Key words
catalysis - photochemistry - radicals - polymers - electron transfer
1
Introduction
Polymers are essential and ubiquitous materials of everyday life, and the evolution
of new chemical techniques to control polymer architecture leads to novel functional
materials and new technologies. Photocontrolled polymerization is a burgeoning research
area that offers great promise for delivering the capacity to tailor material properties
through precise spatiotemporal regulation of polymer chain growth.[1]
[2] The development of photoactive metal-based catalysts (e.g., Ir,[3] Cu,[4,5] Ru,[6] Fe,[7]) has dominated this field and has led to several radical polymerization methods
that give exceptional control over polymerization kinetics and enables the formation
of previously inaccessible structures.[7]
[8]
Although these methods have revolutionized photopolymerizations, the use of metal-based
catalysts can be prohibitively expensive, which restricts their practicality. In addition,
the contamination of final materials with even trace quantities of metal can limit
the use of these methods, especially in electronic or biomaterials applications.[9]
[10] Although strategies have been developed to remove impurities from polymers,[11] they can be time-consuming and costly. These drawbacks have spawned investigations
into the development of organic-based catalysts for photocontrolled, metal-free polymerizations.
Organic photoredox catalysts have seen widespread adoption in organic transformations.[12]
[13] They have been used as drop-in surrogates for metal-based catalysts,[14,15] and in certain cases have provided unique reactivity and led to the development
of new synthetic methods. This review focuses on recently developed organic catalysts
for controlled polymerization reactions that allow photoregulation of polymer chain
growth.[16] Specifically, we examine the development of metal-free variants of photocontrolled
atom-transfer radical polymerization (ATRP) and photoinduced electron transfer-reversible
addition–fragmentation chain transfer polymerization (PET-RAFT). In addition, we highlight
how the unique reactivity of these organic catalysts has enabled the emergence of
photocontrolled reversible complexation-mediated polymerization (RCMP) and photocontrolled
ring-opening metathesis polymerization (ROMP) (Scheme [1]).
Scheme 1 General scheme for the photocontrolled polymerizations discussed in this review,
catalyzed by organic (carbon-based) catalysts. ATRP = atom-transfer radical polymerization;
PET-RAFT = photoinduced electron transfer-reversible addition–fragmentation chain
transfer; RCMP = reversible complexation-mediated polymerization; ROMP = ring-opening
metathesis polymerization
Photocontrolled Atom-Transfer Radical Polymerization (ATRP)
2
Photocontrolled Atom-Transfer Radical Polymerization (ATRP)
ATRP is one of the most widely used controlled radical polymerization (CRP) techniques.
It operates through a redox equilibrium of ligated Cu, Ru, or Fe complexes with halide-capped
polymer chains (Scheme [2]).[17] Advances in this technique have led to highly efficient protocols that give well-controlled
polymerizations with living characteristics. Importantly, the ease of use and excellent
monomer scope of these reactions enables the synthesis of a wide array of functional
materials for a number of applications. Recently, there has been a surge in the development
of photocontrolled ATRP-like processes that allow excellent spatial and temporal regulation
of polymer chain growth.[2] However, metal contamination in the final materials and the requirement of expensive
catalysts (e.g., Ir) remain limiting factors for both traditional and photocontrolled
ATRP processes.
Scheme 2 Traditional Cu-mediated ATRP
Hawker and co-workers[9] addressed these challenges by developing a photocontrolled ATRP process mediated
by light and catalyzed by an organic catalyst. They had previously described a photoregulated
ATRP process that used the photoredox catalyst fac-Ir(ppy)3 and proceeded through the proposed mechanism shown in Scheme [3].[3]
[18] Building on this work, they sought a metal-free variant of Ir(ppy)3 that would operate through a similar mechanism and, ideally, offer the same control
over the polymerization. This organic catalyst also required a highly reducing excited
state similar to that of Ir(ppy)3 [–1.7 eV, Ir(IV)/Ir(III)*; see Scheme [3]]. With an excited state redox potential of –2.1 eV, 10-phenylphenothiazine (PTH)
was found to be a suitable candidate for these polymerizations.
