A new dimer of subphthalocyanine and Seven derivatives ([RPhO-BSubPcOPh] 2 ) of it have been synthesized, characterized and developed for high efficient catalysts to Lithium/thionyl chloride (Li/SOCl 2 ) battery. The stored energy and the capacity of the batteries whose electrolytes contain these compounds as catalysts are increased by approximately 21.4%-33.1% and 15.7%-32.7% than that of the battery in the absence of them. In addition, the results of cyclic voltammetry states that a two-step electron transfer occurs in the reduction process of SOCl 2 .Li/SOCl 2 battery, with high battery voltage and energy density, is a very useful electrochemical power source. 1 It is an ideal candidate for security systems and monitoring systems. 2,3 However, the stored energy and the capacity of the batteries can be still improved to expand the application of them. The using of catalysts can achieve this purpose by extending the discharge time or improving the discharge voltage. To the best of our knowledge, subphthalocyanines used as catalyst in this area have not been reported. Subphthalocyanines (SubPc) 4,5 are cone-shaped, aromatic macrocycles made of three diminoisoindoline units N-fused around a boron atom. Their delocalized 14-π-system characterisc confers them interesting optical properties that have been exploited in the field of dyes, nonlinear optics, organic solar cells and field effect transistors. [6][7][8][9] In this paper, seven different binuclear subphthalocyanines were designed, synthesized and characterized. The catalytic activity of the compounds to Li/SOCl 2 battery was measured. The stored energy and the capacity of the batteries were increased by approximately 21.4%-33.1% and 15.7%-32.7%, respectively. A three-step hypothetical mechanism was proposed and proved by the cyclic voltammetry.
ExperimentalThe synthetic process is described in Scheme 1. Compound 1 was formed by the nucleophilic aromatic substitution reaction of 4-nitrophthalonitrile with 4, 4 -dihydroxybiphenyl in the presence of K 2 CO 3 . 10 Compound 2 was prepared as the method described in literature. 11 Replacement of the bromine atom was prepared by compound 2 reacting with the corresponding phenol. 12 All the compounds were characterized by IR, UV and elemental analysis.