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The intricate interplay between self‐assembly and phase separation orchestrates biomolecular organization inside cells, thereby dictating the formation of vital structures such as protein assemblies and membraneless organelles (MLOs). However, in the context of supramolecular polymerization, these fundamental processes have traditionally been studied separately. This study reevaluates the supramolecular polymerization process to unveil the presence of phase‐separated droplet state. Utilizing the well‐studied benzene‐1,3,5‐tricarboxamide (BTA) supramolecular motif, we explore its thermally driven liquid‐liquid phase separation (LLPS). Thermodynamic and kinetic analysis, employing temperature‐dependent spectroscopic and microscopic techniques, elucidates the distinct BTA states and their evolution towards the thermodynamic fiber state. This research sheds light on the existence of hidden phases of supramolecular monomers, emphasizing the delicate balance of non‐covalent interactions among monomers and with solvents in governing self‐assembly vs. phase separation. This is particularly important in comprehending phase separation in the biological realm such as in MLOs, and for applications such as condensate‐modifying therapeutics. [ABSTRACT FROM AUTHOR]

Multicomponent supramolecular polymers offer versatile dynamic and functional properties; however, the influence of the monomer chemical structures on their structure-dynamics-function relationship remains unclear. In this study, we investigated the subtle variations in monomer interactions using one monomer and its two dopant derivatives, with functionalization away from the self-assembling core. We systematically investigated their multicomponent supramolecular polymers using a combination of spectroscopy and super-resolution microscopy. Our results highlight the significant impact of the supplementary intermolecular interactions, resulting from the functional motifs located away from the core and present in small quantities, on the microstructure and dynamics. Thus, a comprehensive approach, combining spectroscopy, microscopy, and well-designed experiments, is essential for assessing multicomponent supramolecular polymers. These findings have implications for the rational design of functional multicomponent supramolecular materials. [ABSTRACT FROM AUTHOR]

Polyaniline films are under extensive consideration for applications in sensors, memory devices, displays, biomedicals, etc., owing to their unique optical and electronic functional states that are switchable in response to external stimuli. The application arena of these materials could be enhanced by creating active, adaptive, and autonomous systems with preprogramable spatiotemporal control over the functional states. Here, we present a simple approach to achieve autonomous temporal regulation of polyaniline films' optical and electrical states by integrating enzyme-catalyzed biochemical reaction. The enzymatic reaction produces a feedback-induced transient pH profile, and correspondingly, the functional states of polyaniline films give rise to a similar switching profile, whose lifetime could be preprogrammed via enzyme concentration. This autonomous, temporally regulated polymer film system represents an advancement to the existing switchable materials that operate at equilibrium. [ABSTRACT FROM AUTHOR]

The clinical use of irinotecan (IRI), one of the most commonly used antitumor drugs for colon cancer, is limited by its numerous side effects, and it also lacks selectivity and specificity for tumor cells. When conjugated with fullerenes and biotin, this drug may serve as a drug of choice to reduce these side effects. Fullerenes are an allotropic form of carbon with a closed cage-like structure that can act as a drug carrier, and the presence of biotin makes it a promising targeting agent. In this work, we performed release as well as toxicity comparison studies between pure irinotecan and fullerene-biotin-conjugated irinotecan. The release studies were performed by HPLC (High Performance Liquid Chromatography), while the toxicity studies were performed on a model of colon tumors in gopher rats. All animals were divided into four groups, namely normal, control, test and standard groups. Biochemical parameters and histopathological studies were performed to compare the acute toxicity of irinotecan and the conjugate (C60-PEIbiotin/IRI). It was found that IRI alone was unable to reduce the toxicity caused by DMH (1,2-dimethylhydrazine), whereas its conjugate was able to significantly reduce the toxic effects, which was also evident in the histopathological studies. Therefore, the study suggests that the administration of conjugated IRI reduces toxicity and proves to be a potential candidate for a preventive chemo effect. [ABSTRACT FROM AUTHOR]

