Reversible 2D Supramolecular Organic Frameworks encompassing Viologen Cation Radicals and CB[8]

Reversible 2D supramolecular organic frameworks encompassing branched viologen architectures and cucurbit[8]uril (CB[8]) were constructed and investigated. UV-vis investigation clearly indicates the formation and intermolecular dimerization of monocation radicals and their encapsulation into the hydrophobic CB[8] cavity which is further complemented by EPR (electron paramagnetic resonance) spectroscopy. Particle size measurements by dynamic light scattering method showed particle sizes in the range of several µm indicating larger aggregates. Zeta potential measurements suggested the instability of these particles and their tendency to form aggregates. TEM (transmission electron microscope) analysis further revealed the formation of supramolecular polymer (monocation radical with cucurbit[8]uril) whose diameter were in the range of several µm as indicated by DLS measurements; however the oxidized form, i.e., the viologen dication with cucurbit[8]uril showed dotted spots in the range of sub nanometer level. The internal periodicities of the supramolecular polymers were analyzed by SAXs (small angle X-ray scattering) measurements. Additionally, we have demonstrated that these supramolecular organic frameworks can be depolymerized by oxidation in air and again can be polymerized (intermolecular radical dimerization) by reduction under inert atmosphere demonstrating that these systems will be of broad interest.

interactions. Gao et al. reported that 1,1′-binaphthyl inter-connected viologen based tweezer like molecules undergoes reversible modulation upon chemical or photochemical reduction 29,30 . Spectroelectrochemical investigations of different conjugated oligomeric viologens were reported by Zhao and coworkers. The authors illustrated that the viologen radical cations dimerized to linear supramolecular polymers 31 . Zhang et al. reported a two-dimensional viologen based supramolecular assembly formed by viologen radical dimerization which is enhanced by CB [8] 27 . Zhou et al. reported the construction of a three-dimensional viologen based cross-linked supramolecular assembly and they further discussed on the stability of radical dimer with preorganization of rigid building blocks 28 . Very recently Marchini et al. reported the pimerization of tetrahedrally arranged bipyridinium units wherein, reduced viologen units were intermolecularly dimerized, which stabilizedthe system as well asenchanced the supramolecular growth 32 . Following a similar strategy, herein we report the synthesis of star-shaped ethyl terminated viologen (ESV) and newly self-assembled network of different viologens (EV, EDV, ETV & ESV) driven by radical-radical (V +• … •+ V) dimerization. Further these dimerized species forms a supramolecular polymeric network in the presence of CB [8] and these assemblies were subjected to spectroscopic investigations. Figure 1 shows the chemical structure of cucurbit [8]uril host and viologen guest molecules.

Results and Discussion
Synthesis. Ethyl terminated star-shaped viologen (ESV) was synthesized in two steps following a reported procedure as shown in Fig. 2 16 . The synthesis starts with the selective alkylation reaction of 4,4′-bipyridine with 1-bromoethane to obtain the key compound 1 (92%) (Fig. 2) 17,33 . The compound 1 was further reacted with p-xylylene dibromide (five-fold excess) to obtain compound 2 (81%) in the first step. In the second step, compound 2 was reacted with well-known trimer core P 0 3PF 6 34 to afford ESV(65%). The newly synthesized star-shaped viologen was characterized by 1 HNMR, 13 CNMR and DEPT measurements and its purity was cross-checked by elemental analysis.

Methods
General. All starting materials and solvents were purchased from Sigma-Aldrich or Alfa Aesar and used without further purification. All reactions were performed under dry conditions unless otherwise stated. Diethyl viologen dibromide was synthesized following the reported procedure and it was anion exchanged to EV 2PF 6 35 . Cucurbit [8]uril was synthesized following a reported procedure. For measurements in organic media, the as prepared hexafluorophosphate salts were used, and for the measurements in aqueous media, the corresponding PF 6¯ salts were anion exchanged to Br¯ salts by adding TBA.Br in CH 3  Small angle X-ray scattering experiments were conducted on Rigaku (Rigaku Smart Lab) using Cu Kα radiation, the power of X-ray source was operated at 50 mA and 40 kV and the d-spacing values were calculated by the formula d = 2π/q. For SAXs measurement, thin film of the respective polymer solution was dip coated on a glass plate and dried in glove box. The as dried thin films were then measured. [8]]. Reported procedure was followed to obtain CB Synthesis of compound 1. Reported literature is followed, for the sake of data completion, the procedure is presented here 17 .

