Boisdenghien Arnaud, Leveque Julien, Moucheron Cécile, Kirsch-De Mesmaeker Andrée
Service de Chimie Organique et Photochimie, CP 160/08, Université Libre de Bruxelles, (U. L. B.), 50 Avenue F.D. Roosevelt, B-1050, Bruxelles, Belgium.
Dalton Trans. 2007 May 7(17):1705-12. doi: 10.1039/b618645a. Epub 2007 Mar 16.
Three trinuclear elbow-shaped Ru(II) complexes based on the non symmetrical bridging PHEHAT ligand (PHEHAT = 1,10-phenanthrolino[5,6-b]-1,4,5,8,9,12-hexaazatriphenylene) have been prepared and characterized by NMR, electrochemistry, absorption and emission spectroscopy. It is shown that the dichloro trinuclear complex 1 should behave as an excellent precursor for the synthesis of larger species. Indeed, it reacts easily with 1,10-phenanthroline (phen) and 1,4,5,8-tetraazaphenanthrene (TAP) and leads to the trinuclear compounds 2 and 3, respectively. The electrochemical and emission studies indicate that for 2 and 3, there is an intramolecular energy transfer from the center to the periphery of the elbow-shaped trinuclear complex, whereas for complex 1 the energy transfer takes place in the other direction.
基于非对称桥联配体PHEHAT(PHEHAT = 1,10 - 菲咯啉并[5,6 - b]-1,4,5,8,9,12 - 六氮杂三苯撑)制备了三种三核肘形Ru(II)配合物,并通过核磁共振、电化学、吸收光谱和发射光谱对其进行了表征。结果表明,二氯三核配合物1应是合成更大物种的优良前体。实际上,它能轻松与1,10 - 菲咯啉(phen)和1,4,5,8 - 四氮杂菲咯啉(TAP)反应,分别生成三核化合物2和3。电化学和发射研究表明,对于化合物2和3,在肘形三核配合物中存在从中心到外围的分子内能量转移,而对于配合物1,能量转移则发生在相反方向。