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Triphenylene Analogues with B2N2C2 Cores:...
Journal article

Triphenylene Analogues with B2N2C2 Cores: Synthesis, Structure, Redox Behavior, and Photophysical Properties

Abstract

A series of alkyl (1-3), aryl (6), and benzo-annulated (4, 5) heteroaromatic triphenylene analogues with B(2)N(2)C(2) cores have been synthesized via chelation of pyridazine derivatives using difunctional Lewis acidic diborabiphenyl precursors. In contrast to triphenylene, NICS(1) calculations on 1 suggested high aromaticities for the central (-11.3 ppm) and outer borabenzene rings (-7.7 ppm), along with nonaromatic behavior for the pyridazine …

Authors

Jaska CA; Emslie DJH; Bosdet MJD; Piers WE; Sorensen TS; Parvez M

Journal

Journal of the American Chemical Society, Vol. 128, No. 33, pp. 10885–10896

Publisher

American Chemical Society (ACS)

Publication Date

August 1, 2006

DOI

10.1021/ja063519p

ISSN

0002-7863