FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2065493838> ?p ?o ?g. }

• W2065493838 endingPage "576" @default.
• W2065493838 startingPage "569" @default.
• W2065493838 abstract "A new glycerol-based dimethacrylate monomer with an aromatic carboxylic acid, 2-((1,3-bis(methacryloyloxy)propan-2-yloxy)carbonyl)benzoic acid (BMPB), was synthesized, characterized, and proposed as a possible dental co-monomer for dentin adhesives. Dentin adhesives containing 2-hydroxyethyl methacrylate (HEMA) and 2,2-bis[4-(2-hydroxy-3-methacryloxypropoxy) phenyl]propane (BisGMA) in addition to BMPB were formulated with water at 0, 5, 10, and 15 wt % to simulate wet, oral conditions, and photo-polymerized. Adhesives were characterized with regard to viscosity, real-time photopolymerization behavior, dynamic mechanical analysis, and microscale 3D internal morphologies and compared with HEMA/BisGMA controls. When formulated under wet conditions, the experimental adhesives showed lower viscosities (0.04–0.07 Pa s) as compared to the control (0.09–0.12 Pa s). The experimental adhesives showed higher glass transition temperature (146–157°C), degree of conversion (78–89%), and rubbery moduli (33–36 MPa), and improved water miscibility (no voids) as compared to the controls (123–135°C, 67–71%, 15–26 MPa, and voids, respectively). The enhanced properties of these adhesives suggest that BMPB with simple, straightforward synthesis is a promising photocurable co-monomer for dental restorative materials. © 2011 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater 100B: 569–576, 2012." @default.
• W2065493838 created "2016-06-24" @default.
• W2065493838 creator A5017997193 @default.
• W2065493838 creator A5035690766 @default.
• W2065493838 creator A5043513911 @default.
• W2065493838 creator A5044702300 @default.
• W2065493838 creator A5044728655 @default.
• W2065493838 creator A5062950866 @default.
• W2065493838 date "2011-11-24" @default.
• W2065493838 modified "2023-10-16" @default.
• W2065493838 title "Synthesis and evaluation of novel dental monomer with branched aromatic carboxylic acid group" @default.
• W2065493838 cites W1660751430 @default.
• W2065493838 cites W1967102737 @default.
• W2065493838 cites W1972507080 @default.
• W2065493838 cites W1977624432 @default.
• W2065493838 cites W1981455089 @default.
• W2065493838 cites W1990409648 @default.
• W2065493838 cites W1990684715 @default.
• W2065493838 cites W1991383023 @default.
• W2065493838 cites W1993011194 @default.
• W2065493838 cites W1997997645 @default.
• W2065493838 cites W2026535730 @default.
• W2065493838 cites W2050661087 @default.
• W2065493838 cites W2051545426 @default.
• W2065493838 cites W2057559281 @default.
• W2065493838 cites W2073761677 @default.
• W2065493838 cites W2073997136 @default.
• W2065493838 cites W2079193522 @default.
• W2065493838 cites W2081235275 @default.
• W2065493838 cites W2087689999 @default.
• W2065493838 cites W2088056759 @default.
• W2065493838 cites W2088995204 @default.
• W2065493838 cites W2097274883 @default.
• W2065493838 cites W2104572739 @default.
• W2065493838 cites W2115614531 @default.
• W2065493838 cites W2116440357 @default.
• W2065493838 cites W2123947437 @default.
• W2065493838 cites W2132607320 @default.
• W2065493838 cites W2136010571 @default.
• W2065493838 cites W2141065279 @default.
• W2065493838 cites W2142052848 @default.
• W2065493838 cites W2149386396 @default.
• W2065493838 doi "https://doi.org/10.1002/jbm.b.31987" @default.
• W2065493838 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5515472" @default.
• W2065493838 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/22114017" @default.
• W2065493838 hasPublicationYear "2011" @default.
• W2065493838 type Work @default.
• W2065493838 sameAs 2065493838 @default.
• W2065493838 citedByCount "23" @default.
• W2065493838 countsByYear W20654938382012 @default.
• W2065493838 countsByYear W20654938382013 @default.
• W2065493838 countsByYear W20654938382014 @default.
• W2065493838 countsByYear W20654938382015 @default.
• W2065493838 countsByYear W20654938382016 @default.
• W2065493838 countsByYear W20654938382019 @default.
• W2065493838 countsByYear W20654938382020 @default.
• W2065493838 countsByYear W20654938382021 @default.
• W2065493838 countsByYear W20654938382022 @default.
• W2065493838 crossrefType "journal-article" @default.
• W2065493838 hasAuthorship W2065493838A5017997193 @default.
• W2065493838 hasAuthorship W2065493838A5035690766 @default.
• W2065493838 hasAuthorship W2065493838A5043513911 @default.
• W2065493838 hasAuthorship W2065493838A5044702300 @default.
• W2065493838 hasAuthorship W2065493838A5044728655 @default.
• W2065493838 hasAuthorship W2065493838A5062950866 @default.
• W2065493838 hasBestOaLocation W20654938382 @default.
• W2065493838 hasConcept C110884469 @default.
• W2065493838 hasConcept C122865956 @default.
• W2065493838 hasConcept C127413603 @default.
• W2065493838 hasConcept C132050475 @default.
• W2065493838 hasConcept C15487406 @default.
• W2065493838 hasConcept C159985019 @default.
• W2065493838 hasConcept C166940927 @default.
• W2065493838 hasConcept C178790620 @default.
• W2065493838 hasConcept C185592680 @default.
• W2065493838 hasConcept C188027245 @default.
• W2065493838 hasConcept C192562407 @default.
• W2065493838 hasConcept C2778844314 @default.
• W2065493838 hasConcept C2779227376 @default.
• W2065493838 hasConcept C2779263046 @default.
• W2065493838 hasConcept C42360764 @default.
• W2065493838 hasConcept C44228677 @default.
• W2065493838 hasConcept C521977710 @default.
• W2065493838 hasConcept C68928338 @default.
• W2065493838 hasConceptScore W2065493838C110884469 @default.
• W2065493838 hasConceptScore W2065493838C122865956 @default.
• W2065493838 hasConceptScore W2065493838C127413603 @default.
• W2065493838 hasConceptScore W2065493838C132050475 @default.
• W2065493838 hasConceptScore W2065493838C15487406 @default.
• W2065493838 hasConceptScore W2065493838C159985019 @default.
• W2065493838 hasConceptScore W2065493838C166940927 @default.
• W2065493838 hasConceptScore W2065493838C178790620 @default.
• W2065493838 hasConceptScore W2065493838C185592680 @default.
• W2065493838 hasConceptScore W2065493838C188027245 @default.
• W2065493838 hasConceptScore W2065493838C192562407 @default.
• W2065493838 hasConceptScore W2065493838C2778844314 @default.
• W2065493838 hasConceptScore W2065493838C2779227376 @default.
• W2065493838 hasConceptScore W2065493838C2779263046 @default.

• next