Electronically Driven Regioselective Iridium‐Catalyzed C−H Borylation of Donor‐π‐Acceptor Chromophores Containing Triarylboron Acceptors

Abstract: We observed a surprisingly high electronically driven regioselectivity for the iridium‐catalyzed C−H borylation of donor‐π‐acceptor (d‐π‐A) systems with diphenylamino (1) or carbazolyl (2) moieties as the donor, bis (2,6‐bis (trifluoromethyl) phenyl) boryl (B (FXyl) 2) as the acceptor, and 1,4‐phenylene as the π‐bridge. Under our conditions, borylation was observed only at the sterically least encumbered para‐positions of the acceptor group. As boronate esters are versatile building blocks for organic synthesis (C−C coupling, functional group transformations) the C−H borylation represents a simple potential method for post‐functionalization by which electronic or other properties of d‐π‐A systems can be fine‐tuned for specific applications. The photophysical and electrochemical properties of the borylated (1‐(Bpin) 2) and unborylated (1) diphenylamino‐substituted d‐π‐A systems were investigated. Interestingly, the borylated derivative exhibits coordination of THF to the boronate ester moieties, influencing the photophysical properties and exemplifying the non‐innocence of boronate esters.

Standort
Deutsche Nationalbibliothek Frankfurt am Main
Umfang
Online-Ressource
Sprache
Englisch

Erschienen in
Electronically Driven Regioselective Iridium‐Catalyzed C−H Borylation of Donor‐π‐Acceptor Chromophores Containing Triarylboron Acceptors ; volume:26 ; number:46 ; year:2020 ; pages:10626-10633 ; extent:8
Chemistry - a European journal ; 26, Heft 46 (2020), 10626-10633 (gesamt 8)

Urheber

DOI
10.1002/chem.202002348
URN
urn:nbn:de:101:1-2022060308113819946909
Rechteinformation
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Letzte Aktualisierung
15.08.2025, 07:27 MESZ

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