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首页> 外文期刊>Tetrahedron >Alkyl and dialkylammonium tetrafluoroborate catalyzed cis-trans isomerization of 1,3,5-trimethyl-1,3,5-triphenyleyclotrisiloxane
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Alkyl and dialkylammonium tetrafluoroborate catalyzed cis-trans isomerization of 1,3,5-trimethyl-1,3,5-triphenyleyclotrisiloxane

机译:烷基和四氟硼酸二烷基铵催化1,3,5-三甲基-1,3,5-三苯基环三硅氧烷的顺反异构化

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摘要

Alkyl and dialkylammonium tetrafluoroborate promoted cis-trans isomerization of 1,3,5-trimethyl-1,3,5-triphenylcyclotrisiloxane (1) in DMSO-d(6) were studied. The isomerization equilibrium constant K are within the range of 3.74-3.30 from 22 to 47 degreesC. Thermodynamic parameters of DeltaHdegrees and DeltaSdegrees for the isomerization were -0.95 kcal/mol and -0.59 cal/mol-K respectively. The isomerization rate is first order in [cis-1] and second order in [RnNH4-nBF4]. Both components of RnNH4-n+ and BF4- are essential for the catalytic cis-trans isomerization. The catalytic strength follows the decreasing order of +H3N(CH2)(6)NH3+ > n-C8H17NH3+ > n-C16H33NH3+ > Me3CNH3+ > PhCH2NH3+ > Et2NH2+ much greater than Ph2CHNH3+, Et3NH+. Inversion region was observed in the plot of ln(k(f)/T) versus (1/T) with the ceiling located at around 38 degreesC. The positive activation enthalpy of 9 kcal/mol was estimated at 22-32 degreesC. The activation enthalpy turns to be slightly negative at T > 38 degreesC. (C) 2004 Elsevier Ltd. All rights reserved.
机译:研究了烷基和四氟硼酸二烷基铵促进1,3,5-三甲基-1,3,5-三苯基环三硅氧烷(1)在DMSO-d(6)中的顺反异构化。 22〜47℃下的异构化平衡常数K在3.74〜3.30的范围内。用于异构化的ΔH度和ΔS度的热力学参数分别为-0.95kcal / mol和-0.59cal / mol-K。异构化速率在[cis-1]中为一阶,在[RnNH4-nBF4]中为二阶。 RnNH4-n +和BF4-的两个组分对于催化顺反异构化都是必不可少的。催化强度遵循+ H3N(CH2)(6)NH3 +> n-C8H17NH3 +> n-C16H33NH3 +> Me3CNH3 +> PhCH2NH3 +> Et2NH2 +的降序,远大于Ph2CHNH3 +,Et3NH +。在ln(k(f)/ T)与(1 / T)的关系图中可以看到反转区域,最高温度位于38摄氏度左右。在22-32℃下估计为9kcal / mol的正活化焓。在T> 38摄氏度时,激活焓略微变为负。 (C)2004 Elsevier Ltd.保留所有权利。

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