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. 2024 Feb 29;6(7):1917–1925. doi: 10.1039/d3na01140b

Controlling supramolecular copolymerization of alkynylplatinum(ii) terpyridine complexes: from isodesmic to cooperative mechanisms†

Sehee Kim a,‡, Minhye Kim a,‡, Seojeong Woo a, Juyeong Kim a, Sung Ho Jung a,✉, Jong Hwa Jung a,✉
PMCID: PMC10964763  PMID: 38545286

Abstract

Recently, cooperative supramolecular polymerization has garnered considerable attention due to its significant potential for enabling controlled chain-growth polymerization, which offers a route to achieving a well-defined degree of polymerization and low polydispersity. In this study, we synthesized two distinct alkynylplatinum(ii) complexes, one bearing a saturated long alkyl chain (Pt-Sat-C18) and another containing a diacetylene moiety within a long alkyl chain (Pt-DA-C25). Spectroscopic analyses revealed that Pt-Sat-C18 undergoes supramolecular polymerization via an isodesmic pathway, while Pt-DA-C25 assembles cooperatively. Intriguingly, the mechanism of supramolecular copolymerization could be tuned by varying the composition ratios: transitioning from an isodesmic to a cooperative pathway was achieved by increasing the proportion of Pt-DA-C25. Moreover, UV irradiation prompted a shift from an isodesmic to a cooperative assembly mechanism. Morphologically, self-assembled Pt-Sat-C18 resulted in left-handed fibrillar structures, whereas Pt-DA-C25 led to left-handed tubular assemblies. Supramolecular co-assembly further revealed helical ribbon or tubular structures. Photoluminescent properties were also observed, with emission spectra centered at approximately 650 nm, attributed to the formation of excimer species facilitated by strong Pt⋯Pt interactions. To elucidate the mechanisms underlying these supramolecular polymerizations, temperature-dependent UV-visible spectroscopy was conducted during the cooling/heating processes, and thermodynamic parameters for both isodesmic and cooperative pathways were quantitatively assessed through curve fitting.

The supramolecular growth mechanism is controlled by the ratio of coassembly of Pt-Sat-C18 and Pt-DA-C25. The 8 : 2 ratio follows the isodesmic mechanism, while the 4 : 6 ratio follows the cooperative mechanism.graphic file with name d3na01140b-ga.jpg

Introduction

The rational design of monomers capable of self-assembling into dynamically well-ordered structures is critical for the deployment of self-assembled materials across various applications.1–16 Achieving this goal necessitates the precise control of molecular interactions like solvophobic effects, π–π stacking, and intermolecular hydrogen bonding in the realm of supramolecular polymerization. For supramolecular polymers, even minor alterations in molecular structure can result in significant, often unpredictable, changes in the structural and dynamic behavior of aggregates.17–25 Consequently, the rational design of supramolecular polymers remains a formidable challenge, underscoring the need for an in-depth understanding of the intermolecular interactions that drive self-assembly.

In the formation of supramolecular polymers from small molecular building blocks, two primary growth mechanisms are observed: the so-called isodesmic26–28 and cooperative29–39 pathways. In the isodesmic mechanism, the aggregation behavior generally follows a step-growth mechanism, displaying high polydispersity and a degree of polymerization contingent upon a single binding constant.40,41 No distinct transition point neither a critical concentration nor a critical temperature, resulting in an approximate transition from a monomeric to a polymeric state. On the other hand, the cooperative mechanism involves a two-step process governed by two distinct binding constants: nucleation (Kn) and elongation (Ke).42,43 This mechanism is characterized by a lower degree of polydispersity and exhibits a sharp transition point from nucleation to elongation regime, observable at a critical concentration or temperature, unlike the isodesmic mechanism.

Recently, cooperative supramolecular polymerization has garnered significant attention due to its potential for controlled chain growth, leading to high degrees of polymerization, low dispersity, and controllable morphologies. Consequently, the design of the building blocks emerges as a pivotal factor for realizing desired supramolecular polymers with potential applications in material science and supramolecular chemistry.44–55

Platinum(ii) complexes with tridentate π-acceptor ligands are recognized for their outstanding spectroscopic properties and a strong propensity to form supramolecular architectures through Pt⋯Pt and π–π interactions, both in solid and solution states, due to their square-planar configuration.56–73 This has led to significant interest in supramolecular structures based on Pt(ii) complexes, driven by their inherently fascinating physical properties and the diverse morphologies of self-assembled structures. For instance, V. W. W. Yam and coworkers reported various morphologies of supramolecular aggregates derived from mono- and binuclear platinum(ii) complexes, including helical fibers, tubular, and ribbon formations, alongside their spectroscopic characteristics.74,75 They further elucidated the formation mechanisms of these supramolecular structures of platinum(ii) complex through alterations in solvent composition. The supramolecular assembly in aqueous solutions follows an isodesmic model, whereas in acetone and H2O (7 : 1 v/v), it adopts a cooperative growth strategy, characterized by nucleation and elongation mechanisms.76 Furthermore, exploring Pt(ii) complex systems that transition from isodesmic to cooperative supramolecular copolymerization remains a significant challenge. In this work, we report the mechanisms underlying supramolecular copolymerization based on Pt-Sat-C18 and Pt-DA-C25 at varying composition ratios. The copolymerization mechanism was regulated via UV-irradiation, resulting in pronounced morphological changes influenced by composition ratios. Thermodynamic studies further corroborated the self-assembly mechanisms of both isodesmic and cooperative supramolecular copolymers. Pt(ii) complex-based supramolecular polymers can diverse applicative potential spanning molecular recognition, pH sensing and biomolecular labeling, due to special photophysical characteristics.63

Results and discussion

Preparation of ligands

As shown in Scheme S1,† chiral terpyridine ligands, Pt-Sat-C18 and Pt-DA-C25 (Fig. 1), were synthesized via distinct multi-step routes. The synthesis commenced with the preparation of chiral precursor 2, containing an S-alanine moiety, according to a previously reported procedure.77,78 Compound 3 was subsequently synthesized through the reaction of precursor 2 with decanedioyl dichloride and triethylamine in dichloromethane (DCM). The subsequent stage involved the formation of platinum(ii) complex 4, achieved by reacting compound 3 with dichloro(1,5-cyclooctadiene)platinum(ii) in a water–methanol mixture. The target ligand Pt-Sat-C18 was then obtained by reacting complex 4 with phenylacetylene that featured a saturated long alkyl chain, employing DCM as the solvent. In a parallel synthesis, Pt-DA-C25 was synthesized employing a methodology analogous to that used for Pt-Sat-C18, with the key distinction being the utilization of a diacetylene moiety in the long alkyl chain. Comprehensive characterization of all synthesized products was conducted using nuclear magnetic resonance (NMR) spectroscopy, infrared (IR) spectroscopy, and electrospray ionization mass spectrometry (ESI-MS).

Fig. 1. Chemical structures of building blocks used in this works.

