13C同位素作为嗅觉识别振动理论测试的潜力。

ISRN Organic Chemistry Pub Date : 2013-05-26 eCollection Date: 2013-01-01 DOI:10.1155/2013/515810
Karel D Klika
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引用次数: 6

摘要

关于分子形状(“锁和钥匙”)理论与振动理论的气味识别基础的持续争论可能会通过测试(13)c标记的气味剂来解决。本文通过dft计算的红外振动和吉布斯自由能(ΔG)来讨论(13)C同位素体对苯乙酮和辛烷-1-醇的应用,这两种气味剂的(2)D(氘)同位素体先前已被果蝇证明与它们各自的(1)H(正常)同位素体是可分辨的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The Potential of 13C Isotopomers as a Test for the Vibrational Theory of Olfactory Sense Recognition.

The Potential of 13C Isotopomers as a Test for the Vibrational Theory of Olfactory Sense Recognition.

The Potential of 13C Isotopomers as a Test for the Vibrational Theory of Olfactory Sense Recognition.

The Potential of 13C Isotopomers as a Test for the Vibrational Theory of Olfactory Sense Recognition.

The continuing debate over the basis of odorant recognition with respect to the molecular shape ("lock and key") theory versus the vibrational theory could potentially be resolved by the testing of (13)C-labeled odorants. The application of (13)C isotopomers is discussed herein by means of DFT-calculated IR vibrations and Gibbs' free energies (ΔG) for acetophenone and octan-1-ol, two odorants for which the (2)D (deuterium) isotopomers have previously been shown to be discernible from their respective (1)H (normal) counterparts by Drosophila melanogaster.

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