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Halobenzenes astatination

Nucleophilic astatination of halobenzenes CgHjX (X = Cl, Br, I) in homogeneous mixtures with -C4H9NH2, (C2H5)2NH, and (C2Hj>3N at 210° C has led to the formation of astatobenzene with radiochemical yields of 75-90% 143, 144). A two-step process has been postulated [Eqs. (10) and (11)], with the latter reaction [Eq. (11)] as the ratedetermining step ... [Pg.58]

Activation Energies for Nucleophiuc Astatination of Halobenzenes The Influence of Aliphatic Amines... [Pg.59]

TABLE 2. Activation energy for homogeneous halogen exchange by astatine in halobenzenes. Reproduced with permission from Reference 24... [Pg.791]

TABLE 3. Yields and reaction times for homogeneous halogen exchange by astatine from halobenzenes (t = 200 °C)25... [Pg.791]

TABLE 6. Yield and isomer distribution for electrophilic hydrogen replacement by astatine in heterogeneous mixtures of benzene and halobenzenes with HCI04. Reproduced with permission from Reference 50... [Pg.796]


See other pages where Halobenzenes astatination is mentioned: [Pg.123]    [Pg.123]    [Pg.61]    [Pg.795]    [Pg.804]   
See also in sourсe #XX -- [ Pg.56 , Pg.57 , Pg.58 ]




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