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Kondratenko, N.V.1
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N. V. Kondratenko, V. I. Popov, G. N. Timofeeva, N. V. Ignatiev, L. M. Yagupolskii, J. Org. Chem. USSR 1985, 21, 2367-2371; Chem. Abstr. 1985, 102, 220513.
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Wiley-VCH, Weinheim, Germany
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For an overview on the substituent effects of different fluorinated functional groups, see: P. Kirsch, Modern Fluoroorganic Chemistry: Synthesis, Reactivity, Applications, Wiley-VCH, Weinheim, Germany. 2004, p. 239.
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Modern Fluoroorganic Chemistry: Synthesis, Reactivity, Applications
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Kirsch, P.1
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N. V. Kondratenko, V. I. Popov, O. A. Radchenko, N. V. Ignatiev, L. M. Yagupolskii, J. Org. Chem. USSR 1987, 23, 1542-1547; Chem. Abstr. 1987, 107, 39309.
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Kondratenko, N.V.1
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15044364366
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N. V. Kondratenko, V. I. Popov, O. A. Radchenko, N. V. Ignatiev, L. M. Yagupolskii, J. Org. Chem. USSR 1987, 23, 1542-1547; Chem. Abstr. 1987, 107, 39309.
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13
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15044339682
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note
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NI = 92.8 °C, Δε = 5.3, Δn = 0.0964). The extrapolated values are corrected empirically for differences in the order parameter that are induced by the analyte. For the pure substances, the melting points were identified by DSC.
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14
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79960678031
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For the relation between the molecular dipole moment and the dielectric anisotropy (Δε) of the nematic phase, see: a) W. Maier, G. Meier, Z. Naturforsch.Teil A 1961, 16, 262-267;
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Maier, W.1
Meier, G.2
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0003924521
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Spectroscopy with Polarized Light: Solute Alignment by Photoselection
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Wiley-VCH, Weinheim
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c) J. Michl, E. W. Thulstrup, "Spectroscopy with Polarized Light: Solute Alignment by Photoselection", in Liquid Crystals, Polymers, and Membranes, Wiley-VCH, Weinheim, 1995, p. 171-221.
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Liquid Crystals, Polymers, and Membranes
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Michl, J.1
Thulstrup, E.W.2
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17
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0000754995
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For the prediction of the dielectric anisotropy (Δε) and birefringence (Δn) of nematic liquid crystals, see: a) M. Bremer, K. Tarumi, Adv. Mater. 1993, 5, 842-848;
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Bremer, M.1
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0032140890
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b) M. Klasen, M. Bremer, A. Götz, A. Manabe, S. Naemura, K. Tarumi, Jpn. J. Appl. Phys. 1998, 37, L945-L948.
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0004133516
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Gaussian, Inc., Pittsburgh, PA, USA
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a) Calculations: Gaussian 98, Revision A.6: M. J. Frisch, G. W. Trucks, H. B. Schlegel, G. E. Scuseria, M. A. Robb, J. R. Cheeseman, V. G. Zakrzewski, J. A. Montgomery, Jr., R. E. Stratmann, J. C. Burant, S. Dapprich, J. M. Millam, A. D. Daniels, K. N. Kudin, M. C. Strain, O. Farkas, J. Tomasi, V. Barone, M. Cossi, R. Cammi, B. Mennucci, C. Pomelli, C. Adamo, S. Clifford, J. Ochterski, G. A. Petersson, P. Y. Ayala, Q. Cui, K. Morokuma, D. K. Malick, A. D. Rabuck, K. Raghavachari, J. B. Foresman, J. Cioslowski, J. V. Ortiz, B. B. Stefanov, G. Liu, A. Liashenko, P. Piskorz, I. Komaromi, R. Gomperts, R. L. Martin, D. J. Fox, T. Keith, M. A. Al-Laham, C. Y. Peng, A. Nanayakkara, C. Gonzalez, M. Challacombe, P. M. W. Gill, B. Johnson, W. Chen, M. W. Wong, J. L. Andres, C. Gonzalez, M. Head-Gordon, E. S. Replogle, and J. A. Pople, Gaussian, Inc., Pittsburgh, PA, USA, 1998.
