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1
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33845198114
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and references cited therein
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(a) Nakashima, H.; Hashimoto, M.; Sadakane, Y.; Tomohiro, T.; Hatanaka, Y. J. Am. Chem. Soc. 2006, 128, 15092 and references cited therein.
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(2006)
J. Am. Chem. Soc
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, pp. 15092
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Nakashima, H.1
Hashimoto, M.2
Sadakane, Y.3
Tomohiro, T.4
Hatanaka, Y.5
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4
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0036514084
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For general references on photoaffinity labeling, see, for example: a
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For general references on photoaffinity labeling, see, for example: (a) Hatanaka, Y.; Sadakane, Y. Curr. Top. Med. Chem 2002, 2, 271.
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(2002)
Curr. Top. Med. Chem
, vol.2
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Hatanaka, Y.1
Sadakane, Y.2
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7
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0347651056
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(a) Admasu, A.; Gudmundsdottir, A. D.; Platz, M. S.; Watt, D. S.; Kwiatkowski, S.; Crocker, P. J. J. Chem. Soc., Perkin Trans. 2 1998, 1093.
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(1998)
J. Chem. Soc., Perkin Trans. 2
, pp. 1093
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Admasu, A.1
Gudmundsdottir, A.D.2
Platz, M.S.3
Watt, D.S.4
Kwiatkowski, S.5
Crocker, P.J.6
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11
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0019332445
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(e) Brunner, J.; Senn, H.; Richards, F. J. Biol. Chem. 1980, 255, 3313.
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(1980)
J. Biol. Chem
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Brunner, J.1
Senn, H.2
Richards, F.3
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12
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84985433052
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(f) Turro, N. J.; Butcher, J. A., Jr.; Hefferon, G. J. Photochem. Photobiol. 1981, 34, 517.
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(1981)
Photochem. Photobiol
, vol.34
, pp. 517
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Turro, N.J.1
Butcher Jr., J.A.2
Hefferon, G.J.3
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15
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0011574914
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Wasserman, E.; Barash, L.; Yager, W. A. J. Am. Chem. Soc. 1965, 87, 4974.
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(1965)
J. Am. Chem. Soc
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, pp. 4974
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Wasserman, E.1
Barash, L.2
Yager, W.A.3
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18
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4644300149
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For a general description of the matrix isolation instrumentation, see: Sheridan, R. S.; Zuev, P. S. J. Am. Chem. Soc. 2004, 126, 12220 and references cited therein. Irradiation wavelengths were selected by a high-pressure Hg lamp/monochromator assembly, and are ± 5 nm. See the Supporting Information for further matrix deposition and irradiation details.
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For a general description of the matrix isolation instrumentation, see: Sheridan, R. S.; Zuev, P. S. J. Am. Chem. Soc. 2004, 126, 12220 and references cited therein. Irradiation wavelengths were selected by a high-pressure Hg lamp/monochromator assembly, and are ± 5 nm. See the Supporting Information for further matrix deposition and irradiation details.
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19
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34547960833
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All structures were fully optimized by analytical gradient methods using Gaussian 03, Revision C.02: Frisch, M. J, Trucks, G. W, Schlegel, H. B, Scuseria, G. E, Robb, M. A, Cheeseman, J. R, Montgomery, J. A, Jr, Vreven, T, Kudin, K. N, Burant, J. C, Millam, J. M, Iyengar, S. S, Tomasi, J, Barone, V, Mennucci, B, Cossi, M, Scalmani, G, Rega, N, Petersson, G. A, Nakatsuji, H, Hada, M, Ehara, M, Toyota, K, Fukuda, R, Hasegawa, J, Ishida, M, Nakajima, T, Honda, Y, Kitao, O, Nakai, H, Klene, M, Li, X, Knox, J. E, Hratchian, H. P, Cross, J. B, Adamo, C, Jaramillo, J, Gomperts, R, Stratmann, R. E, Yazyev, O, Austin, A. J, Cammi, R, Pomelli, C, Ochterski, J. W, Ayala, P. Y, Morokuma, K, Voth, G. A, Salvador, P, Dannenberg, J. J, Zakrzewski, V. G, Dapprich, S, Daniels, A. D, Strain, M. C, Farkas, O, Malick, D. K, Rabuck, A. D, Raghavachari, K, Foresman, J. B, Ortiz, J. V, Cui, Q, Baboul, A. G, Clifford, S, Cioslowski, J, Stefanov
