Evidence map›Paper›PMID 42737804›Full record

ArticleInternational journal of molecular sciences2026

4-Oxo-7-Halosubstituted Phenanthroline Diamides Bifunctional Reactivity: A Synthetic Pathway to Unsymmetrical Polydentate Ligands.

Roman V Zonov, Nane A Avagyan, Pavel S Lemport, Vitaly A Roznyatovsky, Victor N Khrustalev, Yulia V Nelyubina, Yuri A Ustynyuk, Valentine G Nenajdenko

Abstract read
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In one paragraph

Article in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Roman V ZonovDepartment of Chemistry, Lomonosov Moscow State University, Leninskie Gory 1 Bld. 3, 119991 Moscow, Russia.
Nane A AvagyanDepartment of Chemistry, Lomonosov Moscow State University, Leninskie Gory 1 Bld. 3, 119991 Moscow, Russia.ORCID 0000-0003-0317-9416
Pavel S LemportDepartment of Chemistry, Lomonosov Moscow State University, Leninskie Gory 1 Bld. 3, 119991 Moscow, Russia.ORCID 0000-0002-4210-7901
Vitaly A RoznyatovskyDepartment of Chemistry, Lomonosov Moscow State University, Leninskie Gory 1 Bld. 3, 119991 Moscow, Russia.ORCID 0000-0002-5673-8931
Victor N KhrustalevDepartment of General and Inorganic Chemistry, Peoples' Friendship University of Russia (RUDN University), Miklukho-Maklay Str. 6, 117198 Moscow, Russia.ORCID 0000-0001-8806-2975
Yulia V NelyubinaAdvanced Engineering School, ITMO University, 9 Lomonosova Str., 191002 St. Petersburg, Russia.ORCID 0000-0002-9121-0040
Yuri A UstynyukDepartment of Chemistry, Lomonosov Moscow State University, Leninskie Gory 1 Bld. 3, 119991 Moscow, Russia.
Valentine G NenajdenkoDepartment of Chemistry, Lomonosov Moscow State University, Leninskie Gory 1 Bld. 3, 119991 Moscow, Russia.ORCID 0000-0001-9162-5169

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An efficient approach to unsymmetrical 1,10-phenanthroline-2,9-dicarboxamides based on the bifunctional reactivity of 4-oxo-7-haloderivatives is reported. These substrates exhibit orthogonal reactivity, enabling selective nucleophilic aromatic substitution at the C

Indexed as

PhenanthrolinesLigandsModels, MolecularMolecular StructureLigandsPhenanthrolinesDFTfluorineligandNMRnucleophilic substitutionphenanthrolineX-ray

Identifiers

PMID42737804
PMCPMC13566864

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.