Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Controlling the helicity of π-conjugated oligomers by tuning the aromatic backbone twist

Abstract

The properties of π-conjugated oligomers and polymers are commonly controlled by side group engineering, main chain engineering, or conformational engineering. The last approach is typically limited to controlling the dihedral angle around the interring single bonds to prevent loss of π-conjugation. Here we propose a different approach to conformational engineering that involves controlling the twist of the aromatic units comprising the backbone by using a tether of varying lengths. We demonstrate this approach by synthesizing an inherently twisted building unit comprised of helically locked tethered acenes, bearing acetylene end-groups to enable backbone extension, which was applied in a series of nine helical oligomers with varying backbone length and twist. We find that the optical and electronic properties of π-conjugated systems may be determined by the additive, antagonistic, or independent effects of backbone length and twist angle. The twisted oligomers display chiral amplification, arising from the formation of secondary helical structures.

Introduction

The field of organic electronics relies on π-conjugated oligomers and polymers whose photophysical, chiroptical, and electronic properties can be tuned using synthetic methodologies1,2,3. One way to modify these properties is by side-group engineering, which involves the addition of electron-accepting or donating, solubilizing, or chiral units to the π-conjugated backbone to obtain desired properties (Fig. 1a)4,5,6,7,8,9. Another approach is main-chain engineering, which is commonly achieved by combining different units in the π-conjugated backbone10,11. For example, the inclusion of donor and acceptor systems can result in low bandgap oligomers and polymers, such as those commonly applied in organic solar cells12.

Fig. 1: Approaches for tuning the properties of π-conjugated backbones.
figure 1

a Side-group engineering. Conformational engineering of the backbone by b single bond rotation, and c aromatic backbone twist, as introduced in this work. d Molecular representation of the tethered twistacene π-conjugated oligomers depicted in c. The length of the tether ((CH2)n, where n = 4, 6 or 8 methylene groups; left) determines the primary and secondary structures of the twistacenes by twisting and bending, respectively, and eventually long backbones (polymers) can adopt to a helical conformation with varying degree of helicity. R = CC(CH3)3.

In addition to these two approaches, the properties of π-conjugated materials are also dependent on their conformation13. Conformational engineering commonly involves controlling the degree of rotation around the inter-unit single bond in the backbone (Fig. 1b) via non-covalent interactions (conformational locking) or by the addition of sterically bulky side groups14,15. Rotation around the single bond can result in interesting properties. For example, twisted donor–acceptor systems may have a lower singlet–triplet energy gap than their planar counterparts, which can enable thermally-activated delayed fluorescence (TADF) processes to occur16,17. Such rotation can also induce chirality, leading to chiral conducting polymers with a wide range of possible applications, from spin filters to magneto-optic materials18. However, as the potential energy surface for single bond rotation is relatively flat, it is hard to control the extent of rotation directly. As a result, conformational engineering depends on the nature of the different aggregation states obtained under different synthetic conditions and, consequently, the approach is of limited practical utility19. Moreover, most conformational engineering is applied to avoid rotation around the single bond, with a focus on obtaining a planar conformation20. This is because such rotation significantly decreases π-orbital overlap, which in turn increases the bandgap. Thus, an ideal approach to conformational engineering would avoid rotation around the single bonds in favor of controlled distortion of the planarity of the aromatic units themselves (Fig. 1c).

We have recently introduced diagonally tethered helically twisted acenes (twistacenes) in their enantiopure form21,22. The twist is induced by combining both molecular tethering23,24 and sterics25. The length of the tether controls the degree of backbone twisting, and this in turn affects their photophysical and electronic properties. For example, as twisting increases, absorption shifts bathochromically and the rate of intersystem crossing increases at the expense of fluorescence26. The chiroptical properties (molar circular dichroism and anisotropy) of twistacenes increase linearly with twisting27. We also found that, unlike rotation around a single bond, twisting hardly decreases conjugation28. Thus, a particularly attractive feature of our tethered helical twistacenes is that they offer the possibility of tuning backbone conformation in a highly controlled fashion without impairing π-conjugation. However, the extension of such twistacenes to enable their inclusion in longer conjugated systems posed a significant synthetic challenge.

