Polymerization Mode Research Articles

Flexural Strength of Modern CAD/CAM Restoratives After Artificial Aging.

Before clinical trials are initiated, studying the mechanical performance of modern CAD/CAM restorative materials exposed to aging conditions would provide insights on their performance in service. This study evaluated the impact of thermomechanical aging on various resin composite, ceramic, hybrid, and nano-filled resin composite materials after two polymerization modes. Specimens (3 × 4 × 14 mm3) were fabricated using (n = 12 per group) a universal composite (Filtek Supreme XTE photo-polymerized for either 40 s or 120 s per layer), hybrid ceramics (BRILLIANT Crios, GC Cerasmart, Lava Ultimate, VITA ENAMIC), glass ceramics (IPS e.max CAD, VITA Suprinity PC, Straumann n!ce), or feldspar ceramics (VITABLOCS Mark II, GC Initial LRF). In each group, half of the specimens underwent thermomechanical aging. A three-point bending test was applied to all specimens and the results were statistically analyzed (α = 0.05). Glass ceramics and hybrid ceramics presented higher flexural strength values than feldspar ceramics and the universal composite before and after aging (p < 0.05). Thermomechanical cycling affected the flexural strength of all materials (p < 0.05) except Lava Ultimate, Straumann n!ce, and GC Initial (p > 0.05). The highest decrease in flexural strength after aging was found in the universal composite (40 s polymerization) (p < 0.001) and Vita Enamic (p < 0.001), while the lowest decrease was in the hybrid ceramics, Cerasmart and Lava Ultimate (p < 0.05). Extending polymerization duration reduced the aging effect on the universal composite tested. Thermomechanical aging affected the flexural strength of most materials tested. Universal composites and feldspar ceramics presented similar flexural strength values.

On the physical-mechanical and tribotechnical properties of antifriction carbon fiber based on a modified thermosetting matrix

The physical-mechanical and tribological properties of anti-friction carbon fiber plastic UGET based on low-modulus carbon fabric “Ural T-15R” have been studied in order to increase the magnitude of the ultimate deformation and reduce the elastic modulus through the use of a modified thermosetting matrix ET-4 instead of the traditionally used ET-2.Modes of polymerization and of heat treatment of epoxy binders were selected considering the results of the experiments. Prototypes of prepregs were obtained by solution impregnation on the UPST-1000M line and then processed into PCM by hot pressing. Laboratory samples were made and physical and mechanical tests were carried out to determine the ultimate strength under compression, shear and bending stress under destruction, as well as Charpy impact strength. Steel 20Kh13 and oxidized titanium alloy PT-3V were used as counter body rollers to determine carbon fiber tribosets.It was shown that carbon fiber samples based on chemically modified binder ET-4 with two-stage polymerization and heat treatment mode in the range of 90°C to 180°C both have better physical-mechanical and tribotechnical properties, in contrast with the analogue with a three-stage mode and carbon fiber carbon heat at friction over 20Kh13 steel and oxidized titanium alloy PT-3V.

Effect of Added Salt on the RAFT Polymerization of 2-Hydroxyethyl Methacrylate in Aqueous Media.

We report the effect of added salt on the reversible addition-fragmentation chain transfer (RAFT) polymerization of 2-hydroxyethyl methacrylate (HEMA) in aqueous media. More specifically, poly(2-(methacryloyloxy)ethyl phosphorylcholine) (PMPC26) was employed as a salt-tolerant water-soluble block for chain extension with HEMA targeting PHEMA DPs from 100 to 800 in the presence of NaCl. Increasing the salt concentration significantly reduces the aqueous solubility of both the HEMA monomer and the growing PHEMA chains. HEMA conversions of more than 99% could be achieved within 6 h at 70 °C regardless of the NaCl concentration when targeting PMPC26-PHEMA800 vesicles at 20% w/w solids. Significantly faster rates of polymerization were observed at higher salt concentration owing to the earlier onset of micellar nucleation. Transmission electron microscopy (TEM) was used to construct a pseudo-phase diagram for this polymerization-induced self-assembly (PISA) formulation. High-quality images required cross-linking of the PHEMA chains with glutaraldehyde prior to salt removal via dialysis. Block copolymer spheres, worms, or vesicles can be accessed at any salt concentration up to 2.5 M NaCl. However, only kinetically trapped spheres could be obtained in the presence of 3 M NaCl because the relatively low HEMA monomer solubility under such conditions leads to an aqueous emulsion polymerization rather than an aqueous dispersion polymerization. In this case, dynamic light scattering studies indicated a gradual increase in z-average diameter from 26 to 86 nm when adjusting the target PHEMA degree of polymerization from 200 to 800. When targeting PMPC26-PHEMA800 vesicles, increasing the salt content up to 2.5 M NaCl leads to a systematic reduction in the z-average diameter from 953 to 92 nm. Similarly, TEM analysis and dispersion viscosity measurements indicated a gradual reduction in worm contour length with increasing salt concentration for PMPC26-PHEMA600 worms. This new PISA formulation clearly illustrates the importance of added salt on aqueous monomer solubility and how this affects (i) the kinetics of polymerization, (ii) the morphology of the corresponding diblock copolymer nano-objects, and (iii) the mode of polymerization in aqueous media.

