Linear Backbone Research Articles

Small-Molecule Hole Transport Materials for >26% Efficient Inverted Perovskite Solar Cells.

Chemically modifiable small-molecule hole transport materials (HTMs) hold promise for achieving efficient and scalable perovskite solar cells (PSCs). Compared to emerging self-assembled monolayers, small-molecule HTMs are more reliable in terms of large-area deposition and long-term operational stability. However, current small-molecule HTMs in inverted PSCs lack efficient molecular designs that balance both the charge transport capability and interface compatibility, resulting in a long-standing stagnation of power conversion efficiency (PCE) below 24.5%. Here, we report the comprehensive design of HTMs' backbone and functional groups, which optimizes a simple planar linear molecular backbone with a high mobility exceeding 7.1 × 10-4 cm2 V-1 S-1 and enhances its interface anchoring capability. Owing to the improved surface properties and anchoring effects, the tailored HTMs enhance the interface contact at the HTM/perovskite heterojunction, minimizing nonradiative recombination and transport loss and leading to a high fill factor of 86.1%. Our work has overcome the persistent efficiency bottleneck for small-molecule HTMs, particularly for large-area devices. Consequently, the resultant PSCs exhibit PCEs of 26.1% (25.7% certified) for a 0.068 cm2 device and 24.7% (24.4% certified) for a 1.008 cm2 device, representing the highest PCE for small-molecule HTMs in inverted PSCs.

Alleviation of the degradation of cell wall pectin contributes to the maintenance of integrity of papaya (Carica papaya L.) fruit tissue during abnormal chilling injury behavior

Papaya (Carica papaya L.) is highly susceptible to chilling injury (CI), which primarily causes surface pitting, black scald, susceptibility to fungal infection, and the breakdown of tissue. It developed rapidly at 6 °C but was significantly suppressed at 1 °C, which indicated that the papaya tissue was more solid at a lower temperature. This rare phenomenon is considered to be abnormal CI behavior. The maintenance of fruit tissue integrity during abnormal CI behavior may be related to modifications of the cell wall pectin. The modifications of cell wall pectin were studied during storage at 1 and 6 °C. Storage at 1 °C alleviated the progression of CI and inhibited the degradation of pectin components and cell wall structure of papaya fruit. The increase in water-soluble pectin and the solubilization of cyclohexanediamine tetraacetic acid- (CDTA-) and sodium carbonate (Na2CO3)-soluble pectin was limited at 1 °C. Storage at this temperature limited the detachment of linear backbone chains and minimized the degradation of branching and reticular structure in the pectin molecules. Storage at this temperature also delayed the decrease in the size of pectin backbone and helped to prevent the loss of neutral sugars from the pectin side chains. Thus, alleviation of the degradation of cell wall pectin contributes to the structural integrity of the cell wall and thus helps the maintenance of the tissue integrity of papaya at 1 °C.

Mechanically strong, reprocessable and chemically recyclable furan-based poly(acylhydrazone)s materials with hydrogen-bonding networks

Acylhydrazone linkages are attractive in designing reconfigurable and chemically recyclable polymer due to their reversible characteristics and ease of preparation. We fabricate mechanically strong, thermally stable and chemically recyclable poly(acylhydrazone)s (pDFF-IPDH) using biobased 2,5-diformylfuran (DFF) and dihydrazide compounds as monomers. The linear chains are physically cross-linked via hydrogen bonding between the acylhydrazone moieties. The pDFF-IPDH sample exhibits good mechanical properties, offering both high strength and toughness. The linear and reversible acylhydrazone backbones endow polymers with attractive temperature-dependent dynamic natures, which enables the topological network to rearrange, giving the poly(acylhydrazone)s excellent reprocessability. Moreover, the feasibility of formaldehyde-promoted depolymerization presents an effective recycling pathway, offering promising opportunities in addressing the challenge between recyclability and service performance.

An Integrated Module Performs Selective 'Online' Epoxidation in the Biosynthesis of the Antibiotic Mupirocin.