In this work, we introduce a π-conjugated unit, characterized by tunable end-to-end twist and extendable acetylene end-groups (Fig. 1d). Using this family, we investigate the effect on material properties of the addition of repeating anthracene units with controlled twist, to synthesize a family of twisted π-conjugated oligomers up to the trimer (1-Ant-Cn; 2-Ant-Cn; and 3-Ant-Cn; where Ant refers to the anthracene backbone and Cn indicates the length of the methylene tether, n = 4,6,8). The tether length directly affects the both end-to-end twisting, as well as bending of the anthracene backbone. We map the influence of both variables, namely, backbone twist and length, on key optical and electronic properties. We find that backbone length and twist have synergistic effects on certain properties, such as absorption/emission maxima, while having antagonistic effects on other properties, such as extinction coefficient. By contrast, still other properties are affected primarily by only one of these factors, for example, quantum efficiency is primarily determined by backbone twist angle. Extending the length of the backbone while fully maintaining conjugation strongly amplifies the rate of increase of the molar circular dichroism because of the combined effect of a larger number of twisted units and the gradual formation of a secondary helical structure that exhibits increasing backbone pitch as the oligomer extends. The overall effect is marked chiral amplification with increasing oligomer length. Overall, the method described here constitutes an approach to tailoring the properties of π-conjugated materials: conformational engineering achieved by tuning the backbone twist via the constituent units, rather than via the single interring bond.

Results

Design and synthesis

The main synthetic challenges in the introduction of extendable groups to tethered twistacenes (Ant-Cn) lay in protecting both the extendable groups and the ortho-phenyl groups prior to tethering. The synthetic method is shown in Fig. 2. We protected the extendable acetylene unit with triisopropylsilyl (TIPS) and protected the ortho-phenol groups prior to tethering by using 2-(methoxymethyl ether)phenylboronic acid. Both groups proved to be stable throughout the synthesis and did not undergo undesired deprotection. Starting from anthraquinone 1, a Sonogashira coupling reaction was performed to replace the bromine groups at the 2,6 positions with TIPS-acetylene to yield 2, followed by a Sandmeyer reaction to convert the amine group to iodine to yield 3. This enabled Suzuki-Miyaura coupling using 2-(methoxymethyl ether)phenylboronic acid to produce 4. In this reaction, a mixture of two atropisomers of 4 were obtained, with the methyoxymethyl ether groups in with either syn or anti conformation with respect to each other, of which only the syn isomer successfully reacted in the next steps. Accordingly, heating the mixture of 4 (110 °C in toluene) resulted in equilibration of the two conformers that were then separated using silica gel column chromatography. Compound 4 in the syn conformation was isolated in three such repetitive equilibration and column chromatography cycles.

Fig. 2: Synthesis of twistacene monomer (1-Ant-Cn), dimer (2-Ant-Cn), and trimer (3-Ant-Cn).
figure 2

a HCCSi(iPr)3, Pd(PPh3)2Cl2 (0.1 equiv.), CuI (0.05 equiv.), THF/Et3N (2:1), reflux. b NaNO2, H2SO4, KI. c 2-(Methoxymethyl ether)phenylboronic acid, Pd(PPh3)4, dioxane/water (4/1), 94 °C, 5 d; d (1) (CH3)3CCH, n-BuLi, THF, 0 °C → rt, 10 h; (2) SnCl2, THF, 4 h; e dil. HCl, 40 °C, 16 h. f Br-(CH2)n-Br, K2CO3, DMF, 40–60 °C n = 4, 6, 8; g TBAF, THF, 0 °C, 0.5 h; h 1,4-diiodobenzene, Pd(PPh3)4, Et3N, rt→50 °C, 36 h; i 1-octylazide, CuSO4 ∙ 5H2O, sodium ascorbate, THF:water (4:1), reflux, 48 h; j 1,4-diiodobenzene, Pd(PPh3)4, THF/Et3N (2:1), 65 °C, 22 h; k Pd(PPh3)4, CuI, Et3N/THF, 65 °C, 22 h.

The syn-4 atropisomer was then reacted with 3,3-dimethyl-1-butyne and n-butyllithium, followed by SnCl2 aromatization to afford compound 5. Deprotection with dilute HCl solution yielded molecule 6, also as syn and anti-isomers. The tethering reaction was performed on 6 under moderate conditions using K2CO3 to avoid decomposition (with 60% yield). Removal of the protecting groups produced 8-C4, 8-C6, and 8-C8, where 8 consists of an anthracene core helically locked with a diagonal Cn tether. Synthesis was not successful for 8-C3, perhaps because its short tether meant that the strain energy was prohibitively high29. The racemic mixture of 8-Cn was separated to the M and P enantiomers using preparative chiral HPLC (Chiralpak IB-N and IG columns) with dichloromethane/hexane mixture as eluent (the enantiomers were assigned based on the X-ray structures presented in the next section). Since acetylenes tend to undergo homo-coupling and polymerization, we utilized the “click” copper-catalyzed azide-alkyne cycloaddition (CuAAC) reaction and mild conditions for Sonogashira coupling to produce the monomer 1-Ant-Cn, compound 10-Cn and compound 9-Cn, which were then used for oligomer assembly via another Sonogashira coupling, to obtain dimers and trimers with different twist angles (2-Ant-Cn and 3-Ant-Cn, respectively). The coupling reactions were performed with enantiopure reactants to avoid obtaining a mixture of diastereomers.

