A novel phthalocyanine with two axial fullerene substituents

Tetrahedron Letters

Volumn 46, Issue 40, 2005, Pages 6791-6795

  Kim, Kun Nam ^a   Choi, Chan Soo ^b   Kay, Kwang Yol ^a  

^a Ajou University   (South Korea)

^b Daejeon University   (South Korea)

Author keywords

Absorption spectrum; Electrochemistry; Fullerene; Glassy film; Si phthalocyanine

Indexed keywords

CYANINE DYE; FULLERENE DERIVATIVE; PHTHALOCYANINE; SILICON DERIVATIVE;

ABSORPTION; ABSORPTION SPECTROSCOPY; ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; ELECTROCHEMICAL ANALYSIS; SYNTHESIS; ULTRAVIOLET SPECTROSCOPY;

EID: 27744434914     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2005.08.038     Document Type: Article

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23. -5 M): λmax = 259, 330, 354, 430, 563, 580, 607, 645, 675 nm.
24. -5M): λmax = 259, 277, 358, 381, 563, 580, 610, 647, 676 nm.
25. Differential pulse voltammograms of compound 1 were obtained under the following conditions: 80 mV pulse, 50 ms pulse width, 100 ms periods, and a scan rate of 20 mV/s. The remaining conditions are the same as that of CV measurements. For compound 1: -0.55, -0.72, -1.01, -1.24, -1.33, -1.57, -1.79, -2.08, -2.37, -2.57, -2.77, +1.06, and +1.34 V. For compound 10: -0.54, -0.98, -1.32, -1.55, -1.76, -2.05, and -2.55 V. For compound 11: -1.02 and +1.09 V.
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