Scheme 3 Proposed mechanism for photocontrolled ATRP with a photoredox catalyst
Using 0.1 mol% of PTH, the authors efficiently polymerized methyl methacrylate (MMA)
via irradiation with 380 nm light (Scheme [4]). Significantly, this example was the first of a metal-free ATRP process. Other
organic photoredox catalysts such as eosin Y and methylene blue have shown no polymerization
under similar conditions, an outcome attributed to their oxidizing excited states
and thus inability to activate the alkyl bromide chain end.[19] This observation demonstrated that a highly reducing organocatalyst such as PTH
is needed for photocontrolled ATRP reactions.
Scheme 4 10-Phenylphenothiazine (PTH) catalyzed ATRP of methyl methacrylate (MMA) and 2-(dimethylamino)ethyl
methacrylate (DMAEMA). M
n = number-average molecular weight
This new PTH-based system efficiently produced poly(methyl methacrylate) (PMMA) samples
with narrow dispersity (Đ) values. Đ is the ratio of weight-average (M
w) to number-average (M
n) molecular weights. Additionally, good agreements between experimental and theoretical
M
n values were observed. Similar to Ir-catalyzed photocontrolled ATRP, the PTH polymerization
could effectively be turned on and off by cycling the exposure of the reaction to
light; no background reaction was observed in the dark, and polymerization recommenced
immediately after re-exposure to light (Figure [1a]). Importantly for these cycling studies, a linear relationship between M
n and conversion was observed (Figure [1b]), as were first-order kinetics (Figure [1c]). These results demonstrated that the polymer chain ends were not irreversibly terminating
in the absence of light and showed that similar to traditional ATRP, this polymerization
protocol had living characteristics.
For a further demonstration of the living characteristics of this PTH system, chain-end
fidelity was evaluated. A low-molecular-weight PMMA polymer was synthesized under
PTH conditions and analyzed with electrospray ionization mass spectrometry (ESIMS)
and 1H NMR spectroscopy. The results of ESIMS analysis showed a correlation between observed
molecular weight and the expected values for the individual PMMA oligomers, which
were capped with the desired alkyl bromide.
Although ESIMS data gave evidence for chain-end fidelity, chain extension studies
gave definitive proof that a CRP system had been developed. With PMMA as a macroinitiator,
a benzyl methacrylate (BnMA) block was grown to yield PMMA-b-PBnMA, in which the results of size exclusion chromatography (SEC) showed a clear
shift to higher molecular weight without any observed tailing. This excellent retention
of the alkyl bromide chain end in the PTH system further allowed chain extension with
both Ir-catalyzed and traditional CuBr-based ATRP polymerizations that used methyl
acrylate and styrene, respectively. This result shows that the PTH system is complementary
to other metal-based ATRP methods.
Figure 1 Irradiation cycling studies for the polymerization of MMA with PTH as the catalyst.
Reprinted with permission from Ref 9 (J. Am. Chem. Soc. 2014, 136, 16096). Copyright 2016 American Chemical Society�
Although the use of PTH as an organocatalyst has been critical in eliminating metal
contamination in polymer products, Hawker[9] further showed that the utility of this catalyst goes beyond its metal surrogacy
by demonstrating that its unique reactivity enables new chemistry. Specifically, for
the polymerization of 2-(dimethylamino)ethyl methacrylate (DMAEMA), the use of Ir(ppy)3 resulted in polymers with broad Đ values and poor control over M
n, a likely result of amine oxidation by the excited catalyst.[20] By contrast, PTH, which is more reducing (or less oxidizing) in the excited state
than Ir(ppy)3, yielded poly[2-(dimethylamino)ethyl methacrylate] with good control and narrow Đ values (Scheme [4]). This outcome demonstrated an improvement in monomer scope for these photocontrolled
ATRP processes and laid the groundwork for what could be future transformations that
take advantage of the high reduction potential of this catalyst.
After this work by Hawker, Matyjaszewski and co-workers[10] used the PTH-catalyzed photocontrolled ATRP system for the polymerization of acrylonitriles.