Structure

Figure 3 displays the X-ray structures for all the monomer precursors, 8-Cn. The X-ray structures of 8-C4 to 8-C8 demonstrate the effect of the tether on the backbone twist of a single unit. All monomers were crystallized from their racemic mixtures to yield racemates. Whereas for 8-C8 the backbone is nearly planar, with an end-to-end twist of 4°, this twist increases to 20° for 8-C6 and further increases to 31° for 8-C4. Calculated (DFT-B3LYP/6-31 G(d) structures of 8-Cn display a similar trend, with end-to-end twists of 14°, 24°, and 33° for 8-C8, 8-C6, and 8-C4, respectively. As expected, the difference between the solid state structure and the (calculated) gas phase structure is more pronounced for longer tethers, as these structures are more flexible21. For example, when tethering involves a short chain, deprotection of the acetylene backbone barely affects backbone twist angle, with only a 1° difference in twist angle between TIPS-protected 7-C4 (30°) and its deprotected counterpart 8-C4 (31°). By contrast, with the longer C8 tether, the difference in twist angle following removal of TIPS is greater, with a 3° difference in twist angle between TIPS-protected 7-C8 (1°) and deprotected 8-C8 (4°). In a similar manner, the addition of triazole does not significantly affect the twist angle, with a difference ranging from 1–3° for 1-Ant-Cn compared with 8-Cn (see ESI for the structures of 7-Cn and 1-Ant-Cn). In contrast to 8-Cn, which was crystallized from their racemic mixtures, all 1-Ant-Cn were crystallized as in their enantiopure form (P enantiomer, see ESI for structures), and the P and M absolute configurations was determined based on both X-ray structures, as well as comparison between experimental and computational ECD spectra (Supplementary Fig. 218, see ESI).

Fig. 3: X-ray analysis of twistacenes.
figure 3

a Side view and b end view for the X-ray structures of the anthracene cores of the monomer precursors 8-C8 (top), 8-C6 (middle), and 8-C4 (bottom), with the substituents and Cn tether removed for clarity. The bend angles between B’B and D’D are depicted in blue, and the (calculated) dihedral angles between ABCD are depicted in red. c X-ray structure of the dimer, M,M-2-Ant-C4, displaying both its monomeric units in the syn conformation, with hydrogens, tBu-acetylene, and n-octyl groups removed for clarity. Right: side view with tether removed for clarity. Color scheme: gray, C; blue, N; red, O.

Since the acetylene substituents are positioned diagonally at the 2,6 positions, twisting also affects the relative orientations of the two ends of the tether, that is, the degree of bending, calculated by taking the angle between the vectors D’D and B’B (Fig. 3a). As the tether shortens, the bending increases from 176° for 1-Ant-C8 to 150° for 1-Ant-C4, corresponding to out of plane bending of 2° for 1-Ant-C8 to 15° for 1-Ant-C4. This bending can induce a secondary helical structure (discussed below), in addition to the primary helical structure induced by the end-to-end backbone twist.

The X-ray structure of the dimer, 2-Ant-C4 (Fig. 3c), displays nearly the same twist in each of its anthracene units (30 and 31°) as was found for the corresponding monomer 8-C4 (31°). This indicates that coupling (i.e., backbone extension) does not significantly affect backbone twist; rather, the twist angles are directly affected by the inherent twist of the monomer units, which in turn are affected by the length of the tether. The anthracene backbones are in-plane with the phenyl inter-unit linker, which results in retention of full π-conjugation and provides evidence that the twist stems from the anthracene core rather than from rotation around the single bond. The monomer units are in the syn conformation with respect to each other, and calculation show that both syn and anti-conformers have similar energies, whereas non-conjugated conformers are higher in energy.

