Development and Applications of Sterically Demanding Ligands in Main Group Chemistry

A special issue of Inorganics (ISSN 2304-6740). This special issue belongs to the section "Coordination Chemistry".

Deadline for manuscript submissions: closed (31 October 2024) | Viewed by 1138

Special Issue Editor


E-Mail Website
Guest Editor
EaStCHEM School of Chemistry, University of St Andrews, North Haugh, St Andrews KY16 9ST, UK
Interests: molecular main group of compounds; low-oxidation state complexes; metal–metal-bonded complexes; main group of metal hydride complexes; main group of organometallics; sterically demanding ligands

Special Issue Information

Dear Colleagues,

Many recent advances in main group chemistry have been achieved with compounds bearing highly sterically demanding ligand systems. This has led, for example, to the discovery of complexes with elements in low coordination and novel bonding modes, rare oxidation states, and compounds with unique properties. Many of these compounds have been capable of activating highly inert small molecules under mild conditions, leading to the discovery of novel stoichiometric and catalytic reactivity. The sterically demanding ligands in these complexes can shape compound geometries and properties, facilitate, or prevent certain reaction pathways, and thus enable new forms of chemistry with main group elements.

These endeavours often started with exploratory fundamental studies on sterically demanding ligand systems at main group element centres, leading to a wide range of both broadly anticipated findings and highly surprising discoveries. Many efforts have been made in synthesising, characterising, and studying these compound classes, helping to shape our understanding of the fine balance of steric and electronic effects in these compounds, which is still developing. The synthesis of new sterically demanding ligand systems, their connection to main group fragments, and the further transformations of their complexes can lead to new challenges; however, because of the significant impact of the ligand bulk, in some instances, minor differences in ligand architecture have led to significantly different reaction outcomes and this field still holds many surprises and opportunities for main group chemistry.

In this Special Issue, we welcome contributions to this field that shed light on new findings in main group chemistry with sterically demanding ligand systems.

Dr. Andreas Stasch
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. Inorganics is an international peer-reviewed open access monthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2700 CHF (Swiss Francs). 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

  • sterically demanding ligands
  • ligand design and synthesis
  • s- and p-block complexes
  • low-coordination modes
  • main group synthesis and catalysis

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 (1 paper)

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

Research

14 pages, 2218 KiB  
Article
Synthesis and Characterization of Extremely Bulky Aminopyridinate Ligands and a Series of Their Groups 1 and 2 Metal Complexes
by Arif M. Earsad, Albert Paparo, Matthew J. Evans and Cameron Jones
Inorganics 2024, 12(10), 270; https://doi.org/10.3390/inorganics12100270 - 15 Oct 2024
Viewed by 836
Abstract
High-yielding synthetic routes to five new extremely bulky aminopyridine pro-ligands were developed, viz. (C5H3N-6-Ar1)N(H)Ar2-2; Ar1 = Trip, Ar2 = TCHP (HAmPy1), Ar* (HAmPy2) or Ar (HAmPy3); [...] Read more.
High-yielding synthetic routes to five new extremely bulky aminopyridine pro-ligands were developed, viz. (C5H3N-6-Ar1)N(H)Ar2-2; Ar1 = Trip, Ar2 = TCHP (HAmPy1), Ar* (HAmPy2) or Ar (HAmPy3); Ar1 = TCHP, Ar2 = Ar* (HAmPy4) or Ar (HAmPy5) (Trip = 2,4,6-triisopropylphenyl, TCHP = 2,4,6-tricyclohexylphenyl, Ar* = C6H2(CHPh2)2Me-2,6,4, Ar = C6H2(CHPh2)2Pri-2,6,4. Four of these were deprotonated with LiBun in diethyl ether to give lithium aminopyridinate complexes which were dimeric for the least bulky ligand, [{Li(AmPy1)}2] or monomeric for the bulkier aminopyridinates, i.e., in [Li(AmPy2−4)(OEt2)]. One aminopyridine was deprotonated with MeMgI to give monomeric [Mg(AmPy3)I(OEt2)2]. When treated with sodium or potassium mirrors or 5% w/w Na/NaCl, over-reduction occurred, leading to the alkali metal aminopyridinates, [M(AmPy3)(η6-toluene)] (M = Na or K) or [{Na(AmPy3)}]. An attempted reduction of [Mg(AmPy3)I(OEt2)2] with a dimagnesium(I) compound led only to partial loss of diethyl ether and the formation of [(AmPy3)Mg(μ-I)2Mg(AmPy3)(OEt2)]. All prepared complexes have potential as ligand transfer reagents in salt metathesis reactions with metal halide complexes. Full article
Show Figures

Figure 1

Back to TopTop