Synthesis and Photophysical Properties of Substituted 2,2:6,2-Terpyridine Derivatives and Analogous Compounds with a Central Thiophene Ring

被引:7
|
作者
Hommes, Paul [1 ]
Reissig, Hans-Ulrich [1 ]
机构
[1] Free Univ Berlin, Inst Chem & Biochem, Takustr 3, D-14195 Berlin, Germany
关键词
click chemistry; palladium-catalyzed couplings; terpyridines; thiophenes; UV; Vis spectra; CROSS-COUPLING REACTION; DONOR-ACCEPTOR CYCLOPROPANES; AZIDE-ALKYNE CYCLOADDITION; 1,3-DIPOLAR CYCLOADDITIONS; 1.3-DIPOLARE CYCLOADDITIONEN; FUNCTIONALIZED BODIPYS; TERMINAL ALKYNES; LIGANDS; EFFICIENT; 2,2'/6',2''-TERPYRIDINES;
D O I
10.1002/ajoc.201600215
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
New 2,2:6,2-terpyridine derivatives were prepared by Suzuki-Miyaura coupling of the corresponding 4,4-bis(nonaflate) with the appropriate boronic acid derivatives. The corresponding 4,4-diazido terpyridine derivative allowed a copper(I)-promoted click reaction with phenyl acetylene to provide the bis(triazolyl)-substituted terpyridine in excellent yield. For comparison, analogs or terpyridines with a central thiophene ring were synthesized by applying the well proven cyclocondensation reaction of the bis(-ketoenamide) derived from 2,5-thiophenedicarboxylic acid. The UV/Vis spectra as well as the fluorescence spectra of these new compounds were recorded and compared with related heterocycles.
引用
收藏
页码:1033 / 1040
页数:8
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