Whole body hypoxic preconditioning-mediated multiorgan protection in db/db mice via nitric oxide-BDNF-GSK-3ß-Nrf2 signaling pathway.

The beneficial effects of hypoxic preconditioning are abolished in the diabetes. The present study was designed to investigate the protective effects and mechanisms of repeated episodes of whole body hypoxic preconditioning (WBHP) in db/db mice. The protective effects of preconditioning were explored on diabetesinduced vascular dysfunction, cognitive impairment and ischemia-reperfusion (IR)-induced increase in myocardial injury. Sixteen-week old db/db (diabetic) and C57BL/6 (non-diabetic) mice were employed. There was a significant impairment in cognitive function (Morris Water Maze test), endothelial function (acetylcholineinduced relaxation in aortic rings) and a significant increase in IR-induced heart injury (Langendorff apparatus) in db/db mice. WBHP stimulus was given by exposing mice to four alternate cycles of low (8%) and normal air O2 for 10 min each. A single episode of WBHP failed to produce protection; however, two and three episodes of WBHP significantly produced beneficial effects on the heart, brain and blood vessels. There was a significant increase in the levels of brain-derived neurotrophic factor (BDNF) and nitric oxide (NO) in response to 3 episodes of WBHP. Moreover, pretreatment with the BDNF receptor, TrkB antagonist (ANA-12) and NO synthase inhibitor (LNAME) attenuated the protective effects imparted by three episodes of WBHP. These pharmacological agents abolished WBHP-induced restoration of p-GSK-3ß/GSK-3ß ratio and Nrf2 levels in IR-subjected hearts. It is concluded that repeated episodes of WHBP attenuate cognitive impairment, vascular dysfunction and enhancement in IRinduced myocardial injury in diabetic mice be due to increase in NO and BDNF levels that may eventually activate GSK-3ß and Nrf2 signaling pathway to confer protection.

Elucidating the impact of extreme nanoscale confinement on segmental and chain dynamics of unentangled poly(cis-1,4-isoprene).

Broadband dielectric spectroscopy is employed to probe dynamics in low molecular weight poly(cis-1,4-isoprene) (PI) confined in unidirectional silica nanopores with mean pore diameter, D, of 6.5 nm. Three molecular weights of PI (3, 7 and 10 kg/mol) were chosen such that the ratio of D to the polymer radius of gyration, Rg, is varied from 3.4, 2.3 to 1.9, respectively. It is found that the mean segmental relaxation rate remains bulk-like but an additional process arises at lower frequencies with increasing molecular weight (decreasing D/Rg. In contrast, the mean relaxation rates of the end-to-end dipole vector corresponding to chain dynamics are found to be slightly slower than that in the bulk for the systems approaching D/Rg ∼ 2, but faster than the bulk for the polymer with the largest molecular weight. The analysis of the spectral shapes of the chain relaxation suggests that the resulting dynamics of the 10kg/mol PI confined at length-scales close to that of the Rg are due to non-ideal chain conformations under confinement decreasing the chain relaxation times. The understanding of these faster chain dynamics of polymers under extreme geometrical confinement is necessary in designing nanodevices that contain polymeric materials within substrates approaching the molecular scale.

Influence of side chain isomerism on the rigidity of poly(3-alkylthiophenes) in solutions revealed by neutron scattering.

Using small-angle neutron scattering, we conducted a detailed conformational study of poly(3-alkylthiophene) solutions in deuterated dichlorobenzene. The focus was placed on addressing the influence of the spatial arrangement of side chain constituents on backbone conformation. We demonstrate that by introducing a branch point in the side chain, side chain steric interactions may promote torsional motion between backbone units, resulting in greater chain flexibility. Our findings highlight the key role of topological isomerism in determining the chain rigidity and throw new light on the debate about the effective approaches for optimizing the electronic properties of conducting polymers via side chain engineering.

Systematic investigation of benzodithiophene- and diketopyrrolopyrrole-based low-bandgap polymers designed for single junction and tandem polymer solar cells.

