A N3-geminal Al/P-Based Intramolecular Lewis Pair: Synthesis, Characterization and Reactivity

被引:0
作者
Sun, Xiong [1 ]
Xie, Zhuoyi [2 ]
Zou, Lianghua [3 ]
机构
[1] Wuxi Univ, Sch Environm Sci & Engn, Wuxi 214105, Jiangsu, Peoples R China
[2] Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Coordinat Chem, Jiangsu Key Lab Adv Organ Mat, Nanjing 210023, Peoples R China
[3] Jiangnan Univ, Sch Life Sci & Hlth Engn, Lihu Ave 1800, Wuxi 214122, Jiangsu, Peoples R China
关键词
frustrated Lewis pairs; aluminum; small molecules; trianionic ligand; phosphorus; SMALL-MOLECULE ACTIVATION; HETEROLYTIC DIHYDROGEN ACTIVATION; TRANSITION-METAL; COORDINATION BEHAVIOR; ADDUCT FORMATION; CARBON-DIOXIDE; BOND-CLEAVAGE; ALUMINUM; FLP; COMPLEXES;
D O I
10.1002/ejic.202400842
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Frustrated Lewis pairs (FLPs) play a crucial role in main-group chemistry due to the diverse reactivities towards small molecules and extensive applications in organic transformations. The intramolecular FLP systems known in the literature are mainly consisted of boron-containing Lewis acids and the linkers are almost exclusively based on carbon. Herein, the nitrogen-linked geminal Al/P Lewis pair 1 was readily prepared by salt metathesis reaction between AlBr3 and N[CH2CH2NLi-PtBu2]3 in toluene at room temperature. Further studies confirmed that 1 exhibited typical FLP-type reactivity towards heterocumulenes, isocyanide and transition metal precursors. Single-crystal X-ray diffraction analysis revealed that all the addition products contained a penta-coordinated aluminum atom which was less common in FLP chemistry. This study demonstrated that the resulting Al/P-based system represented an efficient alternative class of FLPs and enriched the linker motifs of intramolecular FLPs.
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页数:7
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