Adenosine triphosphate (ATP) is a molecular unit of energy that drives various processes in the cellular environment. In this Minireview, we discuss the potential of physical and chemical properties of ATP for the development of bio‐inspired, synthetic ATP‐induced supramolecular systems with dynamic, stimuli‐responsive and active assembly characteristics. Molecular design rules for ATP‐induced assemblies with various architectures and their stimuli‐responsive structural and functional response are categorized. Special attention is given to the immense potential of ATP‐fuelled designs in the nascent field of transient/non‐equilibrium supramolecular polymerization for the synthesis of lifelike temporally programmable soft materials. Finally, the existing dearth and fate of ATP‐driven systems for future challenges are discussed. [ABSTRACT FROM AUTHOR]

Transient supramolecular self‐assembly has evolved as a tool to create temporally programmable smart materials. Yet, so far single‐component self‐assembly has been mostly explored. In contrast, multicomponent self‐assembly provides an opportunity to create unique nanostructures exhibiting complex functional outcomes, newer and different than individual components. Even two‐component can result in multiple organizations, such as self‐sorted domains or co‐assembled heterostructures, can occur, thus making it highly complex to predict and reversibly modulate these microstructures. In this study, we attempted to create active bicomponent nanoparticle assemblies of orthogonally pH‐responsive‐group‐functionalized gold and cadmium selenide nanoparticles with temporal microstructural control on their composition (self‐sorted or co‐assembly) in order to harvest their emergent transient photocatalytic activity by coupling to temporal changes in pH. Moving towards multicomponent systems can deliver next level control in terms of structural and functional outcomes of supramolecular systems. [ABSTRACT FROM AUTHOR]

Partially purified β-mannanase was immobilized on the modified matrix of sodium alginate-grafted-β-cyclodextrin. The Fourier-transform infrared spectroscopy (FTIR) and X-ray diffraction characterization proved that β-cyclodextrin (β-CD) was successfully grafted with sodium alginate. After successful immobilization, yield of enzyme was found 91.5%, pH and temperature optima were increased, 6.0 to 7.0 and 50 °C to 55 °C respectively. Immobilized mannanase was able to reuse 15 times and retained its 70% activity, meanwhile the immobilized enzyme showed 60% activity after 30 days of storage at 4 °C. Immobilization also increased the thermostability and half-life of the enzyme when compared to the free mannanase. During the comparison of adsorption isotherm and kinetic models, Langmuir isotherm and pseudo-first order kinetics were observed to be the best fit model for the confirmation of immobilization. [ABSTRACT FROM AUTHOR]

Dissipative systems, that constantly consume energy for sustenance, are ubiquitous and essential to life. In synthetic systems, the phenomenon promises emergent properties and different structure from the ones existing at thermodynamic equilibrium. It can create reconfigurable and temporally programmable life‐like smart materials. In this study, we attempt to create reconfigurable, temporally programmable self‐assembly using the redox chemistry of a core‐substituted naphthalene diimide derivative. As a result, transient reconfiguration of supramolecular assembly from vesicle to sheet along with transient fluorescence switching with fuel‐dependent lifetime is attained. We believe that such a design strategy can advance the synthesis of active, adaptive and autonomous materials. [ABSTRACT FROM AUTHOR]

Plants play an important role in the well-being of human beings and have been witnessed by their presence in the Rigveda and Ayurveda. Among those plants, Morus spp. is the one having versatile nature because of the presence of numerous phytochemicals in its different parts and also termed as 'Kalpa Vruksha'. A wide range of the phytochemicals present in the leaves, fruit, root and wood of Morus because of which they possess wide range of biological functions (antidiabetic, antiobesity, antiinflammatory, anticancer, antibacterial, antioxidant, antiviral, cytoprotective and neuroprotective activities etc.). The plant is being utilised traditionally for development of different food products as well as treatment of various diseases. Recently, the researchers took a shift for the efficient utilisation of different parts of the plant for development of various value-added food products. The fruit-based products includes wine, vinegar, jelly, jam, biscuits, bread, squash, yoghurt, cosmetic cream, whereas, leaf-based products includes tea, toothpaste, pastry etc. However, the plant is still lacking its identity at the commercial scale. However, at commercial scale, a kind concern of the industrialists is required towards its effective and efficient utilisation as food, feed and value-added products with the aim to make it available throughout the year. [ABSTRACT FROM AUTHOR]

