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Crystals
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Halogen-Bonded Cocrystals
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Halogen-Bonded Cocrystals

A special issue of Crystals (ISSN 2073-4352). This special issue belongs to the section "Crystal Engineering".

Deadline for manuscript submissions: closed (30 September 2019) | Viewed by 17642

Special Issue Editor

Dr. Filip Topic

E-Mail Website
Guest Editor
McGill University, Department of Chemistry, Montreal, Canada
Interests: halogen bonding; X-ray crystallography; cocrystals; mechanochemistry; crystal engineering; supramolecular chemistry

Special Issue Information

Dear Colleagues,

Cocrystals encompass, in the broadest sense, solids consisting of two or more different molecular species. They have been intensively studied in the past two decades, not least for the great promise in the development of novel pharmaceutical materials, but also as a means of engineering novel crystalline materials with improved optical, mechanical and other properties.

Halogen bonding, an attractive interaction between an electrophilic region on a halogen atom and a nucleophilic moiety, has similarly experienced a renaissance in the last two decades. Cocrystals have enabled the exploration of the unique behaviour of halogen bonding, at times paralleling yet sometimes contrasting with hydrogen bonding, the competition of halogen bonding with other weak interactions, and the (non-)isomorphous switching of donor halogens between iodine, bromine and chlorine. Similarly, halogen-bonded cocrystals have played a critical role in demonstrating exciting new applications of halogen bonding, such as novel strategies for the preparation of liquid crystals, supramolecular gels and luminescent materials as well as the templating of solid-state reactions. X-ray crystallography has been an essential tool for the structural elucidation of halogen-bonded solids, more and more often supported by solid-state NMR and computational studies.

With this Special Issue on the topic of “Halogen-Bonded Cocrystals” we want to provide a venue for contributions dealing with the structures and properties of halogen-bonded organic solids, with a special focus on cocrystals, while also including closely related systems such as amorphous solids, liquid crystals or gels in which the halogen bonding plays a significant role.

Dr. Filip Topic
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. Crystals 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 2600 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

  • halogen bonding
  • cocrystals
  • molecular solids
  • polymorphs

Published Papers (5 papers)

