Benzoyl germanium derivatives as novel visible light photoinitiators for dental materials

被引:219
作者
Moszner, Norbert [1 ]
Fischer, Urs Karl [1 ]
Ganster, Beate [2 ]
Liska, Robert [2 ]
Rheinberger, Volker [1 ]
机构
[1] Ivoclar Vivadent AG, Res & Dev, FL-9494 Schaan, Liechtenstein
[2] Vienna Univ Technol, Inst Appl Synthet Chem, A-1060 Vienna, Austria
关键词
photopolymerization; camphorquinone; visible light photoinitiator; composites; dimethacrylates;
D O I
10.1016/j.dental.2007.11.004
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objectives. The objective of this study was to investigate the use of benzoyl germanium derivatives as a novel visible light photoinitiator of resin-based dental composites. Selected mechanical properties, such as flexural strength and flexural modulus, setting time, storage stability, and UV light stability, of the composites based on the novel photoinitiators benzoyltrimethylgermane (BTMGe) or dibenzoyldiethylgermane (DBDEGe) were investigated and compared to the properties of materials that are cured with a mixture of camphorquinone (CQ) and ethyl 4-(N,N-dimethylamino)benzoate (EMBO). Methods. The flexural strength and flexural modulus of elasticity were determined according to ISO 4049. For this purpose, test specimens (2 mm x 2 mm x 25 mm) of the composites investigated were prepared in stainless steel moulds and light-cured (150 mW/cm(2), 2 s x 180 s). The flexural strength and flexural modulus of elasticity were measured after immersing the cured specimens in water for 24 h at 37 degrees C and in certain cases, after they had been boiled for 24 h in water. in addition, the setting time, curing depth, storage and UV stability of selected composites were determined. Results. The novel photoinitiators BTMGe or DBDEGe can be used to substitute the binary photoinitiator CQ/EMBO in visible light-cured restorative composites. Especially, DBDEGe showed a significantly higher photocuring activity in composites with a filler load of about 60 wt. % in comparison to that of CQ/EMBO. In addition, composites based on BTMGe or DBDEGe showed an improved UV stability and a storage stability comparable to that of CQ/EMBO-based composites. (c) 2007 Academy of Dental Materials. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:901 / 907
页数:7
相关论文
共 43 条
[21]  
ISODentistry, 2000, ISO 4049, V4049, P1
[22]   Camphorquinone-amines photoinitating systems for the initiation of free radical polymerization [J].
Jakubiak, J ;
Allonas, X ;
Fouassier, JP ;
Sionkowska, A ;
Andrzejewska, E ;
Linden, LÅ ;
Rabek, JF .
POLYMER, 2003, 44 (18) :5219-5226
[23]   Kinetic studies of a new photoinitiator hybrid system based on camphorquinone-N-phenylglicyne derivatives for laser polymerization of dental restorative and stereolithographic (3D) formulations [J].
Kucybala, Z ;
Pietrzak, M ;
Paczkowski, J ;
Linden, LA ;
Rabek, JF .
POLYMER, 1996, 37 (20) :4585-4591
[24]   REACTIVITY OF RADICALS DERIVED FROM DIMETHYLANILINES IN ACRYLIC PHOTOPOLYMERIZATION [J].
MATEO, JL ;
BOSCH, P ;
LOZANO, AE .
MACROMOLECULES, 1994, 27 (26) :7794-7799
[25]   DIRECT OBSERVATION OF GERMYL RADICALS BY A LASER-PHOTOLYSIS OF GERMYL KETONES [J].
MOCHIDA, K ;
ICHIKAWA, K ;
OKUI, S ;
SAKAGUCHI, Y ;
HAYASHI, H .
CHEMISTRY LETTERS, 1985, (09) :1433-1436
[26]   MECHANISMS OF PHOTOCHEMICAL REACTIONS IN SOLUTION .58. PHOTOREDUCTION OF CAMPHORQUINONE [J].
MONROE, BM ;
WEINER, SA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1969, 91 (02) :450-&
[27]   MECHANISMS OF PHOTOCHEMICAL REACTIONS IN SOLUTION .52. PHOTOREDUCTION OF CAMPHORQUINONE [J].
MONROE, BM ;
WEINER, SA ;
HAMMOND, GS .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1968, 90 (07) :1913-&
[28]   Chemical aspects of self-etching enamel-dentin adhesives: A systematic review [J].
Moszner, N ;
Salz, U ;
Zimmermann, J .
DENTAL MATERIALS, 2005, 21 (10) :895-910
[29]  
Moszner N, 1999, MACROMOL CHEM PHYSIC, V200, P1062, DOI 10.1002/(SICI)1521-3935(19990501)200:5<1062::AID-MACP1062>3.0.CO
[30]  
2-#