Fig. 1

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Spectroscopic studies of supramolecular polymer

To explore the formation of supramolecular polymers in mixed solvents of dimethyl sulfoxide (DMSO) and H2O, UV-vis spectral changes of Pt-Sat-C18 and Pt-DA-C25 ligands were measured in varying DMSO/H2O ratios. Optimal conditions for supramolecular polymerization were identified as a 5 : 1 (v/v) mixture of DMSO and H2O. As depicted in Fig. 2A, both Pt-Sat-C18 and Pt-DA-C25 displayed nearly identical absorption spectra, characterized by intense high-energy absorption bands in the 250–320 nm region. These bands are attributed to intraligand [π → π*] transitions within the terpyridine units. Additionally, absorption bands appearing between 450–490 nm were identified, indicative of a metal-to-ligand charge transfer (MLCT) [dπ(Pt) → π*(terpyridine)] transition, compounded with a ligand-to-ligand charge transfer (LLCT) [π(terpyridine) → π*(terpyridine)] character. Notably, in the mixed DMSO and H2O (5 : 1 v/v), a distinct absorption feature was observed in the 520–560 nm range. This phenomenon is ascribed to a metal–metal-to-ligand charge transfer (MMLCT) transition, implicating Pt⋯Pt interactions during the course of supramolecular polymerization. In stark contrast, this MMLCT-associated absorption band was conspicuously absent when the ligands were dissolved in pure DMSO (Fig. S1A†), signifying the absence of Pt⋯Pt interactions under these solvent conditions.

Fig. 2. (A) UV-vis, (B) PL and (C) CD spectra of (a) Pt-Sat-C18 (300 μM) and (b) Pt-DA-C25 (300 μM) in a mixed DMSO and H2O (5 : 1 v/v): the spectra with dot lines in (A) were obtained by curve fitting.

Fig. 2

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To further substantiate the role of metal–metal-to-ligand charge transfer (MMLCT) in supramolecular polymerization, photoluminescence spectra of Pt-Sat-C18 and Pt-DA-C25 were acquired in both a mixed DMSO/H2O solvent system (5 : 1, v/v) and in pure DMSO (Fig. 2B and S1B†). Notably, both Pt-Sat-C18 and Pt-DA-C25 manifested intense emission bands at approximately 650 nm (Fig. 2B). These bands are consistent with the formation of excimer species during supramolecular polymerization.79 A characteristic emission band associated with MMLCT was identified at approximately 610 nm in the context of supramolecular polymerization.69 Emission bands at longer wavelengths were ascribed to robust Pt⋯Pt interactions, as compared to those in previously reported compounds.69,70 Contrastingly, in pure DMSO, emission bands were observed at approximately 560 nm (Fig. S1B†), attributable to metal-to-ligand charge transfer (MLCT). These findings corroborate the monomeric nature of Pt-Sat-C18 and Pt-DA-C25 in a DMSO-only environment. Further credence to this supramolecular polymerization mechanism was lent by circular dichroism (CD) spectroscopy. Pronounced negative CD bands were detected in the 350–600 nm range (Fig. 2C), arising from MLCT and metal–metal charge transfer (MMCT) processes during supramolecular polymerization. The negative CD signals indicative that Pt-Sat-C18 and Pt-DA-C25 form supramolecular polymers with left-handed screw shape. In addition, the strong positive CD band showed at around 300 nm, corresponding to π → π* transitions within the terpyridine unit. These observations imply the formation of helical structures in the supramolecular polymers of Pt-Sat-C18 and Pt-DA-C25. These CD signals also originate from helical supramolecular polymers induced by the S-enantiomeric moiety of building blocks. Notably, no CD signals were observed in pure DMSO (Fig. S1C†), corroborating the absence of supramolecular polymerization and reinforcing the monomeric existence of these Pt(ii) complexes. Hence, our results confirm that Pt-Sat-C18 and Pt-DA-C25 engage in supramolecular polymerization when dissolved in a mixture of DMSO/H2O (5 : 1, v/v).

To elucidate the role of intermolecular hydrogen bonding in the assembly of supramolecular nanostructures, Fourier transform infrared (FT-IR) spectroscopy was employed. When compared to the spectra of monomeric Pt-Sat-C18 and Pt-DA-C25 dissolved in pure DMSO, the FT-IR spectra of the aggregates in a DMSO/H2O mixture (5 : 1, v/v, 1 mM) exhibited a discernible shift in the –NH stretching bands toward lower wavenumbers (Fig. S2†). This shift serves as a clear indicator of the formation of intermolecular hydrogen bonds involving the amide functional groups. Supplementing these observations, 1H NMR studies performed in DMSO-d6 and D2O (5 : 1, v/v) at 298 K showed broadening of the aromatic proton peaks for both Pt-Sat-C18 and Pt-DA-C25 (Fig. S3†), a feature ascribed to the assembly of these molecules into supramolecular polymers. Conversely, at elevated temperature (363 K), these aromatic proton peaks displayed more pronounced low-field shifts and improved resolution, signifying the disassembly into monomeric species. Taken together, these FT-IR and 1H NMR spectral data strongly support the notion that intermolecular hydrogen bonding, along with π–π stacking interactions, serve as the principal driving forces underlying the formation of these supramolecular polymers.

Supramolecular polymerization

To gain a nuanced understanding of self-assembly behavior, we conducted temperature-dependent UV-vis spectroscopic measurements on Pt-Sat-C18 and Pt-DA-C25. These measurements were performed under a controlled temperature change of 1 K min−1 in a DMSO/H2O mixture (5 : 1, v/v). For Pt-Sat-C18, a sigmoidal curve was observed when monitoring absorption intensities at 270 and 550 nm (Fig. 3 and S4†). During the cooling process, the absorption intensity at 550 nm, attributable to metal–metal-to-ligand charge transfer (MMLCT), displayed an increase below 350 K. This observation implies the activation of MMLCT interactions during supramolecular polymerization at below 350 K temperature. Intriguingly, both heating and cooling curves manifested a well-defined sigmoidal shape, with no hysteresis observed (Fig. 3C). These features suggest that Pt-Sat-C18 undergoes supramolecular polymerization via an isodesmic model. In contrast, the cooling curve for Pt-DA-C25 demonstrated a distinctly non-sigmoidal profile (Fig. 3B, D and S5†), indicative of a cooperative self-assembly mechanism featuring successive nucleation and elongation stages. These results indicate that the supramolecular polymers based on Pt-Sat-C18 follow a distinct pathway compared to their Pt-DA-C25 counterpart, likely due to the greater hydrophobicity of the latter and differences in molecular arrangement during supramolecular polymerization. Additionally, we calculated the number-averaged degree of polymerization,41 DPN, for Pt-Sat-C18 and Pt-DA-C15 (Fig. S6†). As shown in Fig. S6,† the number-averaged degree of polymerization for Pt-DA-C25 is higher than that of Pt-Sat-C18 at temperatures below 290 K, indicating that the formation mechanism of Pt-DA-C25 differs from that of Pt-Sat-C18. Corroborating these observations, temperature-dependent circular dichroism (CD) spectral changes were consistent with the UV-vis data (Fig. S7 and S8†). Further supporting these findings, photoluminescence (PL) intensity at 650 nm diminished progressively, while the PL band at 560 nm increased (Fig. S9 and S10†). This behavior is consistent with the dissociation of the MMLCT-driven supramolecular polymers into monomeric species.

