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1.·Ö±ðÑо¿ÁËTpRu(PPh3)2£¨OH£©´ß»¯Ë®»¯ÒÒëæºÍÄ©¶ËȲÌþµÄ·´Ó¦¡££¨1£©´ß»¯Ë®»¯ÒÒëæ£ºÑо¿·¢ÏÖÔÚ¸ÉÔïµÄTHFÈÜÒºÖжÔÒÒëæ½øÐд߻¯Ë®»¯£¬ÒÒëæ²¢Ã»Óз¢Éúת»¯¡£¶øÔÚÌí¼ÓÊÊÁ¿H2Oºó£¬·´Ó¦Éú³ÉÁËÔ¤²âµÄ²úÎïÒÒõ£°·¡£Õâ˵Ã÷£¬Ë®×÷ÓöԴ߻¯Ë®»¯·´Ó¦µÄÓ°ÏìºÜ´ó¡£´ß»¯»úÀí±íÃ÷£¬PPh3ÅäÌåµÄ¿Õ¼äλ×è½Ï´ó£¬Ìí¼ÓµÄÒÒëæÊ×ÏÈÈ¡´úÅäºÏÎïµÄPPh3ÅäÌåÉú³ÉTpRu(PPh3)£¨CH3CN£©£¨OH£©£¬È»ºó¼ÓÈëÊÊÁ¿H2OÓëÅäºÏÎïµÄOHÅäÌåÐγÉÇâ¼ü£¬H2OµÄôÇ»ùÑõÔ­×ÓÇ׺˽ø¹¥ÒÒëæÅäÌåµÄëæ»ù̼ԭ×Ó£¬¾­¹ýÏ©´¼Ê½ÖØÅÅÉú³ÉTpRu(PPh3)(H2O)(NHCOMe)£¬×îºóÒÒëæÈ¡´úH2OÅäÌå¾­¹ýÑ­»··´Ó¦Éú³ÉÒÒõ£°·¡£ÔÚÌí¼ÓPPh3ºÍ¹ýÁ¿H2Oºó£¬¶¼»áÒòΪ×è°­ÒÒëæµÄÈ¡´ú¶ø½µµÍת»¯ÂÊ¡££¨2£©´ß»¯Ë®»¯Ä©¶ËȲÌþ£ºÊµÑ齫TpRu(PPh3)2£¨OH£©ºÍTpRu(PPh3)£¨CH3CN£©£¨OH£©·Ö±ð´ß»¯Ë®»¯±½ÒÒȲºÍÕý¼ºÈ²£¬¾­¹ý¶Ô±È·ÖÎö£¬·¢ÏÖ´ß»¯Ë®»¯´øÓй©µç×Ó»ùÍŵÄÄ©¶ËȲÌþµÄ²úÂÊÒª¸ßÓÚ´øÓÐÎüµç×Ó»ùÍŵÄÄ©¶ËȲÌþ£¬±½ÒÒȲµÄ±½»·ÓëȲÌþ̼ÐγÉP-¦Ð¹²éʹµÃ̼µÄµç¸ºÐÔ±äС²»Ò×ÓëîÉÖÐÐĽáºÏ¡£´ËÍ⣬PPh3ÅäÌåµÄ¿Õ¼äЧӦ×è°­ÁËȲÌþÓëTpRu(PPh3)2£¨OH£©µÄ½áºÏ£¬Ó°Ïì´ß»¯Ë®»¯·´Ó¦µÄ½øÐС£

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3Â¥2011-05-15 09:57:54
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sunxuefei(½ð±Ò+60, ·­ÒëEPI+1): 2011-05-15 14:43:43
the catalytic hydration of  acetonitrile and terminal alkynes byTpRu(PPh3)2£¨OH£©have been studied.(1)the catalytic hydration of  acetonitrile: Researches indicated that the acetonitrile conversion did not happen in the anhydrous THF. while adding some water to THF, Acetamide was formed. this indicated that water plays an important role in this reaction.
2Â¥2011-05-15 09:56:52
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Catalytic mechanism shows that the stereo-hindrance effect of PPh3 is remarkable.TpRu(PPh3)£¨CH3CN£©£¨OH£©was produced by ligand exchange reaction of acetonitrile and PPh3.
4Â¥2011-05-15 10:06:49
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chemistry2228

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then the hydrogen-bond between H2O and OH was formed. after the oxygen atom of water nucleophilic attack the carbon atom of cyano, TpRu(PPh3)(H2O)(NHCOMe) was formed by a phosphoenol rearrangement. finally, Acetamide was produced by Cyclic reaction which nvolved  the exchange of acetonitrile and H2O.
5Â¥2011-05-15 10:21:45
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