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Polymerizable thioureas as innovative reducing agents for self-cured and dual-cured dental materials
To evaluate polymerizable acylthioureas as reducing agents in two-component dental materials. Acylthioureas 1 and 2 were synthesized and characterized by H and C NMR spectroscopy. Self-cured composites based on the redox initiator system cumene hydroperoxide/acylthiourea 1 or 2/copper(II) acetylacet...
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Published in: | Dental materials 2022-07, Vol.38 (7), p.1108-1116 |
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creator | Lamparth, Iris Fässler, Pascal Schnur, Thomas Thetiot, Estelle Lalevée, Jacques Catel, Yohann |
description | To evaluate polymerizable acylthioureas as reducing agents in two-component dental materials.
Acylthioureas 1 and 2 were synthesized and characterized by
H and
C NMR spectroscopy. Self-cured composites based on the redox initiator system cumene hydroperoxide/acylthiourea 1 or 2/copper(II) acetylacetonate were formulated. Various amounts of cumene hydroperoxide, acylthiourea and copper(II) acetylacetonate were used. An equimolar cumene hydroperoxide/acylthiourea ratio was selected for each self-cured composite. The reactivity and the final double-bond conversions obtained with these two-component materials was assessed using RT-FTIR spectroscopy. The flexural strength and modulus were measured using a three-point bending setup, after storage of the specimens for 45 min at 37 °C (dry) and for 24 h in water at 37 °C. The working time of each composite was determined using an oscillating rheometer.
Acylthioureas 1 and 2 were synthesized in three to four steps. In combination with cumene hydroperoxide and copper(II) acetylacetonate, both prepared compounds were found to be effective reducing agents. The higher the amount of cumene hydroperoxide and acylthiourea in the self-cured composite, the higher the flexural modulus and the faster the polymerization (lower working times). Similarly, it was shown that increased copper(II) acetylacetonate amounts result in an acceleration of the curing as well as in an improvement of the mechanical properties. The self-cured composite containing 1.25 wt% of cumene hydroperoxide in the monomer mixture of the first paste and 2.00 wt% of acylthiourea 1 in the monomer mixture of the second one provided excellent mechanical properties as well as an optimal working time.
Polymerizable acylthioureas can be used as reducing agents in two-component dental materials. Due to the presence of the methacrylate group, such structures should be efficiently incorporated into the network during polymerization and should not leach out of the composite after curing. As a result, such dental materials are not expected to exhibit bitterness properties. |
doi_str_mv | 10.1016/j.dental.2022.04.027 |
format | article |
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Acylthioureas 1 and 2 were synthesized and characterized by
H and
C NMR spectroscopy. Self-cured composites based on the redox initiator system cumene hydroperoxide/acylthiourea 1 or 2/copper(II) acetylacetonate were formulated. Various amounts of cumene hydroperoxide, acylthiourea and copper(II) acetylacetonate were used. An equimolar cumene hydroperoxide/acylthiourea ratio was selected for each self-cured composite. The reactivity and the final double-bond conversions obtained with these two-component materials was assessed using RT-FTIR spectroscopy. The flexural strength and modulus were measured using a three-point bending setup, after storage of the specimens for 45 min at 37 °C (dry) and for 24 h in water at 37 °C. The working time of each composite was determined using an oscillating rheometer.
Acylthioureas 1 and 2 were synthesized in three to four steps. In combination with cumene hydroperoxide and copper(II) acetylacetonate, both prepared compounds were found to be effective reducing agents. The higher the amount of cumene hydroperoxide and acylthiourea in the self-cured composite, the higher the flexural modulus and the faster the polymerization (lower working times). Similarly, it was shown that increased copper(II) acetylacetonate amounts result in an acceleration of the curing as well as in an improvement of the mechanical properties. The self-cured composite containing 1.25 wt% of cumene hydroperoxide in the monomer mixture of the first paste and 2.00 wt% of acylthiourea 1 in the monomer mixture of the second one provided excellent mechanical properties as well as an optimal working time.
