JP2008163184A - Two-photon absorption material and its application - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide an organic material with a large absorption cross section which effectively absorbs two photons and sensitively realizes change of a spectrum, index of refraction or polarization, to provide a method for two-photon absorption optical recording and readout which enables readout by irradiating a recorded material with light and detecting the difference in emission intensity after recording is performed by an unrewritable method utilizing two-photon absorption of a two-photon absorption compound, to provide a two-photon absorption optical recording material capable of such the recording and readout, and further to provide a three-dimensional two-photon absorption optical recording material using the same and methods for optical recording and readout of the same. <P>SOLUTION: The two-photon absorption material comprises a porphyrin derivative having four pyrrole rings that optionally have substituents and are bound to each other either directly or via carbon atoms optionally having substituents. Here, the total number of carbon atoms optionally having substituents linking the four pyrrole rings is four, and at least two of the pyrrole rings are directly bound to each other instead of via the carbon atom. <P>COPYRIGHT: (C)2008,JPO&INPIT

Description

  The present invention relates to a two-photon absorption material, a two-photon absorption monomolecular material or a polymer material having a high two-photon absorption cross-section, a three-dimensional memory material, a light limiting material, a curing material for a photocurable resin for stereolithography, photochemotherapy It is applied to applications such as materials for fluorescent materials and fluorescent dye materials for two-photon fluorescence microscopes.

As conventional examples of the two-photon absorption material, there are those disclosed in Patent Documents 1 to 3.
Among others, there are those disclosed in Patent Documents 4 to 9 as conventional examples related to porphyrin derivatives.
In addition, as conventional examples relating to a three-dimensional memory medium (material), there are those disclosed in Patent Documents 10 to 12.
Further, as a conventional example relating to an optical limiting element (material), there is one disclosed in Patent Document 13.
Moreover, there exists a thing of patent document 14 disclosure as a prior art example regarding an optical shaping technique.
Further, as conventional examples of a (fluorescence) microscope using two-photon characteristics, there are those disclosed in Patent Documents 15 to 17. We have also developed and proposed a technology related to two-photon absorption materials (Japanese Patent Application No. 2006-73792, Japanese Patent Application No. 2006-74156, Japanese Patent Application No. 2006-250292, Japanese Patent Application No. 2006-70305). Description etc.).

  The use of the two-photon absorption phenomenon makes it possible to apply to various devices characterized by extremely high spatial resolution, but the two-photon absorption compounds currently available have a low two-photon absorption capability, so two-photon absorption As an excitation light source for inducing light, an expensive and very high-power laser is required. Therefore, in order to realize a practical application using two-photon absorption using an inexpensive and small (low output) laser, development of a highly efficient two-photon absorption material is essential.

JP-A-2005-213434 JP 2005-82507 A JP 2004-168690 A Special Table 2005-500394 JP 2004-16890 A JP 2004-339435 A Japanese Patent Laying-Open No. 2005-267338 JP 2006-178399 A JP 2006-209059 A JP-A-2005-100606 JP 2005-517769 Gazette JP-T-2004-534849 Japanese Patent Laid-Open No. 08-320422 JP 2005-134783 A Japanese Patent Application Laid-Open No. 09-230246 JP 10-142507 A JP 2005-165212 A

  In view of the above prior art, an object of the present invention is to realize an organic material that efficiently absorbs two-photons, that is, an organic material having a large two-photon absorption cross-section, that realizes a change in spectrum, refractive index, or polarization state with high sensitivity. Is to provide.

  Furthermore, an object of the present invention is to have at least a two-photon absorption compound having a large two-photon absorption cross-section, and to record light in a recording material that cannot be rewritten using two-photon absorption of the two-photon absorption compound. It is intended to provide a two-photon absorption optical recording / reproducing method characterized in that reproduction is performed by irradiating a light source and detecting a difference in light emission intensity, and a two-photon absorption optical recording material capable of such recording / reproduction. Furthermore, it is to provide a two-photon absorption three-dimensional optical recording material, a two-photon absorption three-dimensional optical recording method and a reproducing method using them.

As a result of intensive studies, the present inventors have found that the above problems can be solved by a specific porphyrin derivative, and have reached the present invention.
That is, according to the present invention, (1) "in a porphyrin derivative having a structure in which four pyrrole rings which may have a substituent are bonded via a carbon atom which may have a substituent or directly, A two-photon absorption material comprising a porphyrin derivative in which the total number of carbon atoms that may have a substituent connecting the four pyrrole rings is four and at least one pyrrole ring is directly bonded without any carbon atom "
(2) “The two-photon absorption material according to item (1), which is composed of a porphyrin derivative represented by the following formula (1);

式中、R₁〜R₈、X₁〜X₄はそれぞれ独立に水素原子、ハロゲン原子、ニトロ基、シアノ基、水酸基、カルボキシル基、置換もしくは未置換のアルキル基、置換もしくは未置換のアルコキシ基、置換もしくは未置換のアリール基、置換もしくは未置換のアミノ基、置換もしくは未置換のアシル基を表す。
Ｍは２個の水素原子、または酸素、ハロゲンを有してもよい２価、３価、もしくは４価の金属原子、または（ＯＲ₉）p、（ＯＳｉＲ₁₀Ｒ₁₁Ｒ₁₂）q、（ＯＰＯＲ₁₃Ｒ₁₄）r、（ＯＣＯＲ₁₅）sを有してもよい金属原子を表す。Ｒ₉〜Ｒ₁₅は独立に水素原子、置換もしくは未置換の脂肪族、芳香族炭化水素基を表し、p , q , r , sは０〜２の整数を表す。」、
（３）「下記式（２）で示されるポルフィリン誘導体からなることを特徴とする前記第（１）項に記載の二光子吸収材料；

In the formula, R _{1 to} R ₈ and X _{1 to} X ₄ are each independently a hydrogen atom, a halogen atom, a nitro group, a cyano group, a hydroxyl group, a carboxyl group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkoxy group. Represents a substituted or unsubstituted aryl group, a substituted or unsubstituted amino group, or a substituted or unsubstituted acyl group.
M is two hydrogen atoms, or a divalent, trivalent, or tetravalent metal atom which may have oxygen or halogen, or (OR ₉ ) p, (OSiR ₁₀ R ₁₁ R ₁₂ ) q, (OPOR ₁₃ R ₁₄ ) r represents a metal atom which may have (OCOR ₁₅ ) s. R _{9 to} R ₁₅ independently represent a hydrogen atom, a substituted or unsubstituted aliphatic or aromatic hydrocarbon group, and p 1, q 2, r 3 and s represent an integer of 0 to 2. "
(3) “A two-photon absorption material according to item (1), which is composed of a porphyrin derivative represented by the following formula (2);

式中、R₁〜R₈、X₁〜X₄はそれぞれ独立に水素原子、ハロゲン原子、ニトロ基、シアノ基、水酸基、カルボキシル基、置換もしくは未置換のアルキル基、置換もしくは未置換のアルコキシ基、置換もしくは未置換のアリール基、置換もしくは未置換のアミノ基、置換もしくは未置換のアシル基を表す。
Ｍは２個の水素原子、または酸素、ハロゲンを有してもよい２価、３価、もしくは４価の金属原子、または（ＯＲ₉）p、（ＯＳｉＲ₁₀Ｒ₁₁Ｒ₁₂）q、（ＯＰＯＲ₁₃Ｒ₁₄）r、（ＯＣＯＲ₁₅）sを有してもよい金属原子を表す。Ｒ₉〜Ｒ₁₅は独立に水素原子、置換もしくは未置換の脂肪族、芳香族炭化水素基を表し、p , q , r , sは０〜２の整数を表す。」、
（４）「下記式（３）で示されるポルフィリン誘導体からなることを特徴とする前記第（１）項に記載の二光子吸収材料；

In the formula, R _{1 to} R ₈ and X _{1 to} X ₄ are each independently a hydrogen atom, a halogen atom, a nitro group, a cyano group, a hydroxyl group, a carboxyl group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkoxy group. Represents a substituted or unsubstituted aryl group, a substituted or unsubstituted amino group, or a substituted or unsubstituted acyl group.
M is two hydrogen atoms, or a divalent, trivalent, or tetravalent metal atom which may have oxygen or halogen, or (OR ₉ ) p, (OSiR ₁₀ R ₁₁ R ₁₂ ) q, (OPOR ₁₃ R ₁₄ ) r represents a metal atom which may have (OCOR ₁₅ ) s. R _{9 to} R ₁₅ independently represent a hydrogen atom, a substituted or unsubstituted aliphatic or aromatic hydrocarbon group, and p 1, q 2, r 3 and s represent an integer of 0 to 2. "
(4) “Two-photon absorption material according to item (1), comprising a porphyrin derivative represented by the following formula (3);

