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Symmetry
  • Editorial
  • Open Access

11 October 2023

Chemistry: Symmetry/Asymmetry

Department of Organic Chemistry and Technology, Budapest University of Technology and Economics, 1521 Budapest, Hungary
This article belongs to the Section Chemistry: Symmetry/Asymmetry
All kinds of symmetry-related problems in organic and inorganic chemistry may be the subject of papers submitted to Symmetry. One of the most relevant fields includes optical activity that is the consequence of a kind of chirality center, such as an asymmetric C atom, while a heteroatom, like P. Atrop isomerism, may also be a reason. The discussion of problems associated with a stereogene center or centers, like the separation of racemates, enantiomer enrichment or separation, chiral induction, diastereomeric transition states, diastereomers or intermediates, asymmetric (enantioselective) syntheses, or any kind of selective syntheses, is welcome. New transition metal complex catalysts comprising optically active P-ligands and the asymmetric reactions that they allow are also of interest.
Another exciting field that may attract papers for Symmetry is X-ray crystallography. These days, single-crystal X-ray analysis is a routine method that not only allows the elucidation of the stereostructures of individual molecules but also gives insights regarding the crystal structures hiding symmetry/asymmetry-related issues.
Last but not least, theoretical calculations may also include symmetry-related problems [1,2,3,4,5,6,7,8].
The Editorial Office is open to receive research and review papers that report on the following subjects:
  • Asymmetric synthesis;
  • Chiral catalysts and chiral P-ligands;
  • Enantiomer enrichment and separation;
  • Optical resolution (via diastereomer salt formation or derivatization);
  • Theoretical calculations on enantioselective reactions;
  • Chemo-, regio-, and diastereoselective reactions;
  • X-ray crystallography;
  • X-ray structures;
  • Stereostructures determined via X-ray and/or calculations;
  • Crystal structures;
  • Coordination chemistry;
  • Parity effects in molecules;
  • Circular dichroism in spectroscopy;
  • Enantiomer recognition;
  • Homochirality in chemistry and biochemistry;
  • Molecular clusters;
  • Electronic structure calculations;
  • Symmetry and chemistry, symmetry and molecular structure, symmetry and spectroscopy, symmetry and isomerism, and chiral and achiral molecules;
  • Permutational, substitutional, and positional isomers;
  • Magnetic space groups; topological materials, including the topology of band structures; semi-metals; and quantum Hall effect;
  • Symmetry and topology in dynamic stereochemistry and conformational rearrangements;
  • Homochirality in the origin of life;
  • Biocatalysts;
  • Dynamic kinetic resolution;
  • Chirogenesis, chirality induction, optical activity, enantiomeric resolution, chiral memory, chiroptical spectroscopy, polarized light, circular dichroism (CD), electronic circular dichroism (ECD), vibrational circular dichroism (VCD), magnetic circular dichroism (MCD), circularly polarized luminescence (CPL), optical rotatory dispersion (ORD), linear dichroism (LB), refractive index, optical rotation, circular birefringence (CB), and linear birefringence (LB);
  • Structural chemistry, supramolecular interactions, and cluster aggregates

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Ota, K.; Watabe, Y.; Haga, Y.; Iesari, F.; Okajima, T.; Matsumoto, Y. Synthesis, Crystal Structure, Local Structure, and Magnetic Properties of Polycrystalline and Single-Crystalline Ce2Pt6Al15. Symmetry 2023, 15, 1488. [Google Scholar] [CrossRef]
  2. Novikov, A.S. Symmetry in Quantum and Computational Chemistry: Volume 2. Symmetry 2023, 15, 1472. [Google Scholar] [CrossRef]
  3. Rachwalski, M. Special Issue: Asymmetry and Symmetry in Organic Chemistry. Symmetry 2023, 15, 1363. [Google Scholar] [CrossRef]
  4. Faisca Phillips, A.M.; Pombeiro, A.J.L. Atropselective Organocatalytic Synthesis of Chiral Compounds Containing Nitrogen along the Axis of Chirality. Symmetry 2023, 15, 1261. [Google Scholar] [CrossRef]
  5. Pietrusiewicz, K.M.; Kozioł, A.E.; Małuszyńska, H.; Sowa, S. Myrtenal and Myrtanal as Auxiliaries in the Synthesis of Some C,P-Stereogenic Hydroxyphosphine Oxides and Hydroxyphosphine-Boranes Possessing up to Four Contiguous Centers of Chirality. Symmetry 2023, 15, 1172. [Google Scholar] [CrossRef]
  6. Ishihara, S.; Uto, S. Symmetry and Liquid Crystals. Symmetry 2023, 15, 691. [Google Scholar] [CrossRef]
  7. Kolodiazhna, A.O.; Kolodiazhnyi, O.I. Chiral Organophosphorus Pharmaceuticals: Properties and Application. Symmetry 2023, 15, 1550. [Google Scholar] [CrossRef]
  8. Kolodiazhna, A.O.; Kolodiazhnyi, O.I. Catalytic Asymmetric Synthesis of C-Chiral Phosphonates. Symmetry 2022, 14, 1758. [Google Scholar] [CrossRef]
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