The tandem solar cell architecture is an effective way to harvest a broader part of the solar spectrum and make better use of the photonic energy than the single junction cell. Here, we present the design, synthesis, and characterization of a series of new low bandgap polymers specifically for tandem polymer solar cells. These polymers have a backbone based on the benzodithiophene (BDT) and diketopyrrolopyrrole (DPP) units. Alkylthienyl and alkylphenyl moieties were incorporated onto the BDT unit to form BDTT and BDTP units, respectively; a furan moiety was incorporated onto the DPP unit in place of thiophene to form the FDPP unit. Low bandgap polymers (bandgap = 1.4-1.5 eV) were prepared using BDTT, BDTP, FDPP, and DPP units via Stille-coupling polymerization. These structural modifications lead to polymers with different optical, electrochemical, and electronic properties. Single junction solar cells were fabricated, and the polymer:PC(71)BM active layer morphology was optimized by adding 1,8-diiodooctane (DIO) as an additive. In the single-layer photovoltaic device, they showed power conversion efficiencies (PCEs) of 3-6%. When the polymers were applied in tandem solar cells, PCEs over 8% were reached, demonstrating their great potential for high efficiency tandem polymer solar cells.

Photophysical and electronic properties of five PCBM-like C60 derivatives: spectral and quantum chemical view.

By means of transient UV-visible absorption spectra/fluorescence spectra, combined with electronic structure calculations, the present work focuses on characterizing the photophysical and electronic properties of five PCBM-like C(60) derivatives (F1, F2, F3, F4, and F5) and understanding how these properties are expected to affect the photovoltaic performance of polymer solar cells (PSCs) with those molecules as acceptors. Spectral data reveal that the fluorescence quantum yields (Φ(F)) are enhanced and the triplet quantum yields (Φ(T)) are lowered for the five PCBM-like C(60) derivatives as compared to those of the pristine C(60), suggesting that functionalization of a C═C double bond perturbs the fullerene's π-system and breaks the I(h) symmetry of pristine C(60), which results in modifications of photophysical properties of the fullerene derivatives. PBEPBE/6-311G(d,p)//PBEPBE/6-31G(d) level of electronic structure calculations yields the HOMO-LUMO gaps and LUMO energies, showing that the electron-withdrawing effect induced by the side chain functional groups perturbs LUMO energies, from which different open circuit voltages V(oc) are resulted. The predicted V(oc) from our calculation agrees with previous experiment results. Basically, we found that functionalization of a C═C double bond sustains the fullerene structure and its electron affinitive properties. Adducted side chains contribute to adjust the HOMO-LUMO gap and LUMO levels of the acceptors to improve open circuit voltage. The results could provide fundamental insights for understanding how structural modifications influence the photovoltaic performance, which paves a way for guiding the synthesis of new fullerene derivatives with improved performance in polymer solar cells.

Perception of National Park Soundscape and Its Effects on Visual Aesthetics.

Soundscape perception is a very weak link in the national park landscape evaluation system in China. A thorough understanding of soundscapes and their effects on visual aesthetics is important for the management of national park landscapes. In this study, features of soundscapes (e.g., loudness, frequency, preference, and auditory satisfaction) were investigated based on 394 valid questionnaires of residents in the Qianjiangyuan National Park Pilot Area. The effects of soundscape on visual aesthetics were analyzed using the PLS-SEM. The results demonstrated that: (1) Peddling voice and insect sound were the loudest components in the soundscape, running water and birdsong were the most commonly heard and most preferred, religious sound was the quietest and least frequently heard, and horn was the least preferred. Residents in the Pilot Area were generally satisfied with the auditory environment. (2) Both sound frequency and preference have significant effects on auditory satisfaction, but preference (path coefficient = 0.426) has a larger effect than does frequency (path coefficient = 0.228). (3) Loudness has negligible effects on visual aesthetics, but other soundscape characteristics did influence visual aesthetics. Soundscape preference had the most significant effect (path coefficient = 0.305), followed by auditory satisfaction (path coefficient = 0.174), and sound frequency (path coefficient = 0.165). Among them, effects of perception frequency are the indirect utilities.

Reprocessable Polybenzoxazine Thermosets with High Tgs and Mechanical Strength Retentions Using Boronic Ester Bonds as Crosslinkages.

