JP2011157297A - Diethylzinc composition, method for thermal stabilization and compound for thermal stabilization - Google Patents

Diethylzinc composition, method for thermal stabilization and compound for thermal stabilization Download PDF

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JP2011157297A
JP2011157297A JP2010019853A JP2010019853A JP2011157297A JP 2011157297 A JP2011157297 A JP 2011157297A JP 2010019853 A JP2010019853 A JP 2010019853A JP 2010019853 A JP2010019853 A JP 2010019853A JP 2011157297 A JP2011157297 A JP 2011157297A
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diethylzinc
compound
composition
diethyl zinc
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JP5775672B2 (en
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Kenichi Haga
健一 羽賀
Shizuo Tomiyasu
静夫 富安
Koichi Tokutome
功一 徳留
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Tosoh Finechem Corp
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Priority to US13/394,129 priority patent/US8722561B2/en
Priority to KR1020127007704A priority patent/KR101790801B1/en
Priority to CN201080046333.8A priority patent/CN102686597B/en
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Abstract

<P>PROBLEM TO BE SOLVED: To enhance thermal stabilization of diethylzinc used for a polymerization catalyst, a reagent for organic syntheses, a raw material for the formation of a zinc oxide film by an MOCVD method or the like, or the like, and to provide a diethylzinc composition that exhibits excellent thermal stability causing no deposition of a zinc metal particle after longtime handling and improves a problem of remaining of diethylzinc when used and a method for thermally stabilizing diethylzinc. <P>SOLUTION: The diethylzinc composition comprises diethylzinc and, added thereto as an additive, a naphthalene compound having a melting point or a freezing point of 85°C or lower. The method for thermally stabilizing diethylzinc is also provided. <P>COPYRIGHT: (C)2011,JPO&INPIT

Description

本発明は、熱安定性に優れたジエチル亜鉛組成物、ジエチル亜鉛組成物の熱安定化方法および熱安定化用化合物に関する。   The present invention relates to a diethylzinc composition excellent in thermal stability, a method for thermal stabilization of a diethylzinc composition, and a compound for thermal stabilization.

ジエチル亜鉛は、従来、ポリエチレンオキシド、ポリプロピレンオキシド等の重合触媒用途や、医薬、機能性材料等の中間体等の製造において有機合成の反応試薬として用いられており、極めて有用な工業材料として知られている。   Diethyl zinc is conventionally used as a reaction reagent for organic synthesis in polymerization catalyst applications such as polyethylene oxide and polypropylene oxide, and in the production of intermediates such as pharmaceuticals and functional materials, and is known as an extremely useful industrial material. ing.

また近年、原料にジエチル亜鉛と酸化剤として水蒸気を使用してMOCVD(Metal Organic Chemical Vapor Deposition)法と呼ばれる手法等により酸化亜鉛薄膜を形成する方法が検討されている。このMOCVD法により得られた酸化亜鉛薄膜は、CIGS太陽電池のバッファ層、透明導電膜、色素増感太陽電池の電極膜、薄膜Si太陽電池の中間層、透明導電膜等の太陽電池における各種機能膜、光触媒膜、紫外線カット膜、赤外線反射膜、帯電防止膜等の各種機能膜、化合物半導体発光素子、薄膜トランジスタ等の電子デバイス等に使用され、幅広い用途を持つ。   In recent years, a method of forming a zinc oxide thin film by a technique called MOCVD (Metal Organic Chemical Vapor Deposition) using diethyl zinc as a raw material and water vapor as an oxidizing agent has been studied. The zinc oxide thin film obtained by this MOCVD method has various functions in solar cells such as CIGS solar cell buffer layer, transparent conductive film, dye-sensitized solar cell electrode film, thin-film Si solar cell intermediate layer, and transparent conductive film. It is used in various functional films such as films, photocatalytic films, ultraviolet cut films, infrared reflective films, and antistatic films, compound semiconductor light emitting devices, electronic devices such as thin film transistors, etc., and has a wide range of uses.

ジエチル亜鉛は、熱を加えると徐々に分解して金属亜鉛粒子が析出することが知られている(例えば非特許文献1参照)。そのため、ジエチル亜鉛の取り扱い等においては、熱分解で生成した金属亜鉛粒子の析出による製品純度の低下、貯蔵容器の汚染、製造設備配管の閉塞等の問題があった。   It is known that diethyl zinc is gradually decomposed and metal zinc particles are deposited when heat is applied (for example, see Non-Patent Document 1). Therefore, handling of diethyl zinc has problems such as a decrease in product purity due to precipitation of metal zinc particles generated by pyrolysis, contamination of storage containers, and blockage of manufacturing equipment piping.

