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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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