式中、R₁〜R₈、X₁〜X₄はそれぞれ独立に水素原子、ハロゲン原子、ニトロ基、シアノ基、水酸基、カルボキシル基、置換もしくは未置換のアルキル基、置換もしくは未置換のアルコキシ基、置換もしくは未置換のアリール基、置換もしくは未置換のアミノ基、置換もしくは未置換のアシル基を表す。
Ｍは２個の水素原子、または酸素、ハロゲンを有してもよい２価、３価、もしくは４価の金属原子、または（ＯＲ₉）p、（ＯＳｉＲ₁₀Ｒ₁₁Ｒ₁₂）q、（ＯＰＯＲ₁₃Ｒ₁₄）r、（ＯＣＯＲ₁₅）sを有してもよい金属原子を表す。Ｒ₉〜Ｒ₁₅は独立に水素原子、置換もしくは未置換の脂肪族、芳香族炭化水素基を表し、p , q , r , sは０〜２の整数を表す。」、
（５）「下記式（４）で示されるポルフィリン誘導体からなることを特徴とする前記第（１）項に記載の二光子吸収材料；

In the formula, R _{1 to} R ₈ and X _{1 to} X ₄ are each independently a hydrogen atom, a halogen atom, a nitro group, a cyano group, a hydroxyl group, a carboxyl group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkoxy group. Represents a substituted or unsubstituted aryl group, a substituted or unsubstituted amino group, or a substituted or unsubstituted acyl group.
M is two hydrogen atoms, or a divalent, trivalent, or tetravalent metal atom which may have oxygen or halogen, or (OR ₉ ) p, (OSiR ₁₀ R ₁₁ R ₁₂ ) q, (OPOR ₁₃ R ₁₄ ) r represents a metal atom which may have (OCOR ₁₅ ) s. R _{9 to} R ₁₅ independently represent a hydrogen atom, a substituted or unsubstituted aliphatic or aromatic hydrocarbon group, and p 1, q 2, r 3 and s represent an integer of 0 to 2. "
(5) “A two-photon absorption material according to item (1), which is composed of a porphyrin derivative represented by the following formula (4);

式中、R₁〜R₈、X₁〜X₄はそれぞれ独立に水素原子、ハロゲン原子、ニトロ基、シアノ基、水酸基、カルボキシル基、置換もしくは未置換のアルキル基、置換もしくは未置換のアルコキシ基、置換もしくは未置換のアリール基、置換もしくは未置換のアミノ基、置換もしくは未置換のアシル基を表す。
Ｍは２個の水素原子、または酸素、ハロゲンを有してもよい２価、３価、もしくは４価の金属原子、または（ＯＲ₉）p、（ＯＳｉＲ₁₀Ｒ₁₁Ｒ₁₂）q、（ＯＰＯＲ₁₃Ｒ₁₄）r、（ＯＣＯＲ₁₅）sを有してもよい金属原子を表す。Ｒ₉〜Ｒ₁₅は独立に水素原子、置換もしくは未置換の脂肪族、芳香族炭化水素基を表し、p , q , r , sは０〜２の整数を表す。」、
（６）「下記式（５）で示されるポルフィリン誘導体からなることを特徴とする前記第（１）項に記載の二光子吸収材料；

In the formula, R _{1 to} R ₈ and X _{1 to} X ₄ are each independently a hydrogen atom, a halogen atom, a nitro group, a cyano group, a hydroxyl group, a carboxyl group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkoxy group. Represents a substituted or unsubstituted aryl group, a substituted or unsubstituted amino group, or a substituted or unsubstituted acyl group.
M is two hydrogen atoms, or a divalent, trivalent, or tetravalent metal atom which may have oxygen or halogen, or (OR ₉ ) p, (OSiR ₁₀ R ₁₁ R ₁₂ ) q, (OPOR ₁₃ R ₁₄ ) r represents a metal atom which may have (OCOR ₁₅ ) s. R _{9 to} R ₁₅ independently represent a hydrogen atom, a substituted or unsubstituted aliphatic or aromatic hydrocarbon group, and p 1, q 2, r 3 and s represent an integer of 0 to 2. "
(6) “Two-photon absorption material according to item (1), comprising a porphyrin derivative represented by the following formula (5);

式中、R₁〜R₈、X₁〜X₄はそれぞれ独立に水素原子、ハロゲン原子、ニトロ基、シアノ基、水酸基、カルボキシル基、置換もしくは未置換のアルキル基、置換もしくは未置換のアルコキシ基、置換もしくは未置換のアリール基、置換もしくは未置換のアミノ基、置換もしくは未置換のアシル基を表す。
Ｍは２個の水素原子、または酸素、ハロゲンを有してもよい２価、３価、もしくは４価の金属原子、または（ＯＲ₉）p、（ＯＳｉＲ₁₀Ｒ₁₁Ｒ₁₂）q、（ＯＰＯＲ₁₃Ｒ₁₄）r、（ＯＣＯＲ₁₅）sを有してもよい金属原子を表す。Ｒ₉〜Ｒ₁₅は独立に水素原子、置換もしくは未置換の脂肪族、芳香族炭化水素基を表し、p , q , r , sは０〜２の整数を表す。」、
（７）「置換基を有してもよい４つのピロール環が置換基を有してもよい炭素原子又は窒素原子を介して結合した構造を有する下記式（６）で示されるポルフィリン誘導体からなる二光子吸収材料であって、該４つのピロール環を結ぶ置換基を有してもよい原子のうち少なくとも一個が炭素原子及び窒素原子であるポルフィリン誘導体からなる二光子吸収材料；

In the formula, R _{1 to} R ₈ and X _{1 to} X ₄ are each independently a hydrogen atom, a halogen atom, a nitro group, a cyano group, a hydroxyl group, a carboxyl group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkoxy group. Represents a substituted or unsubstituted aryl group, a substituted or unsubstituted amino group, or a substituted or unsubstituted acyl group.
M is two hydrogen atoms, or a divalent, trivalent, or tetravalent metal atom which may have oxygen or halogen, or (OR ₉ ) p, (OSiR ₁₀ R ₁₁ R ₁₂ ) q, (OPOR ₁₃ R ₁₄ ) r represents a metal atom which may have (OCOR ₁₅ ) s. R _{9 to} R ₁₅ independently represent a hydrogen atom, a substituted or unsubstituted aliphatic or aromatic hydrocarbon group, and p 1, q 2, r 3 and s represent an integer of 0 to 2. "
(7) “consisting of a porphyrin derivative represented by the following formula (6) having a structure in which four pyrrole rings which may have a substituent are bonded via a carbon atom or a nitrogen atom which may have a substituent. A two-photon absorption material comprising a porphyrin derivative in which at least one of the atoms which may have a substituent connecting the four pyrrole rings is a carbon atom and a nitrogen atom;

R₁〜R₄は、窒素原子、炭素原子を表し、そのうち少なくとも一個は窒素原子を表す。
X₁〜X₈はそれぞれ独立に水素原子、ハロゲン原子、ニトロ基、シアノ基、水酸基、カルボキシル基、置換もしくは未置換のアルキル基、置換もしくは未置換のアルコキシ基、置換もしくは未置換のアリール基、置換もしくは未置換のアミノ基、置換もしくは未置換のアシル基を表す。
Ｍは２個の水素原子、または酸素、ハロゲンを有してもよい２価、３価、もしくは４価の金属原子、または（ＯＲ₅）p、（ＯＳｉＲ₆Ｒ₇Ｒ₈）q、（ＯＰＯＲ₉Ｒ₁₀）r、（ＯＣＯＲ₁₁）sを有してもよい金属原子を表す。Ｒ₅〜Ｒ₁₁は独立に水素原子、置換もしくは未置換の脂肪族、芳香族炭化水素基を表し、p , q , r , sは０〜２の整数を表す。」、
（８）「式（６）で示されるポルフィリン誘導体のR₁〜R₄のうち、１つが窒素原子であり、残りは炭素原子であるモノアザポルフィリン化合物からなることを特徴とする前記第（７）項に記載の二光子吸収材料」、
（９）「式（６）で示されるポルフィリン誘導体のR₁〜R₄のうち、２つが窒素原子であり、残りは炭素原子であるジアザポルフィリン化合物からなることを特徴とする前記第（７）項に記載の二光子吸収材料」、
（１０）「式（６）で示されるポルフィリン誘導体のR₁、R_３が窒素原子であり、R_２、R₄が炭素原子であるジアザポルフィリン化合物からなる前記第（７）項に記載の二光子吸収材料」、
（１１）「前記第（１）項乃至第（１０）項のいずれかに記載の化合物を含む三次元メモリ材料」、
（１２）「前記第（１）項乃至第（１０）項のいずれかに記載の化合物を含む光制限材料」、
（１３）「前記第（１）項乃至第（１０）項のいずれかに記載の化合物を含む光造形用光硬化樹脂の硬化材料」、
（１４）「前記第（１）項乃至第（１０）項のいずれかに記載の化合物を含む二光子蛍光顕微鏡用蛍光色素材料」、
（１５）「前記第（１）項乃至第（１０）項のいずれかに記載の化合物を記録層中に少なくとも１種含み入射光に対して深さ方向に記録再生可能な三次元記録媒体」、
（１６）「前記第（１）項乃至第（１０）項のいずれかに記載の化合物の少なくとも１種含む光制限素子」、
（１７）「前記第（１）項乃至第（１０）項のいずれかに記載の化合物の少なくとも１種含む光造形システム」、
（１８）「前記第（１）項乃至第（１０）項のいずれかに記載の化合物の少なくとも１種含む二光子蛍光顕微鏡装置」によって達成される。