上記の熱分解で生成した金属亜鉛粒子の析出に関する問題を解決する方法として、例えば、アントラセン、アセナフテン、アセナフチレン等の化合物を添加してジエチル亜鉛を安定化した組成物とするような方法が知られている(例えば特許文献1〜3参照)。   As a method for solving the above-mentioned problems related to the precipitation of metal zinc particles generated by pyrolysis, for example, a method of adding a compound such as anthracene, acenaphthene, or acenaphthylene to obtain a composition in which diethyl zinc is stabilized is known. (For example, refer to Patent Documents 1 to 3).

米国特許第4385003号明細書U.S. Pat. No. 4,385,003 米国特許第4402880号明細書U.S. Pat. No. 4,402,880 米国特許第4407758号明細書U.S. Pat. No. 4,407,758

Yasuo Kuniya et Al.,Applied Organometallic Chemistry、5巻,337〜347頁,1991年発行Yasuo Kuniya et al. , Applied Organometallic Chemistry, 5, 337-347, published in 1991

特許文献1〜3に開示されるように、アントラセン、アセナフテン、アセナフチレンを添加してもジエチル亜鉛を十分に安定化することができず、より熱安定性に優れたジエチル亜鉛が求められる。
また、アントラセン、アセナフテン、アセナフチレンは、それぞれの融点が、216℃、93℃、90〜95℃と高く、一般的な取扱温度である25℃前後の室温では固体の化合物である。一般的に、融点の高い物質は、その蒸気圧が低く、CVD成膜等におけるジエチル亜鉛の使用においては、キャリアガスによるバブリングによってジエチル亜鉛をキャリアガス中の飽和ガスとして供給する際に、これら、アントラセン、アセナフテン、アセナフチレンといった添加物は、気化せずにジエチル亜鉛中に残存する割合が多くなる恐れがある。
As disclosed in Patent Documents 1 to 3, even if anthracene, acenaphthene, and acenaphthylene are added, diethylzinc cannot be sufficiently stabilized, and diethylzinc having higher thermal stability is required.
Anthracene, acenaphthene, and acenaphthylene have high melting points of 216 ° C., 93 ° C., and 90 to 95 ° C., and are solid compounds at room temperature around 25 ° C., which is a general handling temperature. In general, a substance having a high melting point has a low vapor pressure, and in the use of diethyl zinc in CVD film formation or the like, when supplying diethyl zinc as a saturated gas in the carrier gas by bubbling with a carrier gas, Additives such as anthracene, acenaphthene, and acenaphthylene are likely to remain in diethyl zinc without being vaporized.

さらに、これら固体の化合物を添加物として用いてジエチル亜鉛組成物を調整する際には、固体投入機等を用いて添加物の移送を行なうが、移送時の添加物の閉塞等のトラブルの際には、ジエチル亜鉛への不純物の汚染がないように対応が必要である。
この移送に際するトラブルの際の添加物の除去に際して、ジエチル亜鉛への不純物の汚染がないように対応として、添加物自身を加熱して融解するなどの対応を行う場合には、添加物は、より融点の低い化合物であることが望ましい。
このような点から、ジエチル亜鉛の添加物は、より融点の低い化合物であることが望ましい。
Furthermore, when preparing a diethylzinc composition using these solid compounds as additives, the additives are transferred using a solid charging machine or the like, but in the case of troubles such as blocking of the additives during the transfer. Therefore, it is necessary to take measures to prevent contamination of diethyl zinc with impurities.
When removing the additive in the case of trouble during the transfer, in order to prevent contamination of the impurities to the diethylzinc, when taking measures such as heating and melting the additive itself, It is desirable that the compound has a lower melting point.
From this point, it is desirable that the diethylzinc additive is a compound having a lower melting point.

