SRG Inscription in Supramolecular Liquid Crystalline Polymer Film : Replacement of Mesogens

The photoinduced surface relief formation via mass transfer upon irradiation with patterned light has long been a subject of extensive investigation. In azobenzene-containing liquid crystalline materials, UV light irradiation that generates the cis isomer leads to the liquid crystal to isotropic photochemical transition. Due to this phase change, efficiency of the mass transfer to generate a surface relief grating (SRG) becomes markedly greater. We have previously indicated that azobenzene-colored SRG-inscribed film can be bleached by removing a hydrogen-bonded azobenzene mesogen. However, this process largely reduces the height feature of the SRG corrugation. Herein, we propose an extended procedure where a colorless mesogen is filled successively after the removal of the azobenzene side chain. The process involves four stages: (i) SRG inscription in a hydrogen-bonded supramolecular azobenzene material; (ii) crosslinking (insolubilization) of the SRG film; (iii) removal of azobenzene mesogen by rinsing with a solvent, and (iv) stuffing the hollow film with a different mesogen. Although the final stuffing stage was insufficient at the present stage, this work demonstrates the possibility and validity of the strategy of mesogen replacement.

The Az unit is essential for the photo-induced mass migration, but after the relief formation the existence of this strongly light absorbing chromophore can be a drawback for many optical applications.The removal of the strongly colored chromophore of Az is of particular advantage and demand for the applications to optical elements such as waveguide couplers and liquid crystal alignment layers.
applications.The removal of the strongly colored chromophore of Az is of particular advantage and demand for the applications to optical elements such as waveguide couplers and liquid crystal alignment layers.Therefore, detachment of Az moiety after the SRG formation without destroying the relief structure has been attempted by supramolecular strategy [18], heat [19], and photochemical [20] decompositions.
We have previously introduced an Az-containing SCLCP system [18] via the hydrogen-bonding framework proposed by Kato et al. [21][22][23][24] and demonstrated that the selective extraction (detachment) of Az units from the SRG inscribed film can be performed without alternation of the periodic features [18].After the SRG is formed, the undulated film is first subjected to the chemical crosslinking, and the hydrogen-bonded Az side chain is successively detached by rinsing with a suitable solvent.This strategy actually worked in terms of bleaching the SRG film; however, the undulation height different was largely reduced to a one-fourth level after the removal of Az units [18].In this context, we attempted to overcome this drawback by filling the contracted hollow SRG film with another mesogen that is transparent in visible light regions.We expected that the feature of the relief structure would be recovered in this procedure.The chemical structures of materials used in this study and their abbreviations are displayed in Scheme 1.To generate transparent SRG films at visible light wavelengths, the use of cinnamate-containing polymers provides simpler processes [8].Nevertheless, this work newly demonstrates the strategy based on the chemical exchange of the constituents.Scheme 1.Chemical structures and their abbreviations of materials used in this study.

Characterizations of P(Py-EO)-Az
The materials used in this study are indicated in Scheme 1.A random copolymer containing a pyridine-containing methacrylate and oligo(ethylene oxide) containing methacrylate (P(Py-EO)) was synthesized using 2,2′-azobisisobutylonitril (AIBM) as the radical initiator.The feed ratio of Scheme 1.Chemical structures and their abbreviations of materials used in this study.

