溴氯氟甲烷事件。

Enantiomer Pub Date : 2000-01-01
J Crassous, A Collet
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引用次数: 0

摘要

通过对溴氯氟乙酸士的宁盐(FClBrCCO2H)的分馏结晶,合成了具有光学活性的溴氯氟甲烷(CHFClBr)样品。通过x射线晶体学建立了酸的S-(+) (R-(-))绝对构型,并利用拉曼光学活性(ROA)和手性隐烷- c对CHFClBr的对映选择性分子识别过程的分子模型确定了卤仿的S-(+) (R-(-))绝对构型。从这些立体化学分配中可以观察到,分别从S-(+)-和R-(-)- fclbrcco2h得到S-(+)-和R-(-)- chfclbr的脱羧作用发生在构型保留的情况下。最后,对CHFClBr进行了第一次宇称违反(PV)测试,并得出了这种小的立体物理效应的上界。
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The bromochlorofluoromethane saga.

Synthesis of optically active samples of bromochlorofluoromethane (CHFClBr) was performed via fractional crystallisation of the strychnine salts of bromochlorofluoroacetic acid (FClBrCCO2H). The S-(+) (R-(-)) absolute configuration of the acid was established by X-ray crystallography and the S-(+) (R-(-)) absolute configuration of the haloform was determined using Raman Optical Activity (ROA) and molecular modelling of the enantioselective molecular recognition process of CHFClBr by the chiral cryptophane-C. From these stereochemical assignments it was observed that the decarboxylation used to obtain S-(+)- and R-(-)-CHFClBr from respectively S-(+)- and R-(-)-FClBrCCO2H occurred with retention of configuration. Finally, the first parity violation (PV) test on CHFClBr was performed and yielded an upper bound for this small stereophysical effect.

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