Synthesis of unsymmetrical NCN′ and PCN pincer palladacycles and their catalytic evaluation compared with a related SCN pincer palladacycle

12Citations
Citations of this article
20Readers
Mendeley users who have this article in their library.

Abstract

1-(3-(Pyridin-2-yl)phenyl)methanamine derivatives have been synthesized and underwent C-H bond activation to afford unsymmetrical NCN′ pincer palladacycles, which were characterised in the solid state. 2-Pyridinyl-phenol and -benzyl alcohols were then used as precursors to unsymmetrical PCN pincer palladacycles. Catalytic applications, where the palladacycle remains in the Pd(ii) state, have been carried out and show good activity and selectivity.

Cite

CITATION STYLE

APA

Roffe, G. W., Tizzard, G. J., Coles, S. J., Cox, H., & Spencer, J. (2016). Synthesis of unsymmetrical NCN′ and PCN pincer palladacycles and their catalytic evaluation compared with a related SCN pincer palladacycle. Organic Chemistry Frontiers, 3(8), 957–965. https://doi.org/10.1039/c6qo00198j

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free