ANHYDRIDE COMPOUND, POLYIMIDE, AND THIN FILM

Abstract

An anhydride compound, polyimide, and thin film are provided. The anhydride compound has a chemical structure of

##STR00001##

wherein R.sup.1 is

##STR00002##

each of R.sup.4 is independently C.sub.1-6 alkylene group, m is an integer of 0 to 10, and m′ is an integer of 1 to 10; n is an integer of 1 to 10, each of R.sup.2 is independently hydrogen, saturated or unsaturated C.sub.1-6 hydrocarbon group, CF.sub.3, silanol group, silyl group, or Al(OH).sub.3; and R.sup.3 is

##STR00003##

silanol group, silyl group, or Al(OH).sub.3. The anhydride compound can be reacted with a diamine compound to form a polyimide.

Claims

1. An anhydride compound, having a chemical structure of ##STR00040## wherein R.sup.1 is ##STR00041## each of R.sup.4 is independently C.sub.1-6 alkylene group, m is an integer of 0 to 10, and m′ is an integer of 1 to 10; n is an integer of 1 to 10; each of R.sup.2 is independently hydrogen, saturated or unsaturated C.sub.1-6 hydrocarbon group, CF.sub.3, silanol group, silyl group, or Al(OH).sub.3; and R.sup.3 is ##STR00042## silanol group, silyl group, or Al(OH).sub.3.

2. The anhydride compound as claimed in claim 1, having a chemical structure of ##STR00043##

3. The anhydride compound as claimed in claim 1, having a chemical structure of ##STR00044##

4. The anhydride compound as claimed in claim 1, having a chemical structure of ##STR00045##

5. The anhydride compound as claimed in claim 1, having a chemical structure of ##STR00046##

6. A polyimide, being formed by reacting an anhydride compound and a diamine compound; wherein the anhydride compound has a chemical structure of ##STR00047## wherein R.sup.1 is ##STR00048## each of R.sup.4 is independently C.sub.1-6 alkylene group, m is an integer of 0 to 10, and m′ is an integer of 1 to 10; n is an integer of 1 to 10; and each of R.sup.2 is independently hydrogen, saturated or unsaturated C.sub.1-6 hydrocarbon group, CF.sub.3, silanol group, silyl group, or Al(OH).sub.3.

7. The polyimide as claimed in claim 6, wherein the diamine compound has a chemical structure of ##STR00049## wherein p is an integer of 0 to 5; each of R.sup.5 is independently —O—, —NH—, C.sub.1-4 alkylene group, —SO.sub.2—, —CF.sub.2—, —C.sub.2F.sub.4—, —(C═O)O—, —(C═O)—, —(C═O)NH—, or —NH(C═O)—; and each of R.sup.6 is independently H, CH.sub.3, or CF.sub.3.

8. The polyimide as claimed in claim 6, wherein the diamine compound has a chemical structure of ##STR00050##

9. A thin film, comprising the polyimide as claimed in claim 6, wherein the thin film has a thickness of 10 μm to 75 μm, and a dielectric constant of 2.5 to 3 at 10 GHz.

Description

DETAILED DESCRIPTION

[0010] In the following detailed description, for purposes of explanation, numerous specific details are set forth in order to provide a thorough understanding of the disclosed embodiments. It will be apparent, however, that one or more embodiments may be practiced without these specific details.

[0011] One embodiment of the disclosure provides an anhydride compound, having a chemical structure of

##STR00009##

wherein R.sup.1 is

##STR00010##

each of R.sup.4 is independently C.sub.1-6 alkylene group, m is an integer of 0 to 10, and m′ is an integer of 1 to 10; n is an integer of 1 to 10; each of R.sup.2 is independently hydrogen, saturated or unsaturated C.sub.1-6 hydrocarbon group, CF.sub.3, silanol group, silyl group, or Al(OH).sub.3; and R.sup.3 is

##STR00011##

silanol group, silyl group, or Al(OH).sub.3. The anhydride compound can be synthesized in the following steps:

##STR00012##

can react with

##STR00013##

in the presence of acidic catalyst (e.g. AlCl.sub.3, HF, or another acidic catalyst) to form a diol compound, as shown in below formula.

