-
1
-
-
0013595306
-
-
Abstracts of Papers, Boston, Massachusetts, August, 1998; American Chemical Society: Washington, DC, ORGN 55
-
First presented by Necula, A. ; Scott, L. T. Abstracts of Papers, National Meeting of the American Chemical Society, Boston, Massachusetts, August, 1998; American Chemical Society: Washington, DC, 1998; ORGN 55.
-
(1998)
National Meeting of the American Chemical Society
-
-
Necula, A.1
Scott, L.T.2
-
3
-
-
1842494852
-
-
and references therein
-
(b) Lafleur, A. L.; Howard, J. B.; Plummer, E.; Taghizadeh, K.; Necula, A.; Scott, L. T.; Swallow, K. C. Polycyclic Aromat. Compd. 1998, 12, 223-237 and references therein.
-
(1998)
Polycyclic Aromat. Compd.
, vol.12
, pp. 223-237
-
-
Lafleur, A.L.1
Howard, J.B.2
Plummer, E.3
Taghizadeh, K.4
Necula, A.5
Scott, L.T.6
Swallow, K.C.7
-
4
-
-
0007141578
-
-
(a) Pope, C. J.; Marr, J. A.; Howard, J. B. J. Phys. Chem. 1993, 97, 11001-13.
-
(1993)
J. Phys. Chem.
, vol.97
, pp. 11001-11013
-
-
Pope, C.J.1
Marr, J.A.2
Howard, J.B.3
-
5
-
-
0027886950
-
-
(b) Lafleur, A. L.; Howard, J. B.; Marr, J. A.; Yadav, T. J. Phys. Chem. 1993, 97, 13539-43.
-
(1993)
J. Phys. Chem.
, vol.97
, pp. 13539-13543
-
-
Lafleur, A.L.1
Howard, J.B.2
Marr, J.A.3
Yadav, T.4
-
6
-
-
0001011227
-
-
(c) Ahrens, J.; Bachmann, M.; Baum, T.; Griesheimer, J.; Kovacs, R.; Weilmuenster, P.; Homann, K. H. Int. J. Mass Spectrom. Ion Processes 1994, 138, 133-48.
-
(1994)
Int. J. Mass Spectrom. Ion Processes
, vol.138
, pp. 133-148
-
-
Ahrens, J.1
Bachmann, M.2
Baum, T.3
Griesheimer, J.4
Kovacs, R.5
Weilmuenster, P.6
Homann, K.H.7
-
7
-
-
0001189927
-
-
(d) Bachmann, M.; Griesheimer, J.; Homann, K. H. Chem. Phys. Lett. 1994, 223, 506-10.
-
(1994)
Chem. Phys. Lett.
, vol.223
, pp. 506-510
-
-
Bachmann, M.1
Griesheimer, J.2
Homann, K.H.3
-
8
-
-
0001686768
-
-
(e) Lafleur, A. L.; Howard, J. B.; Taghizadeh, K.; Plummer, E. F.; Scott, L. T.; Necula, A.; Swallow, K. C. J. Phys. Chem. 1996, 100, 17421-17428.
-
(1996)
J. Phys. Chem.
, vol.100
, pp. 17421-17428
-
-
Lafleur, A.L.1
Howard, J.B.2
Taghizadeh, K.3
Plummer, E.F.4
Scott, L.T.5
Necula, A.6
Swallow, K.C.7
-
9
-
-
0030354122
-
-
The Combustion Institute
-
(a) Benish, T. G.; Lafeur, A. L.; Taghizadeh, K.; Howard, J. B. 26th Symp. (Int.) Combust 1996, The Combustion Institute, 2319-2326.
-
(1996)
26th Symp. (Int.) Combust
, pp. 2319-2326
-
-
Benish, T.G.1
Lafeur, A.L.2
Taghizadeh, K.3
Howard, J.B.4
-
10
-
-
0030365670
-
-
The Combustion Institute
-
(b) Macadam, S.; Beer, J. M.; Sarofim, A. F.; Hoffmann, A. B. 26th Symp. (Int.) Combust. 1996, The Combustion Institute, 2295-2302.
