Patent Application
20180036209
This application claims priority to German patent application No. 102016214389.1 filed on Aug. 3, 2016, the disclosure of which is incorporated herein by reference in its entirety.
The present invention relates to dental materials based on monofunctional vinylcyclopropanes which have a high reactivity on radical polymerization. The materials are suitable in particular as cements, composites, coating materials, bondings and adhesives. In addition, they are suitable for the stereolithographic production of shaped bodies.
The polymerizable organic matrix of dental resins, cements or composites primarily consists of a mixture of monomers, initiator components, stabilizers and pigments (J. Viohl, K. Dermann, D. Quast, S. Venz, Die Chemie zahnärztlicher Füllungskunststoffe [The chemistry of dental filling plastics], Carl Hanser Verlag, Munich-Vienna 1986, 21-27). Mixtures of dimethacrylates are usually used as resins (cf. A. Peutzfeldt, Resin composites in dentistry: the monomer systems, Eur. J. Oral. Sci. 105 (1997) 97-116; J. W. Nicolson, H. M. Anstice, The chemistry of modern dental filling materials, J. Chem Ed. 76 (1999) 1497-1501; J. W. Stansburry, Curing dental resins and composites by photopolymerization, J. Esthet. Dent., 12 (2000) 300-308; N. Moszner, T. Hirt, New Polymer-Chemical Developments in Clinical Dental Polymer Materials: Enamel-Dentin Adhesives and Restorative Composites, J. Polym. Sci. Part A: Polym. Chem. 50 (2012) 4369-4402).
A main disadvantage of the methacrylates used is that their polymerization is accompanied by a volume contraction, so-called polymerization shrinkage. In the case of dental materials, polymerization shrinkage can lead, among other things, to disadvantageous shrinkage stresses and to marginal gap formation in filling composites, to reduced substrate adhesion in fixing composites or coating materials and to impairment of the dimensional stability of prosthesis plastics. In this connection, radically polymerizable cyclic monomers have received much attention in the preparation of dental materials due to the considerably lower polymerization shrinkage compared with linear monomers, such as e.g. methacrylates (cf. R. K. Sadhir, R. M. Luck, Expanding Monomers, CRC Press, Boca Raton etc. 1992).
With respect to other known ring-opening monomers, such as methylene group-containing spiro orthocarbonates (SOCs), spiro orthoesters (SOEs) or bicyclic orthoesters (BOEs), vinylcyclopropanes are characterized by the fact that the vinylcyclopropyl (VCP) group is not sensitive to moisture and that polymers with high molar masses which contain only hydrolytically stable C—C bonds in the main chain are obtained in their radical polymerization. (N. Moszner, F. Zeuner, T. Völkel, V. Rheinberger, Macromol. Chem. Phys. 200 (1999) 2173).
From DE 198 12 888 A1 vinylcyclopropane derivatives and in particular vinylcyclopropane (meth)acrylates are known which can be copolymerized with acrylates and methacrylates.
Moreover, vinylcyclopropanes with several polymerizable groups are known. F. Sanda, T. Takata, T. Endo, Macromolecules 27 (1994) 3986 describe 1-vinyl-5,7-dioxaspiro[2.5]octan-6-one, a hybrid monomer which contains a vinylcyclopropane group and a cyclic carbonate group, and T. Okazaki, F. Sanda, T. Endo, Macromolecules 28 (1995) 6026 describe 1,10-bis(vinyl)-4,8,12,15-tetraoxatrispiro[2.2.2.2.2.2]pentadecane, a monomer in which two vinylcyclopropane groups are joined to each other via a hydrolysis-sensitive spiroacetal unit. Compared with monofunctional vinylcyclopropanes, these compounds do not have any improved radical copolymerizability with (meth)acrylic compounds.
EP 0 798 286 A1 relates to multifunctional vinylcyclopropane derivatives with two to six vinylcyclopropane groups which enable the preparation of crosslinked polymers.
Using the example of the radical copolymerization of 1,1-bis(ethoxycarbonyl)-2-vinylcyclopropane with methyl methacrylate (MMA), it could be shown (F. Sanda, T. Takata, T. Endo, Macromolecules, 27 (1994) 3982) that compared with methacrylates, vinylcyclopropanes are characterized by a lower radical polymerization capability, which considerably restricts their practical use. It is particularly disadvantageous that the known 1,1-bis(alkoxycarbonyl)-2-vinylcyclopropanes which are easy to obtain have a low photopolymerization activity.
EP 1 413 569 A1 discloses dental materials based on bicyclic cyclopropane derivatives, such as e.g. 2-[bicyclo[3.1.0]hex-1-yl]-acrylic acid methyl ester, which exhibit an improved reactivity on radical polymerization (N. Moszner, F. Zeuner, U.K. Fischer, V. Rheinberger, A. de Meijere, V. Bagutski, Macromol. Rapid. Commun. 24 (2003) 269). However, these more reactive monofunctional bicyclic cyclopropyl acrylates can only be obtained with great difficulty.
The object of the invention is to provide radically polymerizable dental materials which shrink only slightly on radical polymerization and which have a high radical polymerization reactivity, in particular on photopolymerization. The dental materials are to be suitable as adhesives, cements or filling composites as well as for the production of coatings and shaped bodies, for example for the stereolithographic production of shaped bodies. Moreover, the dental materials are to be based on monomers which are easy to obtain synthetically.
Further advantages, details and features may be taken from the following description of an exemplary embodiment of the invention in conjunction with the drawing, in which:
This object is achieved by dental materials which contain at least one vinylcyclopropane with general formulae I:
in which
If X=Y=O, R1≠H and R2≠H then n+m≧1. The compounds of formula I are characterized by the fact that they have groups (CO—NH, OH, COOH) which are suitable for forming hydrogen bridge bonds.
Compounds of formula I in which A and B have the same meaning are preferred. Likewise, those compounds in which X and Y have the same meaning are preferred. R1 and R2 can be the same or preferably different.
Formula I and the remaining formulae shown herein cover all stereoisomeric forms as well as mixtures of different stereoisomeric forms, such as e.g. racemates. The formulae cover only those compounds that are compatible with the chemical valence theory. If, for example R1=H, then m must=0, and if R2=H, then n must=0. If m=0 and R1≠H, the free valence at R1 is saturated by H, and if n=0 and R2≠H, the free valence at R2 is accordingly saturated by H. The indication that a radical can be interrupted by a group or a heteroatom such as 0 is to be understood to mean that the group or the heteroatom is inserted into the carbon chain or the carbon ring of the radical, i.e. is bordered on both sides by carbon atoms. The number of heteroatoms is therefore smaller than the number of carbon atoms by at least 1 and the heteroatoms cannot be terminal. C1 radicals cannot be interrupted. In the case of hydrocarbon radicals which contain carbon and heteroatoms, the number of heteroatoms is always less than the number of carbon atoms irrespective of substituents. The radicals R1 and/or R2 can be interrupted by one or more of the named atoms and groups. Preferred are radicals that are interrupted by one group or one atom, or particularly preferably are not interrupted.
The named cyclic radicals can be mono- or polycyclic groups. R1 and/or R2 can also be formed by a combination of the named radicals, for example by a combination of one or more aliphatic and one or more aromatic groups, e.g. an aliphatic-aromatic C7-C14 radical. Particularly preferred are radicals which contain a tricyclodecane group (TCD).
The compounds of formula I contain a radically polymerizable vinylcyclopropane group. Compounds with only one radically polymerizable group are referred to as monofunctional monomers here.
According to the invention, compounds of formula I are preferred in which the variables have the following meanings:
Particularly preferred are compounds of formula I in which the variables have the following meanings:
The vinylcyclopropanes of formula I and thus also the dental materials based on them are characterized by a low shrinkage and a high reactivity on radical polymerization.
In addition, the vinylcyclopropanes of formula I have a low viscosity and are therefore particularly suitable as diluting monomers for viscous monomers. The monomers of formula I preferably have a viscosity of from 10 to 2000 mPa·s, measured at 23° C. with a rotational viscometer. In addition, monomers with low viscosity permit the preparation of highly fluid dental materials, which can be advantageous e.g. for the preparation of adhesives or for the preparation of materials for the stereolithographic production of shaped bodies. In the case of materials containing filler, such as e.g. filling composites, they make it possible to use higher quantities of filler.
A subject of the present invention is also the use of vinylcyclopropanes of formula I for the preparation of dental materials, in particular dental cements, composites, coating materials, bondings and adhesives, as well as for the preparation of materials for the stereolithographic production of shaped bodies. A further subject of the invention are shaped bodies, polymers and copolymers which can be obtained by homo- or copolymerization of the vinylcyclopropanes of formula I.
Vinylcyclopropanes of general formula I can be easily prepared. The synthesis of 1,1-di(alkoxycarbonyl)-substituted 2-vinylcyclopropanes can take place according to known methods (cf. U.S. Pat. No. 4,713,478 and U.S. Pat. No. 4,713,479) by reacting trans-1,4-dihalogen-but-2-enes with corresponding malonic acid esters:
For example:
From the 1,1-di(alkoxycarbonyl)-substituted 2-vinylcyclopropanes, 2-vinylcyclopropane-1-alkoxycarbonyl-1-carboxylic acids according to the invention can be prepared by partial alkaline hydrolysis:
For example:
From the 2-vinylcyclopropane-1-alkoxycarbonyl-1-carboxylic acids according to the invention, corresponding amides according to the invention can be synthesized by reaction with primary amines in the presence of N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide (EDC*HCl) and 1-hydroxybenzotriazol (HOBt):
For example:
In addition, from the 2-vinylcyclopropane-1-alkoxycarbonyl-1-carboxylic acids according to the invention, the hydroxyalkyl derivatives according to the invention can be obtained by reaction with diols in the presence of dicyclohexylcarbodiimide (DCC) and 4-dimethylaminopyridine (DMAP):
For example:
Furthermore, from 1,1-di(alkoxycarbonyl)-substituted 2-vinylcyclopropanes, 2-vinylcyclopropane-1,1-dicarboxylic acid can be prepared by complete alkaline hydrolysis:
From the 2-vinylcyclopropane-1,1-dicarboxylic acid, the corresponding amides according to the invention can be prepared by reaction with primary amines in the presence of N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide (EDC*HCl) and 1-hydroxybenzotriazole (HOBt):
For example:
Preferred examples of the vinylcyclopropanes according to the invention of general formulae I are:
The polymerizable urethane group-containing vinylcyclopropanes of general formula I are mostly liquid and surprisingly exhibit a considerably improved radical polymerizability, in particular on photopolymerization, compared with 1,1-bis(alkoxycarbonyl)-2-vinylcyclopropanes and a lower polymerization shrinkage compared with non-cyclic methacrylates. Dental materials such as fixing cements or filling composites can thus be prepared likewise with reduced polymerization shrinkage.
The (dental) materials according to the invention preferably contain 2 to 95 wt.-%, particularly preferably 2 to 85 wt.-%, more preferably 5 to 70 wt.-% and most preferably 10 to 50 wt.-% vinylcyclopropane(s) of general formula I, in each case relative to the total mass of the material.
In addition to one or more vinylcyclopropanes of general formula I, the materials preferably contain at least one further radically polymerizable monomer. Other vinylcyclopropanes such as 1,1-di(ethoxycarbonyl)- or 1,1-di(methoxycarbonyl)-2-vinylcyclopropane, bis(2-vinylcyclopropane-1-carboxylic acid ethyl ester-1-carbonamido)-2,2-dimethyl-4-methylhexane, 1,8-bis(2-vinylcyclopropane-1-carboxylic acid ethyl ester-1-carbonyloxy)-3,6-dioxaoctane or the esters of 1-ethoxycarbonyl- or 1-methoxycarbonyl-2-vinylcyclopropane carboxylic acid with ethylene glycol, 1,1,1-trimethylolpropane, 1,4-cyclohexanediol or resorcinol are preferred as further radically polymerizable monomers, such as bis-(2-vinyl-1,1-dicarboxylic acid monoethyl ester) resorcinyl ester, and in particular the 2-vinylcyclopropanes described in N. Moszner, F. Zeuner, V. Rheinberger, Macromol. Rapid Commun. 18 (1997) 775-780, and N. Moszner, F. Zeuner, T. Völkel, U. K. Fischer, V. Rheinberger, J. Appl. Polym. Sci. 72 (1999) 1775-1782. Further preferred are the bicyclic cyclopropane derivatives disclosed in EP 1 413 569 A1, in particular 2-(bicyclo[3.1.0]hex-1-yl)acrylic acid methyl or ethyl ester or disubstitution products thereof in the 3 position, such as (3,3-bis(ethoxycarbonyl)bicyclo[3.1.0]hex-1-yl)acrylic acid methyl or ethyl ester.
Likewise preferred are the cyclopropyl acrylates disclosed in EP 1 688 125 A1, in particular {3,3-bis(ethoxycarbonyl)bicyclo[3.1.0]hexa-1-yl}acrylic acid methyl ester and 2-(3-acetyl-3-ethoxycarbonyl-bicyclo[3.1.0]hexa-1-yl}acrylic acid methyl ester.
In addition, the dental materials can also contain radically polymerizable mono- or polyfunctional (meth)acrylic acid derivatives. By monofunctional monomers is meant herein in all cases compounds with one, by multifunctional monomers compounds with two or more, preferably 2 to 4, radically polymerizable groups.
Preferred mono- or multifunctional methacrylates are methyl, ethyl, 2-hydroxyethyl, butyl, benzyl, tetrahydrofurfuryl or isobornyl (meth)acrylate, p-cumylphenoxyethylene glycol methacrylate (CMP-1E), bisphenol A di(meth)acrylate, bis-GMA (an addition product of methacrylic acid and bisphenol A diglycidyl ether), ethoxylated or propoxylated bisphenol A dimethacrylate, such as e.g. the bisphenol A dimethacrylate 2-[4-(3-methacryloyloxyethoxyethyl)phenyl]-2-[4-(3-methacryloyloxyethyl)phenyl]-propane) (SR-348c) with 3 ethoxy groups or 2,2-bis[4-(2-(meth)acryloxypropoxy)phenyl]propane, UDMA (an addition product of 2-hydroxyethyl methacrylate (HEMA) and 2,2,4-trimethylhexamethylene diisocyanate), TMX-UDMA (an addition product of a mixture of HEMA and hydroxypropyl methacrylate (HPMA) with α,α,α′,α′-tetramethyl-m-xylylene diisocyanate (TMXDI)), di-, tri- or tetraethylene glycol di(meth)acrylate, trimethylolpropane tri(meth)acrylate, pentaerythritol tetra(meth)acrylate, as well as glycerol di- and trimethacrylate, 1,4-butanediol di(meth)acrylate, 1,10-decanediol di(meth)acrylate (D3MA) or 1,12-dodecanediol di(meth)acrylate.
Moreover, the dental materials can advantageously also contain radically polymerizable, acid group-containing monomers, such as e.g. polymerizable carboxylic acids, phosphonic acids and phosphoric acid esters. Preferred examples of polymerizable carboxylic acid monomers are maleic acid, 2-(hydroxymethyl)acrylic acid and 4-(meth)acryloyloxyethyltrimellitic acid anhydride. Preferred examples of suitable phosphonic acid monomers are 2-methacryloyloxyethyl phosphonic acid, 2-methacrylamidoethyl phosphonic acid, 2-[4-(dihydroxyphosphoryl)-2-oxa-butyl]-acrylic acid ethyl or -2,4,6-trimethylphenyl ester. Preferred examples of suitable acidic polymerizable phosphoric acid esters are 2-methacryloyloxypropyl dihydrogen phosphate, 2-methacryloyloxyethyl dihydrogen phosphate, 2-methacryloyloxyethylphenyl hydrogen phosphate, dipentaerythritol pentamethacryloyloxy phosphate, 10-methacryloyloxydecyl dihydrogen phosphate and 6-(methacrylamido)hexyl dihydrogen phosphate. Acidic monomers primarily serve to improve the adhesion of the materials to dentine and/or tooth enamel. The amount of acidic monomers preferably lies in the range of from 0 to 20 wt.-%, preferably 0 to 15 wt.-% and particularly preferably 0 to 10 wt.-%, relative to the total mass of the dental material.
According to the invention, materials are preferred which contain at least one multifunctional radically polymerizable monomer, i.e. materials which contain a monomer with two or more, preferably 2 to 4, radically polymerizable groups.