The delineation of the complex biosynthesis of the potent antibiotic mupirocin, which consists of a mixture of pseudomonic acids (PAs) isolated from Pseudomonas fluorescens NCIMB 10586, presents significant challenges, and the timing and mechanisms of several key transformations remain elusive. Particularly intriguing are the steps that process the linear backbone from the initial polyketide assembly phase to generate the first cyclic intermediate PA-B. These include epoxidation as well as incorporation of the tetrahydropyran (THP) ring and fatty acid side chain required for biological activity. Herein, we show that the mini-module MmpE performs a rare online (ACP-substrate) epoxidation and is integrated ('in-cis') into the polyketide synthase via a docking domain. A linear polyketide fragment with six asymmetric centres was synthesised using a convergent approach and used to demonstrate substrate flux via an atypical KS0 and a previously unannotated ACP (MmpE_ACP). MmpE_ACP-bound synthetic substrates were critical in demonstrating successful epoxidation in vitro by the purified MmpE oxidoreductase domain. Alongside feeding studies, these results confirm the timing as well as chain length dependence of this selective epoxidation. These mechanistic studies pinpoint the location and nature of the polyketide substrate prior to the key formation of the THP ring and esterification that generate PA-B.

Regulating Molecular Structure of S,N‐Heteroacene Non‐fullerene Acceptors to Achieve Efficient Photoelectric Properties†

Comprehensive SummaryThe ternary strategy has demonstrated its efficacy in improving charge transport in organic solar cells (OSCs). Here, three novel non‐fullerene acceptors, SN6C9‐4F, SN6C9‐4Cl and SN6C10‐4F, based on S,N‐heteroacene linear backbone were designed and synthesized. The three acceptors exhibit excellent molecular coplanarity, high crystallinity and possess a deep‐lying lowest unoccupied molecular orbital energy level, which is beneficial for charge transport and injection in organic field‐effect transistors (OFETs). Notably, the OFET devices based on all three acceptors achieved impressive electron mobilities, with SN6C10‐4F achieving up to 0.73 cm2·V–1·s–1, which is one of the highest values among A‐D‐A type small molecules. In addition, the OSCs device based on PBDB‐T:SN6C9‐4F exhibited the best power conversion efficiency of 12.07% owing to its optimal morphology and enhanced charge transport. Moreover, the incorporation of SN6C9‐4F into the efficient PM6:L8‐BO binary system to form ternary OSCs resulted in extended absorption range, enhanced donor crystallization, improved and more balanced charge transport, ultimately leading to an improvement of PCE from 17.78% to 18.32%. This study highlights the potential of developing acceptors with distinct structures from Y‐series acceptors to broaden absorption and regulate donor crystallization, providing a novel approach to enhance the PCE of OSCs.

Beyond Traditional Stimuli: Exploring Salt-Responsive Bottlebrush Polymers-Trends, Applications, and Perspectives.

Bottlebrush polymers represent an important class of high-density side-chain-grafted polymers traditionally with high molecular weights, in which one or more polymeric side chains are tethered to each repeating unit of a linear polymer backbone, such that these macromolecules look like "bottlebrushes". The arrangement of molecular brushes is determined by side chains located at a distance considerably smaller than their unperturbed dimensions, leading to substantial monomer congestion and entropically unfavorable extension of both the backbone and the side chains. Traditionally, the conformation and physical properties of polymers are influenced by external stimuli such as solvent, temperature, pH, and light. However, a unique stimulus, salt, has recently gained attention as a means to induce shape changes in these molecular brushes. While the stimulus has been less researched to date, we see that these systems, when stimulated with salts, have the potential to be used in various engineering applications. This potential stems from the unique properties and behaviors these systems show when exposed to different salts, which could lead to new solutions and improvements in engineering processes, thus serving as the primary motivation for this narrative, as we aim to explore and highlight the various ways these systems can be utilized and the benefits they could bring to the field of engineering. This Review aims to introduce the concept of stimuli-responsive bottlebrush polymers, explore the evolutionary trajectory, delve into current trends in salt-responsive bottlebrush polymers, and elucidate how these polymers are addressing a variety of engineering challenges.

Biobased, catalyst-free non-isocyanate polythiourethane foams: Highly dynamic nature affords fast reprocessability, extrudability and refoamability