Characterizations of P(Py-EO)-Az
The materials used in this study are indicated in Scheme 1.A random copolymer containing a pyridine-containing methacrylate and oligo(ethylene oxide) containing methacrylate (P(Py-EO)) was synthesized using 2,2 -azobisisobutylonitril (AIBM) as the radical initiator.The feed ratio of pyridine monomer was 0.7, and the resulting polymer possessed a copolymerization ratio of 0.48 for pyridine unit as revealed by 1 H-NMR spectroscopy.Meanwhile, an Az derivative having a benzoic acid terminal (8Az4Me-Bz) was synthesized.The P(Py-EO) polymer was mixed with Az in tetrahydrofuran (THF) Crystals 2017, 7, 52 3 of 10 at a 1:1 ratio with respect to the pyridine unit, and the solvent was then evaporated.This mixing procedure gave a hydrogen bonding complex (P(Py-EO)/8Az4Me-Bz) as also shown in Scheme 1.In the molecular design of 8Az4Me-Bz, the alkyl spacer between the Az unit and benzoic acid possessed a methyl branch, which prevented strong dimerization and stacking of Az-containing molecules in the hydrogen-bonded complex.This feature was favorable to effectively attain the hydrogen-bonded complex of P(Py-EO)/8Az4Me-Bz.As demonstrated below, the hydrogen bond complexation between P(Py-EO) and 8Az4Me-Bz was confirmed and characterized by differential scanning calorimetry (DSC), FTIR spectroscopy, and X-ray scattering measurements.
Figure 1 shows the DSC curves for the host polymer (P(Py-EO), 8Az4Me-Bz, and the complex (P(Py-EO)/8Az4Me-Bz). P(Py-EO) gave no appreciable change in the DSC curve.The 8Az4Me-Bz exhibited an exothermic peak at 133 • C and two sharp endothermic peaks at 157 • C and 166 • C in the heating process.In contrast, P(Py-EO)/8Az4Me-Bz exhibited small and broad and thermic peaks at 92 • C and 135 • C, and no peaks ascribed to the pure compound of 8Az4Me-Bz were observed at 157 • C and 166 • C. Therefore, the thermal property of the complexed polymer was fully different.Polarizing optical microscopic observation (POM) indicated that this polymer exhibited a smectic A phase from 92 pyridine monomer was 0.7, and the resulting polymer possessed a copolymerization ratio of 0.48 for pyridine unit as revealed by 1 H-NMR spectroscopy.Meanwhile, an Az derivative having a benzoic acid terminal (8Az4Me-Bz) was synthesized.The P(Py-EO) polymer was mixed with Az in tetrahydrofuran (THF) at a 1:1 ratio with respect to the pyridine unit, and the solvent was then evaporated.This mixing procedure gave a hydrogen bonding complex (P(Py-EO)/8Az4Me-Bz) as also shown in Scheme 1.In the molecular design of 8Az4Me-Bz, the alkyl spacer between the Az unit and benzoic acid possessed a methyl branch, which prevented strong dimerization and stacking of Az-containing molecules in the hydrogen-bonded complex.This feature was favorable to effectively attain the hydrogen-bonded complex of P(Py-EO)/8Az4Me-Bz.As demonstrated below, the hydrogen bond complexation between P(Py-EO) and 8Az4Me-Bz was confirmed and characterized by differential scanning calorimetry (DSC), FTIR spectroscopy, and X-ray scattering measurements.
Figure 1 shows the DSC curves for the host polymer (P(Py-EO), 8Az4Me-Bz, and the complex (P(Py-EO)/8Az4Me-Bz). P(Py-EO) gave no appreciable change in the DSC curve.The 8Az4Me-Bz exhibited an exothermic peak at 133 °C and two sharp endothermic peaks at 157 °C and 166 °C in the heating process.In contrast, P(Py-EO)/8Az4Me-Bz exhibited small and broad and thermic peaks at 92 °C and 135 °C, and no peaks ascribed to the pure compound of 8Az4Me-Bz were observed at 157 °C and 166 °C.Therefore, the thermal property of the complexed polymer was fully different.Polarizing optical microscopic observation (POM) indicated that this polymer exhibited a smectic A phase from 92 °C to 135 °C. Figure 2 displays FTIR spectra in 1600-3200 cm −1 (a) and 1400-1900 cm −1 (b) regions.For a P(Py-EO)/8Az4Me-Bz) film, characteristic bands were observed at 1917 and 2488 cm −1 , which are indicative of the formation of the hydrogen band between carboxylic acid and pyridine [25].These peaks were commonly observed at 25-150 °C (a), showing that the hydrogen bond was not cleaved in these temperature regions.A strong absorption band was observed at 1680 cm −1 assignable to the dimer formation [21,22] between two benzoic acid groups of 8Az4Me-Bz molecules (b, dotted curve).In contrast, P(Py-EO)/8Az4Me-Bz indicated a smaller band at 1699 cm −1 instead of 1680 cm −1 at 25-150 °C [21,22].This also indicates the hydrogen bond formation between the benzoic acid of 8Az4Me-Bz and pyridine of P(Py-EO).Therefore, the hydrogen bonding of 8Az4Me-Bz and P(Py-EO) were firmly formed in the mixture of P(Py-EO)/8Az4Me-Bz films, and the Az unit was introduced as the side chain of P(Py-EO) at all temperatures under investigation.
X-ray scattering measurements were further conducted (Figure 3).At 100 °C and 115 °C, X-ray scattering was observed at 2θ = 2.2° corresponding to a spacing (d) of 4.1 nm.This value should be ascribed to the layer structure of side chain of 8Az4Me-Bz.This layer structure disappeared in the isotropic state at 135 °C.At lower temperatures at 25 °C and 50 °C, a broad scattering was observed at 2θ = 0.68° (d = 13.5 nm).We did not elucidate yet the origin of this larger-scaled regular structure.Figure 2 displays FTIR spectra in 1600-3200 cm −1 (a) and 1400-1900 cm −1 (b) regions.For a P(Py-EO)/8Az4Me-Bz) film, characteristic bands were observed at 1917 and 2488 cm −1 , which are indicative of the formation of the hydrogen band between carboxylic acid and pyridine [25].These peaks were commonly observed at 25-150 • C (a), showing that the hydrogen bond was not cleaved in these temperature regions.A strong absorption band was observed at 1680 cm −1 assignable to the dimer formation [21,22] between two benzoic acid groups of 8Az4Me-Bz molecules (b, dotted curve).In contrast, P(Py-EO)/8Az4Me-Bz indicated a smaller band at 1699 cm −1 instead of 1680 cm −1 at 25-150 • C [21,22].This also indicates the hydrogen bond formation between the benzoic acid of 8Az4Me-Bz and pyridine of P(Py-EO).Therefore, the hydrogen bonding of 8Az4Me-Bz and P(Py-EO) were firmly formed in the mixture of P(Py-EO)/8Az4Me-Bz films, and the Az unit was introduced as the side chain of P(Py-EO) at all temperatures under investigation.
X-ray scattering measurements were further conducted (Figure 3).At 100 • C and 115 • C, X-ray scattering was observed at 2θ = 2.2 • corresponding to a spacing (d) of 4.1 nm.This value should be ascribed to the layer structure of side chain of 8Az4Me-Bz.This layer structure disappeared in the isotropic state at 135 • C. At lower temperatures at 25 • C and 50 • C, a broad scattering was observed at 2θ = 0.68 • (d = 13.5 nm).We did not elucidate yet the origin of this larger-scaled regular structure.

