Synthesis and Photophysics of a 2,7-Disubstituted Donor–Acceptor Pyrene Derivative: An Example of the Application of Sequential Ir-Catalyzed C–H Borylation and Substitution Chemistry-Reference-Cited by-同舟云学术

Synthesis and Photophysics of a 2,7-Disubstituted Donor–Acceptor Pyrene Derivative: An Example of the Application of Sequential Ir-Catalyzed C–H Borylation and Substitution Chemistry

Published:2015-05-14 Issue:11 Volume:80 Page:5658-5665
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Ji Lei¹,Lorbach Andreas¹,Edkins Robert M.¹,Marder Todd B.¹

Affiliation:

1. Institut für Anorganische Chemie, Julius-Maximilians-Universität Würzburg, Am Hubland, 97074 Würzburg, Germany

Funder

Alexander von Humboldt-Stiftung

Bayerisches Staatsministerium für Wissenschaft, Forschung und Kunst

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.5b00618

Reference41 articles.

1. Pyrene-Based Materials for Organic Electronics

2. Synthesis of 2‐ and 2,7‐Functionalized Pyrene Derivatives: An Application of Selective CH Borylation

3. Experimental and Theoretical Studies of the Photophysical Properties of 2- and 2,7-Functionalized Pyrene Derivatives

4. C−H Activation for the Construction of C−B Bonds

5. Selective Ir-catalysed borylation of polycyclic aromatic hydrocarbons: structures of naphthalene-2,6-bis(boronate), pyrene-2,7-bis(boronate) and perylene-2,5,8,11-tetra(boronate) esters

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