Synthesis of Cucurbit[8]uril [CB
4,4ʹ-bipyridine (4.0 g, 25.6 mmol) was dissolved in 20 ml CH 3 CN and stirred at 80 °C. To this solution 1-bromo ethane (0.56 g, 5.12 mmol) dissolved in (10 ml) CH 3 CN was added slowly over 8 h. The progress of the reaction was monitored by TLC (MeOH: HOAc: H 2 O -10:4:1). The reaction mixture was stirred for 24 h in total, and then cooled to room temperature. The reaction mixture was concentrated under reduced pressure and the resulting yellow precipitate was washed with excess diethyl ether to remove unreacted bipyridine. The bromide salt was then dissolved in minimal amount of water, precipitated with 3 M NH 4 PF 6 ,filtered, washed and dried to yield the 1 as a white solid (1.42 g, 84%). 1 13  Synthesis of compound 2. p-xylylene dibromide (2.0 g, 7.57 mmol) was dissolved in 10 mL CH 3 CN and heated to 80 °C under stirring. To this solution, 1 (0.50 g, 1.51 mmol) dissolved in CH 3 CN (10 mL) was added slowly over 8 h. The reaction mixture was stirred for 48 h in total, and then cooled to room temperature. The reaction mixture was concentrated under reduced pressure and the resulting yellow precipitate was washed with excess diethyl ether to remove unreacted dibromide. The bromide salt was then dissolved in minimal amount of water, precipitated with 3 M NH 4 PF 6 , filtered, washed and dried to yield compound 2 as a white solid (0.75 g, 75%). (0.64 g, 64%). 1  Synthesis of compound ETV. Mixture of 1,3,5-tris(bromomethyl)benzene (0.5 g, 1.40 mmol) and (2.0 g, 4.62 mmol) 1 were dissolved in 10 ml CH 3 CN and the reaction mixture was stirred at 80 °C for 24 h. Then the reaction mixture was cooled to RT, and the precipitate was filtered and washed with CH 3 CN and dried. It was then dissolved in water, precipitated with NH 4 PF 6 , filtered, washed and dried to yield the ETV (1.55 g, 72%). 1

UV-Vis.
In UV-Vis, dialkyl bipyridinium salts (viologens) typically show an absorption maxima at 250 nm approx. corresponding to the dication, and its one electron reduced monocation radical (V +• ) shows an absorption maxima at 400 and 600 nm respectively 37 . This monocation radical has the tendency to dimerize i.e., formation of intramolecular charge transfer complex between the reduced monocation radicals and there is an equilibrium between the monocation radical and its dimeric form. A typical UV-Vis measurement shows absorption maxima at 400, 600 nm corresponding to the monocation radical, upon complexation the wavelength shifts to 550 nm (blue shift) 38 corresponding to the monocation radical and an additional 800-1100 nm corresponding to the dimer is observed 16,37,39 . The ratio between these two bands indicates the degree of dimerization.
Ethyl viologen (EV) is used as a model compound in this work. UV-vis spectra of four different ethyl terminated viologen compounds (EV, EDV, ETV & ESV) were recorded in aqueous phosphate buffer (pH = 7) solution containing excess sodium dithionite (50 mM) and are displayed in Fig. 3. [In aqueous solution, sodium dithionite readily reduces viologen (V 2+ ) to monocation radical (V +• )]. All the viologen radical cations (EDV 2+• , ETV 3(+•) , ESV 6(+•) except EV (+•) ) displayed broad and strong absorption bands. EDV 2(+•) showed absorption maxima at 525 and 1020 nm, ETV 3(+•) at 525 and 990 nm, ESV 6(+•) at 590 and >1100 nm corresponding to the monocation radical and its dimer respectively. In the case of EV (+•) , an absorption maxima centered around 600 nm corresponding to the monocation radical was observed (Fig. 3a) and this indicates that the monomer behaves differently than that of the branched architectures. In the case of branched architectures, because of the flexible benzyl interconnection, dimerization is more favored and hence intra/intermolecular CT complexation occurs. All these results strongly suggest that except the monomer EV (+•) , all the other branched viologens (EDV 2(+•) , ETV 3(+•) , ESV 6(+•) ) undergo dimerization. In the presence of CB [8], the affinity to form radical dimer (V +• ) 2 increases as the dimer can be easily encapsulated into the hydrophobic cavity of CB [8] which is additionally stabilized by ion-dipole interactions between the oxygen atoms (16 nos) and radical cation 26,40 . On the other hand, the possibility for intramolecular stacking between radical cations of peripheral viologen units in the projected viologen derivatives is fewer as the intramolecular radical dimerization is mainly distant dependent 16 . Further the presence of rigid benzene core moiety and unfavorable steric interactions suppress the possibilities of intramolecular dimerization. Figure 3b shows the UV-Vis spectra of CB [8] encapsulated viologen radicals. It is clear that all the four molecules are included in the CB [8] cavity in their dimerized form as the intensity of the absorption band at 800-1100 nm is more strong than their corresponding monocation radical spectrum without CB [8]. Even the monocation radical of EV shows an intense band at 1020 nm indicating that it is included in the CB [8] cavity in the dimerized form. These results clearly suggest that in the presence of CB [8] dimerization is more favored and such dimerization can be a result of inter/intramolecular interactions. It is important to note that intramolecular dimerization inhibit the formation of supramolecular polymer. However, the particle size measurements show that we have larger aggregates indicating that they are formed from a long chain linear/hyperbranched supramolecules. Such supramolecular polymerization is a result of intermolecular dimerization between the molecules.
The association constants of all the four molecules were estimated from UV-Vis titrations and the plots are given in the supporting information. Table 1 depicts the physical chemical data of all the four viologen derivatives.

