JP2011237730A - Spectacle lens - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a spectacle lens which can obtain optical transparency by using a porphyrin compound having light absorption performance.SOLUTION: The spectacle lens contains at least a kind of the porphyrin compound represented by the general formula (1).

Description

The present invention relates to a spectacle lens. More specifically, the present invention relates to a spectacle lens that can obtain light transmittance using an organic dye having light absorption performance. Furthermore, the present invention relates to a spectacle lens that is provided and used in, for example, myopia glasses, reading glasses, protective glasses, sunglasses, goggles, polarized sunglasses, polarized goggles, 3D video glasses, and 3D video goggles.

An antireflection film is formed on a spectacle lens in order to suppress a decrease in light transmittance of the lens due to reflection of visible light by the lens. Since the spectacle lens provided with these antireflection films has a high light transmittance, the brightness of light that can be recognized can be increased.
By the way, natural light emitted from the sun contains rays that are harmful to the eyes and makes the eyes feel dazzling. However, in the case of a lens with an antireflection film, diffuse reflection that causes glare is felt. Since the transmittance of light, particularly short-wavelength light that is easily diffusely reflected, is also increased, the perceived glare increases.
Moreover, since short wavelength light is high energy light, it is easy to give stress to eyes. In addition, even when there is no natural light emitted from the sun, short-wavelength light is incident on the eyes by an illuminator installed indoors, and stress is given to the eyes day and night. Furthermore, image display devices such as liquid crystal displays, plasma displays, and 3D displays have been increasing in brightness, and as the amount of light emitted from these devices has increased, the stress experienced by the eyes has continued to increase. Therefore, the problem of an increase in the number of people who complain of eye strain has arisen. The stress experienced by the eye is a serious problem particularly for elderly people whose eyes have declined due to aging, and for eye disease patients having symptoms such as cataracts and glaucoma.
As described above, there is a demand for reducing discomfort associated with glare with respect to visible light, blurring of contrast, and visual fatigue. As one of the countermeasures, there is a method of imparting an appropriate light shielding property, a so-called antiglare function, to the spectacle lens. For example, sunglasses are made for the purpose of suppressing glare by suppressing the transmittance of visible light. However, in an environment such as twilight, there may be a case where the user feels uncomfortable feeling due to dark field of view or unclearness of visual recognition of an object. That is, as a result of trying to suppress glare, the total amount of transmitted light is excessively reduced, and the visibility is unnecessarily lowered. Therefore, there is a need for a formulation that exhibits appropriate light-shielding properties while maintaining as much visibility and brightness as possible.

The prescription is to selectively shield as much as possible the wavelength band that is likely to give glare, and when the spectacle lens contains a rare earth metal compound capable of absorbing visible light in the vicinity of 585 nm in a highly wavelength selective manner. It is known that effective anti-glare properties can be obtained. The rare earth metal compound has a wavelength-selective characteristic in that the peak shape of the absorption spectrum in the absorption wavelength band in the visible light region is extremely sharp, that is, the absorption wavelength region is narrow. This characteristic has high transmittance in the wavelength band necessary for visibility, and selectively absorbs the wavelength band that adversely affects glare, so it has both anti-glare and visibility. As a dazzling spectacle lens, it has extremely desirable characteristics.
As described above, blending a rare earth metal compound, particularly a neodymium compound, for the purpose of imparting antiglare properties or contrast enhancement has been performed by a method of blending a rare earth metal compound into a glass lens (Patent Document 1). With the trend of plasticization of lens materials, recently, lenses in which specific rare earth metal compounds are blended with plastic lens materials have been developed.

However, the method of blending the rare earth metal compound with the lens material has various disadvantageous problems. For example, depending on the lens material, the selection of the rare earth metal compound is greatly limited, so that it is often limited to an expensive compound, and a compound that can be replaced with a rare earth metal compound has been desired from a practical viewpoint.
For this reason, various attempts using dyes have been disclosed for the purpose of imparting the function of selectively blocking light as much as possible in a specific wavelength band. For example, the molded lenses can be prevented by being dyed by immersing them in an aqueous dye solution. A method of imparting glare (Patent Document 2) or a method of curing by adding a cobalt compound or a specific organic dye to a monomer has been proposed (Patent Documents 3 to 5). However, the dyes used for these have an extremely wide absorption bandwidth, and in order to ensure effective anti-glare properties, the transmittance in other visible regions must be shielded more than necessary, and the visibility is greatly increased. It was a sacrifice. Further, although an anti-glare spectacle lens made of a specific organic dye having a maximum extinction coefficient near 575 nm and a relatively sharp peak width has been disclosed, there is a problem with certain restrictions when combining colors. (Patent Document 6).
Therefore, when using organic dyes, the common shortcomings or disadvantages of the past are the extremely wide absorption band, and therefore antiglare and visibility that are worthy of replacement with rare earth metals, and good color tone. An organic dye having a setting property has been desired.

In addition, in a wavelength range of 570 nm or less that easily diffuses and feels particularly dazzling, the shorter the wavelength, the light that gives stress to the human eye. Usually, a spectacle lens having a low transmittance in a wavelength region exceeding this wavelength region is required, and thus a spectacle lens having a particularly low light transmittance of a short wavelength visible ray of 570 nm or less is desired.
Porphyrin compounds are compounds that have been known for a long time, and their application to various functional materials has been proposed. For example, it has been proposed to apply a porphyrin compound to an optical recording material (Patent Document 7). Further, it has been proposed to apply a porphyrin compound to a display filter such as a plasma display (Patent Document 8). However, to date, no report has been made on the application of porphyrin compounds to spectacle lenses.

JP 2000-75128 A Japanese Patent Publication No.53-39910 Japanese Patent Laid-Open No. 5-5860 Japanese Patent Laid-Open No. 5-45610 JP-A-2-254401 Japanese Patent Laid-Open No. 2003-107412 JP-A-5-159410 JP 2004-45887 A

  The subject of this invention is providing the spectacles lens which can obtain light transmittance using the organic pigment | dye which has light absorption performance. More specifically, it is to provide a spectacle lens comprising a porphyrin compound.

As a result of intensive studies on the spectacle lens, the present inventors have completed the present invention. That is, the present invention
(I) a spectacle lens containing at least one porphyrin compound;
(Ii) The eyeglass lens according to (i), wherein the porphyrin compound is a compound represented by the general formula (1):

［式中、Ｘ１〜Ｘ８はそれぞれ独立に、水素原子、ハロゲン原子、直鎖、分岐または環状のアルキル基、直鎖、分岐または環状のアルコキシ基、置換または未置換のエテニル基、置換または未置換のエチニル基、置換または未置換のアリール基、置換または未置換のアリールオキシ基、置換または未置換のアリールオキシカルボニル基、置換または未置換のアルキルチオ基、置換または未置換のアリールチオ基、置換または未置換のアラルキル基、置換または未置換のアラルキルオキシ基、直鎖、分岐または環状のハロゲノアルキル基、直鎖、分岐または環状のハロゲノアルコキシ基、置換または未置換のアシル基、直鎖、分岐または環状のアルコキシアルキル基、直鎖、分岐または環状のアルコキシアルコキシアルキル基、置換または未置換のアリールオキシアルキル基、置換または未置換のアラルキルオキシアルキル基、あるいは直鎖、分岐または環状のハロゲノアルコキシアルキル基から選ばれる置換基であり、さらに、Ｘ１〜Ｘ８から選ばれる互いに隣接する基は互いに結合して、置換している炭素原子と共に、置換または未置換の芳香族環を形成していてもよいを表す。ただし、Ｘ１〜Ｘ８のすべてが水素原子であることはない。Ｒ１〜Ｒ４はそれぞれ独立に、置換または未置換のアリール基を表し、Ｍは２個の水素原子、２個の１価の金属原子、２価の金属原子、３価の置換金属原子、４価の置換金属原子、または酸化金属原子を表す]

[Wherein, X1 to X8 each independently represents a hydrogen atom, a halogen atom, a linear, branched or cyclic alkyl group, a linear, branched or cyclic alkoxy group, a substituted or unsubstituted ethenyl group, substituted or unsubstituted. Ethynyl group, substituted or unsubstituted aryl group, substituted or unsubstituted aryloxy group, substituted or unsubstituted aryloxycarbonyl group, substituted or unsubstituted alkylthio group, substituted or unsubstituted arylthio group, substituted or unsubstituted Substituted aralkyl group, substituted or unsubstituted aralkyloxy group, linear, branched or cyclic halogenoalkyl group, linear, branched or cyclic halogenoalkoxy group, substituted or unsubstituted acyl group, linear, branched or cyclic An alkoxyalkyl group, a linear, branched or cyclic alkoxyalkoxyalkyl group, substituted or unsubstituted Of the aryloxyalkyl group, a substituted or unsubstituted aralkyloxyalkyl group, or a linear, branched or cyclic halogenoalkoxyalkyl group, and the adjacent groups selected from X1 to X8 are It represents that it may combine to form a substituted or unsubstituted aromatic ring together with a substituted carbon atom. However, not all of X1 to X8 are hydrogen atoms. R1 to R4 each independently represents a substituted or unsubstituted aryl group, and M represents two hydrogen atoms, two monovalent metal atoms, a divalent metal atom, a trivalent substituted metal atom, and a tetravalent group. Represents a substituted metal atom or a metal oxide atom]

(Iii) In the general formula (1), X1 to X8 are each independently a halogen atom, a linear, branched or cyclic alkyl group, a linear, branched or cyclic alkoxy group, a substituted or unsubstituted ethenyl group, a substituted or An unsubstituted ethynyl group, a substituted or unsubstituted aryl group, a substituted or unsubstituted aryloxy group, a linear, branched or cyclic halogenoalkyl group, a linear, branched or cyclic halogenoalkoxy group, and X1 to X8 The groups adjacent to each other selected from the above are bonded to each other and are condensed with a substituted carbon atom together with a substituted or unsubstituted benzene ring or naphthalene ring, and R1 to R4 are substituted or unsubstituted aryl. A porphyrin compound in which M is a divalent metal atom, a trivalent substituted metal atom, a tetravalent substituted metal atom, or a metal oxide atom. A Kutomo comprising one (i) ~ (ii), wherein the spectacle lens,

(Iv) In the general formula (1), X1 to X8 are each independently a substituted or unsubstituted ethynyl group, R1 to R4 are substituted or unsubstituted phenyl groups, and M is a divalent metal atom or The spectacle lens according to (i) to (iii), comprising at least one porphyrin compound that is a metal oxide atom,

(V) In the general formula (1), groups adjacent to each other selected from X1 to X8 are substituted or unsubstituted naphthylene rings condensed at the 1st and 8th positions of the naphthalene ring, and R1 to R4 are substituted. Or an eyeglass lens according to (i) to (iii), which is an unsubstituted phenyl group and contains at least one porphyrin compound in which M is a divalent metal atom or a metal oxide atom;

[式中、Ｙ１〜Ｙ８はそれぞれ独立に、水素原子、ハロゲン原子、シアノ基、ニトロ基、直鎖、分岐または環状のアルキル基、直鎖、分岐または環状のアルコキシ基、置換または未置換のアリール基、置換または未置換のアリールオキシ基、置換または未置換のアラルキル基、置換または未置換のアラルキルオキシ基、直鎖、分岐または環状のハロゲノアルキル基、直鎖、分岐または環状のハロゲノアルコキシ基、置換または未置換のアミノ基、直鎖、分岐または環状のアルコキシアルキル基、直鎖、分岐または環状のアルコキシアルコキシアルキル基、置換または未置換のアリールオキシアルキル基、置換または未置換のアラルキルオキシアルキル基、あるいは直鎖、分岐または環状のハロゲノアルコキシアルキル基を表し、さらに、Ｙ１〜Ｙ８から選ばれる互いに隣接する基は互いに結合して、置換している炭素原子と共に、置換または未置換の炭素環式脂肪族環を形成していてもよいを表す。ただし、Ｙ１〜Ｙ８のすべてが水素原子であることはない。Ｍは２個の水素原子、２個の１価の金属原子、２価の金属原子、３価の置換金属原子、４価の置換金属原子、または酸化金属原子を表す]
(Vi) Further, the present invention relates to a spectacle lens according to (i) to (vii), which further contains a tetraazaporphyrin compound represented by the following general formula (2).

[Wherein Y1 to Y8 are each independently a hydrogen atom, a halogen atom, a cyano group, a nitro group, a linear, branched or cyclic alkyl group, a linear, branched or cyclic alkoxy group, substituted or unsubstituted aryl. Group, substituted or unsubstituted aryloxy group, substituted or unsubstituted aralkyl group, substituted or unsubstituted aralkyloxy group, linear, branched or cyclic halogenoalkyl group, linear, branched or cyclic halogenoalkoxy group, Substituted or unsubstituted amino group, linear, branched or cyclic alkoxyalkyl group, linear, branched or cyclic alkoxyalkoxyalkyl group, substituted or unsubstituted aryloxyalkyl group, substituted or unsubstituted aralkyloxyalkyl group Or a straight-chain, branched or cyclic halogenoalkoxyalkyl group, and Y1- The groups adjacent to each other selected from Y8 are bonded to each other to represent a substituted or unsubstituted carbocyclic aliphatic ring together with a substituted carbon atom. However, not all of Y1 to Y8 are hydrogen atoms. M represents two hydrogen atoms, two monovalent metal atoms, a divalent metal atom, a trivalent substituted metal atom, a tetravalent substituted metal atom, or a metal oxide atom]

According to the present invention, it is possible to provide a spectacle lens containing at least one porphyrin compound.

