Photoswitching using visible light: A new class of organic photochromic molecules

Article abstract of DOI:10.1021/ja503016b

A versatile new class of organic photochromic molecules that offers an unprecedented combination of physical properties including tunable photoswitching using visible light, excellent fatigue resistance, and large polarity changes is described. These uniq

Full text of DOI:10.1021/ja503016b

Communication
pubs.acs.org/JACS
Photoswitching Using Visible Light: A New Class of Organic
Photochromic Molecules
Sameh Helmy,† Frank A. Leibfarth,† Saemi Oh,† Justin E. Poelma,‡ Craig J. Hawker,†,‡
and Javier Read de Alaniz*,†
‡
†Department of Chemistry and Biochemistry and Materials Research Laboratory, Materials Department, University of California,
Santa Barbara, California 93106, United States
S
* Supporting Information
(DASAs).6 These derivatives switch from a conjugated, colored,
ABSTRACT: A versatile new class of organic photo-
chromic molecules that offers an unprecedented combi-
nation of physical properties including tunable photo-
switching using visible light, excellent fatigue resistance,
and large polarity changes is described. These unique
features offer significant opportunities in diverse fields
ranging from biosensors to targeted delivery systems while
also allowing non-experts ready synthetic access to these
materials.
and hydrophobic form to a ring-closed, colorless, and
zwitterionic structure on irradiation with visible light and
have high fatigue resistance under ambient conditions (Figure
1). In addition, the potential of this photoswitch in materials
n the field of adaptable and responsive materials, the ability
Iof organic photochromic compounds to reversibly undergo
changes in spectral absorption, volume, and solubility is of
particular importance for applications in energy storage and
chemical sensing and for controlling the conformation and
activity of biomolecules.1 These switches are particularly
valuable because their property changes are triggered by light,
the most widely available, non-invasive, and environmentally
benign external stimulus. Significantly, light also provides
unique opportunities for spatial and temporal resolution.
Among the classes of organic photochromic materials,
azobenzenes, spiropyrans and diarylethenes have received the
most attention because of their excellent performance and
broad utility. Specifically, azobenzene has been extensively
employed for its change in volume, resulting from a trans to cis
isomerization, upon irradiation.2 Similarly, the change in
spectral properties of spiropyrans and diarylethenes upon
photoswitching has been exploited in a number of applica-
tions,3 with spiropyran exhibiting the added benefit of a
solubility switch, or a conversion from a hydrophobic to a
hydrophilic form, upon irradiation.4 Despite their ubiquity and
broad utility, these privileged classes of photochromes typically
all require the use of high-energy UV light to trigger their
photochemical reactions. This hinders their potential use in
biomedical applications and material science because UV light
can be damaging to healthy cells and results in degradation for
many macromolecular systems. Fatigue resistance is also a
primary concern for UV-based photochromic switches.
Figure 1. DASAs, a new platform of visible light organic photo-
switches.
science is highlighted through the synthesis of a functional
amphiphile that displays light-mediated micelle disassembly and
cargo release.
Our interest in the cascade rearrangements of activated
furans7 and a pioneering report by Honda8 played a critical role
in our development of these novel negative (colored to
colorless) photochromic materials.5e,3b The synthetic design of
these DASA photoswitches takes advantage of furfural (1), a
commodity chemical derived from plant byproducts, as a
renewable and readily available starting material and employs
highly efficient reactions amenable to the rapid synthesis of a
broad range of materials. Facile activation of 1 by an “on water”
condensation with cyclic 1,3-dicarbonyl compounds provides
intermediates that undergo ring-opening at room temperature
with a wide variety of secondary amines in the absence of
catalysts or other reagents (Scheme 1).9
The highly modular nature of this approach enables the rapid
synthesis of a library of DASA materials with a variety of furan
activating groups and secondary amines in high yields. For
example, activation of furfural, 1, could be accomplished with
either Meldrum’s acid to form furan 2 or with 1,3-dimethyl
barbituric acid to form 3. Treatment of these activated furans
with secondary aliphatic, cyclic, or functional amine derivatives,
such as diethylamine, diallylamine, and tetrahydroisoquinoline
A common design principle to address this problem is to
make synthetic modifications to these known classes of
photochromic compounds that enable the use of visible
light.5 Herein, we describe a conceptually different approach
in which we designed a new class of visible light activated
photochromes, termed donor−acceptor Stenhouse adducts
Received: March 31, 2014
© XXXX American Chemical Society
A
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Communication
a
Scheme 1
a
(a) Meldrum’s acid, H2O, 75 °C; (b) 1,3-dimethylbarbituric acid,
H2O, rt; (c) amine (1-1.5 equiv), THF, rt. See Table S1 for amine
derivatives investigated.
provide DASA photoswitches with the general structure 4 and
5 (Table S1). These derivatives are routinely accessed at the
multigram scale in yields >85% over the two-step procedure.
