On the chemistry of 1-pyrroline in solution and in the gas phase

Abstract 1-Pyrroline has a highly characteristic odor, which is employed by living organisms for chemical signaling and other purposes, but the mechanism whereby this odor is formed remains poorly understood. Here we used a combination of ambient mass spectrometry (AMS) and nuclear magnetic resonanc...

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Main Authors: Xiaoping Zhang, Konstantin Chingin, Dacai Zhong, Juchao Liang, Yongzhong Ouyang, Huanwen Chen
Format: Article
Language:English
Published: Nature Publishing Group 2017-08-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-017-08217-1
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spelling doaj-88e6c7faa2d54a46a70bc3d23e1690b32020-12-08T01:03:53ZengNature Publishing GroupScientific Reports2045-23222017-08-01711810.1038/s41598-017-08217-1On the chemistry of 1-pyrroline in solution and in the gas phaseXiaoping Zhang0Konstantin Chingin1Dacai Zhong2Juchao Liang3Yongzhong Ouyang4Huanwen Chen5Jiangxi Key Laboratory for Mass Spectrometry and Instrumentation, East China University of TechnologyJiangxi Key Laboratory for Mass Spectrometry and Instrumentation, East China University of TechnologyJiangxi Key Laboratory for Mass Spectrometry and Instrumentation, East China University of TechnologyJiangxi Key Laboratory for Mass Spectrometry and Instrumentation, East China University of TechnologyJiangxi Key Laboratory for Mass Spectrometry and Instrumentation, East China University of TechnologyJiangxi Key Laboratory for Mass Spectrometry and Instrumentation, East China University of TechnologyAbstract 1-Pyrroline has a highly characteristic odor, which is employed by living organisms for chemical signaling and other purposes, but the mechanism whereby this odor is formed remains poorly understood. Here we used a combination of ambient mass spectrometry (AMS) and nuclear magnetic resonance (NMR) spectroscopy to experimentally address the mechanistic aspects of 1-pyrroline volatility and other controversies regarding the chemistry of this compound. Our results indicate that in solution the volatility of the monomer species is significantly higher than that of the trimer species, and 1-pyrroline is evaporated mainly in its monomer state. Neat 1-pyrroline is essentially the pure trimer and displays ca. 100-fold lower evaporation rate than the monomer state in solution. In the gas-phase the trimer species is irreversibly decomposed into monomer species. Under equilibrium conditions the vapor of 1-pyrroline entirely consists of monomer species. The evaporation rate of 1-pyrroline in water has a step-wise dependence on the solution pH, the abrupt increase in volatility (>1,000-fold) occurring around the pKa value of 1-pyrroline (6.8). The pronounced step-wise dependence of 1-pyrroline volatility around neutral pH may also be an important evolutionary factor allowing living systems to regulate the odor strength from very weak to very strong with minimal efforts.https://doi.org/10.1038/s41598-017-08217-1
collection DOAJ
language English
format Article
sources DOAJ
author Xiaoping Zhang
Konstantin Chingin
Dacai Zhong
Juchao Liang
Yongzhong Ouyang
Huanwen Chen
spellingShingle Xiaoping Zhang
Konstantin Chingin
Dacai Zhong
Juchao Liang
Yongzhong Ouyang
Huanwen Chen
On the chemistry of 1-pyrroline in solution and in the gas phase
Scientific Reports
author_facet Xiaoping Zhang
Konstantin Chingin
Dacai Zhong
Juchao Liang
Yongzhong Ouyang
Huanwen Chen
author_sort Xiaoping Zhang
title On the chemistry of 1-pyrroline in solution and in the gas phase
title_short On the chemistry of 1-pyrroline in solution and in the gas phase
title_full On the chemistry of 1-pyrroline in solution and in the gas phase
title_fullStr On the chemistry of 1-pyrroline in solution and in the gas phase
title_full_unstemmed On the chemistry of 1-pyrroline in solution and in the gas phase
title_sort on the chemistry of 1-pyrroline in solution and in the gas phase
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2017-08-01
description Abstract 1-Pyrroline has a highly characteristic odor, which is employed by living organisms for chemical signaling and other purposes, but the mechanism whereby this odor is formed remains poorly understood. Here we used a combination of ambient mass spectrometry (AMS) and nuclear magnetic resonance (NMR) spectroscopy to experimentally address the mechanistic aspects of 1-pyrroline volatility and other controversies regarding the chemistry of this compound. Our results indicate that in solution the volatility of the monomer species is significantly higher than that of the trimer species, and 1-pyrroline is evaporated mainly in its monomer state. Neat 1-pyrroline is essentially the pure trimer and displays ca. 100-fold lower evaporation rate than the monomer state in solution. In the gas-phase the trimer species is irreversibly decomposed into monomer species. Under equilibrium conditions the vapor of 1-pyrroline entirely consists of monomer species. The evaporation rate of 1-pyrroline in water has a step-wise dependence on the solution pH, the abrupt increase in volatility (>1,000-fold) occurring around the pKa value of 1-pyrroline (6.8). The pronounced step-wise dependence of 1-pyrroline volatility around neutral pH may also be an important evolutionary factor allowing living systems to regulate the odor strength from very weak to very strong with minimal efforts.
url https://doi.org/10.1038/s41598-017-08217-1
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