Polymerizable acylthioureas can be used as reducing agents in two-component dental materials. Due to the presence of the methacrylate group, such structures should be efficiently incorporated into the network during polymerization and should not leach out of the composite after curing. As a result, such dental materials are not expected to exhibit bitterness properties.</description><identifier>ISSN: 0109-5641</identifier><identifier>EISSN: 1879-0097</identifier><identifier>DOI: 10.1016/j.dental.2022.04.027</identifier><identifier>PMID: 35589440</identifier><language>eng</language><publisher>England: Elsevier BV</publisher><subject>Bitterness ; Copper ; Cumene ; Cumene hydroperoxide ; Curing ; Dental materials ; Dental restorative materials ; Flexural strength ; Magnetic resonance spectroscopy ; Mechanical properties ; Mixtures ; Modulus of rupture in bending ; Monomers ; NMR ; NMR spectroscopy ; Nuclear magnetic resonance ; Polymerization ; Reducing agents ; Spectroscopy ; Spectrum analysis ; Synthesis ; Working hours</subject><ispartof>Dental materials, 2022-07, Vol.38 (7), p.1108-1116</ispartof><rights>Copyright © 2022 Elsevier Inc. All rights reserved.</rights><rights>Copyright Elsevier BV Jul 2022</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c265t-158831a8e0c0fe0ff4d4424f59467e2e6be722da1c6eda5234c1b5f00cf37ba53</citedby><cites>FETCH-LOGICAL-c265t-158831a8e0c0fe0ff4d4424f59467e2e6be722da1c6eda5234c1b5f00cf37ba53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35589440$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lamparth, Iris</creatorcontrib><creatorcontrib>Fässler, Pascal</creatorcontrib><creatorcontrib>Schnur, Thomas</creatorcontrib><creatorcontrib>Thetiot, Estelle</creatorcontrib><creatorcontrib>Lalevée, Jacques</creatorcontrib><creatorcontrib>Catel, Yohann</creatorcontrib><title>Polymerizable thioureas as innovative reducing agents for self-cured and dual-cured dental materials</title><title>Dental materials</title><addtitle>Dent Mater</addtitle><description>To evaluate polymerizable acylthioureas as reducing agents in two-component dental materials.
Acylthioureas 1 and 2 were synthesized and characterized by
H and
C NMR spectroscopy. Self-cured composites based on the redox initiator system cumene hydroperoxide/acylthiourea 1 or 2/copper(II) acetylacetonate were formulated. Various amounts of cumene hydroperoxide, acylthiourea and copper(II) acetylacetonate were used. An equimolar cumene hydroperoxide/acylthiourea ratio was selected for each self-cured composite. The reactivity and the final double-bond conversions obtained with these two-component materials was assessed using RT-FTIR spectroscopy. The flexural strength and modulus were measured using a three-point bending setup, after storage of the specimens for 45 min at 37 °C (dry) and for 24 h in water at 37 °C. The working time of each composite was determined using an oscillating rheometer.
Acylthioureas 1 and 2 were synthesized in three to four steps. In combination with cumene hydroperoxide and copper(II) acetylacetonate, both prepared compounds were found to be effective reducing agents. The higher the amount of cumene hydroperoxide and acylthiourea in the self-cured composite, the higher the flexural modulus and the faster the polymerization (lower working times). Similarly, it was shown that increased copper(II) acetylacetonate amounts result in an acceleration of the curing as well as in an improvement of the mechanical properties. The self-cured composite containing 1.25 wt% of cumene hydroperoxide in the monomer mixture of the first paste and 2.00 wt% of acylthiourea 1 in the monomer mixture of the second one provided excellent mechanical properties as well as an optimal working time.
Polymerizable acylthioureas can be used as reducing agents in two-component dental materials. Due to the presence of the methacrylate group, such structures should be efficiently incorporated into the network during polymerization and should not leach out of the composite after curing. As a result, such dental materials are not expected to exhibit bitterness properties.</description><subject>Bitterness</subject><subject>Copper</subject><subject>Cumene</subject><subject>Cumene hydroperoxide</subject><subject>Curing</subject><subject>Dental materials</subject><subject>Dental restorative materials</subject><subject>Flexural strength</subject><subject>Magnetic resonance spectroscopy</subject><subject>Mechanical properties</subject><subject>Mixtures</subject><subject>Modulus of rupture in bending</subject><subject>Monomers</subject><subject>NMR</subject><subject>NMR spectroscopy</subject><subject>Nuclear magnetic resonance</subject><subject>Polymerization</subject><subject>Reducing agents</subject><subject>Spectroscopy</subject><subject>Spectrum analysis</subject><subject>Synthesis</subject><subject>Working hours</subject><issn>0109-5641</issn><issn>1879-0097</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNpdkUtLJDEQx8Piso6PbyAS8OKleyvpPLqPIr5A0MPuOaSTivbQD026hdlPvxlm9CAUFAW_-tfjT8gZg5IBU7_Xpcdxtn3JgfMSRAlc_yArVuumAGj0AVkBg6aQSrBDcpTSGgAEb9gvclhJWTdCwIr456nfDBi7f7btkc6v3bREtInm6MZx-rBz94E0ol9cN75Q-5KHJhqmSBP2oXCZ9tSOnvrF9vtytxgd7JyFbZ9OyM-QE57u8zH5e3vz5_q-eHy6e7i-eiwcV3IumKzritkawUFACEF4IbgIshFKI0fVoubcW-YUeit5JRxrZQBwodKtldUxudzpvsXpfcE0m6FLDvvejjgtyXCltG645pDRi2_oOh8-5u0ylZEGQIlMiR3l4pRSxGDeYjfYuDEMzNYFsza7Y83WBQPCZBdy2_lefGkH9F9Nn2-v_gM4X4Yi</recordid><startdate>20220701</startdate><enddate>20220701</enddate><creator>Lamparth, Iris</creator><creator>Fässler, Pascal</creator><creator>Schnur, Thomas</creator><creator>Thetiot, Estelle</creator><creator>Lalevée, Jacques</creator><creator>Catel, Yohann</creator><general>Elsevier BV</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QO</scope><scope>7QP</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>JG9</scope><scope>JQ2</scope><scope>K9.