即ち本発明は、重合触媒や有機合成試薬およびMOCVD法等による酸化亜鉛薄膜製造原料等に使用されるジエチル亜鉛の熱安定性を向上させ、長期間取り扱っても金属亜鉛粒子が析出しない熱安定性に優れ、またジエチル亜鉛の使用時の残存の問題を軽減するジエチル亜鉛組成物及びジエチル亜鉛の熱安定化の方法を提供することを目的とし、添加物として、その融点が前述の公知の添加物よりもより低いもの、即ち、添加物の融点または凝固点が85℃以下の化合物を使用する。   That is, the present invention improves the thermal stability of diethyl zinc used as a raw material for producing a zinc oxide thin film by a polymerization catalyst, an organic synthesis reagent, MOCVD method, etc., and does not precipitate metallic zinc particles even when handled for a long time. It is an object of the present invention to provide a diethylzinc composition and a method for thermal stabilization of diethylzinc that are excellent in reducing the residual problem when using diethylzinc, and the melting point of the additive is the aforementioned known additive. Lower than that of the additive, that is, a compound having a melting point or freezing point of the additive of 85 ° C. or lower.

本発明者は上記課題を解決すべく鋭意研究開発を行った結果、添加物の融点または凝固点が85℃以下の化合物として、融点または凝固点が85℃以下であるナフタレン化合物をジエチル亜鉛(CAS No.557−20−0)に共存させた組成物とすることで熱安定性が著しく向上することを見出し、本発明を完成させた。   As a result of diligent research and development to solve the above-mentioned problems, the present inventor obtained a naphthalene compound having a melting point or freezing point of 85 ° C. or lower as diethyl zinc (CAS No. 557-20-0), the thermal stability was remarkably improved by using the composition coexisting with the composition, and the present invention was completed.

本発明に係るジエチル亜鉛組成物は、ジエチル亜鉛に、添加物として添加する融点または凝固点が85℃以下の化合物として、融点または凝固点が85℃以下であるナフタレン化合物が添加されたジエチル亜鉛組成物である。   The diethylzinc composition according to the present invention is a diethylzinc composition obtained by adding a naphthalene compound having a melting point or freezing point of 85 ° C. or lower as a compound having a melting point or freezing point of 85 ° C. or lower to diethyl zinc. is there.

また本発明に係るジエチル亜鉛組成物において、前述の、ナフタレン化合物としては、下記一般式(1)、一般式(2)および一般式(3)で表される化合物からなる群より選ばれる1つまたは2以上の化合物を含む。   In the diethylzinc composition according to the present invention, the naphthalene compound described above is one selected from the group consisting of compounds represented by the following general formula (1), general formula (2) and general formula (3). Or two or more compounds.

Figure 2011157297
Figure 2011157297
Figure 2011157297
Figure 2011157297
Figure 2011157297
Figure 2011157297

(式(1)、式(2)および式(3)中、Rはそれぞれ独立して、水素、炭素数1〜8の直鎖もしくは分岐したアルキル基(アルキル基にはイソプロピル基も含む)、炭素数1〜8の直鎖もしくは分岐したアルケニル基、炭素数6〜14のアリル基である)。 (In the formula (1), the formula (2) and the formula (3), each R is independently hydrogen, a linear or branched alkyl group having 1 to 8 carbon atoms (the alkyl group includes an isopropyl group), A linear or branched alkenyl group having 1 to 8 carbon atoms and an allyl group having 6 to 14 carbon atoms).

前述の融点または凝固点が85℃以下であるナフタレン化合物として、例えば、式(1)および式(2)の例として、ナフタレン自身や、側鎖にアルキル基を有するものとして、例えば、2−メチルナフタレン、2,6−ジイソプロピルナフタレン、アルケニル基等や、アリル基を有するものとして、1−スチリルナフタレン等、酸素を有するナフタレン化合物である式(3)の例として、例えば、2-メトキシナフタレン等の化合物を挙げることが出来る。   Examples of the naphthalene compound having a melting point or a freezing point of 85 ° C. or lower include, for example, naphthalene itself or those having an alkyl group in the side chain as examples of formula (1) and formula (2), for example, 2-methylnaphthalene 2,6-diisopropylnaphthalene, alkenyl group, etc., those having an allyl group, 1-styrylnaphthalene, etc., as an example of formula (3) which is a naphthalene compound having oxygen, for example, a compound such as 2-methoxynaphthalene Can be mentioned.

これらの芳香族化合物のなかでも、構造が単純であり、工業的に容易に入手可能なもので高い効果が得られる添加物として、前述のナフタレン、2−メチルナフタレン、2,6−ジイソプロピルナフタレン、1−スチリルナフタレンおよび2―メトキシナフタレンを好ましく用いることが出来る。
これらのナフタレン化合物は、85℃以下の融点である。
Among these aromatic compounds, the above-mentioned naphthalene, 2-methylnaphthalene, 2,6-diisopropylnaphthalene, and the like, which have a simple structure and can be easily obtained industrially, have a high effect. 1-styrylnaphthalene and 2-methoxynaphthalene can be preferably used.
These naphthalene compounds have a melting point of 85 ° C. or lower.