##STR00014##

[0012] Subsequently, benzyl bromide (BnBr), chloromethyl methyl ether (MeOCH.sub.2Cl), tert-butyldimethylsilyl ether (TBSCl), methanesulfonyl chloride (MsCl), or dimethyl sulfate is used to protect one alcohol group on one side of the diol compound. Take MsCl as an example, the reaction is shown as below formula.

##STR00015##

[0013] Subsequently, the compound containing the protection group can react with trimellitic anhydride chloride (TMAC) to form an anhydride compound, as shown in below formula.

##STR00016##

[0014] Subsequently, a de-protection reaction is performed, as shown in below formula. The de-protection reagent can be HCl, I.sub.2, F.sup.−, LDA (lithium diisopropylamide), BBr.sub.3, or another suitable reagent.

##STR00017##

[0015] Subsequently, R.sup.3—Cl can be added to perform a substitution reaction to form an anhydride compound, as shown in below formula.

##STR00018##

[0016] In some embodiments, the anhydride compound formed by the above reactions may have a chemical structure of

##STR00019##

[0017] Alternatively, the diol compound can directly react with TMAC to form an anhydride compound, as shown in below formula.

##STR00020##

[0018] In some embodiments, the anhydride compound formed by the above reactions may have a chemical structure of

##STR00021##

[0019] In some embodiments, the diol compound can be firstly hydrogenated. BnBr, MeOCH.sub.2Cl, TBSCl, MsCl, or dimethyl sulfate is then used to protect one alcohol group on one side of the diol compound. Take MSCl as an example, and the reaction is shown as below formula.

##STR00022##

[0020] Subsequently, the compound containing the protection group can react with TMAC to form an anhydride compound, as shown in below formula.

##STR00023##

[0021] Subsequently, a de-protection reaction is performed, as shown in below formula. The de-protection reagent can be HCl, I.sub.2, F.sup.−, LDA, BBr.sub.3, or another suitable reagent.

##STR00024##

[0022] Subsequently, R.sup.3—Cl can be added to perform a substitution reaction to form an anhydride compound, as shown in below formula.

##STR00025##

[0023] In some embodiments, the anhydride compound formed by the above reactions may have a chemical structure of

##STR00026##

[0024] On the other hand, the diol compound can firstly undergo hydrogenation, and then react with TMAC to form the anhydride compound, as shown in below formula.

##STR00027##

[0025] In some embodiments, the anhydride compound formed by the above reactions may have a chemical structure of

##STR00028##

[0026] It should be understood that the above reactions are only for illustrating a possible synthesis path of the anhydride compound, which is not the only applicable synthesis path. One skilled in the art may adopt any applicable synthesis path according to his/her requirements for forming the anhydride compound in the disclosure.

[0027] One embodiment of the disclosure provides a polyimide formed by reacting the described anhydride compound with a diamine compound. Take dianhydride compound as an example, the reaction is shown below:

##STR00029## ##STR00030##

In the above formula, R.sup.7 correspond to the diamine compound type, as described below. x is the repeating number of the repeating unit in the polyimide, which is related to the molecular weight of the polyimide.

[0028] In some embodiments, the diamine compound has a chemical structure of

##STR00031##

wherein p is an integer of 0 to 5; each of R.sup.5 is independently —O—, —NH—, C.sub.1-4 alkylene group, —SO.sub.2—, —CF.sub.2—, —C.sub.2F.sub.4—, —(C═O)O—, —O(C═O)—, —(C═O)NH—, or —NH(C═O)—; and each of R.sup.6 is independently H, CH.sub.3, or CF.sub.3. For example, the diamine compound can be 4,4′-oxydianiline (ODA), which has a chemical structure of

##STR00032##

In some embodiments, the diamine compound can be 4-aminobenzoic acid 4-aminophenyl ester, which has a chemical structure of

##STR00033##

In some embodiments, the diamine compound can be 1,4-bis(4-aminophenoxy)benzene, which has a chemical structure of

##STR00034##

In some embodiments, the diamine compound can be 1,4-benzenedicarboxylic acid bis(4-aminophenyl) ester, which has a chemical structure of

##STR00035##

In some embodiments, the diamine compound can be 4,4′-(4,4′-isopropylidene diphenyl-1,1′-diyldioxy)dianiline, which has a chemical structure of

##STR00036##

[0029] One embodiment of the disclosure provides a thin film, including the described polyimide. The thin film has a thickness of 10 μm to 75 μm, and a dielectric constant of 2.5 to 3 at 10 GHz. The dielectric constant of the polyimide thin film is related to the thickness of the polyimide thin film. If the dielectric constant of the polyimide thin film at 10 GHz is too high, the polyimide thin film cannot meet the requirements for its application as 5G board material.

