Cycloaddition of Alkenes and Alkynes to the P‐centered Singlet Biradical [P(μ‐NTer)] 2
Author:
Affiliation:
1. Anorganische Chemie Institut für Chemie A.‐Einstein‐Straße 3a 18059 Rostock Germany
2. Materialdesign Leibniz‐Institut für Katalyse an der Universität Rostock A.‐Einstein‐Str. 29a 18059 Rostock Germany
Publisher
Wiley
Subject
Inorganic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/zaac.201900191
Reference84 articles.
1. Effects of Spiroconjugation on the Calculated Singlet−Triplet Energy Gap in 2,2-Dialkoxycyclopentane-1,3-diyls and on the Experimental Electronic Absorption Spectra of Singlet 1,3-Diphenyl Derivatives. Assignment of the Lowest-Energy Electronic Transition of Singlet Cyclopentane-1,3-diyls
2. Diradicals
3. Die elektronischen Eigenschaften von Diradikalen
4. Stretching bonds in main group element compounds—Borderlines between biradicals and closed-shell species
5. Topics of 1,3-diphosphacyclobutane-2,4-diyl derivatives: Structural aspects and functionality of isolable heavier congeners of cyclobutane-1,3-diyl and the related molecules
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2. Reversible Single Electron Redox Steps Convert Polycycles with a C3P3 Core to a Planar Triphosphinine;Angewandte Chemie International Edition;2023-02-27
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4. Radical Reactivity of the Biradical [⋅P(μ‐NTer) 2 P⋅] and Isolation of a Persistent Phosphorus‐Cantered Monoradical [⋅P(μ‐NTer) 2 P‐Et];Chemistry – A European Journal;2022-05-19
5. Concerted addition of aldehydes to the singlet biradical [P(μ-NTer)]2;Dalton Transactions;2022
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