EPR. Electron paramagnetic resonance spectroscopy (EPR) gives clear insight on the material with unpaired
electrons. Since we reduced the viologen dication to monocation radical and encapsulated them into the CB [8] cavity, EPR analysis can probe the nature of the radicals and their interaction with CB [8]. In this work, we have investigated the paramagnetic properties as well as the dimerization tendency of four different viologen radical cations such as EV (+•) , EDV 2(+•) , ETV 3(+•) & ESV 6(+•) . The concentration of the monocation radical (0.50 mM) and CB [8] (0.25 mM) were kept constant throughout the experiment. EPR spectra were recorded in sodium phosphate buffer solution (0.1 M) containing sodium dithionite (50 mM). The radical cation of the model compound (EV (+•) ) showed a sharp EPR signal with a g-factor value 2.0046 (Fig. 4a) closer to that of a g-factor of free electron (g = 2.0023) 31 and this is in agreement with the reported values for simple viologen monocation radical indicating the very organic feature of the radical 27,28,32 . The sharp hyperfine splitting of respective viologen radical cations (EV (+•) , EDV 2(+•) , ETV 3(+•) & ESV 6(+•) ) indicated that the radical cations (here after denoted as (V +• )) exclusively gets dimerized (V +• ) 2 as reported by Zhang et al. 27 . However, all these molecules EV (+•) , EDV 2(+•) , ETV 3(+•) & ESV 6(+•) displayed a different behavior than the molecules reported by Zhang et al. EPR spectra of all these radicals displayed hyperfine splitting with high resolution corresponding to a dimer, and we could not detect any weak broad hyperfine signal corresponding to the monocation radical very closer to the radical dimer except in the case of ESV 6(+•) (a small hump is seen) before the addition of CB [8] 27 . These results clearly indicate that the monocation radicals exclusive dimerize under our experimental conditions. Nevertheless, in the case of EV, these results are in conflict with the UV-Vis measurements and this could be related to the equilibration time.
Probably the EV (+•) needs more time for the complex formation and equilibration time under UV-Vis measurement conditions is insufficient.
Under identical conditions CB [8] was added to the solution containing radical dimer, equilibrated and EPR spectrum was recorded as displayed in Fig. 4b. The presence of CB [8] developed a weaker broad hyperfine splitting for the dimer (V +• ) 2 . These broad hyperfine structures specify the encapsulation of viologen dimeric species into the hydrophobic cavity of CB [8]. As a result of encapsulation, electron-electron exchange interaction between the corresponding viologen radicals becomes reduced (dipole-dipole interactions becomes weak) 38 . The strength of the broad hyperfine structure increases in the order EDV 2(+•) > EV (+•) > ETV 3(+•) > ESV 6(+•) (Fig. 4b) indicating the decrease in concentration of dimer species (V +• ) 2 upon complexation with CB [8]. All these results clearly indicate the existence of intermolecular-interactions between the radical dimers (V +• ) 2 which is further enhanced in the presence of CB [8] as indicated by UV-Vis and EPR measurements. Intermolecular interactions in these structure leads to molecular self-assembly in a 2D (EDV 2(+•) , ETV 3(+•) , ESV 6(+•) ) orientation. Addition of CB [8] further enhances the formation of inclusion complexes leading to the construction of a well-defined 2D supramolecular polymers as reported by Zhang et al. 27 and Marchini et al. 32 . These self-assembled architectures are guided through non-covalent interactions and their consequent movements and rotations indicate that the supramolecular network should be polydisperse and hence the order of these polydisperse supramolecular polymers may be ideal or randomly arranged 2D structures 26 . Cyclic voltammetry. Viologens or 4,4′-bipyridinium salts exhibit excellent redox behavior and undergoes two consecutive one electron reduction to form the monocation radical and neutral bipyridinylidene. A standard dialkyl viologen shows redox peaks at −0.4 V and −0.8 V corresponding to the reduction of dication to monocation radical (V 2+ ↔ V +• ) and monocation radical to neutral bipyridinylidene (V +• ↔ V 0 ) respectively. The electrochemical potential required for the redox process of viologens solely depends on N-substitution 16 . The electrochemical properties of four different ethyl terminated viologens (EV, EDV, ETV & ESV) and their inclusion complexation with CB [8] were monitored by cyclic voltammetry (CV) (Fig. 5a-d) in the presence and absence of CB [8]. Model compound ethyl viologen (EV) displayed two reduction peaks at a potential of −0.62 V and −0.89 V. Further the positive and negative potential shifts for the rest of the three viologen compounds were compared with redox potential values of EV. Typically the first reduction, V 2+ ↔ V +• occurs easily, while the second reduction (V +• ↔ V 0 ) becomes more difficult, as more electrical stimuli is required for reducing the monocation radical (V +• ) [there is an equilibrium between the monocation radical and its dimerized form