We have developed a series of reprocessable, re-foamable, biobased, catalyst-free non-isocyanate polythiourethane (NIPTU) network foams crosslinked via the auto-oxidation of the pendant thiol groups into disulfides. Capitalizing on the interplay of fast ring-opening of cyclic thiocabonate to create linear backbones and slightly slower thiol auto-oxidation to create disulfide crosslinks, the gelling reaction synchronized well with the vaporization of the physical blowing agent. Different physical blowing agents were used to achieve facile tunability of morphological and physical properties. In addition, incorporating a small amount of trifunctional crosslinker significantly enhanced the compressive mechanical properties of the foam. Moreover, we leveraged the rapid and catalyst-free disulfide dynamic exchange to achieve both reprocessability and extrudability of the NIPTU foams. We demonstrated that the foams are intrinsically self-healable and reprocessable by compression molding. We observed rapid stress relaxation at temperatures above 160 °C, prompting us to explore continuous processing techniques like extrusion and pseudo-injection molding. Spent foams can be extruded into bulk films at 180 °C with excellent property retention. Additionally, with our NIPTU system we demonstrated, for the first time, foam-to-foam recycling of non-isocyanate polyurethanes. By adding a small amount of sodium bicarbonate blowing agent into the spent foams prior to extrusion, CO2 gas was generated during extrusion, leading to a cellular structure. This work highlights the advantages of NIPTU foams: the catalyst-free, rapid synthesis of foams and property tunability, self-healing capability, and amenability towards a family of reprocessing techniques including compression molding, extrusion into bulk films, and foam-to-foam extrusion.

Bottlebrush Polyethylene Glycol Nanocarriers Translocate across Human Airway Epithelium via Molecular Architecture-Enhanced Endocytosis.

Pulmonary drug delivery is critical for the treatment of respiratory diseases. However, the human airway surface presents multiple barriers to efficient drug delivery. Here, we report a bottlebrush poly(ethylene glycol) (PEG-BB) nanocarrier that can translocate across all barriers within the human airway surface. Guided by a molecular theory, we design a PEG-BB molecule consisting of a linear backbone densely grafted by many (∼1000) low molecular weight (∼1000 g/mol) polyethylene glycol (PEG) chains; this results in a highly anisotropic, wormlike nanocarrier featuring a contour length of ∼250 nm, a cross-section of ∼20 nm, and a hydrodynamic diameter of ∼40 nm. Using the classic air-liquid-interface culture system to recapitulate essential biological features of the human airway surface, we show that PEG-BB rapidly penetrates through endogenous airway mucus and periciliary brush layer (mesh size of 20-40 nm) to be internalized by cells across the whole epithelium. By quantifying the cellular uptake of polymeric carriers of various molecular architectures and manipulating cell proliferation and endocytosis pathways, we show that the translocation of PEG-BB across the epithelium is driven by bottlebrush architecture-enhanced endocytosis. Our results demonstrate that large, wormlike bottlebrush PEG polymers, if properly designed, can be used as a carrier for pulmonary and mucosal drug delivery.

Boosted hydrogen evolution in conjugated polymer photocatalyst by noncovalent conformation-locked architecture

A synergetic effect of noncovalent conformational locks (NCLs) and molecular framework engineering on the performance of polymeric photocatalysts is comprehensively investigated by tuning fluorination as well as framework structure with linear or planar backbone of conjugated polymers on the basis of the 2,2′-bithiophene and pyrene building blocks. Both fluorine-induced NCLs and molecular framework structure have beneficial influence on the electronic structure, photon absorption, nanomorphology and porosity, and charge migration/separation of conjugated polymers. As a result, the noncovalent conformation-locked conjugated polymer Py-2F2T achieves a significant high hydrogen evolution rate of 404.8 mmol h−1 under the conditions of being visible-light-driven and cocatalyst-free, which is 2.5- and 202.4-fold as those of the planar counterpart without NCLs and the linear counterpart with NCLs, respectively. Remarkably, Py-2F2T could show excellent apparent quantum yields of over 25.0 % at 450–600 nm irradiation with the highest value of 39.0 % at 575 nm. Overall, this work demonstrates the significance of the synergy of NCLs and molecular framework engineering for enhancing the photocatalytic activity, and the strategy of “noncovalent conformation-locked architecture” as a novel approach to the rational structure design of high-efficiency polymeric photocatalysts for visible-light-driven hydrogen evolution through water splitting.

Donor-Acceptor Copolymer with a Linear Backbone Induced Ordered and Robust Doping Morphology for Efficient and Stable Organic Electrochemical Devices.

Donor (D)-acceptor (A) copolymer-based organic mixed ionic-electronic conductors (OMIECs) exhibit intrinsic environmental stability for they have tailored energy levels. However, their figure-of-merit (μC*) is still falling behind the D-D polymers because of morphology deterioration during the electrochemical doping process. Herein, we developed two D-A copolymers with precisely regulated backbone curvature, namely PTBT-P and PTTBT-P. Compared to the curved PTBT-P and previously reported copolymers, PTTBT-P better keeps its backbone linear, leading to a long-range ordered doping morphology, which is revealed by the in operando X-ray technique. This optimized doping morphology enables a significantly improved operando charge mobility (μ) of 2.44 cm2 V-1 s-1 and a μC* value of 342 F cm-1 V-1 s-1, one of the highest values in D-A copolymer based on OECTs. Besides, we fabricated PTTBT-P-based electrochemical random-access memories and achieved ideal and robust conductance modulation. This study highlights the critical role of backbone curvature control in the optimization of doping morphology for efficient and robust organic electrochemical devices.