According to the invention, those dental materials which contain at least one monofunctional vinylcyclopropane with general formulae II as comonomer are preferred:
in which
The urethane group optionally present in R1/R2 is preferably a non-N-substituted group of the formula —NH—CO—O—. The radicals R1 and/or R2 of formula II can be interrupted by one or more of the named atoms and groups. Preferred are radicals that are interrupted by one group or one atom, or particularly preferably are not interrupted.
The radical R3 of formula II is substituted n times by the expression in brackets. R3 is a hydrocarbon radical with 1 to 20 carbon atoms which can contain one or more N, O or S atoms. R3 is preferably an aliphatic linear or branched C1-C20 hydrocarbon radical which can be interrupted by O, S or an ester group, an alicyclic or aromatic C6-C14 radical or an aromatic or non-aromatic heterocyclic radical which can contain 4 to 20 carbon atoms and 1 to 6 heteroatoms which are selected from N, O and/or S atoms. The named cyclic radicals can be mono- or polycyclic groups. R3 can also be formed by a combination of the named radicals, for example by a combination of one or more aliphatic and one or more aromatic groups, e.g. an aliphatic-aromatic C7-C20 radical. Particularly preferred are radicals which contain a tricyclodecane group (TCD).
According to the invention, those compounds of formula II are preferred in which the variables have the following meanings:
According to the invention, compounds of formula II are particularly preferred in which the variables have the following meanings:
The dental materials according to the invention preferably furthermore contain an initiator for the radical polymerization. Benzophenone, benzoin and derivatives thereof or α-diketones or derivatives thereof, such as 9,10-phenanthrenequinone, 1-phenyl-propane-1,2-dione, diacetyl or 4,4′-dichlorobenzyl are preferred for the initiation of the radical photopolymerization. Camphorquinone and 2,2-dimethoxy-2-phenyl-acetophenone are particularly preferably used, and quite particularly preferably α-diketones combined with amines as reductants, such as e.g. 4-(dimethylamino)-benzoic acid ethyl ester, N,N-dimethylaminoethyl methacrylate, N,N-dimethyl-sym.-xylidine or triethanolamine. Norrish type I photoinitiators, above all acyl- or bisacylphosphine oxides, such as for example the commercially available compounds 2,4,6-trimethylbenzoyl diphenylphosphine oxide and bis(2,4,6-trimethylbenzoyl)phenylphosphine oxide are also particularly suitable. Monoacyl trialkyl or diacyl dialkyl germanium, triacyl alkyl and tetraacyl germanium compounds, such as e.g. benzoyltrimethylgermanium, dibenzoyldiethylgermanium or bis(4-methoxybenzoyl)diethylgermanium as well as tetrabenzoylgermanium are also particularly suitable. Mixtures of the different photoinitiators can also be used, such as e.g. dibenzoyldiethylgermanium in combination with camphorquinone and 4-dimethylaminobenzoic acid ethyl ester or tetrabenzoylgermanium. Advantageously, initiator combinations can also be used which additionally contain aromatic diaryliodonium or triarylsulfonium salts, for example the commercially available compounds 4-octyloxyphenyl-phenyl-iodonium hexafluoroantimonate or isopropylphenyl-methylphenyl-iodonium tetrakis(pentafluorophenyl)borate.
Preferably, redox-initiator combinations, such as e.g. combinations of benzoyl peroxide with N,N-dimethyl-sym.-xylidine or N,N-dimethyl-p-toluidine, are used as initiators for a polymerization carried out at room temperature. In addition, redox systems consisting of peroxides or hydroperoxides and reducing agents, such as e.g. ascorbic acid, barbiturates, thioureas or sulfinic acids, are also particularly suitable. Moreover, compounds of transition metals which exhibit at least two stable valency stages can be used as redox catalysts. They are, above all, compounds of the elements copper, iron, vanadium, nickel or cobalt, wherein copper compounds are particularly preferred and these are preferably used as highly organosoluble compounds, such as e.g. acetylacetonate, naphthenate or 2-ethylhexanoate.
Dental materials which contain at least one photoinitiator are preferred according to the invention. The materials can additionally contain further initiators.
In addition, the compositions used according to the invention preferably also contain at least one organic or particularly preferably inorganic particulate filler, for example to improve the mechanical properties or to adjust the viscosity.
Preferred inorganic particulate fillers are amorphous spherical materials based on oxides, such as SiO2, ZrO2 and TiO2 or mixed oxides of SiO2, ZrO2 and/or TiO2, nanoparticulate or microfine fillers, such as pyrogenic silica or precipitated silica (weight-average particle size of 10-1000 nm), as well as minifillers, such as quartz, glass ceramic or glass powder with a weight-average particle size of from 0.01 to 1 μm. Further preferred fillers are X-ray opaque fillers, such as ytterbium trifluoride, nanoparticulate tantalum(V) oxide, barium sulfate, mixed oxides of SiO2 with ytterbium(III) oxide or tantalum(V) oxide (weight-average particle size of 10-1000 nm) and X-ray opaque glass powder, e.g. barium or strontium aluminium silicate glasses (weight-average particle size of 0.2-10 μm).
To improve the bond between the filler particles and the crosslinked polymerization matrix, the filler particles can be surface-modified with suitable coupling reagents. For SiO2-based fillers such as SiO2, quartz, glass ceramic or glass powder, trialkoxysilanes, such as e.g. 3-methacryloyloxypropyltrimethoxysilane, are particularly suitable. Trialkoxysilanes which contain vinylcyclopropane groups are preferred, quite particularly the vinylcyclopropanesilanes described in EP 0 867 444 A2, wherein in particular the 1-methoxy- or 1-ethoxycarbonyl-1-[(3-trimethoxy- or 3-triethoxysilyl)propylaminocarbonyl)]-2-vinylcyclopropanes are preferred. Specifically, vinylcyclopropanesilanes with the following structures are particularly suitable:
For the surface-modification of non-silicate fillers, e.g. of ZrO2 or TiO2, functionalized acidic phosphates, such as e.g. 10-methacryloyloxy dihydrogen phosphate can also be used.
Optionally, the compositions used according to the invention can contain one or more further additives, above all solvents, preferably water, ethanol or a mixture thereof, and stabilizers, such as e.g. polymerization stabilizers, flavourings, dyes, microbiocidal active ingredients, fluoride-ion-releasing additives, optical brighteners, plasticizers and/or UV absorbers.
According to the invention, those dental materials are preferred which contain the following components:
The filler content is determined decisively by the desired application of the dental material. Dental materials for use as coating material particularly preferably contain 0 to 40 wt.-%, dental materials for use as cement preferably contain 10-70 wt.-% and dental materials for use as filling material (filling composite) preferably contain 10-85 wt.-% filler(s).
Dental materials for use as filling material particularly preferably have the following composition:
Unless otherwise indicated, all quantities herein relate to the total mass of the material. The individual quantity ranges can be chosen separately.
Those materials which consist of the named components are particularly preferred. Furthermore, those materials in which the individual components are in each case selected from the above-named preferred and particularly preferred substances are preferred.
According to the invention, those dental materials which exclusively contain monomers which have vinylcyclopropyl (VCP) groups as radically polymerizable groups are particularly preferred.
The materials according to the invention are particularly suitable as dental materials, in particular as dental adhesives, cements, filling composites and veneering materials, and as materials for the production of prostheses, artificial teeth, inlays, onlays, crowns and bridges. Compared with materials based on dimethacrylates they are characterized by considerably lower polymerization shrinkage, and compared with known polymerizable cyclopropane derivatives by a better polymerization reactivity, in particular on photopolymerization.
The dental materials are suitable primarily for intraoral application by the dentist for the restoration of damaged teeth (clinical materials), e.g. as dental cements, filling composites and veneering materials. However, they can also be used extraorally, for example in the production or repair of dental restorations, such as prostheses, artificial teeth, inlays, onlays, crowns and bridges (technical materials). The materials are suitable in particular for the production of shaped bodies, for example of dental restorations, by generative processes, in particular by stereolithography or 3D printing (cf. A. Gebhardt, Generative Fertigungsverfahren [Generative manufacturing processes], 3rd ed., Carl Hanser Verlag, Munich 2007).
The invention is explained in more detail in the following with reference to examples.