The effect of backbone length and twist on photophysical, chiroptical, and electronic properties

Our synthesis of a family of π-conjugated oligomers possessing varying tether lengths, backbone lengths, and backbone twist angles provides a means of exploring how oligomer properties are controlled by the number and conformation (length and twist) of their constituent repeat units. Figure 4 shows color maps of various electronic and optical properties by backbone length and twist angle per repeat unit. All values were obtained experimentally. Figure 4a shows that the extinction coefficient decreases with increasing twist and increases with backbone length. This is a direct consequence of the decrease in conjugation arising from the deviation from planarity. However, the effect of twisting is relatively small for the monomer and dimer, as the deviation from planarity does not significantly decrease their conjugation. The extinction coefficient for the longer trimer is significantly more affected by twisting compared with the dimer. Indeed, as twisting increases from 14° to 33°, the extinction coefficient decreases by 37% for the trimer and by 22% for the dimer, which indicates a synergistic effect of backbone length and twist angle. As the extinction coefficient of a conjugated backbone is directly related to the degree of π-orbital overlap, the trimer’s high extinction coefficient indicates that π-conjugation remains strong even with a cumulative end-to-end backbone twist of over 90°.

Fig. 4: The effect of backbone twist and length on the photophysical properties.
figure 4

3D graphs displaying the effect of backbone unit twist (y-axis) and backbone length (x-axis) on a extinction coefficients at maximal absorption; b optical bandgaps (Eg); c absorbance maxima (from the onset of the lowest energy band); d fluorescence maxima; e fluorescence lifetime; and f fluorescence quantum yields (Φf) of Ant-Cn monomers, dimers, and trimers. The colors portray the z-axis value, from lowest (blue) to highest (yellow).

Figure 4b shows that the optical bandgap, Eg(opt), is affected to a much greater extent by conjugation length than by twisting, although both have a marked effect. The bandgap decreases with increasing twist, which was previously explained by the LUMO energy-level stabilizing as mixing between π and σ orbitals increases. The bandgap decreases sharply with increasing backbone length, with the effect of length being cumulative, such that the trimer is more affected by twisting compared with the dimer and monomer. Upon further elongation, increased conjugation is expected to decrease the optical bandgap. In a similar manner, the absorption maxima increase with both twisting and conjugation length (Fig. 4c), reaching a maximal value for the most twisted trimer. Twisting has a greater effect on the fluorescence maxima (Fig. 4d) than on the absorption maxima (Fig. 4c). For example, twisting 3-Ant-Cn shifts its fluorescence maximum by 39 meV whereas it shifts its absorption maximum by only 32 meV, which can be explained by the twist increasing the rigidity of the compound.

The fluorescence lifetime (Fig. 4e) decreases with twist, but this decrease is negligible compared with the strong decrease in fluorescence lifetime with increasing backbone length. In contrast, the fluorescence quantum yield is strongly affected by both backbone twisting and length, but the effect of twisting is greater (Fig. 4f). For a given oligomer length, the fluorescence quantum efficiency decreases 2-fold when moving from a nearly planar to a 31° twisted unit, but decreases only 1.5-fold for a doubling of backbone length from the monomer to the dimer. Different mechanisms produce these differential effects of twisting versus backbone length. The introduction of backbone twist induces a non-radiative intersystem crossing (ISC) pathway, which reduces fluorescence quantum efficiency both by decreasing the singlet–triplet energy gap and by increasing the extent of spin-orbit coupling (SOC)26,30. In the case of increasing backbone length, fluorescence quantum yield decreases because of an increase in the degrees of conformational freedom (due to an increase in the number of rotatable triple bonds), which opens non-radiative decay pathways (internal conversion). Consequently, although the fluorescence lifetime decreases with bakcbone length (Fig. 4e), the introduction of a non-radiative pathway means that fluorescent quantum yield also decreases (Fig. 4f). Overall, when compared with the monomer, extension of the conjugation length does not extinguish the effect of unit twist on the electronic and optical properties, and in some cases even amplifies the trends observed in monomers.

Chiral amplification and secondary structure

As the tether induces a backbone twist, the twistacene adopts helical chirality and therefore interacts with circularly polarized light. We have previously demonstrated that, upon twisting a monomer, the molar circular dichroism increases linearly with increasing backbone twist27. Figure 5a presents the ECD spectra of the M and P enantiomers of 1-, 2-, and 3-Ant-C6 (see ESI for the ECD spectra of the complete 1-, 2-, and 3-Ant-Cn series). The M enantiomers exhibit the expected mirror image of the P enantiomers, an indication that the observed spectrum is not an artifact, but rather the direct result of backbone twist. For oligomers with the same unit twist, the ECD intensity increases with backbone length, likely because of the increase in oscillator strength.