Elongational rheology of 2, 3 and 4 polymer stars connected by linear backbone chains

We consider the elongational rheology of model polystyrene topologies with 2, 3 and 4 stars, which are connected by one (2-star or “Pom-Pom”), two (3-star) and three (4-star) linear backbone chains. The number of arms of each star varies from qa = 3 to 24, the molecular weight of the arms from Mw,a = 25 kg/mol to 300 kg/mol, and the backbone chains from Mw,b = 100 kg/mol to 382 kg/mol. If the length of the arm is shorter than the length of the backbone, i.e. Mw,a < Mw,b, and despite the vastly different topologies considered, the elongational stress growth coefficient can be modeled by the Hierarchical Multi-mode Molecular Stress Function (HMMSF) model, based exclusively on the linear-viscoelastic characterization and a single nonlinear parameter, the dilution modulus. If the length of the arms of the stars is similar or longer than the length of the backbone chain (Mw,a ≥ Mw,b) connecting two stars, the impact of the backbone chain on the rheology vanishes and the elongational stress growth coefficient is dominated by the star topology showing similar features of the elongational stress growth coefficient as those of linear polymers.Graphical

High-frequency low-dielectric-loss in linear-backbone-structured polyimides with ester groups and ether bonds

Polyimides have emerged as promising dielectric materials for communication equipment, owing to their excellent thermal stability and processability. Nonetheless, a pressing need remains to reduce the high-frequency dissipation factor (Df) of polyimides. Here, we synthesized various polyimides featuring linear backbone structures, finding that polyimides that incorporate a combination of ester groups and ether bonds exhibit low Df values of 0.0015-0.0024 at 10 GHz. Even in high humidity and temperature conditions they maintain low Df values of <0.005 at 10 GHz. To gain insight into the factors influencing this behavior, we conduct a comprehensive study involving aggregation structures and hygroscopic properties. Our findings highlight the pivotal role of high orientation and crystallinity in determining the high-frequency Df of polyimide films.

Non‐linear functional polymers containing selective/cleavable bonds: Synthesis and their biomedical applications

AbstractThe growing interest in functional materials has resulted in the emergence of smart polymers, demonstrating practical performance in various applications especially for biomedical purposes. The properties of functional polymers are mainly determined by the presence of functional groups that differ from those in the main chains. While some polymers are naturally active and considered functional, others require modification for enhanced impact and functionality. Many functional polymers typically have a linear backbone, but very recently the attention has been shifted towards those with specific topologies and architecture, for example, bottlebrushes, stars, dendritic polymers, and gels. Over the past few years, there has been a rising emphasis on integrating selective bonds into complex polymer structures to enhance chain scission in single macromolecules. This review captures the most recent and promising approaches to the design of non‐linear functional polymers containing selective/cleavable bonds and discusses the potential of these materials for biomedical applications.

Structural and flow rheological properties of pumpkin pectic polysaccharide extracted by citric acid

The present study aimed to investigate the structural and physicochemical characteristics of acid-extracted pumpkin pectic polysaccharide (AcPP) and to evaluate their flow rheological properties. AcPP was extracted from pumpkin pulp using the citric acid extraction method. The physicochemical and structural properties were analyzed by chemical methods and instrumental analyses. The obtained results showed that AcPP consisted predominantly of GalA (85.99 %) and small amounts of Rha, Gal, and Ara, with the ratio of HG/RG-I being 81.39/16.75. In addition, AcPP had medium DE (45.34 %) and contained four macromolecular populations with different Mw of 106.03 (main), 10.15, 4.99, and 2.90 kDa. The NMR analysis further confirmed that AcPP contained a linear backbone consisting of α-1,4-linked GalA residues, some of which were partially methyl-esterified. Furthermore, AcPP was amorphous in nature and had favorable thermal stability. The effects of extrinsic factors on the flow rheological properties of AcPP were evaluated. In particular, the high concentrations of CaCl2 (8 mM) and MgCl2 (10 mM) were effective in enhancing the viscosity and non-Newtonian shear-thinning behavior of the AcPP solution. This study elucidates the unique molecular structure of AcPP and suggests the potential of AcPP as a rheology modifier in low-viscous and mineral-reinforced beverages.

