Issue 1, 2011

Charge-tagged N-heterocyclic carbenes

Abstract

The interception, formation and characterization of the first stable, long lived charge-tagged N-heterocyclic carbenes of the general type 4x+ (x = 1–3) and analogues is reported. Via ESI(+)-MS of solutions of bromine salts of doubly, triply and quadruply charged imidazolium ion IL (3.Brn, n = 2–4), the isolated 4x+ as well as charged aggregates [3.Br(nx)]x+ likely to be participating in the [3.Br(nx)]x+4x+ + HBr solution equilibrium could be transferred and characterized in the gas phase. Mimicking the solution equilibrium, the gaseous [3.Br(nx)]x+ were found to dissociate nearly exclusively viaHBr loss during thermal activationvia collisions to form gaseous 4x+, which were found to add to acrolein and acetone.

Graphical abstract: Charge-tagged N-heterocyclic carbenes

Supplementary files

Article information

Article type
Paper
Submitted
11 ኤፕሪ 2011
Accepted
12 ጁን 2011
First published
18 ጁላይ 2011

RSC Adv., 2011,1, 73-78

Charge-tagged N-heterocyclic carbenes

Y. E. Corilo, F. M. Nachtigall, P. V. Abdelnur, G. Ebeling, J. Dupont and M. N. Eberlin, RSC Adv., 2011, 1, 73 DOI: 10.1039/C1RA00024A

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements