高区域选择性铑催化烯烃氢甲酰化的含膦树状大分子:积极的“树状效应”

Loïc Ropartz, K. Haxton, Douglas F. Foster, R. Morris, A. Slawin, D. Cole-Hamilton
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引用次数: 48

摘要

用二苯基膦功能化的多面体低聚硅氧烷(POSS)树状大分子作为配体进行了辛-1-烯的铑催化氢甲酰化反应,显示出出乎意料的对直链醛壬胺-1-al的高区域选择性(1∶b = 14∶1)。清楚地证实了这些双齿树突配体的不寻常的选择性,并显示了“积极的树突效应”的发生。这种高选择性是在第一代和第二代树状大分子中只有一个结构(磷原子之间的5个原子间隔层和碳-硅键),而其他框架(P原子之间的3个和7个原子间隔层,或碳-氧-硅键)导致选择性较低。
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Phosphine containing dendrimers for highly regioselective rhodium catalysed hydroformylation of alkenes: a positive ‘dendritic effect’
Diphenylphosphine functionalised polyhedral oligomeric silsesquioxane (POSS) dendrimers are used as ligands for the rhodium catalysed hydroformylation of oct-1-ene showing unexpectedly high regioselectivity to the linear aldehyde nonan-1-al (l ∶ b = 14 ∶ 1). Comparative studies with the small molecule analogues, bis-diphenylphosphinopentane, Me2Si[CH2CH2PPh2]2 and Si[CH2CH2PPh2]4, clearly confirm the unusual selectivity of these bidentate dendritic ligands and show that a ‘positive dendritic effect’ occurs. This high selectivity is obtained with only one structure within the 1st and 2nd generation dendrimer (spacer of five atoms between the phosphorus atoms, and carbon–silicon linkage) whilst other frameworks (spacer of three and seven atoms between the P atoms, or carbon–oxygen–silicon linkage) lead to lower selectivity.
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