Beyond Dehydrocoupling: Group 2 Mediated Boron-Nitrogen Desilacoupling.

نویسندگان

  • David J Liptrot
  • Merle Arrowsmith
  • Annie L Colebatch
  • Terrance J Hadlington
  • Michael S Hill
  • Gabriele Kociok-Köhn
  • Mary F Mahon
چکیده

The alkaline-earth element bis(trimethylsilyl)amides, [Ae{N(SiMe3 )2 }2 (thf)2 ] [Ae=Mg, Ca, Sr], are effective precatalysts for boron-nitrogen bond formation through the desilacoupling of amines, RR'NH (R=alkyl, aryl; R'=H, alkyl, aryl), and pinBSiMe2 Ph. This reactivity also yields a stoichiometric quantity of Me2 PhSiH and provides the first example of a catalytic main-group element-element coupling that is not dependent on the concurrent elimination of H2 .

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Stoichiometric and catalytic Sn-mediated dehydrocoupling of primary phosphines.

The room-temperature reactions of stannocene, Cp*(2)Sn, with a range of primary phosphines, RPH(2), result in diphosphanes [RP(H)P(H)R]. The reactions involving Cp*(2)SnCl(2), however, result in catalytic dehydrocoupling; the first example of main group metal catalysed dehydrocoupling to be identified.

متن کامل

Alkali metal-mediated dehydrocoupling of Me2NH·BH3.

Bis(trimethylsilyl)amide derivatives of the group 1 elements (Li, Na, K) are competent pre-catalysts for the dehydrocoupling of Me2NH·BH3 via the formation of intermediates containing [H3BNMe2BH2Me2N](-) anions.

متن کامل

Boron-oxygen luminescence centres in boron-nitrogen systems.

Closed-shell BO(2)(-) and BO(-) anions are proposed as high-efficiency luminescence centres in boron-nitrogen systems, which makes the anions localized and leads to a radiation transition.

متن کامل

Supramolecular polymers based on dative boron-nitrogen bonds.

Heteroditopic monomers containing an arylboronate ester and a dialkyl-4-aminopyridine group aggregate via dative boron-nitrogen bonds to give main chain supramolecular polymers. The degree of polymerization can be tuned by changing the electronic and steric properties of the boronate ester.

متن کامل

Pyridine-promoted Cyclization of Functionalized N-Silylated Boron-Nitrogen Compounds

Dichloroboryldisilylamines [SiClm(CH3)3−m]N[Si(CH3)3](BCl2) (m = 1 – 3) as well as chloromethylboryl-bis-(chlorodimethylsilyl)amine [SiCl(CH3)2]2N[BCl(CH3)] form 1 : 1 adducts with pyridine (1 – 4). Those with m = 2 and 3 have been converted into functionalized diazadiboretidine derivatives which are still coordinated by pyridine: [(SiClm(CH3)3−m)NBCl · Py]2 (5: m = 2, 6: m = 3). Single-crystal...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Angewandte Chemie

دوره 54 50  شماره 

صفحات  -

تاریخ انتشار 2015