Solar Energy Storage by Molecular Norbornadiene–Quadricyclane Photoswitches: Polymer Film Devices

Abstract Devices that can capture and convert sunlight into stored chemical energy are attractive candidates for future energy technologies. A general challenge is to combine efficient solar energy capture with high energy densities and energy storage time into a processable composite for device application. Here, norbornadiene (NBD)–quadricyclane (QC) molecular photoswitches are embedded into polymer matrices, with possible applications in energy storing coatings. The NBD–QC photoswitches that are capable of absorbing sunlight with estimated solar energy storage efficiencies of up to 3.8% combined with attractive energy storage densities of up to 0.48 MJ kg−1. The combination of donor and acceptor units leads to an improved solar spectrum match with an onset of absorption of up to 529 nm and a lifetime (t 1/2) of up to 10 months. The NBD–QC systems with properties matched to a daily energy storage cycle are further investigated in the solid state by embedding the molecules into a series of polymer matrices revealing that polystyrene is the preferred choice of matrix. These polymer devices, which can absorb sunlight and over a daily cycle release the energy as heat, are investigated for their cyclability, showing multicycle reusability with limited degradation that might allow them to be applied as window laminates.


DOI: 10.1002/advs.201900367
was fossil fuel derived, [1] and environmental impacts necessitates the global community to seek cleaner alternatives. [2] Renewable green energies derived from solar power, wind, or hydroelectric sources are the most commonly implemented. However, daily and seasonal variations in both energy production and consumption compel the development of new energy storage technologies. One solution is to address both light harnessing and storage in a combined technology. This has been shown in molecular solar thermal (MOST) storage [3] also referred to as solar thermal fuel (STF). [4] Here, energy can be stored in a molecular photoswitch through irradiation under sunlight, resulting in the formation of a high energy isomer. This metastable species can be stored until the energy is released as heat, leading to the reformation of the parent form. Such heat release can be prompted by heating or even occur under ambient conditions depending upon the storage life time (t 1/2 ) of the high-energy isomer. Moreover, this process has been shown to occur through a stimulus such as a heterogeneous catalyst, [5] electric potential, [6] or light. [7] Molecular photoswitch systems that have been studied for MOST include azobenzenes, [4,8] tetracarbonylfulvalenediruthenium complexes, [3,9] dihydroazulenes, [10] and NBDs. [11] A promising use for liquid MOST systems is in heating applications, [12] whereas the application of such systems in the solid state could lead to functional windows for climate control and de-icing, [8f,13] thus reducing the energy need for conventional heating and cooling. However, in order to make such coating applications practically viable, there are some requirements for the molecular photoswitch system that must be fulfilled. [11a] These include molecular properties such as a good overlap between the absorbance spectra of the parent molecule with the solar spectrum, where the high-energy metastable isomer should not exhibit a competing absorbance; good quantum yield for the photoisomerization; high energy density, and good cyclability. Lastly, the storage time of the metastable isomer should fit the desired application. For instance, this could be as short as 4-8 hours for a lamination on windows that regulates the interior temperature on a daily basis. On the other hand, long-lived liquid based metastable compounds have a possible preferred application in catalyst controlled heat release Devices that can capture and convert sunlight into stored chemical energy are attractive candidates for future energy technologies. A general challenge is to combine efficient solar energy capture with high energy densities and energy storage time into a processable composite for device application. Here, norbornadiene (NBD)-quadricyclane (QC) molecular photoswitches are embedded into polymer matrices, with possible applications in energy storing coatings. The NBD-QC photoswitches that are capable of absorbing sunlight with estimated solar energy storage efficiencies of up to 3.8% combined with attractive energy storage densities of up to 0.48 MJ kg −1 . The combination of donor and acceptor units leads to an improved solar spectrum match with an onset of absorption of up to 529 nm and a lifetime (t 1/2 ) of up to 10 months. The NBD-QC systems with properties matched to a daily energy storage cycle are further investigated in the solid state by embedding the molecules into a series of polymer matrices revealing that polystyrene is the preferred choice of matrix. These polymer devices, which can absorb sunlight and over a daily cycle release the energy as heat, are investigated for their cyclability, showing multicycle reusability with limited degradation that might allow them to be applied as window laminates.
for domestic heating in extreme seasonal climates. The coating, which could conceivably be the neat molecular photoswitch as a solid or a polymer-based composite, needs to retain the desirable molecular properties of the photoswitch, display excellent cyclability, energy density, and stability, and demonstrate ideal aesthetics in, for instance, window laminate applications.
