-
1
-
-
17144415907
-
-
A. V. Talyzin, Y. O. Tsybin, A. A. Peera, T. M. Schaub, A. G. Marshall, B. Sundqvist, P. Mauron, A. Züttel, W. E. Billups, J. Phys. Chem. B 2005, 109, 5403-5405.
-
(2005)
J. Phys. Chem. B
, vol.109
, pp. 5403-5405
-
-
Talyzin, A.V.1
Tsybin, Y.O.2
Peera, A.A.3
Schaub, T.M.4
Marshall, A.G.5
Sundqvist, B.6
Mauron, P.7
Züttel, A.8
Billups, W.E.9
-
2
-
-
28944431534
-
-
A. Nikitin, H. Ogasawara, D. Mann, R. Denecke, Z. Zhang, H. Dai, K. Cho, A. Nilsson, Phys. Rev. Lett. 2005, 95, 225507.
-
(2005)
Phys. Rev. Lett
, vol.95
, pp. 225507
-
-
Nikitin, A.1
Ogasawara, H.2
Mann, D.3
Denecke, R.4
Zhang, Z.5
Dai, H.6
Cho, K.7
Nilsson, A.8
-
5
-
-
9944253880
-
-
C. Bianchini, V. D. Santo, A. Meli, S. Moneti, M. Moreno, W. Oberhauser, R. Psaro, L. Sordelli, F. Vizza, Angew. Chem. 2003, 115, 2740-2743;
-
(2003)
Angew. Chem
, vol.115
, pp. 2740-2743
-
-
Bianchini, C.1
Santo, V.D.2
Meli, A.3
Moneti, S.4
Moreno, M.5
Oberhauser, W.6
Psaro, R.7
Sordelli, L.8
Vizza, F.9
-
6
-
-
0038112091
-
-
Angew. Chem. Int. Ed. 2003, 42, 2636-2639.
-
(2003)
Angew. Chem. Int. Ed
, vol.42
, pp. 2636-2639
-
-
-
7
-
-
11744385946
-
-
P. Tarakeshwar, J. Y. Lee, K. S. Kim, J. Phys. Chem. A 1998, 102, 2253-2255.
-
(1998)
J. Phys. Chem. A
, vol.102
, pp. 2253-2255
-
-
Tarakeshwar, P.1
Lee, J.Y.2
Kim, K.S.3
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8
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-
0033532686
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Aromatic compounds are reported to undergo reduction by using electropositive metals and a proton source with [emim]Cl-AlCl3; C. J. Adams, M. J. Earle, K. R. Seddon, Chem. Commun. 1999, 1043-1044
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3; C. J. Adams, M. J. Earle, K. R. Seddon, Chem. Commun. 1999, 1043-1044.
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10
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0003412412
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-
6th ed, Wiley, New York
-
M. B. Smith, J. March, March's Advanced Organic Chemistry, 6th ed., Wiley, New York, 2007, p. 717.
-
(2007)
March's Advanced Organic Chemistry
, pp. 717
-
-
Smith, M.B.1
March, J.2
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11
-
-
24644446463
-
-
A. P. Umpierre, G. Machado, G. H. Fecher, J. Morais, J. Dupont, Adv. Synth. Catal. 2005, 347, 1404-1412.
-
(2005)
Adv. Synth. Catal
, vol.347
, pp. 1404-1412
-
-
Umpierre, A.P.1
Machado, G.2
Fecher, G.H.3
Morais, J.4
Dupont, J.5
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12
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55249121250
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Some degradation of the fullerene to give lighter hydrocarbons was observed under these conditions
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Some degradation of the fullerene to give lighter hydrocarbons was observed under these conditions.
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13
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5844345768
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In 1980 Buchanan et al. reported that the stable anthracenium salt, anthracenium]AlCl4 can be generated by mixing anthracene and a Brønsted superacidic melt, HCl/SbCl3/AlCl3; A.C. Buchanan III, A. S. Dworkin, G. P. Smith, J. Am. Chem. Soc. 1980, 102, 5262-5265
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3; A.C. Buchanan III, A. S. Dworkin, G. P. Smith, J. Am. Chem. Soc. 1980, 102, 5262-5265.
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14
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55249086135
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The stable anthracenium salt can also be obtained by mixing anthracene with other quaternary ammonium analogues of 1, such as [NMe 4]Cl-AlCl3 x of AlCl3, 0.67, see the Supporting Information, Figure S1
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3 = 0.67); see the Supporting Information, Figure S1).
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15
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55249093499
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An additional hydrogenation experiment was conducted with the anthracenium salt, bmim]-2-[AlCl4, under the same conditions used for entry 10 in Table 2. As anticipated, the same reduced products were obtained with those formed from entry 10 in Table 2
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4], under the same conditions used for entry 10 in Table 2. As anticipated, the same reduced products were obtained with those formed from entry 10 in Table 2.
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16
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55249084060
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In the case of benzene, the enthalpy of the complex formation between benzene-AlCl3 and [bmim][AlCl4]is 9.3 kcal mol -1. For details, see the Supporting Information
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-1. For details, see the Supporting Information.
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