The Excited Triplet State Properties of Titanyl Phthalocyanine and its Sulfonated Derivatives
Xian-Fu Zhang A B , Jingyao Huang A , Qian Xi A and Yun Wang AA Chemistry Department, Hebei Normal University of Science and Technology, Qinghuangdao, Hebei Province, 066004, China.
B Corresponding author. Email: zhangxianfu@tsinghua.org.cn
Australian Journal of Chemistry 63(10) 1471-1476 https://doi.org/10.1071/CH10076
Submitted: 10 February 2010 Accepted: 9 April 2010 Published: 1 October 2010
Abstract
Titanyl phthalocyanine (TiOPc) is a well-known, excellent photoconductive material for laser printers and photocopying machines. Its organic derivatives have recently been shown to be excellent photosensitizers for singlet oxygen [O2(1Δg)] production. The excited triplet state properties of TiOPc, in homogeneous DMSO solution, were measured in this study for the first time by nanosecond laser flash photolysis. The data enabled comparisons to be drawn with TiOPcS4 and zinc phthalocyanine (ZnPc), ultimately providing a better understanding of the reported observations. Absorption, fluorescence, and O2(1Δg) sensitization were also studied. TiOPcS4 in DMSO shows remarkably different fluorescence properties from that reported in aqueous solution: both the fluorescence quantum yield (Φf = 0.068) and the fluorescence lifetime (τf = 3.71 ns) were much larger than that reported for aqueous solutions (0.012 and 0.09 ns, respectively). The photosensitizing properties of TiOPcS4 in DMSO are also so significantly better than that in aqueous solution, i.e. triplet lifetime (τT) of 252 μs, triplet quantum yield (ΦT) of 0.42, and the quantum yield of O2(1Δg) (ΦΔ) of 0.49; compare with values of 60 μs, 0.32, 0.13 reported in aqueous solution. TiOPc, however, shows comparable photophysical properties to that of ZnPc, a well-recognized photosensitizer. These results suggest that TiOPc and its derivatives are not only good photoconductors but also good photosensitizers of O2(1Δg), which may find application in photodynamic therapies for treatment of cancer.
[1]
C. K. Jang,
J. Y. Jaung,
J. Chem. Res. 2009, 2009, 312.
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