Fig. 3. Temperature-dependent UV-vis spectral changes of (A) Pt-Sat-C18 (300 μM) and (B) Pt-DA-C25 (300 μM) in DMSO and H2O (5 : 1 v/v). Plots for αaggvs. temperatures of (C) Pt-Sat-C18 and (D) Pt-DA-C25 upon heating and cooling at a rate of 1 K min−1 in DMSO and H2O (5 : 1 v/v) at 270 nm. The cooperativity parameter σ, representing the ratio of Kn/Ke, was approximately 1 for the self-assembled Pt-Sat-C18 and 4.5 × 10−3 (during cooling) and 1.3 × 10−2 (during heating) for the self-assembled Pt-DA-C25, respectively. These values were obtained through curve fitting with Matlab.

Fig. 3

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Supramolecular copolymerization by different composition ratios

To explore the intricacies of supramolecular copolymerization, we examined various composition ratios of Pt-Sat-C18 to Pt-DA-C25 in a DMSO/H2O mixture (5 : 1, v/v) (Fig. S13–S18†). Upon cooling, the absorbance changes for supramolecular copolymers formed at 9 : 1 and 8 : 2 ratios of Pt-Sat-C18 to Pt-DA-C25 displayed sigmoidal curves similar to those observed for Pt-Sat-C18 alone (Fig. 4). This evidence points toward the dominance of an isodesmic mechanism for copolymers wherein Pt-Sat-C18 constitutes the major component. Conversely, copolymers formulated at 4 : 6, 6 : 4, and 2 : 8 ratios (Pt-Sat-C18 to Pt-DA-C25) manifested non-sigmoidal cooling curves (Fig. 4). Further quantitative analysis yielded cooperativity parameter σ as the ratio of Kn/Ke ranging from 1.7 × 10−2 to 2.1 × 10−2,26 obtained via curve fitting with Matlab. These observations suggest a transition toward a cooperative assembly mechanism in these copolymer systems. In a mixture of Pt-Sat-C18 : Pt-DA-C25, the nucleation of Pt-DA-C25 proceeds rapidly compared to the supramolecular polymerization of Pt-Sat-C18. The nucleation of Pt-DA-C25 would act as a seed for the elongation of Pt-Sat-C18 and Pt-DA-C25, leading to a cooperative pathway. In the co-assembly process, both Pt-Sat-C18 and Pt-DA-C25 undergo co-assembled nucleation under competitive pathways, leading to a cooperative mechanism. Consequently, as a result of this nucleation formation process, the isodesmic mechanism is transformed into a cooperative mechanism to form a supramolecular copolymer. Notably, the mechanism underlying copolymer formation appears to be readily tunable by adjusting the compositional ratios of the constituent building blocks. Such control is imperative for generating supramolecular copolymers via a cooperative mechanism, which is particularly relevant for the kinetic stabilization of metastable states in the synthesis of multi-block supramolecular copolymers.

Fig. 4. (A) Plots of αagg against temperature for supramolecular copolymers (300 μM) at different composition ratios of Pt-Sat-C18 and Pt-DA-C25 (2 : 8, 6 : 4, 8 : 2 and 9 : 1) at 270 nm. (B) Fitting curve of self-coassembled polymers at different composition ratios (6 : 4 and 9 : 1) of Pt-Sat-C18 and Pt-DA-C25; the composition ratio of 6 : 4 suggests a cooperative pathway, while the composition ratio of 9 : 1 indicates an isodesmic pathway.

Fig. 4

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Subsequently, we probed the role of UV-irradiation in governing the mechanism of supramolecular polymerization. When the supramolecular polymer based on Pt-DA-C25 was cooled in a DMSO and H2O mixture (5 : 1 v/v), a non-sigmoidal cooling curve was observed irrespective of UV-irradiation duration (Fig. S11†). Remarkably, a transition in absorbance behavior was witnessed for co-assembled polymers formed at a 9 : 1 ratio of Pt-Sat-C18 to Pt-DA-C25 upon UV-irradiation for 30 min during the cooling process (Fig. S12 and S13†). These data suggest that UV-irradiation shifts the co-assembled polymer system toward a cooperative assembly pathway, characterized by nucleation–elongation mechanics. We also examined the FT-Raman spectral changes in both the self-assembled pure Pt-DA-C25 and the coassembly of Pt-Sat-C18 and Pt-DA-C25 (at a 9 : 1 ratio) to verify the occurrence of 1,4-addition polymerization of the diacetylene moiety under UV irradiation (Fig. S19†). Prior to irradiation, the self-assembled pure Pt-DA-C25 exhibited vibrational bands at 2083 cm−1 and 1458 cm−1 (νC Created by potrace 1.16, written by Peter Selinger 2001-2019 C). After 30 minutes of irradiation with Hg lamp (Fig. S17A†), the vibrational band at 1458 cm−1 for the diacetylene group shifted to a higher wavenumber, corresponding to the –C Created by potrace 1.16, written by Peter Selinger 2001-2019 C– stretching vibrational region.80 Additionally, the peak at 2083 cm−1 shifted to a shorter wavenumber, indicating increased conjugation (Fig. S20†). These results confirm the effective polymerization of the self-assembled pure Pt-DA-C25 under UV irradiation.

In contrast, following UV irradiation of the coassembly formed at a 9 : 1 ratio of Pt-Sat-C18 to Pt-DA-C25, the vibrational band at 1458 cm−1 exhibited a weak shift compared to the self-assembled pure Pt-DA-C25 (Fig. S19B†). This observation suggests that the 1,4-addition reaction of diacetylene moieties in the coassembly does not occur as effectively as in the self-assembled pure Pt-DA-C25. Notably, these findings unveil the capacity to modulate the assembly mechanism of supramolecular polymers featuring UV-responsive functional groups. Therefore, UV-irradiation emerges as a powerful tool for dictating the structural attributes of complex supramolecular architectures.