[0030] Below, exemplary embodiments will be described in detail so as to be easily realized by a person having ordinary knowledge in the art. The inventive concept may be embodied in various forms without being limited to the exemplary embodiments set forth herein. Descriptions of well-known parts are omitted for clarity.

EXAMPLES

[0031] In the following Examples, the dielectric constant of the thin film at 10 GHz was measured by the standard JISC2565, the dielectric loss of the thin film at 10 GHz was measured by the standard JISC2565, and the moisture absorption of the thin film was measured by the standard means of the follows. First, the film was heated in an oven to 105° C. for 30 mins, then moved to a drying box for cooling down and the weight of the film (W.sub.0) was recorded. Next, the film was soaked in D. I. water for 24 hours and the weight after water absorption (W.sub.1) was recorded. The moisture absorption of the thin film is (W.sub.1−W.sub.0)/W.sub.0×100%.

Example 1

[0032] AlCl.sub.3 (0.10 mole, 13.11 g) serving as an acidic catalyst was added to and dissolved in 2,6-dimethylphenol (DMP, 1.18 mol, 144.15 g) solution, and dicyclopentadiene (DCPD, 0.60 mol, 78.00 g) was then added, and heated to react. After reaction, the solution was allowed to cool down to room temperature, and potassium hydroxide solution (5 wt %, 0.06 mol) was added to the reaction result to neutralize it. The diol compound was then extracted with toluene. The above reaction is shown below:

##STR00037##

[0033] Pyridine (0.13 mol, 13.11 g) was added to trimellitic anhydride chloride (TMAC, 0.33 mol, 70.00 g) solution, which was then dropwise added to the diol compound solution to react for 24 hours. Afterward, the solvent of the reaction result was removed, and the reaction result was further dried in an oven to obtain an anhydride compound. The .sup.1H NMR spectrum of the anhydride compound is shown below: .sup.1H NMR (400 MHz, CDCl.sub.3): δ 2.14 (s, 4H, aliphatic), 2.19 (s, 9H, aliphatic), 2.31 (s, 2H, aliphatic bridge), 7.14 (s, 4H, —Ar), 8.23 (d, 2H, phthalic anhydride, J=7.88 Hz), 8.76 (d, 2H, phthalic anhydride, J=7.88 Hz), 8.88 (s, 2H, phthalic anhydride). The reaction is shown below:

##STR00038##

[0034] The anhydride compound and ODA were allowed to react at 25° C. for 6 hours to form polyimide. The polyimide solution was coated to form a thin film having a thickness of about 50 μm for measuring its dielectric constant at 10 GHz (2.80), dielectric loss at 10 GHz (0.006), and moisture absorption (0.5%).

Comparative Example 1

[0035] p-Phenylenebis(trimellitate anhydride) (TAHQ) and ODA were allowed to react at 25° C. for 6 hours to form polyimide. The polyimide solution was coated to form a thin film having a thickness of about 50 μm for measuring its dielectric constant at 10 GHz (3.5), dielectric loss at 10 GHz (0.007), and moisture absorption (0.6%). TAHQ has a chemical structure of

##STR00039##

[0036] As shown in the comparison between Example 1 and Comparative Example 1, the polyimide formed from the anhydride compound in Example 1 is preferably applied as 5G board material due to its lower dielectric constant, lower dielectric loss, and lower moisture absorption.

[0037] It will be apparent to those skilled in the art that various modifications and variations can be made to the disclosed methods and materials. It is intended that the specification and examples be considered as exemplary only, with the true scope of the disclosure being indicated by the following claims and their equivalents.