Catalytic C-C/C-H Bond Activation Relay for Synthesis of Fluorescent Naphthoquinolizinium Salts

被引:0
|
作者
Ulc, Jan [1 ]
Jacko, Jaroslav [1 ]
Cisarova, Ivana [2 ]
Pospisil, Lubomir [3 ,4 ]
Necas, David [1 ]
Kotora, Martin [1 ]
机构
[1] Charles Univ Prague, Fac Sci, Dept Organ Chem, Hlavova 8, Prague 2, Czech Republic
[2] Charles Univ Prague, Fac Sci, Dept Inorgan Chem, Hlavova 8, Prague 2, Czech Republic
[3] Acad Sci, Inst Organ Chem & Biochem, Flemingovo namesti 2, Prague 16610, Czech Republic
[4] Acad Sci, J Heyrovsky Inst Phys Chem, Dolejskoval 3, Prague 18223, Czech Republic
关键词
catalysis; C-C activation; C-H activation; fluorescence; heterocycles; RH(III)-CATALYZED OXIDATIVE ANNULATION; POLYCYCLIC AROMATIC-HYDROCARBONS; DOPED GRAPHENE SYNTHESIS; ONE-POT SYNTHESIS; POLYHETEROAROMATIC COMPOUNDS; PYRIDINIUM SALTS; INTERNAL ALKYNES; HETEROCYCLES; ROUTE; FUNCTIONALIZATION;
D O I
10.1002/ejoc.202300153
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Herein, we report the design and synthesis of a series of novel cationic nitrogen-embedded polyaromatic hydrocarbons with a planar geometry. The synthetic pathway is based on catalytic C-C/C-H bond activation relay that enabled preparation of regioselectively 5,6,10,11-tetrasubstituted naphtho[2,1,8-ija]quinolizinium salts bearing various types of substituents. Single-crystal X-ray analyses of selected compounds confirmed planarity of the quinolizinium core. Most of the prepared compounds exhibited strong fluorescence (f(s) up to >99 %) ranging from 420-600 nm depending on the substitution pattern. According to DFT calculations LUMO is always distributed over the quinolizinium framework regardless of the attached substituents, whereas delocalization of HOMO is related to the substitution pattern. Electrochemical measurements show irreversible reduction of all compounds, which is supported by the calculated location of LUMO orbitals.
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页数:10
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