JP4902381B2 - Polymer of polymerizable compound - Google Patents
Polymer of polymerizable compound Download PDFInfo
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- JP4902381B2 JP4902381B2 JP2007027557A JP2007027557A JP4902381B2 JP 4902381 B2 JP4902381 B2 JP 4902381B2 JP 2007027557 A JP2007027557 A JP 2007027557A JP 2007027557 A JP2007027557 A JP 2007027557A JP 4902381 B2 JP4902381 B2 JP 4902381B2
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- 0 CC(*)C(O)OCC*C(O)OCCCCCC(CC1*(CCCC2)C2c2ccccc2C1)=CC(C)C(C)OC1*2C=CCCC2C2=CC=CCC12 Chemical compound CC(*)C(O)OCC*C(O)OCCCCCC(CC1*(CCCC2)C2c2ccccc2C1)=CC(C)C(C)OC1*2C=CCCC2C2=CC=CCC12 0.000 description 3
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本発明は、平面表示パネルやこれに用いられるバックライト用の有機発光素子（ＯＬＥＤ）に用いられる高分子系発光材料の前駆体である重合性化合物の重合体に関するものである。 The present invention relates to a polymer of a polymerizable compound which is a precursor of a polymer light emitting material used in a flat display panel or an organic light emitting device (OLED) for a backlight used therein.
有機発光素子は、１９８７年にコダック社のＣ．Ｗ．Ｔａｎｇらにより高輝度の発光が示されて（非特許文献１参照。）以来、材料開発、素子構造の改良が急速に進み、最近になってカーオーディオや携帯電話用のディスプレイなどから実用化が始まった。この有機ＥＬ（エレクトロルミネッッセンス）の用途を更に拡大するために、発光効率向上、耐久性向上のための材料開発、フルカラー表示の開発などが現在活発に行われている。特に、中型パネルや大型パネル、あるいは照明用途への展開を考える上では発光効率の向上による更なる高輝度化と、大面積化に適した量産方法の確立が必要である。 The organic light-emitting device was manufactured by Kodak C.I. W. Since Tang et al. Showed high-luminance light emission (see Non-Patent Document 1), material development and device structure improvements have rapidly progressed, and recently they have been put into practical use from displays for car audio and mobile phones. Was started. In order to further expand the applications of this organic EL (electroluminescence), development of materials for improving luminous efficiency and durability, development of full-color display, and the like are being actively carried out. In particular, when considering expansion to medium-sized panels, large-sized panels, or lighting applications, it is necessary to establish a mass production method suitable for further increase in luminance and increase in area by improving luminous efficiency.
先ず、発光効率に関しては、現在の発光材料で利用されているのは励起一重項状態からの発光、すなわち蛍光であり、非特許文献２によれば、電気的励起における励起一重項状態と励起三重項状態の励起子の生成比が１：３であることから、有機ＥＬにおける発光の内部量子効率は２５％が上限である。 First, regarding light emission efficiency, light emission from an excited singlet state, that is, fluorescence is used in the present light emitting material. According to Non-Patent Document 2, the excited singlet state and excited triplet in electrical excitation are used. Since the generation ratio of the excitons in the term state is 1: 3, the upper limit of the internal quantum efficiency of light emission in the organic EL is 25%.
これに対し、Ｍ．Ａ．Ｂａｌｄｏらは励起三重項状態から燐光発光するイリジウム錯体を用いることにより外部量子効率７．５％を得、これは外部取り出し効率を２０％と仮定すると内部量子効率３７．５％に相当し、蛍光色素を利用した場合の上限値である２５％という値を上回ることが可能なことを示した（非特許文献３、特許文献１参照。）。 In contrast, M.M. A. Baldo et al. Obtained an external quantum efficiency of 7.5% by using an iridium complex that emits phosphorescence from an excited triplet state, which corresponds to an internal quantum efficiency of 37.5% assuming an external extraction efficiency of 20%. It was shown that it is possible to exceed the upper limit of 25% when a dye is used (see Non-Patent Document 3 and Patent Document 1).
次に、パネルの量産方法に関しては、従来から真空蒸着法が用いられてきた。しかし、この方法は真空設備を必要とする点、大面積になるほど有機薄膜を均一の厚さに成膜することが困難になる点などの問題点を有しており、必ずしも大面積パネルの量産に適した方法とは言えない。 Next, as a mass production method for panels, a vacuum deposition method has been conventionally used. However, this method has problems such as requiring vacuum equipment and the difficulty of forming an organic thin film with a uniform thickness as the area becomes larger. This is not a suitable method.
これに対し、大面積化が容易な方法として高分子系発光材料を用いた製造方法、すなわちインクジェット法や印刷法が開発されている。特に、印刷法は連続して長尺の成膜が行え、大面積化と量産性に優れている。 On the other hand, a manufacturing method using a polymer light emitting material, that is, an ink jet method or a printing method has been developed as a method for easily increasing the area. In particular, the printing method can continuously form a long film and is excellent in large area and mass productivity.
上記のように、発光効率が高くかつ大面積の有機発光素子を得るためには、燐光発光性の高分子材料が必要となる。このような燐光発光性の高分子材料としては、ルテニウム錯体を高分子の主鎖または側鎖に組み込んだものがある（非特許文献４参照。）。しかし、これらはイオン性化合物であるため、電圧を印加した場合に電極での酸化還元反応による電気化学発光が起こる。これは応答速度が分オーダーと極めて遅く、通常のディスプレイパネルとしては使用できない。
また、厳密な意味では高分子材料とは言えないが、ポリ（Ｎ−ビニルカルバゾール）に燐光発光性の低分子化合物であるイリジウム錯体を混合したものがある（非特許文献５参照。）。しかし、これは均質な高分子材料に較べて熱安定性が劣り、相分離や偏析を起こす可能性がある。
As described above, in order to obtain an organic light emitting device with high luminous efficiency and a large area, a phosphorescent polymer material is required. As such a phosphorescent polymer material, there is a material in which a ruthenium complex is incorporated in a main chain or a side chain of a polymer (see Non-Patent Document 4). However, since these are ionic compounds, electrochemiluminescence due to an oxidation-reduction reaction at the electrode occurs when a voltage is applied. This is a very slow response speed on the order of minutes and cannot be used as a normal display panel.
In a strict sense, although it cannot be said to be a polymer material, there is a material in which poly (N-vinylcarbazole) is mixed with an iridium complex which is a phosphorescent low-molecular compound (see Non-Patent Document 5). However, this is inferior in thermal stability to a homogeneous polymer material and may cause phase separation or segregation.
上記のように、発光効率が高くかつ大面積の有機発光素子を量産するために必要とされる実用的な高分子系の燐光発光性材料は未だ存在しない。そこで、本発明は上記のような従来技術の問題点を解決し、高発光効率で大面積化が可能であり、かつ量産可能な有機発光素子を得るための高分子系発光材料を提供することを課題とする。 As described above, there is no practical high-molecular phosphorescent material required for mass-producing organic light-emitting devices having high luminous efficiency and a large area. Accordingly, the present invention provides a polymer light-emitting material for solving the problems of the prior art as described above, and for obtaining an organic light-emitting device capable of large area production with high luminous efficiency and mass production. Is an issue.
本発明者らは、上記の課題を解決すべく種々検討した結果、有機発光素子の発光材料として有用なイリジウム錯体部分を有する重合性化合物を得ることに成功し、本発明を完成するに至った。 As a result of various studies to solve the above problems, the present inventors have succeeded in obtaining a polymerizable compound having an iridium complex portion useful as a light-emitting material of an organic light-emitting device, and completed the present invention. .
すなわち、本発明は以下の［１］〜［４２］で示される新規化合物である重合性化合物とこれら重合性化合物の合成に必要な新規化合物である中間体、及びこれら重合性化合物の製造方法に関する。 That is, the present invention relates to a polymerizable compound which is a novel compound represented by the following [1] to [42], an intermediate which is a novel compound necessary for the synthesis of these polymerizable compounds, and a method for producing these polymerizable compounds. .
［１］ 式（１）で示される重合性化合物。
［２］ 前記式（１）におけるＸ1またはＺ1のいずれか一方が重合性官能基を有する置換基である［１］に記載の重合性化合物。 [2] The polymerizable compound according to [1], wherein either X 1 or Z 1 in the formula (1) is a substituent having a polymerizable functional group.
［３］式（２）で示される重合性化合物。
［４］ 重合性官能基が炭素−炭素二重結合である［１］〜［３］のいずれか一つに記載の重合性化合物。 [4] The polymerizable compound according to any one of [1] to [3], wherein the polymerizable functional group is a carbon-carbon double bond.
［５］ 式（３）で示される重合性化合物。
［６］ 重合性官能基がスチリル基である［１］〜［３］のいずれか一つに記載の重合性化合物。 [6] The polymerizable compound according to any one of [1] to [3], wherein the polymerizable functional group is a styryl group.
［７］ 式（４）で示される重合性化合物。
［８］ 重合性官能基がアクリレート基またはメタクリレート基である［１］〜［３］のいずれか一つに記載の重合性化合物。 [8] The polymerizable compound according to any one of [1] to [3], wherein the polymerizable functional group is an acrylate group or a methacrylate group.
［９］ 式（５）で示される重合性化合物。
［１０］ 式（６）で示される重合性化合物。
［１１］ 式（７）で示される重合性化合物。
［１２］式（８）で示される重合性化合物。
［１３］ 式（９）で示される重合性化合物。
［１４］ 式（１０）で示される重合性化合物。
［１５］ 式（１１）で示される重合性化合物。
［１６］ 式（１２）で示される重合性化合物。
［１７］ 式（１３）で示される重合性化合物。
［１８］ 前記式（１）におけるＹ1が重合性官能基を有する置換基である［１］に記載の重合性化合物。 [18] The polymerizable compound according to [1], wherein Y 1 in the formula (1) is a substituent having a polymerizable functional group.
［１９］ 式（１４）で示される重合性化合物。
［２０］ 重合性官能基が炭素−炭素二重結合である［１８］または［１９］に記載の重合性化合物。
［２１］ 重合性官能基がスチリル基である［１８］または［１９］に記載の重合性化合物。
［２２］ 重合性官能基がアクリレート基またはメタクリレート基である［１８］または［１９］に記載の重合性化合物。
[20] The polymerizable compound according to [18] or [19], wherein the polymerizable functional group is a carbon-carbon double bond.
[21] The polymerizable compound according to [18] or [19], wherein the polymerizable functional group is a styryl group.
[22] The polymerizable compound according to [18] or [19], wherein the polymerizable functional group is an acrylate group or a methacrylate group.
［２３］ 式（１５）で示される重合性化合物。
［２４］ 式（１６）で示される重合性化合物。
［２５］ 式（１７）で示されるイリジウム二核錯体と式（１８）で示される重合性官能基を有する化合物を反応させることを特徴とする単核イリジウム錯体部分を含む重合性化合物の製造方法。
［２６］ 前記式（１８）におけるＸ1またはＺ1が重合性官能基を有する置換基である［２５］に記載の単核イリジウム錯体部分を含む重合性化合物の製造方法。
［２７］ 前記式（１８）におけるＹ1が重合性官能基を有する置換基である［２５］に記載の単核イリジウム錯体部分を含む重合性化合物の製造方法。
[26] The method for producing a polymerizable compound containing a mononuclear iridium complex moiety according to [25], wherein X 1 or Z 1 in the formula (18) is a substituent having a polymerizable functional group.
[27] The method for producing a polymerizable compound containing a mononuclear iridium complex moiety according to [25], wherein Y 1 in the formula (18) is a substituent having a polymerizable functional group.
［２８］ 式（１７）で示されるイリジウム二核錯体と式（１９）で示される反応性置換基を有する化合物を反応させた後、得られた単核イリジウム錯体の反応性置換基と重合性官能基を有する化合物を反応させることを特徴とする単核イリジウム錯体部分を含む重合性化合物の製造方法。
［２９］ 式（１９）におけるＸ2またはＹ2が水酸基を有する置換基である［２８］に記載の単核イリジウム錯体部分を含む重合性化合物の製造方法。
［３０］ 式（１９）におけるＹ2が水酸基を有する置換基である請求項２８に記載の単核イリジウム錯体部分を含む重合性化合物の製造方法。
[29] The method for producing a polymerizable compound containing a mononuclear iridium complex moiety according to [28], wherein X 2 or Y 2 in formula (19) is a substituent having a hydroxyl group.
[30] The method for producing a polymerizable compound containing a mononuclear iridium complex moiety according to claim 28, wherein Y 2 in formula (19) is a substituent having a hydroxyl group.
［３１］ 式（２０）で示される化合物。
［３２］ 式（２０）におけるＸ2またはＺ2が水酸基を有する置換基である［３１］に記載の化合物。
[31] The compound represented by the formula (20).
[32] The compound according to [31], wherein X 2 or Z 2 in formula (20) is a substituent having a hydroxyl group.
［３３］ 式（２１）で示される化合物。
［３４］式（２２）で示される化合物。
［３５］ 式（２０）におけるＹ2が水酸基を有する置換基である［３１］に記載の化合物。
[34] A compound represented by formula (22).
[35] The compound according to [31], wherein Y 2 in formula (20) is a substituent having a hydroxyl group.
［３６］ 式（２３）で示される化合物。
［３７］ ［１］〜［２４］のいずれか一つに記載の重合性化合物の重合体。
［３８］ ［１］〜［２４］のいずれか一つに記載の重合性化合物を１種以上含む組成物を重合してなる重合体。
［３９］ ［１］〜［２４］のいずれか一つに記載の重合性化合物を含むことを特徴とする発光材料。
［４０］ ［１］〜［２４］のいずれか一つに記載の重合性化合物を重合してなる発光材料。
［４１］ ［１］〜［２４］のいずれか一つに記載の重合性化合物を１種以上含む組成物を重合してなる発光材料。
［４２］ ［１］〜［２４］のいずれか一つに記載の発光材料を用いた有機発光素子。
[37] A polymer of the polymerizable compound according to any one of [1] to [24].
[38] A polymer obtained by polymerizing a composition containing one or more polymerizable compounds according to any one of [1] to [24].
[39] A light-emitting material comprising the polymerizable compound according to any one of [1] to [24].
[40] A light emitting material obtained by polymerizing the polymerizable compound according to any one of [1] to [24].
[41] A light-emitting material obtained by polymerizing a composition containing one or more polymerizable compounds according to any one of [1] to [24].
[42] An organic light emitting device using the light emitting material according to any one of [1] to [24].
本発明の新規な重合性化合物はイリジウム錯体部分を含む新規な重合体を与え、これを有機発光素子の発光材料として使用することにより励起三重項状態から高効率で発光し、かつ大面積化が可能で量産に適した有機発光素子を提供することができる。
The novel polymerizable compound of the present invention gives a novel polymer containing an iridium complex portion, and by using this as a luminescent material of an organic light-emitting device, it emits light from an excited triplet state with high efficiency and has a large area. An organic light-emitting element that is possible and suitable for mass production can be provided.