V (+•)
. Thus the difficulty in the second reduction i.e., larger shift in the electrochemical potential can be attributed to the dimerization of the monocation radical. The electrochemical potential difference between the two reduction and two oxidation waves in ethyl terminated viologens were investigated by CV, and the potential differences were denoted as ∆E p , ∆E p increases with increase in 4,4′-bipyridinium units in the respective viologen architectures (EV, EDV, ETV and ESV).
Notably, the reduction potential differences were 0.27 V for EV, 0.33 V for EDV, 0.35 V for ETV and 0.46 V for ESV and these shift in potential differences enhance the stability of their respective dimer (V +• ) 2 . On the other hand, the anodic potential increased in the order EV (0.21 V) < EDV (0.24 V) < ETV (0.29 V) < ESV (0.30 V) and such increments can be accounted for the additional stabilization of the dimer. It is noteworthy that in the absence of CB [8], all the four viologens displayed similar CV profile and diffusion behavior. In the presence of CB [8], viologens compounds displayed different behavior, EDV and ESV showed same number of redox waves with obvious positive and negative redox potential shifts. Particularly EDV showed larger ∆E p values of 0.42 V and 0.66 V for the corresponding anodic and cathodic potential differences in the presence of CB [8]. These large difference in the reduction potential could be ascribed to the higher tendency of radical dimerization (V +• ) 2 in the presence of CB [8] and further stacking of such inclusion assembly as probed by particle size measurements. Noteworthy is the very low diffusion current of the ESV-CB [8] complex (approx. 5-7 times lesser) compared to that of the parent compound (ESV) depicting the fact that it forms large molecular aggregates which limits its self-diffusion towards the electrode surface. In all the other cases decrease in diffusion current of approx. 1.5-2 times was observed indicating the formation of inclusion complex. With and without CB [8], the first oxidation peak in all the four cases depicts preferential adsorption of the complex over the electrode surface (except ESV-CB [8]complex which shows normal redox pattern). The other viologens such as the model compound EV and the trimer ETV showed three different reduction waves, wherein the first two reduction peaks are ascribed to the EV 2+ ↔ EV +• and EV 2+ + EV +• → (EV +• ) 2 processes 27 . The third reduction peak is attributed to the conversion of radical cation to its neutral form EV +• ↔ EV o at the potentials of −0.89 (EV) and −0.79 (ETV). The slight potential shifts on both anodic as well as cathodic side is a result of an improved stability of (V +• ) 2 after encapsulation into hydrophobic cavity of CB [8].
Particle size measurements. UV-Vis, EPR and cyclic voltammetric studies clearly revealed the possibility of formation of intermolecular dimerized supramolecular network where the arrangement on 2D depends on the nature of the viologen precursor (EV, EDV, ETV & ESV) with CB [8]. To infer more details into the supramolecular framework, particle size measurements were done for viologen compounds without and with CB [8] in aqueous solutions. These supramolecular framework were constructed by self-stacking the respective viologen radical cations (V +• ) and they exhibit certain hydrodynamic diameter (D H ) (particle size) in water. The D H value of supramolecular entity formed by (V +• ) before the addition of CB [8] was found to be 0.66 μm for EV, 0.53 μm for EDV, 0.85 μm for ETV and 0.35 μm for ESV (Fig. 6). These results clearly specify that the compounds are stacked in to very larger aggregates guided by molecular self-assembly and these results are in contrast to the recent reports on supramolecular assemblies where particle size of several nm were reported 27,28 . The larger aggregates/polydispersely arranged network could stack to form 2D supramolecular assemblies as reported by Zhou et al., Zhang et al. and Marchini et al. 27,28,32 . In the presence of 0.1 mM CB [8], the aqueous solution containing excess of sodium dithionite and EV (•+) produced aggregates with the D H value 1.35 μm which was twice when compared with the value (0.66 μm) without CB [8], denoting that 2:2 or 1:1 complex was formed in the mixture. Further the solution containing 0.2 mM CB [8] and EDV 2(•+) formed aggregates with the D H value of 0.72 μm which is slightly larger compared to the value (D H = 0.53 μm) without CB [8]. This smaller difference in particle size indicates the formation of 2:1 complex between CB species were 0.85 μm and 0.35 μm. These particle size differences indicates the formation of 2:1 and 2:3 complexes of ETV 3(•+) and ESV 6(•+) with CB [8] respectively.
In addition, zeta potential measurements were carried out to study on the stability of these monocation radicals in the absence and presence of CB [8] ( Figure S1). The stability of a colloidal dispersion can be described by zeta potential. In the absence of CB [8], we obtained zeta potential values of −5.8, −3.0, −10.7 and −18.6 mV and in the presence of CB [8], 5.8, 2.4, 9.3 and 15.8 mV were obtained for EV (•+) , EDV 2(•+) , ETV 3(•+) and ESV 6(•+) respectively. All these values indicate high instability/rapid aggregation of these molecules. It is noteworthy that in the absence of CB [8], the zeta potential values were negative and as soon as the intermolecular dimer gets encapsulated in CB [8] cavity, the value becomes positive.

