Proton transfer vs. oligophosphine formation by P–C/P–H σ-bond metathesis: decoding the competing Brønsted and Lewis type reactivities of imidazolio-phosphines
Author:
Affiliation:
1. Institute of Inorganic Chemistry
2. University of Stuttgart
3. 70550 Stuttgart
4. Germany
5. Department of Chemistry
6. University of Helsinki
7. 00014 Helsinki
8. Finland
Abstract
Cationic imidazolio-phosphines show two-sided reactivity towards bases, undergoing either Brønsted-type proton transfer to imidazolio-phosphides or autocatalytic Lewis acid/base reaction cascades to yield P-free imidazolium ions and oligophosphines.
Funder
Deutsche Forschungsgemeinschaft
Ministerium für Wissenschaft, Forschung und Kunst Baden-Württemberg
Publisher
Royal Society of Chemistry (RSC)
Subject
Inorganic Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2020/DT/D0DT03633A
Reference45 articles.
1. Early-Transition-Metal-Mediated Activation and Transformation of White Phosphorus
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3. P4 Activation by Main Group Elements and Compounds
4. Functionalization of P4 through Direct P−C Bond Formation
5. Contributions to the chemistry of phosphorus. 218. Monocyclic and polycyclic phosphines
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1. Reactions of Imidazolio‐Phosphides with Organotin Chlorides: Surprisingly Diverse;European Journal of Inorganic Chemistry;2022-01-13
2. A PH-functionalized dicationic bis(imidazolio)diphosphine;Dalton Transactions;2022
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