Viologen based covalent organic polymer (COP) interfaced with graphene at the nanoscale showed pseudocapacitive energy storage associated with redox‐active moieties. The positively charged viologen moieties endow charge storage as well as easy wetting of the electrode. The non‐conducting COP grown over conducting graphene enhances its performance by extensive interface formation. All the redox states of viologen moieties can be reversibly attained without significant polarization when it is interfaced with graphene. However, the COP (devoid of graphene) shows irreversible/pseudo‐reversible behavior due to lack of electron conducting pathways. The intimate and dense conducting pathways in graphene‐COP composites facilitates the charge transfer across interface leading to effective and reversible participation of redox moieties across the entire range over 1000 cycles. Also, we show that the strategy being universal in nature and aid in electron transfer in dense 3D networks which lacks traditional π‐π stacking of 2D crystalline networks (COF). [ABSTRACT FROM AUTHOR]

Aim: Rhodiola imbricata is an endangered medicinal plant of the trans-Himalayan Leh-Ladakh region belonging to the family Crassulaceae. An efficient propagation and regeneration system via direct shoot organogenesis from leaf explant and evaluation of cinnamyl alcohol (Secondary metabolite) was established in this study. Material and Methods: In vitro grown leaves were inoculated using Murashige and Skoog (MS) medium supplemented with (alpha)- naphtalene acetic acid (NAA) in combination with 6- benzyladenine (BAP) for callus proliferation and regeneration. Results: The highest percentage of rhizogenous callus was induced in medium containing NAA (10.0-15.0 μM). The highest percentage of shoot formation from leaf derived callus was obtained in the medium containing of NAA (5.0 μM) and BAP (2.5 μM) as well as in NAA (1.0 μM), BAP (5.0 μM) (38.88% and 37.49%) respectively. Rooting of regenerated shoots were effective when a lower concentration of NAA (0.5 μM) was used alone. A maximum number of roots (22.0) and higher length (0.6 cm) was observed. The in-vitro plantlets with well-developed shoots and roots were acclimatized successfully to natural field conditions with a survival rate of over 80%. Cinnamyl alcohol (Secondary metabolite) evaluation was also done for the very first time and an upregulation of 49.6% and 30.6% were observed in in-vitro roots and shoots when compared with mother root and shoot respectively. Hence, it was proved that the content of secondary metabolites obtained from in-vitro raised plants is higher than mother plant. Conclusion : These results may lay a foundation for genetic improvement and can be used to determine sequential level of targeted secondary metabolites through cell culture in Rhodiola imbricata. [ABSTRACT FROM AUTHOR]

Natural systems have been an inspiration to synthetic supramolecular chemistry. Synthetic demonstrations of dissipative biological systems such as actin filaments are a formidable scientific challenge in attaining future life-like materials. Dynamic instability of such structures beckons control of self-organization in the temporal regimes. In this study, we present a fuel-dependent helical assembly of a supramolecular polymer. We further attempt the synthetic manifestation of a temporally programmable self-assembly. Additionally, the fuel-induced chiral (re)organization with the employment of various enzymes singularly and in tandem have resulted in designing a multistate transient self-assembly. These parameter modulations result in controllable lifetimes and rates. We thus report, for the first time, a temporally programmed multistate reorganization of self-assembly. [ABSTRACT FROM AUTHOR]

Chirality-driven self-sorting is envisaged to efficiently control functional properties in supramolecular materials. However, the challenge arises because of a lack of analytical methods to directly monitor the enantioselectivity of the resulting supramolecular assemblies. Presented herein are two fluorescent core-substituted naphthalene-diimide-based donor and acceptor molecules with minimal structural mismatch and they comprise strong self-recognizing chiral motifs to determine the self-sorting process. As a consequence, stereoselective supramolecular polymerization with an unprecedented chirality control over energy transfer has been achieved. This chirality-controlled energy transfer has been further exploited as an efficient probe to visualize microscopically the chirality driven self-sorting. [ABSTRACT FROM AUTHOR]

Synthetic manifestations of supramolecular chirality have extensively drawn inspiration from naturally occurring systems. Even though in biological systems conformational changes are dissipative, synthetic systems that change conformation under non-equilibrium conditions have still not been established. Herein, we attempt to alleviate this scenario by reporting a synthetic supramolecular system that undergoes temporal changes in its helical conformation as an active system at the expense of a biologically relevant chemical fuel, ATP. Use of enzymes working in tandem provides transient and switchable helices with modular lifetime and stereomutation rates. [ABSTRACT FROM AUTHOR]

