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Protonolysis is the cleavage of a chemical bond by acids. Many examples are found in organometallic chemistry since the reaction requires polar Mδ+-Rδ- bonds, where δ+ and δ- signify partial positive and negative charges associated with the bonding atoms. When compounds containing these bonds are treated with acid (HX), these bonds cleave: :M-R + HX → M-X + H-R Hydrolysis (X- = OH-) is a special case of protonolysis. Compounds susceptible to hydrolysis often undergo protonolysis. ==Hydrides== The borohydride anion is susceptible to reaction with even weak acids, resulting protonolysis of one or more B-H bonds. Protonolysis of sodium borohydride with acetic acid gives triacetoxyborohydride:〔Gordon W. Gribble, Ahmed F. Abdel-Magid, "Sodium Triacetoxyborohydride" Encyclopedia of Reagents for Organic Synthesis, 2007, John Wiley & Sons.〕 :NaBH4 + 3 HO2CCH3 → NaBH(O2CCH3)3 + 3 H2 Related reactions occur for hydrides of other electropositive elements, e.g. lithium aluminium hydride. 抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)』 ■ウィキペディアで「Protonolysis」の詳細全文を読む スポンサード リンク
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