Suppr超能文献

回应关于“在化学反应过程中跟踪分子迁移:没有主动推进的证据”和“点击反应成分的分子扩散率:扩散增强问题”的评论。

Response to Comment on "Following Molecular Mobility during Chemical Reactions: No Evidence for Active Propulsion" and "Molecular Diffusivity of Click Reaction Components: The Diffusion Enhancement Question".

机构信息

Department of NMR-based Structural Biology, Max Planck Institute for Multidisciplinary Sciences, Am Faßberg 11, D-37077 Göttingen, Germany.

Institut für Physikalische Biologie, Heinrich-Heine-Universität Düsseldorf, Universitätsstraße 1, D-40225 Düsseldorf, Germany.

出版信息

J Am Chem Soc. 2022 Aug 3;144(30):13441-13445. doi: 10.1021/jacs.2c02850.

Abstract

In their Comment (DOI: 10.1021/jacs.2c02965) on two related publications by our group ( , , 1380-1388; DOI: 10.1021/jacs.1c11754) and another ( , , 20884-20890; DOI: 10.1021/jacs.1c09455), Huang and Granick refer to the diffusion NMR measurements of molecules during a copper-catalyzed azide-alkyne cycloaddition (CuAAC) "click" reaction. Here we respond to their comments and maintain that no measurable diffusion enhancement was observed during the reaction. We expand on the physical arguments presented in our original Article regarding the appropriate reference state for the diffusion coefficient and present new data showing that the use of other reference states, as suggested by Huang and Granick, will still support our conclusion that the two reactants and one product of the CuAAC reaction do not exhibit boosted mobility during the reaction.

摘要

在他们对我们小组的两篇相关论文(,, 1380-1388; DOI: 10.1021/jacs.1c11754)和另一篇论文(,, 20884-20890; DOI: 10.1021/jacs.1c09455)的评论中(DOI: 10.1021/jacs.2c02965),Huang 和 Granick 提到了在铜催化叠氮-炔环加成(CuAAC)“点击”反应中扩散 NMR 测量分子的情况。在这里,我们对他们的评论做出回应,并坚持认为在反应过程中没有观察到可测量的扩散增强。我们扩展了我们原始文章中关于扩散系数适当参考状态的物理论点,并提供了新的数据,表明如 Huang 和 Granick 所建议的使用其他参考状态,仍将支持我们的结论,即 CuAAC 反应的两种反应物和一种产物在反应过程中没有表现出增强的迁移率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6a7/9354245/5da70a926a23/ja2c02850_0001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验