Blue Laser for Polymerization of Bulk Fill Composites: Influence on dentin bond strength and temperature rise during curing and co-curing method.

Blue diode lasers are alternative curing devices for dental composites. The aim of this study was to investigate the influence of blue diode laser polymerization on shear bond strength of bulk fill composites to human dentin and temperature rise during two types of polymerization. Composite cylinders of SDR Plus(SDR) and Ever X Flow(EX) were bonded to dentin slabs using Adhese Universal and curing devices blue diode laser (449nm, 1.6 W) and Power Cure LED. For each material and curing device there were two polymerization approaches: 1)conventional: separate curing of adhesive; 2)co-curing: simultaneous adhesive and composite curing. Polymerization modes for each material in conventional and co-curing(c) approach were: blue laser 2000 mW/cm2 for 5s (L5 and L5c); blue laser 1000 mW/cm2 for 10s (L10 and L10c); Power Cure 2000 mW/cm2 for 5s (LED5 and LED5c); Power Cure 1000 mW/cm2 for 10s (LED10 and LED10c). Temeperature was measured using thermal vision camera. For SDR, the highest bond strength was 24.3MPa in L10c, and the lowest 9.2MPa in LED5c. EX exhibited the highest bond strength(21.3MPa) in LED5, and the lowest in L5(7.7MPa). The highest temperature rise for SDR was in L10 and L5 (7.3 and 7.2°C), and the lowest in LED5(0.8°C). For EX, the highest temperature rise was in L5 (13.0°C), and the lowest in LED5 (0.7°C). Temperature rise was higher during blue laser polymerization, especially at high intensity and with conventional curing. Preferable blue laser curing mode is co-curing at 1000mW/cm2 for 10s.

Trisarcglaboids A and B, two cytotoxic lindenane sesquiterpenoid trimers with a unique polymerization mode isolated from Sarcandra glabra

Trisarcglaboids A and B (1 and 2), representing the first example of lindenane sesquiterpenoid trimers repolymerized based on the classical [4 + 2] type dimer, together with known biogenic precursors chlorahololide D (3) and sarcandrolide A (4), were identified as chemical components of the root of Sarcandra glabra. The novel trimeric lindenane sesquiterpenoid skeletons, including their absolute configurations, were characterized using MS, NMR, ECD, and X-ray single crystal diffraction. The proposed Diels-Alder cycloaddition between Δ2(3) of the tiglic acyl group of the classical [4 + 2] type dimer and Δ15(4),5(6) of the third lindenane may serve as the key biogenic step. In addition, compound 1 exerted significant cytotoxicity against five human cancer cell lines with IC50 values ranging from 1 to 7 μM, potentially through blocking Akt phosphorylation and activating the endogenous apoptosis pathway.

Organoboron-mediated polymerizations.