Morphology observation of supramolecular polymers

Morphological characterization of the self-assembled polymers of Pt-Sat-C18 and Pt-DA-C25 in a mixed solvent of DMSO and H2O (5 : 1 v/v) was conducted via scanning electron microscopy (SEM) and transmission electron microscopy (TEM) (Fig. 5). For Pt-Sat-C18, SEM images revealed a well-defined left-handed helical fiber architecture with an approximate diameter of 75 nm (Fig. 5A). Conversely, Pt-DA-C25 exhibited a tubular morphology, which was additionally confirmed to feature a left-handed helical twist by SEM and TEM images (Fig. 5C and F). Intriguingly, supramolecular copolymers comprising different ratios of Pt-Sat-C18 and Pt-DA-C25 (8 : 2 and 4 : 6) manifested left-handed helical tubular or ribbon-like morphologies with diameters around 110–120 nm. Notably, a 4 : 6 ratio coassembly of Pt-Sat-C18 and Pt-DA-C25 yielded a left-handed helical ribbon structure (Fig. 5D), suggesting a morphological transition from a left-handed tubular arrangement. These findings underscore the critical role of the Pt-DA-C25 composition ratio in modulating the resulting morphologies. Additionally, the TEM image in Fig. 5F revealed a clear inner hollow cavity a diameter of approximately 220 nm. In general, the tubular structure in the self-assembling process begins with small vesicular structures.81 Vesicles then grow into ribbon structures. Subsequently, the ribbon structure transforms into a helical tubular structure.81 In this study, the vesicular structure was not observed, which may be due to the rapid morphological transformation in supramolecular polymerization. The tubular structures in Fig. 5 could also originate from small vesicles. Therefore, we conclude that the structural attributes of coassembled polymers can be strategically tuned via altering the composition ratios of Pt-Sat-C18 and Pt-DA-C25.

Fig. 5. SEM and TEM images of the self-assembled polymers obtained by (A) pure Pt-Sat-C18, (B and E) 8 : 2 and (D) 4 : 6 ratios of Pt-Sat-C18 and Pt-DA-C25 and pure (C and F) Pt-DA-C25 in DMSO and H2O (5 : 1 v/v).

Fig. 5

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Thermodynamic study of supramolecular polymers

The temperature-dependent UV-vis spectral changes of Pt-Sat-C18 and Pt-DA-C25 (200–600 μM) at ranges of various concentrations were observed by cooling process at a rate of 1 K min−1 in DMSO and H2O (5 : 1 v/v) (Fig. 6 and S21–S28†). As mentioned early, since the plots of the fraction of aggregated Pt-Sat-C18 molecules (αagg) against temperature for supramolecular polymers based on Pt-Sat-C18 showed sigmodal shapes, the thermodynamic parameters (ΔG, ΔH and ΔS) were calculated by applying isodesmic model (Fig. 6A and B). The binding constant (KI) and Gibbs free energy (ΔG) were calculated to be in the range of 2.6 × 104 to 1.3 × 103 mol−1 and −29.3 kJ mol−1 at 298 K (Tables S1 and S2†), respectively. On the other hand, the plots of αagg against temperature for supramolecular polymer based Pt-DA-C25 showed non-sigmodal curves (Fig. 6C). Through curve fitting by Matlab using basis on cooperative model with a nucleation and elongation mechanism (Fig. 6C and D), the ΔGe, ΔHe and the elongation binding constant (Ke) afforded −24.3 kJ mol−1 at 298 K, −43.0 kJ mol−1 and 1.8 × 104 mol−1 (Table S3†), respectively.

Fig. 6. (A) Plots of αaggvs. concentration of Pt-Sat-C18 in DMSO and H2O (5 : 1 v/v) at different temperatures and corresponding isodesmic fit. (B) Van't Hoff plot for Pt-Sat-C18 in DMSO and H2O (5 : 1 v/v). (C) Plots of Pt-DA-C25 for αaggvs. temperature in DMSO and H2O (5 : 1 v/v) at different concentrations. (D) Van't Hoff plot for Pt-DA-C25 in DMSO and H2O (5 : 1 v/v).

Fig. 6

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The thermodynamic parameters of co-assembled polymers formed at different composition ratios of Pt-Sat-C18 and Pt-DA-C25 (9 : 1 to 2 : 8) were also calculated by curve fitting obtained in the cooling process at a rate of 1 K min−1 in DMSO and H2O (5 : 1 v/v). The ΔGe of co-assembled polymers formed at different composition ratios was −16.8 to −19.7 kJ mol−1 at 298 K (Table S4†), which was smaller than those obtained by Pt-Sat-C18 and Pt-DA-C25. In addition, the ΔGe decreased by increase of concentration of Pt-Sat-C18. This decrease of ΔGe would due to mismatching between two building blocks in formation of supramolecular copolymers. Furthermore, the ΔGe of the self-assembled Pt-DA-C25 (−18.8 kJ mol−1 at 298 K) and co-assembly formed at 9 : 1 ratio (−17.1 kJ mol−1 at 298 K) after UV-irradiation for 30 min were smaller than that the self-assembly before UV-irradiation (Tables S5 and S6†), indicating leading disordering of supramolecular structure in 1,4-addition polymerization process of diacetylene moieties (Fig. S20†). Although UV irradiation did not influence the formation mechanism in the self-assembled Pt-DA-C25 process, the ΔGe of self-assembled Pt-DA-C25 after UV irradiation (ΔGe = −18.8 kJ mol−1) significantly reduced compared to before UV irradiation (ΔGe = −24.3 kJ mol−1). This reduction was attributed to the disordering of the self-assembly. In contrast, the ΔGe of the co-assembly of Pt-Sat-C18 and Pt-DA-C25 (9 : 1) was not influenced by UV irradiation (Tables S4 and S6†). However, the assembly mechanism shifted from isodesmic to cooperative. This change is attributed to a small amount of Pt-DA-C25 undergoing a 1,4-addition reaction upon UV irradiation, leading to co-assembled nucleation through competitive pathways. In particular, exposure to UV irradiation caused a transition from an isodesmic to a cooperative assembly mechanism. This finding implies that UV irradiation offers a novel approach to controlling the self-assembly process.

Conclusions

We have precisely modulated the formation mechanisms of supramolecular polymers derived from alkyne platinum(ii) complexes, each with either a saturated or unsaturated alkyl chain. Photoluminescence spectra of these chiral supramolecular polymers and copolymers prominently feature peaks around 650 nm, attributable to the generation of excimer species facilitated by robust Pt⋯Pt interactions. Notably, Pt-Sat-C18 undergoes polymerization via an isodesmic pathway, whereas Pt-DA-C25 favors a cooperative mechanism incorporating nucleation and elongation stages. Intriguingly, the innate isodesmic polymerization pathway of Pt-Sat-C18 transitions to a cooperative mechanism in the presence of Pt-DA-C25, underscoring the capacity for dynamic control over supramolecular polymerization mechanisms. Morphological studies further support these mechanistic insights. Supramolecular polymers based on Pt-Sat-C18 manifest as helical fibers, whereas copolymers derived from varying composition ratios of Pt-Sat-C18 and Pt-DA-C25 adopt either left-handed ribbon or tubular—morphologies reminiscent of the supramolecular polymers based on Pt-DA-C25 alone. Furthermore, UV irradiation prompted a shift from an isodesmic to a cooperative assembly mechanism. These findings not only demonstrate the feasibility of controlling the self-assembly mechanisms of supramolecular polymers but also offer an innovative strategy for dictating morphology in supramolecular copolymerization processes.