In order to obtain reprocessable polybenzoxazine thermosets with high heat resistance and mechanical strength retentions, network structures without irreversible parts were constructed via crosslinking benzoxazine oligomers using boronic ester cross-linkers. Firstly, the benzoxazine monomer containing carbon-carbon double bonds was synthesized via the Mannich reaction. After thermal ring-opening polymerization, the benzoxazine oligomer containing carbon-carbon double bonds (OBZ) was yielded. Through the thiol-ene click reaction of the OBZ and dithiol cross-linker bearing boronic ester bonds, the polybenzoxazine thermosets using boronic ester bonds as crosslinkages (OBZ-BDB) were successfully synthesized. The structures of OBZ and OBZ-BDB were characterized by SEC, 1H NMR, and FT-IR measurements. Reprocessing experiments showed that OBZ-BDB has remarkable reprocessability. The retention rates of the tensile strengths through three generations of reprocessing were 98%, 95%, and 84%, respectively. Meanwhile, OBZ-BDB cross-linked by boronic ester bonds had brilliant thermal properties. The Tg of the original OBZ-BDB was 224 °C. With the increase of the reprocessing generations, the Tgs basically remained unchanged.

Fullerene derivative acceptors for high performance polymer solar cells.

Polymer solar cells (PSCs) are composed of a blend film of a conjugated polymer donor and a soluble fullerene derivative acceptor sandwiched between a PEDOT : PSS coated ITO positive electrode and a low workfunction metal negative electrode. The conjugated polymer donor and the fullerene derivative acceptor are the key photovoltaic materials for high performance PSCs. For the acceptors, although [6,6]-phenyl-C(61)-butyric acid methyl ester (PC(60)BM) and its corresponding C(70) derivative PC(70)BM are dominantly used as the acceptors in PSC at present, several series of new fullerene derivatives with higher-lying LUMO energy level and better solubility were reported in recent years for further improving the power conversion efficiency of the PSCs. In this perspective paper, we reviewed the recent research progress on the new fullerene derivative acceptors, including various PC(60)BM-like C(60) derivatives, PC(60)BM bisadduct, PC(70)BM bisadduct, indene-C(60) bisadduct and indene-C(70) bisadduct, trimetallic nitride endohedral fullerenes and other C(60) derivatives with multi side chains. The synthesis and physicochemical properties of PC(60)BM and PC(70)BM were also introduced considering the importance of the two fullerene acceptors.

[Spatial distribution and associations of dead woods in natural spruce-fir secondary forests]. / äº‘å†·æ‰å¤©ç„¶æ¬¡ç”Ÿæž—æ­»æœ¨åˆ†å¸ƒæ ¼å±€åŠç©ºé—´å ³è”æ€§.

To reveal the community succession rule of natural secondary forest, we investigated basic characteristics and coordinates of each tree (DBH≥1 cm) within a plot (100 m×100 m) using the adjacent grid method and examined the distribution pattern and spatial associations of dead woods in a natural spruce-fir secondary forest in Jingouling Forest Farm, Wangqing Forestry Bureau, Jilin Province, China. The results showed that the diameter class distribution of dead woods showed the pattern of left single-peak curve, while the logs showed the pattern of multi-peak curve. The relationship between the abundance of dead woods and the standing individuals of a particular species was inconsistent. There was a significant negative exponential relationship between the number of dead woods and mixing degree of trees. The distribution of dead woods was concentrated at the 0-8 m scale. With the increases of scale, it gradually changed to random or uniform, with the random distribution being dominant. The aggregation distribution of dead woods with middle (10 cm≤DBH＜20 cm) and small (1 cm≤DBH＜10 cm) DBH was the main reason for the aggregation distribution of dead woods at small scale below 8 m. The spatial associations between dead woods and stan-ding trees at different diameter classes were significantly different. The relationship between dead woods and saplings (1 cm≤DBH＜5 cm) was closely correlated. The dead woods with large DBH and saplings showed a significant positive association at 2-25 m scale. There was no spatial association between dead woods and small trees (5 cm≤DBH＜15 cm). At the 0-3 m scale, there was a positive association between the middle trees (15 cm≤DBH＜25 cm) and dead woods of small and middle DBH. At the 9, 11-14 and 15, 42-45 m scales, dead woods of small and middle DBH were significantly negatively associated with large trees (DBH≥25 cm). In conclusion, biological traits, diameter class distribution, and spatial distribution affected the abundance and diameter class distribution of dead woods. The species with low mixing degree tended to have more dead woods. The diameter and scale would affect the spatial distribution of dead woods. The spatial correlation between dead woods and standing trees varied across diameter classes and scales.

