[1] J.M. Hogg, F. Coleman, A. Ferrer-Ugalde, M.P. Atkins, M. Swadźba-Kwaśny, Liquid coordination complexes:A new class of Lewis acids as safer alternatives to BF3 in synthesis of polyalphaolefins, Green. Chem. 17(3) (2015) 1831-1841. [2] S. Ray, P.V.C. Rao, N.V. Choudary, Poly-α-olefin-based synthetic lubricants:A short review on various synthetic routes, Lubr. Sci. 24(1) (2012) 23-44. [3] R. Benda, J. Bullen, A. Plomer, Synthetics basics:Polyalphaolefins-base fluids for high-performance lubricants, Lubr. Sci. 13(1) (1996) 41-57. [4] G.D. Yadav, N.S. Doshi, Alkylation of phenol with methyl-tert-butyl ether and tertbutanol over solid acids:Efficacies of clay-based catalysts, Green. Chem. 236(1) (2002) 129-147. [5] J.C. Gee, B.L. Small, K.D. Hope, Behavior of protonated cyclopropyl intermediates during polyalphaolefin synthesis:Mechanism and predicted product distribution, J. Phys. Org. Chem. 25(1) (2012) 1409-1417. [6] H. Ding, B.Y. Zhang, J. Liu, Study on preparation process of lubrication from 1-decene with acidic ionic liquid catalyst, Pet. Sci. Technol. 27(17) (2009) 1919-1925. [7] J. Edward, invs Brenner and S.R.W. Haddonfeld, High viscosity synthetic lubrications from alpha-olefins, U.S.Pat. 3113167(1963). [8] A. De Klerk, Oligomerization of 1-hexene and 1-octene over solid acid catalysts, Ind. Eng. Chem. Res. 44(11) (2005) 3887-3893. [9] R.L. Shubkin, Synthetic lubricants by oligomerization and hydrogenation, U.S.Pat. (1973) 3780128. [10] J.A. Brennan, N.J. Cherry Hill, Dimerization of olefins with boron trifluoride, U.S.Pat. (1973) 3742082. [11] S.S. Scheuermann, S. Eibl, P. Bartl, Detailed characterisation of isomers present in polyalphaolefin dimer and the effect of isomeric distribution on bulk properties, Lubr. Sci. 23(5) (2011) 221-232. [12] Q. Huang, L. Chen, L. Ma, Z. Fu, W. Yang, Synthesis and characterization of oligomer from 1-decene catalyzed by supported Ziegler-Natta catalyst, Eur. Polym. J. 41(12) (2005) 2909-2915. [13] W.D. Jerome, W.W. Lewis, Edward, Jr. and T. Marquis, Feedstocks for the production of synthetic lubricants, U.S. Pat. 4420646(1991). [14] B. Lu, J. Yan, J. Xu, et al., Novel electroactive proton-doped conducting poly (aromatic ethers) with good fluorescence properties via electropolymerization, Macromolecules 43(10) (2010) 4599-4608. [15] B. Lu, Y. Li, J. Xu, Electropolymerization study of benzothiophenes and characterization of novel poly (dibenzothiophene-S, S-dioxide), J. Electroanal. Chem. 643(1-2) (2010) 67-76. [16] Y. Li, J. Xu, Y. Nie, et al., Computational study on the interaction of C4H4Y (Y=O, S, Se) with BX3(X=H, F, Cl), Acta. Chim. Sin. 68(01) (2010) 41-49. [17] J.W. Darden, E.T. Warquis and L.W. Watts, Olefin oligomerization with BF3 alcohol alkoxylate co-catalysts, U.S.Pat. 5068487(1991) [18] M. Clarembeau, Co-oligomerization of 1-dodecene and 1-decene, U.S. Pat. 20030166986(2003). [19] N. Yang, P.J. Nandapurkar, Low viscosity polyalphapolfin based on 1-decene and 1-dodecene, U.S.Pat. 7592497(2009). [20] B.L. Cupples, W.J. Heilman, A. Norman Kresge, P. Hills, Method of making alphaolefin oligomers, U.S.Pat. (1977) 4045508. [21] Akatasu, S. Miyaji and S. Kawamura, Process for producing olefin oligomer, U.S. Pat. 5191140(1993). [22] A.V. Topchiev, S.V. Zavgorodnii, Y.M. Paushkin, in:W. Doe (Ed.), Coordination Compounds of Boron Fluoride with Organic Substances:In the Series on Organic Chemistry, Pergamon Press, UK, 1959. [23] A.D. Becke, Density-functional thermochemistry. III. The role of exact exchange, J. Chem. Phys. 98(1993) 5648-5652. [24] G.K.S. Prakash, T. Mathew, E.R. Marinez, P.M. Esteves, G. Rasul, G.A. Olah, BF3·2CF3CH2OH (BF3·2TFE), an efficient superacidic catalyst for some organic synthetic transformations, J. Org. Chem. 71(10) (2006) 3952-3958. [25] R.J. Gillspie, J.S. Hartman, A nuclear magnetic resonance study of exchange reactions in the system boron trifluoride-methanol. A modified interpretation, Can. J. Chem. 45(19) (1967) 2243-2246. [26] C. Lee, W. Yang, R.G. Parr, Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density, Phys. Rev. B 37(2) (1988) 785. [27] C.P. Kong, R. Jia, Y.G. Zhao, J. Wang, Z.X. Qu, H.X. Zhang, Why HS-and CN-can be detected by different chemosensors with similar structures:A quantum mechanics and molecular dynamics study, RSC. Adv. 6(68) (2016) 663548-663558. |