Cited by 274Chemical Reaction MechanismsOrganophosphorus compounds synthesisPhosphorus compounds and reactions

The Acid Strength of Mono and Diesters of Phosphoric Acid. The n-Alkyl Esters from Methyl to Butyl, the Esters of Biological Importance, and the Natural Guanidine Phosphoric Acids

Kumler, W. D., Eiler, John J.·1943·Journal of the American Chemical Society

Abstract

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTThe Acid Strength of Mono and Diesters of Phosphoric Acid. The n-Alkyl Esters from Methyl to Butyl, the Esters of Biological Importance, and the Natural Guanidine Phosphoric AcidsW. D. Kumler and John J. EilerCite this: J. Am. Chem. Soc. 1943, 65, 12, 2355–2361Publication Date (Print):December 1, 1943Publication History Published online1 May 2002Published inissue 1 December 1943https://pubs.acs.org/doi/10.1021/ja01252a028https://doi.org/10.1021/ja01252a028research-articleACS PublicationsRequest reuse permissionsArticle Views2202Altmetric-Citations220LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-Alertsclose Get e-Alerts

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Crossref · 10.1021/ja01252a028

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  • Methanesulfonate based ionic liquids [C2C1im][MeSO3] and [C4C1im][MeSO3] are stable at 140 °C and only slowly degrade at 200 °C.

    “The same study showed methanesulfonate based ionic liquids [C 2 C 1 im][MeSO 3 ] and [C 4 C 1 im][MeSO 3 ] to be stable at 140 °C and to only slowly degrade at 200 °C.”

    From Deconstruction of lignocellulosic biomass with ionic liquids (2013) · cites this paper as [176]

  • [C2C1im]Cl and [C4C1im]Cl are long-term stable at 120 °C and show signs of decomposition at 140 °C.

    “[C 2 C 1 im]Cl and [C 4 C 1 im]Cl are longterm stable at 120 °C and show signs of decomposition at 140 °C.176”

    From Deconstruction of lignocellulosic biomass with ionic liquids (2013) · cites this paper as [176]

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Authors
Kumler, W. D., & Eiler, J. J.
Venue
Journal of the American Chemical Society
Published
1943-12
Volume
65
Issue
12
Pages
2355-2361
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
OpenAlex
W2062773033
Cited by
274
References
0
Citations by year
2026: 6 · 2025: 6 · 2024: 12 · 2023: 7 · 2022: 7 · 2021: 12 · 2020: 8 · 2019: 6 · 2018: 6 · 2017: 7 · 2016: 12 · 2015: 12 · 2014: 10 · 2013: 10 · 2012: 8
FWCI
2.05
Type
journal article
Language
en
Open access
closed
Locations
Journal of the American Chemical Society (publishedVersion)
Topics
  • Physical Sciences › Chemistry › Organic Chemistry › Chemical Reaction Mechanisms
  • Physical Sciences › Chemistry › Organic Chemistry › Organophosphorus compounds synthesis
  • Physical Sciences › Chemistry › Organic Chemistry › Phosphorus compounds and reactions
Keywords
phosphate esters, acid strength, monoesters, diesters, pKa

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