以下、本発明を具体的に説明する。
本発明により式（１）
According to the invention, the formula (1)
式（１）におけるＸ1、Ｙ1、Ｚ1のうちの重合性官能基を有する置換基は、ラジカル重合性、カチオン重合性、アニオン重合性、付加重合性、縮合重合性のいずれであってもよいが、ラジカル重合性の官能基が好ましい。この重合性官能基としては、ビニル基、アリル基、アルケニル基、アクリレート基、メタクリレート基、メタクリロイルオキシエチルカルバメート基等のウレタン（メタ）アクリレート基、スチリル基及びその誘導体、ビニルアシド基及びその誘導体などを有する置換基を挙げることができる。これらの重合性官能基の中で、その重合性という観点から、アクリレート基、メタアクリレート基、ウレタン（メタ）アクリレート基が好ましい。 The substituent having a polymerizable functional group among X 1 , Y 1 , and Z 1 in formula (1) is any of radical polymerizable, cationic polymerizable, anionic polymerizable, addition polymerizable, and condensation polymerizable. However, a radical polymerizable functional group is preferable. Examples of the polymerizable functional group include a vinyl (ally) group, an alkenyl group, an acrylate group, a methacrylate group, a urethane (meth) acrylate group such as a methacryloyloxyethyl carbamate group, a styryl group and a derivative thereof, a vinyl acid group and a derivative thereof, and the like. The substituent which it has can be mentioned. Among these polymerizable functional groups, an acrylate group, a methacrylate group, and a urethane (meth) acrylate group are preferable from the viewpoint of polymerizability.
各式におけるＸ1、Ｙ1、Ｚ1のうちの重合性官能基を有しない置換基、Ｑ1〜Ｑ3としては水素原子、メチル、エチル、プロピル、イソプロピル、ブチル、イソブチル、ターシャリーブチル、アミル、ヘキシル等のアルキル基、またメトキシ、エトキシ、プロポキシ、イソブトキシ、ターシャリーブトキシ等のアルコキシ基、アセトキシ基、プロポキシカルボニル基などのエステル基、アリール基等の有機基を挙げることができる。 Substituents having no polymerizable functional group among X 1 , Y 1 and Z 1 in each formula, Q 1 to Q 3 are a hydrogen atom, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tertiary butyl, Examples thereof include alkyl groups such as amyl and hexyl, alkoxy groups such as methoxy, ethoxy, propoxy, isobutoxy and tertiary butoxy, ester groups such as acetoxy group and propoxycarbonyl group, and organic groups such as aryl group.
各式におけるＲ1〜Ｒ12およびＲ13〜Ｒ24としては水素原子、ハロゲン原子、ニトロ基、アミノ基、スルホン酸基、スルホン酸メチル等のスルホン酸エステル基、メチル、エチル、プロピル、イソプロピル、ブチル、イソブチル、ターシャリーブチル、アミル、ヘキシル等のアルキル基、またメトキシ、エトキシ、プロポキシ、イソブトキシ、ターシャリーブトキシ等のアルコキシ基、アセトキシ基、プロポキシカルボニル基などのエステル基、アリール基等の有機基を挙げることができる。また、これらの有機基は、更にハロゲン原子、ニトロ基、アミノ基等の置換基を有していてもよい。 R 1 to R 12 and R 13 to R 24 in each formula are hydrogen atom, halogen atom, nitro group, amino group, sulfonic acid group, sulfonic acid ester group such as methyl sulfonate, methyl, ethyl, propyl, isopropyl Organic groups such as alkyl groups such as butyl, isobutyl, tertiary butyl, amyl, hexyl, etc., alkoxy groups such as methoxy, ethoxy, propoxy, isobutoxy, tertiary butoxy, ester groups such as acetoxy group, propoxycarbonyl group, and aryl groups Can be mentioned. Further, these organic groups may further have a substituent such as a halogen atom, a nitro group, or an amino group.
次に、本発明による重合性化合物の合成方法の例を以下に挙げるが、本発明は何らこれらに限定されるものではない。 Next, although the example of the synthesis | combining method of the polymeric compound by this invention is given below, this invention is not limited to these at all.
その第１の合成方法は、式（１７）で示されるイリジウムの二核錯体と式（１８）で示される重合性置換基を有する化合物を反応させることにより単核イリジウム錯体部分を含む重合性化合物を得る方法である。
式（１７）のイリジウムの二核錯体は公知の方法（S. Lamansky et al., Inorganic Chemistry, 40, 1704 (2001)）により合成することができる。式（１７）のＲ1〜Ｒ24としては水素原子、ハロゲン原子、ニトロ基、アミノ基、スルホン酸基、スルホン酸メチル等のスルホン酸エステル基、メチル、エチル、プロピル、イソプロピル、ブチル、イソブチル、ターシャリーブチル、アミル、ヘキシル等のアルキル基、またメトキシ、エトキシ、プロポキシ、イソブトキシ、ターシャリーブトキシ等のアルコキシ基、更にはアセトキシ基、プロポキシカルボニル基などのエステル基等の有機基を挙げることができる。また、これらの有機基は、更にハロゲン原子、ニトロ基、アミノ基等の置換基を有していてもよい。 The binuclear complex of iridium of formula (17) can be synthesized by a known method (S. Lamansky et al., Inorganic Chemistry, 40, 1704 (2001)). R 1 to R 24 in the formula (17) are hydrogen atom, halogen atom, nitro group, amino group, sulfonic acid group, sulfonic acid ester group such as methyl sulfonate, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, Examples include alkyl groups such as tertiary butyl, amyl, and hexyl; alkoxy groups such as methoxy, ethoxy, propoxy, isobutoxy, and tertiary butoxy; and organic groups such as ester groups such as acetoxy and propoxycarbonyl groups. . Further, these organic groups may further have a substituent such as a halogen atom, a nitro group, or an amino group.
式（１８）で示される化合物の置換基Ｘ1、Ｙ1、Ｚ1の少なくとも１つは重合性官能基を有する置換基であり、式（１）の説明と同じものを意味する。また、式（１８）で示される化合物の置換基Ｘ1、Ｙ1、Ｚ1のうちの重合性官能基を有しない置換基も式（１）の場合と同様である。 At least one of the substituents X 1 , Y 1 , and Z 1 of the compound represented by the formula (18) is a substituent having a polymerizable functional group, and means the same as the description of the formula (1). Moreover, the substituent which does not have a polymerizable functional group among the substituents X 1 , Y 1 and Z 1 of the compound represented by the formula (18) is the same as in the case of the formula (1).
本発明による重合性化合物の第２の合成方法は、式（１７）で示されるイリジウムの二核錯体と式（１９）で示される反応性置換基を有する化合物を反応させることにより反応性置換基を有する単核のイリジウム錯体を中間体として得、この中間体の反応性置換基と重合性置換基を有する化合物を反応させることにより単核イリジウム錯体部分を含む重合性化合物を得る方法である。
式（１９）のＸ2、Ｙ2、Ｚ2の少なくとも１つは反応性置換基であり、水酸基などの官能基を有する。官能基としては水酸基、アミノ基、カルボキシル基などを例示することができるが、何らこれに限定されるものではない。これら官能基を有する反応性置換基としては水酸基、ヒドロキシアルキル基、ヒドロキシフェニル基などが挙げられる。 At least one of X 2 , Y 2 and Z 2 in the formula (19) is a reactive substituent and has a functional group such as a hydroxyl group. Examples of the functional group include a hydroxyl group, an amino group, and a carboxyl group, but the functional group is not limited thereto. Examples of the reactive substituent having these functional groups include a hydroxyl group, a hydroxyalkyl group, and a hydroxyphenyl group.
また、この反応性置換基は保護基で保護されていてもよい。尚、この場合は保護基により保護されたまま反応を行って単核イリジウム錯体を得た後、脱保護により反応性置換基を有する単核イリジウム錯体を中間体として得る。その後、この中間体の反応性置換基と重合性官能基を有する化合物と反応させることにより、単核イリジウム錯体部分を含む重合性化合物を得る。なお、これら反応性置換基の官能基としては前述の重合性官能基は除かれる。 Moreover, this reactive substituent may be protected with a protecting group. In this case, the mononuclear iridium complex having a reactive substituent is obtained as an intermediate by deprotection after carrying out the reaction while being protected by the protective group to obtain a mononuclear iridium complex. Then, the polymeric compound containing a mononuclear iridium complex part is obtained by making it react with the compound which has the reactive substituent of this intermediate body, and a polymeric functional group. In addition, the above-mentioned polymerizable functional group is excluded as a functional group of these reactive substituents.
式（１９）で示される化合物の置換基Ｘ2、Ｙ2、Ｚ2のうちの反応性置換基でない置換基としては水素原子、ハロゲン原子、メチル、エチル、プロピル、イソプロピル、ブチル、イソブチル、ターシャリーブチル、アミル、ヘキシル等のアルキル基、またメトキシ、エトキシ、プロポキシ、イソブトキシ、ターシャリーブトキシ等のアルコキシ基、アセトキシ基、プロポキシカルボニル基などのエステル基、アリール基等の有機基を挙げることができる。また、これらの有機基は、更にハロゲン原子等の置換基を有していてもよい。 Of the substituents X 2 , Y 2 , and Z 2 of the compound represented by the formula (19), examples of the substituent that is not a reactive substituent include a hydrogen atom, a halogen atom, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, and tarsia. Examples include alkyl groups such as butyl, amyl, and hexyl; alkoxy groups such as methoxy, ethoxy, propoxy, isobutoxy, and tertiary butoxy; ester groups such as acetoxy and propoxycarbonyl groups; and organic groups such as aryl groups. . Further, these organic groups may further have a substituent such as a halogen atom.
イリジウム二核錯体と反応性置換基を有する式（１９）で示される化合物との反応で得られる反応性置換基を有する単核イリジウム錯体と反応させる重合性官能基を有する化合物は重合性の基以外に式（１９）の反応性置換基Ｘ2、Ｙ2、Ｙ3と反応する基を有する官能基を有して必要がある。本発明による重合性化合物の第２の合成法による場合には式（１７）のＲ1〜Ｒ24は上記の単核イリジウム錯体と反応させる重合性官能基を有する化合物と反応しない基を選択しておく必要がある。 A compound having a polymerizable functional group to be reacted with a mononuclear iridium complex having a reactive substituent obtained by reacting an iridium dinuclear complex with a compound represented by the formula (19) having a reactive substituent is a polymerizable group. In addition, it is necessary to have a functional group having a group that reacts with the reactive substituents X 2 , Y 2 , and Y 3 of formula (19). In the second synthesis method of the polymerizable compound according to the present invention, R 1 to R 24 in the formula (17) are selected from groups that do not react with the compound having a polymerizable functional group to be reacted with the mononuclear iridium complex. It is necessary to keep.
上記単核イリジウム錯体と反応させる重合性官能基を有する化合物としては重合性酸塩化物や重合性イソシアネートを例示することができるが、何らこれらに限定されるものではない。これらの化合物における重合性官能基は、ラジカル重合性、カチオン重合性、アニオン重合性、付加重合性、縮合重合性のいずれであってもよいが、ラジカル重合性の官能基が好ましい。この重合性官能基としてはビニル基、アリル基、アルケニル基、アクリレート基、メタクリレート基、メタクリロイルオキシエチルカルバメート基等のウレタン（メタ）アクリレート基、スチリル基及びその誘導体、ビニルアシド基及びその誘導体など有するものを挙げることができる。これらの重合性官能基の中で、その重合性という観点から、アクリレート基、メタアクリレート基、ウレタン（メタ）アクリレート基が好ましい。具体的には、重合性酸塩化物としてはアクリル酸クロライド、メタクリル酸クロライド等が挙げられ、重合性イソシアネートとしてはメタクリロイルイソシアネート、メタクリロイルオキシエチルイソシアネート等が挙げられる。
なお、本発明の化合物を示す式（１）などの化学式は金属錯体構造を表し、Ｏ−Ｃ−Ｃ−Ｏは共鳴構造を表すが、化学的に許容される構造を含むことは言うまでもない。
Examples of the compound having a polymerizable functional group to be reacted with the mononuclear iridium complex include polymerizable acid chlorides and polymerizable isocyanates, but are not limited thereto. The polymerizable functional group in these compounds may be any of radical polymerizable, cationic polymerizable, anionic polymerizable, addition polymerizable, and condensation polymerizable, but is preferably a radical polymerizable functional group. This polymerizable functional group has a urethane (meth) acrylate group such as vinyl group, allyl group, alkenyl group, acrylate group, methacrylate group, methacryloyloxyethyl carbamate group, styryl group and its derivatives, vinyl acid group and its derivatives, etc. Can be mentioned. Among these polymerizable functional groups, an acrylate group, a methacrylate group, and a urethane (meth) acrylate group are preferable from the viewpoint of polymerizability. Specifically, examples of the polymerizable acid chloride include acrylic acid chloride and methacrylic acid chloride, and examples of the polymerizable isocyanate include methacryloyl isocyanate and methacryloyloxyethyl isocyanate.
In addition, although chemical formulas, such as Formula (1) which show the compound of this invention represent a metal complex structure and O-C-C-O represents a resonance structure, it cannot be overemphasized that the structure accept | permitted chemically is included.
以下に本発明について代表的な例を示し、更に具体的に説明する。尚、これらは説明のための単なる例示であって、本発明は何らこれらに限定されるものではない。 The present invention will be described in more detail below with typical examples. Note that these are merely illustrative examples, and the present invention is not limited to these.
＜測定装置等＞
１）1Ｈ−ＮＭＲ
日本電子（株）製 ＪＮＭ ＥＸ２７０
２７０Ｍｚ 溶媒：重クロロホルムまたは重ジメチルスルホシキド
２）元素分析装置
ＲＥＣ０社製 ＣＨＮＳ−９３２型
<Measurement equipment, etc.>
1) 1H-NMR
JNM EX270 manufactured by JEOL Ltd.
270Mz Solvent: deuterated chloroform or deuterated dimethyl sulfoxide 2) CHNS-932 type manufactured by elemental analyzer REC0
＜試薬類＞
特に断らない限り、市販品（特級）を精製することなく使用した。
<Reagents>
Unless otherwise noted, commercial products (special grade) were used without purification.
（実施例１）重合性化合物：（８−ノネン−２，４−ジオナート）ビス（２−フェニルピリジン）イリジウム（ＩＩＩ）（以下Ｉｒ（ｐｐｙ）2（１−Ｂｕ−ａｃａｃ）と略す）の合成
スキーム（１Ａ）に示すように、常法に従い合成したビス（μ−クロロ）テトラキス（２−フェニルピリジン）ジイリジウム（ＩＩＩ）（以下［Ｉｒ（ｐｐｙ）2Ｃｌ］2と略す）と、公知の方法（H. Gerlach et al.,
Helv. Chim. Acta, 60, 638 (1977)）により合成した８−ノネン−２，４−ジオンを反応させてＩｒ（ｐｐｙ）2（１−Ｂｕ−ａｃａｃ）を合成した。即ち、［Ｉｒ（ｐｐｙ）2Ｃｌ］2 ２６１ｍｇ（０．２４ｍｍｏｌ）を３０ｍｌの窒素ガスで脱気したメタノール中に懸濁させ、８−ノネン−２，４−ジオン８７ｍｇ（０．５６ｍｍｏｌ）とトリエチルアミン７６ｍｇ（０．７５ｍｍｏｌ）を加えて油浴上で3時間加熱還流させた。得られた薄黄色の反応液を室温にまで冷却し、ロータリーエバポレータで濃縮した。次に希塩酸水溶液２００ｍｌとクロロホルム５０ｍｌを加えて激しく攪拌し、クロロホルム層を分取して硫酸マグネシウムで乾燥後、減圧して溶媒を留去した。得られた黄色の残渣をジクロロメタンに溶解し、ジクロロメタンを溶出液とするシリカゲルカラムクロマトグラフィーで薄黄色の主生成物を分取した。この溶液を減圧して濃縮後、少量のヘキサンを加えて−２０℃に冷却し、目的とするＩｒ（ｐｐｙ）2（１−Ｂｕ−ａｃａｃ）２７０ｍｇ（０．４１ｍｍｏｌ）を薄黄色結晶として得た（収率８５％）。同定はＣＨＮ元素分析、1Ｈ−ＮＭＲで行った。
(Example 1) Synthesis of polymerizable compound: (8-nonene-2,4-dionato) bis (2-phenylpyridine) iridium (III) (hereinafter abbreviated as Ir (ppy) 2 (1-Bu-acac)) As shown in Scheme (1A), bis (μ-chloro) tetrakis (2-phenylpyridine) diiridium (III) (hereinafter abbreviated as [Ir (ppy) 2 Cl] 2 ) synthesized according to a conventional method, Method (H. Gerlach et al.,
Ir (ppy) 2 (1-Bu-acac) was synthesized by reacting 8-nonene-2,4-dione synthesized by Helv. Chim. Acta, 60, 638 (1977). That is, 261 mg (0.24 mmol) of [Ir (ppy) 2 Cl] 2 was suspended in methanol degassed with 30 ml of nitrogen gas, and 87 mg (0.56 mmol) of 8-nonene-2,4-dione and triethylamine were suspended. 76 mg (0.75 mmol) was added, and the mixture was heated to reflux on an oil bath for 3 hours. The obtained pale yellow reaction liquid was cooled to room temperature and concentrated by a rotary evaporator. Next, 200 ml of dilute hydrochloric acid solution and 50 ml of chloroform were added and stirred vigorously. The chloroform layer was separated, dried over magnesium sulfate, and the solvent was distilled off under reduced pressure. The obtained yellow residue was dissolved in dichloromethane, and a light yellow main product was fractionated by silica gel column chromatography using dichloromethane as an eluent. The solution was concentrated under reduced pressure, a small amount of hexane was added, and the mixture was cooled to −20 ° C. to obtain 270 mg (0.41 mmol) of target Ir (ppy) 2 (1-Bu-acac) as light yellow crystals. (Yield 85%). Identification was performed by CHN elemental analysis and 1 H-NMR.