R _{1 to} R ₄ represent a nitrogen atom or a carbon atom, and at least one of them represents a nitrogen atom.
X _{1 to} X ₈ are each independently a hydrogen atom, a halogen atom, a nitro group, a cyano group, a hydroxyl group, a carboxyl group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkoxy group, a substituted or unsubstituted aryl group, A substituted or unsubstituted amino group or a substituted or unsubstituted acyl group is represented.
M is two hydrogen atoms, or a divalent, trivalent, or tetravalent metal atom which may have oxygen or halogen, or (OR ₅ ) p, (OSiR ₆ R ₇ R ₈ ) q, (OPOR ₉ R ₁₀ ) r represents a metal atom which may have (OCOR ₁₁ ) s. R ₅ to R ₁₁ are independently a hydrogen atom, an aliphatic substituted or unsubstituted, an aromatic hydrocarbon group, p, q, r, s represents an integer of 0 to 2. "
(8) The above (7), wherein the porphyrin derivative represented by the formula (6) is composed of a monoazaporphyrin compound in which _one of R _{1 to} R ₄ is a nitrogen atom and the remainder is a carbon atom. ) Two-photon absorption material according to item ",
(9) The above-mentioned (7) characterized in that among the porphyrin derivatives represented by formula (6), R _{1 to} R ₄ are diazaporphyrin compounds in which two are nitrogen atoms and the rest are carbon atoms. ) Two-photon absorption material according to item ",
(10) “The porphyrin derivative represented by the formula (6) is a diazaporphyrin compound in which R ₁ and R ₃ are nitrogen atoms, and R ₂ and R ₄ are carbon atoms,” Two-photon absorption material ",
(11) "Three-dimensional memory material containing the compound according to any one of (1) to (10)",
(12) "Optical limiting material containing the compound according to any one of (1) to (10)",
(13) “Curing material of photo-curing resin for optical modeling including the compound according to any one of (1) to (10)”,
(14) "Fluorescent dye material for a two-photon fluorescence microscope containing the compound according to any one of (1) to (10)",
(15) “Three-dimensional recording medium including at least one compound according to any one of items (1) to (10) in a recording layer and capable of recording / reproducing in the depth direction with respect to incident light” ,
(16) "Optical limiting element including at least one compound according to any one of items (1) to (10)",
(17) "Optical modeling system including at least one compound according to any one of (1) to (10)",
(18) This can be achieved by “a two-photon fluorescence microscope apparatus including at least one compound according to any one of (1) to (10)”.

  That is, the present invention relates to a two-photon absorption material, a three-dimensional memory material using the same, a light limiting material, a photocuring resin curing material, and a fluorescent dye material for a two-photon fluorescence microscope. Here, said (1)-(10) shows the basic structure of the two-photon absorption material of this invention, (11)-(14) shows the example of the suitable industrial application material, (15)- (18) shows an application example of a device, apparatus and system containing the compound of the present invention.

  As will be apparent from the following detailed and specific description, the present invention can realize a two-photon absorption compound having a high two-photon absorption transition efficiency, and can be used in practical applications using a small and inexpensive laser (three-dimensional memory material, Light-limiting material, photocuring resin curing material, photochemotherapy material, fluorescent dye material for two-photon fluorescence microscope, etc.) can be realized.

Hereinafter, the present invention will be described in detail.
The two-photon absorption material of the present invention is a material capable of exciting a molecule at a wavelength in a non-resonant region, and a material having an actual excited state at an energy level twice that of a photon used for excitation at this time. That is.
By the way, the two-photon absorption phenomenon is a kind of third-order nonlinear optical effect, which is a phenomenon in which a molecule absorbs two photons simultaneously and transitions from a ground state to an excited state. Since Luc Bredas et al. Elucidated the relationship between molecular structure and mechanism in 1998 (Science, 281, 1653 (1998)), research on materials having two-photon absorption ability has recently advanced.

However, since the transition efficiency of such two-photon simultaneous absorption is extremely low compared to single-photon absorption and requires extremely high power density photons, it is almost neglected in the usual laser light intensity, and peak light intensity It has been confirmed that an ultra-short pulse laser of about femtosecond such as a mode-locked laser having a high (light intensity at the maximum emission wavelength) is used.
The transition efficiency of two-photon absorption is proportional to the square of the applied photoelectric field (the two-photon absorption square characteristic). For this reason, when a laser is irradiated, two-photon absorption occurs only at a position where the electric field strength is high at the center of the laser spot, and no two-photon absorption occurs at a portion where the electric field strength is weak at the peripheral portion. In the three-dimensional space, two-photon absorption occurs only in a region where the electric field strength at the focal point where the laser light is collected by the lens is large, and no two-photon absorption occurs in the region outside the focal point because the electric field strength is weak. Compared to the linear absorption of one photon where excitation occurs at all positions in proportion to the intensity of the applied photoelectric field, the two-photon absorption is excited only at a pinpoint inside the space due to this square characteristic. Therefore, the spatial resolution is significantly improved.

  Utilizing this characteristic, research on a three-dimensional memory for recording bit data by causing a spectral change, a refractive index change or a polarization change by two-photon absorption at a predetermined position of a recording medium is underway. Since two-photon absorption occurs in proportion to the square of the intensity of light, a memory using two-photon absorption can reduce the spot size compared to a memory using one-photon absorption, and super-resolution recording. Is possible. In addition, from the characteristics of high spatial resolution derived from this square characteristic, development for applications such as a light limiting material, a cured material of a photo-curing resin for stereolithography, and a fluorescent dye material for a two-photon fluorescence microscope is being promoted.

  Furthermore, in the case of inducing two-photon absorption, it is possible to use a short-pulse laser in the near-infrared region that has a longer wavelength than the wavelength region in which the linear absorption band of the compound exists and does not have absorption. Since the near-infrared light of the so-called transparent region, which does not have a linear absorption band of the compound, is used, the excitation light can reach the inside of the sample without being absorbed or scattered, and because of the square characteristic of the two-photon absorption, Since pinpoints can be excited with high spatial resolution, two-photon absorption and two-photon emission are also expected in photochemotherapy applications such as two-photon contrast and two-photon photodynamic therapy (PDT) in biological tissues. In addition, research on upconversion lasing has been reported from the viewpoint of a wavelength conversion device because photons with higher energy than the energy of incident photons can be extracted by using two-photon absorption and two-photon emission.

Many inorganic materials have been found so far as two-photon absorption materials. However, inorganic materials are very difficult to put into practical use because so-called molecular design for optimizing desired two-photon absorption characteristics and various physical properties necessary for device manufacture is difficult. On the other hand, organic compounds can be optimized not only for the desired two-photon absorption by molecular design, but also for other physical properties, making it highly practical and a promising two-photon absorption material. It attracts attention.
As conventional organic two-photon absorption materials, pigment compounds such as rhodamine and coumarin, compounds such as dithienothiophene derivatives and oligophenylene vinylene derivatives are known. However, the two-photon absorption cross section showing the two-photon absorption capacity per molecule is small, especially when using a femtosecond pulse laser, the two-photon absorption cross-section is 200 (GM: × 10-50cm4 · s · molecule-1 -Most of those less than photon-1) have not been put into practical use.

