Although hypervalent iodine(III) reagents have become staples in organic chemistry, the exploration of their isoelectronic counterparts, namely hypervalent bromine(III) and chlorine(III) reagents, has been relatively limited, partly due to challenges in synthesizing and stabilizing these compounds. In this study, we conduct a thorough examination of both homolytic and heterolytic bond dissociation energies (BDEs) critical for assessing the chemical stability and functional group transfer capability of cyclic hypervalent halogen compounds using density functional theory (DFT) analysis. A moderate linear correlation was observed between the homolytic BDEs across different halogen centers, while a strong linear correlation was noted among the heterolytic BDEs across these centers. Furthermore, we developed a predictive model for both homolytic and heterolytic BDEs of cyclic hypervalent halogen compounds using machine learning algorithms. The results of this study could aid in estimating the chemical stability and functional group transfer capabilities of hypervalent bromine(III) and chlorine(III) reagents, thereby facilitating their development.
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http://dx.doi.org/10.3762/bjoc.20.127 | DOI Listing |
Chem Commun (Camb)
January 2025
Research School of Chemistry and Applied Biomedical Sciences, Tomsk Polytechnic University, Tomsk 634050, Russian Federation.
We report the synthesis of novel N-coordinated -iodanes as a unique class of hypervalent iodine compounds. X-ray diffraction analysis revealed their intriguing (pseudo)cyclic structure, showcasing distinctive N⋯I-secondary bonding interactions. We demonstrate the generation of reactive diacetoxy derivatives, which exhibits remarkable efficacy in alcohol oxidation reactions.
View Article and Find Full Text PDFJ Org Chem
December 2024
School of Traditional Chinese Medicine, Southern Medical University, Guangzhou 510515, P. R. China.
To date, a general approach for the direct α-acyloxylation of cyclic 1,3-dicarbonyls remains challenging. Herein, we report a Pd-catalyzed α-acyloxylation of cyclic 1,3-dicarbonyl-derived hypervalent iodine compounds with highly abundant carboxylic acids. Our approach utilizes a commercially available Pd(OAc) catalyst, which exhibits mild reaction conditions, scalability, operational simplicity, and robustness against moisture and air.
View Article and Find Full Text PDFBeilstein J Org Chem
November 2024
University of Bristol, School of Chemistry, Bristol, BS8 1TS, UK.
Chemistry
November 2024
Faculty for Chemistry, University of Konstanz, Universitätsstrasse 10, 78457, Konstanz, Germany.
We present a series of six hypervalent bismuth complexes Bi(PDP)X bearing ligands characterized by the pyridine-2,6-bis(pyrrolide) (PDP) structural motif. While bismuth holds considerable potential for facilitating efficient intersystem crossing (ISC), reports on phosphorescent molecular bismuth complexes are still scarce and mostly based on systems that exhibit inter- or intraligand charge transfer character of their optical excitations. Herein, the UV/vis absorptive, luminescent, and electrochemical properties of complexes Bi(PDP)X are explored, where the substituents R and R, as well as the halide ligand X are varied.
View Article and Find Full Text PDFOrg Lett
November 2024
Department of Organic and Medicinal Chemistry, Graduate School of Pharmaceutical Sciences, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.
Stable hypervalent bromine(III) compounds were synthesized via aryl bromine oxidation with -hybridized nitrogen cations generated by oxime N-O bond cleavage in trifluoroacetic acid. The resulting intramolecular N-Br hypervalent bond is effectively stabilized by the planar xanthone structure. The structures and physicochemical properties of these λ-bromanes were characterized by X-ray crystallography, cyclic voltammetry, UV-vis spectroscopy, and computational analysis.
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