Conflicts of interest

There are no conflicts to declare.

Supplementary Material

NA-006-D3NA01140B-s001

Acknowledgments

This research was supported by a National Foundation of Korea (NRF) grant funded by the Korean Government (MSIT) (2021R1A2C2007664 and 2022R1A4A1022252).

†

Electronic supplementary information (ESI) available. See DOI: https://doi.org/10.1039/d3na01140b

Notes and references

  1. Krieg E. Rybtchinski B. Noncovalent water-based materials: robust yet adaptive. Chem.–Eur. J. 2011;17:9016–9026. doi: 10.1002/chem.201100809. [DOI] [PubMed] [Google Scholar]
  2. Stupp S. I. Self-assembly and biomaterials. Nano Lett. 2010;10:4783–4786. doi: 10.1021/nl103567y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Wang Y. Hasegawa T. Matsumoto H. Mori T. Michinobu T. Rational design of high-mobility semicrystalline conjugated polymers with tunable charge polarity: beyond benzobisthiadiazole-based polymers. Adv. Mater. 2017;27:1604608. [Google Scholar]
  4. Liebing P. Wang L. Gilje J. W. Hilfert L. Edelmann F. T. Supramolecular first-row transition metal complexes of 3-(3,5dimethylpyrazol-1-yl)propanamide: three different coordination modes. Polyhedron. 2019;164:228–235. doi: 10.1016/j.poly.2019.02.056. [DOI] [Google Scholar]
  5. Webber M. J. Appel E. A. Meijer E. W. Langer R. Supramolecular biomaterials. Nat. Mater. 2016;15:13–26. doi: 10.1038/nmat4474. [DOI] [PubMed] [Google Scholar]
  6. Gao M. Kwaria D. Norikane Y. Yue Y. Visible-light-switchable azobenzenes: molecular design, supramolecular systems, and applications. Nat. Sci. 2022;3:e220020. doi: 10.1002/ntls.20220020. [DOI] [Google Scholar]
  7. Han H. Zhang D. Zhu Z. Wei R. Xiao X. Wang X. Liu Y. Ma Y. Zhao D. Aromatic stacking mediated spin-spin coupling in cyclophane-assembled diradicals. J. Am. Chem. Soc. 2021;143:17690–17700. doi: 10.1021/jacs.1c08262. [DOI] [PubMed] [Google Scholar]
  8. Tong J. Jia L. M. Shang P. Yu S. Y. Controlled synthesis of supramolecular architectures of homo- and heterometallic complexes by programmable self-assembly. Cryst. Growth Des. 2019;19:30–39. doi: 10.1021/acs.cgd.8b01406. [DOI] [Google Scholar]
  9. Kartha K. K. Allampally N. K. Yagai S. Albuquerque R. Q. Fernandez G. Mechanistic insights into the self-assembly of an acid-sensitive photoresponsive supramolecular polymer. Chem.–Eur. J. 2019;25:9230–9236. doi: 10.1002/chem.201900775. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Saalfrank R. W. Maid H. Scheurer A. Supramolecular coordination chemistry: the synergistic effect of serendipity and rational design. Angew. Chem., Int. Ed. 2008;47:8794–8824. doi: 10.1002/anie.200702075. [DOI] [PubMed] [Google Scholar]
  11. Zhou L. Xu L. Song X. Kang S. M. Liu N. Wu Z. Q. Nickel(II)-catalyzed living polymerization of diazoacetates toward polycarbene homopolymer and polythiophene-block-polycarbene copolymers. Nat. Commun. 2022;13:811. doi: 10.1038/s41467-022-28475-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Chan M. H. Yam V. W. Toward the design and construction of supramolecular functional molecular materials based on metal-metal interactions. J. Am. Chem. Soc. 2022;144:22805–22825. doi: 10.1021/jacs.2c08551. [DOI] [PubMed] [Google Scholar]
  13. Baumer N. Matern J. Fernandez G. Recent progress and future challenges in the supramolecular polymerization of metal-containing monomers. Chem. Sci. 2021;12:12248–12265. doi: 10.1039/D1SC03388C. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Xu L. Wang C. Li Y. X. Xu X. H. Zhou L. Liu N. Wu Z. Q. Crystallization-driven asymmetric helical assembly of conjugated block copolymers and the aggregation induced white-light emission and circularly polarized luminescence. Angew. Chem., Int. Ed. 2020;59:16675–16682. doi: 10.1002/anie.202006561. [DOI] [PubMed] [Google Scholar]
  15. Wang C. Xu L. Zhou L. Liu N. Wu Z. Q. Asymmetric living supramolecular polymerization: precise fabrication of one-handed helical supramolecular polymers. Angew. Chem., Int. Ed. 2022;61:e202207028. doi: 10.1002/anie.202207028. [DOI] [PubMed] [Google Scholar]
  16. Liu N. Gao R. T. Wu Z. Q. Helix-induced asymmetric self-assembly of pi-conjugated block copolymers: from controlled syntheses to distinct properties. Acc. Chem. Res. 2023;56:2954–2967. doi: 10.1021/acs.accounts.3c00425. [DOI] [PubMed] [Google Scholar]
  17. Wang F. Liao R. Wang F. Pathway control of pi-conjugated supramolecular polymers by incorporating donor-acceptor functionality. Angew. Chem., Int. Ed. 2023;62:e202305827. doi: 10.1002/anie.202305827. [DOI] [PubMed] [Google Scholar]
  18. Lim S. A. Jung S. H. Jung J. H. Kinetically controlled chiral metal-coordinated supramolecular polymerization accompanying helical inversion or morphological transformation. Bull. Korean Chem. Soc. 2023;44:322–331. doi: 10.1002/bkcs.12670. [DOI] [Google Scholar]
