References
- J. McFarlane, Jason Richard. Bell, David K. Felde, Robert A. Joseph, III, A. Lou Qualls, and Samuel Paul Weaver, “Performance and Thermal Stability of a Polyaromatic Hydrocarbon in a Simulated Concentrating Solar Power Loop,” AIMS Energy 2, no. 1 (2014): 41–70.
- Rajdip Utane, Sujata Deo, Pratik Patra, and Chaitali Gumgaonkar, “Green Approach towards the Synthesis of Synthesis of 1-Phenyl Naphthalene Lignan and Their Derivatives,” International Journal of Advances in Science Engineering and Technology 1, no. 1 (2015): 43–7.
- Paolo Beltrame, Francesco Demartin, and Giovanni Zuretti, “The Reaction of Naphthalene with Benzyl Chloride over an MCM-41 Solid Acid Catalyst: A Kinetic Study,” Applied Catalysis A: General 232, no. 1-2 (2002): 265–76.
- Ch Ramesh Kumar, K. T Venkateswara Rao, P. S. Sai Prasad, and N. Lingaiah, “Tin Exchanged Heteropoly Tungstate: An Efficient Catalyst for Benzylation of Arenes with Benzyl Alcohol,” Journal of Molecular Catalysis A: Chemical 337, no. 1-2 (2011): 17–24.
- Wenming Hao, Weimin Zhang, Zaibin Guo, Jinghong Ma, and Ruifeng Li, “Mesoporous Beta Zeolite Catalysts for Benzylation of Naphthalene: Effect of Pore Structure and Acidity,” Catalysts 8, no. 11 (2018): 504–13pp.
- Carlos Gutierrez. Blanco, Dolores Casal. Banciella, and M. Dolores Gonz ´Alez Azp´Roz, “Alkylation of Naphthalene Using Three Different Ionic Liquids,” Journal of Molecular Catalysis A: Chemical 253, no. 1-2 (2006): 203–6.
- Jitendra R. Satam, and Radha V. Jayaram, “Liquid Phase Friedel–Crafts Benzylation of Aromatics on a Polymer-Supported 12-Tungstophosphoric Acid Catalyst,” Catalysis Communications 9no. 9 (2008): 1937–40.
- Paolo. Beltrame, and Giovanni. Zuretti, “The Reaction of Naphthalene with Benzyl Alcohol over a Nafion-Silica Composite: A Kinetic Study,” Applied Catalysis A: General 248, no. 1-2 (2003): 75–83.
- Ganapati D. Yadav, and Suraj A. Purandare, “Efficacy of a Novel Mesoporous Solid Acid Catalyst UDCaT-4 in Liquid Phase Benzylation of Naphthalene,” Journal of Molecular Catalysis A: Chemical 263, no. 1-2 (2007): 26–31.
- Vasant R. Choudhary, and Rani Jha, “GaClx- or GaAlClx-Grafted Si-MCM-41: Highly Active and Moisture Insensitive/Stable Catalyst for the Acylation and Benzylation of Benzene, Naphthalene and Substituted Benzenes,” Applied Catalysis A: General 333, no. 1 (2007): 42–8.
- Vasant R. Choudhary, and Rani Jha, “GaAlClx-Grafted Mont.K-10 Clay; Highly Active and Stable Solid Catalyst for the Friedel-Crafts Type Benzylation and Acylation Reactions,” Catalysis Communications 9, no. 6 (2008): 1101–5.
- Qinghua. Zhang, Shiguo Zhang, and Youquan Deng, “Recent Advances in Ionic Liquid Catalysis,” Green Chemistry 13, no. 10 (2011): 2619–37.
- Kenneth N. Marsh, Alex Deev, Alex C.-T. Wu, Emma Tran, and A. Klamt, “Room Temperature Ionic Liquids as Replacements for Conventional Solvents – a Review,” Korean Journal of Chemical Engineering 19, no. 3 (2002): 357–62.