The scientific community has witnessed extensive developments and applications of organoboron compounds as synthetic elements and metal-free catalysts for the construction of small molecules, macromolecules, and functional materials over the last two decades. This review highlights the achievements of organoboron-mediated polymerizations in the past several decades alongside the mechanisms underlying these transformations from the standpoint of the polymerization mode. Emphasis is placed on free radical polymerization, Lewis pair polymerization, ionic (cationic and anionic) polymerization, and polyhomologation. Herein, alkylborane/O2 initiating systems mediate the radical polymerization under ambient conditions in a controlled/living manner by careful optimization of the alkylborane structure or additives; when combined with Lewis bases, the selected organoboron compounds can mediate the Lewis pair polymerization of polar monomers; the bicomponent organoboron-based Lewis pairs and bifunctional organoboron-onium catalysts catalyze ring opening (co)polymerization of cyclic monomers (with heteroallenes, such as epoxides, CO2, CO, COS, CS2, episulfides, anhydrides, and isocyanates) with well-defined structures and high reactivities; and organoboranes initiate the polyhomologation of sulfur ylides and arsonium ylides providing functional polyethylene with different topologies. The topological structures of the produced polymers via these organoboron-mediated polymerizations are also presented in this review mainly including linear polymers, block copolymers, cyclic polymers, and graft polymers. We hope the summary and understanding of how organoboron compounds mediate polymerizations can inspire chemists to apply these principles in the design of more advanced organoboron compounds, which may be beneficial for the polymer chemistry community and organometallics/organocatalysis community.

Triazabicyclodecene: A versatile catalyst for polymer synthesis

AbstractThis comprehensive review aims to provide an in‐depth analysis of the catalytic performance of 1,5,7‐triazabicyclo[4,4,0]dec‐5‐ene (TBD) in polymer synthesis. TBD, a well‐established organic superbase, possesses a distinctive bifunctional character that grants it exceptional capabilities, particularly in processes such as transesterification or transamidation. TBD has garnered considerable attention since its initial report by Hedrick and Waymouth in 2006, and it has played a pivotal role in diverse polymerization reactions. Its versatility spans various polymerization modes, including chain‐growth and step‐growth polymerization, post‐polymerization modification, and network thermoset formation. More recently, its utility has extended to the green chemical recycling of polymers. By providing an encompassing overview of TBD's historical journey, this review delves into its past accomplishments while shedding light on its present and future potential to organocatalysts in polymer science.

Broadband and compact reconfigurable polymeric thermo-optic mode converter based on cascaded Y-junctions

We propose and demonstrate experimentally a thermo-optically reconfigurable mode converter based on cascaded Y-junctions on a polymer waveguide platform. The proposed device, which can achieve reconfigurable mode conversion between the LP01 and LP11a modes, features compact, broadband, and low-power. Our typical fabricated mode converter has a footprint of 1.5 mm × 66.2 μm. The power consumptions of each heater for achieving the LP01-to-LP11a and LP11a-to-LP01 mode conversions are 32 mW and 28 mW, respectively. The mode crosstalks are as low as −20.7 dB and −18.9 dB for the x- and y-polarized LP01 modes over the wavelength range of 1530–1600 nm, respectively. Our proposed mode converter could find applications in reconfigurable mode-division multiplexing optical communication systems.

Insight into the synergistic behaviors of a hydroxyethyl cellulose-based graft copolymer in the mitigation of silica scaling: Combined static and reverse osmosis tests

Silica scaling has become a common problem in membrane systems due to the ubiquity of silica in the natural environment. In this work, a series of N-[3-(dimethylamino)propyl]methacrylamide-grafted hydroxyethyl cellulose (DHEC) with different grafting ratios was designed and used as a silica scaling inhibitor. The performances and mechanisms of DHEC in the inhibition of silica scaling were evaluated in detail by static and reverse osmosis (RO) tests. The maximum inhibition efficiency of DHEC with the grafting ratio of 97% reached as high as 77.20% ± 0.26% in the static test. The permeate flux in the presence of this DHEC gradually decreased and was eventually maintained at 89.12% after 10 h of RO operation. The efficient mitigation of silica scaling was ascribed to the synergistic effect of the grafted copolymer, specifically, the hydrophilic cellulose backbone of DHEC exerted a dispersion effect and the cationic grafted chains acted as aggregators to inhibit silica scaling in the solution and at the membrane surface. This synergistic effect cannot delay the induction time of silica polymerization but can change the dominant mode of polymerization in the solution from the first-order to the second-order reaction as confirmed by the kinetic study. Thus, DHEC is an efficient and environmentally friendly inhibitor with high application potential for membrane fouling control in RO operations.