[Spatial distribution of carbon storage in natural secondary forest based on geographically weighted regression expansion model.] / åŸºäºŽåœ°ç†åŠ æƒå›žå½’æ‹“å±•æ¨¡åž‹çš„å¤©ç„¶æ¬¡ç”Ÿæž—ç¢³å‚¨é‡ç©ºé—´åˆ†å¸ƒ.

To accurately assess carbon storage and its spatial distribution in natural secondary forest at the regional scale, we constructed seven expansion models by modifying the geographically weighted regression (GWR) in aspects of spatial dimension, parameter heterogeneity and residual spatial autocorrelation, based on data collected from 165 bureau level permanent plots in Langxi Forest Farm of Wangqing Forestry Bureau in Jilin Province. Stand factor, topography factor, and soil factor were selected as the influencing factors. The expansion models included geographically and altitudinal weighted regression (GAWR), semiparametric geographically weighted regression (SGWR), semiparametric geographically and altitudinal weighted regression (SGAWR), geographically weighted regression Kriging (GWRK), geographically and altitudinal weighted regression Kriging (GAWRK), semiparametric geographically weighted regression Kriging (SGWRK), and semiparametric geographically and altitudinal weighted regression Kriging (SGAWRK). Coefficient of determination (R2), mean square error (MSE) and Akaike's Information Criterion (AIC) were used to evaluate the fitness of these models. Finally, the spatial distribution diagram of forest carbon storage was drawn with the fitting results of the optimal regression model, and the distribution pattern of forest carbon storage in the research area was analyzed. The stand factor and topographic factor had strong influence on carbon storage of natural secondary forests, among which the average diameter at breast height (DBH) of stands was the dominant variable. There was positive correlation between stand factor and topographic factor. SGWR and SGAWR model could reduce the spatial autocorrelation of the GWR model residual. The geographically regression expansion model could improve the fitting effect of GWR model. Among them, the SGWRK model had the highest R2 and the lowest MSE and AIC. The method with altitude as the spatial weight did not effectively improve the fitting effect of the model. The total forest carbon storage of Langxi Forest Farm was 205×104 t, and the carbon density ranged from 8.56 to 145.74 t·hm-2, with a mean value of 57.98 t·hm-2. Overall, the distribution pattern of carbon storage was high in the northwest and low in the southeast, while high in the edge and low in the interior. By improving the parameter heterogeneity and residual spatial autocorrelation in the GWR model, we can accurately assess the spatial relationship between forest carbon storage and relevant variables in the study area, and improve the estimation accuracy of the forest carbon storage and its spatial distribution at the regional scale.

Structure and function of soil bacterial communities in the monoculture and mixed plantation of Pinus massoniana and Castanopsis hystrix in southern subtropical China.

Establishing monoculture of native broadleaved tree species and mixed coniferous broadleaved plantations is the tendency for forest management in subtropical China. The variations of structure and function of soil bacterial community in monoculture and mixed tree plantations are still not clear. We examined soil bacterial community structure and function under different soil layers (0-20, 20-40 and 40-60 cm) in three planted forests, including broadleaved Castanopsis hystrix, coniferous Pinus massoniana and their mixed plantation, in south subtropical China, using 16S rRNA gene high-throughput sequencing and PICRUSt prediction. The results showed that soil bacterial community structure of mixed plantation and P. massoniana plantation were similar but being significant different from that in C. hystrix plantation. The diversity, biological pathways metabolic function, and nitrogen cycling function of soil bacterial community in C. hystrix plantation were lower than those in P. massoniana plantation and mixed plantation. Soil total nitrogen, nitrate nitrogen and C/N were the main factors driving the variations of soil bacterial community structure and function among different forest types. Our results suggested that the mixed plantation of C. hystrix and P. massoniana is better than C. hystrix plantation in this area in terms of soil bacterial community structure and function.

Indene-C(60) bisadduct: a new acceptor for high-performance polymer solar cells.