SRG Inscription and Replacement of Mesogens
The strategy of this work using P(Py-EO)/8Az4Me-Bz is depicted in Scheme 2. After an SRG structure is inscribed by irradiation with patterned UV light, crosslinking (fixation) of the SRG structure (Process A), removal (dissolving) of the Az mesogen by washing with a suitable solvent (Process B), and finally filling with another mesogen, cyanobiphenyl (CB) unit will be introduced (Process C).More details of the procedures of crosslinking and stuffing the SRG film are displayed in Scheme 3.Both chemical [10,12] and photochemical [26] crosslinking may be achieved for the SRG fixation.In this study, chemical crosslinking was adopted using a formaldehyde vapor to undergo the acetal condensation between two hydroxyl groups in the P(Py-EO) polymer (a).In the process of filling with CB unit, the free pyridine unit after the removal of 8Az4Me-Bz was reacted with CB-Br (see Scheme 1) by the quarternization (b).
Figure 4a shows a time-course profile of the height difference between the top and bottom levels of the SRG structure upon irradiation with line-and-space (10 × 10 μm) patterned non-polarized UV light (365 nm, 2 mW•cm −2 ). Figure 4b,c shows AFM images and surface profiles after UV irradiation for 100 s and 1000 s, respectively.An induction time was observed until 100 s, and after this period, the SRG undulation was efficiently formed until 600 s.The height difference reached 160 nm at 1000 s, which corresponds to twice the thickness of the initial flat film (85 nm).The bottom area almost reached the level of substrate.In this way, very efficient mass migration occurred in this supramolecular film.The efficiency of the motion is comparable with that reported previously for relevant systems of covalently side chain films [10,12].Sufficient mass transfer was observed around 1 J• cm −2 .The motion was directed from un-irradiated areas to irradiated ones (supporting information), which agreed with the previous observations using covalently bonded Az side chains [11].

