4,7-Functionalization of Tetradentate Phenanthroline Ligands via Nucleophilic Substitution of Fluorine Full article
| Journal |
Journal of Organic Chemistry
ISSN: 1520-6904 , E-ISSN: 0022-3263 |
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| Output data | Year: 2026, Volume: 91, Number: 1, Pages: 302-315 Pages count : 14 DOI: 10.1021/acs.joc.5c02395 | ||||||
| Authors |
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| Affiliations |
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Funding (1)
| 1 | N. D. Zelinsky Institute of Organic Chemistry Russian Academy of Sciences |
Abstract:
An effective pathway for the functionalization of 1,10-phenanthroline-2,9-dicarboxamides (DAPhen) to positions 4 and 7 of the heterocyclic backbone by nucleophilic aromatic substitution was developed. The developed approach makes it possible to introduce various functional groups of almost any nature into positions 4 and 7 of the phenanthroline nucleus. The introduction of reactive functional groups, such as the azide group, has allowed for further functionalization. Thus, a set of novel symmetrically or unsymmetrically 4,7-disubstituted DAPhen ligands was prepared.
Cite:
Zonov R.V.
, Avagyan N.A.
, Lemport P.S.
, Khrustalev V.N.
, Roznyatovsky V.A.
, Ustynyuk Y.A.
, Nenajdenko V.G.
4,7-Functionalization of Tetradentate Phenanthroline Ligands via Nucleophilic Substitution of Fluorine
Journal of Organic Chemistry. 2026. V.91. N1. P.302-315. DOI: 10.1021/acs.joc.5c02395 WOS Scopus OpenAlex
4,7-Functionalization of Tetradentate Phenanthroline Ligands via Nucleophilic Substitution of Fluorine
Journal of Organic Chemistry. 2026. V.91. N1. P.302-315. DOI: 10.1021/acs.joc.5c02395 WOS Scopus OpenAlex
Dates:
| Submitted: | Sep 23, 2025 |
| Published online: | Jan 9, 2026 |
Identifiers:
| Web of science: | WOS:001644816300001 |
| Scopus: | 2-s2.0-105027184359 |
| OpenAlex: | W7116663377 |
Citing:
| DB | Citing |
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| OpenAlex | Нет цитирований |
| Scopus | Нет цитирований |