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Cyclic nitrenium ions (CNIs) with five and seven-membered rings are well known, but the CNIs with six-membered rings are rare. Only a few are known as peri-fused six-membered cyclic nitrenium ions (PCNIs) and they are reported to be nitrogen Lewis acids. Preliminary electronic structure analysis indicated that the electronic properties of PCNIs somewhat deviate from the other CNIs (five or seven-membered). Further, these ring systems proved to be non-aromatic (in the triazine ring), whereas the five and seven-membered analogs are aromatic. In this work, an electronic structure analysis was carried out on the newly designed PCNIs to understand their characteristic features. Several analogs of these species were designed to identify PCNIs with improved electronic stability. The PCNIs are electrophilic because of the empty p orbital and the formal positive charge at the central nitrogen atom. The Lewis acidic character of known and designed PCNIs has been evaluated in terms of hydride ion affinity (HIA), fluoride ion affinity (FIA), ΔH and ΔH values. This work helped identify a set of new PCNIs whose electronic stability and Lewis acidity parameters are significantly high. Further, a few of these systems were found to be aromatic in all three rings with notable negative NICS(1) values.
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http://dx.doi.org/10.1002/jcc.70197 | DOI Listing |
J Comput Chem
July 2025
Department of Medicinal Chemistry, National Institute of Pharmaceutical Education and Research (NIPER), S. A. S. Nagar, Punjab, India.
Cyclic nitrenium ions (CNIs) with five and seven-membered rings are well known, but the CNIs with six-membered rings are rare. Only a few are known as peri-fused six-membered cyclic nitrenium ions (PCNIs) and they are reported to be nitrogen Lewis acids. Preliminary electronic structure analysis indicated that the electronic properties of PCNIs somewhat deviate from the other CNIs (five or seven-membered).
View Article and Find Full Text PDFJ Phys Chem A
May 2025
Department of Pharmacoinformatics, National Institute of Pharmaceutical Education and Research, Sector 67, S.A.S. Nagar, Mohali 160062, Punjab, India.
Cyclic nitrenium ions (CNIs) are generally stable and have found applications in chemistry, including biochemistry. Cyclic five-membered 1,2,3-triazolium ions (CFTIs) are a special class of CNIs; such moieties are found in a few medicinally important species. Though they are isoelectronic to N-heterocyclic carbenes (NHCs), they exhibit electrophilic properties (unlike nucleophilic NHCs).
View Article and Find Full Text PDFChemistry
May 2025
Fachbereich Chemie, Philipps-Universität Marburg, Hans-Meerwein-Str. 4, Marburg, 35037, Germany.
Cyclic (alkyl)(amino)carbenes (CAACs) are key compounds en route to a plethora of unprecedented low-valent and radical complexes of transition metals and main group elements. For p-block elements of the sixth period, however, low-valent and radical complexes of CAACs are extremely rare, and even simple adducts with CAACs are difficult to access. Here we report the full characterization of the first adduct between a CAAC and a bismuth trihalide, [BiCl(CAAC)] (1), which has previously only been spectroscopically characterized.
View Article and Find Full Text PDFJ Comput Chem
January 2025
Department of Medicinal Chemistry, National Institute of Pharmaceutical Education and Research (NIPER), S.A.S. Nagar, Punjab, India.
Cyclic nitrenium ions containing five-membered and six-membered rings are available, however, the seven-membered cyclic nitrenium ions (azepinium ions) are rare. The chemistry of these species is related to their stability originating from the aromaticity due to 6π electrons. Very few theoretical and experimental studies have been conducted on the azepinium ions.
View Article and Find Full Text PDFJ Org Chem
February 2021
Institute of Problems of Chemical Physics, Russian Academy of Sciences, Chernogolovka 142432, Russian Federation.
Cyclic oxoammonium salts and DMSO are known as important reagents for their diverse and unique reactivity. In the present work, we have studied the reaction of six- and five-membered oxoammonium salts with DMSO. The reaction includes ∼100% selective transfer of the O atom from the >N═O group to the S atom of DMSO and structural rearrangement of the remaining cationic framework, leading to the formation of hydrolytically unstable iminium salts.
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