Photolytic preparation and isomerization of thionyl imide, thiocyanic acid, thionitrous acid, and nitrogen hydroxide sulfide in an argon matrix: an experimental and theoretical study
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ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTPhotolytic preparation and isomerization of thionyl imide, thiocyanic acid, thionitrous acid, and nitrogen hydroxide sulfide in an argon matrix: an experimental and theoretical studyM. Nonella, J. Robert. Huber, and Tae Kyu. HaCite this: J. Phys. Chem. 1987, 91, 20, 5203–5209Publication Date (Print):September 1, 1987Publication History Published online1 May 2002Published inissue 1 September 1987https://pubs.acs.org/doi/10.1021/j100304a014https://doi.org/10.1021/j100304a014research-articleACS PublicationsRequest reuse permissionsArticle Views257Altmetric-Citations51LEARN 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 options Get e-Alerts
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There are four isomers with the formula HNSO, HOSN, HSNO, HONS and their corresponding anions, and all have been characterized.
“There are four isomers with the same formula (HNSO, HOSN, HSNO, HONS and their corresponding anions, respectively; Eq. 13) [56]), and all have been characterized.”
From On the chemical biology of the nitrite/sulfide interaction (2015) · cites this paper as [56]
In HSNO, the strength of the S-N bond is not substantially different from that in other nitrosothiols.
“Further calculations suggest that in HSNO the strength of the S-N bond is not substantially different from that in other nitrosothiols [55,56].”
From On the chemical biology of the nitrite/sulfide interaction (2015) · cites this paper as [56]
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- Authors
- Nonella, M., Huber, J. R., & Ha, T. K.
- ORCID
- Huber, J. Robert.
- Venue
- The Journal of Physical Chemistry
- Publisher
- American Chemical Society (ACS)
- Published
- 1987-09
- Volume
- 91
- Issue
- 20
- Pages
- 5203-5209
- ISSN
- 0022-3654 (ISSN-L)
- 1541-5740
- OpenAlex
- W1995324248
- Cited by
- 55
- References
- 0
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 3 · 2022: 2 · 2021: 1 · 2020: 3 · 2019: 2 · 2018: 4 · 2017: 5 · 2016: 7 · 2015: 1 · 2014: 3 · 2013: 1 · 2012: 1
- FWCI
- 1.54
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Physical Chemistry (publishedVersion)
- Topics
- Physical Sciences › Chemistry › Physical and Theoretical Chemistry › Chemical Reactions and Mechanisms
- Physical Sciences › Chemistry › Inorganic Chemistry › Inorganic Fluorides and Related Compounds
- Physical Sciences › Chemistry › Organic Chemistry › Synthesis and Reactivity of Sulfur-Containing Compounds
- Keywords
- thiocyanic acid, photolysis, isomerization, argon matrix isolation, sulfur-nitrogen compounds
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