Public reporting burden for this collection of information is estimated to average 1 hour per response, including the time for reviewing instructions, searching existing data sources, gathering and maintaining the data needed, and completing and reviewing this collection of information. Send comments regarding this burden estimate or any other aspect of this collection of information, including suggestions for reducing this burden to Department of Defense, Washington Headquarters Services, Directorate for Information Operations and Reports (0704-0188), 1215 Jefferson Davis Highway, Suite 1204, Arlington, VA 22202-4302. Respondents should be aware that notwithstanding any other provision of law, no person shall be subject to any penalty for failing to comply with a collection of information if it does not display a currently valid OMB control number. PLEASE DO NOT RETURN YOUR FORM TO THE ABOVE ADDRESS.
REPORT DATE (DD-MM-YYYY)2. REPORT TYPE 3. DATES COVERED (From -To)
SPONSORING / MONITORING AGENCY NAME(S) AND ADDRESS(ES) 10. SPONSOR/MONITOR'S ACRONYM(S)Air Force Research Laboratory (AFMC) AFRL/PRS
SPONSOR/MONITOR'S
Pollux Drive
NUMBER(S)Edwards AFB CA 93524-7048 AFRL-PR-ED-JA-2006-178
DISTRIBUTION / AVAILABILITY STATEMENT
Approved for public release; distribution unlimited (AFRL-ERS-PAS-2006-132)
SUPPLEMENTARY NOTESTo be published in the ACS journal Macromolecules.
AbstractA new cyanate ester monomer was prepared from bis(4-cyanatophenyl)-dimethylsilane (SiMCy) and fully characterized by analytical and spectroscopic techniques. The monomer was found to have a melting point about 20 °c lower than that of the commercial bis(4-cyanatophenyl)dimethylmethane (BADCy) with similar melt viscosity, curing kinetics, and post-cure glass transition temperature. Analysis of the single-crystal molecular structure by x-ray diffraction showed that intermolecular packing was dominated by weak hydrogen-bonding attractions between the aromatic rings and the -OCN nitrogen atoms. In contrast, the packing interactions found in BADCy are dominated by dipole-dipole interactions of the OCN groups. These differences may explain the 50% reduction in moisture uptake observed in SiMCy as compared to BADCy during exposure to boiling water. In addition, thermogravimetric analysis revealed that SiMCy exhibited a significantly higher char yield in air than BADCy, presumably due to the formation of silicates at high temperature. The combination of improved thermooxidative stability and reduced moisture absorption without significant loss in ease of processing or mechanical properties makes SiMCy an important potential "drop in" replacement for BADCy, and demonstrates the power of the molecular level approach to designing new hightemperature polymer materials.
SUBJECT TERMS
SECURITY CLASSIFICATION OF:17
Abstract.A new cyanate ester monomer was prepared from bis(4-cyanatophenyl)-dimethylsilane (SiMCy) and fully characterized by analytical and spectroscopic techniques. The monomer was found to have a melting point about 20 °C lower than that ...