  19. Bochicchio D. Salvalaglio M. Pavan G. M. Into the dynamics of a supramolecular polymer at submolecular resolution. Nat. Commun. 2017;8:147. doi: 10.1038/s41467-017-00189-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Baker M. B. Albertazzi L. Voets I. K. Leenders C. M. Palmans A. R. Pavan G. M. Meijer E. W. Consequences of chirality on the dynamics of a water-soluble supramolecular polymer. Nat. Commun. 2015;6:6234. doi: 10.1038/ncomms7234. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Yadav S. Sharma A. K. Kumar P. Nanoscale self-assembly for therapeutic delivery. Front. Bioeng. Biotechnol. 2020;8:127. doi: 10.3389/fbioe.2020.00127. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Zhu X. Jiang Y. Yang D. Zhang L. Li Y. Liu M. Homochiral nanotubes from heterochiral lipid mixtures: a shorter alkyl chain dominated chiral self-assembly. Chem. Sci. 2019;10:3873–3880. doi: 10.1039/C9SC00215D. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Imai Y. Yuasa J. Supramolecular chirality transformation driven by monodentate ligand binding to a coordinatively unsaturated self-assembly based on C3-symmetric ligands. Chem. Sci. 2019;10:4236–4245. doi: 10.1039/C9SC00399A. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Leenders C. M. Albertazzi L. Mes T. Koenigs M. M. Palmans A. R. Meijer E. W. Supramolecular polymerization in water harnessing both hydrophobic effects and hydrogen bond formation. Chem. Commun. 2013;49:1963–1965. doi: 10.1039/C3CC38949A. [DOI] [PubMed] [Google Scholar]
  25. Ghosh G. Dey P. Ghosh S. Controlled supramolecular polymerization of pi-systems. Chem. Commun. 2020;56:6757–6769. doi: 10.1039/D0CC02787A. [DOI] [PubMed] [Google Scholar]
  26. De Greef T. F. A. Smulders M. M. J. Wolffs M. Schenning A. P. H. J. Sijbesma R. P. Meijer E. W. Supramolecular polymerization. Chem. Rev. 2009;109:5687–5754. doi: 10.1021/cr900181u. [DOI] [PubMed] [Google Scholar]
  27. Haino T. Hirao T. Supramolecular polymerization and functions of isoxazolering monomers. Chem. Lett. 2020;49:574–584. doi: 10.1246/cl.200031. [DOI] [Google Scholar]
  28. Casellas N. M. Pujals S. Bochicchio D. Pavan G. M. Torres T. Albertazzi L. Garcia-Iglesias M. From isodesmic to highly cooperative: reverting the supramolecular polymerization mechanism in water by fine monomer design. Chem. Commun. 2018;54:4112–4115. doi: 10.1039/C8CC01259H. [DOI] [PubMed] [Google Scholar]
  29. Kang J. Miyajima D. Mori T. Inoue Y. Itoh Y. Aida T. A rational strategy for the realization of chain-growth supramolecular polymerization. Science. 2015;347:646–651. doi: 10.1126/science.aaa4249. [DOI] [PubMed] [Google Scholar]
  30. Besenius P. Portale G. Bomans P. H. Janssen H. M. Palmans A. R. Meijer E. W. Controlling the growth and shape of chiral supramolecular polymers in water. Proc. Natl. Acad. Sci. U.S.A. 2010;107:17888–17893. doi: 10.1073/pnas.1009592107. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Zhao D. Moore J. S. Nucleation-elongation: a mechanism for cooperative supramolecular polymerization. Org. Biomol. Chem. 2003;1:3471–3491. doi: 10.1039/B308788C. [DOI] [PubMed] [Google Scholar]
  32. ten Eikelder H. M. M. Markvoort A. J. de Greef T. F. A. Hilbers P. A. J. An equilibrium model for chiral amplification in supramolecular polymers. J. Phys. Chem. B. 2012;116:5291–5301. doi: 10.1021/jp300622m. [DOI] [PubMed] [Google Scholar]
  33. Vantomme G. Ter Huurne G. M. Kulkarni C. Ten Eikelder H. M. M. Markvoort A. J. Palmans A. R. A. Meijer E. W. Tuning the length of cooperative supramolecular polymers under thermodynamic control. J. Am. Chem. Soc. 2019;141:18278–18285. doi: 10.1021/jacs.9b09443. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Takahashi S. Yagai S. Harmonizing topological features of self-assembled fibers by rosette-mediated random supramolecular copolymerization and self-sorting of monomers by photo-cross-linking. J. Am. Chem. Soc. 2022;144:13374–13383. doi: 10.1021/jacs.2c05484. [DOI] [PubMed] [Google Scholar]
  35. Su H. Jansen S. A. H. Schnitzer T. Weyandt E. Rosch A. T. Liu J. Vantomme G. Meijer E. W. Unraveling the complexity of supramolecular copolymerization dictated by triazine-benzene interactions. J. Am. Chem. Soc. 2021;143:17128–17135. doi: 10.1021/jacs.1c07690. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Mayoral M. J. Rest C. Stepanenko V. Schellheimer J. Albuquerque R. Q. Fernandez G. Cooperative supramolecular polymerization driven by metallophilic Pd⋯Pd interactions. J. Am. Chem. Soc. 2013;135:2148–2151. doi: 10.1021/ja312628g. [DOI] [PubMed] [Google Scholar]
  37. Krieg E. Weissman H. Shimoni E. Bar On A. Rybtchinski B. Understanding the effect of fluorocarbons in aqueous supramolecular polymerization: ultrastrong noncovalent binding and cooperativity. J. Am. Chem. Soc. 2014;136:9443–9452. doi: 10.1021/ja503906p. [DOI] [PubMed] [Google Scholar]
  38. Chan M. H. Ng M. Leung S. Y. Lam W. H. Yam V. W. Synthesis of luminescent platinum(II) 2,6-bis(N-dodecylbenzimidazol-2'-yl)pyridine foldamers and their supramolecular assembly and metallogel formation. J. Am. Chem. Soc. 2017;139:8639–8645. doi: 10.1021/jacs.7b03635. [DOI] [PubMed] [Google Scholar]
  39. Samanta S. Raval P. Manjunatha Reddy G. N. Chaudhuri D. Cooperative self-assembly driven by multiple noncovalent interactions: investigating molecular origin and reassessing characterization. ACS Cent. Sci. 2021;7:1391–1399. doi: 10.1021/acscentsci.1c00604. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Martin R. B. Comparisons of indefinite self-association models. Chem. Rev. 1996;96:3043–3064. doi: 10.1021/cr960037v. [DOI] [PubMed] [Google Scholar]
  41. Smulders M. M. J. Nieuwenhuizen M. M. L. de Greef T. F. A. van der Schoot P. Schenning A. P. H. J. Meijer E. W. How to distinguish isodesmic from cooperative supramolecular polymerisation. Chem.–Eur. J. 2010;16:362–367. doi: 10.1002/chem.200902415. [DOI] [PubMed] [Google Scholar]
  42. Martinez M. A. Doncel-Gimenez A. Cerda J. Calbo J. Rodriguez R. Arago J. Crassous J. Orti E. Sanchez L. Distance matters: biasing mechanism, transfer of asymmetry, and stereomutation in N-annulated perylene bisimide supramolecular polymers. J. Am. Chem. Soc. 2021;143:13281–13291. doi: 10.1021/jacs.1c06125. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Choi H. Ogi S. Ando N. Yamaguchi S. Dual trapping of a metastable planarized triarylborane pi-system based on folding and lewis acid-base complexation for seeded polymerization. J. Am. Chem. Soc. 2021;143:2953–2961. doi: 10.1021/jacs.0c13353. [DOI] [PubMed] [Google Scholar]