本発明に用いられる添加物は、単独の添加で充分な効果が得られるが、複数を混合して用いても差し支えない。
ここで、添加物の添加量は、ジエチル亜鉛の性能が維持され、熱安定化効果が得られる範囲であれば、特に制限は無いが、通常、ジエチル亜鉛に対して、100ppm〜20wt%、好ましくは500ppm〜10wt%,より好ましくは 2000ppm〜5wt%であれば,熱安定性に優れたジエチル亜鉛組成物を得ることができる。
The additive used in the present invention can provide a sufficient effect when added alone, but a plurality of additives may be used in combination.
Here, the addition amount of the additive is not particularly limited as long as the performance of diethyl zinc is maintained and a thermal stabilization effect is obtained, but usually 100 ppm to 20 wt%, preferably with respect to diethyl zinc. Is 500 ppm to 10 wt%, more preferably 2000 ppm to 5 wt%, a diethylzinc composition having excellent thermal stability can be obtained.

本発明の添加物の添加量が、少なすぎると熱安定性向上の充分な効果が得られない場合があったり、多すぎると、添加量を増加した効果が得られない場合もあるので、熱安定性の所望の効果を得るための適量を添加することが望ましい。   If the amount of the additive of the present invention is too small, a sufficient effect of improving the thermal stability may not be obtained, and if it is too large, the effect of increasing the amount of addition may not be obtained. It is desirable to add an appropriate amount to obtain the desired effect of stability.

本発明に使用されるジエチル亜鉛は、ポリエチレンオキシド、ポリプロピレンオキシド等の重合触媒用途や、医薬、機能性材料等の中間体等の製造において有機合成の反応試薬として用いられている一般に工業材料として知られているものを用いることが出来る。   Diethyl zinc used in the present invention is generally known as an industrial material used as a reaction reagent for organic synthesis in polymerization catalyst applications such as polyethylene oxide and polypropylene oxide, and in the production of intermediates such as pharmaceuticals and functional materials. What is being used can be used.

また、本発明においては、MOCVD法等により酸化亜鉛薄膜を形成する方法で使用され、CIGS太陽電池のバッファ層、透明導電膜、色素増感太陽電池の電極膜、薄膜Si太陽電池の中間層、透明導電膜等の太陽電池における各種機能膜、光触媒膜、紫外線カット膜、赤外線反射膜、帯電防止膜等の各種機能膜、化合物半導体発光素子、薄膜トランジスタ等の電子デバイス等に使用されるような、工業材料よりも高純度のジエチル亜鉛も用いることが出来る。   In the present invention, it is used in a method of forming a zinc oxide thin film by MOCVD or the like, and includes a buffer layer for CIGS solar cells, a transparent conductive film, an electrode film for dye-sensitized solar cells, an intermediate layer for thin-film Si solar cells, Various functional films in solar cells such as transparent conductive films, photocatalytic films, ultraviolet cut films, infrared reflective films, various functional films such as antistatic films, compound semiconductor light emitting devices, electronic devices such as thin film transistors, etc. Diethyl zinc having a purity higher than that of industrial materials can also be used.

本発明のジエチル亜鉛組成物の調製においては、ジエチル亜鉛と本発明の添加物とを混合すればよく、例えば、ジエチル亜鉛に前述の添加物を添加する等、添加の方法においては特に制限は無い。   In preparing the diethylzinc composition of the present invention, diethylzinc and the additive of the present invention may be mixed, and there is no particular limitation on the method of addition, for example, the above-mentioned additive is added to diethylzinc. .

例えば、保存安定性の向上を目的する場合においては、あらかじめ、ジエチル亜鉛に添加物を添加する方法を用いることが出来る。
また、例えば、反応等に使用する場合、使用の直前にジエチル亜鉛に添加物を添加することも可能である。
For example, in order to improve storage stability, a method of adding an additive to diethyl zinc in advance can be used.
Further, for example, when used for a reaction or the like, an additive can be added to diethyl zinc immediately before use.

