Evidence map›Paper›PMID 36770641›Full record

ArticleMolecules (Basel, Switzerland)2023

Differentiation between Isomeric 4,5-Functionalized 1,2,3-Thiadiazoles and 1,2,3-Triazoles by ESI-HRMS and IR Ion Spectroscopy.

Dmitrii M Mazur, Elettra L Piacentino, Giel Berden, Jos Oomens, Victor Ryzhov, Vasiliy A Bakulev, Albert T Lebedev

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Dmitrii M MazurOrganic Chemistry Department, Lomonosov Moscow State University, 119992 Moscow, Russia.ORCID 0000-0002-9780-1490
Elettra L PiacentinoDepartment of Chemistry and Biochemistry, Northern Illinois University, DeKalb, IL 60115, USA.
Giel BerdenFELIX Laboratory, Institute for Molecules and Materials, Radboud University, Toernooiveld 7, 6525 ED Nijmegen, The Netherlands.
Jos OomensFELIX Laboratory, Institute for Molecules and Materials, Radboud University, Toernooiveld 7, 6525 ED Nijmegen, The Netherlands.
Victor RyzhovDepartment of Chemistry and Biochemistry, Northern Illinois University, DeKalb, IL 60115, USA.ORCID 0000-0001-6041-9821
Vasiliy A BakulevTechnology of Organic Synthesis Department, Ural Federal University, 620002 Yekaterinburg, Russia.
Albert T LebedevOrganic Chemistry Department, Lomonosov Moscow State University, 119992 Moscow, Russia.ORCID 0000-0002-6459-9484

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A large variety of 1,2,3-thiadiazoles and 1,2,3-triazoles are used extensively in modern pure and applied organic chemistry as important structural blocks of numerous valuable products. Creation of new methods of synthesis of these isomeric compounds requires the development of reliable analytical tools to reveal the structural characteristics of these novel compounds, which are able to distinguish between isomers. Mass spectrometry (MS) is a clear choice for this task due to its selectivity, sensitivity, informational capacity, and reliability. Here, the application of electrospray ionization (ESI) with ion detection in positive and negative modes was demonstrated to be useful in structural studies. Additionally, interconversion of isomeric 4,5-functionalized 1,2,3-triazoles and 1,2,3-thiadiazoles was demonstrated. Application of accurate mass measurements and tandem mass spectrometry in MS2 and MS3 modes indicated the occurrence of gas-phase rearrangement of 1,2,3-triazoles into 1,2,3-thiadiazoles under (+)ESI-MS/MS conditions, independent of the nature of substituents, in line with the reaction in the condensed phase. Infrared multiple photon dissociation (IRMPD) spectroscopy enabled the establishment of structures of some of the most crucial common fragment ions, including [M+H-N

Indexed as

1,2,3-thiadiazoles1,2,3-triazoleselectrospray ionizationisomer identificationmass spectrometry

Identifiers

PMID36770641
PMCPMC9920699

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