One molecular system that has shown promise in this regard is the norbornadiene-quadricyclane (NBD-QC) couple (Figure 1). The photoswitching properties are highly tunable for MOST, in fact, many derivatives have been shown to exhibit good cyclability and high quantum yields. [11f ] Unfortunately, the absorbance band of unsubstituted N1 does not overlap with the solar spectrum. By introducing a π-conjugated donor-acceptor system across C2 and C3, the absorbance of the NBD can be red-shifted. [5f,11e,g-i] However, a higher degree of polarization through the C2-C3 olefin is typically accompanied by shorter ambient lifetimes for the corresponding QCs. [11h] We have recently shown that this effect can be counterbalanced with subtle structural modifications to the aromatic group at the C3 position of NBD, which allowed significant increases of the storage time (t 1/2 ) by a factor of 100, without compromising the energy release (ΔH storage ) or the absorbance profile. [11h] Furthermore, dimeric molecules having a linear conjugation pathway between the two NBD units through a shared benzene donor display both good solar spectrum overlap and quantum yields. [11g] In addition, the concept of sharing the donor part of the molecule between several NBD units effectively leads to a lower molecular weight per NBD unit and in consequence to a higher energy density; for the double metastable form approaching up to ≈0.93 MJ kg −1 . [11g] In an effort to realize solid state devices for application, the MOST photoswitch will ideally be incorporated into polymers. To this end, Zhitomirsky and Grossman [8e] designed high molecular weight azobenzene derivatives that were able to form solid films, retaining morphology through interconversion processes. In addition, methyl methacrylate-functionalized azobenzene afforded a polymer with high cyclability, with a half-life of longer than two days. [8d] NBD derivatives have also been incorporated into polymers, either by incorporating it into a poly(methyl methacrylate) (PMMA) host [14] or by making it part of the polymer itself. [15] In addition, many NBDs, or their corresponding QCs, are typically liquids. Thus, blending with a polymer makes it possible to create a solid photoactive NBD material, whose mechanical properties are governed by the poly mer matrix in which the NBD has been dispersed. Another advantage of using NBDs for this purpose is that the QC form tends not to absorb visible light, thereby avoiding inner filtering effects or photostationary states, which is more evident for other photochromic systems. Good cyclability has been demonstrated for N2 ( Figure 1) hosted in PMMA, though the reported half-life was less than 5 min, which has a limited practical application. [14a] The focus of the work presented here is to develop an NBD-QC polymer composite system toward applications in windows and coatings where solid-state function is needed. While the NBD system fulfils many of the requirements stated above for molecular entity, few examples of function in the solid state can be found for this system, likely due to the challenge of balancing energy storage time with solar spectrum match. [11g,h] Here, we present the synthesis of a new series of NBD-based molecules with a good solar spectrum match (estimated up to 3.8% solar energy storage efficiency), using the strong acceptor moiety trifluoroacetyl unit in conjunction with carefully selected donor units for the purpose of making NBD derivatives having QCs with half-lives in the range of 4-8 h, applicable for a daily charging/discharging cycle. Furthermore, we investigated the performance of two high-performing derivatives in film configuration for different polymer matrices demonstrating the basic function for a possible future application in MOST coated windows.