また、本発明のジエチル亜鉛組成物の調製の温度においては、ジエチル亜鉛の熱分解の影響が少ない70℃以下が望ましい。通常、−20℃〜35℃で本発明の組成物の調製を行なうことが出来る。また、圧力についても、特に制限は無いが、反応等、特殊な場合を除いては、通常、0.1013MPaなど、大気圧付近でジエチル亜鉛と本発明の組成物の調製を行なうことが出来る。   In addition, the temperature for preparing the diethylzinc composition of the present invention is preferably 70 ° C. or less, which is less affected by the thermal decomposition of diethylzinc. Usually, the composition of the present invention can be prepared at -20 ° C to 35 ° C. Also, the pressure is not particularly limited. Except for special cases such as reaction, diethylzinc and the composition of the present invention can be usually prepared near atmospheric pressure, such as 0.1013 MPa.

本発明のジエチル亜鉛組成物の保管・運搬容器、貯蔵タンク、配管等の設備における使用機材、使用雰囲気はジエチル亜鉛に用いているものをそのまま転用可能である。例えば、前述の使用機材の材質はSUS、炭素鋼、チタン、ハステロイ等の金属や、テフロン(登録商標)、フッ素系ゴム等の樹脂等を用いることができる。また、使用雰囲気は、窒素、ヘリウム、アルゴン等の不活性ガス等がジエチル亜鉛と同様に用いることができる。   The equipment used and the atmosphere used in equipment such as storage / transport containers, storage tanks, and piping for the diethyl zinc composition of the present invention can be used as they are. For example, the material of the above-mentioned equipment can be a metal such as SUS, carbon steel, titanium, or Hastelloy, or a resin such as Teflon (registered trademark) or fluorine rubber. In addition, an inert gas such as nitrogen, helium, or argon can be used in the same manner as diethyl zinc.

また、本発明のジエチル亜鉛組成物は、ジエチル亜鉛の使用に際して用いることが出来る公知の溶媒に溶解して使用することが出来る。前記溶媒の例として、例えば、ペンタン、ヘキサン、ヘプタン、オクタン等の飽和炭化水素や、ベンゼン、トルエン、キシレン等の芳香族炭化水素等の炭化水素化合物、ジエチルエーテル、ジイソプロピルエーテル、テトラヒドロフラン、ジオキサン、ジグライム等のエーテル系化合物等を挙げることが出来る。   The diethyl zinc composition of the present invention can be used by dissolving in a known solvent that can be used when diethyl zinc is used. Examples of the solvent include, for example, saturated hydrocarbons such as pentane, hexane, heptane and octane, hydrocarbon compounds such as aromatic hydrocarbons such as benzene, toluene and xylene, diethyl ether, diisopropyl ether, tetrahydrofuran, dioxane and diglyme. And ether compounds such as

本発明のジエチル亜鉛組成物の用途としては、例えば、ポリエチレンオキシド、ポリプロピレンオキシド等の重合触媒用途や、医薬、機能性材料等の中間体等の製造において有機合成の反応試薬としての用途や、また、MOCVD法等により酸化亜鉛薄膜を形成する方法で使用され、CIGS太陽電池のバッファ層、透明導電膜、色素増感太陽電池の電極膜、薄膜Si太陽電池の中間層、透明導電膜等の太陽電池における各種機能膜、光触媒膜、紫外線カット膜、赤外線反射膜、帯電防止膜等の各種機能膜、化合物半導体発光素子、薄膜トランジスタ等の電子デバイス等に使用されるような酸化物形成用途や、ZnS等、II−VI族の電子デバイス用薄膜形成用途等、これまでジエチル亜鉛が使用されている用途と同様のものを挙げることが出来る。   Examples of the use of the diethylzinc composition of the present invention include use as a polymerization catalyst such as polyethylene oxide and polypropylene oxide, use as a reaction reagent for organic synthesis in the production of intermediates such as pharmaceuticals and functional materials, , Used in a method of forming a zinc oxide thin film by MOCVD method, etc., and CIGS solar cell buffer layer, transparent conductive film, dye-sensitized solar cell electrode film, thin film Si solar cell intermediate layer, transparent conductive film, etc. Various functional films such as various functional films, photocatalytic films, ultraviolet cut films, infrared reflective films, antistatic films, etc. in batteries, oxide forming applications such as compound semiconductor light emitting devices, electronic devices such as thin film transistors, etc., ZnS List the same applications where diethyl zinc has been used so far, such as thin film formation applications for II-VI electronic devices. Can.