  Hereinafter, the present invention will be described in detail. The present invention relates to a spectacle lens containing at least one porphyrin compound (hereinafter abbreviated as a spectacle lens of the present invention). The porphyrin compound according to the present invention may have various substituents on the porphyrin skeleton, and is preferably a porphyrin compound represented by the general formula (1), for example.

［式中、Ｘ１〜Ｘ８はそれぞれ独立に、水素原子、ハロゲン原子、直鎖、分岐または環状のアルキル基、直鎖、分岐または環状のアルコキシ基、置換または未置換のエテニル基、置換または未置換のエチニル基、置換または未置換のアリール基、置換または未置換のアリールオキシ基、置換または未置換のアリールオキシカルボニル基、置換または未置換のアルキルチオ基、置換または未置換のアリールチオ基、置換または未置換のアラルキル基、置換または未置換のアラルキルオキシ基、直鎖、分岐または環状のハロゲノアルキル基、直鎖、分岐または環状のハロゲノアルコキシ基、置換または未置換のアシル基、直鎖、分岐または環状のアルコキシアルキル基、直鎖、分岐または環状のアルコキシアルコキシアルキル基、置換または未置換のアリールオキシアルキル基、置換または未置換のアラルキルオキシアルキル基、あるいは直鎖、分岐または環状のハロゲノアルコキシアルキル基から選ばれる置換基であり、さらに、Ｘ１〜Ｘ８から選ばれる互いに隣接する基は互いに結合して、置換している炭素原子と共に、置換または未置換の芳香族環を形成していてもよいを表す。ただし、Ｘ１〜Ｘ８のすべてが水素原子であることはない。Ｒ１〜Ｒ４はそれぞれ独立に、置換または未置換のアリール基を表し、Ｍは２個の水素原子、２個の１価の金属原子、２価の金属原子、３価の置換金属原子、４価の置換金属原子、または酸化金属原子を表す]

[Wherein, X1 to X8 each independently represents a hydrogen atom, a halogen atom, a linear, branched or cyclic alkyl group, a linear, branched or cyclic alkoxy group, a substituted or unsubstituted ethenyl group, substituted or unsubstituted. Ethynyl group, substituted or unsubstituted aryl group, substituted or unsubstituted aryloxy group, substituted or unsubstituted aryloxycarbonyl group, substituted or unsubstituted alkylthio group, substituted or unsubstituted arylthio group, substituted or unsubstituted Substituted aralkyl group, substituted or unsubstituted aralkyloxy group, linear, branched or cyclic halogenoalkyl group, linear, branched or cyclic halogenoalkoxy group, substituted or unsubstituted acyl group, linear, branched or cyclic An alkoxyalkyl group, a linear, branched or cyclic alkoxyalkoxyalkyl group, substituted or unsubstituted Of the aryloxyalkyl group, a substituted or unsubstituted aralkyloxyalkyl group, or a linear, branched or cyclic halogenoalkoxyalkyl group, and the adjacent groups selected from X1 to X8 are It represents that it may combine to form a substituted or unsubstituted aromatic ring together with a substituted carbon atom. However, not all of X1 to X8 are hydrogen atoms. R1 to R4 each independently represents a substituted or unsubstituted aryl group, and M represents two hydrogen atoms, two monovalent metal atoms, a divalent metal atom, a trivalent substituted metal atom, and a tetravalent group. Represents a substituted metal atom or a metal oxide atom]

  In the porphyrin compound represented by the general formula (1), X1 to X8 are each independently a halogen atom, a linear, branched or cyclic alkyl group, a linear, branched or cyclic alkoxy group, substituted or unsubstituted. An ethenyl group, a substituted or unsubstituted ethynyl group, a substituted or unsubstituted aryl group, a substituted or unsubstituted aryloxy group, a linear, branched or cyclic halogenoalkyl group, a linear, branched or cyclic halogenoalkoxy group, Further, groups adjacent to each other selected from X1 to X8 are bonded to each other and condensed with a substituted or unsubstituted benzene ring or naphthalene ring together with a substituted carbon atom, and R1 to R4 are substituted. Or an unsubstituted aryl group, and M is a divalent metal atom, a trivalent substituted metal atom, a tetravalent substituted metal atom, or a metal oxide atom. It is preferred.

  In the present specification, the aryl group represents, for example, a carbocyclic aromatic group such as a phenyl group or a naphthyl group, for example, a heterocyclic aromatic group such as a furyl group, a thienyl group or a pyridyl group, Represents a carbocyclic aromatic group.

Although the substituent of the porphyrin compound which concerns on this invention is not specifically limited, It illustrates concretely below.
In the porphyrin compound represented by the general formula (1), preferably, X1 to X8 are each independently a hydrogen atom or a halogen atom, such as a fluorine atom, a chlorine atom, or a bromine atom,
Examples of linear, branched or cyclic alkyl groups include, for example, methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, isobutyl group, tert-butyl group, n-pentyl group, isopentyl group, neopentyl group. Group, tert-pentyl group, 1,2-dimethylpropyl group, 1-methylbutyl group, 2-methylbutyl group, n-hexyl group, 2-methylpentyl group, 4-methylpentyl group, 4-methyl-2-pentyl group 1,2-dimethylbutyl group, 2,3-dimethylbutyl group, 2-ethylbutyl group, n-heptyl group, 3-methylhexyl group, 5-methylhexyl group, 2,4-dimethylpentyl group, cyclohexylmethyl group N-octyl group, tert-octyl group, 2-ethylhexyl group, 2-propylpentyl group, 2,5-dimethylhexyl Group, 2,5,5-trimethylhexyl group, 2,2-dimethylheptyl group, 2,6-dimethyl-4-heptyl group, 3,5,5-trimethylhexyl group, n-decyl group, 4-ethyloctyl Group, n-undecyl group, 1-methyldecyl group, n-dodecyl group, 1,3,5,7-tetramethyloctyl group, n-tridecyl group, 1-hexylheptyl group, n-pentadecyl group, n-hexadecyl group , N-heptadecyl group, n-octadecyl group, n-eicosyl group, cyclopentyl group, cyclohexyl group, 4-methylcyclohexyl group, 4-tert-butylcyclohexyl group, cycloheptyl group, cyclooctyl group, etc. A linear, branched or cyclic alkyl group of

  Examples of linear, branched or cyclic alkoxy groups include, for example, methoxy group, ethoxy group, n-propoxy group, isopropoxy group, n-butoxy group, sec-butoxy group, n-pentyloxy group, cyclopentyloxy group, n -Hexyloxy group, 3,3-dimethylbutyloxy group, 2-ethylbutyloxy group, cyclohexyloxy group, n-heptyloxy group, n-octyloxy group, 2-ethylhexyloxy group, n-nonyloxy group, n- Undecyloxy group, n-dodecyloxy group, n-tridecyloxy group, n-tetradecyloxy group, n-pentadecyloxy group, n-hexadecyloxy group, n-heptadecyloxy group, n-octadecyloxy group Straight chain having 1 to 24 carbon atoms such as a group, n-tricosyloxy group, n-tetracosyloxy group, Toki or cyclic alkoxy group,

Examples of the substituted or unsubstituted ethenyl group include those having a linear, branched or cyclic alkyl group having 1 to 24 carbon atoms as a substituent at the 2,2 ′ position of ethenyl,
Examples of the substituted or unsubstituted ethynyl group include those having a linear, branched or cyclic alkyl group having 1 to 24 carbon atoms as a substituent at the 2-position of ethynyl,

  Examples of the substituted or unsubstituted aryl group include a phenyl group, 2-methylphenyl group, 4-methylphenyl group, 3-ethylphenyl group, 4-n-propylphenyl group, 4-n-butylphenyl group, 4 -Isobutylphenyl group, 4-tert-butylphenyl group, 4-n-pentylphenyl group, 4-tert-pentylphenyl group, 4-n-hexylphenyl group, 4-cyclohexylphenyl group, 4-n-octylphenyl group 4-n-nonylphenyl group, 4-n-decylphenyl group, 4-n-dodecylphenyl group, 4-n-tetradecylphenyl group, 4-n-octadecylphenyl group, 2,5-dimethylphenyl group 3,4-dimethylphenyl group, 3,4,5-trimethylphenyl group, 5-indanyl group, 1,2,3,4-tetrahydro 6-naphthyl group, 2-methoxyphenyl group, 3-methoxyphenyl group, 4-ethoxyphenyl group, 4-n-propoxyphenyl group, 4-isopropoxyphenyl group, 4-n-butoxyphenyl group, 4-n- Pentyloxyphenyl group, 4-cyclohexyloxyphenyl group, 4-n-heptyloxyphenyl group, 4-n-octyloxyphenyl group, 4-n-decyloxyphenyl group, 4-n-undecyloxyphenyl group, 4 -N-tetradecyloxyphenyl group, 4-n-hexadecyloxyphenyl group, 2,3-dimethoxyphenyl group, 2,4-dimethoxyphenyl group, 3,5-diethoxyphenyl group, 2-methoxy-4- Methylphenyl group, 2-methyl-4-methoxyphenyl group, 2-fluorophenyl group, 4-fluorophenyl 2-chlorophenyl group, 4-bromophenyl group, 4-trifluoromethylphenyl group, 3-trifluoromethylphenyl group, 2,4-difluorophenyl group, 2,4-dichlorophenyl group, 2-methyl-4-chlorophenyl Group, 2-chloro-4-methoxyphenyl group, 3-fluoro-4-methoxyphenyl group, 2-phenylphenyl group, 3,5-diphenylphenyl group, 1-naphthyl group, 2-naphthyl group, 4-methyl- 1-naphthyl group, 4-ethoxy-1-naphthyl group, 6-n-butyl-2-naphthyl group, 2-furyl group, 2-pyridyl group, 3-pyridyl group, 4-pyridyl group, 4-aminophenyl group 3-aminophenyl group, 2-aminophenyl group, 2- (Nn-butylamino) phenyl group, 4- (N, N-dimethylamino) phenyl group, 4- (N-cyclohexyl-N-methylamino) phenyl group, 4- (N, N-diethylamino) -1-naphthyl group, 4-pyrrolidinophenyl group, 4-piperidinophenyl group, 4-morpholinophenyl Group, 4-pyrrolidino-1-naphthyl group, 4- (N-methyl-N-phenylamino) phenyl group, 4- [N, N-di (4′-methylphenyl) amino] phenyl group, 4- [N , N-di (4′-ethoxyphenyl) amino] phenyl group, 4- [N, N-di (4′-n-hexyloxyphenyl) amino] phenyl group, 4- [N-phenyl-N- (1 A substituted or unsubstituted aryl group having 4 to 30 carbon atoms, such as' -naphthyl) amino] phenyl group and 4- (N-phenoxadiyl) phenyl group;

Examples of the substituted or unsubstituted aryloxy group include a phenyloxy group, a 2-methylphenyloxy group, a 4-methylphenyloxy group, a 4-ethylphenyloxy group, a 4-isopropylphenyloxy group, and a 4-isobutylphenyloxy group. Group, 4-n-pentylphenyloxy group, 4-tert-pentylphenyloxy group, 4-cyclohexylphenyloxy group, 4-n-octylphenyloxy group, 4-n-decylphenyloxy group, 4-n-dodecyl Phenyloxy group, 4-n-hexadecylphenyloxy group, 2,3-dimethylphenyloxy group, 2,5-dimethylphenyloxy group, 3,4-dimethylphenyloxy group, 3,4,5-trimethylphenyloxy Group, 5-indanyloxy group, 1,2,3,4-tetrahydro-6 Naphthyloxy group, 3-methoxyphenyloxy group, 3-ethoxyphenyloxy group, 4-n-propoxyphenyloxy group, 4-n-butoxyphenyloxy group, 4-n-pentyloxyphenyloxy group, 4-cyclohexyloxy Phenyloxy group, 4-n-octyloxyphenyloxy group, 4-n-decyloxyphenyloxy group, 4-n-dodecyloxyphenyloxy group, 4-n-hexadecyloxyphenyloxy group, 2,3-dimethoxy Phenyloxy group, 2,5-dimethoxyphenyloxy group, 3,5-dimethoxyphenyloxy group, 2-methoxy-4-methylphenyloxy group, 3-methoxy-4-methylphenyloxy group, 3-methyl-4- Methoxyphenyloxy group, 2-fluorophenyloxy group, 4-fur Rophenyloxy group, 3-chlorophenyloxy group, 4-bromophenyloxy group, 3-trifluoromethylphenyloxy group, 3,5-difluorophenyloxy group, 3,4-dichlorophenyloxy group, 2-methyl-4- Chlorophenyloxy group, 3-chloro-4-methylphenyloxy group, 3-methoxy-4-fluorophenyloxy group, 3-fluoro-4-methoxyphenyloxy group, 4-phenylphenyloxy group, 3-phenylphenyloxy group 4- (4′-methylphenyl) phenyloxy group, 4- (4′-methoxyphenyl) phenyloxy group, 1-naphthyloxy group, 4-methyl-1-naphthyloxy group, 6-n-butyl-2 -Naphthyloxy group, 7-ethoxy-2-naphthyloxy group, 2-thienyloxy group, 2-pyridylo group A substituted or unsubstituted aryloxy group having 4 to 30 carbon atoms, such as a xyl group and a 4-pyridyloxy group;
Examples of the substituted or unsubstituted aryloxycarbonyl group include phenoxycarbonyl group, 2-methylphenoxycarbonyl group, 4-methylphenoxycarbonyl group, xylyloxycarbonyl group, chlorophenoxycarbonyl group, 4-tert-butylphenoxycarbonyl. A substituted or unsubstituted aryloxycarbonyl group having 7 to 11 carbon atoms such as a group, 2-methoxyphenoxycarbonyl group, 4-isopropylphenoxycarbonyl group, naphthoxycarbonyl group,