Background The transition metal oxide nanoparticles are in focus for their anti-cancer potential. In this study we have synthesized and characterized CuO, NiO and Fe 2 O 3 nanoparticles and, investigated their cytotoxic potential in the heterogeneous tumour microenvironment. Methods Nanoparticles were synthesized by aqueous precipitation method and characterized with UV-Visible spectrophotometer, Fourier transform infrared spectroscopy (FTIR), Scanning electron microscopy (SEM) and X-ray diffraction (XRD). Cell viability of lung cancer cells (A549) grown in normoxia (18%O 2 ) and hypoxia (1%O 2 ) was determined for all nanoparticles. The mechanism of cell death was assessed by nuclear morphological analysis, flow cytometry analysis and western blotting. Generation of intracellular ROS in treated cells and its contribution to cell viability was determined. Results The synthesized metal oxide nanoparticles were successfully characterized with SEM, spectroscopy and X-ray diffraction patterns. Cell viability of lung cancer cells was compromised in both normoxia and hypoxia. ROS generation was shown to contribute to cellular toxicity in CuO, but not NiO and Fe 2 O 3 . Conclusion We have shown the therapeutic potential of CuO, NiO and Fe 2 O 3 nanoparticles in non small cell lung cancer cells cultured in hypoxia, a relevant feature of solid tumors along with normoxia. The newly synthesized nanoparticles showed efficacy in both conditions. General significance Hypoxia drives metabolic alterations and epigenetic modifications in the tumor microenvironment. By using conditions that mimic tumour microenvironment, this study expands the possibility of using metal oxide nanoparticles as a therapeutic agent for lung cancer treatment. [ABSTRACT FROM AUTHOR]

This study aimed for the partial purification, biochemical characterization, determination of bioprocess and thermodynamic parameters of mannanase from newly isolated strain Enterobacter asburiae SD26 under submerged culture. From different variables, locust bean gum and combination of peptone + yeast extract was found as best carbon and nitrogen sources respectively. The profiles of mannanases production and growth kinetics of E. asburiae SD26 were similar. The maximum specific growth rate (μ max) and productivity (γ Pmax) of enzyme was 0.02 h-1 and 0.006 g l -1hr-1. The highest mannanases activity was achieved at pH 6.0 and temperature 50°C. The kinetic parameters of mannanases was K m = 25 mg.ml-1, V max = 2500 μmol.min-1.ml-1 and thermodynamic parameters of enzyme, Δ H d ° , Δ G d ° , Δ S d ° were 67.74 KJmol-1, 105.19 KJmol-1, − 115.89 J.mol-1.K-1 respectively, recorded for mathematical description of the mannanase action at different process conditions. • A bacterial strain Enterobacter asburiae SD26 as mannanase producer was identified. • Bioprocess parameters for growth of bacterial strain and mannanase production were estimated. • Optimum pH and temperature conditions for high mannanase activity were determined. • Kinetics and thermodynamics study of mannanase action were estimated. [ABSTRACT FROM AUTHOR]

Background: Irinotecan is a promising antitumor agent approved by FDA for intravenous use in colon cancer treatment either alone or in combination. It is a topoisomerase inhibitor and by blocking the topoisomerase-I enzyme, it causes DNA damage and results in cell death. However, it lacks selectivity and specificity for tumor cells, resulting in systemic toxicity. Thus, it is essential to reduce its side effects and improve therapeutic efficacy., Objective: The study aimed to improve the therapeutic efficacy and minimize the toxic effects of irinotecan by developing a fullerene functionalized biotin drug delivery system and adsorbing irinotecan on the surface of the functionalized fullerene-biotin complex., Methods: Fullerene (C 60 ) has been observed as a potential drug delivery agent and the aminefunctionalized C 60 -NH 2 was synthesized by functionalizing ethylenediamine on the surface of C 60 . The PEI functionalized C 60 was further synthesized by polymerization of aziridine on the surface of C 60 - NH2. Biotin was attached by an amide linkage to C 60 -PEI and the anti-colon cancer drug irinotecan (IRI) was encapsulated (C 60 -PEI-Biotin/IRI). The C 60 -PEI-Biotin/IRI was characterized and evaluated for in vivo anti-colon cancer activity in rats and the results were compared with the parent drug irinotecan., Results: The results showed that C 60 -PEI-Biotin/IRI conjugate had a controlled release profile according to in vitro HPLC studies. Moreover in vivo anti-tumor studies suggested that the conjugate proved to be less toxic to vital organs and had high efficacy towards tumor cells. Statistical studies confirmed less tumor index and tumor burden in the case of conjugate when compared to irinotecan., Conclusion: It is hypothesized that the conjugate (C 60 -PEI-Biotin/IRI) could cross the cell membrane easily through overexpressed biotin receptors on the cell surface of colon cancer cells and showed better efficacy and less toxicity in comparison to IRI in the colon cancer rat model., (Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.)