本発明の添加物を添加したジエチル亜鉛組成物は、熱安定性に優れ、ジエチル亜鉛が熱分解することにより発生する金属亜鉛粒子の析出が極めて少ない。その結果、製品純度の低下,貯蔵容器の汚染、製造設備配管の閉塞等の問題を防ぐことが可能となる。   The diethyl zinc composition to which the additive of the present invention is added is excellent in thermal stability, and the precipitation of metallic zinc particles generated by the thermal decomposition of diethyl zinc is extremely small. As a result, it is possible to prevent problems such as a decrease in product purity, contamination of storage containers, and blockage of manufacturing equipment piping.

以下に本発明を実施例によってさらに詳細に説明するが、これらの実施例は本発明を限定するものではない。   EXAMPLES The present invention will be described in more detail with reference to examples below, but these examples do not limit the present invention.

[測定機器]
DSC測定(示差走査熱量測定:Differential Scanning Calorimetry)は、DSC6200(セイコーインスツルメンツ株式会社製)を用いて行なった。
[measuring equipment]
DSC measurement (Differential Scanning Calorimetry) was performed using DSC6200 (manufactured by Seiko Instruments Inc.).

[ジエチル亜鉛組成物の調製]
ジエチル亜鉛(東ソー・ファインケム株式会社製)と種々の添加物(市販試薬)とを窒素雰囲気下、室温において所定の濃度でガラス容器に秤量した。添加物をジエチル亜鉛に溶解して、ジエチル亜鉛組成物を調製した。
ジエチル亜鉛への添加物の添加率(重量%)は、以下の式で定義したものを用いた。
添加物の添加率(重量%)=(添加物重量/(添加物重量+ジエチル亜鉛重量))×100
[Preparation of diethyl zinc composition]
Diethyl zinc (manufactured by Tosoh Finechem Co., Ltd.) and various additives (commercial reagents) were weighed into a glass container at a predetermined concentration at room temperature in a nitrogen atmosphere. The additive was dissolved in diethyl zinc to prepare a diethyl zinc composition.
The addition rate (wt%) of the additive to diethyl zinc was defined by the following formula.
Addition rate (% by weight) of additive = (additive weight / (additive weight + diethyl zinc weight)) × 100

前述の方法で調製したジエチル亜鉛組成物について、DSC測定を行ない、添加物の熱安定性効果を評価した。DSC測定の初期発熱温度が高いほど、ジエチル亜鉛に対する熱安定化の効果が高いことを示す。   About the diethyl zinc composition prepared by the above-mentioned method, DSC measurement was performed and the thermal stability effect of the additive was evaluated. It shows that the higher the initial exothermic temperature of the DSC measurement, the higher the heat stabilization effect for diethyl zinc.

[参考例1]
[ジエチル亜鉛のDSC測定による熱安定性試験]
窒素雰囲気下、ジエチル亜鉛を、SUS製DSCセルに秤収して密閉した。得られたサンプルについてDSC測定を、30〜450℃を測定温度範囲として10℃/分の昇温速度で熱分析測定を行なった。それぞれのサンプルの分解温度は、DSC測定の初期発熱温度で観測される。添加物を添加していないジエチル亜鉛のみのサンプルの初期発熱温度を表1に示す。
[Reference Example 1]
[Thermal stability test by DSC measurement of diethyl zinc]
Diethyl zinc was weighed and sealed in a DSC cell made of SUS under a nitrogen atmosphere. The obtained sample was subjected to DSC measurement, and thermal analysis measurement was performed at a temperature increase rate of 10 ° C./min with a temperature range of 30 to 450 ° C. The decomposition temperature of each sample is observed at the initial exothermic temperature of DSC measurement. Table 1 shows the initial exothermic temperature of a sample containing only diethyl zinc with no additive added.

[実施例1〜5]
[ジエチル亜鉛組成物のDSC測定による熱安定性試験]
参考例1と同様にして、窒素雰囲気下、融点または凝固点が85℃以下であるナフタレン化合物として、ナフタレン、2−メチルナフタレン、2,6−ジイソプロピルナフタレン、1−スチリルナフタレンおよび2―メトキシナフタレンをそれぞれ添加したジエチル亜鉛組成物を、SUS製DSCセルに秤収して密閉した。得られたサンプルについてDSC測定を、30〜450℃を測定温度範囲として10℃/分の昇温速度で参考例1と同様の熱分析測定を行なった。各サンプルの初期発熱温度を表1に示す。
[Examples 1 to 5]
[Thermal stability test by DSC measurement of diethyl zinc composition]
In the same manner as in Reference Example 1, naphthalene, 2-methylnaphthalene, 2,6-diisopropylnaphthalene, 1-styrylnaphthalene and 2-methoxynaphthalene were used as naphthalene compounds having a melting point or freezing point of 85 ° C. or lower in a nitrogen atmosphere. The added diethylzinc composition was weighed and sealed in a SUS DSC cell. The obtained sample was subjected to DSC measurement, and the same thermal analysis measurement as in Reference Example 1 was carried out at a rate of temperature increase of 10 ° C./min with 30 to 450 ° C. as the measurement temperature range. Table 1 shows the initial heat generation temperature of each sample.