SRG Inscription and Replacement of Mesogens
The strategy of this work using P(Py-EO)/8Az4Me-Bz is depicted in Scheme 2. After an SRG structure is inscribed by irradiation with patterned UV light, crosslinking (fixation) of the SRG structure (Process A), removal (dissolving) of the Az mesogen by washing with a suitable solvent (Process B), and finally filling with another mesogen, cyanobiphenyl (CB) unit will be introduced (Process C).More details of the procedures of crosslinking and stuffing the SRG film are displayed in Scheme 3.Both chemical [10,12] and photochemical [26] crosslinking may be achieved for the SRG fixation.In this study, chemical crosslinking was adopted using a formaldehyde vapor to undergo the acetal condensation between two hydroxyl groups in the P(Py-EO) polymer (a).In the process of filling with CB unit, the free pyridine unit after the removal of 8Az4Me-Bz was reacted with CB-Br (see Scheme 1) by the quarternization (b).
Figure 4a shows a time-course profile of the height difference between the top and bottom levels of the SRG structure upon irradiation with line-and-space (10 × 10 μm) patterned non-polarized UV light (365 nm, 2 mW•cm −2 ). Figure 4b,c shows AFM images and surface profiles after UV irradiation for 100 s and 1000 s, respectively.An induction time was observed until 100 s, and after this period, the SRG undulation was efficiently formed until 600 s.The height difference reached 160 nm at 1000 s, which corresponds to twice the thickness of the initial flat film (85 nm).The bottom area almost reached the level of substrate.In this way, very efficient mass migration occurred in this supramolecular film.The efficiency of the motion is comparable with that reported previously for relevant systems of covalently side chain films [10,12].Sufficient mass transfer was observed around 1 J• cm −2 .The motion was directed from un-irradiated areas to irradiated ones (supporting information), which agreed with the previous observations using covalently bonded Az side chains [11].