Enhanced N-type Semiconducting Performance of Asymmetric Monochlorinated Isoindigo-based Semiregioregular Polymers under Dynamic Forces.

The asymmetric monochlorination strategy not only effectively addresses the steric issues in conventional dichlorination but also enables the development of promising acceptor units and semiregioregular polymers. Herein, monochlorinated isoindigo (1CIID) is successfully designed and synthesized by selectively introducing single chlorine (Cl) atoms. Furthermore, the 1CIID copolymerizes with two donor counterparts, centrosymmetric 2,2'-bithiophene (2T) and axisymmetric 4,7-di(thiophen-2-yl)benzo[1,2,5]thiadiazole (DTBT), forming two polymers, P1CIID-2T and P1CIID-DTBT. These polymers exhibit notable differences in backbone linearity and dipole moments, influenced by the symmetry of their donor counterparts. In particular, P1CIID-2T, which contains a centrosymmetric 2T unit, demonstrates a linear backbone and a significant dipole moment of 10.20 D. These properties contribute to the favorable film morphology of P1CIID-2T, characterized by highly ordered crystallinity in the presence of fifth-order (500) X-ray diffraction peaks. Notably, P1CIID-2T exhibits a significant improvement in molecular alignment under dynamic force, resulting in over 8-fold improvement in the performance of organic field-effect transistor (OFET) devices, with superior electron mobility up to 1.22 cm2 V-1 s-1. This study represents the first synthesis of asymmetric monochlorinated isoindigo-based conjugated polymers, highlighting the potential of asymmetric monochlorination for developing n-type semiconducting polymers. Moreover, our findings provide valuable insights into the relationship between the molecular structure and properties.

Thermal Conductivity of Bottle-Brush Polymers.

Using molecular dynamics (MD) simulations of a generic model, we investigated heat propagation in bottle-brush polymers (BBP). An architecture is referred to as a BBP when a linear (backbone) polymer is grafted with the side chains of different length Ns and grafting density ρg, which control the bending stiffness of a backbone. Investigating κ-behavior in BBP is of particular interest due to two competing mechanics: increased backbone stiffness, via Ns and ρg, increases the thermal transport coefficient κ, while the presence of side chains provides additional pathways for heat leakage. We show how a delicate competition between these two effects controls κ. These results reveal that going from a weakly grafting (ρg < 1) to a highly grafting (ρg ≥ 1) regime, κ changes non-monotonically that is independent of Ns. The effect of side chain mass on κ and heat flow in the BBP melts is also discussed.

Microbial α-L-arabinofuranosidases: diversity, properties, and biotechnological applications.

Arabinoxylans (AXs) are hemicellulosic polysaccharides consisting of a linear backbone of β-1,4-linked xylose residues branched by high content of α-L-arabinofuranosyl (Araf) residues along with other side-chain substituents, and are abundantly found in various agricultural crops especially cereals. The efficient bioconversion of AXs into monosaccharides, oligosaccharides and/or other chemicals depends on the synergism of main-chain enzymes and de-branching enzymes. Exo-α-L-arabinofuranosidases (ABFs) catalyze the hydrolysis of terminal non-reducing α-1,2-, α-1,3- or α-1,5- linked α-L-Araf residues from arabinose-substituted polysaccharides or oligosaccharides. ABFs are critically de-branching enzymes in bioconversion of agricultural biomass, and have received special attention due to their application potentials in biotechnological industries. In recent years, the researches on microbial ABFs have developed quickly in the aspects of the gene mining, properties of novel members, catalytic mechanisms, methodologies, and application technologies. In this review, we systematically summarize the latest advances in microbial ABFs, and discuss the future perspectives of the enzyme research.

All-Atom Molecular Dynamics Simulations of Uncharged Linear Polymer Bottlebrushes: Effect of the Brush Sizes and the Number of Side-Chain Monomers.

