Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Biradicaloids charge transfer

W. Rettig, F. Marschner, Molecular conformation and biradicaloid charge transfer states in substituted N-pheny 1-pyrroles, NewJ. Chem. 74,819(1990). [Pg.145]

The intermediacy of a species analogous to (i) (Scheme 1.7) that some described as a resonance hybrid of a radical pair and an ion pair and others as an ultrafast equilibrium between radical and ion pair has been proposed in the photoionization reaction of benzyl derivatives [172, 174-176]. Also, interestingly, to explain the driving force behind the rotational motion that leads to an extremely rapid deactivation of S of TAM cations, Vogel and Rettig [177] proposed that SI promptly forms a biradicaloid charge-transfer state. [Pg.22]


See other pages where Biradicaloids charge transfer is mentioned: [Pg.268]    [Pg.268]    [Pg.59]    [Pg.66]    [Pg.165]    [Pg.428]    [Pg.255]    [Pg.214]    [Pg.218]    [Pg.303]    [Pg.120]    [Pg.122]    [Pg.132]    [Pg.444]    [Pg.76]    [Pg.95]    [Pg.151]    [Pg.210]    [Pg.214]    [Pg.218]    [Pg.303]    [Pg.935]    [Pg.18]   
See also in sourсe #XX -- [ Pg.59 ]




SEARCH



Biradicaloid

Biradicaloids

© 2024 chempedia.info