- Raquel F. M. Frade, and Carlos Am Afonso, “Impact of Ionic Liquids in Environment and Humans: An Overview,” Human & Experimental Toxicology 29, no. 12 (2010): 1038–54.
- Mangesh Sakhalkar, Pavankumar Aduri, Sharad Lande, and Sudeshna Chandra, “Single Step Synthesis of Novel Chloroaluminate Ionic Liquid for Green Friedel-Crafts Alkylation Reaction,” Clean Technologies and Environmental Policy 22, no. 1 (2020): 59–71.
- Hadi M. A. Abood, Andrew P. Abbott, Andrew D. Ballantyne, and Karl S. Ryder, “ Do all ionic liquids need organic cations? Characterisation of [AlCl2·nAmide]+ AlCl4(-) and comparison with imidazolium based systems,” Chemical Communications (Cambridge, England) 47, no. 12 (2011): 3523–5.
- Youxing Fang, Kazuki Yoshii, Xueguang Jiang, Xiao-Guang Sun, Tetsuya Tsuda, Nada Mehio, and Sheng Dai, “An AlCl3 Based Ionic Liquid with a Neutral Substituted Pyridine Ligand for Electrochemical Deposition of Aluminium,” Electrochimica Acta. 160, (2015): 82–8.
- ]Andrew P. Abbott, Robert C. Harris, Yi-Ting Hsieh, Karl S. Ryder, and I-Wen Sun, “Aluminium Electrodeposition under Ambient Conditions,” Physical Chemistry Chemical Physics: PCCP 16, no. 28 (2014): 14675–81.
- R. J. Gale, and R. A. Osteryoung, “Infrared Investigation of Room Temperature Aluminium Chloride: Butyl Pyridinium Chloride Melts,” Inorganic Chemistry 19, no. 8 (1980): 2240–2.
- Lucy C. Brown, James M. Hogg, and Małgorzata Swadźba-Kwaśny, “Małgorzata Swadzba-Kwasny; Lewis Acidic Ionic Liquids,” Topics in Current Chemistry (Cham) 375, no. 5 (2017): 78
- Giridhar Pulletikurthi, Bjorn Bodecker, Andriy Borodin, Bernd Weidenfeller, and Frank Endres, “Electrodeposition of Al from a 1-butylpyrrolidine-AlCl3 Ionic Liquid,” Progress in Natural Science: Materials International 25, no. 6 (2015): 603–11.
- Miao Hai-Xia, Ma Li, Ma Jing-Hong, Li Dui-Chun, and Li Rui-Feng, “Benzylation of Naphthalene over a Mesoporous ZSM-5 Zeolite Microsphere Catalyst,” Acta Physico-Chimica Sinica 30, no. 8 (2014): 1518–26.
- Li Chenmin, Qi Xin, and Tang Xiangyang, “Synthesis of 2-Isopropyl Naphthalene Catalyzed by Et3NHCl-AlCl3 Ionic Liquids,” China Petroleum Processing and Petrochemical Technology 16, no. 1 (2014): 60–5.
- Zhongmin Liu, Patrice Moreau, and François Fajula, “Liquid Phase Selective Alkylation of Naphthalene with t-Butanol over Large Pore Zeolites,” Applied Catalysis A: General 159, no. 1-2 (1997): 305–16.
- D. Bhattacharya, A. K. Pandey, and A. P. Singh, “Benzylation of Naphthalene over Zeolite Catalysts,” Studies in Surface Science and Catalysis 113 (1998): 737–41.
- Pengcheng Hu, Wei Jiang, Lijuan Zhong, and Shu-Feng Zhou, “Determination of the Lewis Acidity of Amide–AlCl3 Based Ionic Liquid Analogues by Combined in Situ IR Titration and NMR Methods,” RSC Advances 8, no. 24 (2018): 13248–52.
- Z. Popova, M. Yankov, L. Dimitrov, and I. Chervenkov, “Isomerization and Disproportionation of 1 Methylnaphthalene on Zeolites,” Reaction Kinetics & Catalysis Letters 52, no. 1 (1994): 51–8.