Effect of inorganic fillers on the light transmission through traditional or flowable resin-matrix composites for restorative dentistry

ObjectivesThe aim of this in vitro study was to evaluate the light transmission through five different resin-matrix composites regarding the inorganic filler content.MethodsResin-matrix composite disc-shaped specimens were prepared on glass molds. Three traditional resin-matrix composites contained inorganic fillers at 74, 80, and 89 wt. % while two flowable composites revealed 60 and 62.5 wt. % inorganic fillers. Light transmission through the resin-matrix composites was assessed using a spectrophotometer with an integrated monochromator before and after light curing for 10, 20, or 40s. Elastic modulus and nanohardness were evaluated through nanoindentation’s tests, while Vicker’s hardness was measured by micro-hardness assessment. Chemical analyses were performed by FTIR and EDS, while microstructural analysis was conducted by optical microscopy and scanning electron microscopy. Data were evaluated using two-way ANOVA and Tukey’s test (p < 0.05).ResultsAfter polymerization, optical transmittance increased for all specimens above 650-nm wavelength irradiation since higher light exposure time leads to increased light transmittance. At 20- or 40-s irradiation, similar light transmittance was recorded for resin composites with 60, 62, 74, or 78–80 wt. % inorganic fillers. The lowest light transmittance was recorded for a resin-matrix composite reinforced with 89 wt. % inorganic fillers. Thus, the size of inorganic fillers ranged from nano- up to micro-scale dimensions and the high content of micro-scale inorganic particles can change the light pathway and decrease the light transmittance through the materials. At 850-nm wavelength, the average ratio between polymerized and non-polymerized specimens increased by 1.6 times for the resin composite with 89 wt. % fillers, while the composites with 60 wt. % fillers revealed an increased ratio by 3.5 times higher than that recorded at 600-nm wavelength. High mean values of elastic modulus, nano-hardness, and micro-hardness were recorded for the resin-matrix composites with the highest inorganic content.ConclusionsA high content of inorganic fillers at 89 wt.% decreased the light transmission through resin-matrix composites. However, certain types of fillers do not interfere on the light transmission, maintaining an optimal polymerization and the physical properties of the resin-matrix composites.Clinical significanceThe type and content of inorganic fillers in the chemical composition of resin-matrix composites do affect their polymerization mode. As a consequence, the clinical performance of resin-matrix composites can be compromised, leading to variable physical properties and degradation.Graphical

Effect of Attenuated Light Through Translucent Zirconia on the Interfacial Adaptation and Polymerization of Resin Cements.

The first objective was to determine if dual-curing of resin cement with reduced light could affect interfacial adaptations of zirconia restoration. The second objective was to examine whether cement type and pretreatment method of universal adhesive affected interfacial adaptation. The final objective was to compare the polymerization degree of cement under different reduced-light conditions. Inlay cavities were prepared on extracted third molars. Translucent zirconia restorations were milled using Katana UTML (Kuraray Noritake) in three groups with restoration thicknesses of 1, 2, and 3 mm, respectively. Each group had three subgroups using different cementation methods. For subgroup 1, restorations were cemented with self-adhesive cement. For subgroup 2, universal adhesive was applied and light cured. After the restoration was seated with conventional resin cement, light curing was performed. For subgroup 3, after adhesive was applied, the restoration was seated with conventional resin cement. Light curing was performed for the adhesive and cement simultaneously. After thermocycling, interfacial adaptation at the restoration-tooth interface was investigated using swept-source optical coherence tomography imaging. Finally, polymerization shrinkage of the cement was measured using a linometer and compared under the conditions of different zirconia thicknesses and light-curing durations. Interfacial adaptation varied signficantly depending on the zirconia thickness, pretreatment, polymerization mode and cements used (p < 0.05). The effects of the adhesive and polymerization shrinkage differed signficantly, depending on the reduced light under the zirconia (p < 0.05). Lower curing-light irradiance may lead to inferior adaptation and lower polymerization of the cement. Polymerization of resin cement can differ depending on the light irradiance and exposure duration.

High-durability organic electrochromic devices based on in-situ-photocurable electrochromic materials

