S. Hashimoto et al., Photophysical studies of neutral aromatic species confined in zeolite L: Comparison with cationic dyes, PHYS CHEM P, 3(22), 2001, pp. 5043-5051
The photophysical properties of a few aromatic molecules incorporated into
the straight channels of zeolite L were investigated, mainly by luminescenc
e spectroscopy. Two significant observations were made. (1) Intense room te
mperature phosphorescence (RTP) was observed for 9-ethylcarbazole and other
aromatics included in the dehydrated K+-form of the zeolite L (KL) whereas
RTP was very weak in 47 atom % Na+-exchanged KL (NaKL) and the K+- and Na-forms of zeolite Y (KY and NaY). Previously, observation of RTP was only m
ade in zeolites exchanged with heavy atom cations such as Rb+ and Cs+. For
9-ethylcarbazole, the tight rt into the KL channels and resultant increased
structural rigidity are largely responsible for the remarkable reduction i
n the rate of nonradiative intersystem crossing from T-1 to S-0, leading to
the enhanced phosphorescence lifetime even at room temperature. (2) Anthra
cene, intercalated in the channels, formed dimers that can be detected by t
he excimer emission. It was found that the dimer formed in NaKL has less ov
erlap than that formed in KL. Moreover, the dimer must have a remarkably sh
ort separation between the two rings, comparable to that of anthracenophane
, judging from its distorted absorption spectrum. Formation of naphthalene
dimers with partial overlap in KL was identified from the characteristic fl
uorescence spectrum of the second excimer. No naphthalene dimer was formed
in NaKL even at high loadings. Thus the photophysics of anthracene and naph
thalene in zeolite L is remarkably different from that in solutions and lar
ge-pore faujasite zeolites where the framework exerts only weak conformatio
nal control over the guest molecules. Additionally, the charge compensating
cations in zeolite L were found to have the ability to control the distrib
ution and conformation of the guest species within the channels. The presen
t findings show that the zeolite L is a better host matrix than the large p
ore faujasite zeolites for manipulating the photophysics of neutral guest s
pecies.