<Application to two-dimensional multilayer optical memory using two-photon absorption material>
Recently, networks such as the Internet and high-definition TV are rapidly spreading. In addition, at the time of HDTV (High Definition Television) broadcasting, there is an increasing demand for a large-capacity recording medium for easily and inexpensively recording image information of 50 GB or more, preferably 100 GB or more, for consumer use. Furthermore, for business use such as computer backup use and broadcast backup use, an optical recording medium capable of recording large-capacity information of about 1 TB or more at high speed and at low cost is required. Under such circumstances, the conventional two-dimensional optical recording medium such as DVD ± R is about 25 GB at most even if the recording / reproducing wavelength is shortened due to the physical principle, and is sufficiently large enough to meet future requirements. It cannot be said that capacity can be expected.
Under such circumstances, a three-dimensional optical recording medium has attracted attention as an ultimate high-density, high-capacity recording medium. Three-dimensional optical recording media can be recorded in dozens or hundreds of layers in the three-dimensional (film thickness) direction, resulting in tens or hundreds of times the ultra-high density and ultra-high capacity recording of conventional two-dimensional recording media. That is what we are trying to achieve. In order to provide a three-dimensional optical recording medium, it is necessary to be able to access and write at an arbitrary place in the three-dimensional (film thickness) direction. As a means for this, a method using a two-photon absorption material and holography (interference) There is a method of using. In a three-dimensional optical recording medium using a two-photon absorbing material, so-called bit recording can be performed over tens or hundreds of times based on the principle described above, and higher density recording is possible. It can be said that this is the ultimate high-density, high-capacity optical recording medium.
As a three-dimensional optical recording medium using a two-photon absorption material, a method of reading with fluorescence using a fluorescent substance for recording and reproduction (Lewitch, Eugene, Police, etc., JP 2001-524245 A, Pavel, Eugene, etc.) , JP 2000-520261 A), a method of reading by absorption or fluorescence using a photochromic compound (Korotif, Nikolai Eye et al., JP 2001-522119 JP, Arsenoff, U "Radimir et al., JP 2001-508221 A However, there is no specific two-photon absorption material presented, and examples of two-photon absorption compounds presented abstractly are two-photon absorption compounds with extremely low two-photon absorption efficiency. Is used. Further, since the photochromic compounds used in these patent documents are reversible materials, there are problems in non-destructive reading, long-term storage stability of recording, S / N ratio of reproduction, and the like, a method that is practical as an optical recording medium I can't say that. In particular, in terms of non-destructive readout, long-term storage stability of recording, etc., it is preferable to reproduce by changing the reflectance (refractive index or absorptivity) or emission intensity using an irreversible material, but a two-photon having such a function. There was no example that specifically disclosed the absorbent material.
Also, Kawada Jun, Kawada Yoshimasa, JP-A-6-28672, Kawada Jun, Kawada Yoshimasa et al., JP-A-6-118306 discloses a recording apparatus and a reproducing apparatus for three-dimensional recording by refractive index modulation, Although a reading method and the like are disclosed, there is no description about a method using a two-photon absorption three-dimensional optical recording material.

As mentioned above, the reaction is caused by the excitation energy obtained by non-resonant two-photon absorption, and as a result, the emission intensity when light is irradiated at the laser focus (recording) part and the non-focus (non-recording) part If modulation is possible with a method that cannot be rewritten, it is possible to cause emission intensity modulation with extremely high spatial resolution in any place in three-dimensional space, and it can be applied to three-dimensional optical recording media that are considered to be the ultimate high-density recording medium. It becomes possible. Furthermore, since non-destructive readout is possible and the material is an irreversible material, it can be expected to have good storage stability and is practical.
However, the currently available two-photon absorption compounds have a low two-photon absorption capability, so that a very high-power laser is required as a light source and a long recording time is required. Especially for use in three-dimensional optical recording media, construction of a two-photon absorption three-dimensional optical recording material that can perform recording with two-photon absorption with high sensitivity to achieve a fast transfer rate. Is essential. For that purpose, the difference between the two-photon absorption compound that can absorb two-photons with high efficiency and generate an excited state, and the two-photon absorption optical recording material using a two-photon absorption compound excited state in some way. Although a material containing a recording component that can efficiently form a thin film is effective, such a material has hardly been disclosed so far, and it has been desired to construct such a material.

The two-photon absorption optical recording material of the present invention can be applied directly on the substrate by using a spin coater, roll coater or bar coater, or can be cast as a film and laminated on the substrate by a usual method. Thus, a two-photon absorption optical recording material can be obtained.
Here, “substrate” means any natural or synthetic support, preferably one that can exist in the form of a flexible or rigid film, sheet or plate.
The substrate is preferably polyethylene terephthalate, resin-undercoated polyethylene terephthalate, polyethylene terephthalate treated with flame or electrostatic discharge, cellulose acetate, polycarbonate, polymethyl methacrylate, polyester, polyvinyl alcohol, glass or the like. The substrate may be provided with a guide groove for tracking and address information in advance.
The solvent used can be removed by evaporation during drying. Heating or reduced pressure may be used for evaporation removal.

  Furthermore, a protective layer (intermediate layer) for blocking oxygen and preventing interlayer crosstalk may be formed on the two-photon absorption optical recording material. The protective layer (intermediate layer) is made of a plastic film or plate such as polyolefin such as polypropylene or polyethylene, polyvinyl chloride, polyvinylidene chloride, polyvinyl alcohol, polyethylene terephthalate or cellophane film, and is attached electrostatically using an extruder. Alternatively, the layers may be laminated together or the polymer solution may be applied. Further, a glass plate may be bonded. In addition, an adhesive or a liquid substance may be present between the protective layer and the photosensitive film and / or between the base material and the photosensitive film in order to improve airtightness. Further, the protective layer (intermediate layer) between the photosensitive films may be provided with tracking guide grooves and address information in advance.

  By focusing on an arbitrary layer of the above-described three-dimensional multilayer optical recording medium and performing recording and reproduction, it functions as the three-dimensional recording medium of the present invention. Further, even if the layers are not separated by a protective layer (intermediate layer), three-dimensional recording in the depth direction is possible from the two-photon absorption dye characteristics.

Hereinafter, preferred embodiments (specific examples) of the three-dimensional multilayer optical memory will be described. However, the present invention is not limited to these embodiments, and any structure capable of three-dimensional recording (recording in a plane and a film thickness direction) can be used. Any other structure may be used. A schematic diagram of a recording / reproducing system of a three-dimensional multilayer optical memory is shown in FIG. 1A, and a schematic sectional view of a recording medium is shown in FIG.
In the recording medium (b) in the drawing, a recording layer (3) using the two-photon absorption compound of the present invention on a flat support (substrate (1)), and an intermediate layer (4) for preventing crosstalk ( 50 protective layers) are alternately stacked, and each layer is formed by spin coating. The recording layer (3) preferably has a thickness of 0.01 to 0.5 [mu], and the intermediate layer (4) preferably has a thickness of 0.1 [mu] to 5 [mu]. Terabyte-class ultra-high-density optical recording can be realized with disk size. Further, a substrate (2) (protective layer) similar to the substrate (1) or a reflective layer made of a high reflectance material is formed by a data reproduction method (transmission / or reflection type).
A single beam (5) is used during recording, and in this case, ultrashort pulsed light in the femtosecond order can be used. At the time of reproduction, it is also possible to use a light (6) having a wavelength different from that of the beam (5) used for data recording or the same wavelength with a low output. Recording and reproduction can be performed in either bit units or page units, and parallel recording / reproduction using a surface light source, a two-dimensional detector (7), or the like is effective in increasing the transfer rate.
Note that a three-dimensional multilayer optical memory similarly formed according to the present invention may have a card shape, a plate shape, a tape shape, a drum shape, or the like.

<Application to optical limiting element using two-photon absorption material>
In optical communication and optical information processing, optical control such as modulation and switching is required to carry signals such as information with light. For this type of light control, an electro-light control method using an electric signal has been conventionally employed. However, the electro-optical control method has limitations such as a band limitation due to a CR time constant as in an electric circuit, a processing speed being limited due to a response speed of the element itself and a speed mismatch between an electric signal and an optical signal. In order to make full use of the broadband and high speed, which are the advantages of light, light-light control technology for controlling an optical signal with an optical signal becomes very important. An optical element manufactured by processing the two-photon absorption material of the present invention in response to this requirement utilizes an optical change such as transmittance, refractive index, absorption coefficient, etc. caused by irradiating light, and an electronic circuit. By modulating the intensity and frequency of light without using technology, it can be applied to optical switches in optical communication, optical exchange, optical computers, optical interconnections, and the like.
The optical limiting element of the present invention that utilizes the change in optical characteristics due to two-photon absorption provides an optically limiting element that is formed from a normal semiconductor material and an element that has a much higher response speed than those based on one-photon excitation. be able to. Further, because of the high sensitivity, it is possible to provide an optical limiting element excellent in signal characteristics with a high S / N ratio.

  FIG. 2 shows an optical control element (21) that optically switches signal light having a wavelength that can be excited by one photon by exciting the two-photon absorbing material of the present invention with control light having a wavelength that can be excited by two photons. It is an example. Although the form of the two-photon absorption material sandwiched between the protective layers is shown, this configuration does not limit the present invention.

  JP-A-8-320422 is known as a known document useful for understanding the light limiting element in the present invention. According to this, it is disclosed that a light refractive index material whose refractive index is changed by light irradiation is irradiated with light having a wavelength whose refractive index changes to perform focusing, and used as an optical waveguide for forming a refractive index distribution. . That is, a solid material dispersed in a material having a high two-photon absorption ability, a thin film, or a photocurable resin according to the present invention is arranged as an optical element, and is excited to an excited state by light of one wavelength (λ1). Further, by being excited from the state to another state with light of another wavelength (λ2), it becomes possible to design an optical waveguide using a refractive index change distribution according to the wavelength. Many of the two-photon absorption materials have fluorescence, and a fluorescent substance is disposed at one of the emission ends of the optical device or in the vicinity thereof, and excitation light (λ1) is emitted from the other, thereby exciting light (λ1). And a refractive index distribution can be formed by fluorescence (λ2). In this case, since the fluorescence is usually weaker than the excitation light, it is desirable to increase the sensitivity at the fluorescence wavelength. Examples of the fluorescent substance include those obtained by dispersing a fluorescent dye in a photocurable substance or various resins.

