2010
DOI: 10.1007/s10965-010-9549-3
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Liquid crystalline epoxy resin modified cyanate ester for high performance electronic packaging

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Cited by 33 publications
(19 citation statements)
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“…Furthermore, peaks of ‐OCN group (2270 and 2238 cm −1 ) and epoxy ring (913 cm −1 ) were disappeared during the curing. It should be noted that the presence of peaks at 1570 and 1370 cm −1 corresponding to C─N and CN of triazine indicated homopolymerization of CE and peak at 1730 cm −1 indicated the formation of oxazolidone ring structure which come from the reaction between epoxy ring and cyanate group . Moreover, there are new peaks of 1210 and 1050 cm −1 corresponding to ester group, indicating the reactions between CTBN and CE.…”
Section: Resultsmentioning
confidence: 96%
See 1 more Smart Citation
“…Furthermore, peaks of ‐OCN group (2270 and 2238 cm −1 ) and epoxy ring (913 cm −1 ) were disappeared during the curing. It should be noted that the presence of peaks at 1570 and 1370 cm −1 corresponding to C─N and CN of triazine indicated homopolymerization of CE and peak at 1730 cm −1 indicated the formation of oxazolidone ring structure which come from the reaction between epoxy ring and cyanate group . Moreover, there are new peaks of 1210 and 1050 cm −1 corresponding to ester group, indicating the reactions between CTBN and CE.…”
Section: Resultsmentioning
confidence: 96%
“…It should be noted that the presence of peaks at 1570 and 1370 cm −1 corresponding to C─N and C N of triazine indicated homopolymerization of CE and peak at 1730 cm −1 indicated the formation of oxazolidone ring structure which come from the reaction between epoxy ring and cyanate group. 29,30 Moreover, there are new peaks of 1210 and 1050 cm −1 corresponding to ester group, 31 indicating the reactions between CTBN and CE. Furthermore, the presence of the peaks at 1565 and 1370 cm −1 corresponding to triazine rings in the precured CTBN/EP/CE spectrum indicated that the corresponding reactions had already taken place at the mixing stage of the components.…”
Section: Curing Kinetics Studiesmentioning
confidence: 98%
“…HBPGO has excellent dielectric properties due to the chemical structure of polysiloxane and special unoccupied spaces of hyperbranched polymers as well as the outstanding dielectric properties of GO, so modified DCPDCE systems with higher HBPGO concentration have smaller dielectric constant values. Secondly, the addition of HBPGO into CE resin promotes the self-polymerization of -NCO groups, thus increases the productivity of symmetrical triazine rings [38]. As a result, the modified DCPDCE system tends to form networks with greater symmetry and larger space hinder, which is beneficial for reducing the dielectric constant and loss.…”
Section: Dielectric Properties Of Hbpgo/dcpdce Systemmentioning
confidence: 99%
“…For modifying a thermosetting resin, a suitable LCE must have desirable melting and clearing temperatures to fit the curing procedure of the resin, good compatibility and properties to guarantee the expected performance of the modified resin. 26 LCE can exhibit a mesomorphic state during the curing process, and thus the resultant crosslinked network of modified resin will add to its advantages. Therefore, designing and synthesizing LCEs with desirable molecular structure is a good method for modifying thermosetting resins.…”
Section: Introductionmentioning
confidence: 99%