An aromatic micelle with bent pentacene-based panels: encapsulation of perylene bisimide dyes and graphene nanosheets.

For exploitation of a new class of aromatic micelles, we synthesized a bent pentacene-based amphiphilic molecule through Diels-Alder reaction. The amphiphiles bearing two trimethylammonium tethers assemble into a spherical aromatic micelle, with an average core diameter of 1.5 nm, in water at room temperature. The new aromatic micelle efficiently encapsulates perylene bisimide (PBI) dyes and graphene nanosheets (GNS) in water. The encapsulated PBI dyes form a parallel stacked dimer, exhibiting characteristic absorption and emission bands. In addition, the encapsulated GNS are composed of few-layer graphene sheets with an average lateral size of ∼7 nm, as confirmed by Raman spectroscopy. The resultant, aqueous host-guest complexes are stable even after three weeks in water under ambient conditions. This journal is © The Royal Society of Chemistry 2020.

Introduction

n class="Chemical">Polyacenes provide planar π-electron-rich frameworks with unique photo/electrochemical properties, like typical polyaromatic compounds (e.g., n>n class="Chemical">pyrene and perylene).1 On the other hand, unlike other polyaromatics, their tape-shaped frameworks display characteristic reactivities: the central benzene rings can be easily and selectively functionalized from the side edges or face (Fig. 1a). Pentacene is one of the most appealing polyacenes. Its edge-functionalization has been intensively investigated for the development of advanced photofunctional materials (e.g., chemical sensors, thin film transistors, and solar cells).2,3 However, pentacene-based components, synthesized via face-functionalization, usable for supramolecular systems have been rarely explored so far, despite the facile accessibility by Diels–Alder reaction.4 We thus employed pentacene as a starting material for the design of new face-functionalized, amphiphilic molecule PA (Fig. 1b), capable of forming an aqueous supramolecular container with intriguing host functions.5,6 Here we report the formation of aromatic micelle (PA) from bent pentacene-based amphiphiles PA with two trimethylammonium tethers in water at room temperature and its unusual host abilities toward relatively large perylene bisimide (PBI) dyes7 and graphene nanosheets (GNS) in water.8 In the new host cavity, the encapsulated PBI dyes form a parallel stacked dimer, exhibiting characteristic spectral bands and the encapsulated GNS comprise few-layer sheets with small lateral size (∼7 nm), as confirmed by Raman analysis. The resultant, host–guest complexes remain intact in water under ambient conditions even after three weeks.

Fig. 1

(a) Schematic representation of the edge- and face-functionalization of a polyacene. (b) Bent pentacene-based amphiphilic molecule PA, designed in this work and (c) its optimized structure (side and bottom views). The optimized structure of PA was obtained by DFT calculations (B3LYP/6-31G (d) level, Gaussian 16 Rev A.03).12 (d) Anthracene-based amphiphile AA.

Recently, we have shown that n class="Chemical">anthracene-based amphiphiles AA (Fig. 1d) with bent n>n class="Chemical">dianthrylbenzene frameworks assemble into well-defined, spherical micelles in water through π-stacking interactions and the hydrophobic effect.9 The bent amphiphile is synthesized via Pd-catalyzed cross-coupling reaction (i.e., edge-functionalization) using 9-bromoanthracene. Obtained aromatic micelle (AA) possesses a flexible aromatic cavity capable of binding a wide range of hydrophobic compounds (e.g., fullerenes and carbon nanotubes) in water.6b,10 In contrast to the previous amphiphile, bent pentacene-based amphiphile PA (Fig. 1b) designed herein provides the following three features. (i) The bent aromatic framework is constructed by the transition metal-free and 100% atom-economic Diels–Alder reaction of pentacene and a dienophile. (ii) The framework with a dihedral angle of 120° has a hydrophobic pocket on the concave side (Fig. 1c, left). (iii) Two hydrophilic groups, attached on the convex side, adopt an orthogonal orientation with respect to the bent aromatic framework, facilitating efficient π-stacking interactions (Fig. 1c, right). Although the Diels–Alder reaction is a very simple and useful synthetic tool, its use for the preparation of supramolecular capsules has been limited so far.5,6,11