The substituted or unsubstituted alkylthio group is an alkylthio group which may have a substituent similar to the alkyl group listed above, and examples thereof include a methylthio group, an ethylthio group, an n-propylthio group, an isopropylthio group, an n -Butylthio group, isobutylthio group, sec-butylthio group, tert-butylthio group, n-pentylthio group, isopentylthio group, neopentylthio group, 2-methylbutylthio group, methylcarboxylethylthio group, 2-ethylhexylthio A substituted or unsubstituted alkylthio group having 1 to 10 carbon atoms such as a group, 3,5,5-trimethylhexylthio group, decalylthio group, etc.
The substituted or unsubstituted arylthio group is an arylthio group which may have the same substituent as the above-mentioned aryl group, for example, a phenylthio group, a 4-methylphenylthio group, a 2-methoxyphenylthio group. A substituted or unsubstituted arylthio group having 6 to 10 carbon atoms, such as 4-tert-butylphenylthio group, naphthylthio group, ferrocenylthio group,

  Examples of the substituted or unsubstituted aralkyl group include benzyl group, α-methylbenzyl group, α, α-dimethylbenzyl group, α-phenylbenzyl group, α, α-diphenylbenzyl group, phenethyl group, α-methylphenethyl group. Group, α, α-dimethylphenethyl group, 4-methylphenethyl group, 4-methylbenzyl group, 2-methylbenzyl group, 4-ethylbenzyl group, 4-isopropylbenzyl group, 4-tert-butylbenzyl group, 4- tert-pentylbenzyl group, 4-cyclohexylbenzyl group, 4-n-octylbenzyl group, 4-phenylbenzyl group, 4- (4'-tert-butylphenyl) benzyl group, 4-methoxybenzyl group, 3-methoxybenzyl Group, 2-ethoxybenzyl group, 4-n-butoxybenzyl group, 3,4-dimethoxybenzyl Substituted, unsubstituted aralkyl having 5 to 30 carbon atoms such as a group, 4-fluorobenzyl group, 2-fluorobenzyl group, 4-chlorobenzyl group, 2-chlorobenzyl group, 2-furfuryl group, 1-naphthylmethyl group, etc. Group,

  Examples of the substituted or unsubstituted aralkyloxy group include benzyloxy group, α-methylbenzyloxy group, α-ethylbenzyloxy group, α, α-dimethylbenzyloxy group, α-phenylbenzyloxy group, α, α -Diphenylbenzyloxy group, phenethyloxy group, α-methylphenethyloxy group, β-methylphenethyloxy group, α, α-dimethylphenethyloxy group, 4-methylphenethyloxy group, 4-methylbenzyloxy group, 2-methyl Benzyloxy group, 4-ethylbenzyloxy group, 2-ethylbenzyloxy group, 4-tert-butylbenzyloxy group, 2-tert-butylbenzyloxy group, 4-tert-pentylbenzyloxy group, 4-cyclohexylbenzyloxy Group, 4-n-octylbenzyloxy group, 4 -Phenylbenzyloxy group, 4- (4'-methylphenyl) benzyloxy group, 4- (4'-tert-butylphenyl) benzyloxy group, 4-methoxybenzyloxy group, 2-ethoxybenzyloxy group, 4- n-heptyloxybenzyloxy group, 3,4-dimethoxybenzyloxy group, 4-fluorobenzyloxy group, 3-chlorobenzyloxy group, 3,4-dichlorobenzyloxy group, 2-furfuryloxy group, 2-naphthyl A substituted or unsubstituted aralkyloxy group having 5 to 30 carbon atoms, such as a methyloxy group;

Examples of the linear, branched or cyclic halogenoalkyl group include, for example, a fluoromethyl group, a 3-fluoropropyl group, a 6-fluorohexyl group, an 8-fluorooctyl group, a trifluoromethyl group, and 1,1-dihydro-perfluoro. Ethyl group, 1,1-dihydro-perfluoro-n-propyl group, 2-hydro-perfluoro-2-propyl group, 1,1-dihydro-perfluoro-n-butyl group, 6-fluorohexyl group, 4 -Fluorocyclohexyl group, 1,1-dihydro-perfluoro-n-octyl group, 1,1-dihydro-perfluoro-n-decyl group, 1,1-dihydro-perfluoro-n-dodecyl group, 1,1 -Dihydro-perfluoro-n-hexadecyl group, perfluoroethyl group, perfluoro-n-pentyl group, perfluoro-n-he Straight chain having 1 to 24 carbon atoms such as syl group, 2,2-bis (trifluoromethyl) propyl group, dichloromethyl group, 3-chloropropyl group, 7-chloroheptyl group, 2,2,2-trichloroethyl group, etc. Chain, branched or cyclic halogenoalkyl groups,
Examples of the linear, branched or cyclic halogenoalkoxy group include, for example, a fluoromethyloxy group, a 3-fluoropropyloxy group, a 6-fluorohexyloxy group, a trifluoromethyloxy group, and 1,1-dihydro-perfluoro-n. -Propyloxy group, 1,1,3-trihydro-perfluoro-n-propyloxy group, 2-hydro-perfluoro-2-propyloxy group, 1,1-dihydro-perfluoro-n-butyloxy group, , 1-dihydro-perfluoro-n-hexyloxy group, 4-fluorocyclohexyloxy group, 1,1-dihydro-perfluoro-n-octyloxy group, 1,1-dihydro-perfluoro-n-dodecyloxy group 1,1-dihydro-perfluoro-n-tetradecyloxy group, 1,1-dihydro-perf Oro-n-hexadecyloxy group, perfluoroethyloxy group, perfluoro-n-pentyloxy group, perfluoro-n-hexyloxy group, dichloromethyloxy group, 2-chloroethyloxy group, 4-chlorocyclohexyloxy A straight-chain, branched or cyclic halogenoalkoxy group having 1 to 24 carbon atoms such as a group, 2,2,2-trichloroethyloxy group,

  Examples of the substituted or unsubstituted acyl group include formyl group, acetyl group, ethylcarbonyl group, n-propylcarbonyl group, n-butylcarbonyl group, isobutylcarbonyl group, tert-butylcarbonyl group, n-pentylcarbonyl group, Substitution having 1 to 15 carbon atoms such as isopentylcarbonyl group, 2-methylbutylcarbonyl group, phenacyl group, propylphenacyl group, tert-butylphenacyl group, nitrobenzylcarbonyl group, 3-butoxy-2-naphthoyl group, cinnamoyl group Or an unsubstituted acyl group,

Examples of linear, branched or cyclic alkoxyalkyl groups include methoxymethyl group, ethoxymethyl group, n-butoxymethyl group, n-pentyloxymethyl group, n-hexyloxymethyl group, (2-ethylbutyloxy) Methyl group, n-heptyloxymethyl group, n-octyloxymethyl group, n-dodecyloxymethyl group, 2-methoxyethyl group, 2-ethoxyethyl group, 2-isopropoxyethyl group, 2-n-butoxyethyl group 2-n-hexyloxyethyl group, 2-n-heptyloxyethyl group, 2-n-octyloxyethyl group, 2-n-dodecyloxyethyl group, 2-n-tetradecyloxyethyl group, 2-cyclohexyl Oxyethyl group, 2-methoxypropyl group, 3-methoxypropyl group, 3-ethoxypropyl group, 3- Sopropoxypropyl group, 3-n-butoxypropyl group, 3-n-pentyloxypropyl group, 3- (2′-ethylbutoxy) propyl group, 3-n-octyloxypropyl group, 3-n-decyloxypropyl group Group, 3-cyclohexyloxypropyl group, 4-methoxybutyl group, 4-ethoxybutyl group, 4-n-propoxybutyl group, 4-isopropoxybutyl group, 4-n-butoxybutyl group, 4-n-octyloxy Butyl group, 4-n-decyloxybutyl group, 4-n-dodecyloxybutyl group, 5-methoxypentyl group, 5-ethoxypentyl group, 5-n-pentyloxypentyl group, 6-methoxyhexyl group, 6- Ethoxyhexyl group, 6-n-butoxyhexyl group, 6-n-hexyloxyhexyl group, 6-n-decyloxyhexyl Group, 4-methoxycyclohexyl group, 7-ethoxyheptyl group, 8-methoxyoctyl group, 9-methoxynonyl group, 10-methoxydecyl group, 10-n-butoxydecyl group, 12-methoxydodecyl group, 12-isopropoxy group A linear, branched or cyclic alkoxyalkyl group having 2 to 24 carbon atoms such as a dodecyl group and a tetrahydrofurfuryl group;
Examples of linear, branched or cyclic alkoxyalkoxyalkyl groups include (2-methoxyethoxy) methyl group, (2-ethoxyethoxy) methyl group, (2-n-butyloxyethoxy) methyl group, and (3-methoxy). Propyloxy) methyl group, (3-ethoxypropyloxy) methyl group, (3-n-pentyloxypropyloxy) methyl group, (6-methoxyhexyloxy) methyl group, (10-ethoxydecyloxy) methyl group, 2 -(2'-ethoxyethoxy) ethyl group, 3- (2'-ethoxyethoxy) propyl group, 3- (2'-methoxypropyloxy) propyl group, 3- (3'-methoxypropyloxy) propyl group, etc. A linear, branched or cyclic alkoxyalkoxyalkyl group having 3 to 24 carbon atoms,

  Examples of the substituted or unsubstituted aryloxyalkyl group include phenyloxymethyl group, 4-methylphenyloxymethyl group, 4-ethylphenyloxymethyl group, 4-n-butylphenyloxymethyl group, 4-n-hexyl. Phenyloxymethyl group, 4-n-decylphenyloxymethyl group, 4-methoxyphenyloxymethyl group, 4-butoxyphenyloxymethyl group, 4-n-pentyloxyphenyloxymethyl group, 4-fluorophenyloxymethyl group, 2-fluorophenyloxymethyl group, 3,4-difluorophenyloxymethyl group, 4-chlorophenyloxymethyl group, 4-phenylphenyloxymethyl group, 2-naphthyloxymethyl group, 2-furyloxymethyl group, 1-phenyl Oxyethyl group, 2- (4′-me Ruphenyloxy) ethyl group, 2- (4′-ethylphenyloxy) ethyl group, 2- (4′-methoxyphenyloxy) ethyl group, 2- (4′-n-butoxyphenyloxy) ethyl group, 2- (4′-fluorophenyloxy) ethyl group, 2- (4′-bromophenyloxy) ethyl group, 2- (1′-naphthyloxy) ethyl group, 2-phenyloxypropyl group, 3-phenyloxypropyl group, 3- (4′-methylphenyloxy) propyl group, 4-phenyloxybutyl group, 4- (2′-ethylphenyloxy) butyl group, 4-phenyloxypentyl group, 5- (4′-tert-butylphenyl) Oxy) pentyl group, 6-phenyloxyhexyl group, 8-phenyloxyoctyl group, 10- (3′-methylphenyloxy) decyl group Any substituted or unsubstituted aryloxy group having a carbon number of 5-30,

  Examples of the substituted or unsubstituted aralkyloxyalkyl group include benzyloxymethyl group, phenethyloxymethyl group, 4-methylbenzyloxymethyl group, 4-n-propylbenzyloxymethyl group, 4-n-octylbenzyloxymethyl group. Group, 4-methoxybenzyloxymethyl group, 4-n-butoxybenzyloxymethyl group, 4-fluorobenzyloxymethyl group, 3-fluorobenzyloxymethyl group, 4-chlorobenzyloxymethyl group, 2-benzyloxyethyl group 2-phenethyloxyethyl group, 2- (4′-methylbenzyloxy) ethyl group, 2- (4′-fluorobenzyloxy) ethyl group, 2- (4′-chlorobenzyloxy) ethyl group, 3- ( 4'-methoxybenzyloxy) propyl group, 4-benzyloxy Butyl group, 4- (4'-phenyl benzyloxy) butyl group, 6-benzyl substituted or unsubstituted aralkyloxy group having 6 to 30 carbon atoms such as oxy hexyl group,

  Alternatively, the linear, branched or cyclic halogenoalkoxyalkyl group includes, for example, a fluoromethyloxymethyl group, a 3-fluoro-n-propyloxymethyl group, a trifluoromethyloxymethyl group, and 1,1-dihydro-perfluoroethyl. Oxymethyl group, 1,1-dihydro-perfluoro-n-propyloxymethyl group, 2-hydro-perfluoro-2-propyloxymethyl group, 1,1-dihydro-perfluoro-n-butyloxymethyl group, 1,1-dihydro-perfluoro-n-hexyloxymethyl group, 1,1-dihydro-perfluoro-n-octyloxymethyl group, 1,1-dihydro-perfluoro-n-tetradecyloxymethyl group, 2 , 2-bis (trifluoromethyl) propyloxymethyl group, 2- (8-fluoro n-octyloxy) ethyl group, 2- (1,1,3-trihydro-perfluoro-n-propyloxy) ethyl group, 2- (6-fluoro-n-hexyloxy) ethyl group, 2- (1, 1-dihydro-perfluoro-n-octyloxy) ethyl group, 3- (1,1-dihydro-perfluoroethyloxy) propyl group, 4- (perfluoro-n-hexyloxy) butyl group, 6- (2 And a straight-chain, branched or cyclic halogenoalkoxyalkyl group having 2 to 24 carbon atoms such as (chloroethyloxy) hexyl group.

