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A number of these bases are commercially available by Fluka Chemie AG, Switzerland
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[14p] A number of these bases are commercially available by Fluka Chemie AG, Switzerland.
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71
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33749128340
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Commercially available by Fluka Chemie AG, Switzerland
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Commercially available by Fluka Chemie AG, Switzerland.
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75
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33749134650
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Synthesis 1979, 811-813.
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a polymeric base derived from MTBD is commercially available from Fluka Chemie AG, Switzerland
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[28b] K. Iijima, W. Fukuda, M. Tomoi, J. Macromol. Sci., Pure Appl. Chem. 1992, A 29, 249-261; a polymeric base derived from MTBD is commercially available from Fluka Chemie AG, Switzerland.
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Iijima, K.1
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85085781559
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-
note
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[1b]. We feel that the term "sponge" fits better to an insoluble material.
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81
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33749143456
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commercially available by Fluka Chemie AG, Switzerland
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"Reagent of the Year" 1992; commercially available by Fluka Chemie AG, Switzerland.
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(1992)
Reagent of the Year
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83
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0342293503
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3042988525
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[34] for NH hydrogen gave better results than the corresponding MM2 parameters and were therefore also applied for the phosphazene systems.
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[34] for NH hydrogen gave better results than the corresponding MM2 parameters and were therefore also applied for the phosphazene systems.
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33749120332
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unpublished results
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M. Keller, R. Link, unpublished results. Unfortunately, the quality of the structure was not sufficient to justify a presentation within this paper.
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Keller, M.1
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[37c] L. B. Handy, J. K. Ruff, L. F. Dahl, J. Am. Chem. Soc. 1970, 92, 7327-7337.
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33749149278
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Semiempirical and ab initio calculations on proton affinities of phosphazene bases are on the way: I. A. Koppel, R. W. Taft, R. Kurg, T. Rodima, R. Schwesinger
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Semiempirical and ab initio calculations on proton affinities of phosphazene bases are on the way: I. A. Koppel, R. W. Taft, R. Kurg, T. Rodima, R. Schwesinger.
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94
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33749152355
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Ph. D. Thesis, University of Freiburg
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C. Hasenfratz, Ph. D. Thesis, University of Freiburg, 1995.
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Hasenfratz, C.1
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0041403370
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J. Braun, C. Hasenfratz, R. Schwesinger, H.-H. Limbach, Angew. Chem. 1994, 106, 2302-2304;
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33947482832
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Absolute scale, based on 1,4-diaminobutane = 20.12: J. F. Coetzee, G. R. Padmanabhan, J. Am. Chem. Soc. 1965, 87, 5005-5010;
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85085780747
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note
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[45] employing the hexafluorophosphate salts.
-
-
-
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101
-
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85085780711
-
-
note
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[9,17].
-
-
-
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102
-
-
85085782019
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-
note
-
[9,17,18].
-
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103
-
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85085781016
-
-
note
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[43] from measurements in benzene or fluorobenzene by UV/Vis-spectroscopically controlled deprotonation of triphenylmethane, 9-phenylxanthene, or tetraphenylporphyrine; details will be published elsewhere.
-
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-
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104
-
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85085782498
-
-
note
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[50].
-
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107
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0001475343
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For a discussion of resonance saturation in conjugated hydrocarbon anions see: M. Tolbert, M. E. Ogle, J. Am. Chem. Soc. 1990, 112, 9519-9527.
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110
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33749144322
-
-
note
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[17]. The value for methyl phenyl sulfoxide has been extrapolated from the values for DMSO and for the corresponding sulfones.
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