SRG Inscription and Replacement of Mesogens
The strategy of this work using P(Py-EO)/8Az4Me-Bz is depicted in Scheme 2. After an SRG structure is inscribed by irradiation with patterned UV light, crosslinking (fixation) of the SRG structure (Process A), removal (dissolving) of the Az mesogen by washing with a suitable solvent (Process B), and finally filling with another mesogen, cyanobiphenyl (CB) unit will be introduced (Process C).More details of the procedures of crosslinking and stuffing the SRG film are displayed in Scheme 3.Both chemical [10,12] and photochemical [26] crosslinking may be achieved for the SRG fixation.In this study, chemical crosslinking was adopted using a formaldehyde vapor to undergo the acetal condensation between two hydroxyl groups in the P(Py-EO) polymer (a).In the process of filling with CB unit, the free pyridine unit after the removal of 8Az4Me-Bz was reacted with CB-Br (see Scheme 1) by the quarternization (b).
Figure 4a shows a time-course profile of the height difference between the top and bottom levels of the SRG structure upon irradiation with line-and-space (10 × 10 µm) patterned non-polarized UV light (365 nm, 2 mW•cm −2 ). Figure 4b,c shows AFM images and surface profiles after UV irradiation for 100 s and 1000 s, respectively.An induction time was observed until 100 s, and after this period, the SRG undulation was efficiently formed until 600 s.The height difference reached 160 nm at 1000 s, which corresponds to twice the thickness of the initial flat film (85 nm).The bottom area almost reached the level of substrate.In this way, very efficient mass migration occurred in this supramolecular film.The efficiency of the motion is comparable with that reported previously for relevant systems of covalently side chain films [10,12].Sufficient mass transfer was observed around 1 J•cm −2 .The motion was directed from un-irradiated areas to irradiated ones (supporting information), which agreed with the previous observations using covalently bonded Az side chains [11].The chemical crosslinking was achieved by exposure to a mixed vapor of formaldehyde and hydrochloride.The SRG-inscribed film was placed into a sealed container together with a hydrochloric acid (6 mol•L −1 ) and 30% (by weight) formaldehyde aqueous solutions for 1 h.After this treatment, the SRG film was immersed in pure water to remove the unreacted reagents, and dried in a reduced pressure.Figure 5 indicates AFM images taken before (a) and after (b) the above treatment.As shown, the film surface of SRG became quite coarse (b); however, the height and periodic features was essentially unchanged as indicated in the surface profiles (c).
The sample treated as above was then immersed into tetrahydrofuran (THF) several times.Figure 6 shows the AFM images before (a) and after (b) the THF immersion.After the immersion into THF, the top-to-bottom height difference was reduced to approximately half from 164 nm to 87 nm (c).UV-visible absorption spectra revealed that the ππ* band around 350 nm entirely disappeared after rinsing with this solvent (d).These results clearly indicate that the initial side chain of 8Az4Me-Bz was fully detached from the crosslinked SRG-inscribed film.The chemical crosslinking between the hydroxyl groups was essentially needed for this process because both 8Az4Me-Bz and P(Py-EO) were well dissolved in THF.The retained SRG structure (b) clearly shows that the film became insoluble to THF due to the formation of cross-linked chemical networks.The chemical crosslinking was achieved by exposure to a mixed vapor of formaldehyde and hydrochloride.The SRG-inscribed film was placed into a sealed container together with a hydrochloric acid (6 mol•L −1 ) and 30% (by weight) formaldehyde aqueous solutions for 1 h.After this treatment, the SRG film was immersed in pure water to remove the unreacted reagents, and dried in a reduced pressure.Figure 5 indicates AFM images taken before (a) and after (b) the above treatment.As shown, the film surface of SRG became quite coarse (b); however, the height and periodic features was essentially unchanged as indicated in the surface profiles (c).
The sample treated as above was then immersed into tetrahydrofuran (THF) several times.Figure 6 shows the AFM images before (a) and after (b) the THF immersion.After the immersion into THF, the top-to-bottom height difference was reduced to approximately half from 164 nm to 87 nm (c).UV-visible absorption spectra revealed that the ππ* band around 350 nm entirely disappeared after rinsing with this solvent (d).These results clearly indicate that the initial side chain of 8Az4Me-Bz was fully detached from the crosslinked SRG-inscribed film.The chemical crosslinking between the hydroxyl groups was essentially needed for this process because both 8Az4Me-Bz and P(Py-EO) were well dissolved in THF.The retained SRG structure (b) clearly shows that the film became insoluble to THF due to the formation of cross-linked chemical networks.The chemical crosslinking was achieved by exposure to a mixed vapor of formaldehyde and hydrochloride.The SRG-inscribed film was placed into a sealed container together with a hydrochloric acid (6 mol•L −1 ) and 30% (by weight) formaldehyde aqueous solutions for 1 h.After this treatment, the SRG film was immersed in pure water to remove the unreacted reagents, and dried in a reduced pressure.Figure 5 indicates AFM images taken before (a) and after (b) the above treatment.As shown, the film surface of SRG became quite coarse (b); however, the height and periodic features was essentially unchanged as indicated in the surface profiles (c).
The sample treated as above was then immersed into tetrahydrofuran (THF) several times.Figure 6 shows the AFM images before (a) and after (b) the THF immersion.After the immersion into THF, the top-to-bottom height difference was reduced to approximately half from 164 nm to 87 nm (c).UV-visible absorption spectra revealed that the ππ* band around 350 nm entirely disappeared after rinsing with this solvent (d).These results clearly indicate that the initial side chain of 8Az4Me-Bz Crystals 2017, 7, 52 6 of 10 was fully detached from the crosslinked SRG-inscribed film.The chemical crosslinking between the hydroxyl groups was essentially needed for this process because both 8Az4Me-Bz and P(Py-EO) were well dissolved in THF.The retained SRG structure (b) clearly shows that the film became insoluble to THF due to the formation of cross-linked chemical networks.