In the general formula (1), X1 to X8 are more preferably a fluorine atom, a chlorine atom, a bromine atom, a straight chain having 1 to 16 carbon atoms, a branched or cyclic alkyl group, a straight chain having 1 to 16 carbon atoms, A branched or cyclic alkoxy group, an ethenyl group having a linear, branched or cyclic alkyl group having 1 to 12 carbon atoms as a substituent, and a linear, branched or cyclic alkyl group having 1 to 12 carbon atoms as a substituent An ethynyl group, a substituted or unsubstituted aryl group having 6 to 24 carbon atoms, a substituted or unsubstituted aryloxy group having 6 to 24 carbon atoms, a linear, branched or cyclic halogenoalkyl group having 1 to 16 carbon atoms, or A linear, branched or cyclic halogenoalkoxy group having 1 to 16 carbon atoms is represented.
In the general formula (1), X1 to X8 are more preferably a fluorine atom, a bromine atom, a linear, branched or cyclic alkyl group having 1 to 10 carbon atoms, a linear, branched or cyclic group having 1 to 10 carbon atoms. An ethenyl group having a linear, branched or cyclic alkyl group having 1 to 10 carbon atoms as a substituent, an ethynyl group having a linear, branched or cyclic alkyl group having 1 to 10 carbon atoms as a substituent, A substituted or unsubstituted aryl group having 6 to 16 carbon atoms, a substituted or unsubstituted aryloxy group having 6 to 16 carbon atoms, a linear, branched or cyclic halogenoalkyl group having 1 to 10 carbon atoms, or 1 carbon atom Represents 10 to 10 linear, branched or cyclic halogenoalkoxy groups.

Further, groups adjacent to each other selected from X1 to X8 may be bonded to each other to form a substituted or unsubstituted aromatic ring together with the substituted carbon atom, and preferably selected from X1 to X8 The adjacent groups are bonded to each other, and a substituted or unsubstituted benzene ring or naphthalene ring is condensed together with a substituted carbon atom. The substituent is a chlorine atom, a fluorine atom, or a carbon number of 1 to 10. A linear, branched or cyclic alkyl group, and a linear, branched or cyclic alkoxy group having 1 to 10 carbon atoms. More preferably, groups adjacent to each other selected from X1 to X8 are bonded to each other to form 2- or 3-position, 1-position and 2-position, or 1-position and 8-position of a substituted or unsubstituted benzene ring or naphthalene ring. The substituent of the condensed phenylene ring is a linear, branched or cyclic alkyl group having 1 to 8 carbon atoms, or a linear, branched or cyclic alkoxy group having 1 to 8 carbon atoms. The substituent of the condensed naphthylene ring is a chlorine atom, a fluorine atom, or a linear, branched or cyclic alkyl group having 1 to 8 carbon atoms. More preferably, groups adjacent to each other selected from X1 to X8 are bonded to each other and fused together with the substituted carbon atom at either the 2-position and 3-position or the 1-position and 8-position of the naphthalene ring, The substituent of the condensed naphthylene ring is a chlorine atom, a fluorine atom, or a linear, branched or cyclic alkyl group having 1 to 6 carbon atoms.
In the porphyrin compound represented by the general formula (1), preferably, R1 to R4 are each independently a substituted or unsubstituted aryl group, and the substituted aryl group includes X1 to X1 in the general formula (1). The aryl group which may have the same substituent as the aryl group mentioned by X8 is mentioned.
In the general formula (1), more preferably, R1 to R4 represent a substituted or unsubstituted aryl group having 6 to 24 carbon atoms, and more preferably a substituted or unsubstituted aryl group having 6 to 16 carbon atoms. To express.

In the porphyrin compound represented by the general formula (1), M is two hydrogen atoms, two monovalent metal atoms, a divalent metal atom, a trivalent substituted metal atom, and a tetravalent substituted metal atom. Or a metal oxide atom, more preferably a divalent metal atom, a trivalent substituted metal atom, a tetravalent substituted metal atom or an oxidized metal atom, and more preferably a divalent metal atom or an oxidized metal atom. It is a metal atom.
Examples of the monovalent metal atom represented by M include Na, K, and Li.
Examples of the divalent metal atom represented by M include Cu, Zn, Fe, Co, Ni, Ru, Pd, Pt, Mn, Mg, Ti, Ba, Cd, Hg, Pb, and Sn. Can do.
Examples of the trivalent substituted metal atom represented by M include Al-F, Al-Cl, Al-Br, Al-I, Ga-Cl, In-F, In-Cl, In-I, and Tl-. _{F, Tl-Cl, Al-} C 6 H 5, Al-C 6 H 4 (CH 3), In-C 6 H 5, In-C 6 H 4 (CH 3), Mn (OH), Mn (OC ₆ H ₅₎
, Mn [OSi (CH ₃ ) ₃ ], Fe—Cl, Ru—Cl, and the like.
The tetravalent substituted metal atom represented by M, for _{example, CrCl 2, SiCl 2, SiF} 2, SiI 2, ZrCl 2, ZrI 2, GeBr 2, GeF 2, SnCl 2, SnF 2, TiCl 2, TiBr ₂ , TiF ₂ , Si (OH) ₂ , Zr (OH) ₂ , Mn (OH) ₂ , Sn (OH) ₂ , Cr (Z 1) ₂ , Si (Z 1) ₂ , Sn (Z 1) ₂ Z1 represents an alkyl group, a phenyl group, a naphthyl group, or a derivative thereof], Si (OZ2) ₂ , Sn (OZ2) ₂ , Ti (OZ2) ₂ , Cr (OZ2) ₂ [wherein Z2 represents an alkyl group] group, a phenyl group, a naphthyl group, a trialkylsilyl group, a dialkyl alkoxy silyl group, or a derivative _{thereof], Sn (SZ3) 2, Ge} (SZ3) 2 wherein, Z3 is a Kill group, a phenyl group, a naphthyl group, or the like can be given represent] a derivative thereof. Examples of the metal oxide atom represented by M include VO, MnO, TiO and the like.
In the general formula (1), M is more preferably Cu, Zn, Fe, Co, Ni, Pd, Mn, Mg, Mn (OH), Mn (OH) ₂ , VO, TiO, and more preferably Cu, Ni, Pd, and VO.
More preferable specific examples of the porphyrin compound according to the present invention include compounds represented by the general formula (3) and the general formula (4), but the present invention is not limited thereto. .

［式中、Ｘ１〜Ｘ８はそれぞれ独立に、置換または未置換のエチニル基を表し、置換基を有するエチニル基として、炭素数１〜１０の直鎖、分岐または環状のアルキル基を置換基とするエチニル基、Ｍは２価の金属原子または酸化金属原子を表す]

[Wherein, X1 to X8 each independently represents a substituted or unsubstituted ethynyl group, and the ethynyl group having a substituent is a linear, branched or cyclic alkyl group having 1 to 10 carbon atoms. An ethynyl group, M represents a divalent metal atom or a metal oxide atom]

［式中、Ｑ１〜Ｑ２４はそれぞれ独立に、水素原子、炭素数１〜６の直鎖または分岐のアルキル基を表し、Ｒ１〜Ｒ４はそれぞれ独立に、置換または未置換のアリール基を表し、置換基を有するアリール基として、炭素数１〜１０の直鎖、分岐または環状のアルキル基もしくはアルコキシ基を置換基とするフェニル基、Ｍは２価の金属原子または酸化金属原子を表す]

[Wherein, Q1 to Q24 each independently represents a hydrogen atom or a linear or branched alkyl group having 1 to 6 carbon atoms; R1 to R4 each independently represents a substituted or unsubstituted aryl group; As the aryl group having a group, a phenyl group substituted with a linear, branched or cyclic alkyl group or alkoxy group having 1 to 10 carbon atoms, M represents a divalent metal atom or a metal oxide atom]

  The porphyrin compound according to the present invention can be produced by referring to a method known per se. That is, the compound represented by the general formula (1) includes, for example, the compounds represented by the general formula (5-1) to the general formula (5-4) and the general formula (6-1) to the general formula (6- 4) The compound represented by 4) is subjected to dehydration condensation reaction and oxidation (for example, 2,3-dichloro-5,6-dicyano-) with an acid catalyst (for example, propionic acid, boron trifluoride / ethyl ether complex, trifluoroacetic acid). 1,4-benzoquinone), which is synthesized by a so-called Rothermount reaction, and can be produced by reacting a metal or a metal salt (for example, acetylacetone complex, metal acetate) in an appropriate solvent, if desired [for example, J. et al. Am. Chem. Soc. 61, 2921 (1939), J. Am. Org. Chem. , 32, 476 (1967), Ann. , 745, 135 (1971), J.A. Am. Chem. Soc. , 118, 8767 (1996)].

〔式中、Ｘ１〜Ｘ８、及びＲ１〜Ｒ４は一般式(１)の場合と同じ意味を表す〕
又、例えば、メソ−テトラフェニルポルフィリン化合物のピロール部の３，４位をハロゲン化し、次いで置換することで所望の一般式（１）で表される化合物法を製造することができる。
なお、本明細書においては、一般式（１）で表されるポルフィリン化合物は、実際には、１種または２種以上の異性体から成る混合物を表している。このような複数の異性体から成る混合物の構造の記載に際しても、本明細書においては、便宜上、例えば、一般式（１）で表される一つの構造式を記載しているものである。

[Wherein, X1 to X8 and R1 to R4 represent the same meaning as in the general formula (1)]
For example, the compound method represented by the desired general formula (1) can be produced by halogenating the pyrrole part of the meso-tetraphenylporphyrin compound at positions 3 and 4 and then substituting it.
In the present specification, the porphyrin compound represented by the general formula (1) actually represents a mixture composed of one or more isomers. In describing the structure of such a mixture of a plurality of isomers, in this specification, for example, one structural formula represented by the general formula (1) is described for convenience.

  In the spectacle lens of the present invention, the porphyrin compound according to the present invention may be used alone or in combination. Furthermore, a mixture of one or more isomers can be used. Further, if desired, each isomer can be separated from the mixture, and one of the isomers can be used, and a plurality of isomers having an arbitrary ratio can be used in combination. The porphyrin compound according to the present invention includes not only crystals but also amorphous (amorphous).

  Considering the required characteristics of the spectacle lens of the present invention, the porphyrin compound according to the present invention preferably absorbs in the wavelength region between 440 and 570 nm among the compounds represented by the general formula (1). A compound having a maximum wavelength, specifically, an absorption spectrum measured at a concentration of 0.01 g / L toluene solution at an optical path length of 10 mm, and a half-value width of an absorption peak of 10 nm or more and less than 40 nm, more preferably 15 nm or more and less than 35 nm More preferably, among the compounds represented by the general formula (3), among the compounds represented by the general formula (4), compounds having an absorption maximum wavelength in a wavelength region between 440 to 510 nm, A compound having an absorption maximum wavelength in a wavelength region between 520 to 570 nm can be used for the spectacle lens of the present invention.

In this specification, the half width is the full width at half maximum, and in the absorption spectrum, a straight line parallel to the horizontal axis and the peak drawn with a value half of the extinction coefficient value (εg) at the absorption maximum wavelength. Expressed by the distance (nm) between two intersections formed by.
Since the porphyrin compound according to the present invention has an absorption peak half width of 10 nm or more and less than 40 nm, more preferably 15 nm or more and less than 35 nm, a plurality of dyes are combined while maintaining selective light absorption characteristics in the visible light wavelength region. In other words, when the lens material has various color tones, the light absorption factor in the wavelength range other than the selective light wavelength range is as small as possible. It is easy to obtain a color tone with a wider range and less dullness.

Furthermore, since it has an absorption maximum in a wavelength region between 440 and 510 nm, which is highly phototoxic to the retina, it is effective for cataract accompanying aging.
This is due to the fact that a small number of small protein fragments appear in the lens as it ages, and it becomes turbid. The same applies if you feel dazzling when you look at the light during the day or under a brighter light source than before.
As a cause of this, there has been a report that retinal photoinjury caused by light having a short wavelength of 400 to 500 nm induces age-related cataracts. It is said that the main component AE2 of lipofuscin is highly sensitive to short wavelength light, and free radicals generated by absorption of short wavelength light cause cell death of RPE.
Thus, the porphyrin compound according to the present invention has an absorption maximum in a wavelength region between 440 and 510 nm, which is a wavelength region in which retinal photoinjury is likely to be induced. .