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Research

15 pages, 3826 KiB  
Article
Anion Influence on the Packing of 1,3-Bis(4-Ethynyl-3-Iodopyridinium)-Benzene Halogen Bond Receptors
by Daniel A. Decato, Asia Marie S. Riel and Orion B. Berryman
Crystals 2019, 9(10), 522; https://0-doi-org.brum.beds.ac.uk/10.3390/cryst9100522 - 11 Oct 2019
Cited by 5 | Viewed by 2926
Abstract
Rigid and directional arylethynyl scaffolds have been widely successful across diverse areas of chemistry. Utilizing this platform, we present three new structures of a dicationic 1,3-bis(4-ethynyl-3-iodopyridinium)-benzene halogen bonding receptor with tetrafluoroborate, nitrate, and hydrogen sulfate. Structural analysis focused on the receptor conformation, anion [...] Read more.
Rigid and directional arylethynyl scaffolds have been widely successful across diverse areas of chemistry. Utilizing this platform, we present three new structures of a dicationic 1,3-bis(4-ethynyl-3-iodopyridinium)-benzene halogen bonding receptor with tetrafluoroborate, nitrate, and hydrogen sulfate. Structural analysis focused on the receptor conformation, anion shape, solvation, and long range packing of these systems. Coupled with our previously reported structures, we concluded that anions can be classified as building units within this family of halogen bonding receptors. Two kinds of antiparallel dimers were observed for these dicationic receptors. An off-centered species was most frequent, present among geometrically diverse anions and assorted receptor conformations. In contrast, the centered antiparallel dimers were observed with receptors adopting a bidentate conformation in the solid-state. While anions support the solid-state formation of dimers, the molecular geometry and characteristics (planarity, rigidity, and directionality) of arylethynyl systems increase the likelihood of dimer formation by limiting efficient packing arrangements. The significantly larger cation may have considerable influence on the solid-state packing, as similar cationic arylethynyl systems also display these dimers. Full article
(This article belongs to the Special Issue Halogen-Bonded Cocrystals)
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10 pages, 1230 KiB  
Article
Extended Assemblies of Ru(bpy)(CO)2X2 (X = Cl, Br, I) Molecules Linked by 1,4-Diiodotetrafluoro-Benzene (DITFB) Halogen Bond Donors
by Xin Ding, Matti Tuikka, Kari Rissanen and Matti Haukka
Crystals 2019, 9(6), 319; https://0-doi-org.brum.beds.ac.uk/10.3390/cryst9060319 - 24 Jun 2019
Cited by 8 | Viewed by 3565
Abstract
The ruthenium carbonyl compounds, Ru(bpy)(CO)2X2 (X = Cl, Br or I) act as neutral halogen bond (XB) acceptors when co-crystallized with 1,4-diiodotetrafluoro-benzene (DITFB). The halogen bonding strength of the Ru-X⋅⋅⋅I halogen bonds follow the nucleophilic character of the halido ligand. [...] Read more.
The ruthenium carbonyl compounds, Ru(bpy)(CO)2X2 (X = Cl, Br or I) act as neutral halogen bond (XB) acceptors when co-crystallized with 1,4-diiodotetrafluoro-benzene (DITFB). The halogen bonding strength of the Ru-X⋅⋅⋅I halogen bonds follow the nucleophilic character of the halido ligand. The strongest halogen bond occurs between the chlorido ligand and the iodide atoms of the DITFB. All three halogen bonded complexes form polymeric assemblies in the solid state. In Ru(bpy)(CO)2Cl2⋅DITFB (1) and in Ru(bpy)(CO)2Br2⋅DITFB (2) both halido ligands are halogen bonded to only one DITFB donor. In Ru(bpy)(CO)2I2⋅DITFB (3) only one of the halido ligands is involved in halogen bonding acting as ditopic center for two DITFB donors. The polymeric structures of 1 and 2 are isomorphic wave-like single chain systems, while the iodine complexes form pairs of linear chains attached together with weak F⋅⋅⋅O≡C interactions between the closest neighbors. The stronger polarization of the iodide ligand compared to the Cl or Br ligands favors nearly linear C-I⋅⋅⋅I angles between the XB donor and the metal complex supporting the linear arrangement of the halogen bonded chain. Full article
(This article belongs to the Special Issue Halogen-Bonded Cocrystals)
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10 pages, 3114 KiB  
Article
Adenine as a Halogen Bond Acceptor: A Combined Experimental and DFT Study
by Yannick Roselló, Mónica Benito, Elies Molins, Miquel Barceló-Oliver and Antonio Frontera
Crystals 2019, 9(4), 224; https://0-doi-org.brum.beds.ac.uk/10.3390/cryst9040224 - 25 Apr 2019
Cited by 16 | Viewed by 3591
Abstract
In this work, we report the cocrystallization of N9-ethyladenine with 1,2,4,5-tetrafluoro-3,6-diiodobenzene (TFDIB), a classical XB donor. As far as our knowledge extends, this is the first cocrystal reported to date where an adenine derivative acts as a halogen bond acceptor. In [...] Read more.