1H NMR (CDCl3): d 8.49 (d, J = 5.7 Hz, 2 H,
ppy), 7.83 (t, J = 7.8 Hz, 2 H, ppy), 7.70 (m, 2 H, ppy), 7.54 (t, J = 6.8 Hz,
2 H, ppy), 7.10 (m, 2 H, ppy), 6.80 (t, J = 7.3 Hz, 2 H, ppy), 6.68 (m, 2 H,
ppy), 6.35 (d, J = 6.2 Hz, 1 H, ppy), 6.25 (d, J = 6.2 Hz, 1 H, ppy), 5.61 (m,
1 H, -CH=CH2), 5.19 (s, 1
H, diketonate-methine), 4.86 (m, 2 H, -CH=CH2), 1.99 (t, J = 7.3 Hz, 2 H, methylene), 1.79 (s, 3 H, CH3), 1.72 (m, 2 H, methylene), 1.38
(m, 2 H, methylene). E.A.: Calcd for C31H29IrN2O2: C, 56.95; H, 4.47; N, 4.28. Found: C, 55.84; H,
4.32; N, 3.97.
1 H NMR (CDCl 3 ): d 8.49 (d, J = 5.7 Hz, 2 H,
ppy), 7.83 (t, J = 7.8 Hz, 2 H, ppy), 7.70 (m, 2 H, ppy), 7.54 (t, J = 6.8 Hz,
2 H, ppy), 7.10 (m, 2 H, ppy), 6.80 (t, J = 7.3 Hz, 2 H, ppy), 6.68 (m, 2 H,
ppy), 6.35 (d, J = 6.2 Hz, 1 H, ppy), 6.25 (d, J = 6.2 Hz, 1 H, ppy), 5.61 (m,
1 H, -CH = CH 2 ), 5.19 (s, 1
H, diketonate-methine), 4.86 (m, 2 H, -CH = CH 2 ), 1.99 (t, J = 7.3 Hz, 2 H, methylene), 1.79 (s, 3 H, CH 3 ), 1.72 (m , 2 H, methylene), 1.38
(m, 2 H, methylene). EA: Calcd for C 31 H 29 IrN 2 O 2 : C, 56.95; H, 4.47; N, 4.28. Found: C, 55.84; H,
4.32; N, 3.97.
（実施例２）重合性化合物：［６−（４−ビニルフェニル）−２，４−ヘキサンジオナート］ビス（２−フェニルピリジン）イリジウム（ＩＩＩ）（以下Ｉｒ（ｐｐｙ）2［１−（Ｓｔ−Ｍｅ）−ａｃａｃ］と略す）の合成
スキーム（２Ａ）に示すように、アセチルアセトンと４−ビニルベンジルクロライドを反応させて６−（４−ビニルフェニル）−２，４−ヘキサジオンを合成した。即ち、水素化ナトリウム１．２３ｇ（６０％ ｉｎ ｏｉｌ）（３１ｍｍｏｌ）を窒素雰囲気下で秤量し、これに乾燥テトラヒドロフラン（以下ＴＨＦと略す）６０ｍｌを加えて氷浴で０℃に冷却した。この懸濁液にアセチルアセトン２．５ｇ（２４ｍｍｏｌ）とヘキサメチルホスホリックトリアミド１ｍｌの混合溶液を滴下すると無色の沈殿が生成した。０℃で１０分間攪拌した後、ｎ−ブチルリチウムのヘキサン溶液（１．６Ｍ）１７．５ｍｌ（２８ｍｍｏｌ）を滴下すると沈殿が溶解し、更に０℃で２０分間攪拌した。得られた薄黄色の溶液に４−ビニルベンジルクロライド４．０ｇ（２６ｍｍｏｌ）を滴下し、反応液を室温に戻して２０分間攪拌後、希塩酸を加えて水層を酸性にした。有機層を飽和塩化ナトリウム水溶液で洗浄し、硫酸マグネシウムで乾燥した後、ロータリーエバポレータで溶媒を留去した。得られた反応混合物をシリカゲルカラムに加えてヘキサン／ジクロロメタンの１：１（体積比）混合溶媒で展開し、主生成物を分取した。得られた溶液から減圧で溶媒を留去することにより、目的とする６−（４−ビニルフェニル）−２，４−ヘキサジオン３．０ｇ（１４ｍｍｏｌ）を褐色の液体として得た。収率５６％。同定はＣＨＮ元素分析、1Ｈ−ＮＭＲで行った。
(Example 2) Polymerizable compound: [6- (4-vinylphenyl) -2,4-hexanedionate] bis (2-phenylpyridine) iridium (III) (hereinafter Ir (ppy) 2 [1- (St Synthesis of -Me) -acac]) As shown in the scheme (2A), acetylacetone and 4-vinylbenzyl chloride were reacted to synthesize 6- (4-vinylphenyl) -2,4-hexadione. That is, 1.23 g (60% in oil) (31 mmol) of sodium hydride was weighed under a nitrogen atmosphere, 60 ml of dry tetrahydrofuran (hereinafter abbreviated as THF) was added thereto, and the mixture was cooled to 0 ° C. in an ice bath. When a mixed solution of 2.5 g (24 mmol) of acetylacetone and 1 ml of hexamethylphosphoric triamide was added dropwise to this suspension, a colorless precipitate was formed. After stirring at 0 ° C. for 10 minutes, 17.5 ml (28 mmol) of n-butyllithium in hexane (1.6M) was added dropwise to dissolve the precipitate, and the mixture was further stirred at 0 ° C. for 20 minutes. To the obtained pale yellow solution, 4.0 g (26 mmol) of 4-vinylbenzyl chloride was added dropwise, the reaction solution was returned to room temperature and stirred for 20 minutes, and diluted hydrochloric acid was added to acidify the aqueous layer. The organic layer was washed with a saturated aqueous sodium chloride solution and dried over magnesium sulfate, and then the solvent was distilled off with a rotary evaporator. The obtained reaction mixture was added to a silica gel column and developed with a 1: 1 (volume ratio) mixed solvent of hexane / dichloromethane to fractionate the main product. The solvent was distilled off from the resulting solution under reduced pressure to obtain 3.0 g (14 mmol) of the intended 6- (4-vinylphenyl) -2,4-hexadione as a brown liquid. Yield 56%. Identification was performed by CHN elemental analysis and 1 H-NMR.
1H NMR (CDCl3): enol; d 7.33 (d, J = 8.1 Hz, 2 H,
aromatic), 7.14 (d, J = 8.4 Hz, 2 H, aromatic), 6.68 (dd, J = 8.1 Hz, 1 H,
vinylic), 5.70 (d, J = 17.0 Hz, 1 H, vinylic), 5.46 (s, 1 H,
diketonate-methine), 5.20 (d, J = 11.1 Hz, 1 H, vinylic), 2.91 (t, J = 5.7 Hz,
2 H, methylene), 2.58 (t, J = 7.3 Hz, 2 H, methylene), 2.03 (s, 3 H,
methyl). keto; d 7.33 (d, J = 8.1 Hz, 2 H, aromatic), 7.14 (d, J = 8.4 Hz, 2 H,
aromatic), 6.68 (dd, J = 8.1 Hz, 1 H, vinylic), 5.70 (d, J = 17.0 Hz, 1 H,
vinylic), 5.20 (d, J = 11.1 Hz, 1 H, vinylic), 3.53 (s, 2 H, C(=O)CH2C(=O)), 2.89 (m, 4 H, ethylene),
2.19 (s, 3 H, methyl). enol : keto = 6 : 1. E.A.: Calcd for C14H9O2:
C, 77.75; H, 7.46. Found: C, 77.49; H, 7.52.
1 H NMR (CDCl 3 ): enol; d 7.33 (d, J = 8.1 Hz, 2 H,
aromatic), 7.14 (d, J = 8.4 Hz, 2 H, aromatic), 6.68 (dd, J = 8.1 Hz, 1 H,
vinylic), 5.70 (d, J = 17.0 Hz, 1 H, vinylic), 5.46 (s, 1 H,
diketonate-methine), 5.20 (d, J = 11.1 Hz, 1 H, vinylic), 2.91 (t, J = 5.7 Hz,
2 H, methylene), 2.58 (t, J = 7.3 Hz, 2 H, methylene), 2.03 (s, 3 H,
methyl) .keto; d 7.33 (d, J = 8.1 Hz, 2 H, aromatic), 7.14 (d, J = 8.4 Hz, 2 H,
aromatic), 6.68 (dd, J = 8.1 Hz, 1 H, vinylic), 5.70 (d, J = 17.0 Hz, 1 H,
vinylic), 5.20 (d, J = 11.1 Hz, 1 H, vinylic), 3.53 (s, 2 H, C (= O) CH 2 C (= O)), 2.89 (m, 4 H, ethylene),
2.19 (s, 3 H, methyl) .enol: keto = 6: 1.EA: Calcd for C 14 H 9 O 2 :
C, 77.75; H, 7.46. Found: C, 77.49; H, 7.52.
次いで、スキーム（２Ｂ）に示すように、この６−（４−ビニルフェニル）−２，４−ヘキサンジオンと常法に従い合成した［Ｉｒ（ｐｐｙ）2Ｃｌ］2を反応させてＩｒ（ｐｐｙ）2［１−（Ｓｔ−Ｍｅ）−ａｃａｃ］を合成した。即ち、［Ｉｒ（ｐｐｙ）2Ｃｌ］2３４２ｍｇ（０．３２ｍｍｏｌ）、炭酸ナトリウム１５８ｍｇ（１．５ｍｍｏｌ）および２，６−ジ−ｔｅｒｔ−ブチル−４−メチルフェノール５ｍｇ（０．０２３ｍｍｏｌ）を5 mlのＮ，Ｎ−ジメチルホルムアミド（以下ＤＭＦと略す）に溶解し、これに６−（４−ビニルフェニル）−２，４−ヘキサンジオン２１０ｍｇ（０．９７ｍｍｏｌ）を加えて６５℃で1時間加熱攪拌した。次に室温まで冷却した反応溶液に希塩酸水溶液を加えた後、薄黄色の成分をクロロホルムで抽出した。ロータリーエバポレータを用いて溶媒を留去後、残渣を少量のジクロロメタンに溶解し、シリカゲルカラムクロマトグラフィー(展開液：ジクロロメタン)で黄色の主生成物を分取した。この溶液を減圧乾固し、ジクロロメタン−ヘキサン混合溶液を加えて−２０℃で再結晶を行い、目的とするＩｒ（ｐｐｙ）2［１−（Ｓｔ−Ｍｅ）−ａｃａｃ］３５４ｍｇ（０．４９ｍｍｏｌ）を薄黄色結晶として得た。収率７８％。同定はＣＨＮ元素分析、1Ｈ−ＮＭＲで行った。 Next, as shown in Scheme (2B), this 6- (4-vinylphenyl) -2,4-hexanedione was reacted with [Ir (ppy) 2 Cl] 2 synthesized according to a conventional method to give Ir (ppy) 2 [1- (St-Me) -acac] was synthesized. That is, 5 ml of [Ir (ppy) 2 Cl] 2 342 mg (0.32 mmol), sodium carbonate 158 mg (1.5 mmol) and 2,6-di-tert-butyl-4-methylphenol 5 mg (0.023 mmol) Was dissolved in N, N-dimethylformamide (hereinafter abbreviated as DMF), 210 mg (0.97 mmol) of 6- (4-vinylphenyl) -2,4-hexanedione was added thereto, and the mixture was heated and stirred at 65 ° C. for 1 hour. did. Next, a diluted hydrochloric acid aqueous solution was added to the reaction solution cooled to room temperature, and the light yellow component was extracted with chloroform. After distilling off the solvent using a rotary evaporator, the residue was dissolved in a small amount of dichloromethane, and the yellow main product was fractionated by silica gel column chromatography (developing solution: dichloromethane). This solution was dried under reduced pressure, a dichloromethane-hexane mixed solution was added, and recrystallization was performed at −20 ° C. to obtain 354 mg (0.49 mmol) of target Ir (ppy) 2 [1- (St-Me) -acac]. Was obtained as pale yellow crystals. Yield 78%. Identification was performed by CHN elemental analysis and 1 H-NMR.
1H NMR (CDCl3): d 8.47 (d, J = 5.7 Hz, 1 H,
ppy), 8.21 (d, J = 5.7 Hz, 1 H, ppy), 7.9 – 7.5 (m, 6 H, ppy), 7.18
(d, J = 8.1 Hz, 2 H, stylyl-aromatic), 7.00 (m, 2 H, ppy), 6.89 (d, J = 8.1 Hz,
2 H, stylyl-aromatic), 6.75 (m, 5 H, ppy and vinylic), 6.28 (t, J = 7.3 Hz, 2
H, ppy), 7.67 (d, J = 17.6 Hz, 1 H, vinylic), 5.19 (d, J = 9.5 Hz, 1 H,
vinylic), 5.17 (s, 1 H, diketonate-methine), 2.60 (t, J = 7.3 Hz, 2 H,
ethylene), 2.36 (m, 2 H, ethylene), 1.75 (s, 3 H, methyl). E.A.: Calcd for C36H31IrN2O2: C, 60.40; H, 4.36; N, 3.91.
Found: C, 61.35; H, 4.34; N, 3.83.
1 H NMR (CDCl 3 ): d 8.47 (d, J = 5.7 Hz, 1 H,
ppy), 8.21 (d, J = 5.7 Hz, 1 H, ppy), 7.9 – 7.5 (m, 6 H, ppy), 7.18
(d, J = 8.1 Hz, 2 H, stylyl-aromatic), 7.00 (m, 2 H, ppy), 6.89 (d, J = 8.1 Hz,
2 H, stylyl-aromatic), 6.75 (m, 5 H, ppy and vinylic), 6.28 (t, J = 7.3 Hz, 2
H, ppy), 7.67 (d, J = 17.6 Hz, 1 H, vinylic), 5.19 (d, J = 9.5 Hz, 1 H,
vinylic), 5.17 (s, 1 H, diketonate-methine), 2.60 (t, J = 7.3 Hz, 2 H,
ethylene), 2.36 (m, 2 H, ethylene), 1.75 (s, 3 H, methyl) .EA: Calcd for C 36 H 31 IrN 2 O 2 : C, 60.40; H, 4.36; N, 3.91.
