Six-fold C-H borylation of hexa-peri-hexabenzocoronene

23Citations
Citations of this article
19Readers
Mendeley users who have this article in their library.

Abstract

Hexa-peri-hexabenzocoronene (HBC) is known to be a poorly soluble polycyclic aromatic hydrocarbon for which direct functionalization methods have been very limited. Herein, the synthesis of hexaborylated HBC from unsubstituted HBC is described. Iridiumcatalyzed six-fold C-H borylation of HBC was successfully achieved by screening solvents. The crystal structure of hexaborylated HBC was confirmed via X-ray crystallography. Optoelectronic properties of the thus-obtained hexaborylated HBC were analyzed with the support of density functional theory calculations. The spectra revealed a bathochromic shift of absorption bands compared with unsubstituted HBC under the effect of the ó-donation of boryl groups.

Cite

CITATION STYLE

APA

Nagase, M., Kato, K., Yagi, A., Segawa, Y., & Itami, K. (2020). Six-fold C-H borylation of hexa-peri-hexabenzocoronene. Beilstein Journal of Organic Chemistry, 16, 391–397. https://doi.org/10.3762/bjoc.16.37

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