ijms-logo

Journal Browser

Journal Browser

Advanced Ligands for Coordination Chemistry

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Physical Chemistry and Chemical Physics".

Deadline for manuscript submissions: closed (30 September 2023) | Viewed by 4401

Special Issue Editor


E-Mail Website
Guest Editor
Department of Chemistry, Lomonosov Moscow State University, 119991 Moscow, Russia
Interests: organic chemistry; synthesis; fluorine; nitrogen; heterocycle; isocyanide; multicomponent reaction
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues, 

Coordination chemistry is a huge and very important field in modern chemical science. Coordination compounds are integral in modern catalytic transformations, material science, separation technologies, biological processes, and other fields. In principle, the classical coordination compound consists of two parts: the metal cation and the ligand(s). The Periodic Table displays a restricted amount of metals. In contrast, the design and synthesis of new ligands have established new frontiers in coordination chemistry. Therefore, this Special Issue focuses on the ligands used for coordination chemistry. All fundamental or practically oriented aspects of this field within this Special Issue include the design, synthesis, and study of coordination properties of ligands; their use for separation techniques; the photo-physical properties of ligands and their complexes; and many others. All colleagues active in this field are invited to contribute to this Special Issue by presenting original papers or short reviews in the field.

Prof. Dr. Valentine G. Nenajdenko
Guest Editor

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. International Journal of Molecular Sciences is an international peer-reviewed open access semimonthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. There is an Article Processing Charge (APC) for publication in this open access journal. For details about the APC please see here. Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • ligand
  • complex
  • separation
  • coordination chemistry
  • extraction
  • lanthanide
  • actinide
  • metal

Benefits of Publishing in a Special Issue

  • Ease of navigation: Grouping papers by topic helps scholars navigate broad scope journals more efficiently.
  • Greater discoverability: Special Issues support the reach and impact of scientific research. Articles in Special Issues are more discoverable and cited more frequently.
  • Expansion of research network: Special Issues facilitate connections among authors, fostering scientific collaborations.
  • External promotion: Articles in Special Issues are often promoted through the journal's social media, increasing their visibility.
  • e-Book format: Special Issues with more than 10 articles can be published as dedicated e-books, ensuring wide and rapid dissemination.

Further information on MDPI's Special Issue polices can be found here.

Published Papers (2 papers)

Order results
Result details
Select all
Export citation of selected articles as:

Research

19 pages, 8552 KiB  
Article
First 24-Membered Macrocyclic 1,10-Phenanthroline-2,9-Diamides—An Efficient Switch from Acidic to Alkaline Extraction of f-Elements
by Pavel S. Lemport, Valentine S. Petrov, Petr I. Matveev, Uliana M. Leksina, Vitaly A. Roznyatovsky, Igor P. Gloriozov, Alexandr V. Yatsenko, Viktor A. Tafeenko, Pavel V. Dorovatovskii, Viktor N. Khrustalev, Gleb S. Budylin, Evgeny A. Shirshin, Vitaliy Yu. Markov, Alexey A. Goryunkov, Vladimir G. Petrov, Yuri A. Ustynyuk and Valentine G. Nenajdenko
Int. J. Mol. Sci. 2023, 24(12), 10261; https://doi.org/10.3390/ijms241210261 - 17 Jun 2023
Cited by 6 | Viewed by 2151
Abstract
A reaction of acyl chlorides derived from 1,10-phenanthroline-2,9-dicarboxylic acids with piperazine allows the preparation of the corresponding 24-membered macrocycles in good yield. The structural and spectral properties of these new macrocyclic ligands were thoroughly investigated, revealing promising coordination properties towards f-elements (Am, Eu). [...] Read more.
A reaction of acyl chlorides derived from 1,10-phenanthroline-2,9-dicarboxylic acids with piperazine allows the preparation of the corresponding 24-membered macrocycles in good yield. The structural and spectral properties of these new macrocyclic ligands were thoroughly investigated, revealing promising coordination properties towards f-elements (Am, Eu). It was shown that the prepared ligands can be used for selective extraction of Am(III) from alkaline–carbonate media in presence of Eu(III) with an SFAm/Eu up to 40. Their extraction efficiency is higher than calixarene-type extraction of the Am(III) and Eu(III) pair. Composition of macrocycle–metal complex with Eu(III) was investigated by luminescence and UV-vis spectroscopy. The possibility of such ligands to form complexes of L:Eu = 1:2 stoichiometry is revealed. Full article
(This article belongs to the Special Issue Advanced Ligands for Coordination Chemistry)
Show Figures

Figure 1

14 pages, 3837 KiB  
Article
Pyrrolidine-Derived Phenanthroline Diamides: An Influence of Fluorine Atoms on the Coordination of Lu(III) and Some Other f-Elements and Their Solvent Extraction
by Nane A. Avagyan, Pavel S. Lemport, Mariia V. Evsiunina, Petr I. Matveev, Svetlana A. Aksenova, Yulia V. Nelyubina, Alexandr V. Yatsenko, Viktor A. Tafeenko, Vladimir G. Petrov, Yuri A. Ustynyuk, Xihe Bi and Valentine G. Nenajdenko
Int. J. Mol. Sci. 2023, 24(6), 5569; https://doi.org/10.3390/ijms24065569 - 14 Mar 2023
Cited by 8 | Viewed by 1936
Abstract
Three pyrrolidine-derived phenanthroline diamides were studied as ligands for lutetium trinitrate. The structural features of the complexes have been studied using various spectral methods and X-ray. The presence of halogen atoms in the structure of phenanthroline ligands has a significant impact on both [...] Read more.
Three pyrrolidine-derived phenanthroline diamides were studied as ligands for lutetium trinitrate. The structural features of the complexes have been studied using various spectral methods and X-ray. The presence of halogen atoms in the structure of phenanthroline ligands has a significant impact on both the coordination number of lutetium and the number of solvate water molecules in the internal coordination sphere. The stability constants of complexes with La(NO3)3, Nd(NO3)3, Eu(NO3)3, and Lu(NO3)3 were measured to demonstrate higher efficiency of fluorinated ligands. NMR titration was performed for this ligand, and it was found that complexation with lutetium leads to an approximately 13 ppm shift of the corresponding signal in the 19F NMR spectrum. The possibility of formation of a polymeric oxo-complex of this ligand with lutetium nitrate was demonstrated. Experiments on the liquid–liquid extraction of Am(III) and Ln(III) nitrates were carried out to demonstrate advantageous features of chlorinated and fluorinated pyrrolidine diamides. Full article
(This article belongs to the Special Issue Advanced Ligands for Coordination Chemistry)
Show Figures

Graphical abstract

Back to TopTop