It is also effective as a spectacle lens that can partially cut off visible light in the wavelength region between 440 and 510 nm. Can be reduced.
In the spectacle lens according to the present invention, if necessary, the porphyrin compound according to the present invention and a light absorbing compound can be used in combination. Examples of the light absorbing compound include compounds having desired absorption in the visible light region in consideration of further antiglare property and contrast enhancement for the effects of the present invention.
For example, a tetraazaporphyrin compound represented by the general formula (2) can be given.

[式中、Ｙ１〜Ｙ８はそれぞれ独立に、水素原子、ハロゲン原子、シアノ基、ニトロ基、直鎖、分岐または環状のアルキル基、直鎖、分岐または環状のアルコキシ基、置換または未置換のアリール基、置換または未置換のアリールオキシ基、置換または未置換のアラルキル基、置換または未置換のアラルキルオキシ基、直鎖、分岐または環状のハロゲノアルキル基、直鎖、分岐または環状のハロゲノアルコキシ基、置換または未置換のアミノ基、直鎖、分岐または環状のアルコキシアルキル基、直鎖、分岐または環状のアルコキシアルコキシアルキル基、置換または未置換のアリールオキシアルキル基、置換または未置換のアラルキルオキシアルキル基、あるいは直鎖、分岐または環状のハロゲノアルコキシアルキル基を表し、さらに、Ｙ１〜Ｙ８から選ばれる互いに隣接する基は互いに結合して、置換している炭素原子と共に、置換または未置換の炭素環式脂肪族環を形成していてもよいを表す。ただし、Ｘ１〜Ｘ８のすべてが水素原子であることはない。Ｍは２個の水素原子、２個の１価の金属原子、２価の金属原子、３価の置換金属原子、４価の置換金属原子、または酸化金属原子を表す]

[Wherein Y1 to Y8 are each independently a hydrogen atom, a halogen atom, a cyano group, a nitro group, a linear, branched or cyclic alkyl group, a linear, branched or cyclic alkoxy group, substituted or unsubstituted aryl. Group, substituted or unsubstituted aryloxy group, substituted or unsubstituted aralkyl group, substituted or unsubstituted aralkyloxy group, linear, branched or cyclic halogenoalkyl group, linear, branched or cyclic halogenoalkoxy group, Substituted or unsubstituted amino group, linear, branched or cyclic alkoxyalkyl group, linear, branched or cyclic alkoxyalkoxyalkyl group, substituted or unsubstituted aryloxyalkyl group, substituted or unsubstituted aralkyloxyalkyl group Or a straight-chain, branched or cyclic halogenoalkoxyalkyl group, and Y1- The groups adjacent to each other selected from Y8 are bonded to each other to represent a substituted or unsubstituted carbocyclic aliphatic ring together with a substituted carbon atom. However, not all of X1 to X8 are hydrogen atoms. M represents two hydrogen atoms, two monovalent metal atoms, a divalent metal atom, a trivalent substituted metal atom, a tetravalent substituted metal atom, or a metal oxide atom]

Although the substituent of the tetraazaporphyrin compound which concerns on this invention is not specifically limited, It illustrates concretely below.
In the tetraazaporphyrin compound represented by the general formula (2), preferably, Y1 to Y8 are each independently a hydrogen atom, a cyano group, a nitro group, or a halogen atom, such as a fluorine atom, a chlorine atom, or a bromine atom. Linear, branched or cyclic alkyl group, linear, branched or cyclic alkoxy group, substituted or unsubstituted aryl group, substituted or unsubstituted aryloxy group, substituted or unsubstituted aralkyl group, substituted or Unsubstituted aralkyloxy group, linear, branched or cyclic halogenoalkyl group, linear, branched or cyclic halogenoalkoxy group, substituted or unsubstituted amino group, linear, branched or cyclic alkoxyalkyl group, linear Branched or cyclic alkoxyalkoxyalkyl groups, substituted or unsubstituted aryloxyalkyl groups, substituted or unsubstituted As the unsubstituted aralkyloxy group or a linear, branched or cyclic halogenoalkoxy group, include the same substituents as X1~X8 in Formula (1),

  Examples of the substituted or unsubstituted amino group include an amino group, N-methylamino group, N-ethylamino group, N-cyclohexylamino group, Nn-octylamino group, N-benzylamino group, N- ( 3-methylphenyl) amino group, N- (4-methoxyphenyl) amino group, N- (3-fluorophenyl) amino group, N- (4-chlorophenyl) amino group, N- (2-naphthyl) amino group, N, N-dimethylamino group, N, N-di-n-butylamino group, N, N-di-n-decylamino group, N-methyl-N-ethylamino group, N-ethyl-Nn-butyl Amino group, N-methyl-N-phenylamino group, Nn-butyl-N-phenylamino group, N-benzyl-N-phenylamino group, N, N-di (3-methylphenyl) amino group, N , N-di 4-ethylphenyl) amino group, N, N-di (4-tert-butylphenyl) amino group, N, N-di (4-methoxyphenyl) amino group, N, N-di (4-ethoxyphenyl) amino Group, N, N-di (4-n-hexyloxyphenyl) amino group, N, N-di (2-naphthyl) amino group, N-phenyl-N- (4-methylphenyl) amino group, N-phenyl -N- (4-methoxyphenyl) amino group, N-phenyl-N- (4-n-hexyloxyphenyl) amino group, N-phenyl-N- (1-naphthyl) amino group, N-phenyl-N- A substituted or unsubstituted amino group having 1 to 30 carbon atoms such as (2-naphthyl) amino group, N-phenyl-N- (4-phenylphenyl) amino group, N-phenoxadiyl group, and N-phenothiadiyl group; Raising It is possible.

  In the general formula (2), more preferably, Y1 to Y8 are a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom, a cyano group, a linear, branched or cyclic alkyl group having 1 to 16 carbon atoms, and 1 carbon atom. -16 linear, branched or cyclic alkoxy group, substituted or unsubstituted aryl group having 4 to 24 carbon atoms, linear, branched or cyclic halogenoalkyl group having 1 to 16 carbon atoms, 1 to 16 carbon atoms Linear, branched or cyclic halogenoalkoxy group, linear, branched or cyclic alkoxyalkyl group having 2 to 16 carbon atoms, linear, branched or cyclic alkoxyalkoxyalkyl group having 3 to 16 carbon atoms, carbon number 5 to 5 24 substituted or unsubstituted aryloxyalkyl groups, substituted or unsubstituted aralkyloxyalkyl groups having 6 to 24 carbon atoms, or linear, branched or cyclic groups having 2 to 16 carbon atoms It represents a halogenoalkoxy group.

In the general formula (2), more preferably, Y1 to Y8 are a hydrogen atom, a chlorine atom, a fluorine atom, a cyano group, a linear, branched or cyclic alkyl group having 1 to 10 carbon atoms, or a carbon atom having 1 to 10 carbon atoms. A straight, branched or cyclic alkoxy group, a substituted or unsubstituted aryl group having 6 to 16 carbon atoms, a straight chain having 1 to 10 carbon atoms, a branched or cyclic halogenoalkoxy group, or a straight chain having 2 to 10 carbon atoms Represents a branched or cyclic alkoxyalkyl group. Further, groups adjacent to each other selected from Y1 to Y8 may be bonded to each other to form a substituted or unsubstituted carbocyclic aliphatic ring together with a substituted carbon atom, preferably total carbon A substituted or unsubstituted carbocyclic aliphatic ring having 4 to 20 carbon atoms may be formed, and more preferably a substituted or unsubstituted carbocyclic aliphatic ring having 6 to 10 carbon atoms in total is formed. And more preferably a cyclopentane ring or a cyclohexane ring may be formed. In the general formula (2), M is the same as M in the general formula (1), more preferably Cu, Zn. Fe, Co, Ni, Pd, Mn, Mg, VO and TiO, and more preferably Cu, Pd and VO.
Specific examples of the tetraazaporphyrin compound according to the present invention include, for example, compounds represented by the general formula (7), but the present invention is not limited thereto.

［式中、Ｙ１、Ｙ３、Ｙ５、Ｙ７はそれぞれ独立に水素原子を表し、Ｙ２、Ｙ４、Ｙ６、Ｙ８はそれぞれ炭素数１〜６の直鎖、分岐または環状のアルキル基を表し、Ｍは２価の金属原子または酸化金属原子を表す]
本発明に係るテトラアザポルフィリン化合物は、それ自体公知の方法を参考にして製造することができる。すなわち、一般式（２）で表される化合物は、例えば、一般式（８−１）〜一般式（８−４）で表される化合物と、金属あるいは金属塩（例えば、ハロゲン化金属、カルボン酸金属）とを、所望により塩基（例えば、モリブデン酸アンモニウム、１，８−ジアザビシクロ［５．４．０］−７−ウンデセン、１，５−ジアザビシクロ［４．３．０］−５−ノネン、トリアルキルアミン、アンモニア）の存在下で反応させることにより製造することができる〔例えば、米国特許２８５０５０５号、英国特許６８９３８７号、英国特許７６３０８５号、Ｊ．Ｇｅｎ．Ｃｈｅｍ．ＵＳＳＲ，４７、１９５４（１９７７）、Ｊ．Ｏｒｇ．Ｃｈｅｍ．ＵＳＳＲ，１５、９６２（１９７９）、Ｊ．Ｏｒｇ．Ｃｈｅｍ．ＵＳＳＲ，２８、１７２３（１９９２）、Ｃｈｅｍ．Ｈｅｔｅｒｏｃｙｃｌｉｃ Ｃｏｍｐ．，１８、１２６９（１９８２）、Ｓｙｎｔｈｅｓｉｓ，６８７（１９９１）、特開平１１−１１０１５号公報、特開平１１−４３６１９号公報、特開平１１−１００５２０号公報、特開平１１−１１６５７４号公報、特開平１１−１３０９７１号公報、特開２００２−１２９０５２号公報、特開２００６−３２１９２５号公報に記載の方法に従って製造することができる〕。

[Wherein Y1, Y3, Y5 and Y7 each independently represent a hydrogen atom, Y2, Y4, Y6 and Y8 each represent a linear, branched or cyclic alkyl group having 1 to 6 carbon atoms, and M is 2 Represents a valent metal atom or a metal oxide atom]
The tetraazaporphyrin compound according to the present invention can be produced with reference to a method known per se. That is, the compound represented by the general formula (2) includes, for example, a compound represented by the general formula (8-1) to the general formula (8-4), a metal or a metal salt (for example, a metal halide, a carboxyl Acid metal) and optionally a base (eg, ammonium molybdate, 1,8-diazabicyclo [5.4.0] -7-undecene, 1,5-diazabicyclo [4.3.0] -5-nonene, (E.g., U.S. Pat. No. 2,850,505, British Patent No. 689387, British Patent No. 763085, J. Pat. Gen. Chem. USSR, 47, 1954 (1977), J. MoI. Org. Chem. USSR, 15, 962 (1979), J. MoI. Org. Chem. USSR, 28, 1723 (1992), Chem. Heterocyclic Comp. 18, 1269 (1982), Synthesis, 687 (1991), Japanese Patent Application Laid-Open No. 11-11015, Japanese Patent Application Laid-Open No. 11-43619, Japanese Patent Application Laid-Open No. 11-1000052, Japanese Patent Application Laid-Open No. 11-116574, and Japanese Patent Application Laid-Open No. 11-116574. -130971, JP-A No. 2002-129052 and JP-A No. 2006-321925].

なお、本明細書においては、一般式（２）で表されるテトラアザポルフィリン化合物は、実際には、１種または２種以上の異性体から成る混合物を表している。このような複数の異性体から成る混合物の構造の記載に際しても、本明細書においては、便宜上、例えば、一般式（２）で表される一つの構造式を記載しているものである。
本発明の眼鏡レンズにおいては、本発明に係るテトラアザポルフィリン化合物は、１種を単独で使用してもよく、あるいは複数を併用してもよい。さらに、１種または２種以上の異性体から成る混合物を使用することができる。また、所望により、該混合物から各異性体を分離し、異性体の内の１種の化合物を用いることができ、さらには、任意の割合から成る複数の異性体を併用することができる。尚、本発明に係るテトラアザポルフィリン化合物とは、結晶は勿論であるが、無定型（アモルファス体）をも包含するものである。
要求される本発明の眼鏡レンズの特性を考慮し、本発明に係るテトラアザポルフィリン化合物としては、好ましくは、一般式（２）で表される化合物の中で、より好ましくは、５８０〜６０５ｎｍに吸収極大を有する化合物が、本発明の眼鏡レンズに使用することができる。

In the present specification, the tetraazaporphyrin compound represented by the general formula (2) actually represents a mixture composed of one or more isomers. In describing the structure of such a mixture composed of a plurality of isomers, in this specification, for example, one structural formula represented by the general formula (2) is described for convenience.
In the spectacle lens of the present invention, the tetraazaporphyrin compound according to the present invention may be used alone or in combination. Furthermore, a mixture of one or more isomers can be used. Further, if desired, each isomer can be separated from the mixture, and one of the isomers can be used, and a plurality of isomers having an arbitrary ratio can be used in combination. The tetraazaporphyrin compound according to the present invention includes not only crystals but also amorphous (amorphous).
Considering the required characteristics of the spectacle lens of the present invention, the tetraazaporphyrin compound according to the present invention is preferably a compound represented by the general formula (2), more preferably 580 to 605 nm. A compound having an absorption maximum can be used in the spectacle lens of the present invention.