<Application to stereolithography materials>
A schematic diagram of a two-photon stereolithography apparatus is shown in FIG. 3 and described below.
A shutter (32), an ND filter (33) that controls the amount of light emitted from the near-infrared pulse laser light source (31) in time, and a light beam conversion system (34a) that controls the size of the light beam (light intensity) to a desired level. ) Is passed through a mirror scanner (34), then condensed into a photocurable resin liquid (39) using a condenser lens (35), and a laser spot is scanned to induce two-photon absorption. This is a two-photon micro stereolithography method in which the resin is cured only in the vicinity of the focal point to form an arbitrary three-dimensional structure. In the figure, reference numeral 36 denotes a Z stage, and reference numeral 38 denotes a computer monitor for controlling these devices.
The pulse laser beam is condensed by the lens (35), and a region with high photon density is formed in the vicinity of the condensing point. At this time, since the total number of photons passing through each cross section of the beam is constant, when the beam is scanned two-dimensionally within the focal plane, the total light intensity in each cross section is constant. However, since the probability of occurrence of two-photon absorption is proportional to the square of the light intensity, a region where the generation of two-photon absorption is high is formed only near the condensing point where the light intensity is high. Thus, by condensing the pulsed laser light with the lens and inducing two-photon absorption, it is possible to limit the light absorption near the condensing point and to cure the resin in a pinpoint manner. Since the condensing point can be freely moved in the photocurable resin liquid by the Z stage (36) and the galvanometer mirror, a desired three-dimensional workpiece can be freely formed in the photocurable resin liquid. .

The features of the two-photon stereolithography include the following items.
1) Processing resolution exceeding the diffraction limit: Processing resolution exceeding the diffraction limit of light can be realized by the nonlinearity of the two-photon absorption with respect to the light intensity.
2) Ultra-high speed modeling: When two-photon absorption is used, the photocurable resin does not cure in principle in the region other than the focal point. For this reason, the light intensity to be irradiated can be increased, and the beam scanning speed can be increased. For this reason, modeling speed can be improved about 10 times.
3) Three-dimensional processing: The photocurable resin is transparent to near-infrared light that induces two-photon absorption. Therefore, even when the focused light is condensed deeply into the resin, internal curing is possible. In the conventional SIH, when the beam is condensed deeply, the light intensity at the condensing point is reduced by light absorption, and the internal curing becomes difficult. In the present invention, these problems can be solved reliably. .
4) High yield: In the conventional method, there is a problem that the molded object is damaged or deformed due to the viscosity or surface tension of the resin. However, in this method, the problem is solved because the modeling is performed inside the resin.
5) Application to mass production: By using ultra-high speed modeling, it is possible to manufacture a large number of parts or movable mechanisms continuously in a short time.

  The photocurable resin for two-photon stereolithography is a resin having a characteristic of causing a two-photon polymerization reaction when irradiated with light and changing from a liquid to a solid. The main components are a resin component consisting of an oligomer and a reactive diluent and a photopolymerization initiator (including a photosensitizing material as required). An oligomer is a polymer having a degree of polymerization of about 2 to 20, and has a large number of reactive groups at its ends. Further, a reactive diluent is added to adjust the viscosity, curability and the like. When irradiated with light, the polymerization initiator or photosensitizing material absorbs this two-photon, and a reactive species is generated directly from the polymerization initiator or through the photosensitizing material, to the reactive group of the oligomer or reactive diluent. React and initiate polymerization. Thereafter, a chain polymerization reaction takes place between them to form a three-dimensional cross-link, and in a short time, a solid resin having a three-dimensional network structure is formed.

Photocurable resins are used in fields such as photocurable inks, photoadhesives, and layered three-dimensional modeling, and resins having various characteristics have been developed. Especially in layered 3D modeling (1) Reactivity is good,
(2) Deposition shrinkage during curing is small,
(3) Excellent mechanical properties after curing,
Etc. are important. These characteristics are equally important in this method. Therefore, resins developed for layered three-dimensional modeling that have two-photon absorption characteristics are also used as photocurable resins for two-photon photofabrication in this method. it can. As specific examples, acrylate-based and epoxy-based photocurable resins are often used, and urethane acrylate-based photocurable resins are particularly preferable.

  Japanese Patent Application Laid-Open No. 2005-134873 is a known document useful for understanding the optical modeling in the present invention. According to this, pulsed laser light is subjected to interference exposure on the surface of the photosensitive polymer film without passing through a mask. It is important that the pulsed laser beam is a pulsed laser beam in a wavelength region that allows the photosensitive polymer film to exhibit a photosensitive function. Therefore, the wavelength region of the pulsed laser light can be appropriately selected according to the type of the photosensitive polymer or the type of group or site that exhibits the photosensitive function in the photosensitive polymer. In particular, even if the wavelength of the pulsed laser light emitted from the light source is not in a wavelength region that causes the photosensitive polymer film to exhibit a photosensitive function, by utilizing a multiphoton absorption process upon irradiation with the pulsed laser light, The photosensitive polymer film can exhibit a photosensitive function. Specifically, when the pulsed laser light emitted from the light source is condensed and irradiated with the condensed pulsed laser light, multiphoton absorption (for example, two-photon absorption, three-photon absorption, four-photon absorption, Photosensitive polymer film even if the wavelength of the pulsed laser light emitted from the light source is not in a wavelength region that causes the photosensitive polymer film to perform a photosensitive function. Is substantially irradiated with a pulsed laser beam in a wavelength region that causes the photosensitive polymer film to exhibit a photosensitive function. As described above, the pulsed laser beam for the interference exposure may be substantially a pulsed laser beam in a wavelength region that causes the photosensitive polymer film to exhibit the photosensitive function, and the wavelength is appropriately selected depending on the irradiation conditions. can do. For example, the high-efficiency two-photon absorbing material of the present invention is used as a photosensitizing material, dispersed in an ultraviolet curable resin, etc., and a photosensitive solid, and only the focal spot is cured using the two-photon absorption ability of the photosensitive solid. It is possible to obtain an ultra-precise three-dimensional structure using

  The two-photon absorption material of the present invention can be used as a two-photon absorption polymerization initiator or a two-photon absorption photosensitizer. Compared to conventional two-photon absorption materials (two-photon absorption polymerization initiators or two-photon absorption photosensitizers), the two-photon absorption sensitivity is high, so high-speed modeling is possible, and the laser light source is small and inexpensive as an excitation light source. Can be used for practical applications that can be mass-produced.

<Application to two-photon fluorescence microscope using two-photon absorption material>
A two (multi) photon excitation laser scanning microscope collects and scans a near-infrared pulse laser on the sample surface, and detects fluorescence generated by excitation by two (multi) photon absorption there. It is a microscope to obtain

A schematic diagram of the basic configuration of the two-photon excitation laser scanning microscope is shown in FIG.
Laser light source (41) that emits sub-picosecond monochromatic coherent light pulses of near-infrared wavelength, light beam conversion optical system (42) that changes the light beam from the laser light source to a desired size, and light beam conversion optical system A scanning optical system (43) for condensing and scanning the light beam on the image plane of the objective lens, an objective lens system (44) for projecting the collected converted light beam onto the sample surface (45), and a dichroic mirror ( 46) and a photodetector (47).
The pulse laser beam passes through the dichroic mirror (46), is condensed by the light beam conversion optical system (42) and the objective lens system (44), and is focused on the sample surface (45). Fluorescence induced by two-photon absorption is generated in the photon-absorbing fluorescent material. The sample surface is scanned with a laser beam, the fluorescence intensity at each location is detected by a light detection device such as a light detector (47), and plotted on a computer based on the obtained position information. A fluorescent image is obtained. As the scanning mechanism, for example, a laser beam may be scanned using a movable mirror such as a galvanometer mirror, or a sample including a two-photon absorption material placed on a stage may be moved.
With such a configuration, it is possible to obtain high resolution in the optical axis direction by utilizing the nonlinear effect of two-photon absorption itself. In addition, if a confocal pinhole plate is used, higher resolution (both in-plane and in the optical axis direction) can be obtained.

  Fluorescent dyes for two-photon fluorescence microscopy are used by staining or dispersing specimens, and can be used not only for industrial applications but also for three-dimensional imaging microimaging of biological cells, etc. Compounds with absorption cross sections are desired

  JP-A-9-230246 is a known document useful for understanding the photon fluorescence microscope of the present invention. For example, a scanning fluorescent microscope includes a laser irradiation optical system that emits collimated light expanded to a desired size, and a substrate on which a plurality of condensing elements are formed. A beam splitter that transmits a long wavelength and reflects a short wavelength is disposed between the substrate on which the light condensing element is formed and the objective lens system, so as to coincide with the image position of the system. The surface is characterized by generating fluorescence by multiphoton absorption. With such a configuration, it is possible to obtain high resolution in the optical axis direction by utilizing the nonlinear effect of multiphoton absorption itself. In addition, if a confocal pinhole plate is used, higher resolution (both in-plane and in the optical axis direction) can be obtained. Such a two-photon optical element uses, as the optical element, a solid material dispersed in a material having a high two-photon absorption ability, a thin film, or a photocurable resin of the present invention, just like the above-described light control element. Is possible.

