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Transition metal-lead single bond reactivity

C. Reactivity of the Transition Metal Lead Single Bond. 1312... [Pg.1242]

The C—H bond activation of benzene leading to equimolar amounts of metal hydride and metal phenyl products resembles the oxidative addition mechanism by late transition metal complexes, in which a single, mixed metal hydride phenyl product forms. The intriguing reactivity and its generality for rare-earth metals prompted a detailed mechanistic study. Inspired by previous reports of inverse-sandwich rare-earth metal arene com-plexes and taking into account the capacity ofbenzene to accept elec-... [Pg.61]

See other pages where Transition metal-lead single bond reactivity is mentioned: [Pg.421]    [Pg.115]    [Pg.43]    [Pg.3813]    [Pg.118]    [Pg.4]    [Pg.172]    [Pg.3812]    [Pg.207]    [Pg.155]    [Pg.25]    [Pg.452]    [Pg.610]    [Pg.890]    [Pg.263]    [Pg.104]   
See also in sourсe #XX -- [ Pg.1312 , Pg.1313 ]

See also in sourсe #XX -- [ Pg.1312 , Pg.1313 ]



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Bonding single bonds

Lead metal

Metallic lead

Metals reactivity

Single bonds

Single metals

Transition metal reactivity

Transition metal-lead single bond

Transition reactive

Transition reactivity

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