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Gaussian 98, Revision A.6
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Frisch, M.J.1
Trucks, G.W.2
Schlegel, H.B.3
Scuseria, G.E.4
Robb, M.A.5
Cheeseman, J.R.6
Zakrzewski, V.G.7
Montgomery Jr., J.A.8
Stratmann, R.E.9
Burant, J.C.10
Dapprich, S.11
Millam, J.M.12
Daniels, A.D.13
Kudin, K.N.14
Strain, M.C.15
Farkas, O.16
Tomasi, J.17
Barone, V.18
Cossi, M.19
Cammi, R.20
Mennucci, B.21
Pomelli, C.22
Adamo, C.23
Clifford, S.24
Ochterski, J.25
Petersson, G.A.26
Ayala, P.Y.27
Cui, Q.28
Morokuma, K.29
Malick, D.K.30
Rabuck, A.D.31
Raghavachari, K.32
Foresman, J.B.33
Cioslowski, J.34
Ortiz, J.V.35
Stefanov, B.B.36
Liu, G.37
Liashenko, A.38
Piskorz, P.39
Komaromi, I.40
Gomperts, R.41
Martin, R.L.42
Fox, D.J.43
Keith, T.44
Al-Laham, M.A.45
Peng, C.Y.46
Nanayakkara, A.47
Gonzalez, C.48
Challacombe, M.49
Gill, P.M.W.50
Johnson, B.51
Chen, W.52
Wong, M.W.53
Andres, J.L.54
Gonzalez, C.55
Head-Gordon, M.56
Replogle, E.S.57
Pople, J.A.58
more..
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20
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0004215507
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Swiss Center for Scientific Computing, Manno, Switzerland
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The energies of the conformers A, B, and C were calculated at the B3LYP/6-31G*//B3LYP/ 6-31G* level of theory, including zero point energy correction, b) Pictures: MOLEKEL 4.2: P. Flükinger, H. P. Lüthi, S. Portmann, J. Weber, Swiss Center for Scientific Computing, Manno, Switzerland, 2002.
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MOLEKEL 4.2
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Flükinger, P.1
Lüthi, H.P.2
Portmann, S.3
Weber, J.4
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21
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85022698109
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US 2862029, 1958
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a) Reaction of S,S-difluoro-N-phenylsulfimide with phenyllithium: W. C. Smith, US 2862029, 1958; Chem. Abstr. 1959, 53, 51019;
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Chem. Abstr.
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Smith, W.C.1
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22
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0001721129
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b) Reaction of Martin sulfurane dehydration reagent with aniline: J. A. Franz, J. C. Martin, J. Am. Chem. Soc. 1975, 97, 583-589;
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J. Am. Chem. Soc.
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Franz, J.A.1
Martin, J.C.2
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0000611910
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c) Reaction of S,S-diphenylsulfimide with an activated haloarene: M. Abou-Gharbia, D. M. Ketcha, D. E. Zacharias, D. Swern, J. Org. Chem. 1985, 50, 2224-2228.
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J. Org. Chem.
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Abou-Gharbia, M.1
Ketcha, D.M.2
Zacharias, D.E.3
Swern, D.4
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24
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15044361043
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note
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-1, R(F) = 4.90% for 3075 observed independent reflections (4.35° ≤ θ ≤ 26.37°);
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25
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15044357986
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note
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-1, R(F) = 5.55% for 4096 observed independent reflections (3.16° ≤ θ 30.05°);
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26
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15044353039
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c) CCDC-242383 (8) and -242384 (9) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/ data_request/cif.
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27
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0037955629
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For a detailed discussion on arene-perfluoroarene interactions, see: E. A. Meyer, R. K. Castellano, F. Diederich, Angew. Chem. 2003, 115, 1244-1287; Angew. Chem. Int. Ed. 2003, 42, 1210-1250.
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Angew. Chem.
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Meyer, E.A.1
Castellano, R.K.2
Diederich, F.3
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28
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0242417008
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For a detailed discussion on arene-perfluoroarene interactions, see: E. A. Meyer, R. K. Castellano, F. Diederich, Angew. Chem. 2003, 115, 1244-1287; Angew. Chem. Int. Ed. 2003, 42, 1210-1250.
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(2003)
Angew. Chem. Int. Ed.
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, pp. 1210-1250
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