Under the optimized conditions, polyacrylonitrile was efficiently synthesized with
good control over M
n and Đ values of ~1.5. Matyjaszewski hypothesized that the broad Đ values could indicate slow deactivation due to low deactivator concentration or rate
constants. Despite these broader distributions, good chain-end fidelity of polyacrylonitrile
was demonstrated through chain extensions with an MMA macroinitiator for which SEC
analysis showed a clear shift to higher molecular weight without any apparent tailing.
Matyjaszewski also explored the variation of N-aryl derivatives of PTH for these polymerizations (Scheme [5]), which showed activities comparable to those of the parent catalyst. Although PTH
gave the best results, this key exploration of structure set the stage for future
generations of efficient phenothiazine-derived catalysts.
Scheme 5 PTH-catalyzed ATRP of acrylonitrile and PTH derivatives
Concurrently with Hawker’s original report, Miyake and Theriot[21] disclosed an ATRP protocol that used perylene as an organic photoredox catalyst
(Scheme [6]). Using 0.1 mol% of perylene under white light irradiation, the authors synthesized
PMMA and poly(n-butyl acrylate) with varying Đ values (1.29 to 1.85) and moderate control over M
n. Matrix-assisted laser desorption ionization time-of-flight mass spectrometry analysis
demonstrated that a large number of the resulting polymers had alkyl bromide chain
ends, however, it also showed that termination through radical–radical coupling and
hydrogen abstraction were competitive processes. Alkyl bromide fidelity was further
explored through the formation of block copolymers with a PMMA macroinitiator. Chain
extensions with n-butyl methacrylate, butyl acrylate, styrene, and MMA were achieved, with some tailing
observed in all cases.
Scheme 6 Perylene-catalyzed ATRP of MMA
These polymerizations with perylene were photoregulated, with little to no polymerization
observed in the dark and first-order kinetics under light exposure (Figure [2]). M
w, however, did not grow linearly with conversion, and Đ increased as the reaction proceeded. Miyake[21] hypothesized that these outcomes were a consequence of the low initiator efficiencies
in these reactions. Although full control over polymerization was not observed for
the perylene-based system, these reactions laid the groundwork for further discoveries
with perylene-like catalysts.
Figure 2 Conversion vs time (A) and M
w vs conversion (B) for the polymerization of MMA with perylene as the catalyst. Adapted
with permission from Ref 21 (Macromolecules 2014, 47, 8255). Part C of the original figure removed. Copyright 2016 American Chemical Society�
Three systems have been developed in the pursuit of photocontrolled ATRP processes
using organic photoredox catalysts. Importantly, these reports were the first of metal-free
ATRP, which overcomes the long-standing issue of metal contamination in the final
polymers and should enable new applications of these ATRP methods. Moreover, we anticipate
that further exploration of these systems will provide access to a wider monomer scope
and open the door for the synthesis of architecturally distinct polymers with precisely
controlled properties.
Photocontrolled Reversible Addition–Fragmentation Chain Transfer (RAFT)
3
Photocontrolled Reversible Addition–Fragmentation Chain Transfer (RAFT)
Similar to ATRP, RAFT is a widely used CRP method with living characteristics that
enables the polymerization of a range of monomers.[22] RAFT protocols use chain transfer agents (CTAs) such as dithioesters, thiocarbamates,
xanthates, and trithiocarbonates that enable degenerative chain transfer after radical
initiation to give well-controlled polymerization processes (Scheme [7a]). In contrast to ATRP, RAFT does not require a catalyst; instead, a thermal initiator
or photoinitiator such as 2,2′-azobis(isobutyronitrile) (AIBN) is used to establish
degenerative chain transfer. To achieve spatiotemporal control over chain growth,
researchers have recently focused on the use of photoredox catalysts to initiate polymerization
reversibly (Scheme [7b]).