The two-photon absorption material of the present invention can be used as a two-photon absorption fluorescent material for a two-photon excitation laser scanning microscope. Compared to conventional two-photon absorption fluorescent materials, it has a large two-photon absorption cross-sectional area, so that it exhibits high two-photon absorption characteristics at a low concentration. Therefore, according to the present invention, not only a highly sensitive two-photon absorption material can be obtained, but there is no need to increase the intensity of light applied to the material, and deterioration and destruction of the material can be suppressed. The adverse effect on the properties of other components can also be reduced.
The two-photon absorption material of the present invention can be applied to various devices by itself or in a thin film mixed with various resins, or in bulk.
For example, in an optical disc, the thin film is in contact with a substrate, and the substrate material is polyethylene terephthalate, polycarbonate, polymethyl methacrylate, polyester, polyvinyl alcohol, glass or the like. In the case of stacking, the surface of the thin film is in contact with the intermediate layer (partition layer). Specific examples of the intermediate layer include polyolefins such as polypropylene and polyethylene, polyvinyl chloride, polyvinylidene chloride, polyvinyl alcohol, plastic films such as polyethylene terephthalate or cellophane film, and various photo-curing resins.

Next, even when applied to various optical devices and optical modeling devices, they are mixed with various resins or mixed with a photocurable resin.
Accordingly, the use requirement of the two-photon absorption material of the present invention is that the material is mixed with various resins or glass, or the interface of the two-photon absorption material layer is in contact with various resins or glass.
In other words, the two-photon absorption material of the present invention is in contact with various resins or glass at the micro level or the macro level.

The porphyrin derivative of the present invention will be described.
These porphyrin derivatives are large aromatic rings like porphyrins.
Porphyrin is a compound in which each pyrrole ring, which may have four substituents, is bonded by one carbon atom (meso position carbon atom) which may have a substituent. The specific porphyrin derivative has a structure in which the total number of carbon atoms that may have a substituent connecting four pyrrole rings is four, and at least one part has a structure in which the pyrrole ring is directly bonded without intervening carbon atoms. A compound.
When the number of carbon atoms that may have 4 substituents to which the pyrrole ring that may have substituents is bonded is represented by [a, b, c, d], the compound used in the present invention is [ a, b, c, d] = 4, and any of a, b, c, d is 0 ([1, 1, 1, 1] = 4 in the case of porphyrin).
According to this notation method, the compound of the chemical formula (1) according to claim 1 of the present invention is [2, 0, 2, 0], the compound of the chemical formula (2) is [2, 1, 1, 0], The compound of formula (3) is [2, 1, 0, 1], the compound of formula (4) is [3, 0, 1, 0], and the compound of formula (5) is [3, 0, 1, 0]. It is.
In the formulas (1) to (5), R _{1 to} R ₈ and X _{1 to} X ₄ are each independently a hydrogen atom, halogen atom, nitro group, cyano group, hydroxyl group, carboxyl group, substituted or unsubstituted alkyl. A group, a substituted or unsubstituted alkoxy group, a substituted or unsubstituted aryl group, a substituted or unsubstituted amino group, or a substituted or unsubstituted acyl group;
M is two hydrogen atoms, or a divalent, trivalent, or tetravalent metal atom which may have oxygen or halogen, or (OR ₉ ) p, (OSiR ₁₀ R ₁₁ R ₁₂ ) q, (OPOR ₁₃ R ₁₄ ) r represents a metal atom which may have (OCOR ₁₅ ) s. R _{9 to} R ₁₅ independently represent a hydrogen atom, a substituted or unsubstituted aliphatic or aromatic hydrocarbon group, and p 1, q 2, r 3 and s represent an integer of 0 to 2.

The second specific porphyrin derivative of the present invention is a porphyrin derivative represented by a structure in which four pyrrole rings which may have a substituent are bonded via a carbon atom or a nitrogen atom which may have a substituent. A compound in which at least one of the atoms which may have a substituent connecting the four pyrrole rings is a carbon atom and a nitrogen atom.
R _{1 to} R _{4 represent} a nitrogen atom or a carbon atom, and at least one of them represents a carbon atom and a nitrogen atom.

In formula (6), X _{1 to} X ₈ are each independently a hydrogen atom, a halogen atom, a nitro group, a cyano group, a hydroxyl group, a carboxyl group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkoxy group, A substituted or unsubstituted aryl group, a substituted or unsubstituted amino group, or a substituted or unsubstituted acyl group is represented.
M is two hydrogen atoms, or a divalent, trivalent, or tetravalent metal atom which may have oxygen or halogen, or (OR ₅ ) p, (OSiR ₆ R ₇ R ₈ ) q, (OPOR ₉ R ₁₀ ) r represents a metal atom which may have (OCOR ₁₁ ) s. R ₅ to R ₁₁ are independently a hydrogen atom, an aliphatic substituted or unsubstituted, an aromatic hydrocarbon group, p, q, r, s represents an integer of 0 to 2.

Examples of the unsubstituted alkyl group and the alkyl group in the unsubstituted alkoxy group include a linear or branched alkyl group. The substituted alkyl group and the substituted alkyl group in the substituted alkoxy group include 2 -Hydroxy-substituted alkyl groups such as hydroxyethyl group, 3-hydroxypropyl group, 4-hydroxybutyl group and 2-hydroxypropyl group; carboxy-substituted alkyl groups such as carboxymethyl group, 2-carboxyethyl group and 3-carboxypropyl group Cyano-substituted alkyl groups such as 2-cyanoethyl group and cyanomethyl group; amino-substituted alkyl groups such as 2-aminoethyl group; 2-chloroethyl group, 3-chloropropyl group, 2-chloropropyl group, 2,2,2- Halogen atom-substituted alkyl groups such as trifluoroethyl group; benzyl group, p-chloro Phenyl-substituted alkyl groups such as benzyl group and 2-phenylethyl group; 2-methoxyethyl group, 2-ethoxyethyl group, 2- (n) propoxyethyl group, 2- (iso) propoxyethyl group, 2- (n) Alkoxy-substituted alkyl groups such as butoxyethyl group, 2- (iso) butoxyethyl group, 2- (2-ethylhexyloxy) ethyl group, 3-methoxypropyl group, 4-methoxybutyl group, 2-methoxypropyl group; (2-methoxyethoxy) ethyl group, 2- (2-ethoxyethoxy) ethyl group, 2- (2- (n) propoxyethoxy) ethyl group, 2- (2- (iso) propoxyethoxy) ethyl group, 2- (2- (n) butoxyethoxy) ethyl group, 2- (2- (iso) butoxyethoxy) ethyl group, 2- {2- (2-ethylhexyl) Xoxy) alkoxyalkoxy-substituted alkyl groups such as ethoxy} ethyl group; substituted alkyl groups such as allyloxyethyl group, 2-phenoxyethyl group, 2-benzyloxyethyl group; 2-acetyloxyethyl group, 2-propionyloxyethyl group , 2- (n) butyryloxyethyl group, 2- (iso) butyryloxyethyl group, 2-trifluoroacetyloxyethyl group and other acyloxy-substituted alkyl groups; methoxycarbonylmethyl group, ethoxycarbonylmethyl group, (n ) Propoxycarbonylmethyl group, (iso) propoxycarbonylmethyl group, (n) butoxycarbonylmethyl group, (iso) butoxycarbonylmethyl group, 2-ethylhexyloxycarbonylmethyl group, benzyloxycarbonylmethyl group, furfuryloxycarbonyl Methyl group, tetrahydrofurfuryloxycarbonylmethyl group, 2-methoxycarbonylethyl group, 2-ethoxycarbonylethyl group, 2- (n) propoxycarbonylethyl group, 2- (iso) propoxycarbonylethyl group, 2- (n) Substituted or unsubstituted butoxycarbonylethyl group, 2- (iso) butoxycarbonylethyl group, 2- (2-ethylhexyloxycarbonyl) ethyl group, 2-benzyloxycarbonylethyl group, 2-furfuryloxycarbonylethyl group, etc. Alkoxycarbonyl-substituted alkyl group; 2-methoxycarbonyloxyethyl group, 2-ethoxycarbonyloxyethyl group, 2- (n) propoxycarbonyloxyethyl group, 2- (iso) propoxycarbonyloxyethyl group, 2- (n) butoxyca Substitution of bonyloxyethyl group, 2- (iso) butoxycarbonyloxyethyl group, 2- (2-ethylhexyloxycarbonyloxy) ethyl group, 2-benzyloxycarbonyloxyethyl group, 2-furfuryloxycarbonyloxyethyl group, etc. Or an unsubstituted alkoxycarbonyloxy-substituted alkyl group; a heterocyclic-substituted alkyl group such as a furfuryl group and a tetrahydrofurfuryl group; and the like.
Examples of the cycloalkyl group include a cyclopentyl group and a cyclohexyl group.