Synthesis
With a target of MOST window laminates possessing a daily charging/discharging cycle in mind, we designed a series of NBD-based molecules which should possess a good solar spectrum match and target half-lives in the range of 4-8 h. Scheme 1 shows the structures of previously studied NBDs with the cyano acceptor N5a-d and NN5e and parent NBD with the trifluoroacetyl acceptor moiety N4a. Based on our previous studies, [11h,i] we chose to investigate the properties of better aromatic donors used in conjunction with the strong trifluoroacetyl acceptor N4b-d and the double NBD analogs NN4e. These NBD derivatives were made using a Diels-Alder methodology between a selection of trifluoroacetylphenyl acetylenes with cyclopentadiene. The acetylenic precursors 3b-e were made following a literature procedure from their corresponding terminal alkynes. [16] Dienophiles 3b-e could be heated in the presence of cyclopentadiene to form N4b-d and NN4e in excellent Adv. Sci. 2019, 6,1900367  yields (Scheme 1), primarily due to the strong trifluoroacetyl acceptor activating the alkyne toward the [4+2π] cycloaddition. The potential for extended conjugation of the C2-C3 substituents was confirmed through a single crystal X-ray structure for N4c, which revealed near coplanarity of these substituents, although there is some disorder between the bridge C7 and the double bond of C5-C6 ( Figure 3).

Photochemical Properties
To determine whether the newly synthesized NBD-QC photoswitches had the correct physical properties for polymer incorporation and daily cycle laminate applications, all NBDs were studied by UV-vis spectroscopy in toluene ( Table 1). This also included measuring the quantum yield of photoconversion and kinetic stabilities all QCs. Comparing the previously made NBDs N5b-d bearing a cyano acceptor group to analogs N4b-d with trifluoroacetyl acceptor group, the latter experienced redshifting for the NBD absorbance spectra of 70-100 nm. This gave NBD products with an improved overlap with the most intense region of the solar spectrum, especially N4c, which had an onset of absorbance at 529 nm. Meanwhile, there appeared to be no observable trend between the quantum yields for photo conversion between series N4b-d and N5b-d when measured using the high concentration regime (Abs >2). [17] Using the molecular absorptivity, quantum yield of photoisomerization and energy storage density (ΔH storage ) (see below) of the isomers as input parameters, we can estimate the fraction of the solar spectrum that can be captured and stored by these compounds. The estimates reveal energy capture efficiencies of 2.9%, 1.5%, and 3.8% for N4b, N4d, and NN4e respectively, (see the Supporting Information for details) rendering these the series of compounds with best solar capture efficiencies reported from our group so far.
Adv. Sci. 2019, 6,1900367 Scheme 1. a) Previously studied NBDs (N5a-d, NN5e, and N4a) and compounds made for this study (N4b-d and NN4e). b) Reaction protocol used to form N4b-d and NN4e. c) A representation of the structure of N4c obtained by X-ray crystallography on crystals grown from dichloromethane/ n-heptane. The disorder of the NBD moiety (major/minor 0.59:0.41) is shown but hydrogen atoms are omitted. The conformation obtained by solving the crystal structure highlights that the C carbonyl -C2 NBD -C3 NBD -C aryl dihedral angle is 11.5° for the major form, indicating that the aryl and trifluoroacetyl groups are nearly coplanar.  The kinetic decay for all QCs was measured at three different temperatures and from exponential fits, the rate constants and life-times were obtained. From Arrhenius plots (see the Supporting Information), the room temperature life-times were determined in toluene by extrapolation. Not surprisingly, the larger the dipole moment through the C2-C3 olefin for the NBD, the lower the life-time for the corresponding QC forms. Metastable forms Q4b and Q4c exhibited markedly shorter half-lives than Q4a, in the order of a few days for previously reported Q4a to around 7 h for Q4b and less than an 1 h for Q4c. In fact, parallel trends for the half-lives of Q5a-d with a cyano group as the acceptor were noticed. Exchanging the cyano for trifluoroacetyl unit proportionately afforded an ≈20-fold increase in the back-conversion rate to the corresponding NBD (Figure 2a). Importantly, the effect of having a substituent at the ortho position was evident in the trifluoroacetyl acceptor series, stabilizing the QC and showing a similar trend in previously reported for Q5d and other 2-cyano-3-arylNBDs. [11h] As