The spectacle lens of the present invention comprises a compound in a substrate, and the compound contains at least one porphyrin compound represented by the general formula (1). The tetraazaporphyrin compound represented may be contained (hereinafter abbreviated as a compound according to the present invention). In addition, it contains in the base material as used in the field of this invention, of course, the state apply | coated to the surface of a base material, the state pinched | interposed between the base materials, etc. .
The substrate may be either a glass lens or a plastic lens. Since plastic is lighter than glass, is hard to break and has high safety, plastic lenses are particularly frequently used. The plastic lens base material may be either a thermoplastic resin or a thermosetting resin, and is not particularly limited. However, the plastic lens base material has a high light transmittance and can be molded, for example, a (meth) acrylic resin or a styrene resin. , Polycarbonate resin, allyl resin, allyl carbonate resin such as diethylene glycol bisallyl carbonate resin (CR-39), vinyl resin, polyester resin, polyether resin, polyurethane obtained by polymerization reaction of isocyanate compound and hydroxy compound such as diethylene glycol Resin, polythiourethane resin obtained by polymerization reaction of isocyanate compound and polythiol compound, transparent resin obtained by curing polymerizable composition containing (thio) epoxy compound having one or more disulfide bonds in the molecule, etc. It can be exemplified.
Preferably, a polycarbonate resin, a polyurethane resin, a polythiourethane resin, or a polyamide resin can be used.

Polycarbonate resin is a typical polymer that is obtained by the phosgene method in which dihydroxydiaryl compounds and phosgene are reacted as a main method, or the ester exchange method in which dihydroxydiaryl compounds are reacted with carbonic esters such as diphenyl carbonate. And polycarbonate resin produced from 2,2-bis (4-hydroxyphenyl) propane (bisphenol A).
The viscosity average molecular weight of the polycarbonate resin is usually 10,000 to 100,000, preferably 10,000 to 400,000.
A typical example of the polythiourethane resin is a polythiourethane resin produced from metaxylylene diisocyanate and pentaerythritol tetrakis (3-mercaptopropionate).

The polyamide resin is a resin having a dehydration polycondensate structure of a diamine compound containing an aromatic or aliphatic group and a dicarboxylic acid compound containing an aromatic or aliphatic group. Here, the aliphatic group also includes an alicyclic aliphatic group. The resin having the structure of the dehydration polycondensate of the diamine compounds and dicarboxylic acid compounds is not necessarily limited to those obtained from the dehydration polycondensation reaction. For example, ring opening of one or more lactam compounds It can also be obtained from polymerization or the like.
In particular, an amorphous polyamide resin is preferable from the viewpoint of transparency, and is generally referred to as transparent nylon. For example, Emamide's Grillamide TR-55, Grillamide TR-90, Grillamide TR-XE3805, or Hulus's Trogamide CX -7233 etc. can be illustrated.
These may be used alone or in combination. For example, a thermoplastic resin in which a polyamide resin is mixed with 30 to 0.5 parts by weight, preferably 20 to 1 part by weight, more preferably 15 to 2 parts by weight, with 100 parts by weight of a polycarbonate resin can be used.

  The compound according to the present invention contains at least one porphyrin compound represented by the general formula (1) and may contain a tetraazaporphyrin compound represented by the general formula (2). The porphyrin compound represented by the general formula (1) has an oil-soluble property, and has a maximum absorption peak between 440 nm and 570 nm in a visible light absorption spectrum measured with a chloroform or toluene solution, The absorption coefficient of the maximum absorption peak is 0.5 × 10 5 (ml / g · cm) or more, the half width is 80 nm or less, and the tetraazaporphyrin compound represented by the general formula (2) is oil-soluble. And has a maximum absorption peak between 580 nm and 605 nm in a visible light absorption spectrum measured with a chloroform or toluene solution, and the absorption coefficient of the maximum absorption peak is 0.5 × 10 5 (ml / g · Cm) or more and the half width is 80 nm or less.

The spectacle lens will be specifically described below.
The spectacle lens of the present invention can be manufactured by a conventional method according to the material of the lens.
For example, in the case of a glass lens, it can be produced by forming a film containing the compound according to the present invention on a lens molded into a predetermined shape. The film formation can be performed by a conventional coating method. For example, as a method for coating the lens surface, a method in which the compound according to the present invention is dissolved in a binder resin and an organic solvent to form a paint can be mentioned. .
As binder resins, aliphatic ester resins, acrylic resins, melamine resins, urethane resins, aromatic ester resins, polycarbonate resins, aliphatic polyolefin resins, aromatic polyolefin resins, polyvinyl resins, polyvinyl alcohol resins, polyvinyl resins. Examples thereof include system-modified resins (PVB, EVA, etc.) or copolymer resins thereof.
Examples of the solvent include halogen-based, alcohol-based, ketone-based, ester-based, aliphatic hydrocarbon-based, aromatic hydrocarbon-based, ether-based solvents, and mixtures thereof.
The concentration of the compound according to the present invention varies depending on the absorption coefficient, coating thickness, target absorption strength, target visible light transmittance, etc., but is usually 0.1 ppm to 30% by weight with respect to the weight of the binder resin. is there. The resin concentration is usually 1 to 50% by weight with respect to the whole paint. The coating material produced by the above method can form a film on a glass lens by a coating method such as a bar coder, a blade coater, a spin coater, a reverse coater, a die coater, or a spray. The film may be formed of a plurality of layers including an infrared absorber.

In carrying out the present invention, for example, in the case of a plastic lens whose base material is a thermosetting resin, a method of polymerizing and curing a monomer that usually forms a target polymer is included. Examples include, but are not limited to, curing of diethylene glycol diallyl carbonate monomer, diallyl phthalate monomer, mixtures of isocyanate compounds and polyols and polythiols, and monomers used in the manufacture of corrective lenses such as acrylic monomers. Things. The polymerization method is not particularly limited, but usually cast polymerization is employed. At that time, the compound according to the present invention is blended in the thermosetting resin compound, and the resin compound is supplied to a lens casting mold to perform a polymerization reaction and to mold into a spectacle lens. A method of supplying the lens casting mold to the lens casting mold is not particularly limited. For example, a method of injecting the resin compound by passing it through a thin tube is used. The resin blend may be defoamed in advance by a method such as decompression, or cast polymerization may be performed in a state where air environmental factors are substantially eliminated.
The lens casting mold in the present invention is generally composed of two molds held by a gasket. A mold release agent may be applied to the mold in order to improve the releasability of the obtained lens. Further, a coating liquid for imparting hard coating performance to the lens material may be applied to the mold.
The method for adding the compound according to the present invention to the thermosetting resin composition will be specifically described below. The thermosetting resin composition used for polymerization and curing is roughly composed of a monomer mixture, a compound according to the present invention, a catalyst, and other additives.

Additives include catalysts such as dibutyltin dichloride, UV absorbers, internal mold release agents such as acidic phosphate esters, light stabilizers, antioxidants, reaction initiators such as radical initiators, chain extenders, and crosslinking Known resin modifiers for adjusting or improving the physical properties such as refractive index, Abbe number, heat resistance, specific gravity, and mechanical strength such as impact resistance, etc. Examples thereof include hydroxy compounds, thiol compounds, epoxy compounds, episulfide compounds, organic acids and anhydrides thereof, and olefin compounds including (meth) acrylate compounds.
If the component to be mixed in mixing the compound according to the present invention is liquid at 0 ° C. or higher, the selection is not particularly limited, and it is appropriately selected in consideration of operability, safety, convenience and the like. For example, a method in which the monomer mixture is mixed with one of the monomer groups constituting the monomer mixture and then the monomer mixture is mixed, a method in which the monomer mixture and other additives are mixed, and then a catalyst is added, or the monomer mixture, catalyst, and The method of mixing with the mixture which consists of another additive is mentioned.

In mixing the compound according to the present invention, the compound according to the present invention is directly mixed, or the compound according to the present invention is dissolved in an organic solvent having a low boiling point in advance, and the organic solvent solution is used as the component to be mixed. After mixing, the organic solvent may be removed by evaporation under conditions such as heating and / or reduced pressure. Examples of the organic solvent used in this case include hexane, heptane, acetone, methyl ethyl ketone, benzene, toluene, dichloromethane, chloroform, etc., but are chemically inert to the resin composition and have a moderately low boiling point. If it is a thing, it will not specifically limit.
In addition, the resin composition may be mixed so that an amount corresponding to the concentration of the compound according to the present invention required for the plastic lens is contained, and any of the monomer mixture and the resin composition may be used. Prepare a master batch containing the compound according to the present invention in a concentration higher than the target concentration in any of the components, add other components to be blended as necessary, and dilute to obtain the target concentration according to the present invention. Examples of the method include a compound.
Further, in dissolving the compound according to the present invention, it can be heated within a range where there is no problem in practice in terms of deterioration of the resin composition and pot life. In mixing the compound according to the present invention, for example, usual methods such as stirring, shaking and bubbling can be mentioned. Furthermore, it is often preferable to carry out defoaming treatment under reduced pressure, filtration treatment under pressure, reduced pressure, or the like after the dissolution of the compound according to the present invention, if necessary.

Next, for example, in the case of a plastic lens whose base material is a thermoplastic resin, generally known methods such as a compression molding method, a transfer molding method, an injection molding method, and a compression injection molding method are employed. That is, the thermoplastic resin to be supplied is heated to a melting temperature or higher, introduced into a mold having the shape of a target plastic lens, and then cooled and solidified to obtain a plastic lens. At this time, a so-called insert method in which a plastic film having a target function such as a polarizing film is set in a mold in advance and the functional plastic film is integrated in the plastic lens molded by the above method is also the present invention. It does not exceed the range.
In that case, the compound which concerns on this invention is previously mix | blended with a thermoplastic resin. Although there is no restriction | limiting in particular as a compounding method, For example, the compound which concerns on this invention, and a thermoplastic resin pellet are mixed mechanically below the melting temperature of a pellet, and the compound which concerns on this invention is hold | maintained on this pellet surface As another method, using a suitable kneader, the compound according to the present invention and the thermoplastic resin pellet are kneaded at a temperature equal to or higher than the melting temperature of the pellet to convert the compound according to the present invention into the thermoplastic resin pellet. It can be included.
In supplying the thermoplastic resin to the molding machine, a drying process may be performed in advance under known conditions as necessary in order to reduce the amount of water contained in the thermoplastic resin.

The concentration of the compound according to the present invention relative to the thermosetting resin is in the range of 0.0002 to 0.05% by weight, preferably 0.0002 to 0.01% by weight, more preferably 0.0004 to 0.01% by weight. Yes, the setting of the compounding amount of the compound according to the present invention for the thermosetting resin composition for setting this concentration is easily experimentally based on the fact that it is usually approximately the same as the target concentration for the plastic lens. Can be determined.
The compound according to the present invention is preferably localized in a range of 500 μm or less from at least one surface of the thermosetting or thermoplastic lens.
The method for incorporating the compound according to the present invention into the thermoplastic resin composition will be specifically described below. The concentration of the compound according to the present invention with respect to the thermoplastic resin is 0.0002 to 0.05% by weight, preferably 0.0002 to 0.01% by weight, more preferably 0.0004 to 0.01% by weight. The setting of the compounding amount of the compound according to the present invention with respect to the thermoplastic resin composition to make the concentration can be easily determined based on the fact that it is usually approximately the same as the target concentration for the plastic lens.

Further, an amount corresponding to the concentration of the compound according to the present invention required for the thermoplastic resin may be blended in the thermoplastic resin supplied by the above method, and the present invention is required. The compound according to the present invention at the target concentration is finally contained in the plastic lens. A so-called master batch method that is set as described above can also be adopted. At that time, the compound-free thermoplastic resin according to the present invention may be supplied in combination for the purpose of dilution. Alternatively, the thermoplastic resin mixed in the predetermined amount may be mixed in advance by a method such as melt kneading, and may be supplied to a molding machine after prescription such as pelletization as necessary.
In addition, in the thermosetting or thermoplastic plastic lens of the present invention, the present invention is applied to at least one component layer constituting a single layer or a multi-layer stack applied as a lens member on at least one surface of the plastic lens as necessary. The compound which concerns on this can be made into the plastic lens which has the target wavelength-selective light absorptivity.
In forming a single layer or a multilayer laminate on at least one surface of the thermosetting or thermoplastic plastic lens, it can be formed by attaching a sheet layer, but usually an organic compound containing the compound according to the present invention. It is formed by applying a resin coating agent.