本発明の種々の添加物を添加したジエチル亜鉛組成物のサンプルの初期発熱温度は、参考例で得られたジエチル亜鉛のみのサンプルの初期発熱温度よりも高く、本発明の組成物は、ジエチル亜鉛のみのサンプルよりも分解の開始温度が高い。本結果より添加物を添加したジエチル亜鉛組成物の高い熱安定性が確認された。これらの添加物のそれぞれの融点は、ナフタレン:80℃、2−メチルナフタレン:31℃、2,6−ジイソプロピルナフタレン:70℃、1−スチリルナフタレン:70℃および2―メトキシナフタレン:73℃と公知の添加物の融点よりも低い。   The initial exothermic temperature of the sample of diethyl zinc composition to which various additives of the present invention were added was higher than the initial exothermic temperature of the sample of only diethyl zinc obtained in the reference example, and the composition of the present invention The decomposition start temperature is higher than that of the sample alone. From this result, the high thermal stability of the diethyl zinc composition to which the additive was added was confirmed. The melting points of these additives are known as naphthalene: 80 ° C, 2-methylnaphthalene: 31 ° C, 2,6-diisopropylnaphthalene: 70 ° C, 1-styrylnaphthalene: 70 ° C, and 2-methoxynaphthalene: 73 ° C. Lower than the melting point of the additive.

[比較例1〜3]
実施例1〜5と同様にして、特許文献1〜3に記載の化合物であるアントラセン、アセナフテン、アセナフチレンを添加したジエチル亜鉛組成物について同様の検討を行った。それぞれのサンプルの初期発熱温度を表1に示す。
[Comparative Examples 1-3]
In the same manner as in Examples 1 to 5, the same study was performed on a diethyl zinc composition to which anthracene, acenaphthene, and acenaphthylene, which are compounds described in Patent Documents 1 to 3, were added. Table 1 shows the initial heat generation temperature of each sample.

これらのサンプルのうち、アントラセン、アセナフテンは、本発明の添加物を添加したジエチル亜鉛組成物のサンプルの初期発熱温度よりも低く、既存の添加物の添加した組成物は本発明の組成物よりも熱安定性が劣っていた。アセナフチレンを添加したジエチル亜鉛組成物については、熱安定性効果は本発明の添加物よりも若干高いが、これら、公知の添加物のそれぞれの融点は、アントラセン:216℃、アセナフテン:93℃、アセナフチレン90〜95℃といずれも本発明の添加物よりも高い。   Among these samples, anthracene and acenaphthene are lower than the initial exothermic temperature of the sample of the diethyl zinc composition to which the additive of the present invention is added, and the composition to which the existing additive is added is more than the composition of the present invention. Thermal stability was poor. The diethylzinc composition added with acenaphthylene has a slightly higher thermal stability effect than the additive of the present invention. The melting points of these known additives are anthracene: 216 ° C., acenaphthene: 93 ° C., acenaphthylene. 90-95 degreeC and all are higher than the additive of this invention.

Figure 2011157297
Figure 2011157297

Claims (9)

ジエチル亜鉛に添加物として、融点または凝固点が85℃以下であるナフタレン化合物が添加されたジエチル亜鉛組成物。   A diethyl zinc composition in which a naphthalene compound having a melting point or a freezing point of 85 ° C. or lower is added as an additive to diethyl zinc. 請求項1記載のジエチル亜鉛組成物において、前記融点または凝固点が85℃以下であるナフタレン化合物として、下記一般式(1)、一般式(2)および一般式(3)で表される化合物からなる群より選ばれる1つまたは2以上の化合物であることを特徴とするジエチル亜鉛組成物。
Figure 2011157297
Figure 2011157297

