Trisubstituted geminal diazaalkene derived transient 1,2-carbodications.

Autor: Mandal, Debdeep, Stein, Felix, Chandra, Shubhadeep, Neuman, Nicolás I., Sarkar, Pallavi, Das, Shubhajit, Kundu, Abhinanda, Sarkar, Arighna, Rawat, Hemant, Pati, Swapan K., Chandrasekhar, Vadapalli, Sarkar, Biprajit, Jana, Anukul
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Zdroj: Chemical Communications; 7/28/2020, Vol. 56 Issue 59, p8233-8236, 4p
Abstrakt: The coulombic repulsion between two adjacent cation centres of 1,2-carbodications is known to decrease with π- and/or n-donor substituents by a positive charge delocalization. Here we report the delocalization of the positive charge of transient 1,2-carbodications having one H-substituent by an intramolecular base-coordination. N-heterocyclic olefin (NHO) derived 2-pyrrolidinyl appended trisubstituted geminal diazaalkenes were used for the generation of transient 1,2-carbodications through a 2-e chemical oxidation process. We have also studied the 1-e oxidation reaction of trisubstituted geminal diazaalkenes (electrochemically and chemically) and also studied them using in situ EPR spectroscopy. [ABSTRACT FROM AUTHOR]
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