Results and discussion

Formation of a bent pentacene-based micelle

New amphiphile PA, synthesized in five steps, assembled into aromatic micelle n class="Chemical">(PA) in n>n class="Chemical">water in a spontaneous and quantitative manner. The Diels–Alder reaction of pentacene and dimethyl acetylenedicarboxylate gave rise to a hydrophobic, bent pentacene framework in 62% yield. The subsequent transformation of the methyl groups into hydrophilic trimethylammonium groups afforded PA, whose monomeric structure was confirmed by NMR and MS analyses (Fig. S1–S14†).12 Once a white solid of PA (6.4 mg, 10 μmol) was added to water (0.5 mL) at room temperature, aromatic micelle (PA) was quantitatively formed within 1 min through π-stacking interactions and the hydrophobic effect (Fig. 2a). In 1H NMR spectra, upon formation of (PA) in D2O (20.0 mM based on PA), the bent pentacene signals Hc and Hd of PA were remarkably shifted upfield as compared with those observed in CD3OD (Δδ = –0.49 and –0.44 ppm, respectively; Fig. 2b and c). The average size (core diameter) of the product was estimated to be 1.5 nm by DOSY NMR (Fig. 2d) and DLS analyses (Fig. 2e).13 Molecular modeling studies suggested that the size corresponds well to that of spherical pentamer (PA)5, featuring the average core and outer diameters of ∼1.6 and ∼2.6 nm, respectively (Fig. 2f).

Fig. 2

(a) Schematic representation of the formation of aromatic micelle (PA) from amphiphile PA in water. 1H NMR spectra (500 MHz, r.t.) of (b) PA in CD3OD and (c) (PA) in D2O (20 mM based on PA), and (d) their DOSY NMR spectra (500 MHz, 25 °C). (e) DLS chart (H2O, r.t.) and (f) optimized structure (n = 5) of (PA). The optimized structure was obtained by molecular mechanics (MM) calculations (Forcite module, Materials Studio, ver. 5.5.3).12

The concentration-dependent 1H NMR and DLS studies of n class="Chemical">(PA) in n>n class="Chemical">water indicated the critical micelle concentration (CMC) being <∼20 mM based on PA (Fig. S18 and S20†). Unlike the similar UV-visible absorption bands of (PA) and PA, the fluorescence band of PA (λmax = 343 nm in methanol) was largely bathochromically shifted (Δλ = +33 nm) upon micelle formation (20.0 mM based on PA in water; Fig. S19†).

Encapsulation of perylene bisimide dyes

To explore the characteristic host functions of aromatic micelle n class="Chemical">(PA), we focused on n>n class="Chemical">perylene bisimides (PBIs), which are an important class of organic dyes frequently employed as supramolecular building blocks,7 exhibiting strong absorption bands in the visible region. Without directing groups, the planar core frameworks of the PBI dyes usually aggregate randomly in the solid state as well as in aqueous solution. 3,5-Dimethylphenyl-substituted perylene bisimide PBI-1, known as Pigment Red 149, is insoluble in water and hardly soluble in common organic solvents (e.g., CHCl3, acetone, and DMSO) owing to its strong aggregation. Nevertheless, aromatic micelle (PA) could readily solubilize PBI-1 in water at room temperature upon encapsulation. As an optimized protocol, red solid PBI-1 was ground with amphiphile PA in a 1 : 2 molar ratio for 5 min using a small mortar and pestle. After sequential water addition, centrifugation, and filtration, host–guest complex (PA)·(PBI-1) was obtained as a clear, red aqueous solution (Fig. 3a, right).12,14 The UV-visible spectrum showed broadened yet intense absorption bands in the range of 400 to 600 nm (Fig. 3b), which indicates the concentration of solubilized PBI-1 in water being 0.54 mM. The absorption bands of (PA)·(PBI-1) are comparable to those of solid PBI-1 (ref. 15) so that encapsulated (PBI-1) dyes (m > 2) adopt random aggregates even within (PA). The host–guest complex remains almost intact (≥96%) in water under ambient conditions even after four months (Fig. S23†).16

Fig. 3

(a) Encapsulation of PBI-1 dyes by amphiphiles PA and AA in water and the photographs of the resultant solutions. Procedures: (i) manual grinding (5 min), (ii) water addition, (iii) high-speed centrifugation (16 000g, ∼10 min), and (iv) membrane filtration (200 nm in pore size). (b) UV-visible spectra (H2O, r.t., 1.0 mM based on the amphiphiles) of (PA)·(PBI-1), (AA)·(PBI-1), and (SDS)·(PBI-1).

