Region of the Spectrum." Proceedings of the Southwest State University. Series: Engineering and Technology 14, no. 1 (2024): 88–103. http://dx.doi.org/10.21869/2223-1528-2024-14-1-88-103.

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Purpose. Investigation of Raman scattering of light in liquid arenas and their halogenated ones in the low-frequency range of the spectrum, taking into account the clustering processes in their structure.Methods. Raman spectroscopy methods were used, as well as a modeling method using cluster representations of the structure of liquids. Raman spectra of light in the low-frequency range from 17 to 500 cm–1 were obtained using a LabRAM HR Evolution spectrometer at room temperature (23°C).Results. The analysis of theoretical and experimental work on the properties of dimeric configurations of ben

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33

Lin, Ming-Fu, Cheng-Liang Huang, Vadim V. Kislov, A. M. Mebel, Yuan T. Lee, and Chi-Kung Ni. "H and CH3 eliminations in the photodissociation of chlorotoluene." Journal of Chemical Physics 119, no. 15 (2003): 7701–4. http://dx.doi.org/10.1063/1.1609393.

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34

Nair, K. P. R., J. Demaison, G. Wlodarczak, and I. Merke. "Millimeterwave rotational spectrum and internal rotation in o-chlorotoluene." Journal of Molecular Spectroscopy 237, no. 2 (2006): 137–42. http://dx.doi.org/10.1016/j.jms.2006.03.011.

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35

Dobslaw, Daniel, and Karl-Heinrich Engesser. "Degradation of 2-chlorotoluene by Rhodococcus sp. OCT 10." Applied Microbiology and Biotechnology 93, no. 5 (2011): 2205–14. http://dx.doi.org/10.1007/s00253-011-3543-5.

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36

Hanson, C., A. N. Patel, and D. K. Chang-Kakoti. "Separation of o- and p- chlorotoluene by solvent extraction." Journal of Applied Chemistry 18, no. 3 (2007): 89–91. http://dx.doi.org/10.1002/jctb.5010180304.

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37

Fyfe, C. A., H. Strobl, H. Gies, and G. T. Kokotailo. "High-resolution solid-state NMR investigation of the nature of the interaction between organic substrates and the zeolite ZSM-5 lattice." Canadian Journal of Chemistry 66, no. 8 (1988): 1942–47. http://dx.doi.org/10.1139/v88-313.

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The compounds p-xylene, p-chlorotoluene, and p-dichlorobenzene induce essentially identical changes in the 29Si MAS NMR spectrum of zeolite ZSM-5, indicating that the major contribution to the induced phase change of the lattice structure in these cases is the size and shape of the sorbed organic molecules. Based on these results, p-dichlorobenzene may be used as a model system in future diffraction studies of the sorbate/lattice structure greatly facilitating these investigations.

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38

Cook, Earl W. F., Christopher B. Lavery, Craig A. Wheaton, Robert McDonald, and Mark Stradiotto. "Sulfur-containing DalPhos ligand variants: synthesis and application in Buchwald−Hartwig amination." Canadian Journal of Chemistry 93, no. 3 (2015): 326–33. http://dx.doi.org/10.1139/cjc-2014-0403.

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We report herein on our synthetic, structural, and catalytic investigations of new P,S-DalPhos ligands featuring pairings of phosphorus and sulfur donor groups as well as new sulfur-containing analogues of the previously reported P,N-ligands Me-DalPhos and Mor-DalPhos, featuring a 2,3-disubstituted thiophenyl backbone. In examining the catalytic performance of these new sulfur-containing ligands in the Buchwald–Hartwig amination of octylamine, aniline, or ammonia with 4-chlorotoluene, noteworthy differences in reactivity behavior relative to Me-DalPhos and Mor-DalPhos were observed.

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39

Pavan Kumar, G., Ch Praveen Babu, K. Samatha, A. N. Jyosthna, and K. Showrilu. "Acoustical Studies of Binary Liquid Mixtures of p-Chlorotoluene in Benzene at Different Temperatures." International Letters of Chemistry, Physics and Astronomy 29 (March 2014): 25–37. http://dx.doi.org/10.18052/www.scipress.com/ilcpa.29.25.

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Ultrasonic velocities (U), densities (ρ), and coefficient of viscosities (η) are measured for binary mixtures containing (i) p-chlorotoluene and (ii) benzene at 303.15 K, 308.15 K, 313.15 K and 318.15 K to understand the molecular interaction. Various acoustical parameters such as adiabatic compressibility (βad), free length (Lf), acoustic impedance (Z), free volume (Vf), molar volume (Vm), Rao’s constant (R), Wada’s constant (W) and internal pressure (πi), are calculated from the measured values of U, ρ, and η. The trend in acoustical parameters also substantiates to asses strong molecular in

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40

Pavan Kumar, G., Ch Praveen Babu, K. Samatha, A. N. Jyosthna, and K. Showrilu. "Acoustical Studies of Binary Liquid Mixtures of p-Chlorotoluene in Benzene at Different Temperatures." International Letters of Chemistry, Physics and Astronomy 29 (March 3, 2014): 25–37. http://dx.doi.org/10.56431/p-e2u618.