Crystals 2017, 7, 52 6 of 10 Having these results, we next attempted to undergo a reaction with the free pyridine moiety of the crosslinked hollow P(Py-EO) with CB-Br by the quarternization reaction.The Az-free SRG film was immersed in a THF solution containing CB-Br at the boiling temperature (66 °C) for 5 days.After this procedure, this sample was immersed into pure THF several times to remove unreacted CB-Br.Then, the resulting film was subjected to measurements of UV-visible absorptions and AFM.Crystals 2017, 7, 52 6 of 10 Having these results, we next attempted to undergo a reaction with the free pyridine moiety of the crosslinked hollow P(Py-EO) with CB-Br by the quarternization reaction.The Az-free SRG film was immersed in a THF solution containing CB-Br at the boiling temperature (66 °C) for 5 days.After this procedure, this sample was immersed into pure THF several times to remove unreacted CB-Br.Then, the resulting film was subjected to measurements of UV-visible absorptions and AFM.In Figure 7, AFM images before (a) and after (b) the quarternization reaction are displayed.The height was slightly increased by the attachment of CB mesogen.The surface profile (c) indicates that 10%-20% increase of the height difference.The UV-visible absorption spectra (Figure 7d) indicated that the ππ* band around 300 nm appeared after the reaction (red line).The CB group was actually reacted with the pyridine moiety and introduced to the crosslinked hollow P(Py-EO) matrix.However, the recovery of the height difference was obviously insufficient.In this way, the strategy of the stuffing process was partly successful but not satisfactorily at the present stage.The molar extinction coefficients of Az and CB compounds employed were comparable, 3.0 × 10 4 L•mol −1 •cm −1 at 352 m and 2.5 × 10 4 L•mol −1 •cm −1 at 298 nm, respectively.A recovery amount of mesogen can be roughly estimated by comparing the absorption spectra in Figure 6d and Figure 7d.Seemingly, approximately a half amount of mesogens was reconstituted in the quarternization process, although the height recovery ratio was apparently less, only by 10%-20%.This discrepancy may be ascribed to the difference in the molecular orientation of mesogens.In the initial Az-containing film, the mesogens are oriented homeotropically to some extent.A reduced intensity of the ππ* band of Az around 350 nm relative to that at 250 nm (Figure 6d, black line) indicates the tendency of homeotropic orientation [15].The stuffing with CB by the chemical reaction in solvent may reduce the molecular packing and disturb the mesogen orientation, providing larger absorbance.The reasons for the insufficient reactivity of CB-Br with the pyridine residues could be ascribed to (i) the formation of denser crosslinking at the surface area that inhibits the penetration of CB-Br; and (ii) the existence of buried pyridine residues that repels the access of CB-Br.We expect that the optimization of the crosslinking conditions, reaction solvent, and conditions for the quarternization process will improve the recovery ratio in the mesogen stuffing.Having these results, we next attempted to undergo a reaction with the free pyridine moiety of the crosslinked hollow P(Py-EO) with CB-Br by the quarternization reaction.The Az-free SRG film was immersed in a THF solution containing CB-Br at the boiling temperature (66 • C) for 5 days.After this procedure, this sample was immersed into pure THF several times to remove unreacted CB-Br.Then, the resulting film was subjected to measurements of UV-visible absorptions and AFM.
In Figure 7, AFM images before (a) and after (b) the quarternization reaction are displayed.The height was slightly increased by the attachment of CB mesogen.The surface profile (c) indicates that 10%-20% increase of the height difference.The UV-visible absorption spectra (Figure 7d) indicated that the ππ* band around 300 nm appeared after the reaction (red line).The CB group was actually reacted with the pyridine moiety and introduced to the crosslinked hollow P(Py-EO) matrix.However, the recovery of the height difference was obviously insufficient.In this way, the strategy of the stuffing process was partly successful but not satisfactorily at the present stage.The molar extinction coefficients of Az and CB compounds employed were comparable, 3.0 × 10 4 L•mol −1 •cm −1 at 352 m and 2.5 × 10 4 L•mol −1 •cm −1 at 298 nm, respectively.A recovery amount of mesogen can be roughly estimated by comparing the absorption spectra in Figures 6d and 7d.Seemingly, approximately a half amount of mesogens was reconstituted in the quarternization process, although the height recovery ratio was apparently less, only by 10%-20%.This discrepancy may be ascribed to the difference in the molecular orientation of mesogens.In the initial Az-containing film, the mesogens are oriented homeotropically to some extent.A reduced intensity of the ππ* band of Az around 350 nm relative to that at 250 nm (Figure 6d, black line) indicates the tendency of homeotropic orientation [15].The stuffing with CB by the chemical reaction in solvent may reduce the molecular packing and disturb the mesogen orientation, providing larger absorbance.The reasons for the insufficient reactivity of CB-Br with the pyridine residues could be ascribed to (i) the formation of denser crosslinking at the surface area that inhibits the penetration of CB-Br; and (ii) the existence of buried pyridine residues that repels the access of CB-Br.We expect that the optimization of the crosslinking conditions, reaction solvent, and conditions for the quarternization process will improve the recovery ratio in the mesogen stuffing.
The number-averaged molecular weight (Mn) and polydispersity index (Mw/Mn) were determined by gel permeation chromatography (GPC) using Shodex DS-4 (UV detector) with columns of KF 803F and KF 805L (eluent solvent: THF).Mn and Mw/Mn P(Py-EO) used in this work were found to be 8.9 × 10 3 and 1.24, respectively.The content of pyridine unit in the resulting copolymer was determined by 1 H-NMR using a JNM-GSX270 (JEOL).The copolymerization ratio of pyridine used in this work was 0.48.The detailed synthetic procedures and characterizations are described in the supporting information.