The n class="Chemical">water solubilizing ability of n>n class="Chemical">(PA) toward PBI-1 was compared with a typical micelle and previous aromatic micelle, consisting of linear alkane-based amphiphile, sodium dodecylsulfonate (SDS), and bent anthracene-based amphiphile AA (Fig. 1d), respectively. The treatment of PBI-1 with SDS in the same way afforded a pale red solution with very weak absorption bands for (PBI-1) within (SDS). On the basis of the band intensity of the encapsulated dyes at 473 nm, the water solubilization of PBI-1 by PA was estimated to be 17 times higher than that by SDS, most probably due to the efficient host–guest π-stacking interactions. An apparent red solution including (AA)·(PBI-1) was also obtained from AA and PBI-1 (Fig. 3a, left). In the UV-visible spectra, the observed guest bands were virtually overlapped with those of (PA)·(PBI-1) (Fig. 3b) and thus PA and AA exhibit an equal water solubilizing ability toward PBI-1.17

In sharp contrast to (n class="Chemical">PBI-1) within aromatic micelles n>n class="Chemical">(PA) and (AA), sterically demanding, 2,6-diisopropylphenyl-substituted perylene bisimide PBI-2, known as Perylene Orange, displayed host-dependent spectroscopic features in water at room temperature. In a manner similar to (PA)·(PBI-1), aqueous host–guest complex (PA)·(PBI-2) was formed through the grinding protocol using PA and PBI-2 (Fig. 4a, right). The resultant red solution showed relatively sharp absorption bands with slight bathochromic shifts (Δλmax = +9 nm) relative to those of PBI-2 in CH2Cl2 (Fig. 4b), indicating multiple stacks of the dyes. The formation of the stacked (PBI-2) species was further confirmed by a significant bathochromic shift (Δλ = +108 nm) of the emission band of PBI-2 upon encapsulation (Fig. 4c). It is worthy of note that the same protocol employing AA and PBI-2 generated a red purple aqueous solution of (AA)·(PBI-2) with broadened absorption bands in the range of 420 to 670 nm (Fig. 4a, left and Fig. 4b). The fluorescence spectrum of the resultant host–guest complex showed a couple of broad emission bands with significant bathochromic shifts (Fig. 4c). Therefore, the stacking conformation of (PBI-2) and its spectroscopic properties could be modulated upon encapsulation by the aromatic micelles in water.

Fig. 4

(a) Encapsulation of PBI-2 dyes by amphiphiles PA and AA in water and the photographs of the resultant solutions. Procedures: (i) manual grinding (5 min), (ii) water addition, (iii) high-speed centrifugation, and (iv) membrane filtration. (b) UV-visible and (c) fluorescence spectra (H2O, r.t., 1.0 mM based on the amphiphiles, λex = 498 nm) of (PA)·(PBI-2) and (AA)·(PBI-2). (d) DLS chart (H2O, r.t.) and (e) optimized structure (n = 6, m = 2) of (PA)·(PBI-2). The optimized structure was obtained by MM calculations (Forcite module).12

To gain structural insights into n class="Chemical">(PA)·(n>n class="Chemical">PBI-2), the product composition and size were revealed by NMR and DLS analyses. After lyophilization of the aqueous (PA)·(PBI-2) solution, the average PA : PBI-2 ratio was determined to be 3 : 1 by integration of the sharp 1H NMR signals of the product mixture in DMSO-d6 (Fig. S26†). The DLS analysis of (PA)·(PBI-2) suggested an average diameter of 2.0 nm for the product (Fig. 4d). The combination of the obtained NMR and DLS data as well as the spectroscopic findings (Fig. 4b and c) indicates the selective formation of a (PA)6·(PBI-2)2 complex, in which the parallel stacked (PBI-2)2 are surrounded by the bent pentacene panels of (PA)6.7 The optimized structure bearing the hydrophobic guest core and an amphiphilic host shell provides an average core diameter of ∼2 nm (Fig. 4e).