Inherent in the versatility and overall usefulness of these DASA
photoswitches is the high yielding and simple nature of the
synthetic procedures, which allows nonexperts easy access to
more complex or functional substrates that are attractive for
tailored applications in materials science. Having efficient access
to the triene derivatives, the photophysical properties were
examined with the diethyl amine derived adducts as model
systems (Scheme 2).
Figure 2. (A) Conversion of 4a to 4b by 1H NMR in CD3OD over 4
h. (B) Absorption spectra of 5a to 5b on irradiation with visible light
in CH3OH. (C) Expanded view of absorption spectra of 5a to 5b
between 250 and 280 nm.
ideal, providing conversion of the triene to cyclopentenone
upon irradiation with visible light with thermal reversion from
the meta-stable cyclopentenone back to the triene when
irradiation is stopped.
With reversible conditions identified, the relative rates of
interconversion between the triene and cyclopentenone isomer
were evaluated in toluene for the two photoswiches (4a and
5a) bearing different acceptor groups. As illustrated in Figure
3A both derivatives undergo conversion from the open triene
isomer (4a and 5a) to the closed zwitterionic cyclopentenone
isomer (4b and 5b) at approximately the same rate. A more
dramatic rate difference was observed in the thermal
recoloration, upon cessation of irradiation, where the 1,3-
dimethyl barbituric acid derivative (5a) reverted back
Scheme 2. Photoswitching and Thermal Reversion of
Trienes 4a and 5a to Cyclopentenones 4b and 5b
We began by examining the unidirectional conversion of the
colored triene 4a to its colorless zwitterionic cyclopentenone
isomer 4b using NMR spectroscopy in a deuterated methanolic
solution (Figure 2A). Exposure of 4a to a standard
incandescent bulb or hand-held fluorescent lamp results in a
decrease over the course of 4 h in the NMR peaks
corresponding to 4a and a concomitant increase in the peaks
for 4b. Similarly, this process was also studied using UV−visible
spectroscopy for 5a in methanol (Figure 2B). Again, irradiation
with visible light leads to a decrease of the absorption of 5a as it
is converted to 5b over 50 min.10 The isosbestic point was
determined to occur at 280 nm for both compounds (see
Supporting Information (SI) for absorption spectra of 4a to
4b).
Having controlled access to both structural forms, we next
determined conditions that would facilitate rapid, quantitative,
and fully reversible switching between the triene and
cyclopentenone forms. Similar to spiropyrans and diary-
lethenes, reversible photoswitching of DASAs was found to
be solvent dependent.11 We found aromatic solvents to be
Figure 3. (A) In situ kinetic plot of the switching cycle of 4a and 5a in
PhMe, monitored at λmax of 545 and 570 nm, respectively. (B)
Multiple photoswitching cycles of 5a in PhMe (0.16 mM), alternative
irradiation at 570 nm (red) and dark (black). (C) Photographs
illustrating the concomitant photoswitching and phase transfer of 4a
upon irradiation with visible light. (D) ORTEP drawings of 4a (top)
and 4b (bottom) (50% probability ellipsoids, hydrogen atoms omitted
for clarity).
B
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Journal of the American Chemical Society
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Figure 4. (A) Photoswitching of micelle-forming polymer amphiphile. (B) Schematic of micelle formation and hydrophobic cargo encapsulation by
functional amphiphile 7a and micelle disruption and cargo release on visible light irradiation. (C) Fluorescence intensity (Em at 588 nm) vs log
concentration (mg/mL) of 7a. (D) Fluorescence emission spectra of Nile Red in 0.50 mg/mL 7a in water at various times of visible light irradiation.
approximately twice as fast. This process is solvent and
temperature dependent (details in SI),12 but it is worth noting
that in polar protic solvent thermal reversion was not observed.
We also found that the choice of acceptor group has an effect
on the λmax and associated color of the triene. For example, in
toluene the Meldrum’s acid derived triene 4 displays a λmax of
545 nm, changing the acceptor to the more electron-
withdrawing 1,3-dimethyl barbituric acid, 5, results in a
bathochromic shift to 570 nm. In both cases these derivatives
are excellent organic dyes with extinction coefficients
determined to be ∼100,000 M−1 cm−1 for the triene form
(details in SI).
Fatigue resistance is a key characteristic for gauging the
potential of photochromic materials, thus the performance of
DASA photoswitches was tested (Figure 3B).13 Rapid and
complete switching of 5a was consistently observed when
irradiating with visible light centered at the λmax of our DASA
with negligible material degradation (<0.05% loss per cycle), as
measured by the intensity of absorbance.14,1b Fatigue experi-
ments were conducted in ambient conditions without the need
to exclude oxygen or water, demonstrating the robust nature of
this process.
A powerful aspect of the modular design of DASAs is the
ability to rapidly modify their structure, critical for the adoption
of these photoswitches into complex systems that require on-
demand property changes. Accordingly, we sought to develop a
functional polymer system to exploit the visible-light-mediated
solubility switch of DASAs. The development of a general,
stimuli-responsive micellar system with external control over
assembly has been a long-standing goal in polymer chemistry
with potential applications in biological settings.15 The
characteristics of these photoswitches are therefore perfectly
suited to provide such a function, as visible light mediates
structural and property changes from the hydrophobic, linear
derivative to the fully hydrophilic, cyclic derivative.
