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2.4- Dimethylenecyclobutane-1,3-diyl

BBB = bismethylenebiscyclobutylidene DMCBD = 2,4-dimethylenecyclobutane-1,3-diyl I/O = input and output HL = Heitler and London SC = spin-coupled. [Pg.2672]

The sequential removal of H and H+ from isobutene-type structural units (so-called H2+ abstraction ) was also used to generate the radical anion of non-Kekule benzene , i.e. l,3-dimethylenecyclobutane-l,3-diyl (39) (Scheme 11). As shown by Hill and Squires161, this highly unusual, distonic C(,II(, isomer can be produced in pure form by reaction of O with 1,3-dimethylenecyclobutane (38). Working in a flowing afterglow mass spectrometer, subsequent reactions were again used to characterize this radical anion and differentiate it from other ( VdL, isomers. [Pg.26]

Spin-coupled Description of Cyclobutadiene and 2,4-Dimethylenecyclobutane-l,3-diyls Antipairs. [Pg.94]


See other pages where 2.4- Dimethylenecyclobutane-1,3-diyl is mentioned: [Pg.513]    [Pg.200]    [Pg.200]    [Pg.513]    [Pg.1224]    [Pg.1224]    [Pg.300]   
See also in sourсe #XX -- [ Pg.200 ]




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1.4- diyl

2.4- Dimethylenecyclobutane-l,3-diyl

Dimethylenecyclobutanes

Diyls

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