Organic Compounds
Carboxylic Acid Derivatives: Overview
Aryldiazonium Salts to Azo Dyes: Diazo Coupling
Substituent Effects on Acidity of Carboxylic Acids
Diazonium Group Substitution: –OH and –H
Structures of Carboxylic Acid Derivatives
You might also read
Articles linked to this work by shared authors, journal, and citation graph.
Updated: Dec 20, 2025

2-Methacryloyloxyethyl Phosphorylcholine Polymer Treatment of Complete Dentures to Inhibit Denture Plaque Deposition
Published on: December 26, 2016
Evgeniy M Chistyakov1, Natalya Kolpinskaya1, Vera Posokhova2
1D.Mendeleev University of Chemical Technology of Russia, Miusskaya sq. 9, 125047 Moscow, Russia.
This study introduces a new dental composite modifier made from cyclotriphosphazene compounds with specific functional groups. The modifier was tested for its ability to improve adhesion and reduce water absorption in dental restorations. Using NMR and mass spectrometry, the researchers confirmed the modifier's structure. They found that adding the modifier increased adhesion to dental tissues and reduced water sorption. Mechanical properties like elastic modulus and microhardness also improved with higher modifier content. The modified compositions met international standards for dental materials. These findings suggest that this new modifier could lead to more durable and effective dental restorations.
08:26Development of Amelogenin-chitosan Hydrogel for In Vitro Enamel Regrowth with a Dense Interface
Published on: July 10, 2014
08:20Systematic Approach to Identify Novel Antimicrobial and Antibiofilm Molecules from Plants' Extracts and Fractions to Prevent Dental Caries
Published on: March 31, 2021
Area of Science:
Background:
Current dental restorative materials face limitations in adhesion and water resistance. While bis-GMA and TGM-3 are widely used, their performance is constrained by insufficient bonding to dental tissues and high water sorption. Prior research has shown that modifying dental composites can improve mechanical and chemical properties. However, no prior work had resolved the specific impact of arylphosphazene derivatives on these properties. This gap motivated the development of a new modifier to enhance adhesion and reduce water absorption. The need for durable, biocompatible dental composites remains unmet in clinical settings. No prior work had tested the effects of β-carboxyethenylphenoxy moieties in dental compositions. The challenge lies in balancing mechanical strength with hydrophobicity. This study addresses these limitations through a novel chemical approach.
Purpose Of The Study:
The study aimed to develop a dental composition modifier using cyclotriphosphazene derivatives with specific functional groups. The goal was to improve adhesion and reduce water sorption in dental restorations. The research focused on evaluating the effects of arylphosphazene compounds on composite properties. The authors sought to determine optimal mixing conditions using thermal analysis. They also aimed to assess compliance with ISO 4049:2019 standards. The study's motivation was to address known limitations in current dental materials. The authors proposed that arylphosphazene could enhance mechanical and chemical stability. This approach was intended to provide a practical solution for clinical use.
Main Methods:
The modifier was synthesized using cyclotriphosphazene compounds with 4-allyl-2-methoxyphenoxy and β-carboxyethenylphenoxy groups. Structural confirmation was achieved through 1H and 13C NMR spectroscopy. MALDI-TOF mass spectrometry was used to verify molecular weight and purity. The modifier was combined with bis-GMA and TGM-3 dental mixtures. Differential scanning calorimetry (DSC) determined optimal mixing conditions. Cured compositions were tested for mechanical and chemical properties. Compliance with ISO 4049:2019 was evaluated through standardized methods. The study focused on adhesion, water sorption, and mechanical strength.
Main Results:
The modified dental compositions showed increased adhesion to dental tissues and deeper cure depth. Water sorption and solubility were significantly reduced compared to unmodified samples. Elastic modulus values increased with higher modifier content. Destructive compressive stress and microhardness also improved. The optimal modifier concentration was determined through DSC analysis. The compositions met the ISO 4049:2019 requirements for restorative dental materials. Structural analysis confirmed successful synthesis of the modifier. The study demonstrated that arylphosphazene derivatives enhance key dental composite properties.
Conclusions:
The authors concluded that the arylphosphazene modifier improves adhesion and reduces water absorption in dental composites. They proposed that this enhancement is due to the functional groups in the modifier. The study showed that increasing modifier content correlates with better mechanical properties. The authors suggested that these findings could lead to more durable dental restorations. They emphasized that the modified compositions comply with ISO standards. No prior work had demonstrated such a direct relationship between modifier content and performance. The results suggest practical applications in clinical dentistry. The authors proposed further investigation into long-term biocompatibility.
The modifier contains functional groups that enhance bonding to dental tissues, as shown by increased adhesion in modified compositions.
Structure was verified using <sup>1</sup>H and <sup>13</sup>C NMR spectroscopy and MALDI-TOF mass spectrometry.
DSC was used to determine optimal mixing conditions for the modifier and dental composite base materials.
Adhesion, water sorption, solubility, elastic modulus, compressive stress, and microhardness were assessed.
Higher modifier content increased elastic modulus, compressive stress, and microhardness values.
The authors suggest that these modifications could lead to longer-lasting dental restorations due to improved adhesion and water resistance.