Encapsulation of fullerene and graphene nanosheets

We next investigated the host functions of n class="Chemical">(PA) toward n>n class="Chemical">fullerene C60 (C) and graphene nanosheets as typical and uncommon nanocarbon guests, respectively.18 Anthracene-based amphiphile AA has been revealed to be a superior water-solubilizing agent for various fullerenes upon encapsulation.14 Similar solubilizing ability of PA was found toward C. Simply grinding a mixture of PA and C (2 : 1 molar ratio) for 5 min and subsequent addition of water to the resultant solid generated a brown aqueous solution of host–guest complex (PA)·(C). After removal of the excess guest, the UV-visible spectrum of the product solution showed clear absorption bands assignable to encapsulated (C) around 340 and 450 nm (Fig. 5a). The band intensity is comparable to that of (AA)·(C) prepared in the same way. The amphiphile-fullerene ratio (n = 6, m = 1) and size (1.7 nm in core diameter) of (PA)·(C) were confirmed by UV-visible and DLS analyses (Fig. 5b).

Fig. 5

(a) UV-visible spectra (H2O, r.t., 1.0 mM based on PA or AA) and the photographs of (PA)·(C) and (AA)·(C). (b) DLS chart (H2O, 1.0 mM based on PA, r.t.) of (PA)·(C) and optimized structure of (PA)6·C. The optimized structure was obtained by MM calculations (Forcite module).12

The encapsulation test for well-defined n class="Chemical">fullerene prompted us to examine the encapsulation and n>n class="Chemical">water-solubilization of large nanocarbon sheets with various dimensions by pentacene-based micelle (PA). Graphene nanosheets (GNS) employed here are multilayer sheets in a platelet morphology (2–10 nm in thickness and 5 μm in width), which are sparingly soluble in water using additives (e.g., SDS and sodium dodecylbenzenesulfonate).12,18 The combination of grinding and sonication operations with PA enabled the efficient formation of host–guest complex (PA)·GNS in water (Fig. 6a, right). A mixture of PA (0.6 mg, 1.0 μmol) and GNS (0.3 mg) was ground for 5 min and the resultant black solid was sonicated in H2O (1.0 mL) for 10 min at room temperature. The high-speed centrifugation (16 000g for 30 min) and membrane filtration (200 nm in pore size) of the obtained suspension gave a clear black aqueous solution.12 The UV-visible-NIR, DLS, and Raman analyses of the black solution revealed the formation of (PA)·GNS. The UV-visible-NIR spectrum displayed wide-ranging, very broadened absorption bands without characteristic peaks, derived from encapsulated GNS (Fig. 6b). The high stability of the host–guest structure was clarified by the absorption spectrum after three weeks (Fig. S32†). The DLS chart showed a single peak with an average diameter of 5.2 nm and a relatively narrow size distribution (Fig. 6c), suggesting the selective encapsulation of small graphene sheets.

Fig. 6

(a) Schematic representation of the encapsulation of GNS by amphiphiles PA, AA, and SDS in water and the photographs of the resultant solutions. Procedures: (i) manual grinding (5 min), (ii) water addition, (iii) sonication (40 kHz, 10 min), (iv) high-speed centrifugation (16 000g, ∼30 min), and (v) membrane filtration (200 nm in pore size). (b) UV-visible-NIR spectra (H2O, r.t., 1.0 mM based on the amphiphiles) of (PA)·GNS, (AA)·GNS, (PA)·SG, and (SDS)·GNS. (c) DLS charts (H2O, r.t.) and (d) optimized structure (n = 66, 3-layer graphene sheet) of (PA)·GNS. The optimized structure was obtained by MM calculations (Forcite module).12

