Abstract The present invention provides a process for converting a hydrophobic siloxane diacrylate, an aromatic fluorinated diacrylate and a hydrophilic polyethylene glycol diacrylate to their respective multifunctional oligomers. Bis(4-acryloxybutyl)tetramethyldisiloxane, prepared from the corresponding diol, is converted to relatively low viscosity, multifunctional oligomers with the use of DMSO. The hydrophilic monomer, polyethylene glycol 400 diacrylate, formed more viscous, water soluble oligomeric products without the need for a solvent. Characterization of these oligomers by infrared spectroscopy and 1 H NMR supports the assigned structures. Because of the predominant 1,6-arrangement of double bonds in these oligomers, they have a propensity to undergo cyclopolymerization as well as the usual crosslinking associated with the free radical polymerization of multifunctional monomers and oligomers. These novel oligomeric monomers have potential use in dental composites, sealants, adhesives, dentures, contact lenses, biomedical prostheses, cements, drug delivery systems, coatings and caulks.
A process for synthesizing multifunctional acrylate monomers and oligomers, comprising the steps of: providing a reactant acrylate compound selected from a group consisting of siloxane diacrylate, a polyethylene glycol diacrylate, an aromatic fluorinated diacrylate, and a hydroxylated aliphatic diacrylate; and exposing the acrylate compound to reaction conditions comprising a temperature within the range of about 90° C. to about 95° C. for a time within about 6 hours to about 20 hours effective for resulting in multifunctional acrylate monomers and oligomers having predominant 1,6-arrangement of double bonds.
Claim 2
Dependent Claim
87 words
A process for synthesizing multifunctional acrylate monomers and oligomers, comprising the steps of: providing a reactant acrylate compound selected from a group consisting of siloxane diacrylate, a polyethylene glycol diacrylate, an aromatic fluorinated diacrylate, and a hydroxylated aliphatic diacrylate; and exposing the acrylate compound to reaction conditions comprising a temperature within the range of about 90° C. to about 95° C. for a time within about 6 hours to about 20 hours effective for resulting in multifunctional acrylate monomers and oligomers having predominant 1,6-arrangement of double bonds.
Claim 3
Dependent Claim
12 words
The process of claim 1 wherein said acrylate compound is siloxane diacrylate.
Claim 4
Dependent Claim
13 words
The process of claim 1 wherein said acrylate compound is aromatic fluorinated diacrylate.
Claim 5
Dependent Claim
13 words
The process of claim 1 wherein said acrylate compound is polyethylene glycol diacrylate.
Claim 6
Dependent Claim
14 words
The process of claim 1 wherein said acrylate compound is a hydroxylated aliphatic diacrylate.
Claim 7
Dependent Claim
12 words
The process of claim 1 wherein DMSO is used as a solvent.
Claim 8
Dependent Claim
12 words
The process of claim 3, wherein DMSO is used as a solvent.