Fig. 5: Chiroptical properties and secondary helical structures of twistacenes.
figure 5

a Electronic circular dichroism (ECD) spectra of enantiopure n-Ant-C6 (n = 1–3), measured in chloroform. b Maximal molar circular dichroism (Δεmax) for n-Ant-C measured experimentally (solid lines, left y-axis) and computationally (dashed lines, right y-axis). c Calculated electronic transition dipole moment (μe, dashed lines) and magnetic transition dipole moment (μm, solid lines) for 2-Ant-Cn (green) and 3-Ant-Cn (blue). The backbone twist angles were determined computationally. d Calculated rotation energy around the inter-unit acetylene bond of 2-Ant-C6. Calculated at the B3LYP-D3/6-31G(d) level of theory. e Measured (dark blue) and calculated (light blue) ECD spectra, consisting of averaged syn and anti conformers. f Optimized (B3LYP/6-31G(d)) structures of anthracene-phenyl skeleton, in syn or anti conformations, with each anthracene unit twisted in 10° (top) or 40° (bottom).

Within a series consisting of the same number of units, the maximal molar circular dichroism (Δεmax) also increases with increasing twist, despite a decrease in the molar extinction coefficient (ε) that occurs as the magnetic transition dipole moment (μm) increases. However, the increase in molar circular dichroism (Δε) with twist is more significant as length increases. This difference is expressed in the observed slope in Fig. 5b, with the steepest slope observed for the trimer, 3-Ant-Cn. The ECD spectra for the backbone (with no substituents and tether) were calculated for the dimer and trimer with varying unit twists, from 10° to 40°, at the TD-DFT/CAM-B3LYP/6-31G(d) level of theory. The slope for the trimer is larger compared with the dimer (Fig. 5b, dashed lines), which is in good agreement with the experimental values (In order to verify that chiral amplification is pesistent for longer oligomers, we have calculated the ECD spectra up to the hexamer. The trend clearly shows that as the length extends, the molar circular dichroism is increasingly affected by the backbone twist, as depicted by increasing slope with backbone length. See Supplementary Fig. 219 in ESI).

The chiral amplification observed both computationally and experimentally cannot be explained as arising solely from a helical primary structure31. As oligomer length extends, the backbone is expected to adopt a secondary helical structure. Whereas in the vast majority of helical conjugated polymers, secondary helical structures stem from the effect of auxiliary side chains32, in the current case they arise from the intrinsic backbone chirality, inducing increasing twist and bend as the tether length decreases. The presence of a secondary structure is known to increase the molar circular dichroism in a non-linear fashion31,33,34,35. As the molar circular dichroism effect is proportional to the electric and magnetic transition dipole moments (denoted as μe and μm, respectively), we followed the calculated values of μe and μm for the skeletons of 2- and 3-Ant-Cn (Fig. 5c). Although μe decreases and μm increases with twist in both the dimer and trimer, the extent of increase in μm with increasing twist is significantly greater for 3-Ant-Cn, whose slope is almost five times larger compared with that of 2-Ant-Cn. (Fig. 5c). Such an increase can only be explained by a contribution from a secondary helical structure.

The barrier of free rotation around inter-unit acetylene bond was calculated at the B3LYP-D3/6-31G(d) level of theory (Fig. 5d)36. The Boltzmann population of both syn and anti conformers is dominant, while conformers with rotation around the acetylenic bond is negligible. Since the ECD spectrum is very sensitive to conformation, we utilized the predicted spectra to elucidate the dominant conformation in solution, as was previously applied by Diederich37,38. We simulated the ECD spectrum for 2-Ant-C6 for different torsion angles around the alkyne bond (Supplementary Fig. 222). The weighted spectra according to the Boltzmann distribution, consisting of syn and anti conformers matches the experimental spectra of 2-Ant-C6 (Fig. 5e, for similar treatment of 2-Ant-C4 see Supplementary Fig. 223). We therefore consider both the syn and anti conformers when discussing a secondary helical structure.

To model the effect of different bridge lengths on the structure of long π-conjugated polymers, we extended the optimized structure of trimers of Ant-Cn to a 9-mer long chain, in either syn or anti conformation. Whereas backbones composed of Ant-C8 are only slightly curved, backbones composed of Ant-C4 display a helical structure, with a half turn after five repeat units (Fig. 5f). Such helical secondary structure observed for both syn and anti conformers. Therefore, twisting the π-conjugated backbone results both in twisting of the acene building block and the formation of a secondary helical structure. Consequently, the tether length controls both the extent of helicity of the primary structure (acene end-to-end twist) and the pitch of the helical secondary structure. Whereas for a 40° end-to-end twist a loop is completed after nine units, for a 10° twist it requires 38 units. Overall, the primary structure accounts for the linear increase in the molar circular dichroism for a given monomer twist, and the secondary structure accounts for the amplification of chiroptical properties with backbone length, resulting in the non-linear increase. While chiral amplification of π-conjugated materials is commonly observed for supramolecular assemblies39,40,41, this study demonstrates that chiral amplification can be induced by both primary and secondary structures of π-conjugated backbones.