To a stirred solution of 1-ethoxycarbonyl-2-vinylcyclopropane carboxylic acid (VCP 3, 2.76 g, 15.0 mmol), which was prepared by partial hydrolysis of 1,1-bis(ethoxycarbonyl)-2-vinylcyclopropane (VCP 4) (cf. N. Moszner, F. Zeuner, V. Rheinberger, Macromol. Rapid. Commun. 18 (1997) 775-780) in anhydrous methylene chloride (20.0 ml), 1-hydroxybenzotriazol (HOBt, 2.03 g, 15.0 mmol) was added under argon. The solution was cooled to 0° C. and then ethylamine was added (2.0 M in THF, 7.5 ml, 15.0 mmol). A solution of N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide (EDC*HCl, 3.45 g, 18.0 mmol) in anhydrous methylene chloride (40.0 ml) was added dropwise to the reaction mixture. It was stirred at 0° C. for 1 h and at RT for 15 h. The mixture was washed with a saturated sodium hydrogen carbonate solution (2×50 ml). The organic phase was dried over anhydrous sodium sulfate. The solvent was distilled off in a vacuum and the crude product was purified by chromatography (flash silica gel with ethyl acetate/hexane: 2/8). 2.63 g (83% yield) of a colourless liquid was obtained as a mixture of diastereoisomers (ratio: approx. 9/1).
NMR analysis of the main isomer: 1H NMR (400 MHz, CDCl3): δ=1.17 (t, 3JHH=7.4 Hz, 3H, NHCH2CH3); 1.29 (t, 3JHH=7.1 Hz, 3H, OCH2CH3); 1.85 (dd, 2JHH=4.2 Hz, 3JHH=7.9 Hz, 1H, CH2CHCH═CH2); 2.05 (dd, 2JHH=4.2 Hz, 3JHH=9.1 Hz, 1H, CH2CHCH═CH2); 2.53 (q, 3JHH=8.6 Hz, 1H, CH2CHCH═CH2); 3.24-3.41 (m, 2H, CH2NH); 4.11-4.26 (m, 2H, CH2O); 5.12-5.19 (m, 1H, CH2═CH); 5.29-5.37 (m, 1H, CH2═CH); 5.59-5.71 (m, 1H, CH2═CH); 8.34 (s, NH). 13C NMR (101 MHz, CDCl3): δ=14.2 (CH3); 14.7 (CH3); 21.2 (CH2CHCH═CH2); 34.2 (COCCO); 34.8 (CH2NH); 36.7 (CH2CHCH═CH2); 61.4 (CH2O); 119.4 (CH2═CH); 133.4 (CH2=CH); 167.7 (OC═O); 171.4 (NHC═O).
To a stirred solution of 1-ethoxycarbonyl-2-vinylcyclopropane carboxylic acid (VCP 3, 36.8 g, 200 mmol), ethylene glycol (49.7 g, 800 mmol) and 4-dimethylaminopyridine (DMAP, 1.22 g, 1.0 mmol) in anhydrous methylene chloride (30.0 ml), dicyclohexylcarbodiimide (DCC, 41.2 g, 200 mmol) was added in portions under argon. It was stirred at 0° C. for 30 min and at RT for 15 h. The reaction mixture was suctioned over a frit and the residue was washed with methylene chloride (3×40 ml). The organic phase was washed with water (150 ml) and the aqueous phase extracted with dichloromethane (DCM) (2×30 ml). The combined organic phases were dried over anhydrous sodium sulfate. The solvent was distilled off in a vacuum and the crude product was purified by chromatography (flash silica gel with ethyl acetate/hexane: 1/3). 32.44 g (71% yield) of a colourless liquid was obtained as a mixture of diastereoisomers (ratio: approx. 9/1).
NMR analysis of the main isomer: 1H NMR (400 MHz, CDCl3): δ=1.27 (t, 3JHH=7.1 Hz, 3H, OCH2CH3); 1.60 (dd, 2JHH=5.0 Hz, 3JHH=9.0 Hz, 1H, CH2CHCH═CH2); 1.77 (dd, 2JHH=5.0 Hz, 3JHH=7.7 Hz, 1H, CH2CHCH═CH2); 2.62 (q, 3JHH=8.5 Hz, 1H, CH2CHCH═CH2); 3.82 (t, 3JHH=4.6 Hz, CH2OH); 4.14-4.29 (m, 3H, CH2OCO); 4.38 (dt, 2JHH=10.7 Hz, 3JHH=4.8 Hz, 1H, CH2OCO); 5.13-5.20 (m, 1H, CH2═CH); 5.27-5.37 (m, 1H, CH2═CH); 5.41-5.53 (m, 1H, CH2═CH). 13C NMR (101 MHz, CDCl3): δ=14.2 (CH3); 20.8 (CH2CHCH═CH2); 31.8 (CH2CHCH═CH2); 35.7 (COCCO); 60.9 (CH2OH); 61.6 (CH2OCO); 67.1 (CH2OCO); 119.0 (CH2═CH); 132.7 (CH2═CH); 167.4 (C═O); 169.9 (C═O).
