IR-Spectroscopic and X-ray-Structural Study of Vinyl-Type Carbocations in Their Carborane Salts
Author:
Affiliation:
1. N.N. Vorozhtsov Institute of Organic Chemistry, Siberian Branch of Russian Academy of Sciences, Novosibirsk 630090, Russia
Funder
Ministry of Science and Higher Education of the Russian Federation
Publisher
American Chemical Society (ACS)
Subject
General Chemical Engineering,General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acsomega.2c03025
Reference33 articles.
1. Contemporary Carbocation Chemistry: Applications in Organic Synthesis
2. Why Are Vinyl Cations Sluggish Electrophiles?
3. The Mechanism of High Reactivity of Benzyl Carbocation, C 6 H 5 CH 2 + , during Interaction with Benzene
4. Are Vinyl Cations Finally Coming of Age?
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2. A new type of C+⋯Hδ−(C=) bond in adducts of vinyl carbocations with alkenes;Scientific Reports;2024-04-10
3. Substitution of H Atoms in Unsaturated (Vinyl-Type) Carbocations by Cl or O Atoms;International Journal of Molecular Sciences;2023-06-27
4. Interaction of Vinyl-Type Carbocations, C3H5+ and C4H7+ with Molecules of Water, Alcohols, and Acetone;Molecules;2023-01-23
5. Spontaneous Transition of Alkyl Carbocations to Unsaturated Vinyl-Type Carbocations in Organic Solutions;International Journal of Molecular Sciences;2023-01-16
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