Fascinating properties are displayed by synthetic multicomponent supramolecular systems that comprise a manifold of competitive interactions, thereby mimicking natural processes. We present the integration of two reentrant phase transitions based on an unexpected dilution-induced assembly process using supramolecular polymers and surfactants. The co-assembly of the water-soluble benzene-1,3,5-tricarboxamide (BTA-EG 4 ) and a surfactant at a specific ratio yielded small-sized aggregates. These interactions were modeled using the competition between self-sorting and co-assembly of both components. The small-sized aggregates were transformed into supramolecular polymer networks by a twofold dilution in water without changing their ratio. Kinetic experiments show the in situ growth of micrometer-long fibers in the dilution process. We were able to create systems that undergo fully reversible hydrogel-solution-hydrogel-solution transitions upon dilution by introducing another orthogonal interaction.

Fullerenes are the allotropic form of carbon consisting of a cage-like structure due to which they have attained special attention from researchers since their discovery in 1985. The unique chemical and physical properties of fullerene have attracted researchers to develop a variety of its biomedical applications. The closed cage structure of fullerenes can be used for various drug delivery applications and can also act as a medium for controlled release formulations. The development of targeted anticancer drug and drug delivery systems is one of the most challenging fields, which is widely studied and researched. In this review, we aim to provide a comprehensive review on the most recent advances in fullerenes as targeted anticancer drug delivery systems along with their therapeutic applications and challenges, thus serving the pharmaceutical and biotechnology community., (Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.)

Background: Camptothecin is a naturally occurring alkaloid obtained from the stem wood of the Chinese tree, Camptotheca acuminata. It exerts pharmacological effects due to its ability to selectively inhibit the type-I topoisomerase DNA nuclear enzyme. Several semisynthetic analogs of camptothecin have been synthesized to date possessing antitumor activity., Objective: Camptothecin (CPT) is one of the most promising anticancer drugs but it produces various side effects because of its non-selectivity towards cancer cells. To overcome these adverse effects, we synthesized biotin conjugate of camptothecin, which was linked via a self-immolative disulfide linker (CPT-SS-Biotin)., Methods: Biotin conjugated camptothecin linked through a disulfide bond was synthesized following schemes, and the structural characterization was carried out. The stability and drug release studies were performed in the presence of glutathione (GSH) while in vitro studies were performed on 4T1 tumor cell lines. In vivo pharmacological investigation was done using an antitumor Wistar rat model., Results: The stability and drug release studies were performed in the presence of glutathione (GSH), and CPT-SSBiotin was found to be physiologically stable moiety and can only be cleaved in the presence of GSH to release free CPT. The CPT-SS-Biotin showed higher toxicity in the biotin-overexpressing 4T1 tumor cell line with a lower IC50 value (8.44 μM) compared to camptothecin alone (IC 50 > 30 μM). CPT-SS-Biotin also showed 10.6% higher cellular uptake by cells in comparison to free camptothecin. The CPT-SS-Biotin was delivered to cells by binding to the biotin receptors on the cell surface, followed by energy-dependent endocytosis and internalization to cause cellular toxicity., Conclusion: In-vivo tumor suppression studies and in vitro cell line studies along with serological parameters and histopathological studies showed that conjugate produced a high therapeutic effect and remarkably reduced toxic effects in comparison to free CPT. The results suggested that biotinylation of camptothecin via disulfide linker can be a safe and efficacious method in cancer therapeutics., (Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.)

