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38949106877
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Compare: Emond, S. J.; Debroy, P.; Rathore, R. Org. Lett. 2008, 10, 389.
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Compare: Emond, S. J.; Debroy, P.; Rathore, R. Org. Lett. 2008, 10, 389.
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26
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64249132063
-
-
With the exception of the slight broadening in the first spectrum in Figure 1 with 0.2 equiv of Ag, which may arise due to the low concentration of [SB2, Ag+, the other spectra in Figure 1 did not show any significant line broadening to allow the extraction of a reliable Kd value. Compare: Rathore, R, Chebny, V. J, Abdelwahed, S. H. J. Am. Chem. Soc. 2004, 127, 8012
-
d value. Compare: Rathore, R.; Chebny, V. J.; Abdelwahed, S. H. J. Am. Chem. Soc. 2004, 127, 8012.
-
-
-
-
28
-
-
84869263228
-
-
3Ag in anhydrous dichloromethane (in the absence of methanol) produced a colored solution of the SB4 cation radical as judged by spectrophotometric analysis.
-
3Ag in anhydrous dichloromethane (in the absence of methanol) produced a colored solution of the SB4 cation radical as judged by spectrophotometric analysis.
-
-
-
-
29
-
-
64249086950
-
-
Owing to the poor solubility of SB1, it was not utilized in the subsequent studies.
-
(b) Owing to the poor solubility of SB1, it was not utilized in the subsequent studies.
-
-
-
-
30
-
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0032558126
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Rathore, R.; Lindeman, S. V.; Kumar, A. S.; Kochi, J. K. J. Am. Chem. Soc. 1998, 120, 6931.
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85178352889
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+ using a larger counter anion, e.g., see: Nelsen, S. F.; Ismagilov, R. F.; Powell, D. R. J. Am. Chem. Soc. 1997, 119, 10213.
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+ using a larger counter anion, e.g., see: Nelsen, S. F.; Ismagilov, R. F.; Powell, D. R. J. Am. Chem. Soc. 1997, 119, 10213.
-
-
-
-
34
-
-
84869279414
-
-
The ideal values for the sum of the intracyclic bond angles for the planar rings are the following: 3 × 60 = 180° for 3-membered cycles, 4 × 90 = 360° for 4-membered cycles, 5 × 108 = 540° for 5-membered cycles, 6 × 120 = 720° for 6-rnemhered cycles, etc. A deviation from the ideal value of the sum of the intracyclic bond angles results either in the nonplanar conformations (e.g., the chair conformation of cyclohexane) or distortion of the bonds (e.g., the banana bonds in cyclopropane).
-
The ideal values for the sum of the intracyclic bond angles for the planar rings are the following: 3 × 60 = 180° for 3-membered cycles, 4 × 90 = 360° for 4-membered cycles, 5 × 108 = 540° for 5-membered cycles, 6 × 120 = 720° for 6-rnemhered cycles, etc. A deviation from the ideal value of the sum of the intracyclic bond angles results either in the nonplanar conformations (e.g., the chair conformation of cyclohexane) or distortion of the bonds (e.g., the "banana" bonds in cyclopropane).
-
-
-
-
38
-
-
35348838961
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Comparera Banerjee, M.; Emond, S. J.; Lindeman, S. V.; Rathore, R J. Org. Chem. 2007, 72, 8054.
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Comparera) Banerjee, M.; Emond, S. J.; Lindeman, S. V.; Rathore, R J. Org. Chem. 2007, 72, 8054.
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39
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0037414526
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34447122719
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Banerjee, M.; Lindeman, S. V.; Rathore, R. J. Am. Chem. Soc. 2007, 129, 8070.
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41
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33947091062
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For example
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For example: Momicchioli, F.; Bruni, M. C.; Baraldi, I. J. Phys. Chem. 1972, 26, 3983.
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