•Organic electrochromic materials with in situ photocuring features were proposed •The electrochromic film and device showed attractive durability and calendar life •A high-resolution electrochromic photolithographic patterning was demonstrated Electrochromic materials can undergo electrochemically driven redox processes resulting in optical signal changes, and they have shown attractive application potential in smart windows, wearable electronics, electronic papers, etc. However, their research and development (R&D) are still limited due to the lack of suitable materials and processing strategies to achieve high durability. Here, in-situ-photocurable electrochromic molecules were designed and synthesized to overcome the aforementioned challenges. Compared with the existing doping mode and polymerization mode, in-situ-photocured electrochromic films and devices showed superior durability (e.g., adhesion, multi-dimension stability, and full-contrast calendar life of >120 days) and remarkable overall performance (e.g., transparency = ∼90%, optical modulation = 72.7%, and full-contrast cycle life > 21,000). Furthermore, a high-resolution electrochromic photolithography for micro-nano patterning (recognizable pattern size: ∼2 μm, the best electrochromic resolution to date) was successfully achieved. Based on this, some potential applications in multi-level information encryption and tunable secondary colors were demonstrated. Electrochromic materials can undergo electrochemically driven redox processes resulting in optical signal changes, and they have shown attractive application potential in smart windows, wearable electronics, electronic papers, etc. However, their research and development (R&D) are still limited due to the lack of suitable materials and processing strategies to achieve high durability. Here, in-situ-photocurable electrochromic molecules were designed and synthesized to overcome the aforementioned challenges. Compared with the existing doping mode and polymerization mode, in-situ-photocured electrochromic films and devices showed superior durability (e.g., adhesion, multi-dimension stability, and full-contrast calendar life of >120 days) and remarkable overall performance (e.g., transparency = ∼90%, optical modulation = 72.7%, and full-contrast cycle life > 21,000). Furthermore, a high-resolution electrochromic photolithography for micro-nano patterning (recognizable pattern size: ∼2 μm, the best electrochromic resolution to date) was successfully achieved. Based on this, some potential applications in multi-level information encryption and tunable secondary colors were demonstrated.

Interfacial Dynamics and Growth Modes of β2-Microglobulin Dimers.

Protein aggregation is a complex process, strongly dependent on environmental conditions and highly structurally heterogeneous, both at the final level of fibril structure and intermediate level of oligomerization. Since the first step in aggregation is the formation of a dimer, it is important to clarify how certain properties of the latter (e.g., stability or interface geometry) may play a role in self-association. Here, we report a simple model that represents the dimer's interfacial region by two angles and combine it with a simple computational method to investigate how modulations of the interfacial region occurring on the ns-μs time scale change the dimer's growth mode. To illustrate the proposed methodology, we consider 15 different dimer configurations of the β2m D76N mutant protein equilibrated with long Molecular Dynamics simulations and identify which interfaces lead to limited and unlimited growth modes, having, therefore, different aggregation profiles. We found that despite the highly dynamic nature of the starting configurations, most polymeric growth modes tend to be conserved within the studied time scale. The proposed methodology performs remarkably well taking into consideration the nonspherical morphology of the β2m dimers, which exhibit unstructured termini detached from the protein's core, and the relatively weak binding affinities of their interfaces, which are stabilized by nonspecific apolar interactions. The proposed methodology is general and can be applied to any protein for which a dimer structure has been experimentally determined or computationally predicted.

3D-2D microleakage assessment of preheated bulk-fill composite resin applied with different parameters: a micro-CT analysis.

This study evaluated microleakage from class II cavities filled with bulk-fill composite preheated to different temperatures, applied at different thicknesses, and with different polymerization modes. A total of 60 mesio-occlusal cavity were drilled into the extracted human third molars at 2mm and 4mm thickness. Preheated bulk-fill composite resin (Viscalor; VOCO, Germany) was applied to the cavities at 68°C and 37°C after the adhesive resin was applied, and cured using standard and high-power light-curing modes of a VALO light-curing unit. An incrementally applied microhybrid composite was used as the control. The teeth were subjected to 2000 cycles of heating to 55°C and cooling to 5°C with a 30-s hold time. Then, they were immersed in a 50% silver nitrate solution for 24h and scanned with micro-computed tomography. Scanned data were processed using the CTAn software. Two (2D) and three (3D) dimensional analyses of leached silver nitrate were performed. The data's normality was assessed using the Shapiro-Wilk test before comparisons using a three-way analysis of variance. In both 2D and 3D analysis, bulk-fill composite resin preheated to 68°C and applied at 2mm thickness showed less microleakage. In the 3D analysis, restorations applied at 37°C and 4mm thickness in high-power mode showed significantly higher values (p < 0.001). Preheated bulk-fill composite resin can be applied at 68°C and effectively cured at both 2mm and 4mm thickness.

Neogrisphenol A, a Potential Ovarian Cancer Inhibitor from a New Record Fungus Neohelicosporium griseum.