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Ultrasonic velocities (U), densities (ρ), and coefficient of viscosities (η) are measured for binary mixtures containing (i) p-chlorotoluene and (ii) benzene at 303.15 K, 308.15 K, 313.15 K and 318.15 K to understand the molecular interaction. Various acoustical parameters such as adiabatic compressibility (βad), free length (Lf), acoustic impedance (Z), free volume (Vf), molar volume (Vm), Rao’s constant (R), Wada’s constant (W) and internal pressure (πi), are calculated from the measured values of U, ρ, and η. The trend in acoustical parameters also substantiates to asses strong molecular in

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41

ZHAO, Junli, Guang QIAN, Fengyun LI, Jie ZHU, Shengfu JI, and Lei LI. "Catalytic Selective Oxidation of 4-Chlorotoluene by Bi-MCM-41." Chinese Journal of Catalysis 33, no. 4-6 (2012): 771–76. http://dx.doi.org/10.1016/s1872-2067(11)60367-7.

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42

Okutsu, Tetsuo, Naomi Kounose, Hiroaki Nakatsuka, Tadashi Suzuki, Teijiro Ichimura, and Hiroshi Hiratsuka. "Excited state dynamics of p-chlorotoluene in rigid glass matrices." Journal of Photochemistry and Photobiology A: Chemistry 115, no. 3 (1998): 243–47. http://dx.doi.org/10.1016/s1010-6030(98)00270-6.

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43

Lablanquie, Pascal, Kazuhiko Ohashi, and Nobuyuki Nishi. "Laser photodissociation of C7H7+created through multiphoton ionization ofpara‐chlorotoluene." Journal of Chemical Physics 98, no. 1 (1993): 399–408. http://dx.doi.org/10.1063/1.464633.

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44

Ichimura, Teijiro, Masayoshi Iwai, and Yuji Mori. "Formation of methylanisole in the photolysis of chlorotoluene in methanol." Journal of Photochemistry 39, no. 1 (1987): 129–34. http://dx.doi.org/10.1016/0047-2670(87)80011-4.

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Dahiya, H. P., P. P. Singh, and Shashi Dagar. "Thermodynamics of molecular interactions in aromatic hydrocarbons + o-chlorotoluene mixtures." Fluid Phase Equilibria 33, no. 1-2 (1987): 191–205. http://dx.doi.org/10.1016/0378-3812(87)87011-5.

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Terrill, James B., Merrel Robinson, Gary W. Wolfe, and Leonard H. Billups. "Subacute and Subchronic Oral Toxicity of p-Chlorotoluene in the Rat." Journal of the American College of Toxicology 9, no. 5 (1990): 487–95. http://dx.doi.org/10.3109/10915819009078757.

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Abstract:

p-Chlorotoluene was administered by corn oil gavage for 14 and 90 days to male and female Sprague-Dawley-derived rats at dosages of 200, 600, and 1800 mg/kg per day and 50, 200, and 800 mg/kg per day, respectively. In the 14-day study, 8 of 10 animals of each sex in the high-dose group died due to treatment. Other treatment-related signs for these animals included an adverse effect upon body weight and clinical signs of salivation, tremors, and prostration. In the 200 and 600 mg/kg per day groups there were no apparent treatment-related effects. In the 90-day study, 4 of 10 males and 2 of 10 f

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Kim, Y., M. Lee, K. Park, and Y. Choi. "P13-09 Subacute inhalation toxicity study of 2-chlorotoluene in rats." Toxicology Letters 368 (September 2022): S202. http://dx.doi.org/10.1016/j.toxlet.2022.07.548.

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Liu, Ya-Jun, and Sten Lunell. "Multireference calculations of the fluorescence, phosphorescence and photodissociation of p-chlorotoluene." Physical Chemistry Chemical Physics 7, no. 23 (2005): 3938. http://dx.doi.org/10.1039/b510601j.

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Deng, Wei-Qiao, Ke-Li Han, Ji-Ping Zhan, Guo-Zhong He, and Nan-Quan Lou. "The intramolecular hydrogen atom transfer in the photodissociation of o-chlorotoluene." Chemical Physics Letters 285, no. 5-6 (1998): 404–9. http://dx.doi.org/10.1016/s0009-2614(97)01447-4.

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Roberge, D. M., and W. F. Hölderich. "Catalytic and non-catalytic formation of 4,4′-dimethylbiphenyl using p-chlorotoluene." Applied Catalysis A: General 194-195 (March 2000): 341–57. http://dx.doi.org/10.1016/s0926-860x(99)00380-4.

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