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Indole, Azaindole and Indazole Derivatives and Their Compounds with Metal Ions

A special issue of Molecules (ISSN 1420-3049). This special issue belongs to the section "Organometallic Chemistry".

Deadline for manuscript submissions: closed (30 April 2022) | Viewed by 3085

Special Issue Editor


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Guest Editor
Institute of Chemistry, Faculty of Science and Technology, Jan Dlugosz University, Armii Krajowej 13/15, 42-200 Czestochowa, Poland
Interests: coordination chemistry; structural chemistry; spectroscopy, in particular vibrational spectroscopy; computational chemistry; heterocycles as ligands
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Special Issue Information

Dear Colleagues,

Indole, azaindole, and indazole derivatives are the subject of intense research owing to their wide range of biological activity. These heterocycles, depending on the type of substituent and its position in the five- and six-membered rings, can form hetero- and homoleptic coordination compounds including coordination polymers and metal–organic compounds with interesting structures and properties. This Special Issue shall cover new research and review works developed so far in the field of the title compounds, with the aim of making an important contribution to the community. A combination of experimental and theoretical studies, also including the potential application of both ligands and their compounds with metal ions, are welcome.

Prof. Dr. Barbara Morzyk-Ociepa
Guest Editor

Manuscript Submission Information

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Keywords

  • Multidentate ligands
  • Coordination compounds
  • Coordinate polymers
  • Metal–organic compounds
  • X-ray
  • Spectroscopy
  • DFT
  • Applications

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Published Papers (1 paper)

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Research

16 pages, 1895 KiB  
Article
Visible-Light-Induced, Graphene Oxide-Promoted C3-Chalcogenylation of Indoles Strategy under Transition-Metal-Free Conditions
by Qing Huang, Xiangjun Peng, Hong Li, Haiping He and Liangxian Liu
Molecules 2022, 27(3), 772; https://doi.org/10.3390/molecules27030772 - 25 Jan 2022
Cited by 14 | Viewed by 2467
Abstract
An efficient and general method for the synthesis of 3-sulfenylindoles and 3-selenylindoles employing visible-light irradiation with graphene oxide as a promoter at room temperature has been achieved. The reaction features are high yields, simple operation, metal-free and iodine-free conditions, an easy-to-handle oxidant, and [...] Read more.
An efficient and general method for the synthesis of 3-sulfenylindoles and 3-selenylindoles employing visible-light irradiation with graphene oxide as a promoter at room temperature has been achieved. The reaction features are high yields, simple operation, metal-free and iodine-free conditions, an easy-to-handle oxidant, and gram-scalable synthesis. This simple protocol allows one to access a wide range of 3-arylthioindoles, 3-arylselenylindoles, and even 3-thiocyanatoindoles with good to excellent yields. Full article
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