Specific examples of the alkyl group in the alkyl group and the alkoxy group include the following. In addition, these alkyl groups may be substituted with a substituent such as a halogen atom. Methyl group, ethyl group, n-propyl group, n-butyl group, isobutyl group, n-pentyl group, neopentyl group, isoamyl group, 2-methylbutyl group, n-hexyl group, 2-methylpentyl group, 3-methylpentyl Group, 4-methylpentyl group, 2-ethylbutyl group, n-heptyl group, 2-methylhexyl group, 3-methylhexyl group, 4-methylhexyl group, 5-methylhexyl group, 2-ethylpentyl group, 3- Ethylpentyl group, n-octyl group, 2-methylheptyl group, 3-methylheptyl group, 4-methylheptyl group, 5-methylheptyl group, 2-ethylhexyl group, 3-ethylhexyl group, n-nonyl group, n- Primary alkyl group such as decyl group, n-dodecyl group; isopropyl group, sec-butyl group, 1-ethylpropyl group, 1-methylbutyl group, , 2-dimethylpropyl group, 1-methylheptyl group, 1-ethylbutyl group, 1,3-dimethylbutyl group, 1,2-dimethylbutyl group, 1-ethyl-2-methylpropyl group, 1-methylhexyl group, 1-ethylheptyl group, 1-propylbutyl group, 1-isopropyl-2-methylpropyl group, 1-ethyl-2-methylbutyl group, 1-propyl-2-methylpropyl group, 1-methylheptyl group, 1-ethylhexyl Group, 1-propylpentyl group, 1-isopropylpentyl group, 1-isopropyl-2-methylbutyl group, 1-isopropyl-3-methylbutyl group, 1-methyloctyl group, 1-ethylheptyl group, 1-propylhexyl group Secondary alkyl groups such as 1-isobutyl-3-methylbutyl group; tert-butyl group, tert-hexyl group, Tertiary alkyl groups such as ert-amyl group and tert-octyl group; cyclohexyl group, 4-methylcyclohexyl group, 4-ethylcyclohexyl group, 4-tert-butylcyclohexyl group, 4- (2-ethylhexyl) cyclohexyl group, bornyl And cycloalkyl groups such as an isobornyl group and an adamantane group.
As the aryl group, phenyl group, methylphenyl group, dimethylphenyl group, trimethylphenyl group, ethylphenyl group, tert-butylphenyl group, di (tert-butyl) phenyl group, butylphenyl group, methoxyphenyl group, dimethoxyphenyl group , Trimethoxyphenyl group, butoxyphenyl group and the like, and these aryl groups may be substituted with a substituent such as halogen.

In the chemical formulas (1) to (5), M is two hydrogen atoms, or a divalent, trivalent, or tetravalent metal atom that may have oxygen or halogen, or (OR ₉ ) p, (OSiR). ₁₀ R ₁₁ R ₁₂ ) q, (OPOR ₁₃ R ₁₄ ) r, (OCOR ₁₅ ) s represents a metal atom which may have. R _{9 to} R ₁₅ independently represent a hydrogen atom, a substituted or unsubstituted aliphatic or aromatic hydrocarbon group, and p 1, q 2, r 3 and s represent an integer of 0 to 2.
Specifically, as M, Ib group, IIa group, IIb group, IIIa group, IVa group, IVb group, Vb group, VIb group, VIIb group, VIII metal, oxides of these metals, There are halides or hydroxides of these metals, and there are those having the above-mentioned substituents

Examples of the metal include Cu, Zn, Mg, Al, Ge, Ti, Sn, Pb, Cr, Mo, Mn, Fe, Co, Ni, In, Pt, and Pd. As the oxide, TiO, VO and the like, halides include AlCl, GeCl ₂ , SiCl ₂ , FeCl, SnCl ₂ , InCl and the like, and hydroxides include Al (OH), Si (OH) ₂ , Ge (OH) ₂ , Sn (OH) _{2 and the} like.
Further, when the metal has a substituent, the metal includes Al, Ti, Si, Ge, Sn, etc., and the substituent includes an aryloxyl group, an alkoxyl group, a trialkylsiloxyl group, and a triarylsiloxyl. Group, trialkoxysiloxyl group, triaryloxysiloxyl group, trityloxyl group or acyloxyl group.

  Examples of porphyrin derivatives used in the present invention are shown below.

  These porphyrin isomers themselves and their synthesis methods are known in the art, for example, by using the method described in Angew. Chem. Int. Ed. Engl. 1993, 32, No. 11, pp. 1600-1604. can do.

  EXAMPLES Hereinafter, the present invention will be described more specifically with reference to examples. However, the present invention is not limited by these examples unless it exceeds the gist.

(Example 1)
A dimethylformamide solution of the above porphyrin derivative example [Chemical Formula 7] was prepared, and the two-photon absorption cross section was measured by the following two-photon absorption cross-section evaluation method.
The measurement results of the two-photon absorption cross section are shown in Table 2, and the two-photon absorption spectrum is shown in FIG.

(Examples 2 to 5)
Similarly, the two-photon absorption cross sections of [Chemical Formula 10], [Chemical Formula 15], [Chemical Formula 28], and [Chemical Formula 30] were measured.
The measurement result of the two-photon absorption cross section is shown in Table 2, and the two-photon absorption spectrum is shown in FIGS.

(Examples 6 to 10)
Similarly, the two-photon absorption cross sections of [Chemical 9], [Chemical 12], [Chemical 24], [Chemical 32], and [Chemical 36] were measured.
Table 2 shows the measurement results of the two-photon absorption cross section.

(Comparative Example 1)
A tetrahydrofuran solution of the compound represented by the following formula (ratio 1) was prepared, and the two-photon absorption cross section was measured by the following two-photon absorption cross-section evaluation method.
The measurement results are shown in Table 2.

(Comparative Example 2)
Dimethylformamide of a compound represented by (ratio 2), which is a typical typical porphyrin structure, was prepared, and its two-photon absorption cross section was measured in the same manner.
The measurement results are shown in Table 2.

[Evaluation method of two-photon absorption cross section]
A schematic diagram of the measurement system is shown in FIG.
Measurement light source: Femtosecond titanium sapphire laser Wavelength: 720-920nm Pulse width: 100fs
Repeat: 80MHz Optical power: 800mW
Measurement method: Z scan method Light source wavelength: 780-900nm Cuvette inner diameter: 1mm
Measurement optical power: Approximately 500mW Repeat frequency: 80MHz
Condensing lens: f = 75mm Condensing diameter: ~ 40μm
A quartz cell filled with the sample solution was placed in the collected optical path portion, and Z-scan measurement was performed by moving the position along the optical path.

  The transmittance was measured, and the nonlinear absorption coefficient was determined from the result by the following theoretical formula (I).

（上記式中、Ｔは透過率（％）、Ｉ0は励起光密度［ＧＷ／ｃｍ^２］、Ｌ0は試料セル長［ｃｍ］、βは非線形吸収係数［ｃｍ／ＧＷ］を示す。）

(In the above formula, T represents transmittance (%), I 0 represents excitation light density [GW / cm ² ], L 0 represents sample cell length [cm], and β represents nonlinear absorption coefficient [cm / GW].)

From this nonlinear absorption coefficient, a two-photon absorption cross-sectional area σ2 was determined by the following formula (II).
(The unit of σ2 is 1GM = 1 × 10 ⁻⁵⁰ cm ⁴ · s · photon ⁻¹ .)

（上記式中、ｈはプランク定数［Ｊ・ｓ］、νは入射レーザ光の振動数［ｓ^−１］、ＮAはアボガドロ数、Ｃは溶液濃度［ｍｏｌ／Ｌ］を示す。）

(In the above formula, h represents Planck's constant [J · s], ν represents the frequency [s ⁻¹ ] of incident laser light, NA represents the Avogadro number, and C represents the solution concentration [mol / L].)

<Evaluation results>

■ 二光子吸収の遷移効率が従来材料に比較し、二桁高い二光子吸収化合物が得られた。
■ 通常のポルフィリン構造では二光子吸収能を示さないが、本発明のポルフィリン誘導体では大きな二光子吸収断面積が得られる。
■ 本発明の優れた二光子吸収特性を有する化合物を適用すれば、より高品位の三次元メモリ材料、光制限材料、光造形用光硬化樹脂の硬化材料、光化学療法用材料、二光子蛍光顕微鏡用蛍光色素材料が実現できる。

■ A two-photon absorption compound with a transition efficiency of two-photon absorption that is two orders of magnitude higher than conventional materials was obtained.
(2) Although the ordinary porphyrin structure does not show the two-photon absorption ability, the porphyrin derivative of the present invention provides a large two-photon absorption cross section.
■ If the compound having excellent two-photon absorption characteristics of the present invention is applied, a higher-quality three-dimensional memory material, light-limiting material, photocuring resin curing material for photofabrication, photochemotherapy material, two-photon fluorescence microscope Fluorescent dye material can be realized.