TEM & HR-TEM analysis. TEM (transmission electron microscope) analysis of viologen trimer further
revealed the formation of supramolecular polymer (ETV 3(•+) with cucurbit [8]uril) whose diameter were in the range of several µm as indicated by DLS measurements; however the oxidized form, i.e., the viologen dication with cucurbit [8]uril showed dotted spots in the range of sub nanometer level (Fig. 7). It is very clear from TEM experiments that these samples show a characteristic difference in their morphology before and after reduction.
HR-TEM images of the samples were given in supporting information (Figures S10 and S11). SAD (selected area diffraction) analysis by HR-TEM reveals the semi-crystalline nature of these supramolecular polymers (EDV, ETV and ESV).

SAXs measurements.
The internal periodicities of the samples were measured by SAXs (small angle X-ray scattering) measurements and are shown in Fig. 8. The following conclusions can be drawn from the SAXs measurements (i) EDV showed a broad scattering peak with a d-spacing value of 4.4 nm corresponding to {200} facet 41 . (ii) ETV showed relatively less scattered broad peak with a d-spacing value of 5.7 nm corresponding to {100} facet (iii) ESV showed a sharp peak with a d-spacing value of 6.8 nm corresponding to {100} facet 41 .
The internal periodicities of these samples clearly reflect the fact that they form 2D architecture 27 . This is further confirmed by SAD pattern measured from the TEM analysis.
Based on UV-Vis studies, SAXs measurements and particle size measurements, we propose the following scheme to illustrate the supramolecular self-assembly process as shown in Fig. 9. The whole process is accompanied by two key processes, i) supramolecular polymer formation and ii) aggregation. The model compound diethyl viologen is involved in dimer formation and aggregation, whereas all the other three compounds form supramolecular polymer network and its aggregates. For simplicity, only for dimer we have given the mechanism of aggregate formation and whole mechanism, in the case of trimer and star shaped viologens, the mechanism is complex and the pictographical representation of such complex would be tedious.