Scheme 7 General mechanism for reversible addition–fragmentation chain transfer (RAFT) polymerization
highlighting the degenerative chain transfer process that takes place after initiation
Scheme 8 General mechanism for PET-RAFT catalyzed by eosin Y (EY)
Efforts to control RAFT through photoredox chemistry (PET-RAFT) have been pioneered
by Boyer and co-workers. Their original systems used Ir and Ru photoredox catalysts
for reversible initiation of the RAFT process (Scheme [7b]).[23]
[24] The proposed PET-RAFT mechanism was similar to that of photocontrolled ATRP, in
which an excited photoredox catalyst reduces the CTA chain end to give the propagating
radical, which can then undergo the degenerative chain transfer process (Scheme [8]). These systems allowed excellent photoregulation of polymerization, however, the
use of a non-metal catalyst was desirable for reasons similar to those discussed for
photo-ATRP (vide supra).
Figure 3 Substrate scope for PET-RAFT catalyzed by eosin Y. MAA = methacrylic acid; HEMA =
hydroxyethyl methacrylate; GMA = glycidyl methacrylate; DMAEMA = 2-(dimethylamino)ethyl
methacrylate; OEGMA = oligoethylene glycol methyl ether methacrylate; HPMA = hydroxypropyl
methacrylamide; PFPMA = pentafluorophenyl methacrylate
Boyer and co-workers[25] reported the use of the organic dye, eosin Y, as an efficient catalyst for these
PET-RAFT processes (Scheme [8]). Eosin Y was chosen for its excited state redox potential that efficiently reduces
the CTA to give the desired alkyl radical.[19] Moreover, because CTAs can themselves degrade under UV light, the use of an organocatalyst
that absorbs light in the visible region was advantageous.[26]
[27] Using 0.01 mol% of eosin Y (Scheme [8]) irradiated under 461 nm light, Boyer and colleagues polymerized MMA and multiple
methacrylate derivatives (Figure [3]) to obtain polymers with narrow Đ values and good agreement between observed and theoretical M
n’s. Importantly, the eosin Y system showed improved monomer scope compared with that
of the Ir-based catalysts (specifically, DMAEMA and glycidyl methacrylate) previously
used for these PET-RAFT polymerizations. Linear growth between M
n and conversion as well as first-order kinetics and photocontrol were demonstrated
for this method. Furthermore, chain-end fidelity was illustrated through efficient
chain extensions of both MMA and oligoethylene glycol methyl ether methacrylate with
a PMMA macroinitiator.
In addition to having a broad monomer scope and living characteristics, this catalytic
system worked in the presence of oxygen. Importantly, good control was maintained
when the reaction was exposed to oxygen, however, the reaction rates were slower than
those of the anaerobic system. Boyer proposed that these reduced rates were due to
oxygen quenching of the catalyst excited state, a well-known pathway for these photocatalysts.[28]
Boyer and co-workers performed the first PET-RAFT polymerizations under metal-free
conditions with eosin Y as an organic catalyst. This approach enabled the visible-light-controlled
synthesis of well-defined polymers from a variety of functionally diverse monomers,
even in the presence of oxygen.
To increase the efficiency of the electron transfer process in these photocontrolled
RAFT polymerizations, Boyer and colleagues[29] developed CTA initiators that were covalently bound to the organic dye, tetraphenylporphyrin
(TPP). They reasoned that this strategy would increase the effective concentration
of the catalyst relative to that of the CTA and improve the efficiency of the photoactivation,
thereby leading to the traditional RAFT process (Scheme [9]). The use of 0.01 mol% of the tethered photocatalyst, TPP–3-benzylsulfanylthiocarbonylthiosulfanyl
propionic acid (TPP–BSTP) with additional external CTA and 2-(n-butyltrithiocarbonate)propionic acid (BTPA) resulted in 56% conversion of MMA into
a well-defined polymer (Figure [4]). Interestingly, in the control reaction in which TPP was not covalently bound to
the CTA, only 3% conversion of MMA was detected after the same reaction time. These
results corroborated Boyer’s hypothesis and illustrated that the electron transfer
process was more efficient with the covalently bound catalyst/trithiocarbonate (TTC)
system.
