Cited by 18Synthesis and Reactivity of Sulfur-Containing CompoundsInorganic and Organometallic ChemistrySynthesis and characterization of novel inorganic/organometallic compounds

Untersuchung der Umsetzung von Schwefel mit Natriumnitrit in DMF, DMSO und HMPT

Seel, F., Simon, G., Schuh, J., Wagner, M., Wolf, B., Ruppert, I., Wieckowski, A. B.·1986·Zeitschrift für anorganische und allgemeine Chemie

Abstract

Abstract Durch VIS/UV‐, IR‐,15N‐NMR‐ und ESR‐spektrometrische Messungen, sowie chromatographische und Gas‐Analysen ist der Mechanismus der Titelreaktion aufgeklärt worden. Der Verlauf der komplexen Umsetzung und die groβe Anzahl von Produkten — Distickstoffoxid, Stickstoffmonoxid, Natriumthiosulfat, Sulfat, Polysulfide, Polythionate, Nitrat — können mit der Annahme erklärt werden, daß zunächst Natriumperthionitrate NaSxNO2entstehen, die sich in Distickstoffoxid und Thiosulfat zersetzen, oder auch mit Nitrit zu Nitrat und Perthionitrit, NaSSNO, reagieren, das reversibel in Stickoxid und Natriumtrisulfid(1—) dissoziiert. (Bezüglich der Einzelheiten der konkurrierenden und aufeinander folgenden Reaktionsschritte vgl. Tab. 2.) Der charakteristische Farbwechsel während der Titelreaktion von blau‐grün über braun nach orangerot ist auf die Entstehung zweier Farbträger zurückzuführen: S3−(blau, λmax= 620 nm, g = 2,029) und ONSS−(rot, λmax= 448 nm, δ(15N) = 334 ppm, bez. auf K15NO3).

Integrity signals

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Crossref · 10.1002/zaac.19865380718

Cites

16 of 16 references verified0 citation errors · 0 not checkable

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  • The reaction of nitrite with polysulfide or sulfur in aqueous solution does not occur, although it is predicted to be thermodynamically favorable and highly exothermic.

    “The reaction of nitrite with polysulfide or sulfur in aqueous solution, although predicted to be thermodynamically favorable and highly exothermic [68], does not occur.”

    From On the chemical biology of the nitrite/sulfide interaction (2015) · cites this paper as [68]

  • Nitrite reacts very efficiently with elemental sulfur in polar aprotic solvents under deaerated conditions, and the reaction leads to formation of NO and N2O.

    “Indeed nitrite reacts very efficiently with elemental sulfur in polar aprotic solvents (albeit not in water [66][67][68]) under deaerated conditions [66,67], and according to Seel et al. [68], the reaction leads to formation of NO and N2O.”

    From On the chemical biology of the nitrite/sulfide interaction (2015) · cites this paper as [68]

  • The NO-containing yellow compound formed from nitrite and S8 is assigned to be nitrosopersulfide, SSNO-.

    “Based on Seel's earlier findings [58,68,69] we assign this product to be nitrosopersulfide, SSNO - [19].”

    From On the chemical biology of the nitrite/sulfide interaction (2015) · cites this paper as [68]

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Authors
Seel, F., Simon, G., Schuh, J., Wagner, M., Wolf, B., Ruppert, I., & Wieckowski, A. B.
Affiliations
  • Saarland University (DE)
  • University of Bonn (DE)
Corresponding author
Seel, F.
Venue
Zeitschrift für anorganische und allgemeine Chemie
Publisher
Wiley
Published
1986-07
Volume
538
Issue
7
Pages
177-190
ISSN
  • 0044-2313 (ISSN-L)
  • 1521-3749
OpenAlex
W2058090379
Cited by
18
References
16
Citations by year
2025: 2 · 2024: 1 · 2022: 1 · 2020: 1 · 2018: 1 · 2017: 2 · 2016: 2 · 2014: 1
FWCI
0.56
Type
journal article
Language
en
Open access
closed
Locations
Zeitschrift für anorganische und allgemeine Chemie (publishedVersion)
Topics
  • Physical Sciences › Chemistry › Organic Chemistry › Synthesis and Reactivity of Sulfur-Containing Compounds
  • Physical Sciences › Chemistry › Organic Chemistry › Inorganic and Organometallic Chemistry
  • Physical Sciences › Chemistry › Inorganic Chemistry › Synthesis and characterization of novel inorganic/organometallic compounds
Keywords
sodium nitrite, reaction mechanism, polysulfides, polythionates, sodium thiosulfate, dinitrogen monoxide, nitric oxide, 15N NMR, electron spin resonance, color change, DMF, dimethyl sulfoxide, HMPT

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