DMPC (dimyristoyl-L-alpha-phosphatidylcholine) liposomes are used as artifi
cial photosynthetic media to study the behavior of carotenoids. 8'-Apo-beta
-caroten-8'-al (I) and beta-carotene (II) degrade faster under irradiation
in DMPC liposomes than in organic solvents, which is possibly because vibra
tional deactivation of carotenoid excited states is less efficient in rigid
lipid membranes. The lifetime of the first excited singlet state (SI) of I
in DMPC liposomes is 27.2 ps, very close to that in 3-methylpentane (26.4
ps), but longer than its lifetime in EtOH (17.1 ps) or CH2Cl2 (14.1 ps). Th
e lifetime of the S-1 state of I in DMPC liposomes is as expected for an al
kane environment. The lifetime of the S-1 state of II in DMPC liposomes is
10.3 ps, very close to its lifetimes in 3-methylpentane (8.1 ps), EtOH (9.2
ps), and CH2Cl2 (8.5 ps). This independence of the S-1 state lifetime of I
I from the matrix agrees with earlier conclusions. Carotenoid I can suppres
s the photodegradation of chlorophyll a (Chl a) in liposomes, which shows t
he protection role of I on Chl cr under strong irradiation. In liposomes, C
hi a fluorescence quenching by I is observed when using either the Q(y) ban
d or the Soret band of Chi a as the excitation line.