Reversibility Studies by UV-Vis spectroscopy.
It is well-known that the viologen dication undergoes two electron reductions to produce monocation radical and a neutral species and such reduced species can be reoxidized chemically/electrochemically. Throughout this study, we employed reduced monocation radical to study its dimerization and subsequent formation of supramolecular organic framework. Hence it is possible to reoxidize this species by aerial oxidation or by passing O 2 gas.
To probe more on the reversibility of supramolecular polymerization, we performed five subsequent cycles of UV-V is measurements by consecutive oxidation and reduction of the same solution (Fig. 10). The fully reduced solution containing viologen monocation radical/dimer V +• /V (+•) 2 with CB [8] was oxidized by bubbling O 2 and the spectra was recorded which showed typical viologen dication (V 2+ ) absorption at 220-260 nm. This solution was again degassed with N 2 and reduced with sodium dithionite. The corresponding UV-Vis spectra showed typical bands for the monocation radical and the dimerized species. Likewise, the experiment was repeated for five consecutive cycles and the system was found to be reversible. Thus, the supramolecular polymerization can be reversed by bubbling oxygen and can be formed again by degassing with N 2 and reducing with sodium dithionite.  Under our experimental conditions, we were able to repeat this cycle for at least five times without much decrease in the redox activity and hence we believe that these supramolecular polymerization can be reversed i.e., depolymerized. Once oxidized, the dicationic viologens exhibit electrostatic repulsion and hence they unwind from CB [8] cavity, where only one viologen unit remain encapsulated in the CB [8] cavity. Thus the system becomes monomeric. Again the reduction with sodium dithionite under inert atmosphere yields monocation radical which can undergo facile intermolecular dimerization into the CB [8] cavity forming supramolecular polymeric network. Thus oxidation leads to depolymerization of the network and subsequent reduction yields the supramolecular polymeric network.

Conclusion
In summary, we reported the 2D supramolecular organic framework formed between the different viologen guest molecules (EV, EDV, ETV and ESV) and CB [8] and the interactions were probed spectroscopically in detail by employing UV-Vis spectroscopy, cyclic voltammetry, EPR spectroscopy and particle size measurements. The mechanism of self-assembly was: (i) strong stacking of viologen radical cations (V +• ) in aqueous/phosphate buffer solution containing excess of sodium dithionite, (ii) the dimerized species (V +• ) 2 can be included in to hydrophobic cavity of CB [8] which additionally stabilizes the (V +• ) 2 species. UV-vis investigation clearly proves that the radical cations were involved in intermolecular dimerization and the dimerized species were encapsulated into CB [8] cavity. This inclusion behavior was nicely supplemented by UV-Vis spectroscopy in the region  of 800-1100 nm. EPR studies also revealed that the addition of CB [8] enhanced the dimerization. Particle size measurements showed a particle size in the range of several µm indicating larger aggregates and strongly supported the formation of 2D single -assembly as reported by Zhou et al. and Zhang et al. However, our results partly vary from their previous reports in terms of particle size. Zeta potential measurements suggested that these particles are highly unstable and have the tendency to form aggregates readily, and notably zeta potential value changed from negative to positive upon encapsulation with CB [8]. In addition, we have demonstrated that these supramolecular organic frameworks can be depolymerized by oxidation in air and again can be polymerized (intermolecular radical dimerization) by reduction under inert atmosphere. Such reversible systems are of broad interest as they show advantages over irreversible systems. A key point of these newly-assembled processes are high stability of radical cations with formation of larger aggregates leading to the formation of 2D assembly as indicated by TEM. SAXs profile of the supramolecular polymer samples showed broad scattering peaks indicating the internal periodicity of the supramolecular polymer. Thus the dimerization of radical cations can be considered as a new strong non-covalent force to construct highly ordered supramolecular ensembles for wide range of applications. Future studies will focus on the photophysical and spectroelectrochemical investigations on these systems towards reversible electron/charge storage properties.