Differences in the stability of zirconium(IV) complexes related to catalytic phosphine dehydrocoupling reactions.
نویسندگان
چکیده
Relating to the catalytic dehydrocoupling of secondary phosphine substrates, zirconium phosphide complexes supported by triamidoamine and pentamethylcyclopentadienyl ligands exhibit different stability that is attributed to β-hydride elimination.
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ورودعنوان ژورنال:
- Dalton transactions
دوره 40 30 شماره
صفحات -
تاریخ انتشار 2011