  44. Nie Z. Petukhova A. Kumacheva E. Properties and emerging applications of self-assembled structures made from inorganic nanoparticles. Nat. Nanotechnol. 2010;5:15–25. doi: 10.1038/nnano.2009.453. [DOI] [PubMed] [Google Scholar]
  45. Mai Y. An Z. Liu S. Self-assembled materials and applications. Macromol. Rapid Commun. 2022;43:e2200481. doi: 10.1002/marc.202200481. [DOI] [PubMed] [Google Scholar]
  46. Ten Eikelder H. M. M. Adelizzi B. Palmans A. R. A. Markvoort A. J. Equilibrium model for supramolecular copolymerizations. J. Phys. Chem. B. 2019;123:6627–6642. doi: 10.1021/acs.jpcb.9b04373. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Sarkar A. Sasmal R. Empereur-Mot C. Bochicchio D. Kompella S. V. K. Sharma K. Dhiman S. Sundaram B. Agasti S. S. Pavan G. M. George S. J. Self-sorted, random, and block supramolecular copolymers via sequence controlled, multicomponent self-assembly. J. Am. Chem. Soc. 2020;142:7606–7617. doi: 10.1021/jacs.0c01822. [DOI] [PubMed] [Google Scholar]
  48. Katoono R. Kawai H. Fujiwara K. Suzuki T. Dynamic molecular propeller: supramolecular chirality sensing by enhanced chiroptical response through the transmission of point chirality to mobile helicity. J. Am. Chem. Soc. 2009;131:16896–16904. doi: 10.1021/ja906810b. [DOI] [PubMed] [Google Scholar]
  49. Karayianni M. Pispas S. Block copolymer solution self-assembly: Recent advances, emerging trends, and applications. J. Polym. Sci. 2021;59:1874–1898. doi: 10.1002/pol.20210430. [DOI] [Google Scholar]
  50. Kim S. Kim K. Y. Jung J. H. Jung S. H. Supramolecular polymerization based on the metalation of porphyrin nanosheets in aqueous media. Inorg. Chem. Front. 2022;9:1630–1635. doi: 10.1039/D2QI00106C. [DOI] [Google Scholar]
  51. Li X. Liu X. Liu X. Self-assembly of colloidal inorganic nanocrystals: nanoscale forces, emergent properties and applications. Chem. Soc. Rev. 2021;50:2074–2101. doi: 10.1039/D0CS00436G. [DOI] [PubMed] [Google Scholar]
  52. Yeom J. Guimaraes P. P. G. Ahn H. M. Jung B. K. Hu Q. McHugh K. Mitchell M. J. Yun C. O. Langer R. Jaklenec A. Chiral supraparticles for controllable nanomedicine. Adv. Mater. 2020;32:e1903878. doi: 10.1002/adma.201903878. [DOI] [PMC free article] [PubMed] [Google Scholar]
  53. Pugliese R. Fontana F. Marchini A. Gelain F. Branched peptides integrate into self-assembled nanostructures and enhance biomechanics of peptidic hydrogels. Acta Biomater. 2018;66:258–271. doi: 10.1016/j.actbio.2017.11.026. [DOI] [PubMed] [Google Scholar]
  54. Zhang F. Hu C. Kong Q. Luo R. Wang Y. Peptide-/drug-directed self-assembly of hybrid polyurethane hydrogels for wound healing. ACS Appl. Mater. Interfaces. 2019;11:37147–37155. doi: 10.1021/acsami.9b13708. [DOI] [PubMed] [Google Scholar]
  55. Song W. Zhang X. Song Y. Fan K. Shao F. Long Y. Gao Y. Cai W. Lan X. Enhancing photothermal therapy efficacy by in situ self-assembly in glioma. ACS Appl. Mater. Interfaces. 2023;15:57–66. doi: 10.1021/acsami.2c14413. [DOI] [PMC free article] [PubMed] [Google Scholar]
  56. Poon J. K. Chen Z. Leung S. Y. Leung M. Y. Yam V. W. Geometrical manipulation of complex supramolecular tessellations by hierarchical assembly of amphiphilic platinum(II) complexes. Proc. Natl. Acad. Sci. U. S. A. 2021;118:e2022829118. doi: 10.1073/pnas.2022829118. [DOI] [PMC free article] [PubMed] [Google Scholar]
  57. Cho Y. J. Kim S. Y. Son H. J. Cho D. W. Kang S. O. Steric effect on excimer formation in planar Pt(ii) complexes. Phys. Chem. Chem. Phys. 2017;19:5486–5494. doi: 10.1039/C6CP08651A. [DOI] [PubMed] [Google Scholar]
  58. Wong E. K. Chan M. H. Tang W. K. Leung M. Y. Yam V. W. Molecular alignment of alkynylplatinum(II) 2,6-bis(benzimidazol-2-yl)pyridine double complex salts and the formation of well-ordered nanostructures directed by Pt⋯Pt and donor-acceptor interactions. J. Am. Chem. Soc. 2022;144:5424–5434. doi: 10.1021/jacs.1c12994. [DOI] [PubMed] [Google Scholar]
  59. Schulte T. R. Holstein J. J. Krause L. Michel R. Stalke D. Sakuda E. Umakoshi K. Longhi G. Abbate S. Clever G. H. Chiral-at-metal phosphorescent square-planar Pt(II)-complexes from an achiral organometallic ligand. J. Am. Chem. Soc. 2017;139:6863–6866. doi: 10.1021/jacs.7b03963. [DOI] [PubMed] [Google Scholar]
  60. Leung F. C. Leung S. Y. Chung C. Y. Yam V. W. Metal-metal and pi-pi interactions directed end-to-end assembly of gold nanorods. J. Am. Chem. Soc. 2016;138:2989–2992. doi: 10.1021/jacs.6b01382. [DOI] [PubMed] [Google Scholar]
  61. Poirier S. Lynn H. Reber C. Tailleur E. Marchivie M. Guionneau P. Probert M. R. Variation of M⋯H-C interactions in square-planar complexes of nickel(II), palladium(II), and platinum(II) probed by luminescence spectroscopy and X-ray diffraction at variable pressure. Inorg. Chem. 2018;57:7713–7723. doi: 10.1021/acs.inorgchem.8b00724. [DOI] [PubMed] [Google Scholar]
  62. Po C. Ke Z. Tam A. Y. Chow H. F. Yam V. W. A platinum(II) terpyridine metallogel with an L-valine-modified alkynyl ligand: interplay of Pt⋯Pt, pi-pi and hydrogen-bonding interactions. Chemistry. 2013;19:15735–15744. doi: 10.1002/chem.201302702. [DOI] [PubMed] [Google Scholar]
  63. Haque A. Xu L. Al-Balushi R. A. Al-Suti M. K. Ilmi R. Guo Z. Khan M. S. Wong W. Y. Raithby P. R. Cyclometallated tridentate platinum(ii) arylacetylide complexes: old wine in new bottles. Chem. Soc. Rev. 2019;48:5547–5563. doi: 10.1039/C8CS00620B. [DOI] [PubMed] [Google Scholar]