Scheme 9 General mechanism of intramolecular electron transfer in the tethered porphyrin/chain
transfer agent (CTA) system, which leads to a photocontrolled RAFT process. Adapted
with permission from Ref 29 (ACS Macro Lett. 2015, 4, 926). Copyright 2016 American Chemical Society�
In further support of their postulate, Boyer and colleagues showed that the addition
of linkers between the porphyrin and the CTA (TPP–C2–BSTP) (Figure [4]) resulted in reaction rates slower than those with TPP–BSTP. This result was attributed
to the limitation of electron transfer by the increased distance between the TPP and
CTA species. Furthermore, the synthesis of TPP–C2–2-(n-butyltrithiocarbonate)propionic acid, in which fragmentation and polymerization occurred
between the catalyst and the CTA, resulted in even slower reaction rates. In this
example, the distance between the CTA and TPP grew as polymerization proceeded, which
decreased the electron transfer efficiency. Together the results of these control
experiments elegantly show that the high activity of TPP–BSTP is due to an efficient
intramolecular electron transfer process.
The end-group fidelity of these polymerizations was evaluated with chain extension
experiments. Conveniently, no additional catalyst was required for these reactions
because the photocatalyst was present at the chain end. Poly(methyl acrylate)-b-poly(N,N-dimethylamide) diblock copolymers were efficiently formed with this method.
This study by Boyer[29] shows that interaction between the CTA and the photoredox catalyst is necessary
for efficient photocontrolled RAFT polymerization. This knowledge could enable the
design of more effective systems that allow better control of the synthesis of varying
polymer architectures.
Scheme 10 Photocontrolled RAFT polymerization based on a bifunctional trithiocarbonate (TTC)
initiator with PTH as the catalyst
Complementary to Boyer’s work,[23]
[25]
[30] and as an extension from their original work[31] with UV-activated TTC initiators, Johnson and co-workers[32] developed a visible-light-controlled RAFT process based on bifunctional TTC iniferters
and catalyzed by PTH (Scheme [10]). With 0.4 mol% of TTC and 0.02 mol% of PTH, N-isopropyl acrylamide was polymerized to give polymers with narrow Đ values and observed M
n’s matching theoretical data. M
n also increased linearly with conversion, following first-order kinetics when illuminated
with light. These conditions also produced high-molecular-weight polymers up to 159
kg/mol that were not achievable with a previous method Johnson had developed using
UV light. These results illustrate that PTH is an effective catalyst for multiple
photocontrolled CRPs.
Figure 4 Tetraphenylporphyrin (TTP)/CTA organocatalyst complexes used by Boyer and co-workers.
BSTP = 3-benzylsulfanylthiocarbonylthiosulfanyl propionic acid; BTPA = 2-(n-butyltrithiocarbonate)propionic acid
Johnson further demonstrated chain-end fidelity in this system through extensions
with poly(N,N-dimethylamide) macroinitiators that yielded triblock copolymers (Scheme [10]). Extensions were performed via three methods: (1) the organocatalyzed process discussed
herein with N-isopropyl acrylamide, (2) UV irradiation to activate the macro-TTC initiator with
ethoxy methyl ether acrylate as the monomer, and (3) traditional RAFT with AIBN as
an initiator with t-butyl acrylate. This approach demonstrated that this method[32] was complementary to other RAFT processes and showed that it could be used to make
well-defined functional materials.
Multiple organocatalyzed RAFT processes that are truly photoregulated have been developed
and give excellent control over final polymer structures. Similar to organocatalyzed
photocontrolled ATRP, these processes are likely to see further development and widespread
use.