Examples of the organic resin coating agent include (meth) acrylic resin, polyester resin, polyether resin, polyurethane resin, silicone resin, melamine resin, or the like. Alternatively, a copolymerized resin or the like may be used. As the resin, either a thermoplastic type or a thermosetting type is adopted depending on the purpose.
In application to the plastic lens, the resin is dissolved in a solvent-free or normally in a solvent to obtain a coating solution. Solvents include water, ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone, cyclohexanone, diacetone alcohol, isophorone, esters such as methyl acetate, ethyl acetate, butyl acetate, isobutyl acetate, amyl acetate, ethylene glycol monomethyl ether , Alcohols / esters such as ethylene glycol monoethyl ether and ethylene glycol monobutyl ether, alcohols such as methyl alcohol, ethyl alcohol, isopropyl alcohol, n-butyl alcohol, isobutyl alcohol, amyl alcohol, 2-ethylhexyl alcohol, dibutyl ether, Ethers such as tetrahydrofuran, aromatic hydrocarbons such as benzene, toluene, xylene, n-hexane, n-hept Aliphatic such as down, can alicyclic compounds, such as is illustrated, such as cyclohexane, solvent obtained by mixing two or more solvents selected from these may be used. The selection of these solvents is determined from the viewpoint according to the purpose, such as the solubility of the resin component, the degree of reactivity with the resin component, the boiling point, environmental harmony, and price.
Application of the coating solution to the plastic lens can be performed by a commonly used method such as a dipping method, a spray method, a spin coating method, a dip spin coating method, or a roll coating method. If necessary, the surface of the lens wafer to be coated can be previously subjected to plasma treatment, corona discharge treatment, ultraviolet irradiation treatment, chemical treatment with a silane coupling agent, sodium hydroxide, or the like. In the coating solution, a leveling agent such as silicone or fluorine can be used in combination as required.
When the organic resin coating agent is a thermoplastic resin, a thermoplastic resin component layer containing the compound according to the present invention can be obtained by evaporating and drying the solvent after coating.

In the case where the organic resin coating agent is a thermosetting resin system, after application, the solvent is evaporated and dried, and then the compound according to the present invention is contained by a curing reaction using means such as heat, ultraviolet light, and electron beam. A thermosetting resin component layer can be obtained. Solvent drying conditions and curing reaction conditions can be applied simultaneously.
The thickness of the formed component layer is 0.05 to 100 μm, preferably 0.1 to 50 μm, more preferably 0.5 to 30 μm, and particularly preferably 0.5 to 10 μm. The concentration of the compound according to the present invention contained in the component layer is 0.02 to 5% by weight, preferably 0.05 to 3% by weight.
The compound according to the present invention may be contained only in the plastic lens, or may be contained only in the hard coat layer, primer layer, or other component layer formed on one or both surfaces of the plastic lens. When there are a plurality of component layers, at least one of them may contain the compound according to the present invention. Moreover, you may make the compound which concerns on this invention contain in both a plastic lens and a component layer.
As the primer layer, an aqueous acrylic-urethane resin or polyester-based thermoplastic elastomer that can improve the impact resistance of the plastic lens, is excellent in water resistance and light resistance, and has excellent adhesion to the hard coat layer described later. preferable.
The formation of the component layer containing the compound according to the present invention will be described below with specific examples. In a frequently practiced form, a primer layer is formed on at least one surface of the thermosetting or thermoplastic lens, and a hard coat is applied to the surface to impart mechanical properties such as scratch resistance to the lens material surface. Is done. Furthermore, if necessary, a predetermined inorganic multilayer film is applied to the surface of the hard coat layer to impart antireflection performance. The primer layer not only contributes to the adhesion between the lens surface and the hard coat layer, but the main purpose is to reduce the impact resistance degradation of the lens itself caused by the hard coat and antireflection layer being applied through the buffering action of stress. It can be improved.

The compound according to the present invention can be contained in the hard coat layer or primer layer to exhibit the selective light-shielding property required in the present invention. As the primer layer, a known method, for example, block type polyisocyanate and polyol are blended so that the equivalent ratio of isocyanate and hydroxyl group is about 0.8 to 1.25, diluted with a solvent, and a trace amount of tin-based catalyst and leveling are mixed. The compound according to the present invention is added to the solution to which the agent is added at 0.5 to 2% by weight with respect to the resin component to obtain a primer solution. For example, both surfaces of a thiourethane thermosetting resin lens are used with the primer solution. After dipping, the polyurethane primer layer containing the compound according to the present invention can be formed by thermally curing the solvent after evaporation and drying at about 120 to 140 ° C.
In the formation of the primer layer, a polyurethane-based primer layer not containing the compound according to the present invention can be formed, and a hard coat layer containing the compound according to the present invention can be formed thereon. Known hard coat agents can be used.
50-200 Angstrom average such as colloidal silicon oxide, colloidal aluminum oxide, colloidal antimony oxide, colloidal zirconium oxide, colloidal tungsten oxide, colloidal titanium oxide, colloidal zinc oxide, colloidal tin oxide, etc. Co-hydrolyzing a compound containing inorganic oxide particles having a particle diameter or a metal compound having no functional group such as an alkoxy metal compound having no functional group and a silane compound having a functional group such as an epoxy group or a methacryl group Examples thereof include a composition mainly composed of decomposed components. Examples of the silane compound having a functional group include γ-glycidoxypropyltrimethoxysilane, γ-glycidoxypropyl-methyl-diethoxysilane, and γ-methacryloyloxypropyltrimethoxysilane. In addition to the components exemplified above, the hard coat agent can be used as a hard coat solution by being diluted with a solvent substantially inert with the components exemplified above as necessary.

  The hard coat liquid is applied on the primer-coated surface of at least one surface of a plastic lens, and is usually cured by heating at 60 to 140 ° C., preferably 70 to 130 ° C. At that time, if necessary, a catalyst such as an inorganic acid may be contained in the hard coat solution. The curing reaction can also be performed by irradiating light such as ultraviolet rays. In that case, it is more preferable that the surface of the colloidal inorganic oxide surface is modified with a vinyl group-containing organic group such as a (meth) acryl group, or combined with a photoinitiator. The thickness of the hard coat layer after curing is 1 to 10 μm, preferably 2 to 5 μm.

Thus, for example, the compound according to the present invention is added in advance to the hard coat solution in an amount of 0.5 to 2% by weight with respect to the resin content, and a leveling agent is further added to prepare a dye-containing hard coat solution. The thermosetting resin lens having a primer layer on both sides is dipped on both sides with the dye-containing hard coat solution, evaporated to dryness, and then cured at 120 ° C. for 3 hours, for example, via a polyurethane primer layer. Thus, a plastic lens having a hard coat layer containing the compound according to the present invention is obtained.
The compound-containing plastic lens according to the present invention may be subjected to functional treatments that are possible within the conventional technical range, such as multi-coating (antireflection layer), antifogging treatment, water repellent treatment, or antistatic treatment, if necessary. Good. Further, by using a spectacle lens, a myopia lens or a presbyopia lens can be obtained. By using the spectacle lens of the present invention as a presbyopia lens, it can be suitably used as protective glasses for the elderly with weak eyes.

EXAMPLES Hereinafter, although an Example demonstrates this invention further in detail, this invention is not limited to these.
In all examples, synthesis examples, and comparative examples, the absorption spectrum was measured using a U-3500 type self-recording spectrophotometer manufactured by Hitachi, Ltd. with a toluene solution and a chloroform solution having a concentration of 0.01 g / L as measuring instruments. And an optical path length of 10 mm.

(Synthesis Example 1)
A compound represented by the following formula (1-1) was synthesized according to the method described in Example 1 of International Publication WO2006 / 046497. Table 1 shows the maximum absorption wavelength (λmax), gram extinction coefficient (εg), and solubility of the absorption spectrum of this compound.

(Synthesis Example 2)
In Synthesis Example 1, the same operation as in Synthesis Example 1 was performed except that copper acetate was used instead of p-pentoxybenzaldehyde and nickel acetate instead of p-decyloxybenzaldehyde, and the following formula (1-2) The compound represented by this was synthesized. Table 1 shows the maximum absorption wavelength (λmax), gram extinction coefficient (εg), and solubility of the absorption spectrum of this compound.

(Synthesis Example 3)
In Synthesis Example 1, the same procedure as in Synthesis Example 1 was carried out except that p-hexyloxybenzaldehyde and copper acetate were used instead of p-decyloxybenzaldehyde, and the following formula (1-3) The compound represented by this was synthesized. Table 1 shows the maximum absorption wavelength (λmax), gram extinction coefficient (εg), and solubility of the absorption spectrum of this compound.

(Synthesis Example 4)
A compound represented by the following formula (1-4) was synthesized according to the method described in Example 1 of JP-A-2008-239592. Table 1 shows the maximum absorption wavelength (λmax), gram extinction coefficient (εg), and solubility of the absorption spectrum of this compound.

(Synthesis Example 5)
A compound represented by the following formula (1-5) was synthesized according to the method described in Example 2 of JP-A-2008-239592. Table 1 shows the maximum absorption wavelength (λmax), gram extinction coefficient (εg), and solubility of the absorption spectrum of this compound.

Table 1 shows the measurement results of absorption maximum wavelength (λmax), gram extinction coefficient (εg), and solubility of the compounds synthesized in Synthesis Examples 1 to 5 together with these compounds. Here, λmax and εg are values in a chloroform solution, and the solubility is wt% with respect to each solvent.
(Note) Solubility ○: Completely dissolved ×: Undissolved

(Synthesis Example 6)
A tetra (tert-butyl) tetraazaporphyrin vanadyl complex (2-1) was synthesized according to the method described in Example 2 of JP-A-2006-321925. Table 2 shows the absorption maximum wavelength (λmax), Gram extinction coefficient (εg), and half-value width in the absorption spectrum of this compound.

(Synthesis Example 7)
A tetra (tert-butyl) tetraazaporphyrin copper complex (2-2) was synthesized according to the method described in Example 3 of JP-A-2006-321925. Table 2 shows the absorption maximum wavelength (λmax), Gram extinction coefficient (εg), and half-value width in the absorption spectrum of this compound.

Example 1
In a 500 mL separable flask equipped with a thermometer, a stirrer, and a nitrogen seal tube, 200 parts of polyoxytetramethylene glycol (Hodogaya Chemical Industry: PTG-1000N) with an average molecular weight of 1014 is taken and stirred in a nitrogen stream. The mixture was heated and dehydrated for 1 hour under a reduced pressure of 100 to 110 ° C./3 to 5 mmHg. After dehydration, 170 parts of 4,4′-methylene-bis (cyclohexyl isocyanate) (manufactured by Sumitomo Bayer Urethane: Desmodur W) was added and reacted at 120 to 130 ° C. for 2 hours to produce a prepolymer. The obtained prepolymer was a colorless transparent liquid, and had an NCO content of 9.9%, a viscosity of 8600 mPa · s / 30 ° C., and 750 mPa · s / 60 ° C.
After heating 100 parts by weight of the obtained prepolymer to 70 ° C., 0.10 parts by weight of the compound (1-4) shown in Table 1 prepared in Synthesis Example 4 was added and mixed, and then melted at 120 ° C. The mixture was defoamed and mixed with 31.4 parts by weight of 4,4′-methylene-bis (2-chloroaniline). This mixture was poured into a mold preheated at 100 ° C. and heat-cured at 100 ° C. for 24 hours to produce a spectacle lens having a lens thickness of about 2.6 mm.
In the observation through the obtained lens, for example, the lines of the twigs of trees under clear weather and the contrast of red, yellow and green looked very clear.

(Example 2)
In Example 1, in place of the compound (1-4) described in Table 1 manufactured in Synthesis Example 4, 0.10 parts by weight of the compound (1-5) described in Table 1 manufactured in Synthesis Example 5 was added. A lens mixture for use in lens casting was prepared in the same manner as in Example 1 except that it was cast, and further cast, and a spectacle lens was obtained in the same manner as in Example 1 except that the blended pigments were different. It was.
In any spectacle lens, when observed through the obtained lens, for example, the lines of the twigs of trees under clear weather and the contrast of red, yellow, and green looked very clear.

(Example 3)
In Example 1, instead of the compound (1-4) described in Table 1 prepared in Synthesis Example 4, 0.05 part by weight of the compound (1-5) described in Table 1 manufactured in Synthesis Example 5 was used. The monomer mixture used for lens casting was prepared in the same manner as in Example 1 except that 0.05 part by weight of the compound (1-3) shown in Table 1 produced in Synthesis Example 3 was added. Was cast and spectacle lenses were obtained in the same manner as in Example 1 except that the blended pigments were different.
In any spectacle lens, when observed through the obtained lens, for example, the lines of the twigs of trees under clear weather and the contrast of red, yellow, and green looked very clear.

Example 4
In Example 1, instead of the compound (1-4) described in Table 1 prepared in Synthesis Example 4, 0.05 part by weight of the compound (1-5) described in Table 1 manufactured in Synthesis Example 5 was used. The monomer mixture used for lens casting was prepared in the same manner as in Example 1 except that 0.05 part by weight of the compound (1-1) shown in Table 1 produced in Synthesis Example 1 was added. Was cast and spectacle lenses were obtained in the same manner as in Example 1 except that the blended pigments were different.
In any spectacle lens, when observed through the obtained lens, for example, the lines of the twigs of trees under clear weather and the contrast of red, yellow, and green looked very clear.

(Example 5)
In Example 1, instead of the compound (1-4) described in Table 1 prepared in Synthesis Example 4, 0.05 part by weight of the compound (1-5) described in Table 1 manufactured in Synthesis Example 5 was used. The monomer mixture used for lens casting was prepared in the same manner as in Example 1 except that 0.05 part by weight of the compound (1-2) shown in Table 1 produced in Synthesis Example 2 was added. Was cast and spectacle lenses were obtained in the same manner as in Example 1 except that the blended pigments were different.
In any spectacle lens, when observed through the obtained lens, for example, the lines of the twigs of trees under clear weather and the contrast of red, yellow, and green looked very clear.