-
(1996)
26th Symp. (Int.) Combust.
, pp. 2295-2302
-
-
Macadam, S.1
Beer, J.M.2
Sarofim, A.F.3
Hoffmann, A.B.4
-
13
-
-
0002244636
-
-
(b) Marr, J. A.; Giovane, L. M.; Longwell, J. P.; Howard, J. B.; Lafleur, A. L. Combust. Sci. Technol. 1994, 101, 301-9.
-
(1994)
Combust. Sci. Technol.
, vol.101
, pp. 301-309
-
-
Marr, J.A.1
Giovane, L.M.2
Longwell, J.P.3
Howard, J.B.4
Lafleur, A.L.5
-
15
-
-
0344014698
-
-
(b) Ladaki, M.; Szwarc, M. Proc. K. Soc. London, A 1953, A219, 341.
-
(1953)
Proc. K. Soc. London, A
, vol.A219
, pp. 341
-
-
Ladaki, M.1
Szwarc, M.2
-
18
-
-
0029835973
-
-
For a detailed description of the apparatus and the procedure, see: Scott, L. T.; Bratcher, M. S.; Hagen, S. J. Am. Chem. Soc. 1996, 118, 8743-8744.
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 8743-8744
-
-
Scott, L.T.1
Bratcher, M.S.2
Hagen, S.3
-
19
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0342315915
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note
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1H NMR spectra of the crude pyrolysates; errors are estimated to be ±5%.
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20
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84971019111
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-
Brown, R. F. C; Eastwood, F. W.; Jackman, G. P. Aust. J. Chem. 1977, 30, 1757-67.
-
(1977)
Aust. J. Chem.
, vol.30
, pp. 1757-1767
-
-
Brown, R.F.C.1
Eastwood, F.W.2
Jackman, G.P.3
-
22
-
-
0033594519
-
-
Cioslowski, J.; Schimeczek, M.; Piskorz, P.; Moncrieff, D. J. Am. Chem. Soc. 1999, 121, 3773-3778.
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 3773-3778
-
-
Cioslowski, J.1
Schimeczek, M.2
Piskorz, P.3
Moncrieff, D.4
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23
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0342750727
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note
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In cases where no further isomerization is possible, the arylacetylene survives, e.g., copyrolysis of bromobenzene and maleic anhydride at 1100 °C gives phenyl acetylene and benzene as the only significant products. The volatility of these two hydrocarbons precluded an accurate determination of their relative abundances in our apparatus.
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25
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33845184733
-
-
(b) Chen, R. H.; Kafafi, S. A.; Stein, S. E. J. Am. Chem. Soc. 1989, 111, 1418-1423.
-
(1989)
J. Am. Chem. Soc.
, vol.111
, pp. 1418-1423
-
-
Chen, R.H.1
Kafafi, S.A.2
Stein, S.E.3
-
26
-
-
85021622022
-
-
(c) Scott, L. T.; Hashemi, M. M.; Bratcher, M. S. J. Am. Chem. Soc. 1992, 114, 1920-1.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 1920-1921
-
-
Scott, L.T.1
Hashemi, M.M.2
Bratcher, M.S.3
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29
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0342315912
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note
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In the absence of more facile competing reactions, ethynyl group migration does occur on the naphthalene ring system: FVP of 2-ethynyl-naphthalene (1100 °C, 0.2 mmHg) gives a 2:1 mixture of acenaphthylene and starting material, presumably by the sequence 2-EN → 1-EN → AN.
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31
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0002043353
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(b) Sarobe, M.; Flink, S.; Jenneskens, L. W.; Zwikker, J. W.; Wesseling, J. J. Chem. Soc. Perkin Trans. 2 1996, 2125-2131.
-
(1996)
J. Chem. Soc. Perkin Trans. 2
, pp. 2125-2131
-
-
Sarobe, M.1
Flink, S.2
Jenneskens, L.W.3
Zwikker, J.W.4
Wesseling, J.5
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