Found: C, 61.35; H, 4.34; N, 3.83.
（実施例３）重合性化合物：（９−アクリロイルオキシ−２，４−ノナンジオナート）ビス（２−フェニルピリジン）イリジウム（ＩＩＩ）（以下Ｉｒ（ｐｐｙ）2［１−（Ａ−Ｂｕ）−ａｃａｃ］と略す）の合成
スキーム（３Ａ）に示すように、常法に従い、（９−ヒドロキシ−２，４−ノナンジオナート）ビス（２−フェニルピリジン）イリジウム（以下Ｉｒ（ｐｐｙ）2［１−（ＯＨ−Ｂｕ）−ａｃａｃ］と略す）を合成した。即ち、実施例１と同様にして合成したＩｒ（ｐｐｙ）2（１−Ｂｕ−ａｃａｃ）１６７ｍｇ（０．２６ｍｍｏｌ）をＴＨＦ１０ｍｌに溶解し、これに９−ボラビシクロ［３．３．１］ノナン（以下９−ＢＢＮと略す）の０．５Ｍ ＴＨＦ溶液１．０ｍｌ（０．５ｍｍｏｌ）を滴下した。この溶液を２５分間加熱還流した後、得られた反応混合物に３Ｍ
ＮａＯＨ水溶液０．２ｍｌ（０．６０ｍｍｏｌ）と３５％Ｈ2Ｏ2溶液０．０６０ｍｌ（０．６２ｍｍｏｌ）を順に加えて室温で１２時間攪拌した。次に２０ｍｌの水を加えてロータリーエバポレータで濃縮し、クロロホルムを加えてよく振盪した後、有機層を減圧乾固した。得られた黄色固体を少量のジクロロメタンに溶解してシリカゲルカラムに加え、まずジクロロメタンを流して溶出した不純物を除いた。引き続きジクロロメタン／酢酸エチルの１：１（体積比）混合溶媒を流すと薄黄色の錯体が溶出した。これを回収して減圧乾燥し、ジクロロメタン／ヘキサン混合溶液から−２０℃で再結晶することによりＩｒ（ｐｐｙ）2［１−（ＯＨ−Ｂｕ）−ａｃａｃ］ ２３ｍｇ（０．０３４ｍｍｏｌ）を薄黄色の固体として得た。収率１３％。同定はＣＨＮ元素分析、1Ｈ−ＮＭＲで行った。
(Example 3) Polymerizable compound: (9-acryloyloxy-2,4-nonandionate) bis (2-phenylpyridine) iridium (III) (hereinafter Ir (ppy) 2 [1- (A-Bu) -acac] As shown in scheme (3A), (9-hydroxy-2,4-nonandionato) bis (2-phenylpyridine) iridium (hereinafter referred to as Ir (ppy) 2 [1- (OH— (Bu) -acac]) was synthesized. That is, 167 mg (0.26 mmol) of Ir (ppy) 2 (1-Bu-acac) synthesized in the same manner as in Example 1 was dissolved in 10 ml of THF, and 9-borabicyclo [3.3.1] nonane (hereinafter referred to as “nonane”). 1.0 ml (0.5 mmol) of 0.5 M THF solution of 9-BBN) was added dropwise. The solution was heated to reflux for 25 minutes and then the resulting reaction mixture was added to 3M.
Aqueous NaOH (0.2 ml, 0.60 mmol) and 35% H 2 O 2 solution (0.060 ml, 0.62 mmol) were sequentially added, followed by stirring at room temperature for 12 hours. Next, 20 ml of water was added and concentrated with a rotary evaporator. After adding chloroform and shaking well, the organic layer was dried under reduced pressure. The obtained yellow solid was dissolved in a small amount of dichloromethane and added to a silica gel column. First, dichloromethane was flowed to remove the eluted impurities. Subsequently, when a mixed solvent of dichloromethane / ethyl acetate 1: 1 (volume ratio) was passed, a light yellow complex was eluted. This was recovered, dried under reduced pressure, and recrystallized from a dichloromethane / hexane mixed solution at −20 ° C. to obtain 23 mg (0.034 mmol) of Ir (ppy) 2 [1- (OH-Bu) -acac] as a pale yellow Obtained as a solid. Yield 13%. Identification was performed by CHN elemental analysis and 1 H-NMR.
1H NMR (CDCl3): d 8.50 (d, J = 5.9 Hz, 2 H,
ppy), 7.82 (t, J = 7.0 Hz, 2 H, ppy), 7.72 (t, J = 7.3 Hz, 2 H, ppy), 7.55 (t,
J = 7.0 Hz, 2 H, ppy), 7.12 (t, J = 5.9 Hz, 2 H, ppy), 6.81 (t, J = 7.6 Hz, 2
H, ppy), 6.69 (t, J = 7.3 Hz, 2 H, ppy), 6.31 (d, J = 5.9 Hz, 1 H, ppy), 6.26
(d, J = 5.9 Hz, 1 H, ppy), 5.19 (s, 1 H, diketonate-methine), 3.44 (t, J = 7.0
Hz, 2 H, CH2OH), 1.98 (t,
J = 7.0 Hz, 2 H, methylene), 1.79 (s, 3 H, methyl), 1.34 (m, 4 H, methylene),
1.05 (m, 2 H, methylene). E.A.: Calcd for C31H31IrN2O3: C, 55.42; H, 4.65; N, 4.17. Found: C, 55.76; H,
4.71; N, 4.19.
1 H NMR (CDCl 3 ): d 8.50 (d, J = 5.9 Hz, 2 H,
ppy), 7.82 (t, J = 7.0 Hz, 2 H, ppy), 7.72 (t, J = 7.3 Hz, 2 H, ppy), 7.55 (t,
J = 7.0 Hz, 2 H, ppy), 7.12 (t, J = 5.9 Hz, 2 H, ppy), 6.81 (t, J = 7.6 Hz, 2
H, ppy), 6.69 (t, J = 7.3 Hz, 2 H, ppy), 6.31 (d, J = 5.9 Hz, 1 H, ppy), 6.26
(d, J = 5.9 Hz, 1 H, ppy), 5.19 (s, 1 H, diketonate-methine), 3.44 (t, J = 7.0
Hz, 2 H, CH 2 OH), 1.98 (t,
J = 7.0 Hz, 2 H, methylene), 1.79 (s, 3 H, methyl), 1.34 (m, 4 H, methylene),
1.05 (m, 2 H, methylene). EA: Calcd for C 31 H 31 IrN 2 O 3 : C, 55.42; H, 4.65; N, 4.17. Found: C, 55.76; H,
4.71; N, 4.19.
次いで、スキーム（３Ｂ）に示すように、このＩｒ（ｐｐｙ）2［１−（ＯＨ−Ｂｕ）−ａｃａｃ］とアクリル酸クロライドを反応させることによりＩｒ（ｐｐｙ）2［１−（Ａ−Ｂｕ）−ａｃａｃ］を合成した。即ち、Ｉｒ（ｐｐｙ）2［１−（ＯＨ−Ｂｕ）−ａｃａｃ］ ９５ｍｇ（０．１４ｍｍｏｌ）をジクロロメタン１０ｍｌに溶解し、これにトリエチルアミン０．１０ｍｌ（０．７２ｍｍｏｌ）を加えた。この溶液にアクリル酸クロライド０．０６０ｍｌ（０．７４ｍｍｏｌ）を加えて室温で30分間攪拌した。次にメタノール１ｍｌを加えた後、減圧下、溶媒を留去した。残渣をシリカゲルカラムに通して（展開液：ジクロロメタン）最初に溶出した黄色の溶液を分取して減圧乾固し、ジクロロメタン−ヘキサン混合溶液から−２０℃で再結晶することにより目的とするＩｒ（ｐｐｙ）2［１−（Ａ−Ｂｕ）−ａｃａｃ］ ９９ｍｇ（０．１４ｍｍｏｌ）を
薄黄色の固体として得た。収率９６％。同定はＣＨＮ元素分析、1Ｈ−ＮＭＲで行った。
Next, as shown in Scheme (3B), Ir (ppy) 2 [1- (OH-Bu) -acac] is reacted with acrylic acid chloride to react with Ir (ppy) 2 [1- (A-Bu). -Acac] was synthesized. That is, 95 mg (0.14 mmol) of Ir (ppy) 2 [1- (OH-Bu) -acac] was dissolved in 10 ml of dichloromethane, and 0.10 ml (0.72 mmol) of triethylamine was added thereto. To this solution, 0.060 ml (0.74 mmol) of acrylic acid chloride was added and stirred at room temperature for 30 minutes. Next, 1 ml of methanol was added, and then the solvent was distilled off under reduced pressure. The residue was passed through a silica gel column (developing solution: dichloromethane), the yellow solution eluted first was separated, dried under reduced pressure, and recrystallized from a dichloromethane-hexane mixed solution at −20 ° C. to obtain the target Ir ( ppy) 2 [1- (A-Bu) -acac] 99 mg (0.14 mmol) was obtained as a pale yellow solid. Yield 96%. Identification was performed by CHN elemental analysis and 1 H-NMR.
1H NMR (CDCl3): d 8.50 (d, J = 5.9 Hz, 2 H,
ppy), 7.80 (m, 4 H, ppy), 7.51 (t, J = 7.3 Hz, 2 H, ppy), 7.18 (t, J = 5.9 Hz,
2 H, ppy), 6.84 (t, J = 7.3 Hz, 2 H, ppy), 6.70 (t, J = 7.6 Hz, 2 H, ppy), 6.25
(m, 3 H, ppy + vinylic), 6.12 (dd, J = 15.6, 9.3 Hz, 1 H, vinylic), 5.75 (d, J
= 9.3 Hz, 1 H, vinylic), 5.17 (s, 1 H, diketonate-methine), 4.05 (t, J = 7.0
Hz, 2 H, -COOCH2-), 1.84
(t, J = 7.0 Hz, 2 H, methylene), 1.80 (s, 3 H, methyl), 1.34 (m, 4 H,
methylene), 1.06 (m, 2 H, methylene). E.A.: Calcd for C34H33IrN2O4: C, 56.26; H, 4.58; N, 3.86.
Found: C, 56.55; H, 4.53; N, 3.60.
1 H NMR (CDCl 3 ): d 8.50 (d, J = 5.9 Hz, 2 H,
ppy), 7.80 (m, 4 H, ppy), 7.51 (t, J = 7.3 Hz, 2 H, ppy), 7.18 (t, J = 5.9 Hz,
2 H, ppy), 6.84 (t, J = 7.3 Hz, 2 H, ppy), 6.70 (t, J = 7.6 Hz, 2 H, ppy), 6.25
(m, 3 H, ppy + vinylic), 6.12 (dd, J = 15.6, 9.3 Hz, 1 H, vinylic), 5.75 (d, J
= 9.3 Hz, 1 H, vinylic), 5.17 (s, 1 H, diketonate-methine), 4.05 (t, J = 7.0
Hz, 2 H, -COOCH 2- ), 1.84
(t, J = 7.0 Hz, 2 H, methylene), 1.80 (s, 3 H, methyl), 1.34 (m, 4 H,
methylene), 1.06 (m, 2 H, methylene) .EA: Calcd for C 34 H 33 IrN 2 O 4 : C, 56.26; H, 4.58; N, 3.86.
Found: C, 56.55; H, 4.53; N, 3.60.
（実施例４）
重合性化合物：｛１−［４−（２−メタクリロイルオキシ）カルバモイルオキシフェニル］−３−フェニル−１，３−プロパンジオナート｝ビス（２−フェニルピリジン）イリジウム（ＩＩＩ）（以下Ｉｒ（ｐｐｙ）2（ＭＯＩ−Ｐｈ−ａｃａｃ）と略す）の合成
スキーム（４Ａ）に示すように、常法に従い合成したビス（μ−クロロ）テトラキス（２−フェニルピリジン）ジイリジウム（ＩＩＩ）（［Ｉｒ（ｐｐｙ）2Ｃｌ］2）と、公知の方法（M. Cushman
et al., Tetrahedron Lett., 31, 6497 (1990)）を参考に合成したｐ−ヒドロキシ−ジベンゾイルメタンを反応させて［１−（４−ヒドロキシフェニル）−３−フェニル−１，３−プロパンジオナート］ビス（２−フェニルピリジン）イリジウム（ＩＩＩ）（以下Ｉｒ（ｐｐｙ）2（ＯＨ−Ｐｈ−ａｃａｃ）と略す）を合成した。即ち、［Ｉｒ（ｐｐｙ）2Ｃｌ］2 １１２ｍｇ（０．１０ｍｍｏｌ）と炭酸ナトリウム６４ｍｇ（０．６０ｍｍｏｌ）およびｐ−ヒドロキシ−ジベンゾイルメタン７６ｍｇ（０．３２ｍｍｏｌ）をＤＭＦ１０ｍｌに溶解し、６０℃で０．５時間加熱攪拌した。得られた反応溶液を１００ｍｌの希塩酸水溶液中に注ぎ、クロロホルムでイリジウム錯体を抽出した。ロータリーエバポレータを用いてクロロホルムを留去し、残渣を少量のジクロロメタンに溶解してシリカゲルカラムに加えた。ジクロロメタン／アセトンの３０：１０（体積比）混合溶媒で展開するとオレンジ色の成分が溶出してくるため、これを回収して減圧乾固した。得られた固体を少量のジエチルエーテルに溶解し、ヘキサンを加えて析出した錯体沈殿物を濾取して減圧乾燥することにより、目的とするＩｒ（ｐｐｙ）2（ＯＨ−Ｐｈ−ａｃａｃ）１１１ｍｇ（０．１５ｍｍｏｌ）をオレンジ色の固体として得た。収率７２％。同定はＣＨＮ元素分析、1Ｈ−ＮＭＲで行った。
Example 4
Polymerizable compound: {1- [4- (2-methacryloyloxy) carbamoyloxyphenyl] -3-phenyl-1,3-propanedionate} bis (2-phenylpyridine) iridium (III) (hereinafter referred to as Ir (ppy)) 2 (abbreviated as MOI-Ph-acac)) As shown in Scheme (4A), bis (μ-chloro) tetrakis (2-phenylpyridine) diiridium (III) ([Ir (ppy) ) 2 Cl] 2 ) and known methods (M. Cushman
et al., Tetrahedron Lett., 31, 6497 (1990)) was reacted with p-hydroxy-dibenzoylmethane to produce [1- (4-hydroxyphenyl) -3-phenyl-1,3-propane. Dionate] bis (2-phenylpyridine) iridium (III) (hereinafter abbreviated as Ir (ppy) 2 (OH-Ph-acac)) was synthesized. That is, 112 mg (0.10 mmol) of [Ir (ppy) 2 Cl] 2, 64 mg (0.60 mmol) of sodium carbonate and 76 mg (0.32 mmol) of p-hydroxy-dibenzoylmethane were dissolved in 10 ml of DMF, and 0 ° C. at 60 ° C. The mixture was heated and stirred for 5 hours. The obtained reaction solution was poured into 100 ml of dilute hydrochloric acid aqueous solution, and the iridium complex was extracted with chloroform. Chloroform was distilled off using a rotary evaporator, and the residue was dissolved in a small amount of dichloromethane and added to a silica gel column. When developed with a 30:10 (volume ratio) mixed solvent of dichloromethane / acetone, an orange component was eluted, and this was collected and dried under reduced pressure. The obtained solid was dissolved in a small amount of diethyl ether, and the complex precipitate deposited by adding hexane was collected by filtration and dried under reduced pressure to obtain 111 mg of the desired Ir (ppy) 2 (OH-Ph-acac) ( 0.15 mmol) was obtained as an orange solid. Yield 72%. Identification was performed by CHN elemental analysis and 1 H-NMR.