observed for N4b-d the dimer NN4e also exhibited a red-shifted onset for the absorbance relative to NN5e. Previously synthesized NN5e displayed stepwise photoconversions by irradiation at 405 nm, where an NQ5e intermediate could be identified. [11g] In comparison, NN4e did not experience any sequential photoswitching events. However, stepwise kinetics did occur for the back-conversion for QQ4e. It was found that the first conversion (QQ4e→NQ4e) was significantly faster than the second step (NQ4e→NN4e) (Figure 2c), which is surprising since it is opposite to what we observed for previously explored double systems. [11g] This could be clearly observed from the progressive change in the maxima for the absorbance profile during a kinetic experiment. As seen in Figure 2b, the absorbance maximum initially remains unchanged, where the conversion of QQ4e to NQ4e had occurred relatively fast, and thereafter the maximum started to slowly red-shift, a result of NQ4e to NN4e. Indeed, this progressive behavior was substantiated by following the back-conversion by NMR (see the Supporting Information). Two different half-lives were also observed for dimer NN5e, though in this case the conversion for NQ5e to NN5e was found to be faster than the conversion from QQ5e to NQ5e.
The quantum yields for the two processes in this photoconversion were examined at both 340 and 405 nm, where the former wavelength was close to the absorption maximum for NQ4e and the latter favored the absorbance of the NN4e. At both these wavelengths, comparable results were obtained, both showing a linear fit for the change in concentration versus irradiation time, and so the quantum yields for both processes were 77%. The light-harvesting properties for NN4e were superior to NN5e, which had sequential quantum yields of 73% for the first photoconversion (QQ5e→NQ5e) and 51% for the second event (NQ5e→NN5e).

Incorporation of NBDs into Polymers
With the new NBD-QC photoswitches and analysis of the photo chemistry in hand, the study focused on the incorporation of the identified NBDs into a polymer matrix to assess possible applications in climate control for window laminating. Ideally, laminated films for temperature regulation require the NBD to have a half-life in the order of 4-8 h. To investigate this, N4b was selected as it has a good solar spectrum overlap (λ onset = 457 nm) and a good quantum yield (Φ = 68%), but most importantly a half-life of just under 7 h in toluene. This photoswitch was incorporated into four different polymers with the aim of investigating the effect of the matrix polymer on the switching properties of the incorporated NBD. This included the use of atactic polystyrene (PS), which was identified as a comparable host medium to solution based studies in toluene. Also, included in this study was atactic PMMA as it has been reported previously that the incorporation of NBD derivatives Adv. Sci. 2019, 6,1900367  into PMMA resulted in composites with good cyclability. To compliment this investigation, more polar polymer matrices such as polycarbonate (PC) and polyvinylidene chloride (PVDC) were also tested. PVDC was chosen as it provides a good barrier for molecular oxygen, and it was evident from former work that molecular oxygen can affect the stability of NBD undergoing several cycles. [11f ] Each polymer film was prepared by allowing a dichloromethane solution containing 0.1 wt% N4b. All composites of N4b@polymer gave free standing films of yellow-colored plastic, and when subjected to irradiation these materials went colorless, through the formation of Q4b.
The absorbance profile for N4b within the polymer matrices were slightly redshifted compared to solution characterization in toluene (order of 3 nm). Figure 3a shows the UV-vis absorption profile found for N4b@PS before and after irradiation. In addition, cycling studies were performed on these films, and the results for the activity of N4b in the different hosts can be seen in Figure 3b. Each cycle consisted of measuring absorbance followed by irradiation of the sample until the color of the film had faded and the peak at 379 nm in the UV-vis absorption spectrum had disappeared. The sample was then left in the dark, and the UV-vis absorption spectrum was periodically measured until no change in the spectra was observed.
The stability of N4b was indeed dependent upon the host polymer. For instance, composite N4b@PVDC after one cycle had lost some 20% of its activity, whereas N4b@PS formed a much more robust film, experiencing very little degradation after four cycles.