Polymer solar cells (PSCs) are commonly composed of a blend film of a conjugated polymer donor and a soluble C(60) derivative acceptor sandwiched between an ITO anode and a low-workfunction metal cathode. Poly(3-hexylthiophene) (P3HT) and [6,6]-phenyl-C-61-butyric acid methyl ester (PCBM) are the most widely used donor and acceptor materials, respectively. However, the low LUMO energy level of PCBM limits the open circuit voltage (V(oc)) of the P3HT-based PSCs to ca. 0.6 V. Here we synthesized a new soluble C(60) derivative, indene-C(60) bisadduct (ICBA), with a LUMO energy level 0.17 eV higher than that of PCBM. The PSC based on P3HT with ICBA as acceptor shows a higher V(oc) of 0.84 V and higher power conversion efficiency (PCE) of 5.44% under the illumination of AM1.5, 100 mW/cm(2), while the PSC based on P3HT/PCBM displays a V(oc) of 0.58 V and PCE of 3.88% under the same experimental conditions. The results indicate that ICBA is an alternative high-performance acceptor and could be widely used in high-performance PSCs.

Combination of indene-C60 bis-adduct and cross-linked fullerene interlayer leading to highly efficient inverted polymer solar cells.

A poly(3-hexylthiophene) (P3HT)-based inverted solar cell using indene-C60 bis-adduct (ICBA) as the acceptor achieved a high open-circuit voltage of 0.82 V due to ICBA's higher-lying lowest unoccupied molecular orbital level, leading to an exceptional power-conversion efficiency (PCE) of 4.8%. By incorporating a cross-linked fullerene interlayer, C-PCBSD, to further modulate the interface characteristics, the ICBA:P3HT-based inverted device exhibited an improved short-circuit current and fill factor, yielding a record high PCE of 6.2%.

Effect of branched conjugation structure on the optical, electrochemical, hole mobility, and photovoltaic properties of polythiophenes.

Four branched polythiophenes (PTs) with different ratios of conjugated terthiophene-vinylene side chains, PT-TThV10 to PT-TThV40, were synthesized by Stille coupling reaction. The polymers exhibited reversible p-doping/dedoping (oxidation/re-reduction) and n-doping/dedoping (reduction/reoxidation) processes. The absorption spectra, hole mobility, and photovoltaic properties of the polymers were much improved in comparison with the PT derivative without the terthiophene-vinylene side chain and were influenced by the content of the conjugated side chains. With the increase of the content of the conjugated side chains, the absorption peak of the branched PTs enhanced and blue-shifted. The maximum hole mobility reached 6.35 x 10(-4) cm2/V.s (SCLC method) and the maximum power conversion efficiency of the polymer solar cell reached 1.91% under the illumination of AM 1.5, 100 mW/cm2, for the polymer with 20% terthiophene-vinylene side chains. The results indicate that the branched PTs with suitable content of the terthiophene-vinylene side chains could be promising photovoltaic materials.

Preparation, characterization and application of magnetic Fe3O4-CS for the adsorption of orange I from aqueous solutions.

Fe3O4 (Fe3O4-CS) coated with magnetic chitosan was prepared as an adsorbent for the removal of Orange I from aqueous solutions and characterized by FTIR, XRD, SEM, TEM and TGA measurements. The effects of pH, initial concentration and contact time on the adsorption of Orange I from aqueous solutions were investigated. The decoloration rate was higher than 94% in the initial concentration range of 50-150 mg L(-1) at pH 2.0. The maximum adsorption amount was 183.2 mg g-1 and was obtained at an initial concentration of 400 mg L(-1) at pH 2.0. The adsorption equilibrium was reached in 30 minutes, demonstrating that the obtained adsorbent has the potential for practical application. The equilibrium adsorption isotherm was analyzed by the Freundlich and Langmuir models, and the adsorption kinetics were analyzed by the pseudo-first-order and pseudo-second-order kinetic models. The higher linear correlation coefficients showed that the Langmuir model (R(2) = 0.9995) and pseudo-second-order model (R(2) = 0.9561) offered the better fits.

The isotopic effects of deuteration on optoelectronic properties of conducting polymers.