Discussion

We introduce a methodology to control the properties of π-conjugated backbones by conformational engineering of the aromatic units rather than of the interring single bond. This was achieved by the synthesis of enantiopure tethered twisted acenes with tunable twist in which acetylenes serve as extension groups. The twistacenes, which exhibit increasing backbone twisting and bending, were utilized as the building unit to construct oligomers with controllable backbone length and twist. We found that their electronic and optical properties can be tuned by controlling both backbone length and twist. Some properties, such as the optical bandgap and the fluorescence maxima, arise from the synergistic effect of increasing backbone length and twist, whereas for other properties, such as the extinction coefficient, the effects of increasing twist and backbone length are antagonistic. For fluorescence quantum efficiency, the effect of backbone twist is more significant than the effect of backbone length.

Oligomers consisting of twisted acene units display strong chiroptical properties, with the molar circular dichroism increasing as either twist or backbone length increase, and a synergistic effect observed when both increase. The non-linear increase in the molar circular dichroism effect suggests chiral amplification, which is explained by the combination of primary and secondary helical structures, both controlled by the tether length.

Overall, the extendable twistacenes with controllable twist presented here can serve as building units for π-conjugated oligomers and polymers whose electronic and optical properties can be tuned while maintaining π-conjugation, and that can be used to introduce chirality directly into the conjugated backbone. We are currently embedding our twistacene units in donor–acceptor systems in order to study the effect of backbone twisting on energy transfer and charge delocalization processes.

Methods

“The full Methods for this manuscript can be found within the Supplementary Information file which accompanies this paper.”

Data availability

Crystallographic data for the structures reported in this article have been deposited at the Cambridge Crystallographic Data Centre, under deposition numbers CCDC 2099695 (7-C8), 2099696 (7-C4), 2099699 (8-C8), 2099700 (8-C6), 2099701 (8-C4), 2099698 (P-1-Ant-C8), 2099697 (P-1-Ant-C6), 2099197 (P-1-Ant-C4) and 2099196 (M,M-2-Ant-C4). Copies of the data can be obtained free of charge via https://www.ccdc.cam.ac.uk/structures/. Synthetic and characterization data for all reported compounds as well as computational details and coordinates for optimized structures are included in the Supplementary Information.

References

  1. Mei, J., Diao, Y., Appleton, A. L., Fang, L. & Bao, Z. Integrated materials design of organic semiconductors for field-effect transistors. J. Am. Chem. Soc. 135, 6724–6746 (2013).

    CAS  Article  Google Scholar 

  2. Beaujuge, P. M. & Fréchet, J. M. J. Molecular design and ordering effects in π-functional materials for transistor and solar cell applications. J. Am. Chem. Soc. 133, 20009–20029 (2011).

    CAS  Article  Google Scholar 

  3. Wang, C., Dong, H., Hu, W., Liu, Y. & Zhu, D. Semiconducting π-conjugated systems in field-effect transistors: a material odyssey of organic electronics. Chem. Rev. 112, 2208–2267 (2012).

    CAS  Article  Google Scholar 

  4. Lei, T., Dou, J.-H. & Pei, J. Influence of alkyl chain branching positions on the hole mobilities of polymer thin-film transistors. Adv. Mater. 24, 6457–6461 (2012).

    CAS  Article  Google Scholar 

  5. Akkerman, H. B. et al. Effects of odd–even side chain length of alkyl-substituted diphenylbithiophenes on first monolayer thin film packing structure. J. Am. Chem. Soc. 135, 11006–11014 (2013).

    CAS  Article  Google Scholar 

  6. Sharma, A. et al. Side-chain engineering of diketopyrrolopyrrole-based hole-transport materials to realize high-efficiency perovskite solar cells. ACS Appl. Mater. Interfaces 13, 7405–7415 (2021).

    CAS  Article  Google Scholar 

  7. Liu, Z., Zhang, G. & Zhang, D. Modification of side chains of conjugated molecules and polymers for charge mobility enhancement and sensing functionality. Acc. Chem. Res. 51, 1422–1432 (2018).