  64. Sun C. Y. To W. P. Hung F. F. Wang X. L. Su Z. M. Che C. M. Metal-organic framework composites with luminescent pincer platinum(ii) complexes: (3)MMLCT emission and photoinduced dehydrogenation catalysis. Chem. Sci. 2018;9:2357–2364. doi: 10.1039/C7SC04528J. [DOI] [PMC free article] [PubMed] [Google Scholar]
  65. Park G. Kim H. Yang H. Park K. R. Song I. Oh J. H. Kim C. You Y. Amplified circularly polarized phosphorescence from co-assemblies of platinum(ii) complexes. Chem. Sci. 2019;10:1294–1301. doi: 10.1039/C8SC04509G. [DOI] [PMC free article] [PubMed] [Google Scholar]
  66. Tam A. Y. Wong K. M. Wang G. Yam V. W. Luminescent metallogels of platinum(II) terpyridyl complexes: interplay of metal⋯metal, pi-pi and hydrophobic-hydrophobic interactions on gel formation. Chem. Commun. 2007;20:2028–2030. doi: 10.1039/B705062C. [DOI] [PubMed] [Google Scholar]
  67. Wan Q. Xiao X. S. To W. P. Lu W. Chen Y. Low K. H. Che C. M. Counteranion- and solvent-mediated chirality transfer in the supramolecular polymerization of luminescent platinum(II) complexes. Angew. Chem., Int. Ed. 2018;57:17189–17193. doi: 10.1002/anie.201811943. [DOI] [PubMed] [Google Scholar]
  68. Kim K. Y. Kim J. Moon C. J. Liu J. Lee S. S. Choi M. Y. Feng C. Jung J. H. Co-assembled supramolecular nanostructure of platinum(II) complex through helical ribbon to helical tubes with helical inversion. Angew. Chem., Int. Ed. 2019;58:11709–11714. doi: 10.1002/anie.201905472. [DOI] [PubMed] [Google Scholar]
  69. Kang S. G. Kim K. Y. Cho Y. Jeong D. Y. Lee J. H. Nishimura T. Lee S. S. Kwak S. K. You Y. Jung J. H. Circularly polarized luminescence active supramolecular nanotubes based on Pt(II) complexes that undergo dynamic morphological transformation and helicity inversion. Angew. Chem., Int. Ed. 2022;61:e202207310. doi: 10.1002/anie.202207310. [DOI] [PubMed] [Google Scholar]
  70. Kim M. Ok M. Li C. Go K. Kim S. Kim J. Jung J. H. Jung S. H. Supramolecular architectures based on binuclear Pt(ii) complexes consisting of different ligands and circular and helical fiber structures. Inorg. Chem. Front. 2023;10:768–775. doi: 10.1039/D2QI02130G. [DOI] [Google Scholar]
  71. Bailey J. A. Hill M. G. Marsh R. E. Miskowski V. M. Schaefer W. P. Gray H. B. Electronic spectroscopy of chloro(terpyridine)platinum(II) Inorg. Chem. 1995;34:4591–4599. doi: 10.1021/ic00122a015. [DOI] [Google Scholar]
  72. Miskowski V. M. Houlding V. H. Che C. Wang Y. Electronic spectra and photophysics of platinum (II) complexes with -diimine ligands. mixed complexes with halide ligands. Inorg. Chem. 1993;32:2518–2524. doi: 10.1021/ic00063a052. [DOI] [Google Scholar]
  73. Eryazici I. Moorefield C. N. Newkome G. R. Square-planar Pd(II), Pt(II), and Au(III) terpyridine complexes: their syntheses, physical properties, supramolecular constructs, and biomedical activities. Chem. Rev. 2008;108:1834–1895. doi: 10.1021/cr0781059. [DOI] [PubMed] [Google Scholar]
  74. Leung S. Y. Evariste S. Lescop C. Hissler M. Yam V. W. W. Supramolecular assembly of a phosphole-based moiety into nanostructures dictated by alkynylplatinum(ii) terpyridine complexes through non-covalent Pt⋯Pt and pi-pi stacking interactions: synthesis, characterization, photophysics and self-assembly behaviors. Chem. Sci. 2017;8:4264–4273. doi: 10.1039/C7SC00041C. [DOI] [PMC free article] [PubMed] [Google Scholar]
  75. Chan M. H. Leung S. Y. Yam V. W. W. Controlling self-assembly mechanisms through rational molecular design in oligo( p-phenyleneethynylene)-containing alkynylplatinum(II) 2,6-bis( N-alkylbenzimidazol-2’-yl)pyridine amphiphiles. J. Am. Chem. Soc. 2018;140:7637–7646. doi: 10.1021/jacs.8b03628. [DOI] [PubMed] [Google Scholar]
  76. Zheng X. Chan M. H. Chan A. K. Cao S. Ng M. Sheong F. K. Li C. Goonetilleke E. C. Lam W. W. Y. Lau T. C. Huang X. Yam V. W. Elucidation of the key role of Pt⋯Pt interactions in the directional self-assembly of platinum(II) complexes. Proc. Natl. Acad. Sci. U. S. A. 2022;119:e2116543119. doi: 10.1073/pnas.2116543119. [DOI] [PMC free article] [PubMed] [Google Scholar]
  77. Ok M. Kim K. Y. Choi H. Kim S. Lee S. S. Cho J. Jung S. H. Jung J. H. Helicity-driven chiral self-sorting supramolecular polymerization with Ag(+): right- and left-helical aggregates. Chem. Sci. 2022;13:3109–3117. doi: 10.1039/D1SC06413D. [DOI] [PMC free article] [PubMed] [Google Scholar]
  78. Park S. H. Jung S. H. Ahn J. Lee J. H. Kwon K. Y. Jeon J. Kim H. Jaworski J. Jung J. H. Reversibly tunable helix inversion in supramolecular gels trigged by Co(2+) Chem. Commun. 2014;50:13495–13498. doi: 10.1039/C4CC05699J. [DOI] [PubMed] [Google Scholar]
  79. Pander P. Sil A. Salthouse R. J. Harris C. W. Walden M. T. Yufit D. S. Williams J. A. G. Dias F. B. Excimer or aggregate? near infrared electro- and photoluminescence from multimolecular excited states of N^C^N-coordinated platinum(II) complexes. J. Mater. Chem. C. 2022;10:15084–15095. doi: 10.1039/D2TC01511K. [DOI] [Google Scholar]
  80. Huo J. Hu Z. He G. Hong X. Yang Z. Luo S. Ye X. Li Y. Zhang Y. Zhang M. Chen H. Fan T. Zhang Y. Xiong B. Wang Z. Zhu Z. Chen D. High temperature thermochromic polydiacetylenes: Design and colorimetric properties. Appl. Surf. Sci. 2017;423:951–956. doi: 10.1016/j.apsusc.2017.06.198. [DOI] [Google Scholar]
  81. Nakashima N. Asakuma S. Kunitake T. Optical microscopic study of helical superstructures of chiral bilayer membranes. J. Am. Chem. Soc. 1985;107:509–510. doi: 10.1021/ja00288a043. [DOI] [Google Scholar]

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