Versatile Palladium-catalyzed intramolecular cyclization to access new luminescent azaphosphaphenalene motifs

被引:0
|
作者
Simoens, Andreas [1 ]
Kaczmarek, Anna M. [2 ]
Machado, Ian P. [2 ]
Van Hecke, Kristof [3 ]
Stevens, Christian V. [1 ]
机构
[1] Univ Ghent, Dept Green Chem & Technol Synth, Bioresources & Bioorgan Chem Res Grp, Coupure Links 653, B-9000 Ghent, Belgium
[2] Univ Ghent, Dept Chem, NanoSensing Grp, Krijgslaan 281,S3, B-9000 Ghent, Belgium
[3] Univ Ghent, Dept Chem, XStruct, Krijgslaan 281,S3, B-9000 Ghent, Belgium
基金
比利时弗兰德研究基金会; 欧洲研究理事会;
关键词
Phosphorus; Phosphine oxides; Pd-catalysis; Luminescence; Cross coupling reaction; Polyaromatic; BIOLOGICALLY-ACTIVE QUINOLINE; DIRECT ARYLATION; ORGANOPHOSPHORUS; DEHYDROGENATION; DERIVATIVES; COMPLEXES; DESIGN; BOND;
D O I
10.1002/chem.202303072
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Using a straightforward sequence of diphosphonylation and a Pd-catalysed concerted-metalation-deprotonation (CMD), a synthetic strategy towards polyaromatic phosphorus containing heterocycles was developed. Herein, we report the synthesis and characterization of new azaphosphaphenalenes, using easily accessible palladium catalysts and starting materials. The key tetrahydroquinoline intermediates of the reaction were synthesised via a fast and effective procedure and could be isolated as such, or further reacted towards the target polyaromatic structures. The obtained products showed interesting luminescent properties and their emission, excitation and quantum yields were evaluated. Herein a swift and versatile palladium cyclization is presented using readily accessible catalysts and starting materials to produce new azaphosphaphenalene motifs. The luminescent properties of these products were evaluated and some of the key compounds had their structure unambiguously confirmed by X-ray analysis. The phosphorus atom offers interesting possibilities for post functionalization. image
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页数:9
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