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All structures were fully optimized by analytical gradient methods using Gaussian 03, Revision C.02: Frisch, M. J.; Trucks, G. W.; Schlegel, H. B.; Scuseria, G. E.; Robb, M. A.; Cheeseman, J. R.; Montgomery, J. A., Jr.; Vreven, T.; Kudin, K. N.; Burant, J. C.; Millam, J. M.; Iyengar, S. S.; Tomasi, J.; Barone, V.; Mennucci, B.; Cossi, M.; Scalmani, G.; Rega, N.; Petersson, G. A.; Nakatsuji, H.; Hada, M.; Ehara, M.; Toyota, K.; Fukuda, R.; Hasegawa, J.; Ishida, M.; Nakajima, T.; Honda, Y.; Kitao, O.; Nakai, H.; Klene, M.; Li, X.; Knox, J. E.; Hratchian, H. P.; Cross, J. B.; Adamo, C.; Jaramillo, J.; Gomperts, R.; Stratmann, R. E.; Yazyev, O.; Austin, A. J.; Cammi, R.; Pomelli, C.; Ochterski, J. W.; Ayala, P. Y.; Morokuma, K.; Voth, G. A.; Salvador, P.; Dannenberg, J. J.; Zakrzewski, V. G.; Dapprich, S.; Daniels, A. D.; Strain, M. C.; Farkas, O.; Malick, D. K.; Rabuck, A. D.; Raghavachari, K.; Foresman, J. B.; Ortiz, J. V.; Cui, Q.; Baboul, A. G.; Clifford, S.; Cioslowski, J.; Stefanov, B. B.; Liu, G.; Liashenko, A.; Piskorz, P.; Komaromi, I.; Martin, R. L.; Fox, D. J.; Keith, T.; Al-Laham, M. A.; Peng, C. Y.; Nanayakkara, A.; Challacombe, M.; Gill, P. M. W.; Johnson, B.; Chen, W.; Wong, M. W.; Gonzalez, C.; Pople, J. A. Gaussian 03, Revision C.02; Gaussian, Inc.: Wallingford, CT, 2004. Energies were corrected for zero-point energy differences (ZPVE) (unsealed).
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20
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34547937015
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Details of the syntheses, calculations, and several additional theroetical and experimental spectra are given in the Supporting Information
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Details of the syntheses, calculations, and several additional theroetical and experimental spectra are given in the Supporting Information.
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22
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0001151072
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(b) Sander, W.; Bucher, G.; Wierlacher, S. Chem. Rev. 1993, 93, 1583.
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(1993)
Chem. Rev
, vol.93
, pp. 1583
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Sander, W.1
Bucher, G.2
Wierlacher, S.3
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23
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34547938018
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Although matrices are rigid at 10 K, enabling characterization of highly reactive molecules in the presence of small amounts of trapping agents <5, warming to approximately 30 K permits diffusion of small dopants. For general details of low-temperature trapping experiments, see, for example: Bally, T. In Reactive Intermediate Chemistry; Moss, R. A, Platz, M. S, Jones, M. J, Jr, Eds, John Wiley & Sons: Hoboken, NJ, 2004; p 797
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Although matrices are rigid at 10 K, enabling characterization of highly reactive molecules in the presence of small amounts of trapping agents (<5%), warming to approximately 30 K permits diffusion of small dopants. For general details of low-temperature trapping experiments, see, for example: Bally, T. In Reactive Intermediate Chemistry; Moss, R. A., Platz, M. S., Jones, M. J., Jr., Eds.; John Wiley & Sons: Hoboken, NJ, 2004; p 797.
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25
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33947633367
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Woodcock, H. L.; Moran, D.; Brooks, B. R.; Schleyer, P.v.R.; Schaefer, H. F. J. Am. Chem. Soc. 2007, 129, 3763.
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(2007)
J. Am. Chem. Soc
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, pp. 3763
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Woodcock, H.L.1
Moran, D.2
Brooks, B.R.3
Schleyer, P.V.R.4
Schaefer, H.F.5
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26
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34547951018
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2, to lie 3.8 kcal/mol below the singlet. However, the singlet benzofuryl carbene (S replaced by O) corresponding to 2a lies 3.9 kcal/mol below the triplet. Jian Wang, unpublished results.
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2, to lie 3.8 kcal/mol below the singlet. However, the singlet benzofuryl carbene (S replaced by O) corresponding to 2a lies 3.9 kcal/mol below the triplet. Jian Wang, unpublished results.
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