化学
位阻效应
药物化学
加合物
异丙基
镁
氟苯
苯
立体化学
配体(生物化学)
有机化学
生物化学
受体
作者
Thomas Xaver Gentner,Bastian Rösch,Gerd Ballmann,Jens Langer,Holger Elsen,Sjoerd Harder
标识
DOI:10.1002/anie.201812051
摘要
Abstract The steric bulk of the well‐known DIPP BDI ligand (CH[C(CH 3 )N‐DIPP] 2 , DIPP=2,6‐diisopropylphenyl) was increased by replacing isopropyl for isopentyl groups. This very bulky DIPeP BDI ligand could not stabilize the radical species ( DIPeP BDI)Mg . : reduction of ( DIPeP BDI)MgI with Na gave ( DIPeP BDI) 2 Mg 2 with a rather long Mg‐Mg bond of 3.0513(8) Å. Addition of TMEDA prior to reduction gave complex ( DIPeP BDI) 2 Mg 2 (C 6 H 6 ), which could also be obtained as its THF adduct. It is speculated that combination of a bulky spectator ligand and TMEDA prevents dimerization of the intermediate Mg I radical, which then reacts with the benzene solvent. Complex ( DIPeP BDI) 2 Mg 2 (C 6 H 6 ), which formally contains the anti ‐aromatic anion C 6 H 6 2− , reacted with t BuOH as a Brønsted base to 1,3‐ and 1,4‐cyclohexadiene and with H 2 as a two electron donor to ( DIPeP BDI) 2 Mg 2 H 2 and C 6 H 6 . It also reductively cleaved the C−F bond in fluorobenzene and gave ( DIPeP BDI)MgPh, ( DIPeP BDI)MgF, and C 6 H 6 .
科研通智能强力驱动
Strongly Powered by AbleSci AI