The attractive optoelectronic properties of conducting polymers depend sensitively upon intra- and inter-polymer chain interactions, and therefore new methods to manipulate these interactions are continually being pursued. Here, we report a study of the isotopic effects of deuterium substitution on the structure, morphology and optoelectronic properties of regioregular poly(3-hexylthiophene)s with an approach that combines the synthesis of deuterated materials, optoelectronic properties measurements, theoretical simulation and neutron scattering. Selective substitutions of deuterium on the backbone or side-chains of poly(3-hexylthiophene)s result in distinct optoelectronic responses in poly(3-hexylthiophene)/[6,6]-phenyl-C61-butyric acid methyl ester (PCBM) photovoltaics. Specifically, the weak non-covalent intermolecular interactions induced by the main-chain deuteration are shown to change the film crystallinity and morphology of the active layer, consequently reducing the short-circuit current. However, side-chain deuteration does not significantly modify the film morphology but causes a decreased electronic coupling, the formation of a charge transfer state, and increased electron-phonon coupling, leading to a remarkable reduction in the open circuit voltage.

High performance low band gap polymer solar cells with a non-conventional acceptor.

A novel C70 fullerene derivative was designed and synthesized by [4+2] cyclic addition reaction between indene derivative (methyl 1H-indene-3-carboxylate) and C70. The absorption and photoluminescence of H120 and its mixed films with different polymer donor materials were investigated, as well as its electrochemical property and electron mobility. It was found that H120 has 0.05 eV higher LUMO level than that of PC(70)BM. Its electron mobility reached 6.32 × 10(-4) cm(2) V(-1) s(-1), which is slightly lower than 9.55 × 10(-4) cm(2) V(-1) s(-1) of PC(70)BM. The photovoltaic devices based on P3HT, and two high efficiency low band gap polymers, PBDTTT-C and PBDTTDPP as donors, with H120 as an acceptor gave power conversion efficiencies of 4.2%, 6.0% and 6.2%, respectively.

6.5% Efficiency of polymer solar cells based on poly(3-hexylthiophene) and indene-C(60) bisadduct by device optimization.

A power conversion efficiency of 6.48% was achieved for polymer solar cells based on poly(3-hexylthiophene) (P3HT) as donor and indene-C60 bisadduct (ICBA) as acceptor with an open-circuit voltage of 0.84 V, a short-circuit current of 10.61 mA/cm², and a fill factor of 72.7% under irradiation at AM1.5G, 100 mW/cm² at the optimized conditions of P3HT:ICBA = 1:1 (w/w), solvent annealing and pre-thermal annealing at 150 °C for 10 minutes.

Spatial conformation and charge recombination properties of polythiophene derivatives with thienylene-vinylene side chains investigated by static and femtosecond spectroscopy.

We report herein the photophysics of three two-dimensional polythiophene derivatives, with different lengths of thienylene-vinylene conjugated side chains, in comparison with regioregular poly(3-hexylthiophene) (P3HT). In solution, an evolution from stimulated emission to photoinduced absorption (PIA) at emission peak is discovered with increasing length of side chains, indicating larger steric hindrance by longer side chains. The exciton lifetime is reduced by a factor of five when the thienylene-vinylene side chain is prolonged to three units. In the film form, we investigate the dynamics of the two PIA bands, assigned to intrachain exciton and interchain polaron pairs, respectively. The analysis of the dynamics suggests that their intrachain exciton decays are similar to the one-dimensional P3HT. The recombination possibility of delocalized interchain polaron pairs occurring in 0.9 ps is reduced with longer thienylene-vinylene side chain samples. Compared with regioregular P3HT film, which self-organizes to form lamellae crystal morphology, the morphologies of these three two-dimensional polythiophenes are amorphous, attributed to the large steric hindrance caused by the existence of side chains. This design of polythiophene derivatives provides the reduction of recombination possibility for delocalized interchain polaron pairs generated in the polymer.

Low bandgap polymers by copolymerization of thiophene with benzothiadiazole.

Three low bandgap copolymers of thiophene and benzothiadiazole with electron-donating and electron-withdrawing substituents, P1, P2, and P3, have been synthesized by Pd-catalyzed Stille-coupling. Electronic energy levels of the polymers are estimated by cyclic voltammetry. The polymer films show a broad absorption band in the wavelength range from 300 to 750 nm. Among the polymers, the polymer that contains the 5,6-dinitrobenzothiadiazole unit, P3, possesses the smallest bandgap of 1.55 eV calculated from its absorption band-edge at ≈800 nm. With the increase of the electron-withdrawing ability of the substituents on the benzothiadiazole unit, the energy bandgap of the polymers decreased in the order P1 > P2 > P3. The results indicate that stronger electron-withdrawing substituents on the acceptor unit can effectively decrease the bandgap of the polymers.