Abstract

A series of ester-linked diamines, with different lengths and substituents, was synthesized to obtain poly(ester imide)s (PEsIs) having improved properties. A substituent-free ester-linked diamine (AB-HQ) was poorly soluble in N-methyl-2-pyrrolidone at room temperature, which forced the need for polyaddition by adding tetracarboxylic dianhydride solid into a hot diamine solution. This procedure enabled the smooth progress of polymerization, however, accompanied by a significant decrease in the molecular weights of poly(amic acid)s (PAAs), particularly when using hydrolytically less stable pyromellitic dianhydride. On the other hand, the incorporation of various substituents (–CH3, –OCH3, and phenyl groups) to AB-HQ was highly effective in improving diamine solubility, which enabled the application of the simple polymerization process without the initial heating of the diamine solutions, and led to PAAs with sufficiently high molecular weights. The introduction of bulkier phenyl substituent tends to increase the coefficients of thermal expansion (CTE) of the PEsI films, in contrast to that of the small substituents (–CH3, –OCH3). The effects of ester-linked diamines, consisting of longitudinally further extended structures, were also investigated. However, this approach was unsuccessful due to the solubility problems of these diamines. Consequently, the CTE values of the PEsIs, obtained using longitudinally further extended diamines, were not as low as we had expected initially. The effects of substituent bulkiness on the target properties, and the dominant factors for water uptake (WA) and the coefficients of hygroscopic expansion (CHE), are also discussed in this study. The PEsI derived from methoxy-sustituted AB-HQ analog and 3,3′,4,4′-biphenyltetracarboxylic dianhydride achieved well-balanced properties, i.e., a very high Tg (424 °C), a very low CTE (5.6 ppm K−1), a low WA (0.41%), a very low CHE value (3.1 ppm/RH%), and sufficient ductility, although the 26 μm-thick film narrowly missed certification of the V-0 standard in the UL-94V test. This PEsI film also displayed a moderate εr (3.18) and a low tan δ (3.14 × 10−3) at 10 GHz under 50% RH and at 23 °C. Thus, this PEsI system is a promising candidate as a novel dielectric substrate material for use in the next generation of high-performance flexible printed circuit boards operating at higher frequencies (≥10 GHz).

Highlights

  • The importance of heat-resistant polymers as electrical insulation materials has increased significantly in a variety of electrical and microelectronic applications

  • (–CH3, –OCH3, and phenyl groups) to AB-HQ was highly effective in improving diamine solubility, which enabled the application of the simple polymerization process without the initial heating of the diamine solutions, and led to poly(amic acid)s (PAAs) with sufficiently high molecular weights

  • AB-HQ was not sufficiently soluble in common amide solvents (NMP, DMAc), at room temperature, in order to begin the PAA polymerization without heating

Read more

Summary

Introduction

The importance of heat-resistant polymers as electrical insulation materials has increased significantly in a variety of electrical and microelectronic applications. Ing and fact,dimensional it is difficult to achieve absorption and further decrease conventional water uptake,monomers dielectric constants (εr), and targetwater/moisture properties simultaneously by to combining for PIs (tetracarboxylic dissipation factors (tan δ) at higher operating frequencies It is new dianhydrides and diamines) and even by copolymerization using multiple monomers. These results motivated us to high applyflame a similar retardancy, sufficient film ductility, and a low tan δ at GHz [14] These results motivated us to structural modification approach to diamine monomers [Figure 1(right)]. Prominent positive substituent effects observed in our previous studies [15,16,17]

Our strategies forfor obtaining high-temperature dielectric substrate
Experimental Section
C21 H18analysis
Polymerization and Thermal Imidization for PEsI Film Preparation
Inherent Viscosities
Glass Transition Temperatures
Water Absorption
Birefringence
Mechanical Properties
Flame Retardancy
Dielectric Constants and Dissipation Factors
Polymerizability of AB-HQ
Film Properties
Isomer Effects
PEsIs Derived from withofSmall
PEsIs Derived from AB-HQ Analogs with Bulky Substituents
Influence of Side Group Bulkiness on Tg and CTE
Influence of the Position of Ester-linked Aromatic unit on Properties
Correlation of WA and Imide Group Content
Correlation of W A and Imide Group Content
Correlation of CHE and WA
11. This is reasonable because tensile
Dielectric Properties
Performance Balance of the PEsIs for Use in High-performance FPCs
Conclusions
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.