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Prototropic Tautomerism of 3-Nitro- and 5-Nitrosalicylidene-3-picolylimines

Prototropic Tautomerism of 3-Nitro- and 5-Nitrosalicylidene-3-picolylimines

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2676582149

Prototropic Tautomerism of 3-Nitro- and 5-Nitrosalicylidene-3-picolylimines

About this item

Full title

Prototropic Tautomerism of 3-Nitro- and 5-Nitrosalicylidene-3-picolylimines

Publisher

Moscow: Pleiades Publishing

Journal title

Russian journal of general chemistry, 2022-05, Vol.92 (5), p.750-758

Language

English

Formats

Publication information

Publisher

Moscow: Pleiades Publishing

More information

Scope and Contents

Contents

Synthesis, X-ray diffraction and spectroscopic analysis (IR,
1
H,
13
C,
15
N NMR) of azomethines derived from 3-nitro- and 5-nitrosalicylic aldehyde and 3-picolylamine were carried out. In crystals both molecules are realized in ketoamine (quinoid) tautomeric form. The structures of azomethines are stabilized by strong intramolecu...

Alternative Titles

Full title

Prototropic Tautomerism of 3-Nitro- and 5-Nitrosalicylidene-3-picolylimines

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_journals_2676582149

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2676582149

Other Identifiers

ISSN

1070-3632

E-ISSN

1608-3350

DOI

10.1134/S1070363222050024

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