Abstract:UV-Vis absorption spectras of six series (18 kinds) of tetra- azo-aromaticoxy substituted metallophthalocyanines (R4PcM, R=4-pyridyloxy,8-quinolinoxy,2-methyl-8-quinolinoxy;substitution position:α position and β position;M=Ni(Ⅱ), Cu(Ⅱ), Zn(Ⅱ)) were measured. The effects of central mentals,the kinds and the positions of substitution groups, and solvents on the metallophthalocyanines’ λmax in Q-band were discussed. Experimental data show:The λmax in Q-band of title complexes is about 680 nm. In contrast with substitution-free metallophthalocyanines(669-671 nm), the λmax in Q-band of the title complexes with the same central metal exhibits a different red-shift. The effect of substitution group’s kinds on λmax in Q-band of the title complexes is more obvious in α position than in β position, and with the same substitution group and central metal, λmax in Q-band of α position substituted complexes exhibits more obvious red-shift than β position substituted complexes. The effects of central metal and solvent on λmax in Q-band of the title complexes aren’t obvious.
[1] Lever A B P, Pickens S R, Minor P C, et al. J. Am. Chem. Soc., 1981, 103:6800. [2] Danilo Dini, Michael Hanack. J. Porphyrins and Phthalocyanines, 2004, 8: 915. [3] XUE Jin-ping, HONG Hu-ming, CAI Sen-lin, et al(薛金萍, 洪湖铭, 蔡森林, 等). Chinese J. Inorg. Chem.(无机化学学报), 2005, 21(6): 810. [4] HONG Hu-ming, XUE Jin-ping, SUN Gang-chun, et al(洪湖铭, 薛金萍, 孙纲春, 等). J. of Fuzhou University·Natural Science Edition(福州大学学报·自然科学版), 2005, 33(3): 382. [5] HUANG Jin-ling, PENG Yi-ru,CHEN Nai-sheng(黄金陵, 彭亦如, 陈耐生). Spectroscopy and Spectral Analysis(光谱学与光谱分析),2001, 21(1):1. [6] HUANG Jian-dong,LIU Er-sheng,YANG Su-ling, et al(黄剑东, 刘尔生, 杨素苓, 等). Spectroscopy and Spectral Analysis(光谱学与光谱分析),2000, 20(1): 95. [7] SHEN Shu-yin,LIU Kai,DING Xi-ming, et al(沈淑引, 刘 恺, 丁西明,等). Applied Chemistry(应用化学),1997,14(5):43.