The characterization of newly synthesized materials is a cornerstone of all chemistry and nanotechnology laboratories. For this purpose, a wide array of analytical techniques have been standardized and are used routinely by laboratories across the globe. With these methods we can understand the structure, dynamics and function of novel molecular architectures and their relations with the desired performance, guiding the development of the next generation of materials. Moreover, one of the challenges in materials chemistry is the lack of reproducibility due to improper publishing of the sample preparation protocol. In this context, the recent adoption of the reporting standard MIRIBEL (Minimum Information Reporting in Bio-Nano Experimental Literature) for material characterization and details of experimental protocols aims to provide complete, reproducible and reliable sample preparation for the scientific community. Thus, MIRIBEL should be immediately adopted in publications by scientific journals to overcome this challenge. Besides current standard spectroscopy and microscopy techniques, there is a constant development of novel technologies that aim to help chemists unveil the structure of complex materials. Among them super-resolution microscopy (SRM), an optical technique that bypasses the diffraction limit of light, has facilitated the study of synthetic materials with multicolor ability and minimal invasiveness at nanometric resolution. Although still in its infancy, the potential of SRM to unveil the structure, dynamics and function of complex synthetic architectures has been highlighted in pioneering reports during the last few years. Currently, SRM is a sophisticated technique with many challenges in sample preparation, data analysis, environmental control and automation, and moreover the instrumentation is still expensive. Therefore, SRM is currently limited to expert users and is not implemented in characterization routines. This perspective discusses the potential of SRM to transition from a niche technique to a standard routine method for material characterization. We propose a roadmap for the necessary developments required for this purpose based on a collaborative effort from scientists and engineers across disciplines., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

Modern agriculture has entered an era of technological plateau where intervention of smarter technology like nanotechnology is imminently required for making this sector economically and environmentally sustainable. Throughout the world, researchers are trying to exploit the novel properties of several nanomaterials to make agricultural practices more efficient. Core/shell nanoparticles (CSNs) have attracted much attention because of their multiple attractive novel features like high catalytic, optical, and electronic properties for which they are being widely used in sensing, imaging, and medical applications. Though it also has the promise to solve a number of issues related to agriculture, its full potential still remains mostly unexplored. This review provides a panoramic view on application of CSNs in solving several problems related to crop production and precision farming practices where the wastage of resources can be minimized. This review also summarizes different classes of CSNs and their synthesis techniques. It emphasizes and analyzes the probable potential applications of CSNs in the field of crop improvement and crop protection, detection of plant diseases and agrochemical residues, and augmentation of chloroplast mediated photosynthesis. In a nutshell, there is enormous scope to formulate and design CSN-based smart tools for applications in agriculture, making this sector more sustainable.

Multicomponent supramolecular copolymerization promises to construct complex nanostructures with emergent properties. However, even with two monomeric components, various possible outcomes such as self-sorted supramolecular homopolymers, a random (statistical) supramolecular copolymer, an alternate supramolecular copolymer, or a complex supramolecular block copolymer can occur, determined by their intermolecular interactions and monomer exchange dynamics and hence structural prediction is extremely challenging. Herein, we target this challenge and demonstrate unprecedented two-component sequence controlled supramolecular copolymerization by manipulating thermodynamic and kinetic routes in the pathway complexity of self-assembly of the constitutive monomers. Extensive molecular dynamics simulations provided useful mechanistic insights into the monomer exchange rates and free energy of interactions between the monomers that dictate the self-assembly pathway and sequence. The fluorescent nature of core-substituted naphthalene diimide monomers has been further utilized to characterize the three sequences via Structured Illumination Microscopy (SIM).

The air-water interface is an ideal platform to produce two-dimensional (2D) structures involving anything from simple organic molecules to supramolecular moieties by exploiting hydrophobic-hydrophilic interactions. Here, we show, using grazing incidence X-ray scattering, the formation of a 2D ordered structure of a charge-transfer (C-T) complex, namely, dodecyl methyl viologen (DMV) as acceptor and coronene tetracarboxylate potassium salt (CS) as donor, at the air-water interface. We have observed a phase transition in the 2D ordered structure as the area per molecule is decreased with increasing surface pressure in a Langmuir trough. The high-pressure ordering of the hydrocarbon chains associated with DMV destroys long-range C-T conjugation of DMV and CS at the air-water interface. Our results also explain the formation of DMV-CS cylindrical reverse micelles and eventually long nanowires that get formed in the self-assembly process in the bulk medium to preserve both the C-T conjugation and the organic tail-tail organization.