Notably, n class="Chemical">water-solubilizing ability of n>n class="Chemical">(PA) toward GNS was higher than that of (AA) and (SDS). The same grinding and sonication protocols using AA and SDS instead of PA yielded black and colorless solutions, respectively, showing very broadened absorption bands in the UV-visible-NIR spectra (Fig. 6a and b). The band intensities of encapsulated GNS (at 660 nm) indicate that the water solubilizing ability of PA is 1.4- and 18-fold higher than that of AA and SDS, respectively. The observed, high solubilizing ability of PA most probably arises from efficient π-stacking interactions between the bent pentacene framework and the graphene surface (Fig. S35†). The concentration of GNS in the resultant (PA)·GNS solution (1.0 mM based on PA) was calculated at 0.18 mg mL–1.12 In a manner similar to (PA)·GNS, a black aqueous solution of (PA)·SG was efficiently obtained using PA and synthetic graphite (SG; 10 μm in average size).12 The UV-visible-NIR spectrum and DLS chart of the product (Fig. 6b and c) resembles those of (PA)·GNS, assuming the incorporation of small graphene sheets into the micelle cavity in water.

Finally, the detailed structures of n class="Chemical">GNS and SG within aromatic micelle n>n class="Chemical">(PA) were elucidated by Raman spectroscopic analysis. The Raman spectrum of (PA)·GNS (532 nm laser wavelength) exhibited clear peaks at 1348, 1584, 1623, and 2692 cm–1, corresponding to the typical D, G, D′, and 2D bands of graphenes, respectively (Fig. 7a), in Raman-inactive water at room temperature. On the basis of the ratio of the observed D and G band intensities (i.e., ID/IG = 2.62), the lateral guest size of (PA)·GNS was estimated to be 7.3 nm (Fig. 7e).12,19a The shape and position of the observed 2D band indicate the presence of few-layer graphene sheets, particularly monolayer sheets as a major component.19b,c The relatively large peak width (i.e., full width at half maximum (FWHM) = 62 cm–1) of the 2D band agrees with the presence of defect-rich graphene sheets and thus indicates the formation of the small graphene sheets (Fig. 7f). The combination of the present Raman data with the UV-visible-NIR and DLS findings concluded that aromatic micelle (PA) could efficiently exfoliate and encapsulate the few-layer nanosheets of GNS through simple grinding and sonication protocols.

Fig. 7

Raman spectra (H2O, DPSS laser, λ = 532 nm, r.t.) of (a) (PA)·GNS, (b) (AA)·GNS, (c) (PA)·SG, and (d) GNS (solid). (e) Expanded and its deconvoluted D and G bands of (PA)·GNS. Raman spectra (H2O, λ = 532 nm, r.t.) of the expanded 2D bands of (f) (PA)·GNS, (g) ground and sonicated GNS (solid), and (h) pristine GNS (solid).

The Raman spectra of (AA)·n class="Chemical">GNS (Fig. 7b) and (PA)·SG (Fig. 7c) in water also indicated the exfoliation and encapsulation of similar graphene sheets (6.9 and 6.1 nm in lateral size, respectively; Table S1†) by the aromatic micelles. It is worth noting that the Raman analysis of a pristine GNS sample, bearing large lateral size (e.g., ID/IG = ∼0.4; Fig. 7d and S40†) and wide-ranging thickness, remains almost unchanged after sequential grinding (5 min) and sonicating (30 min) in the absence of PA (Fig. 7f–h). Accordingly, aromatic micelle (PA) captured small graphene sheets (1–3 layers) in a selective fashion from a complex mixture of GNS (Fig. 6d).

Conclusions

We have designed and synthesized a bent n class="Chemical">pentacene-based amphiphilic molecule through Diels–Alder reaction as a key face-functionalization step. The amphiphiles spontaneously and quantitatively assemble into a spherical aromatic micelle (∼2 nm in diameter) in n>n class="Chemical">water at room temperature. The new class of aromatic micelles displays efficient encapsulation abilities toward relatively large perylene bisimide (PBI) dyes and graphene nanosheets (GNS) in water. The resultant, highly water-soluble and stable host–guest complexes accommodate the parallel stacked dimer of a bulky PBI dye and small few-layer nanosheets of GNS, respectively, in a selective fashion. As relevant challenges and future prospects, thanks to the non-covalent host–guest interactions, the encapsulated PBI and GNS guests could potentially be released from the host cavity,14 which prompts us to develop novel functional solid materials through the present, pentacene-based aromatic micelle.

Conflicts of interest

There are no conflicts to declare.

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