Figure 2011157297

(式(1)、式(2)および式(3)中、Rはそれぞれ独立して、水素、炭素数1〜8の直鎖もしくは分岐したアルキル基(アルキル基にはイソプロピル基も含む)、炭素数1〜8の直鎖もしくは分岐したアルケニル基、炭素数6〜14のアリル基である)。
The diethyl zinc composition according to claim 1, wherein the naphthalene compound having a melting point or a freezing point of 85 ° C or lower is composed of a compound represented by the following general formula (1), general formula (2) and general formula (3). A diethylzinc composition, which is one or more compounds selected from the group.
Figure 2011157297
Figure 2011157297

Figure 2011157297

(In the formula (1), the formula (2) and the formula (3), each R is independently hydrogen, a linear or branched alkyl group having 1 to 8 carbon atoms (the alkyl group includes an isopropyl group), A linear or branched alkenyl group having 1 to 8 carbon atoms and an allyl group having 6 to 14 carbon atoms).
請求項1または請求項2に記載のジエチル亜鉛組成物において、前記添加物が、ナフタレン、2−メチルナフタレン、2,6−ジイソプロピルナフタレン、1−スチリルナフタレンおよび2―メトキシナフタレンからなる群より選ばれる1つまたは2以上の化合物であることを特徴とするジエチル亜鉛組成物。   The diethyl zinc composition according to claim 1 or 2, wherein the additive is selected from the group consisting of naphthalene, 2-methylnaphthalene, 2,6-diisopropylnaphthalene, 1-styrylnaphthalene and 2-methoxynaphthalene. A diethylzinc composition characterized in that it is one or more compounds. ジエチル亜鉛への添加物の添加率が100ppm〜20wt%である、請求項1〜請求項3のいずれかに記載のジエチル亜鉛組成物。   The diethyl zinc composition in any one of Claims 1-3 whose addition rate of the additive to diethyl zinc is 100 ppm-20 wt%. 請求項1〜4のいずれかに記載のジエチル亜鉛組成物において、前記ジエチル亜鉛組成物を構成する添加物とは異なる種類の炭素数5〜25の飽和及び/または不飽和炭化水素及び炭素数6〜30の芳香族炭化水素化合物あるいはエーテル系化合物が共存することを特徴とするジエチル亜鉛組成物。   The diethylzinc composition according to any one of claims 1 to 4, wherein the saturated and / or unsaturated hydrocarbons having 5 to 25 carbon atoms and / or carbon atoms of 6 kinds different from the additive constituting the diethylzinc composition. A diethylzinc composition characterized in that -30 aromatic hydrocarbon compounds or ether compounds coexist. ジエチル亜鉛の熱安定性を向上させる方法であって、添加物として請求項1〜3のいずれかに記載の化合物を用い、請求項4に記載した添加率で添加することを特徴とするジエチル亜鉛の熱安定化方法。   A method for improving the thermal stability of diethylzinc, wherein the compound according to any one of claims 1 to 3 is used as an additive and added at the addition rate according to claim 4. Heat stabilization method. 請求項6記載のジエチル亜鉛の安定化方法において、前記ジエチル亜鉛組成物を構成する添加物とは異なる種類の炭素数5〜25の飽和及び/または不飽和炭化水素及び炭素数6〜30の芳香族炭化水素化合物あるいはエーテル系化合物をジエチル亜鉛に共存させることを特徴とするジエチル亜鉛の熱安定化方法。   7. The method for stabilizing diethylzinc according to claim 6, wherein the saturated and / or unsaturated hydrocarbon having 5 to 25 carbon atoms and a fragrance having 6 to 30 carbon atoms are different from the additive constituting the diethylzinc composition. A method for thermally stabilizing diethylzinc, characterized in that an aromatic hydrocarbon compound or an ether compound is allowed to coexist in diethylzinc. ジエチル亜鉛の熱安定性を向上させるために添加する化合物であって、請求項1〜3のいずれかに記載の構造を有することを特徴とする熱安定化用化合物。   A compound to be added to improve the thermal stability of diethyl zinc, the compound for heat stabilization having the structure according to any one of claims 1 to 3. 請求項8記載の熱安定化用化合物において、前記ジエチル亜鉛組成物を構成する添加物とは異なる種類の炭素数5〜25の飽和及び/または不飽和炭化水素及び炭素数6〜30の芳香族炭化水素化合物あるいはエーテル系化合物が共存することを特徴とする熱安定化用化合物。   The compound for thermal stabilization according to claim 8, wherein the saturated and / or unsaturated hydrocarbon having 5 to 25 carbon atoms and an aromatic having 6 to 30 carbon atoms are different from the additive constituting the diethyl zinc composition. A compound for thermal stabilization, wherein a hydrocarbon compound or an ether compound coexists.
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