Abstract
Structural variations of different 2 π-aromatic three-membered ring systems of main group elements, especially group 14 and 13 elements as compared to the classical description of cyclopropenyl cation has been reviewed in this article. The structures of heavier analogues as well as group 13 analogues of cyclopropenyl cation showed an emergence of dramatic structural patterns which do not conform to the general norms of carbon chemistry. Isolobal analogies between the main group fragments have been efficiently used to explain the peculiarities observed in these three-membered ring systems.
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We thank the Supercomputer Education and Research Centre (SERC), Indian Institute of Science, Bangalore and the Centre for Modelling Simulation and Design (CMSD), University of Hyderabad for computational facilities. EDJ thanks the Department of Science and Technology (DST) for J C Bose Fellowship.
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MALLICK, D., JEMMIS, E.D. Structural variations in aromatic 2π-electron three-membered rings of the main group elements. J Chem Sci 127, 183–196 (2015). https://doi.org/10.1007/s12039-015-0777-2
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DOI: https://doi.org/10.1007/s12039-015-0777-2