    CAS  Article  Google Scholar 

  8. Mei, J. & Bao, Z. Side chain engineering in solution-processable conjugated polymers. Chem. Mater. 26, 604–615 (2014).

    ADS  CAS  Article  Google Scholar 

  9. Kulkarni, C. et al. Molecular design principles for achieving strong chiroptical properties of fluorene copolymers in thin films. Chem. Mater. 31, 6633–6641 (2019).

    CAS  Article  Google Scholar 

  10. Beaujuge, P. M. & Reynolds, J. R. Color control in π-conjugated organic polymers for use in electrochromic devices. Chem. Rev. 110, 268–320 (2010).

    CAS  Article  Google Scholar 

  11. Higashihara T. Strategic design and synthesis of π-conjugated polymers suitable as intrinsically stretchable semiconducting materials. Polym. J. 53, 1061–1071 (2021).

  12. Lee, C., Lee, S., Kim, G.-U., Lee, W. & Kim, B. J. Recent advances, design guidelines, and prospects of all-polymer solar cells. Chem. Rev. 119, 8028–8086 (2019).

    CAS  Article  Google Scholar 

  13. Noriega, R., Salleo, A. & Spakowitz, A. J. Chain conformations dictate multiscale charge transport phenomena in disordered semiconducting polymers. Proc. Natl. Acad. Sci. USA 110, 16315 (2013).

    ADS  CAS  Article  Google Scholar 

  14. Meyer, D. L. et al. Side-chain engineering of conjugated polymers: distinguishing its impact on film morphology and electronic structure. J. Phys. Chem. C 123, 20071–20083 (2019).

    CAS  Article  Google Scholar 

  15. Huang, H., Yang, L., Facchetti, A. & Marks, T. J. Organic and polymeric semiconductors enhanced by noncovalent conformational locks. Chem. Rev. 117, 10291–10318 (2017).

    CAS  Article  Google Scholar 

  16. Bryden, M. A. & Zysman-Colman, E. Organic thermally activated delayed fluorescence (TADF) compounds used in photocatalysis. Chem. Soc. Rev. 50, 7587–7680 (2021).

    CAS  Article  Google Scholar 

  17. Liu, Y., Li, C., Ren, Z., Yan, S. & Bryce, M. R. All-organic thermally activated delayed fluorescence materials for organic light-emitting diodes. Nat. Rev. Mater. 3, 18020 (2018).

    ADS  CAS  Article  Google Scholar 

  18. Wang, P. et al. Insights into magneto-optics of helical conjugated polymers. J. Am. Chem. Soc. 140, 6501–6508 (2018).

    CAS  Article  Google Scholar 

  19. Langeveld-Voss, B. M. W., Christiaans, M. P. T., Janssen, R. A. J. & Meijer, E. W. Inversion of optical activity of chiral polythiophene aggregates by a change of solvent. Macromol. 31, 6702–6704 (1998).

    ADS  CAS  Article  Google Scholar 

  20. Jackson, N. E. et al. Controlling conformations of conjugated polymers and small molecules: the role of nonbonding interactions. J. Am. Chem. Soc. 135, 10475–10483 (2013).

    CAS  Article  Google Scholar 

  21. Bedi, A., Shimon, L. J. W. & Gidron, O. Helically locked tethered twistacenes. J. Am. Chem. Soc. 140, 8086–8090 (2018).

    CAS  Article  Google Scholar 

  22. Bedi, A. & Gidron, O. The consequences of twisting nanocarbons: lessons from tethered twisted acenes. Acc. Chem. Res. 52, 2482–2490 (2019).

    CAS  Article  Google Scholar 

  23. Ghasemabadi, P. G., Yao, T. & Bodwell, G. J. Cyclophanes containing large polycyclic aromatic hydrocarbons. Chem. Soc. Rev. 44, 6494–6518 (2015).

    CAS  Article  Google Scholar 

  24. Ahrens, L. et al. (Aza)pentacenes clipped into a ring: stabilization of large (Aza)acenes. Angew. Chem. Int. Ed. 60, 9270–9273 (2021).

    CAS  Article  Google Scholar 

  25. Pascal, R. A. Twisted acenes. Chem. Rev. 106, 4809–4819 (2006).

    CAS  Article  Google Scholar 

  26. Tait, C. E., Bedi, A., Gidron, O. & Behrends, J. Photoexcited triplet states of twisted acenes investigated by electron paramagnetic resonance. Phys. Chem. Chem. Phys. 21, 21588–21595 (2019).

