• Watanabe, N. et al.: Ecotoxic. Env. Safety, 11, 174 (2009)
• Radeva, E. et al.: J. Optoelec. Adv. Mat., 11, 1432 (2009)
• Gandhiraman, R.P. et al.: Plama Proc. Polym., 11, 1432 (2009)
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Reacts with P2O5 to give trimethylsilyl polyphosphate ('PPSE'), a milder and more convenient dehydrating agent then polyphosphoric acid. For examples, and related reagents, see Phosphorus(V) oxide, A13348.• In the presence of FeCl3, reacts with benzotrichlorides to give substituted benzoyl chlorides in good yields: J. Chem. Soc., Chem. Commun., 808 (1977).
• Silylates primary and sec-alcohols and phenols, in the presence of p-TsOH as catalyst. If the substrate contains acid-sensitive groups, PPTS can be used: Tetrahedron Lett., 4261 (1978). See Appendix 4.