The half-lives of Q4b in PMMA, PC, and PS at room temperature were carried out and summarized in Table 2. It was found that the rate of back-conversion for Q4b→N4b was significantly influenced by the polymer host. Composite Q4b@ PMMA exhibited a fast rate of conversion with a half-life of only 20 min, while for Q4b@PS and Q4b@PC, the photoswitch exhibited markedly longer half-lives. In fact for Q4b@PS and Q4b@PC, studies of the switching kinetics revealed that the back-conversion did not follow a first order kinetics, and fitting of the absorbance as a function of time instead agreed with a double exponential decay. For instance, Q4b@PS exhibited two half-life times of 40 min and of 5.8 h for the second cycle. Similar results for other photoswitches in polymer films have been reported [10c] and could be explained by the inhomogeneous nature of local environment in the polymer composites. From these results, we can determine that polystyrene was the most suitable matrix polymer for the fabrication of N4b-polymer composites on the account of its high durability and a high lifetime stability for the QC form. In addition, this aggregation does not appear to affect the stability of the photoswitch in PS. This makes N4b@PS a promising material for window tinting applications. However, this is complicated by the changing rates after successive cycles. Due to the low stability of this photo switch in PVDC, no attempt was made to analyze the back-conversion kinetics for this material.
Given that PS was the optimal host for N4b and best preserved the properties of the photoswitch, longer cycling studies were necessary to ascertain the effects on NBD@PS, and most importantly on the kinetics for the back-reaction. To quantify the effect on the rate of conversion over successive cycles we selected N4c, which has a faster rate of back-conversion and therefore should allow for faster cycling. This investigation was also undertaken using different loadings of N4c (0.005-0.5 wt%) into PS to probe whether the concentration of the photoswitch also played a role. Composite N4c@PS was more colored than N4b@PS on the account of a greater degree of polarization in the π-system and had a higher extinction coefficient. Compound Q4c has a shorter half-life, which made it difficult to obtain a spectrum of fully converted Q4c@PS.
Photoswitch N4c was loaded into PS at four different concentrations, and the cyclability showed a decomposition per cycle of 0.02-0.45% for the system (Figure 4b); however, this was not proportionate to the amount of N4c introduced to PS. Unlike for N4b@PS, it was not possible to obtain full conversion for the more concentrated samples, as the rate of back-conversion Adv. Sci. 2019, 6,1900367   is too fast. More surprising was the change in the conversion rate going from Q4c@PS→N4c@PS. As seen with N4b@PS, the back-conversion rate slowed down over several cycles, and gradually reached a plateau ( Figure 4c) and was independent of the relative concentration of N4c. This could be a result of progressive structural rearrangement of the NBD within the material as Q4c should occupy less space than N4c. After several cycles there are still two rate constants, which average out at t ½ 1:22 min and t ½ 2:178 min for the half-lives for Q4c@PS at all measured concentrations. When examining the films with an optical microscope, it was found that small crystallites had formed within the composite films, suggestive of photoswitches aggregation, which could be related to the change in rate of back-conversion. It should be noted that the measurements were performed at ambient temperature, well below the glass transition (T g ) of polystyrene (T g (PS) ≈ 100 °C).
