Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Organic Compounds03:02

Organic Compounds

55.9K
All living things are formed mostly of carbon compounds called organic compounds. The category of organic compounds includes both natural and synthetic compounds that contain carbon. Although a single, precise definition has yet to be identified by the chemistry community, most agree that a defining trait of organic molecules is the presence of carbon as the principal element, bonded to hydrogen and other carbon atoms. However, some carbon-containing compounds such as carbonates, cyanides, and...
55.9K
Carboxylic Acid Derivatives: Overview01:15

Carboxylic Acid Derivatives: Overview

5.0K
Carboxylic acid derivatives are formed by replacing the hydroxyl group of carboxylic acids with a different functional group. The most common carboxylic acid derivatives are:
5.0K
Aryldiazonium Salts to Azo Dyes: Diazo Coupling01:11

Aryldiazonium Salts to Azo Dyes: Diazo Coupling

3.5K
The reaction of weakly electrophilic aryldiazonium (also called arenediazonium) salts with highly activated aromatic compounds leads to the formation of products with an —N=N— link, called an azo linkage. This reaction, presented in Figure 1, is known as diazo coupling and occurs without the loss of the nitrogen atoms of the aryldiazonium salt. Highly activated aromatic compounds such as phenols or arylamines favor the diazo coupling reaction. The coupling generally occurs at the para...
3.5K
Substituent Effects on Acidity of Carboxylic Acids01:31

Substituent Effects on Acidity of Carboxylic Acids

7.6K
The acidity of carboxylic acids is influenced by the nature of the substituents bounded to the functional group. The acid strength is determined by the stability of the carboxylate anion—the conjugate base formed by dissociating the corresponding carboxylic acid.
7.6K
Diazonium Group Substitution: –OH and –H01:19

Diazonium Group Substitution: –OH and –H

3.2K
Nitrous acid, a weak acid, is prepared in situ via the reaction of sodium nitrite with a strong acid under cold conditions. This nitrous acid prepared in situ reacts with primary arylamines to form arenediazonium salts. Such reactions are known as diazotization reactions. As shown in Figure 1, the formation of arenediazonium salts begins with the decomposition of nitrous acid in an acidic solution to give nitrosonium ions.
3.2K
Structures of Carboxylic Acid Derivatives01:28

Structures of Carboxylic Acid Derivatives

3.6K
Structure of Carboxylic Acid Derivatives
Carboxylic acid derivatives contain an acyl group attached to a heteroatom such as chlorine, oxygen, or nitrogen. The carbonyl carbon and oxygen are both sp2-hybridized with an unhybridized p orbital.
The three sp2 orbitals of the carbonyl carbon form three σ bonds, one each with the carbonyl oxygen, the α carbon, and the heteroatom, whereas the other two sp2 orbitals of the carbonyl oxygen are occupied by the lone pairs. Further, the unhybridized p...
3.6K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Hexaallylaminocyclotriphosphazene-Modified Dental Compositions for 3D Printing of Dental Crowns.

Polymers·2026
Same author

Wound Gel with Antimicrobial Effects Based on Polyvinyl Alcohol and Functional Aryloxycyclotriphosphazene.

Polymers·2023
Same author

Curing of DER-331 Epoxy Resin with Arylaminocyclotriphosphazenes Based on o-, m-, and p-methylanilines.

Polymers·2022
Same author

Nanoaggregates of Biphilic Carboxyl-Containing Copolymers as Carriers for Ionically Bound Doxorubicin.

Materials (Basel, Switzerland)·2022
Same author

Polymeric Dental Nanomaterials: Antimicrobial Action.

Polymers·2022
Same author

Luminescent Coatings Based on (3-Aminopropyl)triethoxysilane and Europium Complex β-Diketophosphazene.

Polymers·2022

Related Experiment Video

Updated: Dec 20, 2025

2-Methacryloyloxyethyl Phosphorylcholine Polymer Treatment of Complete Dentures to Inhibit Denture Plaque Deposition
06:02

2-Methacryloyloxyethyl Phosphorylcholine Polymer Treatment of Complete Dentures to Inhibit Denture Plaque Deposition

Published on: December 26, 2016

10.7K

Dental Composition Modified with Aryloxyphosphazene Containing Carboxyl Groups.

Evgeniy M Chistyakov1, Natalya Kolpinskaya1, Vera Posokhova2

  • 1D.Mendeleev University of Chemical Technology of Russia, Miusskaya sq. 9, 125047 Moscow, Russia.

Polymers
|May 24, 2020
PubMed
Summary

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.

Keywords:
adhesioncomposite materialmodificationphosphazenerestorative dentistrydental composite materialsphosphazene dental modifiersdental adhesion enhancementwater sorption reduction

Frequently Asked Questions

More Related Videos

Development of Amelogenin-chitosan Hydrogel for In Vitro Enamel Regrowth with a Dense Interface
08:26

Development of Amelogenin-chitosan Hydrogel for In Vitro Enamel Regrowth with a Dense Interface

Published on: July 10, 2014

15.4K
Systematic Approach to Identify Novel Antimicrobial and Antibiofilm Molecules from Plants' Extracts and Fractions to Prevent Dental Caries
08:20

Systematic Approach to Identify Novel Antimicrobial and Antibiofilm Molecules from Plants' Extracts and Fractions to Prevent Dental Caries

Published on: March 31, 2021

6.7K

Related Experiment Videos

Last Updated: Dec 20, 2025

2-Methacryloyloxyethyl Phosphorylcholine Polymer Treatment of Complete Dentures to Inhibit Denture Plaque Deposition
06:02

2-Methacryloyloxyethyl Phosphorylcholine Polymer Treatment of Complete Dentures to Inhibit Denture Plaque Deposition

Published on: December 26, 2016

10.7K
Development of Amelogenin-chitosan Hydrogel for In Vitro Enamel Regrowth with a Dense Interface
08:26

Development of Amelogenin-chitosan Hydrogel for In Vitro Enamel Regrowth with a Dense Interface

Published on: July 10, 2014

15.4K
Systematic Approach to Identify Novel Antimicrobial and Antibiofilm Molecules from Plants' Extracts and Fractions to Prevent Dental Caries
08:20

Systematic Approach to Identify Novel Antimicrobial and Antibiofilm Molecules from Plants' Extracts and Fractions to Prevent Dental Caries

Published on: March 31, 2021

6.7K

Area of Science:

  • Dental materials science
  • Polymer chemistry in restorative dentistry
  • Biocompatible material development

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.