1H NMR (CDCl3): d 8.58 (d, 2 H, ppy), 7.9 – 6.7 (m, 21 H,
ppy + phenyl), 6.52 (s, 1 H, diketonate-methine), 6.37 (d, 2 H, ppy), 4.91 (s,
1 H, OH). E.A.: Calcd for C37H27IrN2O3:
C, 60.07; H, 3.68; N, 3.79. Found: C, 60.77; H, 3.75; N, 3.62.
1 H NMR (CDCl 3 ): d 8.58 (d, 2 H, ppy), 7.9 – 6.7 (m, 21 H,
ppy + phenyl), 6.52 (s, 1 H, diketonate-methine), 6.37 (d, 2 H, ppy), 4.91 (s,
1 H, OH). EA: Calcd for C 37 H 27 IrN 2 O 3 :
C, 60.07; H, 3.68; N, 3.79. Found: C, 60.77; H, 3.75; N, 3.62.
次いで、スキーム（４Ｂ）に示すように、このＩｒ（ｐｐｙ）2（ＯＨ−Ｐｈ−ａｃａｃ）とメタクリロイルオキシエチルイソシアネート（商品名：ＭＯＩ、昭和電工製）を反応させることによりＩｒ（ｐｐｙ）2（ＭＯＩ−Ｐｈ−ａｃａｃ）を合成した。即ち、Ｉｒ（ｐｐｙ）2（ＯＨ−Ｐｈ−ａｃａｃ）１１０ｍｇ（０．１５ｍｍｏｌ）をトルエン５０ｍｌに溶解し、これに２，６−ジ−ｔｅｒｔ−ブチル−４−メチルフェノール（以下ＢＨＴと略す）５ｍｇ（０．０２３ｍｍｏｌ）、ジブチル錫（ＩＶ）ジラウレート（以下ＤＢＴＬと略す）３２ｍｇ（０．０５１ｍｍｏｌ）及びＭＯＩ １２１ｍｇ（０．７８ｍｍｏｌ）を加えて７０℃で6時間加熱攪拌した。得られた反応混合物を室温にまで空冷してシリカゲルカラムに加え、ジクロロメタン／アセトンの２０：１（体積比）混合溶媒で展開すると橙色の化合物が溶出した。この溶液をロータリーエバポレータで減圧乾固し、得られた固体を少量のジクロロメタンに溶解してヘキサンを少しずつ加えると橙色の沈殿が析出した。これを濾取して減圧乾燥することにより、目的とするＩｒ（ｐｐｙ）2（ＭＯＩ−Ｐｈ−ａｃａｃ）１００ｍｇ（０．１１ｍｍｏｌ）を橙色の固体として得た。収率７５％。同定はＣＨＮ元素分析、1Ｈ−ＮＭＲで行った。 Next, as shown in Scheme (4B), Ir (ppy) 2 (OH-Ph-acac) is reacted with methacryloyloxyethyl isocyanate (trade name: MOI, manufactured by Showa Denko) to give Ir (ppy) 2 ( MOI-Ph-acac) was synthesized. Specifically, 110 mg (0.15 mmol) of Ir (ppy) 2 (OH-Ph-acac) was dissolved in 50 ml of toluene, and 5 mg of 2,6-di-tert-butyl-4-methylphenol (hereinafter abbreviated as BHT) was dissolved therein. (0.023 mmol), dibutyltin (IV) dilaurate (hereinafter abbreviated as DBTL) 32 mg (0.051 mmol) and MOI 121 mg (0.78 mmol) were added, and the mixture was heated and stirred at 70 ° C. for 6 hours. The obtained reaction mixture was air-cooled to room temperature, added to a silica gel column, and developed with a 20: 1 (volume ratio) mixed solvent of dichloromethane / acetone to elute an orange compound. This solution was dried under reduced pressure using a rotary evaporator. The obtained solid was dissolved in a small amount of dichloromethane, and hexane was added little by little to precipitate an orange precipitate. This was collected by filtration and dried under reduced pressure to obtain 100 mg (0.11 mmol) of the target Ir (ppy) 2 (MOI-Ph-acac) as an orange solid. Yield 75%. Identification was performed by CHN elemental analysis and 1 H-NMR.
1H NMR (CDCl3): d 8.60 (d, 2 H, ppy), 7.9 – 6.7 (m, 21 H,
ppy and phenyl), 6.56 (s, 1 H, diketonate-methine), 6.39 (d, 2 H, ppy), 6.18
(s, 1 H, olefinic), 5.65 (s, 1 H, olefinic), 5.29 (s, 1 H, NH), 4.31 (t, 2 H,
ethylene), 3.59 (t, 2 H, ethylene), 2.00 (s, 3 H, methyl). E.A.: Calcd for C44H36IrN3O6: C, 59.05; H, 4.05; N, 4.70.
Found: C, 59.79; H, 4.05; N, 4.64.
1 H NMR (CDCl 3 ): d 8.60 (d, 2 H, ppy), 7.9 – 6.7 (m, 21 H,
ppy and phenyl), 6.56 (s, 1 H, diketonate-methine), 6.39 (d, 2 H, ppy), 6.18
(s, 1 H, olefinic), 5.65 (s, 1 H, olefinic), 5.29 (s, 1 H, NH), 4.31 (t, 2 H,
ethylene), 3.59 (t, 2 H, ethylene), 2.00 (s, 3 H, methyl) .EA: Calcd for C 44 H 36 IrN 3 O 6 : C, 59.05; H, 4.05; N, 4.70.
Found: C, 59.79; H, 4.05; N, 4.64.
（実施例５）重合性化合物：［６−（４−メタクリロイルオキシフェニル）−２，４−ヘキサンジオナート］ビス（２−フェニルピリジン）イリジウム（ＩＩＩ）（以下Ｉｒ（ｐｐｙ）2［１−（ＭＡ−Ｐｈ−Ｍｅ）−ａｃａｃ］と略す）の合成
スキーム（５Ａ）に示すように、アセチルアセトンと、公知の方法（C. Cativiela, et al., J. Org. Chem., 60, 3074 (1995)）により合成した４−ベンジルオキシベンジルイオダイドを反応させて６−（ベンジルオキシフェニル）−２，４−ヘキサンジオンを合成した。即ち、水素化ナトリウム（６０％ ｉｎ ｏｉｌ）０．３０ｇ（７．５ｍｍｏｌ）を窒素雰囲気下で秤量し、これにＴＨＦ２０ｍｌを加えて水浴で０℃に冷却した。この懸濁液にアセチルアセトン０．７５ｇ（７．５ｍｍｏｌ）とヘキサメチルホスホリックトリアミド０．５ｍｌの混合溶液を滴下すると無色の沈殿が生成した。０℃で１０分間攪拌後、ｎ−ブチルリチウムのヘキサン溶液（１．６Ｍ）４．６ｍｌ（７．５ｍｍｏｌ）を滴下し、更に０℃で２０分間攪拌した。得られた薄黄色の透明な溶液に、４−ベンジルオキシベンジルイオダイド２．２８ｇ（７．０ｍｍｏｌ）をＴＨＦ１０ｍｌに溶かした溶液を滴下した。反応溶液を室温で1時間攪拌し、再び０℃に冷却した後、希塩酸を加えて中和した。有機層を飽和塩化ナトリウム水溶液で洗浄後、ロータリーエバポレータで溶媒を留去した。残渣をシリカゲルカラムに通し（展開液：ジクロロメタン／ヘキサンの１：１（体積比）混合溶媒）、主生成物を分取して減圧乾固することにより、目的とする６−（ベンジルオキシフェニル）−２，４−ヘキサンジオン１．３１ｇ（４．４ｍｍｏｌ）を薄黄色の固体として得た。収率６３％。同定はＣＨＮ元素分析、1Ｈ−ＮＭＲで行った。
Example 5 Polymerizable Compound: [6- (4-Methacryloyloxyphenyl) -2,4-hexanedionate] bis (2-phenylpyridine) iridium (III) (hereinafter Ir (ppy) 2 [1- ( Synthesis of MA-Ph-Me) -acac]) As shown in Scheme (5A), acetylacetone and a known method (C. Cativiela, et al., J. Org. Chem., 60, 3074 (1995) 4-benzyloxybenzyl iodide synthesized by)) was reacted to synthesize 6- (benzyloxyphenyl) -2,4-hexanedione. That is, 0.30 g (7.5 mmol) of sodium hydride (60% in oil) was weighed under a nitrogen atmosphere, 20 ml of THF was added thereto, and the mixture was cooled to 0 ° C. in a water bath. When a mixed solution of 0.75 g (7.5 mmol) of acetylacetone and 0.5 ml of hexamethylphosphoric triamide was added dropwise to this suspension, a colorless precipitate was formed. After stirring at 0 ° C. for 10 minutes, 4.6 ml (7.5 mmol) of a n-butyllithium hexane solution (1.6 M) was added dropwise, and the mixture was further stirred at 0 ° C. for 20 minutes. To the obtained pale yellow transparent solution, a solution of 2.28 g (7.0 mmol) of 4-benzyloxybenzyl iodide in 10 ml of THF was added dropwise. The reaction solution was stirred at room temperature for 1 hour, cooled again to 0 ° C., and neutralized with dilute hydrochloric acid. The organic layer was washed with a saturated aqueous sodium chloride solution, and then the solvent was distilled off with a rotary evaporator. The residue is passed through a silica gel column (developing solution: dichloromethane / hexane 1: 1 (volume ratio) mixed solvent), the main product is separated and dried under reduced pressure to give the desired 6- (benzyloxyphenyl) Obtained 1.31 g (4.4 mmol) of -2,4-hexanedione as a pale yellow solid. Yield 63%. Identification was performed by CHN elemental analysis and 1 H-NMR.
1H NMR (CDCl3): enol; d 7.5 – 6.8 (m, 9 H,
aromatic), 5.46 (s, 1 H, enol-methine), 5.04 (s, 2 H, -O-CH2-), 2.88 (t, J = 7.6 Hz, 2 H,
ethylene), 2.55 (t, J = 8.4 Hz, 2 H, ethylene), 2.04 (s, 3 H, methyl).
keto; d 7.5 – 6.8 (m, 9 H, aromatic), 5.04 (s, 2 H, -O-CH2-), 3.53 (s, 2 H, C(=O)CH2C(=O)), 2.84 (m, 4 H, ethylene),
2.19 (s, 3 H, methyl). enol : keto = 5 : 1. E.A.: Calcd for C19H20O3:
C, 77.00; H, 6.86. Found: C, 77.46; H, 6.77.
1 H NMR (CDCl 3 ): enol; d 7.5 – 6.8 (m, 9 H,
aromatic), 5.46 (s, 1 H, enol-methine), 5.04 (s, 2 H, -O-CH 2- ), 2.88 (t, J = 7.6 Hz, 2 H,
ethylene), 2.55 (t, J = 8.4 Hz, 2 H, ethylene), 2.04 (s, 3 H, methyl).
keto; d 7.5 – 6.8 (m, 9 H, aromatic), 5.04 (s, 2 H, -O-CH 2- ), 3.53 (s, 2 H, C (= O) CH 2 C (= O)), 2.84 (m, 4 H, ethylene),
2.19 (s, 3 H, methyl) .enol: keto = 5: 1.EA: Calcd for C 19 H 20 O 3 :
C, 77.00; H, 6.86. Found: C, 77.46; H, 6.77.
次いで、スキーム（５Ｂ）に示すように、この６−（ベンジルオキシフェニル）−２，４−ヘキサンジオンを水素化することにより６−（ヒドロキシフェニル）−２，４−ヘキサンジオンを生成した。即ち、窒素雰囲気下でＰｄ−活性炭（１０％）１．５ｇを秤量し、ジクロロメタン２０ｍｌと６−（ベンジルオキシフェニル）−２，４−ヘキサンジオン１．３１ｇ（４．４ｍｍｏｌ）を加えた。反応系内を1気圧の水素で置換し、室温で１１時間攪拌した。得られた反応溶液を濾過して不溶物を除き、減圧で溶媒を留去した。残渣をシリカゲルカラムに加えてまずジクロロメタンで展開し、副生成物を除いた。続いてアセトン／ヘキサンの１：１（体積比）混合溶媒で溶出した化合物を含む溶液を減圧乾燥することにより目的とする６−（ヒドロキシフェニル）−２，４−ヘキサンジオン０．７０ｇ（３．４ｍｍｏｌ）を薄黄色の固体として得た。収率７７％。同定はＣＨＮ元素分析、1Ｈ−ＮＭＲで行った。 Then, as shown in Scheme (5B), 6- (hydroxyphenyl) -2,4-hexanedione was produced by hydrogenating the 6- (benzyloxyphenyl) -2,4-hexanedione. That is, 1.5 g of Pd-activated carbon (10%) was weighed under a nitrogen atmosphere, and 20 ml of dichloromethane and 1.31 g (4.4 mmol) of 6- (benzyloxyphenyl) -2,4-hexanedione were added. The reaction system was replaced with 1 atm of hydrogen and stirred at room temperature for 11 hours. The obtained reaction solution was filtered to remove insoluble matters, and the solvent was distilled off under reduced pressure. The residue was added to a silica gel column and first developed with dichloromethane to remove by-products. Subsequently, a solution containing the compound eluted with a 1: 1 (volume ratio) mixed solvent of acetone / hexane is dried under reduced pressure to obtain 0.70 g (3. 4 mmol) was obtained as a pale yellow solid. Yield 77%. Identification was performed by CHN elemental analysis and 1 H-NMR.
1H NMR (CDCl3): enol; d 7.04 (d, J = 8.4 Hz, 2 H,
aromatic), 6.65 (d, J = 8.4 Hz, 2 H, aromatic), 5.55 (br, 1 H, OH), 5.47 (s, 1
H, enol-methine), 2.86 (t, J = 7.3 Hz, 2 H, ethylene), 2.55 (t, J = 7.3 Hz, 2
H, ethylene), 2.04 (s, 3 H, methyl). keto; d 7.04 (d, J = 8.4 Hz, 2 H,
aromatic), 6.65 (d, J = 8.4 Hz, 2 H, aromatic), 5.55 (br, 1 H, OH), 3.55 (s, 2
H, C(=O)CH2C(=O)), 2.83
(m, 4 H, ethylene), 2.19 (s, 3 H, methyl). enol : keto = 5 : 1.
E.A.: Calcd for C12H14O3: C, 69.88; H, 6.84. Found: C, 69.67; H, 6.79.
1 H NMR (CDCl 3 ): enol; d 7.04 (d, J = 8.4 Hz, 2 H,
aromatic), 6.65 (d, J = 8.4 Hz, 2 H, aromatic), 5.55 (br, 1 H, OH), 5.47 (s, 1
H, enol-methine), 2.86 (t, J = 7.3 Hz, 2 H, ethylene), 2.55 (t, J = 7.3 Hz, 2
H, ethylene), 2.04 (s, 3 H, methyl) .keto; d 7.04 (d, J = 8.4 Hz, 2 H,
aromatic), 6.65 (d, J = 8.4 Hz, 2 H, aromatic), 5.55 (br, 1 H, OH), 3.55 (s, 2
H, C (= O) CH 2 C (= O)), 2.83
(m, 4 H, ethylene), 2.19 (s, 3 H, methyl) .enol: keto = 5: 1.
EA: Calcd for C 12 H 14 O 3 : C, 69.88; H, 6.84. Found: C, 69.67; H, 6.79.
スキーム（５Ｃ）に示すように、この６−（４−ヒドロキシフェニル）−２，４−ヘキサンジオンと、常法に従い合成したビス（μ−クロロ）テトラキス（２−フェニルピリジン）ジイリジウム（ＩＩＩ）（［Ｉｒ（ｐｐｙ）2Ｃｌ］2）を反応させて［６−（４−ヒドロキシフェニル）−２，４−ヘキサンジオナート］ビス（２−フェニルピリジン）イリジウム（ＩＩＩ）（以下Ｉｒ（ｐｐｙ）2［１−（ＯＨ−Ｐｈ−Ｍｅ）−ａｃａｃ］と略す）を合成した。即ち、［Ｉｒ（ｐｐｙ）2Ｃｌ］2）７１ｍｇ（０．０６６ｍｍｏｌ）と炭酸ナトリウム４７ｍｇ（０．４４ｍｍｏｌ）の混合物に、６−（４−ヒドロキシフェニル）−２，４−ヘキサンジオン４１ｍｇ（０．２０ｍｍｏｌ）をＤＭＦ５ｍｌに溶かした溶液を加えて６５℃で1時間加熱攪拌した。得られた反応溶液に希塩酸とクロロホルムを加えてよく振盪し、分離した有機層を硫酸マグネシウムで乾燥して減圧下溶媒留去した。残渣をシリカゲルカラムに通し(展開液：ヘキサン／酢酸エチルの１：１（体積比）混合溶媒)、少量の薄黄色の副生成物の次に溶出した薄黄色の溶液を回収して減圧乾固した。得られた固体を少量のジクロロメタンに溶解し、ヘキサンを加えて−２０℃に冷却することにより、目的とするＩｒ（ｐｐｙ）2［１−（ＯＨ−Ｐｈ−Ｍｅ）−ａｃａｃ］８６ｍｇ（０．１２ｍｍｏｌ）を薄黄色の固体として得た。収率９２％。同定はＣＨＮ元素分析、1Ｈ−ＮＭＲで行った。 As shown in Scheme (5C), this 6- (4-hydroxyphenyl) -2,4-hexanedione and bis (μ-chloro) tetrakis (2-phenylpyridine) diiridium (III) synthesized according to a conventional method ([Ir (ppy) 2 Cl] 2 ) is reacted to produce [6- (4-hydroxyphenyl) -2,4-hexanedionate] bis (2-phenylpyridine) iridium (III) (hereinafter Ir (ppy) 2 [abbreviated as 1- (OH-Ph-Me) -acac]). That is, to a mixture of [Ir (ppy) 2 Cl] 2 ) 71 mg (0.066 mmol) and sodium carbonate 47 mg (0.44 mmol), 6- (4-hydroxyphenyl) -2,4-hexanedione 41 mg (0. 20 mmol) in 5 ml of DMF was added and stirred at 65 ° C. for 1 hour. Diluted hydrochloric acid and chloroform were added to the obtained reaction solution and shaken well. The separated organic layer was dried over magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was passed through a silica gel column (developing solution: 1: 1 (volume ratio) mixed solvent of hexane / ethyl acetate), and a light yellow solution eluted after a small amount of light yellow by-product was recovered and dried under reduced pressure. did. The obtained solid was dissolved in a small amount of dichloromethane, hexane was added, and the mixture was cooled to −20 ° C., whereby 86 mg (0. 0) of the target Ir (ppy) 2 [1- (OH-Ph-Me) -acac] was obtained. 12 mmol) was obtained as a pale yellow solid. Yield 92%. Identification was performed by CHN elemental analysis and 1 H-NMR.
1H NMR (CDCl3): d 8.48 (d, J = 6.2 Hz, 1 H,
ppy), 8.23 (d, J = 5.9 Hz, 1 H, ppy), 7.9 – 7.6 (m, 4 H, ppy), 7.53
(t, J = 7.3 Hz, 2 H, ppy), 7.11 (t, J = 7.0 Hz, 1 H, ppy), 6.99 (t, J = 7.0 Hz,
1 H, ppy), 6.8 – 6.4 (m, 8 H, ppy + C6H4OH), 6.27 (t, J = 8.1 Hz, 2 H, ppy),
5.18 (s, 1 H, diketonate-methine), 5.10 (br, 1 H, OH), 2.54 (t, J = 7.0 Hz, 2
H, methylene), 2.31 (m, 2 H, methylene), 1.75 (s, 3 H, methyl). E.A.:
Calcd for C34H29IrN2O3:
C, 57.86; H, 4.14; N, 3.97. Found: C, 58.03; H, 4.11; N, 3.86.
1 H NMR (CDCl 3 ): d 8.48 (d, J = 6.2 Hz, 1 H,
ppy), 8.23 (d, J = 5.9 Hz, 1 H, ppy), 7.9 – 7.6 (m, 4 H, ppy), 7.53
(t, J = 7.3 Hz, 2 H, ppy), 7.11 (t, J = 7.0 Hz, 1 H, ppy), 6.99 (t, J = 7.0 Hz,
1 H, ppy), 6.8 – 6.4 (m, 8 H, ppy + C 6 H 4 OH), 6.27 (t, J = 8.1 Hz, 2 H, ppy),
5.18 (s, 1 H, diketonate-methine), 5.10 (br, 1 H, OH), 2.54 (t, J = 7.0 Hz, 2
H, methylene), 2.31 (m, 2 H, methylene), 1.75 (s, 3 H, methyl). EA:
Calcd for C 34 H 29 IrN 2 O 3 :
C, 57.86; H, 4.14; N, 3.97. Found: C, 58.03; H, 4.11; N, 3.86.
次いで、スキーム（５Ｄ）に示すように、このＩｒ（ｐｐｙ）2［１−（ＯＨ−Ｐｈ−Ｍｅ）−ａｃａｃ］とメタクリル酸クロライドを反応させることによりＩｒ（ｐｐｙ）2［１−（ＭＡ−Ｐｈ−Ｍｅ）−ａｃａｃ］を合成した。即ち、窒素雰囲気下でＩｒ（ｐｐｙ）2［１−（ＯＨ−Ｐｈ−Ｍｅ）−ａｃａｃ］１６９ｍｇ（０．２４ｍｍｏｌ）をジクロロメタン１０ｍｌに溶解し、トリエチルアミン０．３０ｍｌ（２．２ｍｍｏｌ）を加えた。この溶液にメタクリル酸クロライド０．０６０ｍｌ（０．６１ｍｍｏｌ）を加えると速やかに生成物を生じた。更に少量のメタノールを加えた後、減圧で溶媒を留去した。残渣をヘキサン／ジクロロメタン／アセトンの混合溶媒（１０：１０：１（体積比））を用いてシリカゲルカラムに通し、黄色の主生成物を分取した。減圧で溶媒留去後、ジクロロメタン−ヘキサン混合溶液から再結晶することにより目的とするＩｒ（ｐｐｙ）2［１−（ＭＡ−Ｐｈ−Ｍｅ）−ａｃａｃ］１４１ｍｇ（０．１８ｍｍｏｌ）を黄色の固体として得た。収率７６％。同定はＣＨＮ元素分析、1Ｈ−ＮＭＲで行った。 Next, as shown in Scheme (5D), Ir (ppy) 2 [1- (OH-Ph-Me) -acac] is reacted with methacrylic acid chloride to react with Ir (ppy) 2 [1- (MA- Ph-Me) -acac] was synthesized. Specifically, 169 mg (0.24 mmol) of Ir (ppy) 2 [1- (OH-Ph-Me) -acac] was dissolved in 10 ml of dichloromethane under a nitrogen atmosphere, and 0.30 ml (2.2 mmol) of triethylamine was added. When 0.060 ml (0.61 mmol) of methacrylic acid chloride was added to this solution, a product was rapidly formed. After adding a small amount of methanol, the solvent was distilled off under reduced pressure. The residue was passed through a silica gel column using a mixed solvent of hexane / dichloromethane / acetone (10: 10: 1 (volume ratio)) to fractionate a yellow main product. After distilling off the solvent under reduced pressure, recrystallization from a dichloromethane-hexane mixed solution gave 141 mg (0.18 mmol) of the target Ir (ppy) 2 [1- (MA-Ph-Me) -acac] as a yellow solid. Obtained. Yield 76%. Identification was performed by CHN elemental analysis and 1 H-NMR.
1H NMR (CDCl3): d 8.48 (d, J = 5.1 Hz, 1 H,
ppy), 8.27 (d, J = 5.9 Hz, 1 H, ppy), 7.9 – 7.5 (m, 6 H, ppy), 7.12
(t, J = 7.0 Hz, 1 H, ppy), 7.04 (t, J = 7.0 Hz, 1 H, ppy), 6.9 – 6.6 (m, 8 H,
aromatic), 6.33 (s, 1 H, olefinic), 6.27 (d, J = 7.6 Hz, 2 H, ppy), 5.74 (s, 1
H, olefinic), 5.17 (s, 1 H, diketonate-methine), 2.61 (t, J = 7.0 Hz, 2 H,
ethylene), 2.34 (m, 2 H, ethylene), 2.07 (s, 3 H, methacryl-methyl), 1.76 (s, 3
H, diketonate-methyl). E.A.: Calcd for C38H33IrN2O4: C, 58.98; H, 4.30; N, 3.62. Found: C, 58.69; H,
4.17; N, 3.81.
1 H NMR (CDCl 3 ): d 8.48 (d, J = 5.1 Hz, 1 H,
ppy), 8.27 (d, J = 5.9 Hz, 1 H, ppy), 7.9 – 7.5 (m, 6 H, ppy), 7.12
(t, J = 7.0 Hz, 1 H, ppy), 7.04 (t, J = 7.0 Hz, 1 H, ppy), 6.9 – 6.6 (m, 8 H,
aromatic), 6.33 (s, 1 H, olefinic), 6.27 (d, J = 7.6 Hz, 2 H, ppy), 5.74 (s, 1
H, olefinic), 5.17 (s, 1 H, diketonate-methine), 2.61 (t, J = 7.0 Hz, 2 H,
ethylene), 2.34 (m, 2 H, ethylene), 2.07 (s, 3 H, methacryl-methyl), 1.76 (s, 3
H, diketonate-methyl) .EA: Calcd for C 38 H 33 IrN 2 O 4 : C, 58.98; H, 4.30; N, 3.62. Found: C, 58.69; H,
4.17; N, 3.81.
（実施例６）重合性化合物：（１−メタクリロイルオキシ−２，４−ペンタンジオナート）ビス（２−フェニルピリジン）イリジウム（ＩＩＩ）（以下Ｉｒ（ｐｐｙ）2（１−ＭＡ−ａｃａｃ）と略す）の合成
スキーム（６Ａ）に示すように、常法に従い合成したビス（μ−クロロ）テトラキス（２−フェニルピリジン）ジイリジウム（ＩＩＩ）（［Ｉｒ（ｐｐｙ）2Ｃｌ］2）と、公知の方法（欧州特許ＥＰ０５１４２１７）を参考に合成した１−（ｔｅｒｔ−ブチルジメチルシリルオキシ）−２，４−ペンタジオンを反応させて（１−ヒドロキシ−２，４−ペンタンジオナート）ビス（２−フェニルピリジン）イリジウム（ＩＩＩ）（以下Ｉｒ（ｐｐｙ）2（１−ＯＨ−ａｃａｃ）と略す）を合成した。即ち、［Ｉｒ（ｐｐｙ）2Ｃｌ］2４９２ｍｇ（０．４６ｍｍｏｌ）と炭酸ナトリウム１３９ｍｇ（１．３１ｍｍｏｌ）をＤＭＦ１０ｍｌ中に溶解し、１−（ｔｅｒｔ−ブチルジメチルシリルオキシ）−２，４−ペンタジオン（１−ＴＢＤＭＳＯ−２，４−ペンタジオン）３２１ｍｇ（１．３９ｍｍｏｌ）を加えて７０℃で1時間加熱撹拌した。得られた反応混合物を室温にまで冷却した後、１００ｍｌの飽和塩化アンモニウム水溶液および５０ｍｌのクロロホルムを加えてよく振盪した。有機層を硫酸マグネシウムで乾燥して減圧で溶媒留去し、残渣をジクロロメタンを溶出液とするシリカゲルカラムに通し黄色の溶液を得た。これを減圧乾燥した後に得られた黄色の固体をＴＨＦ２０ｍｌ中に溶解し、テトラ−ｎ−ブチルアンモニウムフルオライド（以下Ｂｕn 4ＮＦと略す）の１．０Ｍ ＴＨＦ溶液０．４６ｍｌ（０．４６ｍｍｏｌ）を激しく撹拌しながら滴下した。この反応溶液を室温で０．５時間撹拌後、減圧で溶媒留去した。残渣をシリカゲルカラムに通し（溶出液：ヘキサン／ジクロロメタン／アセトンの１：３：１（体積比）の混合溶媒）、溶出した黄色の主生成物を回収して減圧乾燥した。得られた粗生成物をジクロロメタン／ヘキサン混合溶液から再結晶することにより、目的とするＩｒ（ｐｐｙ）2（１−ＯＨ−ａｃａｃ）３８９ｍｇ（０．６３ｍｍｏｌ）を黄色の固体として得た。収率６９％。同定はＣＨＮ元素分析、1Ｈ−ＮＭＲで行った。
(Example 6) Polymerizable compound: (1-methacryloyloxy-2,4-pentanedionate) bis (2-phenylpyridine) iridium (III) (hereinafter abbreviated as Ir (ppy) 2 (1-MA-acac)) As shown in Scheme (6A), bis (μ-chloro) tetrakis (2-phenylpyridine) diiridium (III) ([Ir (ppy) 2 Cl] 2 ) synthesized according to a conventional method, 1- (tert-Butyldimethylsilyloxy) -2,4-pentadione synthesized by referring to the method (European Patent EP0514217) was reacted to give (1-hydroxy-2,4-pentanedionate) bis (2-phenylpyridine) ) Iridium (III) (hereinafter abbreviated as Ir (ppy) 2 (1-OH-acac)) was synthesized. Specifically, 492 mg (0.46 mmol) of [Ir (ppy) 2 Cl] 2 and 139 mg (1.31 mmol) of sodium carbonate were dissolved in 10 ml of DMF, and 1- (tert-butyldimethylsilyloxy) -2,4-pentadione ( 321 mg (1.39 mmol) of 1-TBDDMSO-2,4-pentadione) was added, and the mixture was heated and stirred at 70 ° C. for 1 hour. After cooling the resulting reaction mixture to room temperature, 100 ml of saturated aqueous ammonium chloride solution and 50 ml of chloroform were added and shaken well. The organic layer was dried over magnesium sulfate, the solvent was distilled off under reduced pressure, and the residue was passed through a silica gel column using dichloromethane as an eluent to obtain a yellow solution. The yellow solid obtained after drying this under reduced pressure was dissolved in 20 ml of THF, and 0.46 ml (0.46 mmol) of 1.0 M THF solution of tetra-n-butylammonium fluoride (hereinafter abbreviated as Bu n 4 NF). Was added dropwise with vigorous stirring. The reaction solution was stirred at room temperature for 0.5 hour, and the solvent was distilled off under reduced pressure. The residue was passed through a silica gel column (eluent: mixed solvent of hexane / dichloromethane / acetone 1: 3: 1 (volume ratio)), and the eluted yellow main product was collected and dried under reduced pressure. The obtained crude product was recrystallized from a dichloromethane / hexane mixed solution to obtain 389 mg (0.63 mmol) of target Ir (ppy) 2 (1-OH-acac) as a yellow solid. Yield 69%. Identification was performed by CHN elemental analysis and 1 H-NMR.
1H NMR (CDCl3): d 8.48 (d, J = 5.7 Hz, 1 H,
ppy), 8.42 (d, J = 5.7 Hz, 1 H, ppy), 7.86 (m, 2 H, ppy), 7.74 (t, J = 7.6 Hz,
2 H, ppy), 7.54 (t, J = 5.9 Hz, 2 H, ppy), 7.14 (t, J = 5.9 Hz, 2 H, ppy), 6.82
(t, J = 7.3 Hz, 2 H, ppy), 6.69 (m, 2 H, ppy), 6.28 (d, J = 6.8 Hz, 1 H, ppy),
6.23 (d, J = 6.5 Hz, 1 H, ppy), 5.17 (s, 1 H, diketonate-methine), 3.88 (dd, J
= 8.1, 5.4 Hz, 1 H, -CHH’-O-), 3.78 (dd, J = 8.1, 4.3 Hz, 1 H, -CHH’-O-), 3.10 (t, J = 4.6 Hz,
1 H, OH), 1.82 (s, 3 H, methyl). E.A.: Calcd for C27H23IrN2O3: C, 52.67; H, 3.77; N, 4.55.
Found: C, 52.45; H, 3.68; N, 4.79.
1 H NMR (CDCl 3 ): d 8.48 (d, J = 5.7 Hz, 1 H,
ppy), 8.42 (d, J = 5.7 Hz, 1 H, ppy), 7.86 (m, 2 H, ppy), 7.74 (t, J = 7.6 Hz,
2 H, ppy), 7.54 (t, J = 5.9 Hz, 2 H, ppy), 7.14 (t, J = 5.9 Hz, 2 H, ppy), 6.82
(t, J = 7.3 Hz, 2 H, ppy), 6.69 (m, 2 H, ppy), 6.28 (d, J = 6.8 Hz, 1 H, ppy),
6.23 (d, J = 6.5 Hz, 1 H, ppy), 5.17 (s, 1 H, diketonate-methine), 3.88 (dd, J
= 8.1, 5.4 Hz, 1 H, -CHH'-O-), 3.78 (dd, J = 8.1, 4.3 Hz, 1 H, -CHH'-O-), 3.10 (t, J = 4.6 Hz,
1 H, OH), 1.82 (s, 3 H, methyl) .EA: Calcd for C 27 H 23 IrN 2 O 3 : C, 52.67; H, 3.77; N, 4.55.
Found: C, 52.45; H, 3.68; N, 4.79.
次いで、スキーム（６Ｂ）に示すように、このＩｒ（ｐｐｙ）2（１−ＯＨ−ａｃａｃ）とメタクリル酸クロライドを反応させることによりＩｒ（ｐｐｙ）2（１−ＭＡ−ａｃａｃ）を合成した。即ち、Ｉｒ（ｐｐｙ）2（１−ＯＨ−ａｃａｃ）２００ｍｇ（０．３２ｍｍｏｌ）を乾燥ジクロロメタン１５ｍｌに溶解し、トリエチルアミン０．２５ｍｌ（１．８ｍｍｏｌ）と０．２０ｍｌのメタクリル酸クロライド０．２０ｍｌ（２．０ｍｍｏｌ）を加えて室温で1時間撹拌した。次に反応溶液を炭酸ナトリウム水溶液２０ｍｌで洗浄し、減圧で溶媒を留去した。残渣を再びジクロロメタンに溶解してシリカゲルカラム上部に加え、ヘキサン／ジクロロメタン／アセトンの２：４：１（体積比）の混合溶媒で展開した。最初に得られる黄色溶液を回収して減圧で乾燥することにより、目的とするＩｒ（ｐｐｙ）2（１−ＭＡ−ａｃａｃ）１６５ｍｇ（０．２４ｍｍｏｌ）を黄色の固体として得た。収率７４％。同定はＣＨＮ元素分析、1Ｈ−ＮＭＲで行った。 Next, as shown in Scheme (6B), Ir (ppy) 2 (1-OH-acac) was reacted with methacrylic acid chloride to synthesize Ir (ppy) 2 (1-MA-acac). That is, 200 mg (0.32 mmol) of Ir (ppy) 2 (1-OH-acac) was dissolved in 15 ml of dry dichloromethane, and 0.25 ml (1.8 mmol) of triethylamine and 0.20 ml of 0.20 ml of methacrylic acid chloride (2 0.0 mmol) was added and stirred at room temperature for 1 hour. Next, the reaction solution was washed with 20 ml of an aqueous sodium carbonate solution, and the solvent was distilled off under reduced pressure. The residue was dissolved again in dichloromethane, added to the top of the silica gel column, and developed with a mixed solvent of hexane / dichloromethane / acetone 2: 4: 1 (volume ratio). The initially obtained yellow solution was collected and dried under reduced pressure to obtain 165 mg (0.24 mmol) of the target Ir (ppy) 2 (1-MA-acac) as a yellow solid. Yield 74%. Identification was performed by CHN elemental analysis and 1 H-NMR.
1H NMR (CDCl3): d 8.53 (d, J = 5.7 Hz, 1 H,
ppy), 8.48 (d, J = 5.4 Hz, 1 H, ppy), 7.84 (d, J = 7.8 Hz, 2 H, ppy), 7.73 (t,
J = 7.0 Hz, 2 H, ppy), 7.53 (t, J = 6.8 Hz, 2 H, ppy), 5.14 (m, 2 H, ppy), 6.79
(m, 2 H, ppy), 6.69 (m, 2 H, ppy), 6.29 (d, J = 7.6 Hz, 1 H, ppy), 6.23 (d, J =
7.6 Hz, 1 H, ppy), 6.04 (s, 1 H, olefinic), 5.51 (s, 1 H, olefinic), 5.31 (s, 1
H, diketonate-methine), 4.38 (d, J = 15.4 Hz, 1 H, -CHH¢-OC(=O)-), 4.27 (d, J =
14.9 Hz, 1 H, -CHH¢-OC(=O)-), 1.87 (s, 3 H, methacryl-methyl), 1.82 (s, 3 H,
diketonate-methyl). E.A.: Calcd for C31H27IrN2O4: C, 54.45; H, 3.98; N, 4.10. Found: C, 54.18; H,
3.96; N, 4.33.
1 H NMR (CDCl 3 ): d 8.53 (d, J = 5.7 Hz, 1 H,
ppy), 8.48 (d, J = 5.4 Hz, 1 H, ppy), 7.84 (d, J = 7.8 Hz, 2 H, ppy), 7.73 (t,
J = 7.0 Hz, 2 H, ppy), 7.53 (t, J = 6.8 Hz, 2 H, ppy), 5.14 (m, 2 H, ppy), 6.79
(m, 2 H, ppy), 6.69 (m, 2 H, ppy), 6.29 (d, J = 7.6 Hz, 1 H, ppy), 6.23 (d, J =
7.6 Hz, 1 H, ppy), 6.04 (s, 1 H, olefinic), 5.51 (s, 1 H, olefinic), 5.31 (s, 1
H, diketonate-methine), 4.38 (d, J = 15.4 Hz, 1 H, -CHH ¢ -OC (= O)-), 4.27 (d, J =
14.9 Hz, 1 H, -CHH ¢ -OC (= O)-), 1.87 (s, 3 H, methacryl-methyl), 1.82 (s, 3 H,
diketonate-methyl). EA: Calcd for C 31 H 27 IrN 2 O 4 : C, 54.45; H, 3.98; N, 4.10. Found: C, 54.18; H,
3.96; N, 4.33.
（実施例７）重合性化合物：［６−（４−ビニルフェニル）−２，４−ヘキサンジオナート］ビス［２−（２，４−ジフルオロフェニル）ピリジン］イリジウム（ＩＩＩ）（以下Ｉｒ（２，４−Ｆ−ｐｐｙ）2［１−（Ｓｔ−Ｍｅ）ａｃａｃ］と略す）の合成
スキーム（７Ａ）に示すように、常法に従い２−（２，４−ジフルオロフェニル）ピリジンを合成した。即ち、アルゴン気流下において２−ブロモピリジン８．６９ｇ（５５．０ｍｍｏｌ）を脱水テトラヒドロフラン２００ｍｌに溶解して−７８℃まで冷却し、１．６Ｍ ｎ−ブチルリチウムのヘキサン溶液３８．７ｍｌ（６１．９ｍｍｏｌ）を３０分かけて滴下した。滴下後、さらに塩化亜鉛７．５ｇ（５５．０ｍｍｏｌ）を脱水テトラヒドロフラン５０ｍｌに溶解した溶液を３０分かけて滴下した。滴下後、０℃までゆっくりと昇温し、１−ブロモ−２，４−ジフルオロベンゼン９．６５ｇ（５５．０ｍｍｏｌ）とテトラキス（トリフェニルホスフィン）パラジウム（０） ２．３１ｇ（２．０ｍｍｏｌ）を加え、還流下に６時間攪拌した後、反応液に飽和食塩水２００ｍｌを加えジエチルエーテルで抽出した。抽出液を乾燥後、濃縮し、カラムクロマトグラフィー（シリカゲル；クロロホルム／ヘキサン（１／１：体積比））で精製することにより、２−（２，４−ジフルオロフェニル）ピリジン６．００ｇ（３１．４ｍｍｏｌ）を無色透明のオイルとして得た。収率６３％。同定は1Ｈ ＮＭＲとＣＨＮ元素分析で行った。
(Example 7) Polymerizable compound: [6- (4-vinylphenyl) -2,4-hexanedionate] bis [2- (2,4-difluorophenyl) pyridine] iridium (III) (hereinafter referred to as Ir (2) , 4-F-ppy) 2 [abbreviated as 1- (St-Me) acac]) As shown in scheme (7A), 2- (2,4-difluorophenyl) pyridine was synthesized according to a conventional method. That is, 8.69 g (55.0 mmol) of 2-bromopyridine was dissolved in 200 ml of dehydrated tetrahydrofuran under an argon stream, cooled to −78 ° C., and 38.7 ml (61.9 mmol) of a 1.6 M n-butyllithium hexane solution. ) Was added dropwise over 30 minutes. After the dropwise addition, a solution in which 7.5 g (55.0 mmol) of zinc chloride was dissolved in 50 ml of dehydrated tetrahydrofuran was further added dropwise over 30 minutes. After the dropwise addition, the temperature was slowly raised to 0 ° C., and 9.65 g (55.0 mmol) of 1-bromo-2,4-difluorobenzene and 2.31 g (2.0 mmol) of tetrakis (triphenylphosphine) palladium (0) were added. After stirring for 6 hours under reflux, 200 ml of saturated brine was added to the reaction solution, and the mixture was extracted with diethyl ether. The extract is dried, concentrated, and purified by column chromatography (silica gel; chloroform / hexane (1/1: volume ratio)) to give 6.00 g (31. 2) of 2- (2,4-difluorophenyl) pyridine. 4 mmol) was obtained as a clear colorless oil. Yield 63%. Identification was performed by 1 H NMR and CHN elemental analysis.
1H NMR(270 MHz, CDCl3), ppm: 8.71(d, 1H, J 4.6 Hz),
8.00(td, 1H, J 8.9, 6.5 Hz), 7.8 - 7.7(m, 2H), 7.3 - 7.2(over wrapped with CHCl3, 1H), 7.1 - 6.8(m, 2H). E. A.
: Found: C 68.98, H 3.80, N 7.31. Calcd: C 69.11, H 3.69, N 7.33.
1 H NMR (270 MHz, CDCl 3 ), ppm: 8.71 (d, 1H, J 4.6 Hz),
8.00 (td, 1H, J 8.9, 6.5 Hz), 7.8-7.7 (m, 2H), 7.3-7.2 (over wrapped with CHCl 3 , 1H), 7.1-6.8 (m, 2H) .EA
: Found: C 68.98, H 3.80, N 7.31.Calcd: C 69.11, H 3.69, N 7.33.
次いで、スキーム（７Ｂ）に示すように、この２−（２，４−ジフルオロフェニル）ピリジンとヘキサクロロイリジウム（ＩＩＩ）酸ナトリウムｎ水和物を反応させることによりビス（μ−クロロ）テトラキス［２−（２，４−ジフルオロフェニル）ピリジン］ジイリジウム（ＩＩＩ）（以下［Ｉｒ（２，４−Ｆ−ｐｐｙ）2Ｃｌ］2と略す）を合成した。即ち、２−（２，４−ジフルオロフェニル）ピリジン０．９６ｇ（５．０ｍｍｏｌ）とヘキサクロロイリジウム（ＩＩＩ）酸ナトリウムｎ水和物１．００ｇを２−エトキシエタノール：水＝３：１（体積比）の混合溶媒４０ｍｌに溶解し、３０分間アルゴンガスを吹き込んだ後、還流下に５時間攪拌した。生じた沈殿を濾取し、エタノールと少量のアセトンで洗浄し、真空下で５時間乾燥することにより、目的とする［Ｉｒ（２，４−Ｆ−ｐｐｙ）2Ｃｌ］2０．７９ｇ（０．６５ｍｍｏｌ）を黄色粉末として得た。収率８６％。同定は1Ｈ ＮＭＲとＣＨＮ元素分析で行った。 Next, as shown in Scheme (7B), this 2- (2,4-difluorophenyl) pyridine is reacted with sodium hexachloroiridium (III) n-hydrate to give bis (μ-chloro) tetrakis [2- (2,4-Difluorophenyl) pyridine] diiridium (III) (hereinafter abbreviated as [Ir (2,4-F-ppy) 2 Cl] 2 ) was synthesized. Namely, 0.96 g (5.0 mmol) of 2- (2,4-difluorophenyl) pyridine and 1.00 g of sodium hexachloroiridium (III) n-hydrate were mixed with 2-ethoxyethanol: water = 3: 1 (volume ratio). ) Was dissolved in 40 ml of a mixed solvent, and argon gas was blown in for 30 minutes, followed by stirring under reflux for 5 hours. The resulting precipitate was collected by filtration, washed with ethanol and a small amount of acetone, and dried under vacuum for 5 hours to obtain 0.79 g (0) of the desired [Ir (2,4-F-ppy) 2 Cl] 2. .65 mmol) as a yellow powder. Yield 86%. Identification was performed by 1 H NMR and CHN elemental analysis.
1H NMR(270 MHz, CDCl3), ppm: 9.12(d, 4H, J = 5.7 Hz),
8.31(d, 4H, J = 8.6 Hz), 7.83(dd, 4H, J = 7.6, 7.6 Hz), 6.82(dd, 4H, J = 7.3, 7.3 Hz), 6.34(ddd, 4H, J =
11.6, 10.0, 2.4 Hz), 5.29(dd, 4H, J = 9.5, 2.4 Hz). Anal. Found: C 43.39, H 2.03,
N 4.55. Calcd: C 43.46, H 1.99, N 4.61.
1 H NMR (270 MHz, CDCl 3 ), ppm: 9.12 (d, 4H, J = 5.7 Hz),
8.31 (d, 4H, J = 8.6 Hz), 7.83 (dd, 4H, J = 7.6, 7.6 Hz), 6.82 (dd, 4H, J = 7.3, 7.3 Hz), 6.34 (ddd, 4H, J =
11.6, 10.0, 2.4 Hz), 5.29 (dd, 4H, J = 9.5, 2.4 Hz). Anal. Found: C 43.39, H 2.03,
N 4.55.Calcd: C 43.46, H 1.99, N 4.61.
次いで、スキーム（７Ｃ）に示すように、この［Ｉｒ（２，４−Ｆ−ｐｐｙ）2Ｃｌ］2と６−（４−ビニルフェニル）−２，４−ヘキサジオンを反応させることによりＩｒ（２，４−Ｆ−ＰＰｙ）2［１−（ＳＴ−Ｍｅ）ａｃａｃ］を合成した。即ち、［Ｉｒ（２，４−Ｆ−ｐｐｙ）2Ｃｌ］2 ２４３ｍｇ（０．２０ｍｍｏｌ）、炭酸ナトリウム２１２ｍｇ（２．００ｍｍｏｌ）、２，６−ジ−ｔｅｒｔ−ブチル−４−メチルフェノール１．３ｍｇ、実施例２と同様に合成した６−（４−ビニルフェニル）−２，４−ヘキサジオン１３０ｍｇ（０．６０ｍｍｏｌ）をアルゴン気流下にＤＭＦ２０ｍｌに溶解し、８０℃で２時間攪拌した後、反応液に水を加え、クロロホルムで抽出した。抽出液を乾燥後、濃縮し、カラムクロマトグラフィー（シリカゲル；クロロホルム）で精製し、さらにクロロホルム／ヘキサン溶液から再結晶することにより、Ｉｒ（２，４−Ｆ−ＰＰｙ）2［１−（ＳＴ−Ｍｅ）ａｃａｃ］２６１ｍｇ（０．３３ｍｍｏｌ）を黄色結晶として得た。収率８３％。同定はＣＨＮ元素分析、1Ｈ−ＮＭＲで行った。 Next, as shown in scheme (7C), Ir [2 (2-F-ppy) 2 Cl] 2 is reacted with 6 (4-vinylphenyl) -2,4-hexadione to give Ir (2 , 4-F-PPy) 2 [1- (ST-Me) acac] was synthesized. That is, [Ir (2,4-F-ppy) 2 Cl] 2 243 mg (0.20 mmol), sodium carbonate 212 mg (2.00 mmol), 2,6-di-tert-butyl-4-methylphenol 1.3 mg Then, 130 mg (0.60 mmol) of 6- (4-vinylphenyl) -2,4-hexadione synthesized in the same manner as in Example 2 was dissolved in 20 ml of DMF under an argon stream and stirred at 80 ° C. for 2 hours. Water was added to and extracted with chloroform. The extract was dried, concentrated, purified by column chromatography (silica gel; chloroform), and recrystallized from a chloroform / hexane solution to give Ir (2,4-F-PPy) 2 [1- (ST- Me) acac] 261 mg (0.33 mmol) was obtained as yellow crystals. Yield 83%. Identification was performed by CHN elemental analysis and 1 H-NMR.
1H NMR(270 MHz, CDCl3), ppm: 8.39(d, 1H, J = 5.7 Hz), 8.3
- 8.2(m, 2H), 8.04(d, 1H, J = 5.7 Hz), 7.8 - 7.7(m, 2H), 7.19(d, 2H, J = 7.8
Hz), 7.15(dd, 1H, J = 6.6, 6.6 Hz), 6.97(dd, 1H, J = 6.6, 6.6 Hz), 6.89(d, 2H,
J = 7.8 Hz), 6.67(dd, 1H, J = 17.6, 10.8 Hz), .6.4 - 6.2(m, 2H), 5.7 - 5.6(m,
3H), 5.22(s, 1H), 5.21(d, 1H, J = 11.1 Hz), 2.62(t, 2H, J = 7.0 Hz), 2.39(m,
2H), 1.78(s, 3H). Anal. Found: C 54.82, H 3.50, N 3.49. Calcd: C 54.88, H
3.45, N 3.56.
1 H NMR (270 MHz, CDCl 3 ), ppm: 8.39 (d, 1H, J = 5.7 Hz), 8.3
-8.2 (m, 2H), 8.04 (d, 1H, J = 5.7 Hz), 7.8-7.7 (m, 2H), 7.19 (d, 2H, J = 7.8
Hz), 7.15 (dd, 1H, J = 6.6, 6.6 Hz), 6.97 (dd, 1H, J = 6.6, 6.6 Hz), 6.89 (d, 2H,
J = 7.8 Hz), 6.67 (dd, 1H, J = 17.6, 10.8 Hz), .6.4-6.2 (m, 2H), 5.7-5.6 (m,
3H), 5.22 (s, 1H), 5.21 (d, 1H, J = 11.1 Hz), 2.62 (t, 2H, J = 7.0 Hz), 2.39 (m,
2H), 1.78 (s, 3H). Anal. Found: C 54.82, H 3.50, N 3.49.Calcd: C 54.88, H
3.45, N 3.56.
（実施例８）重合性化合物：｛３−［４−（２−メタクリロイルオキシエチル）カルバモイルオキシフェニルメチル］−２，４−ペンタンジオナート｝ビス（２−フェニルピリジン）イリジウム（ＩＩＩ）（以下Ｉｒ（ｐｐｙ）2［３−（ＭＯＩ−Ｐｈ−Ｍｅ）−ａｃａｃ］と略す）の合成
スキーム（８Ａ）に示すように、常法に従い合成したビス（μ−クロロ）テトラキス（２−フェニルピリジン）ジイリジウム（ＩＩＩ）（［Ｉｒ（ｐｐｙ）2Ｃｌ］2）と３−（４−ヒドロキシフェニルメチル）−２，４−ペンタンジオンを反応させて［３−（４−ヒドロキシフェニルメチル）−２，４−ペンタンジオナート］ビス（２−フェニルピリジン）イリジウム（ＩＩＩ）（以下Ｉｒ（ｐｐｙ）2［１−（ＯＨ−Ｐｈ−Ｍｅ）−ａｃａｃ］と略す）を合成した。即ち、［Ｉｒ（ｐｐｙ）2Ｃｌ］2）５６ｍｇ（０．０５２ｍｍｏｌ）および炭酸ナトリウム４４ｍｇ（０．４２ｍｍｏｌ）をＤＭＦ５ｍｌに溶解した。この溶液に、公知の方法（C. Cativiela et al., J. Org. Chem., 60, 3074 (1995)）により合成した３−（４−ヒドロキシフェニルメチル）−２，４−ペンタンジオン３０ｍｇ（０．１５ｍｍｏｌ）をＤＭＦ５ｍｌに溶解した溶液を加えて８０℃で１．５時間加熱攪拌した。次に、室温にまで冷却した反応溶液に希塩酸とクロロホルムを加えてよく振とうし、有機層を分取してロータリーエバポレータで溶媒を留去した。残渣をヘキサン／酢酸エチルの１：１（体積比）混合溶媒を展開液とするシリカゲルカラムに通し、主生成物のバンドを分取した。得られた薄黄色の溶液から減圧で溶媒を留去し、ジクロロメタン／ヘキサンの混合溶液から再結晶することによりＩｒ（ｐｐｙ）2［１−（ＯＨ−Ｐｈ−Ｍｅ）−ａｃａｃ］３４ｍｇ（０．０４８ｍｍｏｌ）を薄黄色の固体として得た。収率４６％。同定はＣＨＮ元素分析、1Ｈ−ＮＭＲで行った。
Example 8 Polymerizable Compound: {3- [4- (2-Methacryloyloxyethyl) carbamoyloxyphenylmethyl] -2,4-pentanedionate} bis (2-phenylpyridine) iridium (III) (hereinafter Ir Synthesis of (ppy) 2 [abbreviated as 3- (MOI-Ph-Me) -acac]) As shown in Scheme (8A), bis (μ-chloro) tetrakis (2-phenylpyridine) di synthesized according to a conventional method Iridium (III) ([Ir (ppy) 2 Cl] 2 ) and 3- (4-hydroxyphenylmethyl) -2,4-pentanedione are reacted to produce [3- (4-hydroxyphenylmethyl) -2,4 - pentanedionate] bis (2-phenylpyridine) iridium (III) (hereinafter Ir (ppy) 2 [1- ( OH-Ph-Me) -acac] substantially ) Was synthesized. That is, [Ir (ppy) 2 Cl] 2 ) 56 mg (0.052 mmol) and sodium carbonate 44 mg (0.42 mmol) were dissolved in 5 ml of DMF. To this solution, 30 mg of 3- (4-hydroxyphenylmethyl) -2,4-pentanedione synthesized by a known method (C. Cativiela et al., J. Org. Chem., 60, 3074 (1995)) ( 0.15 mmol) dissolved in 5 ml of DMF was added and stirred with heating at 80 ° C. for 1.5 hours. Next, dilute hydrochloric acid and chloroform were added to the reaction solution cooled to room temperature and shaken well. The organic layer was separated, and the solvent was distilled off with a rotary evaporator. The residue was passed through a silica gel column using a 1: 1 (volume ratio) mixed solvent of hexane / ethyl acetate as a developing solution to separate the main product band. The solvent was distilled off from the obtained pale yellow solution under reduced pressure, and recrystallization from a mixed solution of dichloromethane / hexane gave Ir (ppy) 2 [1- (OH-Ph-Me) -acac] 34 mg (0. 048 mmol) was obtained as a pale yellow solid. Yield 46%. Identification was performed by CHN elemental analysis and 1 H-NMR.
1H NMR (CDCl3): d 8.58 (d, J = 5.9 Hz, 2 H,
ppy), 7.84 (d, J = 7.8 Hz, 2 H, ppy), 7.73 (t, J = 6.5 Hz, 2 H, ppy), 7.55 (d,
J = 7.6 Hz, 2 H, ppy), 7.1 – 6.6 (m, 10 H, aromatic), 6.27 (d, J = 7.6 Hz, 2 H, ppy), 4.86
(br-s, 1 H, OH), 3.62 (s, 2 H, benzyl), 1.80 (s, 6 H, methyl). E.A.: Calcd
for C34H29IrN2O3:
C, 57.86; H, 4.14; N, 3.97. Found: C, 57.97; H, 4.22; N, 4.15.
1 H NMR (CDCl 3 ): d 8.58 (d, J = 5.9 Hz, 2 H,
ppy), 7.84 (d, J = 7.8 Hz, 2 H, ppy), 7.73 (t, J = 6.5 Hz, 2 H, ppy), 7.55 (d,
J = 7.6 Hz, 2 H, ppy), 7.1 – 6.6 (m, 10 H, aromatic), 6.27 (d, J = 7.6 Hz, 2 H, ppy), 4.86
(br-s, 1 H, OH), 3.62 (s, 2 H, benzyl), 1.80 (s, 6 H, methyl). EA: Calcd
for C 34 H 29 IrN 2 O 3 :
C, 57.86; H, 4.14; N, 3.97. Found: C, 57.97; H, 4.22; N, 4.15.
次いで、スキーム（８Ｂ）に示すように、このＩｒ（ｐｐｙ）2［１−（ＯＨ−Ｐｈ−Ｍｅ）−ａｃａｃ］とメタクリロイルオキシエチルイソシアネート（ＭＯＩ：商品名、昭和電工製）を反応させることによりＩｒ（ｐｐｙ）2［１−（ＭＯＩ−Ｐｈ−Ｍｅ）−ａｃａｃ］を合成した。即ち、Ｉｒ（ｐｐｙ）2［１−（ＯＨ−Ｐｈ−Ｍｅ）−ａｃａｃ］７１ｍｇ（０．１０ｍｍｏｌ）と２，６−ジ−ｔｅｒｔ−ブチル−４−メチルフェノール３ｍｇ（０．０１４ｍｍｏｌ）、ジブチル錫（ＩＶ）ジラウレート２７ｍｇ（０．１２ｍｍｏｌ）及びＭＯＩ ５５ｍｇ（０．３５ｍｍｏｌ）をＴＨＦ１０ｍｌに溶解し、７０℃で2時間加熱攪拌した。得られた反応混合物をロータリーエバポレータで減圧乾固し、残渣をヘキサン／酢酸エチルの１：１（体積比）混合溶媒を展開液とするシリカゲルカラムに通した。最初に溶出する薄黄色の副生成物の次に溶出する薄黄色の溶液を回収して減圧乾固した。得られた固体を少量のジクロロメタンに溶解し、ヘキサンを加えて生成した沈殿を濾取して減圧で乾燥することにより目的とするＩｒ（ｐｐｙ）2［３−（ＭＯＩ−Ｐｈ−Ｍｅ）−ａｃａｃ］５９ｍｇ（０．０６９ｍｍｏｌ）を薄黄色の固体として得た。収率６８％。同定はＣＨＮ元素分析、1Ｈ−ＮＭＲで行った。1H NMR
(CDCl3): d 8.58 (d, J =
5.9 Hz, 2 H, ppy), 7.88 (d, J = 7.8 Hz, 2 H, ppy), 7.76 (t, J = 6.5 Hz, 2 H,
ppy), 7.57 (d, J = 7.6 Hz, 2 H, ppy), 7.2 – 6.6 (m, 10 H, aromatic),
6.27 (d, J = 7.6 Hz, 2 H, ppy), 6.16 (s, 1 H, olefinic), 5.63 (s, 1 H,
olefinic), 5.31 (br-s, 1 H, NH), 4.31 (m, 2 H, ethylene), 3.69 (s, 2 H,
benzyl), 3.59 (m, 2 H, ethylene), 1.98 (s, 3 H, methacryl-methyl), 1.80 (s, 6
H, diketonate-methyl). E.A.: Calcd for C41H38IrN3O6:
C, 57.20; H, 4.45; N, 4.88. Found: C, 57.36; H, 4.43; N, 4.91.
Next, as shown in Scheme (8B), this Ir (ppy) 2 [1- (OH-Ph-Me) -acac] is reacted with methacryloyloxyethyl isocyanate (MOI: trade name, manufactured by Showa Denko). Ir (ppy) 2 [1- (MOI-Ph-Me) -acac] was synthesized. That is, Ir (ppy) 2 [1- (OH-Ph-Me) -acac] 71 mg (0.10 mmol), 2,6-di-tert-butyl-4-methylphenol 3 mg (0.014 mmol), dibutyltin (IV) 27 mg (0.12 mmol) of dilaurate and 55 mg (0.35 mmol) of MOI were dissolved in 10 ml of THF and heated and stirred at 70 ° C. for 2 hours. The obtained reaction mixture was dried under reduced pressure using a rotary evaporator, and the residue was passed through a silica gel column using a 1: 1 (volume ratio) mixed solvent of hexane / ethyl acetate as a developing solution. The pale yellow solution eluting after the first pale yellow by-product was collected and evaporated to dryness. The obtained solid is dissolved in a small amount of dichloromethane, hexane is added, and the resulting precipitate is collected by filtration and dried under reduced pressure to give the desired Ir (ppy) 2 [3- (MOI-Ph-Me) -acac. ] 59 mg (0.069 mmol) were obtained as a pale yellow solid. Yield 68%. Identification was performed by CHN elemental analysis and 1 H-NMR. 1 H NMR
(CDCl 3 ): d 8.58 (d, J =
5.9 Hz, 2 H, ppy), 7.88 (d, J = 7.8 Hz, 2 H, ppy), 7.76 (t, J = 6.5 Hz, 2 H,
ppy), 7.57 (d, J = 7.6 Hz, 2 H, ppy), 7.2 – 6.6 (m, 10 H, aromatic),
6.27 (d, J = 7.6 Hz, 2 H, ppy), 6.16 (s, 1 H, olefinic), 5.63 (s, 1 H,
olefinic), 5.31 (br-s, 1 H, NH), 4.31 (m, 2 H, ethylene), 3.69 (s, 2 H,
benzyl), 3.59 (m, 2 H, ethylene), 1.98 (s, 3 H, methacryl-methyl), 1.80 (s, 6
H, diketonate-methyl) .EA: Calcd for C 41 H 38 IrN 3 O 6 :
C, 57.20; H, 4.45; N, 4.88. Found: C, 57.36; H, 4.43; N, 4.91.
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