Methods and Measurements
P(Py-EO) and 8Az4Me-Bz was dissolved and mixed at a 1:1 (Py/Az) ratio in THF and slowly evaporated at 60 °C to obtain a complexed powder.Polymer films were obtained by spincasting at 2000 rpm for 30 s from a THF solution.The photo-triggered mass transfer was induced by UV (365 nm) light irradiation through a 10 × 10 μm line-and-space photomask at 120 °C.UV light irradiation was performed with a Supercure-203S (Sanei Electronic) passing through combinations of Toshiba optical filters, UV35 and V44, for 365 nm.Detailed procedures are described in the supporting information.Non-polarized light was used for the induction of SRG.
UV-visible absorption spectra were taken on an Agilent 8453 diode array spectrometer.Fourier transform infrared (FTIR) spectra were taken on a FTS 6000 (Biorad) with a DTGS detector.The resolution was 4 cm −1 .DSC measurements were carried out with a DSC 200 (Seiko Instrument).The surface morphology was evaluated by AFM using a Nanopics 2100 (Seiko Instruments) equipped with a DMS/SS mode cantilever (NPX1CT004).X-ray analyses were performed with a NANO Viewer (Rigaku) using a Cu Kα beam.POM observations were made using a BX-51 (Olympus).
The number-averaged molecular weight (M n ) and polydispersity index (M w /M n ) were determined by gel permeation chromatography (GPC) using Shodex DS-4 (UV detector) with columns of KF 803F and KF 805L (eluent solvent: THF).M n and M w /M n P(Py-EO) used in this work were found to be 8.9 × 10 3 and 1.24, respectively.The content of pyridine unit in the resulting copolymer was determined by 1 H-NMR using a JNM-GSX270 (JEOL).The copolymerization ratio of pyridine used in this work was 0.48.The detailed synthetic procedures and characterizations are described in the supporting information.