Reversible Complexation-Mediated Polymerization (RCMP)
4
Reversible Complexation-Mediated Polymerization (RCMP)
Whereas ATRP and RAFT are well-established methods, RCMP, recently developed by Kaji
and co-workers,[28]
[33]
[34] is a new CRP method that uses photoactive organic catalysts. RCMP is similar in
mechanism to iodine-transfer polymerization, although it gives significantly improved
control through its distinct activation pathway and non-reliance on degenerative chain
transfer.[2,35] Kaji and colleagues originally published a method that used tributylamine as the
catalyst and an alkyl iodide as the initiator for the polymerization of MMA (Scheme
[11]).[36] They proposed that the amine and alkyl iodide formed a complex through halogen bonding
that in turn caused homolytic C–I bond cleavage upon UV irradiation to give the propagating
radical. Compared with traditional iodine transfer polymerization, this reversible
activation resulted in PMMA with significantly narrower Đ values (~1.2) and better control over M
n. Furthermore, these processes were efficiently regulated with light and did not require
the use of metal-based catalysts.
More recently, Kaji and co-workers[37] reported a similar method with various catalysts with absorption maxima within the
red to near-UV region of the electromagnetic spectrum (Scheme [11]). This method enabled efficient photocontrolled polymerizations in which the wavelength
of light used in the reaction could be selected by choosing a specific catalyst. In
contrast to photo-ATRP and PET-RAFT, which proceed through electron transfer mechanisms,
these reactions reportedly used energy transfer processes exclusively to allow for
controlled polymerization.
In all cases, the authors disclosed well-behaved reactions yielding polymers with
narrow Đ values and controlled molecular weights. Moreover, the polymerization scope for this
method was quite broad, with suitable monomers found in a wide array of functional
methacrylate derivatives (Figure [5]). Furthermore, the chain-end fidelity of the system was evaluated through elemental
analysis and suggested that 99% and 91% of the polymers were capped with iodine at
30% and 81% conversion, respectively. Additionally, these data were corroborated through
1H NMR analysis with an 800 MHz spectrometer, which showed ~99% chain-end fidelity
at 30% conversion. Block copolymer synthesis with PMMA macroinitiators was also performed,
and SEC analysis showed clear shifts to higher M
n values. The controlled kinetics and good chain-end fidelity of this RCMP process
broadens the scope of organocatalyzed photoredox polymerizations in general.
Scheme 11 Organocatalyzed RCMP of MMA and the organic catalysts used for these transformations.
TBA = tributylamine; C1-DCI = 1,1′-diethyl-2,2′-cyanine iodide; DHMI = 1′,3′-dihydro-8-methoxy-1′,3′,3′-trimethyl-6-nitrospiro[2H-1-benzopyran-2,2′-(2H)-indole]; C3-DCI = 1,1′-diethyl-4,4′-carbocyanine iodide; CP-I = 2-cyanopropyl iodide
Figure 5 Monomer scope for RCMP. PEGMA = poly(ethylene glycol methyl ether) methacrylate;
EHMA = ethylhexyl methacrylate
The ability to select a specific wavelength of light for these polymerizations will
likely be highly advantageous. For example, it will enable the polymerization of monomers
sensitive to photodegradation. Moreover, this capability has the potential to permit
the temporal control of two different photomediated processes in a single reaction
vessel through the appropriate selection of wavelength. Kaji and co-workers illustrated
this concept with a one-pot block copolymer formation that relied on two different
light-promoted reactions. With an alkyl iodide initiator functionalized with a pendant
alcohol, they used 602 nm light to synthesize a PMMA block with RCMP. The irradiation
wavelength was then adjusted to 350 nm and a poly(valerolactone) block was grown from
the free alcohol with a photoacid generator as the catalyst (Scheme [12]).[37]
[38] This example shows that appropriate wavelength selection can give temporal control
over separate reactions in the same vessel.
Scheme 12 One-pot synthesis of poly(δ-lactone)-b-poly(methyl methacrylate) through selective photoactivation of DHMI and a triarylsulfonium
hexafluorophosphate photoacid generator
In a manner similar to that of RCMP with alkyl iodides, Qiao reported[39] a process using tertiary amines to photocatalytically activate CTAs for RAFT polymerizations
(Scheme [13]). The polymers obtained with this method exhibited narrow Đ values (1.26 to 1.31), and the approach offered good control over molecular weight.
