Oubaha Hamid, Demitri Nicola, Rault-Berthelot Joëlle, Dubois Philippe, Coulembier Olivier, Bonifazi Davide
Department of Chemistry , University of Namur , Rue de Bruxelles 61 , 5000 Namur , Belgium.
Laboratory of Polymeric and Composite Materials (LPCM), Center of Innovation and Research in Materials and Polymers (CIRMAP) , University of Mons , Place du Parc 23 , 7000 Mons , Belgium.
J Org Chem. 2019 Jul 19;84(14):9101-9116. doi: 10.1021/acs.joc.9b01046. Epub 2019 Jul 8.
In this paper, we describe synthetic routes for preparing a novel switchable BNC-based chromophore, composed of a borazine core peripherally functionalized with azobenzene moieties. Capitalizing on the Pd-catalyzed Suzuki cross-coupling reaction between a tris-triflate borazine and an organoboron azobenzene derivative, a photoswtichable azo-borazine derivative was successfully prepared. The molecule showed reversible / photoisomerization upon irradiation at the maximum of the intense π-π* absorption feature (360 nm). X-ray crystallographic investigations revealed a nonplanar orientation of the three azobenzene moieties and the trans configuration of the -N═N- bonds. Building on the synthetic versatility of the borazine-azobenzene derivative, we used this photoactive scaffold to engineer soluble BN-doped polythiophene polymers. Photophysical characterization performed in solvents of different polarity suggested that the polymer undergoes intramolecular charge transfer (ICT).
在本文中,我们描述了一种新型可切换的基于硼氮苯的发色团的合成路线,该发色团由一个被偶氮苯基团外围功能化的硼嗪核心组成。利用三(三氟甲磺酸酯)硼嗪与有机硼偶氮苯衍生物之间的钯催化铃木交叉偶联反应,成功制备了一种光可切换的偶氮硼嗪衍生物。该分子在强烈的π-π*吸收特征峰(360 nm)处照射时表现出可逆的光异构化。X射线晶体学研究揭示了三个偶氮苯基团的非平面取向以及-N═N-键的反式构型。基于硼嗪-偶氮苯衍生物的合成多功能性,我们使用这种光活性支架设计了可溶性硼氮掺杂聚噻吩聚合物。在不同极性溶剂中进行的光物理表征表明,该聚合物发生分子内电荷转移(ICT)。