Literature DB >> 23955798

Heteroleptic alkyl and amide iminoanilide alkaline earth and divalent rare earth complexes for the catalysis of hydrophosphination and (cyclo)hydroamination reactions.

Bo Liu1, Thierry Roisnel, Jean-François Carpentier, Yann Sarazin.   

Abstract

[{N^N}M(X)(thf)n] alkyl (X=CH(SiMe3)2) and class="Chemical">amide (X=N(SiMe3)2) comclass="Chemical">plexes of alkaline earths (M=Ca, Sr, class="Chemical">pan class="Chemical">Ba) and divalent rare earths (Yb(II) and Eu(II) ) bearing an iminoanilide ligand ({N^N}(-)) are presented. Remarkably, these complexes proved to be kinetically stable in solution. X-ray diffraction studies allowed us to establish size-structure trends. Except for one case of oxidation with [{N^N}Yb(II){N(SiMe3)2}(thf)], all these complexes are stable under the catalytic conditions and constitute effective precatalysts for the cyclohydroamination of terminal aminoalkenes and the intermolecular hydroamination and intermolecular hydrophosphination of activated alkenes. Metals with equal sizes across alkaline earth and rare earth families display almost identical apparent catalytic activity and selectivity. Hydrocarbyl complexes are much better catalyst precursors than their amido analogues. In the case of cyclohydroamination, the apparent activity decreases with metal size: Ca>Sr>Ba, and the kinetic rate law agrees with R(CHA) =k[precatalyst](1)[aminoalkene](1). The intermolecular hydroamination and hydrophosphination of styrene are anti-Markovnikov regiospecific. In both cases, the apparent activity increases with the ionic radius (Ca<Sr<Ba) but the rate laws are different, and obey R(HA) =k[styrene](1)[amine](1)[precatalyst](1) and R(HP) =k[styrene](1)[HPPh2 ](0)[precatalyst](1), respectively. Mechanisms compatible with the rate laws and kinetic isotopic effects are proposed. [{N^N}Ba{N(SiMe3)2}(thf)2] (3) and [{N^N}Ba{CH(SiMe3)2}(thf)2] (10) are the first efficient Ba-based precatalysts for intermolecular hydroamination and hydrophosphination, and display activity values that are above those reported so far. The potential of the precatalysts for C-N and C-P bond formation is detailed and a rare cyclohydroamination-intermolecular hydroamination "domino" sequence is presented.
Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  alkaline earth metals; hydroamination reactions; hydrophosphination reactions; rare earths; reaction mechanisms

Year:  2013        PMID: 23955798     DOI: 10.1002/chem.201301464

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  4 in total

Review 1.  s-Block Metal Catalysts for the Hydroboration of Unsaturated Bonds.

Authors:  Marc Magre; Marcin Szewczyk; Magnus Rueping
Journal:  Chem Rev       Date:  2022-03-07       Impact factor: 72.087

Review 2.  Lithium-Aluminate-Catalyzed Hydrophosphination Applications.

Authors:  Victoria A Pollard; Allan Young; Ross McLellan; Alan R Kennedy; Tell Tuttle; Robert E Mulvey
Journal:  Angew Chem Int Ed Engl       Date:  2019-07-25       Impact factor: 15.336

3.  Enantiopure Calcium Iminophosphonamide Complexes: Synthesis, Photoluminescence, and Catalysis.

Authors:  Bhupendra Goswami; Thomas J Feuerstein; Ravi Yadav; Ralf Köppe; Sergei Lebedkin; Manfred M Kappes; Peter W Roesky
Journal:  Chemistry       Date:  2021-02-02       Impact factor: 5.236

4.  Versatile Visible-Light-Driven Synthesis of Asymmetrical Phosphines and Phosphonium Salts.

Authors:  Percia Beatrice Arockiam; Ulrich Lennert; Christina Graf; Robin Rothfelder; Daniel J Scott; Tillmann G Fischer; Kirsten Zeitler; Robert Wolf
Journal:  Chemistry       Date:  2020-10-30       Impact factor: 5.236

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.