In this work, we report the cocrystallization of N9-ethyladenine with 1,2,4,5-tetrafluoro-3,6-diiodobenzene (TFDIB), a classical XB donor. As far as our knowledge extends, this is the first cocrystal reported to date where an adenine derivative acts as a halogen bond acceptor. In the solid state, each adenine ring forms two centrosymmetric H-bonded dimers: one using N1···HA6–N6 and the other N7···HB6–N6. Therefore, only N3 is available as a halogen bond acceptor that, indeed, establishes an N···I halogen bonding interaction with TFDIB. The H-bonded dimers and halogen bonds have been investigated via DFT (Density Functional Theory) calculations and the Bader’s Quantum Theory of Atoms In Molecules (QTAIM) method at the B3LYP/6-311+G* level of theory. The influence of H-bonding interactions on the lone pair donor ability of N3 has also been analyzed using the molecular electrostatic potential (MEP) surface calculations. Full article
(This article belongs to the Special Issue Halogen-Bonded Cocrystals)
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12 pages, 3394 KiB  
Article
Synthesis, Structures and Co-Crystallizations of Perfluorophenyl Substituted β-Diketone and Triketone Compounds
by Takumi Kusakawa, Shunichiro Sakai, Kyosuke Nakajima, Hidetaka Yuge, Izabela I. Rzeznicka and Akiko Hori
Crystals 2019, 9(3), 175; https://0-doi-org.brum.beds.ac.uk/10.3390/cryst9030175 - 25 Mar 2019
Cited by 7 | Viewed by 3570
Abstract
Perfluorophenyl-substituted compounds, 3-hydroxy-1,3-bis(pentafluorophenyl)-2- propen-1-one (H1) and 1,5-dihydroxy-1,5-bis(pentafluorophenyl)-1,4-pentadien-3-one (H22), were prepared in 56 and 30% yields, respectively, and only the enol forms were preferentially obtained among the keto-enol tautomerism. Molecular conformations and tautomerism of the fluorine-substituted compounds were certified [...] Read more.
Perfluorophenyl-substituted compounds, 3-hydroxy-1,3-bis(pentafluorophenyl)-2- propen-1-one (H1) and 1,5-dihydroxy-1,5-bis(pentafluorophenyl)-1,4-pentadien-3-one (H22), were prepared in 56 and 30% yields, respectively, and only the enol forms were preferentially obtained among the keto-enol tautomerism. Molecular conformations and tautomerism of the fluorine-substituted compounds were certified based on X-ray crystallographic studies and density functional calculations. The solvent dependency of the absorption spectra was only observed for the fluorinated compounds. The compounds H1 and H22 quantitatively formed co-crystals with the corresponding non-perfluorinated compounds, dibenzoylmethane (H3) and 1,5-dihydroxy-1,5-diphenyl-1,4-pentadien-3-one (H24), respectively, through the arene–perfluoroarene interaction to give the 1:1 co-crystals H1•H3 and H22•H24, which were characterized by X-ray crystallographic and elemental analysis studies. Full article
(This article belongs to the Special Issue Halogen-Bonded Cocrystals)
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12 pages, 1443 KiB  
Article
New Crystal Forms for Biologically Active Compounds. Part 1: Noncovalent Interactions in Adducts of Nevirapine with XB Donors
by Mariya A. Kryukova, Alexander V. Sapegin, Alexander S. Novikov, Mikhail Krasavin and Daniil M. Ivanov
Crystals 2019, 9(2), 71; https://0-doi-org.brum.beds.ac.uk/10.3390/cryst9020071 - 30 Jan 2019
Cited by 15 | Viewed by 3449
Abstract
Stabilization of specific crystal polymorphs of an active pharmaceutical ingredient is crucial for preventing uncontrollable interconversion of various crystalline forms, which affects physicochemical properties as well as physiological activity. Co-crystallization with various excipients is an emerging productive way of achieving such stabilization in [...] Read more.
Stabilization of specific crystal polymorphs of an active pharmaceutical ingredient is crucial for preventing uncontrollable interconversion of various crystalline forms, which affects physicochemical properties as well as physiological activity. Co-crystallization with various excipients is an emerging productive way of achieving such stabilization in the solid state. In this work, we identified an opportunity for co-crystallization of antiviral drug nevirapine (NVP) with a classical XB donor, 1,2,4,5-tetrafluoro-3,6-diiodobenzene (1,4-FIB), as well as 1,3-diiodobenzene (1,3-DIB), which has been seldom employed as an XB donor to date. In the X-ray structures of NVP·1,4-FIB and NVP·1,3-DIB co-crystals, different hydrogen and halogen bonding modes were detected and further investigated via DFT calculations as well as topological analysis of the electron density distribution within the framework of the QTAIM method at the M06/DZP-DKH level of theory. Estimated energies of these supramolecular contacts vary from 0.6 to 5.7 kcal/mol. Full article
(This article belongs to the Special Issue Halogen-Bonded Cocrystals)
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