In order to demonstrate that these composites can not only absorb sunlight but also release the energy as heat, four different QC@PS films were prepared with a higher loading of the active molecule. Four NBDs were selected consisting of N4b-d and the symmetric dimer NN4e. Each sample was firstly irradiated under a solar simulator and immediately measured by differential scanning calorimetry (DSC). The polymer composite was recovered from the DSC pan to investigate the cyclability, then placed in a new DSC pan and subjected to two further irradiation-heat release cycles. The heat release was measured using a gradient of 2 °C min −1 and the results are summarized in Table 3. The DSC analysis method was conducted at a markedly slower heating rate than what is normally used for measuring of heat release of neat QCs so as to avoid heating the sample above the temperatures where phase changes of the material could interfere with the anticipated exotherm. For N4b@PS, it was found that the heat release performance of corresponding QC remained unaffected after three cycles, when each DSC cycle heated the material to 90 °C, which is just below the glass transition temperature of the polystyrene matrix. Not surprisingly, it was not possible to obtain and analyze Q4c@PS, as the material back-converted too rapidly. Material Q4d@PS was also measured in the DSC, though this sample could not be cycled as N4b@PS, as heating of the compound to 90 °C did not result in a full back-conversion of N4b. Upon heating to 110 °C, we observed a full release in the DSC; however, the cyclability of the switching process diminished significantly. This could be related to softening of the polymer matrix at temperatures higher than the T g , which facilitates phase separation and the formation of NBD aggregates within the polymer matrix. Composite QQ4e@PS was also prepared, and the heat release of the material could be measured in a similar fashion to that of Q4d@PS. Collectively, these materials exhibited energy densities between 30 and 50 kJ kg −1 (see Table 3), though this was dependent on the amount of NBD in PS. For the sake of direct comparison, molar enthalpies for the heat release are also summarized. In all examples, the energy release per mole of QC was similar. Molecule QQ4e, possessing two photochromic units, leads to a higher energy density (0.48 MJ kg −1 ). We note that it was not possible to measure the heat release of the neat QCs due to their fast back-conversion in their neat forms; however, the molar heat release could be calculated from the polymer samples. These values were found to be similar to those found for cyano analogs Q5b,d, and QQ5e (Table 3).
To illustrate the potential of NBD-polystyrene composites for the lamination on windows, N4b@PS (0.8 wt% N4b) were cast  onto glass substrates (see Figure 5) resulting in a film thickness of 70 µm (±5 µm). To prevent delamination of the N4b@PS coating we used either glass substrates which were subjected to a surface treatment with hexamethyldisilazane, or RadiSurf substrates, which comprise of a PS adhesion layer. These films converted within seconds upon exposure to sunlight, illustrating how the windows would work in real life (see Video SI in the Supporting Information).

Conclusions
In this work, new NBDs furnished with the powerful electronwithdrawing trifluoroacetyl acceptor have been synthesized, having redshifted onset of absorbance compared to analogs with the cyano group acceptor but at the cost of shorter QC lifetimes. As a result, these new derivatives are more suited for a day to day cycling purposes, as well as having a good overlap with the solar spectrum. Nevertheless, the effect of shorter lifetimes could be mitigated by the introduction of aryl donors with steric effects in the ortho position, such as the 1-naphthyl substituent, leading to systems with very long lifetimes (t 1/2 = 10 months). Moreover, double systems bearing two NBD units attached to a central phenylene bridge lead to a good quantum yield and unlike former observations of similar compounds, [11g] the second photoconversion isomerization did not experience lowered quantum yields. Further, the combination of improved solar spectrum match, quantum yield, and energy storage leads to an estimated solar energy storage efficiency of up to 3.8%. Amount the new synthesized NBDs, photochemical properties ideally matched to a daily charge/discharge cycle compounds were studied in polymer films, and it was found that polystyrene provided an attractive host, where the photoswitches could be subjected to multiple cycling without experiencing significant degradation. Molar energy storage enthalpies for the photoswitch-PS composite were comparable to the neat NBDs, which have energy storage enthalpies in the range of 105-198 kJ mol −1 per NBD unit, corresponding to energy densities in the 0.34-0.48 MJ kg −1 range for the neat NBDs and 2.7-3.8 kJ kg −1 in the 0.8 wt% composites.
This study has demonstrated that NBD dispersed in a polystyrene matrix can absorb sunlight, and over time release the energy as heat. This is the first step in making window tinting that contains NBD MOST systems, and shows great promise for implementation of such a technology with the aim of energy saving.

