100649-32-9Relevant articles and documents
Cerium-Hydride Secondary Building Units in a Porous Metal-Organic Framework for Catalytic Hydroboration and Hydrophosphination
Ji, Pengfei,Sawano, Takahiro,Lin, Zekai,Urban, Ania,Boures, Dean,Lin, Wenbin
, p. 14860 - 14863 (2016)
We report the stepwise, quantitative transformation of CeIV6(μ3-O)4(μ3-OH)4(OH)6(OH2)6 nodes in a new Ce-BTC (BTC = trimesic acid) metal-organic framework (
Phosphinoalkylnitriles: Synthesis and coordination behaviour at palladium centres
Pitter, Stephan,Dinjus, Eckhard,Jung, Beate,Go?rls, Helmar
, p. 934 - 946 (2007/10/03)
Phosphinoalkylnitriles R2P-(CH2)n-CN {R = isopropyl (ipr), phenyl (ph), cyclohexyl (chex), n = 3, 6, 10} have been prepared starting from the corresponding secondary phosphines in an easy three step synthesis. All new compounds were characterized by their 1H-, 13C and 31P NMR data. Some of these new P, N ligands were used to prepare complexes [{R2P-(CH2)n-CN}2PdCl2] which were also identified by their NMR data. In addition the crystal structures of three derivatives, [{ipr2P-(CH2)3-CN} 2PdCl2] 7a, [{ph2P-(CH2)3-CN}2PdCl2] 7b and [{ph2P-(CH2)6-CN}2PdCl2] 8b were determined by X-ray analysis. The coordination mode of the phosphinoalkylnitriles in these complexes was found to be P-bonded resulting in a trans configuration. Palladium catalysts with 5a as ligund show high activies in the co-oligomerization of butadiene and carbon dioxide. The δ-lactone 11a is formed under very mild conditions.