</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20220701</creationdate><title>Polymerizable thioureas as innovative reducing agents for self-cured and dual-cured dental materials</title><author>Lamparth, Iris ; Fässler, Pascal ; Schnur, Thomas ; Thetiot, Estelle ; Lalevée, Jacques ; Catel, Yohann</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c265t-158831a8e0c0fe0ff4d4424f59467e2e6be722da1c6eda5234c1b5f00cf37ba53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Bitterness</topic><topic>Copper</topic><topic>Cumene</topic><topic>Cumene hydroperoxide</topic><topic>Curing</topic><topic>Dental materials</topic><topic>Dental restorative materials</topic><topic>Flexural strength</topic><topic>Magnetic resonance spectroscopy</topic><topic>Mechanical properties</topic><topic>Mixtures</topic><topic>Modulus of rupture in bending</topic><topic>Monomers</topic><topic>NMR</topic><topic>NMR spectroscopy</topic><topic>Nuclear magnetic resonance</topic><topic>Polymerization</topic><topic>Reducing agents</topic><topic>Spectroscopy</topic><topic>Spectrum analysis</topic><topic>Synthesis</topic><topic>Working hours</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lamparth, Iris</creatorcontrib><creatorcontrib>Fässler, Pascal</creatorcontrib><creatorcontrib>Schnur, Thomas</creatorcontrib><creatorcontrib>Thetiot, Estelle</creatorcontrib><creatorcontrib>Lalevée, Jacques</creatorcontrib><creatorcontrib>Catel, Yohann</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Dental materials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lamparth, Iris</au><au>Fässler, Pascal</au><au>Schnur, Thomas</au><au>Thetiot, Estelle</au><au>Lalevée, Jacques</au><au>Catel, Yohann</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Polymerizable thioureas as innovative reducing agents for self-cured and dual-cured dental materials</atitle><jtitle>Dental materials</jtitle><addtitle>Dent Mater</addtitle><date>2022-07-01</date><risdate>2022</risdate><volume>38</volume><issue>7</issue><spage>1108</spage><epage>1116</epage><pages>1108-1116</pages><issn>0109-5641</issn><eissn>1879-0097</eissn><abstract>To evaluate polymerizable acylthioureas as reducing agents in two-component dental materials.
Acylthioureas 1 and 2 were synthesized and characterized by
H and
C NMR spectroscopy. Self-cured composites based on the redox initiator system cumene hydroperoxide/acylthiourea 1 or 2/copper(II) acetylacetonate were formulated. Various amounts of cumene hydroperoxide, acylthiourea and copper(II) acetylacetonate were used. An equimolar cumene hydroperoxide/acylthiourea ratio was selected for each self-cured composite. The reactivity and the final double-bond conversions obtained with these two-component materials was assessed using RT-FTIR spectroscopy. The flexural strength and modulus were measured using a three-point bending setup, after storage of the specimens for 45 min at 37 °C (dry) and for 24 h in water at 37 °C. The working time of each composite was determined using an oscillating rheometer.
Acylthioureas 1 and 2 were synthesized in three to four steps. In combination with cumene hydroperoxide and copper(II) acetylacetonate, both prepared compounds were found to be effective reducing agents. The higher the amount of cumene hydroperoxide and acylthiourea in the self-cured composite, the higher the flexural modulus and the faster the polymerization (lower working times). Similarly, it was shown that increased copper(II) acetylacetonate amounts result in an acceleration of the curing as well as in an improvement of the mechanical properties. The self-cured composite containing 1.25 wt% of cumene hydroperoxide in the monomer mixture of the first paste and 2.00 wt% of acylthiourea 1 in the monomer mixture of the second one provided excellent mechanical properties as well as an optimal working time.
Polymerizable acylthioureas can be used as reducing agents in two-component dental materials. Due to the presence of the methacrylate group, such structures should be efficiently incorporated into the network during polymerization and should not leach out of the composite after curing. As a result, such dental materials are not expected to exhibit bitterness properties.</abstract><cop>England</cop><pub>Elsevier BV</pub><pmid>35589440</pmid><doi>10.1016/j.dental.2022.04.027</doi><tpages>9</tpages></addata></record> |
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subjects | Bitterness Copper Cumene Cumene hydroperoxide Curing Dental materials Dental restorative materials Flexural strength Magnetic resonance spectroscopy Mechanical properties Mixtures Modulus of rupture in bending Monomers NMR NMR spectroscopy Nuclear magnetic resonance Polymerization Reducing agents Spectroscopy Spectrum analysis Synthesis Working hours |
title | Polymerizable thioureas as innovative reducing agents for self-cured and dual-cured dental materials |
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