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Cited by 375

The DOI matches its Crossref record; 32 of the 32 references it cites were found in a registry or an index.

Determining the π-Acceptor Properties of N-Heterocyclic Carbenes by Measuring the 77Se NMR Chemical Shifts of Their Selenium Adducts

Liske, Annika, Verlinden, Kathrin, Buhl, Hannes, Schaper, Klaus, Ganter, Christian·2013·Organometallics

Abstract

A new method for the assessment of the π-acceptor strength of N-heterocyclic carbenes is presented. The 77 Se chemical shifts of the easily available selenium carbene adducts 1 ·Se– 7 ·Se correlate with the π-acceptor character of the respective carbenes. The observed δ( 77 Se) values cover a range of almost 800 ppm, with increasing π-acidity leading to a downfield shift of the signal.

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Metadata

Authors
Liske, A., Verlinden, K., Buhl, H., Schaper, K., & Ganter, C.
Venue
Organometallics
Published
2013-09-24
Volume
32
Issue
19
Pages
5269-5272
ISSN
  • 0276-7333 (ISSN-L)
  • 1520-6041
OpenAlex
W2325339364
Cited by
375
References
32
FWCI
10.39
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Determining the π-Acceptor Properties of N-Heterocyclic Carbenes by Measuring the 77Se NMR Chemical Shifts of Their Selenium Adducts. https://app.cochat.ai/papers/10.1021/om400858y
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Liske, A., Verlinden, K., Buhl, H., Schaper, K., & Ganter, C. (2013). Determining the π-Acceptor Properties of N-Heterocyclic Carbenes by Measuring the 77Se NMR Chemical Shifts of Their Selenium Adducts. Organometallics. https://doi.org/10.1021/om400858y

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