The facile and modular synthesis of DASA-functionalized
amphiphilic polymer is detailed in the SI, briefly, a DASA
bearing a terminal azide and 1,3-di-n-octyl barbituric acid, was
coupled to alkyne terminated monomethyl poly(ethylene
glycol) (PEG) (Mw = 3000 g/mol, PDI = 1.1) to form the
desired end-functionalized polymer, 7a (Figure 4A). The
amphiphilic nature of 7a induced micelle formation in aqueous
environments (Figure 4B), as determined by Nile Red
encapsulation experiments and dynamic light scattering,
confirming that Nile Red is successfully encapsulated and
solubilized in water and that the critical micelle concentration
for this system is 49 μM (Figure 4C, see SI for details). Upon
visible light irradiation, the absorption peak of 7a at 550 nm
decreased steadily, indicating the photoswitching of the DASA
to its cyclic, hydrophilic state (details in SI). Concurrently, the
fluorescence emission of encapsulated Nile Red showed a sharp
decrease in intensity and red shift, indicating that the
hydrophobic dye was released into the aqueous phase (Figure
4D).16 These results are consistent with a disruption in the
micellar structure and a release of hydrophobic cargo caused by
the light-induced photoswitching of 7a to the fully hydrophilic
derivative 7b. This simple but powerful application of DASAs
illustrates the significant potential of these photochromic
moieties.
From related studies, the mechanism of switching is
proposed to occur via a reversible Nazarov-type 4π electro-
cyclization.7 Importantly, conversion to the zwitterionic
cyclopentenone (4 and 5) results in bleaching of all derivatives
studied, providing colorless, water-soluble materials. A dramatic
realization of this solubility change is demonstrated through
dynamic phase transfer. Derivative 4a dissolved in toluene was
layered over water; the biphasic system was then irradiated with
visible light (Figure 3C). The highly colored organic phase
underwent rapid loss of color, correlating to the formation of
4b. Complete migration of 4b to the aqueous phase was
1
confirmed by H NMR analysis of the layers after photo-
switching.
Further structural characterization of the two isomeric states
was provided by single crystal X-ray diffraction (Figure 3D),
which revealed the ring-open Stenhouse adduct 4a to be a
conjugated, linear, hydrophobic material with an amine “donor”
and a 1,3-dicarbonyl “acceptor”. In contrast, the water-soluble
cyclopentenone 4b is a zwitterion, with the amine substituent
protonated and one of the ester (or amide) functionalities in
the 1,3-dicarbonyl moiety being a formal enolate.
In conclusion, we have introduced a new class of photo-
switchable molecules that are synthetically versatile and exhibit
a unique combination of physical and chemical properties.
These DASAs show reverse photochromism under visible light,
which is complementary to previous classes of photoswitches,
and display excellent fatigue resistance under ambient
C
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Journal of the American Chemical Society
Communication
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science was demonstrated through the synthesis of a functional
amphiphile that displays on-demand light-mediated disassembly
and cargo release.
(10) The difference in the rate of conversion between the triene and
the zwitterionic cyclopentenone isomers was governed by concen-
tration (1H NMR required high concentration to obtain adequate data,
dilute conditions were used for UV−vis experiment) and not the
nature of the derivative or solvent employed.
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ASSOCIATED CONTENT
* Supporting Information
■
S
Synthetic procedures and experimental details. This material is
available free of charge via the Internet at http://pubs.acs.org.
(12) Swansburg, S.; Buncel, E.; Lemieux, R. P. J. Am. Chem. Soc.
2000, 122, 6594.
AUTHOR INFORMATION
Corresponding Author
javier@chem.ucsb.edu
■
(13) Bertelson, R. In Organic Photochromic and Thermochromic
Compounds; Crano, J., Guglielmetti, R., Eds.; Springer: New York,
2002; p 11.
(14) As a comparison, when cycled with a broadband light source, a
∼0.25% loss in efficiency was observed per cycle due to unfiltered UV
light from the broadband source.
Notes
The authors declare no competing financial interest.
́ ́
(15) (a) Rodríguez-Hernandez, J.; Checot, F.; Gnanou, Y.;
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■
S.H. thanks UCSB LSAMP Bridge to the Doctorate (award no.
0929836) for financial support. F.A.L., S.O., C.J.H., and J.R.A
thank the National Science Foundation (MRSEC program
DMR-1121053) and the Institute for Collaborative Biotechnol-
ogies through grant W911NF-09-0001 from the U.S. Army
Research Office (S.O. and C.J.H), the Department of Defense
(NDSEG Fellowship), and the Dow Materials Institute for
financial support. We also thank Dr. Guang Wu (UCSB) for X-
ray analysis.
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