Experimental and Theoretical Study on One-pot, Synthesis of Some 4-Aryl-1,3,4,6,7,8-hexahydroquinazolin-2,5(1H,6H)-diones Derivatives (HHQs) using Nano K3AlF6
Subject Areas : PolymerMasoumeh Mehrabi 1 , Asadollah Farhadi 2 , Alireza Kiassat 3
1 - Department of Chemistry, Khuzestan Science and Research Branch, Islamic Azad University,
Ahvaz, Iran
Department of Chemistry, Ahvaz Branch, Islamic Azad University, Ahvaz, Iran
3
2 - Department of Chemistry, Ahvaz Branch, Islamic Azad University, Ahvaz, Iran
Petroleum University of Technology, Faculty of Science, Ahvaz, Iran
3 - Department of chemistry, Ahvaz Branch, Islamic Azad University, Ahvaz, Iran
Chemistry Department, College of Science, Shahid Chamran University, Ahvaz, Iran
Keywords: 1, DFT, 4, 6, 7, 3, Zeta Potential, 4-Aryl-1, 8-hexahydroquinazolin-2, 5(1H, 6H)-diones (HHQs), 3-cyclohexadione, Nano K3AlF6, Solvation Gibbs energies,
Abstract :
[1]. N. Nakamichi, Y. Kawashita, M. Hayashi, J. Org. Lett., 4, 3955 (2002).
[2]. N. Nakamichi, Y. Kawashita, M. Hayashi, Synthesis,1015 (2004).
[3]. P. Biginelli, Gazz.Chim. Ital., 23, 360 (1893).
[4]. B. Jauk, T. Pernat, C.O. Kappe, Molecules, 5, 227 (2000).
[5]. V. K. Yadav, K. K. Kapoor, Tetrahedron Lett., 52, 3659 (1996).
[6]. C. T. Kresge, M. E. Leonowicz, W. J. Roth, J. C. Vartulie, J. S. Beck,Nature, 359, 710-712
(1992).
[7]. A. Farhadi, T. Hamoule, M. A. Takassi, T. Arizavipour,Bulg. Chem. Comm., 47, 101 (2015).
[8]. M. Rimaz, J. Khalafy, H. Mousavi, Res. Chem. Int., 42, 8185 (2016).
[9]. Z. Benzekri, H. Serrar, S. Boukhris, A. Ouasri, A. Hassikou, A. Rhandour, Fr. Ukr. J. Chem.,
560 (2017).
[10]. J. M. Fraile, J. I. Garcia, J. A. Matoral, F. Figueras, Tetrahedron Lett., 37, 5995 (1996).
[11]. F. Hoffmann, M. Frӧba, Chem. Soc. Rev., 40, 608 (2011).
[12]. M. Soleymani, Curr. Org. Chem., 22, 890 (2018).
[13]. M. Mehrabi, A. Farhadi, A. kiasat, Int. J. Org. Chem.,7, 240 (2017).
[14]. J. Yamawaki, T. Ando, T. Hanafusa, Chem. Lett., 10, 1143 (1981).
[15]. A. Farhadi, M. A. Takassi, L. Hejazi, J. Iran. Chem. Commun., 5, 35 (2017).
[16]. A. Farhadi, M. A. Takassi, L. Hejazi, Z. Naturforsch, 68b, 51 (2013).
[17]. A. Farhadi, J. Noei, R. H. Aliyari, M. Albakhtiyari, M. A. Takassi, Res. Chem. Int, 42, 1401
(2016).
[18]. A. Farhadi, M. Ramyar, M. A. Takassi, Iran. Chem. Commun., 6, 266 (2018).
[19]. S. X. Wang, L. Ji-Tai, Y. Wen-Zhi, L. Tong-Shuang, Ultrason. Sonochem., 9, 159 (2002).
[20]. N. Schultz, G. Metreveli, M. Franzreb, F. H. Frimmel, C. Syldatk, Colloid Surface B., 66, 39
(2008).
[21]. K. Cai, M. Frant, J. Bossert, G. Hildebrand, K. Liefeith, K. D. Jandt, Colloid Surface B., 50, 1
(2006).
[22]. A. M. Abakumov, M. D. Rossell, A. M. Alekseeva, S. Yu. Vassiliev, S. N. Mudrezova, G. V.
Tendeloo, E. V. Antipov, J. Solid State Chem., 179, 421 (2006).
[23]. J. H. Clark, D. G. Cork, M. S. Robertson, Chem. Lett., 12, 1145 (1983).
[24]. S. Ghassamipour, A. R. Sardarian, J. Iran. Chem. Soc.,7, 237 (2010).
[25]. D. C. Young, John Wiley & Sons New-York, (2001).
[26]. G. Uray,P. Verdino,F. Belaj, C. O. Kappe, W. M. F. Fabian, J. Org. Chem.,66, 6685 (2001).
[27]. S. K. Rathwa, M. S. Vasava, M. N. Bhoi, M. A. Borad, H. D. Patel, Synth. Commun., 48, 963
(2018).
[28]. A. B. Sannigrahi, S. Scheiner, Theochem., 427, 79 (1998).
[29]. A. Farhadi, M. A. Takassi, P. Madmoli, J. Am. Sci., 8, 1024 (2012).
[30]. M. J. Frisch, G. W. Trucks, H. B. Schlegel and et.al., Gaussian, Inc., Wallingford CT, Gussian
(2009)
[31]. H. R Memarian, H. Sabzyan, A. Farhadi, Mont. Chem., 141, 1203 (2010).
[32]. A. Farhadi, M. A. Takassi, Front. Chem. China., 6, 142 (2011).
[33]. S. Subhashandrabose, R. Akhil, R. Krishnan, H. Saleem, R. Parameswari, Spectrochim. Acta
A., 77, 877 (2010).
[34]. A. R. Krishanan, H. Saleem, S. Subhashandrabose, N. Sundaraganesan, S. Sebastian,
Spetrochim. Acta A., 78, 582 (2011).
[35]. J. N. Liu, Z. R. Chen, S. F. Yuan, J. Zhejiang Uni. Sci. B., 6, 584 (2005).
[36]. N. Seif, A. Farhadi, R. Badri, A. R. Kiasat, Iran. J. Chem. Chem. Eng., 39, 21 (2020)
[37]. S. Sebastian, N. Sundaraganesan, Specrochim. Acta A., 75, 941 (2010).
