Host–Guest Complexation-Mediated Supramolecular Photon Upconversion
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https://figshare.com/articles/dataset/Host_Guest_Complexation-Mediated_Supramolecular_Photon_Upconversion/12968049
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资源简介:
The
phenomenon of photon upconversion, in which a system absorbs
two or more photons of lower energy and emits a photon of higher energy,
has been used in numerous applications, including non-destructive
bioimaging, deep-penetrating photodynamic therapy, catalysis, and
photovoltaic devices. To date, photon upconversion has been observed
typically in inorganic nanocrystals, nanoparticles, metal–organic
frameworks, supramolecular assemblies, and organic dyads. Herein,
we demonstrate a new strategy for harnessing photon upconversionsupramolecular
upconversionbased on host–guest chemistry. We have
identified a box-like fluorescent tetracationic host incorporating
a thiazolothiazole emitter, which can accommodate a guest-sensitizer,
5,15-diphenylporphyrin, inside its cavity, and demonstrated
that the host–guest inclusion complex displays triplet-fusion
upconversion when the guest is excited with low-energy light. The
strategy of supramolecular upconversion has been employed successfully
in two other host–guest complexeswith hosts comprised
of anthracene emitters and a 5,15-diphenylporphyrin guestcorroborating
the fact that this strategy is a general one and can be applied to
the design of a new family of host–guest complexes for photon
upconversion. More importantly, supramolecular upconversion
is accessible in solution under dilute conditions (μM) compared
to most of the existing approaches that require significantly higher
concentrations (mM) of emitters and/or sensitizers. Transient absorption
spectroscopy and density functional theory have been employed in order
to confirm a triplet-fusion upconversion mechanism. Host–guest
complexation-mediated supramolecular photon upconversion eliminates
multiple issues in the existing systems related to high working concentrations,
high incident laser power, and low optical penetration depths.
创建时间:
2020-08-31