(Examples 6 to 10)
Except for using the dyes shown in the following Table 3 and parts by weight thereof, the monomer mixture to be used for lens casting was prepared in the same manner as in Example 1 and further cast, and the blended dyes were different. Except for the above, a spectacle lens was obtained in the same manner as in Example 1.
In any spectacle lens, when observed through the obtained lens, for example, the lines of the twigs of trees under clear weather and the contrast of red, yellow, and green looked very clear.

(Example 11)
In a 500 mL separable flask equipped with a thermometer, a stirrer, and a nitrogen seal tube, 200 parts of polyoxytetramethylene glycol (Hodogaya Chemical Industry: PTG-1000N) with an average molecular weight of 1014 was taken and stirred in a nitrogen stream. The mixture was heated and dehydrated for 1 hour under a reduced pressure of 100 to 110 ° C./3 to 5 mmHg. After dehydration, 131 parts of isophorone diisocyanate (Bayer's Desmodule I) was added and reacted at 120 to 130 ° C. for 2 hours to prepare a prepolymer. The obtained prepolymer was a colorless and transparent liquid, and had an NCO content of 9.7%, a viscosity of 6900 mPa · s / 30 ° C., and 900 mPa · s / 60 ° C.
After 100 parts by weight of the obtained prepolymer was heated to 70 ° C., 0.10 parts by weight of the compound (1-4) shown in Table 1 prepared in Synthesis Example 4 was added and mixed, and then at 120 ° C. Defoamed and mixed with 36.5 parts by weight of molten 4,4'methylene-bis (2,6-diethylaniline) This mixture is poured into a mold preheated at 100 ° C., and molding is quickly completed according to a pot life of several minutes, and heat curing is performed at 100 ° C. for 24 hours. Manufactured.
Subsequently, after mixing 626 parts of methanol and 221.8 parts of aqueous emulsion polyurethane (manufactured by Nikka Chemical: Neo sticker 700, solid content concentration 37%), methanol-dispersed titanium dioxide antimony pentoxide-silicon dioxide composite fine particle sol (catalyst) A primer composition was produced by mixing 309.6 parts of Kasei Kogyo Co., Ltd. (solid content concentration: 20 wt%) and 0.25 parts of a silicon surfactant (manufactured by Nippon Unicar Co., Ltd .: L-7604) and stirring well.
This primer composition was applied onto the spectacle lens by a dipping method (pickup speed: 15 cm / min). The applied spectacle lens was heat-cured at 100 ° C. for 20 minutes to form a primer layer having a film thickness of 1.0 μm and a refractive index of 1.67 on the substrate.

Further, 78 parts of methanol, 100.3 parts of butyl cellosolve, 1380.9 parts of methanol-dispersed titanium dioxide antimony pentoxide-silicon dioxide composite fine particle sol, methanol-dispersed colloidal silica (manufactured by Catalyst Kasei Kogyo Co., Ltd .: Oscar 1132 solid content concentration 30% by weight ) After 61.42 parts were mixed, 289.9 parts of γ-glycidoxypropyltrimethoxysilane were mixed. To this mixed solution, 80.1 parts of 0.05N hydrochloric acid aqueous solution was added dropwise with stirring. After further stirring for 4 hours, the mixture was aged overnight. In this solution, 4.4 parts of magnesium perchlorate, 0.6 parts of a silicon surfactant (manufactured by Nihon Unicar: L-7001) and 2.3 parts of a hindered amine light stabilizer (Sankyo LS-770) are added. The mixture was added and stirred for 4 hours, and then aged for a whole day and night to prepare a hard coat composition.
This hard coat composition was applied on the primer layer obtained by forming the primer layer by a dipping method (pickup speed 25 cm / min). The applied spectacle lens was heat-cured at 80 ° C. for 30 minutes and then heat-cured at 120 ° C. for 180 minutes. Thus, a hard coat layer having a thickness of 2.2 μm and a refractive index of 1.67 was formed on the primer layer.
In the observation through the obtained lens, for example, the lines of the twigs of trees under clear weather and the contrast of red, yellow and green looked very clear.

(Examples 12 to 20)
Except for using the dyes shown in the following formula Table 4 and parts by weight thereof, the monomer mixture to be used for lens casting was prepared in the same manner as in Example 11 and further cast, and the blended dyes were different. Except for the above, a spectacle lens having a primer layer and a hard coat layer was obtained in the same manner as in Example 11. In any spectacle lens, when observed through the obtained lens, for example, the lines of the twigs of trees under clear weather and the contrast of red, yellow, and green looked very clear.

(Example 21)
In a 500 mL separable flask equipped with a thermometer, a stirrer, and a nitrogen seal tube, 200 parts of 1,6-hexanediol adipate (Nippon Polyurethane Co., Ltd .: Nipponporan 164) with an average molecular weight of 1007 was placed in a separable flask and placed in a nitrogen stream. The mixture was heated with stirring at 100 to 110 ° C./3 to 5 mmHg and dehydrated for 1 hour. After dehydration, 170 parts of 4,4′-methylene-bis (cyclohexyl isocyanate) was added and reacted at 120 to 130 ° C. for 2 hours to prepare a prepolymer. The obtained prepolymer was a colorless and transparent liquid, and had an NCO content of 9.0%, a viscosity of 19000 mPa · s / 30 ° C., and 2000 mPa · s / 60 ° C.
After 100 parts by weight of the obtained prepolymer was heated to 70 ° C., 0.10 parts by weight of the compound (1-4) shown in Table 1 prepared in Synthesis Example 4 was added and mixed, and then at 120 ° C. The mixture was defoamed and mixed with 44.6 parts by weight of melted 4,4 ′ methylene-bis (3-chloro-2,6-diethylaniline). When this mixture is poured into a mold pre-heated at 100 ° C., a polycarbonate polarizing film (Plastic plastic industry: PGC-1301) is sandwiched and cast quickly, and cured by heating at 100 ° C. for 24 hours. A lens for polarizing glasses having a thickness of about 2.2 mm was manufactured.
In the observation through the obtained lens, for example, the lines of the twigs of trees under clear weather and the contrast of red, yellow and green looked very clear.

(Examples 22 to 30)
Except for using the dyes shown in the following formula Table 5 and parts by weight thereof, the monomer mixture to be used for lens casting was prepared in the same manner as in Example 21, and further casting was performed, and the blended dyes were different. A polarized glasses lens was obtained in the same manner as Example 21 except for the above.
In any of the polarizing eyeglass lenses, the observation through the obtained lens, for example, the lines of the twigs of trees under the clear sky and red, yellow, and green contrasts were seen very clearly.

(Example 31)
0.05 parts by weight of the compound (1-4) shown in Table 1 prepared in Synthesis Example 4 was mixed with 100 parts by weight of polycarbonate resin pellets (Teijin Chemicals: Panlite L-1250VX) and extruded with an extruder. Thereafter, a drying treatment was performed at 120 ° C. for 12 hours, and an eyeglass lens having an outer diameter of 80φ and a center thickness of 2 mm was molded using an injection molding machine in which the temperature was adjusted to 260 to 300 ° C.
In the observation through the obtained lens, for example, the lines of the twigs of trees under clear weather and the contrast of red, yellow and green looked very clear.

(Examples 32 to 40)
A spectacle lens was obtained in the same manner as in Example 31 except that the coloring matter shown in the following Table 6 and its weight part were used.
In any spectacle lens, when observed through the obtained lens, for example, the lines of the twigs of trees under clear weather and the contrast of red, yellow, and green looked very clear.

(Example 41)
After mixing 0.05 parts by weight of the compound (1-4) shown in Table 1 with 100 parts by weight of polyamide resin pellets (produced by Emschemy Japan: Grilamid TR90) in Synthesis Example 4, and extruding it with an extruder, A drying treatment was performed at 80 ° C. for 12 hours, and an eyeglass lens having an outer diameter of 73 φ and a center thickness of 2 mm was molded using an injection molding machine whose temperature was adjusted to 250 to 290 ° C.
In the observation through the obtained lens, for example, the lines of the twigs of trees under clear weather and the contrast of red, yellow and green looked very clear.

(Examples 41 to 50)
A spectacle lens was obtained in the same manner as in Example 31 except that the coloring matter shown in the following Table 7 and its weight part were used. In any spectacle lens, in the observation through the obtained lens, for example, the lines of the twigs of trees under clear sky and red, yellow, and green contrasts were seen very clearly.

A spectacle lens containing a porphyrin compound is capable of reducing discomfort associated with glare with respect to visible light, blurring of contrast, and visual fatigue.

Claims (6)

An eyeglass lens containing at least one porphyrin compound.
The spectacle lens according to claim 1, wherein the porphyrin compound is represented by the general formula (1).

[Wherein, X1 to X8 each independently represents a hydrogen atom, a halogen atom, a linear, branched or cyclic alkyl group, a linear, branched or cyclic alkoxy group, a substituted or unsubstituted ethenyl group, substituted or unsubstituted. Ethynyl group, substituted or unsubstituted aryl group, substituted or unsubstituted aryloxy group, substituted or unsubstituted aryloxycarbonyl group, substituted or unsubstituted alkylthio group, substituted or unsubstituted arylthio group, substituted or unsubstituted Substituted aralkyl group, substituted or unsubstituted aralkyloxy group, linear, branched or cyclic halogenoalkyl group, linear, branched or cyclic halogenoalkoxy group, substituted or unsubstituted acyl group, linear, branched or cyclic An alkoxyalkyl group, a linear, branched or cyclic alkoxyalkoxyalkyl group, substituted or unsubstituted Of the aryloxyalkyl group, a substituted or unsubstituted aralkyloxyalkyl group, or a linear, branched or cyclic halogenoalkoxyalkyl group, and the adjacent groups selected from X1 to X8 are It represents that it may combine to form a substituted or unsubstituted aromatic ring together with a substituted carbon atom. However, not all of X1 to X8 are hydrogen atoms. R1 to R4 each independently represents a substituted or unsubstituted aryl group, and M represents two hydrogen atoms, two monovalent metal atoms, a divalent metal atom, a trivalent substituted metal atom, and a tetravalent group. Represents a substituted metal atom or a metal oxide atom]
In formula (1), X1 to X8 are each independently a halogen atom, a linear, branched or cyclic alkyl group, a linear, branched or cyclic alkoxy group, a substituted or unsubstituted ethenyl group, a substituted or unsubstituted An ethynyl group, a substituted or unsubstituted aryl group, a substituted or unsubstituted aryloxy group, a linear, branched or cyclic halogenoalkyl group, a linear, branched or cyclic halogenoalkoxy group, and further selected from X1 to X8 The groups adjacent to each other are bonded to each other and fused together with a substituted carbon atom with a substituted or unsubstituted benzene ring or naphthalene ring, and R1 to R4 are substituted or unsubstituted aryl groups , M is at least a porphyrin compound selected from a divalent metal atom, a trivalent substituted metal atom, a tetravalent substituted metal atom, or a metal oxide atom Claim 1-2, wherein the spectacle lens comprising seeds.
In the general formula (1), X1 to X8 are each independently a substituted or unsubstituted ethynyl group, R1 to R4 are substituted or unsubstituted phenyl groups, and M is a divalent metal atom or a metal oxide atom. The spectacle lens according to claim 1, comprising at least one porphyrin compound.
The groups adjacent to each other selected from X1 to X8 in the general formula (1) are substituted or unsubstituted naphthylene rings condensed at the 1-position and 8-position of the naphthalene ring, and R1 to R4 are substituted or unsubstituted. The spectacle lens according to claims 1 to 3, comprising at least one porphyrin compound which is a phenyl group and M is a divalent metal atom or a metal oxide atom.
Furthermore, the tetraazaporphyrin compound represented by following General formula (2) is contained, For spectacle lenses of Claims 1-5 characterized by the above-mentioned.

[Wherein Y1 to Y8 are each independently a hydrogen atom, a halogen atom, a cyano group, a nitro group, a linear, branched or cyclic alkyl group, a linear, branched or cyclic alkoxy group, substituted or unsubstituted aryl. Group, substituted or unsubstituted aryloxy group, substituted or unsubstituted aralkyl group, substituted or unsubstituted aralkyloxy group, linear, branched or cyclic halogenoalkyl group, linear, branched or cyclic halogenoalkoxy group, Substituted or unsubstituted amino group, linear, branched or cyclic alkoxyalkyl group, linear, branched or cyclic alkoxyalkoxyalkyl group, substituted or unsubstituted aryloxyalkyl group, substituted or unsubstituted aralkyloxyalkyl group Or a straight-chain, branched or cyclic halogenoalkoxyalkyl group, and Y1- The groups adjacent to each other selected from Y8 are bonded to each other to represent a substituted or unsubstituted carbocyclic aliphatic ring together with a substituted carbon atom. However, not all of Y1 to Y8 are hydrogen atoms. M represents two hydrogen atoms, two monovalent metal atoms, a divalent metal atom, a trivalent substituted metal atom, a tetravalent substituted metal atom, or a metal oxide atom]