    CAS  Article  Google Scholar 

  27. Bedi, A. & Gidron, O. Chiroptical properties of twisted acenes: experimental and computational study. Chem. Eur. J. 25, 3279–3285 (2019).

    CAS  Article  Google Scholar 

  28. Bedi, A., Carmieli, R. & Gidron, O. Radical cations of twisted acenes: chiroptical properties and spin delocalization. Chem. Commun. 55, 6022–6025 (2019).

    CAS  Article  Google Scholar 

  29. Bedi, A., Shimon, L. J. W., Bogoslavsky, B. & Gidron, O. Easier to twist than bend: the scope of the bridge formation approach to naphthalenophane synthesis. Org. Mater. 02, 323–329 (2020).

    Article  Google Scholar 

  30. Nagarajan, K., Mallia, A. R., Muraleedharan, K. & Hariharan, M. Enhanced intersystem crossing in core-twisted aromatics. Chem. Sci. 8, 1776–1782 (2017).

    CAS  Article  Google Scholar 

  31. Yashima, E. et al. Supramolecular helical systems: helical assemblies of small molecules, foldamers, and polymers with chiral amplification and their functions. Chem. Rev. 116, 13752–13990 (2016).

    CAS  Article  Google Scholar 

  32. Kane-Maguire, L. A. P. & Wallace, G. G. Chiral conducting polymers. Chem. Soc. Rev. 39, 2545–2576 (2010).

    CAS  Article  Google Scholar 

  33. Ito, H., Furusho, Y., Hasegawa, T. & Yashima, E. Sequence- and chain-length-specific complementary double-helix formation. J. Am. Chem. Soc. 130, 14008–14015 (2008).

    CAS  Article  Google Scholar 

  34. Takata, T. et al. Optically active poly(aryl carbonates) consisting of axially chiral units. Chiral binaphthyl group induced helical polymer. J. Am. Chem. Soc. 120, 4530–4531 (1998).

    CAS  Article  Google Scholar 

  35. Amemiya, R., Saito, N. & Yamaguchi, M. Hetero-double-helix formation by an ethynylhelicene oligomer possessing perfluorooctyl side chains. J. Org. Chem. 73, 7137–7144 (2008).

    CAS  Article  Google Scholar 

  36. Che, Y. & Perepichka, D. F. Quantifying planarity in the design of organic electronic materials. Angew. Chem. Int. Ed. 60, 1364–1373 (2021).

    CAS  Article  Google Scholar 

  37. Rivera-Fuentes, P. et al. Amplification of chirality in monodisperse, enantiopure alleno-acetylenic oligomers. Angew. Chem. Int. Ed. 49, 2247–2250 (2010).

    CAS  Article  Google Scholar 

  38. Nakano, T. & Okamoto, Y. Synthetic helical polymers:  conformation and function. Chem. Rev. 101, 4013–4038 (2001).

    CAS  Article  Google Scholar 

  39. Pijper, D. & Feringa, B. L. Control of dynamic helicity at the macro- and supramolecular level. Soft Matter 4, 1349–1372 (2008).

    ADS  CAS  Article  Google Scholar 

  40. Palmans, A. R. A. & Meijer, E. W. Amplification of chirality in dynamic supramolecular aggregates. Angew. Chem. Int. Ed. 46, 8948–8968 (2007).

    CAS  Article  Google Scholar 

  41. Liu, M., Zhang, L. & Wang, T. Supramolecular chirality in self-assembled systems. Chem. Rev. 115, 7304–7397 (2015).

    CAS  Article  Google Scholar 

Download references

Acknowledgements

This research was supported by the European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation program (grant agreement no. 850836, ERC Starting Grant “PolyHelix”, O.G.).

Author information

Authors and Affiliations

Authors

Contributions

A.B., A.M.A. and O.G. designed experiments. A.B., A.M.A., Y.D.-P., B.B. and O.G. performed experiments and analyzed the data. A.B., A.M.A. and O.G. prepared this manuscript.

Corresponding author

Correspondence to Ori Gidron.

Ethics declarations

Competing interests

The authors declare no competing interests.

Peer review

Peer review information

Nature Communications thanks Michel Rickhaus and the other, anonymous, reviewer(s) for their contribution to the peer review of this work.

Additional information

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Bedi, A., Manor Armon, A., Diskin-Posner, Y. et al. Controlling the helicity of π-conjugated oligomers by tuning the aromatic backbone twist. Nat Commun 13, 451 (2022). https://doi.org/10.1038/s41467-022-28072-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1038/s41467-022-28072-7

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing