1361129-60-3Relevant academic research and scientific papers
R-allyl nickel(II) complexes with chelating N-heterocyclic carbenes: Synthesis, structural characterization, and catalytic activity
Benitez Junquera, Lourdes,Puerta, M. Carmen,Valerga, Pedro
, p. 2175 - 2183 (2012)
The N-heterocyclic carbene (NHC) nickel complexes [(L)Ni(NHC)][BAr F4] (ArF = 3,5-bis(trifluoromethyl)phenyl; L = allyl (1), methylallyl (2); NHC = 1-(2-picolyl)-3-methylimidazol-2-ylidene (a), 1-(2-picolyl)-3-isopropylimidazol-2-ylidene (b), 1-(2-picolyl)-3-n- butylimidazol-2-ylidene (c), 1-(2-picolyl)-3-phenylimidazol-2-ylidene (d), 1-(2-picolyl)-3-methylbenzoimidazol-2-ylidene (e), 1-(2-picolyl)-4,5-dichloro-3- methylimidazol-2-ylidene (f)) have been obtained in high yields and characterized by NMR spectroscopy. Furthermore, 1d was unambiguously characterized by single-crystal X-ray crystallography. Complexes 1a-f/2a-f have shown catalytic activity toward dimerization and hydrosilylation of styrenes. In particular, 1a proved to be the most efficient catalyst in the dimerization of styrene derivatives in the absence of cocatalyst. Also, complexes 1a,d showed high selectivity and moderate to good yields in hydrosilylation reactions.
Preparation method and application of 2, 9-diaryl-substituted phenanthroline and 2, 9-diaryl-substituted phenanthroline iron complex
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Paragraph 0135; 0136; 0137; 0138; 0139, (2018/04/02)
The present invention relates to a preparation method and application of 2, 9-diaryl-substituted phenanthroline and a 2, 9-diaryl-substituted phenanthroline iron complex. Specifically, the substitutedphenanthroline is prepared by Suzuki coupling reaction
Cobalt-Catalyzed Regiodivergent Hydrosilylation of Vinylarenes and Aliphatic Alkenes: Ligand- and Silane-Dependent Regioselectivities
Wang, Chao,Teo, Wei Jie,Ge, Shaozhong
, p. 855 - 863 (2017/06/07)
We report a regiodivergent hydrosilylation of alkenes catalyzed by catalysts generated in situ from bench-stable Co(acac)2 and phosphine- or nitrogen-based ligands. A wide range of vinylarenes and aliphatic alkenes reacted to afford either branched (45 examples) or linear (37 examples) organosilanes in high isolated yields (average: 84%) and high regioselectivities (from 91:9 to >99:1). This transformation tolerates a variety of functional groups including ether, silyloxy, thioether, epoxide, halogen, amine, ester, boronic ester, acetal, cyano, and ketone moieties. Mechanistic studies suggested that the hydrosilylation of alkenes catalyzed by the cobalt/bisphosphine system follows the Chalk-Harrod mechanism (with a Co-H intermediate), and the hydrosilylation of alkenes catalyzed by the cobalt/pyridine-2,6-diimine system follows the modified Chalk-Harrod mechanism (with a Co-Si intermediate). Systematic studies with sterically varied silanes revealed that the steric properties of silanes play a pivotal role in controlling the regioselectivity of vinylarene hydrosilylation and the chemoselectivity of the reactions of aliphatic alkenes and silanes catalyzed by the cobalt/pyridine-2,6-diimine system.
