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Open-Shell Benzenoid Polycyclic Hydrocarbons

Polycyclic Arenes and Heteroaren Synthesis, Propaties, and Applications, First Edition. Edited by Qian Miao. 2016 Wiley-VCH Verlag GmbH Co. KGaA. Published 2016 by JWley-VCHVerlag GmbH Co. KGaA. [Pg.3]

Most benzenoid PHs actually can be characterized by a closed-shell electronic configuration accommodating their % electrons only in bonding orbitals. However, researchers faced difficulties for certain types of PHs due to their high reactivity. An important work by Bendikov et al. came into spotlight in 2004 when their computational study on oligoacenes supported that the longer acenes [Pg.4]

Theoretically, the diradical character (y) (0 y l, where 0 = closed-shell, [Pg.5]

The synthesis and study of open-shell PHs have become a rising hot topic nowadays, so we aim to provide a brief overview on recent advancements including theoretical studies and experimental characterizations of a series of benzenoid PH-based diradicaloids comprising higher order acenes, bis(phenalenyl)s. [Pg.5]

See other pages where Open-Shell Benzenoid Polycyclic Hydrocarbons is mentioned: [Pg.3]    [Pg.4]    [Pg.6]    [Pg.8]    [Pg.10]    [Pg.12]    [Pg.16]    [Pg.20]    [Pg.22]    [Pg.24]    [Pg.26]    [Pg.30]    [Pg.34]    [Pg.36]    [Pg.3]    [Pg.4]    [Pg.6]    [Pg.8]    [Pg.10]    [Pg.12]    [Pg.16]    [Pg.20]    [Pg.22]    [Pg.24]    [Pg.26]    [Pg.30]    [Pg.34]    [Pg.36]    [Pg.215]    [Pg.3]   


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Benzenoids

Hydrocarbon, benzenoid

Open shell

Polycyclic benzenoid

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