Bottlebrush polymers (BBPs), characterized by grafted polymer side chains on linear backbone polymer chain, have emerged as a unique and versatile class of macromolecules with extensive applications in the fields of material science, electronics, battery materials, self-healing technology, etc. In this paper, we employ all-atom molecular dynamics (MD) simulations to present a comprehensive study of poly(methyl methacrylate)-g-poly(2-ethyl-2-oxazoline) (PMMA-g-PEtOx) BBP and its structural and hydration properties for varying number of backbone monomers (NBB) and side chain monomers (NSC), as well as properties of water molecules supported by the BBP. We find that the radius of gyration follows a scaling of Rg ∼NSC0.36 for smaller grafts and Rg ∼ NSC0.52-0.58 for longer grafts. We also find that the overall shape of the bottlebrush goes from a rod to sphere-like shape with the increase in NSC. Both the hydration per side chain monomer and hydrogen bonds (HBs) per oxygen and nitrogen of the side chain monomer reduce with an increase in NSC, caused by a corresponding enhancement in localization of the side chain monomers in the interior of the BBP. Furthermore, steric influences ensure the number of water-oxygen HBs is much more than the number of water-nitrogen HBs (with oxygen and nitrogen atoms belonging to the monomer side chains). Also, the BBP-supported water molecules demonstrate two distinctly ordered domains with one more structured and one less structured. The more structured domain disappears with an increase in NSC that causes more side chain monomers to localize in the interior of the BBPs. Finally, we observe that despite the highly negative partial charges of the oxygen and nitrogen atoms (of the side chain monomers), the dipole orientation distributions of water molecules around these atoms exhibit the presence of a neutral environment rather than an anionic environment. Overall, we anticipate that our study will generate significant interest in probing the various BBP systems in greater atomistic detail.

Preparation of superstructured comb polymers based on tadpole-shaped single-chain nanoparticles.

Compared with the formation of individual elements, the creation of superstructures often yields exceptional properties. This approach has been applied to assemble diverse synthetic building blocks (molecules, macromolecules, inorganic nanoparticles, etc.) into highly organized constructs. In the present study, a novel comb polymer superstructure is developed via the grafting of tadpole-shaped single-chain nanoparticles (T-SCNPs) onto a high-molecular-weight linear backbone (H-LP). The resulting superstructure (comb of T-SCNPs), which utilizes T-SCNPs as building blocks, exhibits distinct rheological behavior in solution. The influences of the microstructure and related parameters (specifically the relaxation time (τ R) and mesh size (ξ) of the entangled chains) on the macroscopic properties (modulus and viscosity) of this complex topological structure in solution are investigated. Compared with conventional comb macromolecules (comb of F-LPs) and blends of SCNPs with high-molecular-weight polymers (SCNPs&H-LP), T-SCNP combs exhibit significantly reduced chain entanglement, faster τ R, and larger ξ in solution, resulting in a substantially decreased viscosity (up to 90%). Furthermore, our research underscores the intricate relationship between these rheological properties and the size and concentration of grafted T-SCNPs. As the size or concentration of T-SCNPs increases, the mesh size of the entangled chains expands, which leads to increased τ R and decreased viscosity.

Cartilage extracellular matrix polymers: hierarchical structure, osmotic properties, and function.

Proteoglycans are hierarchically organized structures that play an important role in the hydration and the compression resistance of cartilage matrix. In this study, the static and dynamic properties relevant to the biomechanical function of cartilage are determined at different levels of the hierarchical structure, using complementary osmotic pressure, neutron scattering (SANS) and light scattering (DLS) measurements. In cartilage proteoglycans (PGs), two levels of bottlebrush structures can be distinguished: the aggrecan monomer, which consists of a core protein to which are tethered charged glycosaminoglycan (GAG) chains, and complexes formed of the aggrecan monomers attached around a linear hyaluronic acid backbone. The principal component of GAG, chondroitin sulfate (CS), is used as a baseline in this comparison. The osmotic modulus, measured as a function of the proteoglycan concentration, follows the order CS < aggrecan < aggrecan-HA complex. This order underlines the benefit of the increasing complexity at each level of the molecular architecture. The hierarchical bottlebrush configuration, which prevents interpenetration among the bristles of the aggrecan monomers, enhances both the mechanical properties and the osmotic resistance. The osmotic pressure of the collagen solution is notably smaller than in the proteoglycan systems. This is consistent with its known primary role to provide tensile strength to the cartilage and to confine the aggrecan-HA complexes, as opposed to load bearing. The collective diffusion coefficient D governs the rate of recovery of biological tissue after compressive load. In CS solutions the diffusion process is fast, D ≈ 3 × 10-6 cm2 s-1 at concentrations comparable with that of the GAG chains inside the aggrecan molecule. In CS solutions D is a weakly decreasing function of calcium ion concentration, while in aggrecan and its complexes with HA, the relaxation rate is insensitive to the presence of calcium.