From the rice fermentation product of a new record fungus, Neohelicosporium griseum, two new polyketides, neogrisphenol A (1) and neogrisphenol B (2), one new isochroman-1-one, (S)-6-hydroxy-7-methoxy-3,5-dimethylisochroman-1-one (3), and four known compounds (4-7) were isolated. Their structures were determined using 1D- and 2D-NMR, mass spectrometry, and chemical calculations. The C-3~C-2' polymerization mode between the two α-naphthalenone derivative moieties is uncommon in compounds 1 and 2. Meanwhile, compounds 1-2 and 5 exhibited antibacterial activity against Bacillus subtilis, Clostridium perfringens, Staphylococcus aureus, and Staphylococcus aureus, with MIC values ranging between 16 and 31 µg/mL. In addition, compound 5 showed antifungal activity against Sclerotinia sclerotiorum and Phytophthora nicotianae var. nicotianae, with respective IC50 values of 88.14 ± 2.21 µg/mL and 52.36 ± 1.38 µg/mL. Compound 1 showed significant cytotoxicity against A2780, PC-3, and MBA-MD-231 cell lines with respective IC50 values of 3.20, 10.68, and 16.30 µM, and the cytotoxicity against A2780 cells was even higher than that of cisplatin (CDDP). With an IC50 value of 10.13 µM, compound 2 also exhibited cytotoxicity against A2780. The in vitro results showed that compound 1 inhibited A2780 cell proliferation, induced apoptosis, and arrested the cell cycle at the S-phase in a concentration-dependent manner.

Effect of polymerization mode on shrinkage kinetics and degree of conversion of dual-curing bulk-fill resin composites

ObjectivesTo assess the behavior of dual-cure and conventional bulk-fill composite materials on real-time linear shrinkage, shrinkage stress, and degree of conversion.Materials and methodsTwo dual-cure bulk-fill materials (Cention, Ivoclar Vivadent (with ion-releasing properties) and Fill-Up!, Coltene) and two conventional bulk-fill composites (Tetric PowerFill, Ivoclar Vivadent; SDR flow + , Dentsply Sirona) were compared to conventional reference materials (Ceram.x Spectra ST (HV), Dentsply Sirona; X-flow; Dentsply Sirona). Light curing was performed for 20 s, or specimens were left to self-cure only. Linear shrinkage, shrinkage stress, and degree of conversion were measured in real time for 4 h (n = 8 per group), and kinetic parameters were determined for shrinkage stress and degree of conversion. Data were statistically analyzed by ANOVA followed by post hoc tests (α = 0.05). Pearson’s analysis was used for correlating linear shrinkage and shrinkage force.ResultsSignificantly higher linear shrinkage and shrinkage stress were found for the low-viscosity materials compared to the high-viscosity materials. No significant difference in degree of conversion was revealed between the polymerization modes of the dual-cure bulk-fill composite Fill-Up!, but the time to achieve maximum polymerization rate was significantly longer for the self-cure mode. Significant differences in degree of conversion were however found between the polymerization modes of the ion-releasing bulk-fill material Cention, which also exhibited the significantly slowest polymerization rate of all materials when chemically cured.ConclusionsWhile some of the parameters tested were found to be consistent across all materials studied, heterogeneity increased for others.Clinical relevanceWith the introduction of new classes of composite materials, predicting the effects of individual parameters on final clinically relevant properties becomes more difficult.

The Effect of Different Immersion Media, Polymerization Modes, and Brushing on the Color Stability of Different Composite Resins.

