Photophysical properties of 5,10,15,20-tetrakis(m-hydroxyphenyl)porphyrin-(m-THPP), 5,10,15,20-tetrakis(m-hydroxyphenyl)chlorin (m-THPC) and 5,10,15,20-tetrakis(m-hydroxyphenyl)bacteriochlorin (m-THPBC): a comparative study
R. Bonnett et al., Photophysical properties of 5,10,15,20-tetrakis(m-hydroxyphenyl)porphyrin-(m-THPP), 5,10,15,20-tetrakis(m-hydroxyphenyl)chlorin (m-THPC) and 5,10,15,20-tetrakis(m-hydroxyphenyl)bacteriochlorin (m-THPBC): a comparative study, J CHEM S P2, (2), 1999, pp. 325-328
Citations number
24
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2
For the tumour photosensitisers m-THPP, m-THPC,and m-THPBC in methanol the
following photophysical properties have been measured. absorption and fluor
escence spectra, E-s, Stokes shift, Phi(f), Phi(T), tau(T), dioxygen quench
ing rates, and Phi(Delta) for air-saturated and oxygen-saturated solutions.
The properties of the first excited triplet-state are quite uniform across
this series. The quantum yields of singlet oxygen formation are high, bein
g 0.43-0.46 in air-saturated methanol, and 0.59-0.62 in oxygen-saturated me
thanol; For a constant substitution pattern and a standard given light dose
, tumour photonecrosis in vivo appears to parallel the product of drug dose
and the molar extinction at the irradiation wavelength in the red region o
f the visible spectrum.