Polymerization did not occur without irradiation, and uncontrolled polymerization
was observed when the reaction was carried out in the absence of the tertiary amine
catalyst. The authors proposed that this outcome occurred owing to the degradation
of the CTA upon UV irradiation. This report combined RCMP and PET-RAFT in a photocontrolled
polymerization process.
Scheme 13 A tertiary-amine-catalyzed PET-RAFT process. Me6TREN = tris[2-(dimethylamino)ethyl]amine; PMDETA = N,N,N′,N′,N′′-pentamethyldiethylenetriamine; Et3N = triethylamine
Scheme 14 Metal-catalyzed ROMP
Photocontrolled Ring-Opening Metathesis Polymerization (ROMP)
5
Photocontrolled Ring-Opening Metathesis Polymerization (ROMP)
ROMP is a living chain-growth process that typically uses Ru- or Mo-based catalysts
for efficient polymerization of cyclic olefins (Scheme [14]).[40]
[41] The excellent control and broad functional group tolerance of this method has facilitated
its use in a number of applications. Recently, Boydston and co-workers[42] developed a method for photocontrolling these ROMP processes through the use of
an organic-based photoredox catalyst.
Unlike the other methods that we have discussed thus far, traditional ROMP does not
proceed through a radical mechanism, which makes it difficult to envisage the use
of a photoredox catalyst to promote these reactions. The approach to metal-free photocontrolled
ROMP by Boydston and colleagues resulted in a mechanism switch to initiate a radical
process. With a pyrylium salt as the photocatalyst and a vinyl ether as the initiator,
norbornene was efficiently polymerized under irradiation with blue light. They hypothesized
that the excited photocatalyst oxidized the vinyl ether to give a radical cation that
underwent a [2+2] cycloaddition with the norbornene monomer (Scheme [15]). Fragmentation of this intermediate to relieve ring strain yielded a cyclopentane
appended with an oxidized vinyl ether. This outcome enables further [2+2]/fragmentation
cycles to give a chain growth polymerization. Importantly, the photocatalyst reversibly
activated the vinyl ether chain end to give rise to a controlled photoregulated process.
Scheme 15 Photocontrolled ROMP catalyzed by an organic catalyst [pyrylium salt (PYR)]
The optimized conditions of the Boydston and co-workers approach yielded polymers
with Đ values ranging from 1.3 to 1.7, and the final molecular weight could be relatively
well-controlled by varying the stoichiometry of vinyl ether to norbornene. Over the
course of polymerization, an increase in M
n with conversion was observed, verifying the chain growth nature of this photoregulated
ROMP. Although the collected data showed that the photoregulated ROMP was less controlled
than traditional metal-catalyzed processes, the authors indicated that the poly(norbornene)
polymers prepared with both methods had similar glass-transition temperatures, which
indicated that the physical properties of the polymers were not significantly different.
Additionally, temporal control of polymer chain growth was demonstrated by cycling
the exposure of the reactions to visible light; no polymerization was observed in
the dark.
This work by Boydston and colleagues is the first example of metal-free ROMP and achieves
a radical process catalyzed by a photoactive catalyst. Notably, a recent study reported
that this reaction can be used to synthesize metal-free cross-linked networks that
are difficult to access through traditional means.[43] The photocontrol of this method also allows the spatiotemporal control of cyclic
olefin polymerization, and we anticipate that this process will enable future applications
of ROMP.
Conclusion and Future Outlook
6
Conclusion and Future Outlook
Organic-based photoredox catalysts offer practical and cost-effective alternatives
to their metal-based counterparts, and they display distinctive and interesting reactivities
that can lead to new transformations. This review discusses metal-free catalysts that
have been successfully developed for photocontrolled ATRP and PET-RAFT. In addition
to being highly efficient for these reactions, these catalysts provide alternative
reactivity that has broadened the substrate scope for both types of polymerization.
Furthermore, organic catalysts have led the way to the development of photocontrolled
RCMP and ROMP, both of which were previously inaccessible. We anticipate that further
advances in this field will increase the practicality of these reactions and lead
to new types of polymerization. Altogether, research in this area will further our
ability to synthesize functional materials and lead to new discoveries.