This in vitro study investigated color stability of two photo-polymerized nano-filled and nano-hybrid composite resins in different polymerization modes immersed in different staining solutions before and after brushing. Disc-shaped specimens (n = 120) were prepared from two composite resins based on filler particle size: nano-filled (Filtek Z350, shade A1, 3M ESPE) and nano-hybrid (Spectra ST-HV, shade A1, Dentsply Sirona) composite resins (n = 60 per composite type). Specimens of each resin type were photopolymerized using the following polymerization modes: LED conventional, ramp, and pulse (n = 20 specimens per resin type and LED mode). After preparation, baseline color of the specimens was evaluated using a spectrophotometer (Easyshade V, VITA), and color change was evaluated using the CIE L*a*b* formula. Specimens were soaked in distilled water for 4 weeks in separate containers. The specimens from each polymerization-mode group were separated into two groups of 10 specimens; one group was stored in tea and the other group was stored in cola, each 1 hour daily for 4 weeks. After 4 weeks, the color was measured again. The specimens were brushed for 2 minutes under 200-g weight using an electronically powered toothbrush on the polymerized side of the specimen. The color was reevaluated immediately after brushing. Color-difference data (ΔE) between groups were analyzed by one-way analysis of variance for main comparison and by independent t test for color change after brushing. Nano-filled composite resin was more color-stable than nano-hybrid composite resin (P < .001), regardless of the staining media. For both composite resin types, the conventional polymerization method produced a more color-stable result (P < .0001). ΔE after brushing was reduced significantly (P < .0001). Both staining solutions have significant effects on color change, with tea staining more than cola (P < .0001). Nanofilled composite resin had greater color stability than nano-hybrid composite resin after immersion in staining solutions. Polymerization mode influences the color stability of both composite resin types. Int J Periodontics Restorative Dent 2023;43:247-255. doi: 10.11607/prd.6427.

A Scoping Review on the Polymerization of Resin-Matrix Cements Used in Restorative Dentistry.

In dentistry, clinicians mainly use dual-cured or light-cured resin-matrix cements to achieve a proper polymerization of the organic matrix leading to enhanced physical properties of the cement. However, several parameters can affect the polymerization of resin-matrix cements. The main aim of the present study was to perform a scoping review on the degree of conversion (DC) of the organic matrix, the polymerization, and the light transmittance of different resin-matrix cements used in dentistry. A search was performed on PubMed using a combination of the following key terms: degree of conversion, resin cements, light transmittance, polymerization, light curing, and thickness. Articles in the English language published up to November 2022 were selected. The selected studies' results demonstrated that restorative structures with a thickness higher than 1.5 mm decrease the light irradiance towards the resin-matrix cement. A decrease in light transmission provides a low energy absorption through the resin cement leading to a low DC percentage. On the other hand, the highest DC percentages, ranging between 55 and 75%, have been reported for dual-cured resin-matrix cements, although the polymerization mode and exposure time also influence the DC of monomers. Thus, the polymerization of resin-matrix cements can be optimized taking into account different parameters of light-curing, such as adequate light distance, irradiance, exposure time, equipment, and wavelength. Then, optimum physical properties are achieved that provide a long-term clinical performance of the cemented restorative materials.

Photoinitiated Cationic Ring-Opening Polymerization of Octamethylcyclotetrasiloxane.

Photochemical techniques have recently been revitalized as they can readily be adapted to different polymerization modes to yield a wide range of complex macromolecular structures. However, the implementation of the photoinduced cationic methods in the polymerization of cyclic siloxane monomers has scarcely been investigated. Octamethylcyclotetrasiloxane (D4) is an important monomer for the synthesis of polydimethylsiloxane (PDMS) and its copolymers. In this study, the cationic ring-opening polymerization (ROP) of D4, initiated by diphenyl iodonium hexafluorophosphate (DPI), has been studied. Both direct and indirect initiating systems acting at broad wavelength using benzophenone and pyrene were investigated. In both systems, photochemically generated protonic acids and silylium cations are responsible for the polymerization. The kinetics of the polymerization are followed by viscosimetry and GPC analyses. The reported approach may overcome the problems associated with conventional methods and therefore represents industrial importance for the fabrication of polysiloxanes.

Self-Adaptive Re-Organization Enables Polythiophene as an Extraordinary Cathode Material for Aluminum-Ion Batteries with a Cycle Life of 100 000 Cycles.

Aluminum-ion batteries (AIBs) have attracted great attentions in recent years. Organic materials such as polythiophene (PT) are promising cathode for AIBs. However, the capacity and cyclic stability of conventional organic cathode such as PT are limited by the inadequate degree of reaction and the unstable nature of organic materials. To obtain high-performance organic cathode, a new PT with the ability of self-adaptive re-organization was prepared. During cycling, its molecular chain can be re-organized, and the polymerization mode will change from Cα -Cα (α-PT) to Cβ -Cβ (β-PT). This change leads to smaller steric hindrance and faster kinetics during ion insertion which can lower the reaction energy barrier and stabilize the molecular structure. Benefited by this, AIBs with this cathode can deliver a specific capacity of 180 mAh g-1 (@2 A g-1 ) and a superb stability of 100 000 cycles at 10 A g-1 . High energy density and power density can also be achieved with this cathode.