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. Author manuscript; available in PMC: 2011 May 12.
Published in final edited form as: Chem Rev. 2010 May 12;110(5):2579–2619. doi: 10.1021/cr900301e

Table 5.

Spectroscopic Properties of Selected Polyenesa

# Name Solvent λmax (ε) λem Φ τ
4.34b Retinol MeOH - - 0.007 1.5
cyclohexane 325 520 0.020 5.0
4.35c cis-PnA MeOH 318.6, 303.8 (79)b ‘432’d 0.017 1.3
decane 320,8, 305.8 (74) 432 0.054 5.2
4.36e trans-PnA MeOH 313.0, 298.6 (92) ‘422’d 0.031 <1
decane 315.3, 300.7 (88) 422 0.009 3.1
4.37d trans-PA EtOH 344.7 (103) 468 0.075 10.7
dioxane 348.9 (81) 468 0.14 13.7
4.38e trans-PdA CHCl3 353 (92), 335 (95), 320 (60) 474 0.14g -
a

λ, ε, and τ are given in nm, 103 M−1cm−1, and ns respectively

b

Data from Radda and Smith.205

c

Data from Diamond et al.213

d

The emission maximum as virtually solvent independent.213

e

Data from Acuna et al., average lifetimes given.214

f

Data from Acuna et al.215

g

Quantum yield in DMPC vesicles.215