Experimental Section
General Experimental: Cyclopentadiene was distilled by cracking dicyclopentadiene over iron filings and storing at −80 °C prior to use. Tetrahydrofuran used was distilled over a sodium/benzophenone couple. All other chemicals were used as purchased from commercial sources. Cold baths at −84 and −41 °C were made from liquid nitrogen/ ethyl acetate and liquid nitrogen/acetonitrile slurries respectively, while −78 °C was made from dry ice and acetone. Purification of products was carried out by flash chromatography on silica gel (40−63 µm, 60 Å). Thin layer chromatography (TLC) was carried out using aluminum sheets precoated with silica gel. Infrared (IR) spectra recorded on a Perkin-Elmer Frontier FT-IR instrument as films evaporated from CDCl 3 onto an ATR attachment. 1 H NMR (400 MHz) and 13 C NMR (100 MHz) spectra were recorded on a Varian 400 MHz instrument, or 1 H NMR (500 MHz) and 13 C NMR (125 MHz) spectra were recorded on a Varian 500 MHz instrument, or 1 H NMR (800 MHz) spectra were recorded on a Bruker 500 MHz instrument, using the residual solvent as the internal standard (CDCl 3 , 1 H = 7.26 ppm and 13 C = 77.16 ppm, or toluene-d 8, 1 H = 2.090 ppm and 13 C = 20.400 ppm). All NMR experiments were acquired at 298 K unless specified. All chemical shifts are quoted on the δ scale (ppm), and all coupling constants (J) are expressed in Hz. All solution based spectroscopic measurements were performed in a 1 cm path length cuvette on either a Cary 60 Bio or a Cary 100 UVvis spectrophotometer, scanning the wavelength from 600 to 290 nm coupled with Peltier temperature control. Photoswitching experiments were performed using a Vilber Lourmet TLC lamp with a wavelength at 365 nm at 610 µw cm −3 or Thorlabs LED M365F1. Photoswitching for wavelengths 340, 405, and 455 nm were performed using Thorlabs LED M340L4, M405L3, and M455L3, respectively. The thermal back-reaction was performed by heating the sample (cuvette) by a Peltier unit in the UV-vis spectrophotometer. Quantum Yields were measured by the published procedure using a high concentration regime (absorbance Adv. Sci. 2019, 6,1900367  www.advancedscience.com above 2 at wavelength of irradiation) using potassium ferrioxalate and tris-phenanthroline iron(II) complex as a chemical actinometer. [17] Polystyrene (M W = 192 000 g mol −1 ), poly(Bisphenol A carbonate) (M W ≈ 45 000 g mol −1 ), and polyvinylidenechloride (GoodFellow, powder, mean particle size <180 µm) were purchased from Sigma Aldrich. The molecular weight of polyvinylidenechloride (M W = 52 700 g mol −1 ) was measured in 1,2,4-trichlorobenzene with Snatox stabilizer at 150 °C using an Agilent PL-GPC 220 Integrated HT-GPC with a refractive index detector and online viscometer using three Plgel 10 µm MIXED-B LS 300 × 7.5 mm columns with a universal calibration against polystyrene standards. Polymethylmethacrylate (M W = 100 000 g mol −1 ) was purchased from Polysciences Inc. NBDpolymer composites were fabricated by mixing of the respective NBD into a solution of the respective polymer in dichloromethane (c = 100 g L −1 ). The mixtures were poured into petri dishes and were allowed to dry at 25 °C overnight. All polymer based spectroscopic measurements were performed by attaching the polymer samples to a sample holder, ensuring the measurements were made at the exact same spot of the polymer sample every time, using a Cary 60 Bio UV-vis spectrophotometer, scanning the wavelength from 600 to 300 nm. All melting points and heat release of polymer samples were recorded with a Mettler Toledo DSC 2 apparatus, with a heating rate of 2 °C min −1 . HRMS spectra by either atmospheric pressure chemical ionization (APCI) or electrospray ionization (ESI) were acquired using an Agilent 1260 Infinity instrument fitted with an Agilent 6120 quadrupole. Elemental analyses were performed at London Metropolitan University. Terminal alkyne precursors to 3a,c-e, [18] 3b [16] were made by their respective literature methods.

Supporting Information
Supporting Information is available from the Wiley Online Library or from the author.