Methods and Measurements
P(Py-EO) and 8Az4Me-Bz was dissolved and mixed at a 1:1 (Py/Az) ratio in THF and slowly evaporated at 60 • C to obtain a complexed powder.Polymer films were obtained by spincasting at 2000 rpm for 30 s from a THF solution.The photo-triggered mass transfer was induced by UV (365 nm) light irradiation through a 10 × 10 µm line-and-space photomask at 120 • C. UV light irradiation was performed with a Supercure-203S (Sanei Electronic) passing through combinations of Toshiba optical filters, UV35 and V44, for 365 nm.Detailed procedures are described in the supporting information.Non-polarized light was used for the induction of SRG.
UV-visible absorption spectra were taken on an Agilent 8453 diode array spectrometer.Fourier transform infrared (FTIR) spectra were taken on a FTS 6000 (Biorad) with a DTGS detector.The resolution was 4 cm −1 .DSC measurements were carried out with a DSC 200 (Seiko Instrument).The surface morphology was evaluated by AFM using a Nanopics 2100 (Seiko Instruments) equipped

Figure 1 .
Figure 1.DSC profiles in the heating process.

Figure 1 .
Figure 1.DSC profiles in the heating process.

Crystals 2017, 7 , 52 5 of 10 Scheme 2 .Scheme 3 .
Scheme 2. Strategic scheme of the overall process in this work.Process A: chemical crosslinking (acetal formation) of polymer backbone in SRG-inscribed film; Process B: removal of hydrogen-bonded Az side chain by rinsing with a solvent; Process C: filling with CB derivative (CB-Br) by a chemical reaction.

Scheme 2 . 10 Scheme 2 .Scheme 3 .
Scheme 2. Strategic scheme of the overall process in this work.Process A: chemical crosslinking (acetal formation) of polymer backbone in SRG-inscribed film; Process B: removal of hydrogen-bonded Az side chain by rinsing with a solvent; Process C: filling with CB derivative (CB-Br) by a chemical reaction.

Scheme 3 .
Scheme 3. Schematic illustrations of chemical crosslinking between two hydroxyl groups of oligo(ethylene oxide) side chain of P(Py-EO) with formaldehyde ((a), Process B in Scheme 2), and reconstitution with a CB compound (CB-Br) by the quarternization reaction in the hollow P(Py-EO) film ((b), Process C in Scheme 2).

Figure 5 .
Figure 5.Chemical crosslinking (Process A in Scheme 2).AFM images before (a) and after (b) the acetal formation, and their surface profiles (c).

Figure 5 .
Figure 5.Chemical crosslinking (Process A in Scheme 2).AFM images before (a) and after (b) the acetal formation, and their surface profiles (c).

Figure 5 .
Figure 5.Chemical crosslinking (Process A in Scheme 2).AFM images before (a) and after (b) the acetal formation, and their surface profiles (c).

Figure 6 .
Figure 6.Removal of hydrogen-bonded Az side chain (Process B in Scheme 2).AFM images before (a) and after (b) washing with THF; surface profiles (c); and UV-visible absorption spectra (d) before (black) and after (red) the rinsing procedure.

Figure 6 .
Figure 6.Removal of hydrogen-bonded Az side chain (Process B in Scheme 2).AFM images before (a) and after (b) washing with THF; surface profiles (c); and UV-visible absorption spectra (d) before (black) and after (red) the rinsing procedure.

Figure 7 .
Figure 7. Filling with CB derivative (Process C in Scheme 2) into the hollow P(Py-EO) matrix.AFM images before (a) and after (b) filling with the CB derivative, surface profiles ((c), black and red lines correspond to the profile before and after the reaction with CB-Br); and UV-visible absorption spectra (d) before (black) and after (red) filling with CB.

Figure 7 .
Figure 7. Filling with CB derivative (Process C in Scheme 2) into the hollow P(Py-EO) matrix.AFM images before (a) and after (b) filling with the CB derivative, surface profiles ((c), black and red lines correspond to the profile before and after the reaction with CB-Br); and UV-visible absorption spectra (d) before (black) and after (red) filling with CB.