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This optical absorption measurement of 5,10,15-Triphenylcorrole were made by M. Taniguchi on 10-01-2004 using a HP 8453. The absorption values were collected using a spectral bandwidth of 1.0 nm.
These measurements were scaled to make the molar extinction coefficient match the value of 110,000cm-1/M at 415.0nm (Paolesse, 2001).
The fluorescence emission spectrum of 5,10,15-Triphenylcorrole dissolved in dichloromethane. The quantum yield of this molecule is 0.14 (Dixon, 2005). This spectrum was collected by on 10-01-2004 using a PTI QM-4/2003 SE. The excitation and emission monochromators were set at 0.25 mm, giving a spectral bandwidth of 1 nm. The data interval was 1 nm and the integration time was 1 sec.
Samples were prepared in 1cm pathlength quartz cells with absorbance less than 0.1 at the excitation and all emission wavelengths to uniformly illuminate across the sample, and to avoid the inner-filter effect. The dark counts were subtracted and the spectra were corrected for wavelength-dependent instrument sensitivity.
Dixon, J. M., M. Taniguchi and J. S. Lindsey (2005), "PhotochemCAD 2. A Refined Program with Accompanying Spectral Databases for Photochemical Calculations, Photochem. Photobiol., 81, 212-213.
Du, H., R.-C. A. Fuh, J. Li, L. A. Corkan and J. S. Lindsey (1998) PhotochemCAD: A computer-aided design and research tool in photochemistry. Photochem. Photobiol. 68, 141-142.
Ka, J.-W., W.-S. Cho and C.-H. Lee (2000) Expedient synthesis of corroles by oxidant-mediated, direct a-a' coupling of tetrapyrromethanes. Tetrahedron Lett. 41, 8121-8125.
Paolesse, R., S. Nardis, F. Sagone and R. G. Khoury (2001) Synthesis and functionalization of meso-aryl-substituted corroles. J. Org. Chem. 66, 550-556.