The reactivity of 1-ethoxycarbonyl-1-ethylcarbamoyl-2-vinylcyclopropane (VCP 1), 1-(2-hydroxyethoxycarbonyl)-1-ethoxycarbonyl-2-vinylcyclopropane (VCP 2), 1-ethoxycarbonyl-2-vinylcyclopropane carboxylic acid (VCP 3) and 1,1-bis(ethoxycarbonyl)-2-vinylcyclopropane (VCP 4) was investigated. In each case 0.5 mol % bis(4-methoxybenzoyl) diethylgermanium (Ivocerin®, Ivoclar Vivadent AG) was added to each monomer. Each mixture was polymerized in a Diamond Differential Scanning calorimeter (Perkin Elmer) with photopolymerization attachment by irradiation with an LED lamp (Bluephase, Ivoclar Vivadent AG) for 2 min at 37° C. The results are reproduced in
Using a kneader, paste-like composites with the compositions stated in Table 1, based on monomers VCP 5/VCP 1 (8/2: wt./wt.), VCP 5/VCP 3 (8/2: wt./wt.) and UDMA/AAEMA (8/2: wt./wt.), were prepared. 1,6-Bis(2-vinylcyclopropane-1-carboxylic acid ethyl ester-1-carbonamido)-2,2-dimethyl-4-methylhexane (VCP 5) was synthesized from VCP 3 and 2,2,4-trimethylhexamethylenediamine (cf. P. P. Contreras, C. Kuttner, A. Fery, U. Stahlschmidt, V. Jerome, R. Freitag, S. Agarwal, Chem. Commun. 51 (2015) 11899-11902).
Corresponding test pieces were prepared from the materials, irradiated twice for 3 mins with a dental light source (Spectramat®, Ivoclar Vivadent AG) and thus cured. The flexural strength and the flexural modulus of elasticity were determined according to ISO standard 4049 (Dentistry—Polymer-based filling, restorative and luting materials) (Table 2). The measurements were carried out after 24 h storage in water (37° C.). The shrinkage was determined according to the buoyancy method (Table 2). Composites A and B based on the vinylcyclopropanes according to the invention VCP 1 and VCP 3 have a considerably lower polymerization shrinkage than the methacrylate-based composite C with comparable mechanical properties.
1)Urethane dimethacrylate from 2 mol 2-hydroxyethyl methacrylate and 1 mol 2,2,4-trimethylhexamethylene diisocyanate-1,6
2)2-(Methacryloyloxy)ethyl acetoacetate
3)Glass powder GM 27884, 1 μm, silanized (Schott)
4)Tokoyama Soda
5)Auer Remy
6)Evonik
7)Bis(4-methoxybenzoyl)diethylgermanium (Ivoclar Vivadent AG)
Preparation of Composites with Improved Mechanical Properties
The composite pastes based on bis-(2-vinyl-1,1-dicarboxylic acid monoethylester)resorcinylester (VCP 6) were prepared analogously to Example 4 (Table 3).
VCP 1, VCP 3 and VCP 4 were used as diluents. The results of the mechanical properties are reproduced in Table 4 and demonstrate that the highly reactive vinylcyclopropanes VCP 1 and VCP 3 (Composites D and E) lead to an improvement in the mechanical properties compared with the vinylcyclopropane VCP 4 (Composite F), which corresponds to the state of the art.
3)Glass powder GM 27884, 1 μm, silanized (Schott)
4)Tokoyama Soda
5)Auer Remy
7)Bis(4-methoxybenzoyl)diethylgermanium (Ivoclar Vivadent AG)
8)Composite filler, weight-average particle size 30-40 μm (Ivoclar Vivadent AG)
| Number | Date | Country | Kind |
|---|---|---|---|
| 102016214389. 1 | Aug 2016 | DE | national |