(A) is a schematic diagram of a recording / reproducing system of a three-dimensional multilayer optical memory, and (b) is a schematic sectional view of a recording medium. It is the figure which showed an example of the optical control element which optically switches the signal light of the wavelength which can carry out one-photon excitation by carrying out the two-photon excitation of the two-photon absorption material of this invention with the control light of the wavelength which can carry out two-photon excitation. . It is the schematic of the apparatus of the two-photon stereolithography. It is the schematic of the basic composition of a two-photon excitation laser scanning microscope. 1 is a schematic diagram of a measurement system used in the present invention. It is the figure which showed the two-photon absorption spectrum used by [Chemical Formula 7] of this invention. It is the figure which showed the two-photon absorption spectrum used by [Chemical Formula 10] of this invention. It is the figure which showed the two-photon absorption spectrum used by [Chemical 15] of this invention. It is the figure which showed the two-photon absorption spectrum used by [Chemical Formula 28] of this invention. It is the figure which showed the two-photon absorption spectrum used by [Chemical 30] of this invention.

Explanation of symbols

1 Support (substrate)
2 Substrate (protective layer)
3 Recording layer 4 Intermediate layer 5 Single light beam for recording 6 Single light beam for reproduction (reading) 7 Two-dimensional detector 21 Light control element 30 Light modeling object 31 Near-red having transparency to photocurable resin liquid Light source 32 of external pulsed laser light Shutter 33 for controlling excess light temporally ND filter 34 Mirror scanner 34a Light flux conversion system 35 for controlling the magnitude of light flux (light intensity) to a desired level Lens 36 as a focusing means Z stage 37 monitor 38 computer 39 photocurable resin liquid 41 laser light source 42 light beam conversion optical system 43 scanning optical system 44 objective lens system 45 sample surface 46 dichroic mirror 47 photodetector

Claims (18)

In a porphyrin derivative having a structure in which four pyrrole rings which may have a substituent are bonded to each other via a carbon atom which may have a substituent, or have a substituent which connects the four pyrrole rings A two-photon absorption material comprising a porphyrin derivative in which the total number of carbon atoms may be four and at least one pyrrole ring is directly bonded without carbon atoms. The two-photon absorption material according to claim 1, comprising a porphyrin derivative represented by the following formula (1).

In the formula, R _{1 to} R ₈ and X _{1 to} X ₄ are each independently a hydrogen atom, a halogen atom, a nitro group, a cyano group, a hydroxyl group, a carboxyl group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkoxy group. Represents a substituted or unsubstituted aryl group, a substituted or unsubstituted amino group, or a substituted or unsubstituted acyl group.
M is two hydrogen atoms, or a divalent, trivalent, or tetravalent metal atom which may have oxygen or halogen, or (OR ₉ ) p, (OSiR ₁₀ R ₁₁ R ₁₂ ) q, (OPOR ₁₃ R ₁₄ ) r represents a metal atom which may have (OCOR ₁₅ ) s. R _{9 to} R ₁₅ independently represent a hydrogen atom, a substituted or unsubstituted aliphatic or aromatic hydrocarbon group, and p 1, q 2, r 3 and s represent an integer of 0 to 2. It consists of a porphyrin derivative shown by following formula (2), The two-photon absorption material of Claim 1 characterized by the above-mentioned.

In the formula, R _{1 to} R ₈ and X _{1 to} X ₄ are each independently a hydrogen atom, a halogen atom, a nitro group, a cyano group, a hydroxyl group, a carboxyl group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkoxy group. Represents a substituted or unsubstituted aryl group, a substituted or unsubstituted amino group, or a substituted or unsubstituted acyl group.
M is two hydrogen atoms, or a divalent, trivalent, or tetravalent metal atom which may have oxygen or halogen, or (OR ₉ ) p, (OSiR ₁₀ R ₁₁ R ₁₂ ) q, (OPOR ₁₃ R ₁₄ ) r represents a metal atom which may have (OCOR ₁₅ ) s. R _{9 to} R ₁₅ independently represent a hydrogen atom, a substituted or unsubstituted aliphatic or aromatic hydrocarbon group, and p 1, q 2, r 3 and s represent an integer of 0 to 2. It consists of a porphyrin derivative shown by following formula (3), The two-photon absorption material of Claim 1 characterized by the above-mentioned.

In the formula, R _{1 to} R ₈ and X _{1 to} X ₄ are each independently a hydrogen atom, a halogen atom, a nitro group, a cyano group, a hydroxyl group, a carboxyl group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkoxy group. Represents a substituted or unsubstituted aryl group, a substituted or unsubstituted amino group, or a substituted or unsubstituted acyl group.
M is two hydrogen atoms, or a divalent, trivalent, or tetravalent metal atom which may have oxygen or halogen, or (OR ₉ ) p, (OSiR ₁₀ R ₁₁ R ₁₂ ) q, (OPOR ₁₃ R ₁₄ ) r represents a metal atom which may have (OCOR ₁₅ ) s. R _{9 to} R ₁₅ independently represent a hydrogen atom, a substituted or unsubstituted aliphatic or aromatic hydrocarbon group, and p 1, q 2, r 3 and s represent an integer of 0 to 2. It consists of a porphyrin derivative shown by following formula (4), The two-photon absorption material of Claim 1 characterized by the above-mentioned.

In the formula, R _{1 to} R ₈ and X _{1 to} X ₄ are each independently a hydrogen atom, a halogen atom, a nitro group, a cyano group, a hydroxyl group, a carboxyl group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkoxy group. Represents a substituted or unsubstituted aryl group, a substituted or unsubstituted amino group, or a substituted or unsubstituted acyl group.
M is two hydrogen atoms, or a divalent, trivalent, or tetravalent metal atom which may have oxygen or halogen, or (OR ₉ ) p, (OSiR ₁₀ R ₁₁ R ₁₂ ) q, (OPOR ₁₃ R ₁₄ ) r represents a metal atom which may have (OCOR ₁₅ ) s. R _{9 to} R ₁₅ independently represent a hydrogen atom, a substituted or unsubstituted aliphatic or aromatic hydrocarbon group, and p 1, q 2, r 3 and s represent an integer of 0 to 2. It consists of a porphyrin derivative shown by following formula (5), The two-photon absorption material of Claim 1 characterized by the above-mentioned.

In the formula, R _{1 to} R ₈ and X _{1 to} X ₄ are each independently a hydrogen atom, a halogen atom, a nitro group, a cyano group, a hydroxyl group, a carboxyl group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkoxy group. Represents a substituted or unsubstituted aryl group, a substituted or unsubstituted amino group, or a substituted or unsubstituted acyl group.
M is two hydrogen atoms, or a divalent, trivalent, or tetravalent metal atom which may have oxygen or halogen, or (OR ₉ ) p, (OSiR ₁₀ R ₁₁ R ₁₂ ) q, (OPOR ₁₃ R ₁₄ ) r represents a metal atom which may have (OCOR ₁₅ ) s. R _{9 to} R ₁₅ independently represent a hydrogen atom, a substituted or unsubstituted aliphatic or aromatic hydrocarbon group, and p 1, q 2, r 3 and s represent an integer of 0 to 2. Two-photon absorption material comprising a porphyrin derivative represented by the following formula (6) having a structure in which four pyrrole rings which may have a substituent are bonded via a carbon atom or a nitrogen atom which may have a substituent A two-photon absorption material comprising a porphyrin derivative in which at least one of the atoms which may have a substituent connecting the four pyrrole rings is a carbon atom and a nitrogen atom.

R _{1 to} R ₄ represent a nitrogen atom or a carbon atom, and at least one of them represents a nitrogen atom.
X _{1 to} X ₈ are each independently a hydrogen atom, a halogen atom, a nitro group, a cyano group, a hydroxyl group, a carboxyl group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkoxy group, a substituted or unsubstituted aryl group, A substituted or unsubstituted amino group or a substituted or unsubstituted acyl group is represented.
M is two hydrogen atoms, or a divalent, trivalent, or tetravalent metal atom which may have oxygen or halogen, or (OR ₅ ) p, (OSiR ₆ R ₇ R ₈ ) q, (OPOR ₉ R ₁₀ ) r represents a metal atom which may have (OCOR ₁₁ ) s. R ₅ to R ₁₁ are independently a hydrogen atom, an aliphatic substituted or unsubstituted, an aromatic hydrocarbon group, p, q, r, s represents an integer of 0 to 2. 8. The two-photon according to claim 7, wherein _one of R _{1 to} R ₄ of the porphyrin derivative represented by the formula (6) is a monoazaporphyrin compound in which one is a nitrogen atom and the remainder is a carbon atom. Absorbing material. 8. The two-photon according to claim 7, wherein two of R _{1 to} R ₄ of the porphyrin derivative represented by the formula (6) are diazaporphyrin compounds in which two are nitrogen atoms and the rest are carbon atoms. Absorbing material. The two-photon absorption material according to claim 7, comprising a diazaporphyrin compound in which R ₁ and R ₃ of the porphyrin derivative represented by the formula (6) are nitrogen atoms and R ₂ and R ₄ are carbon atoms. A three-dimensional memory material comprising the compound according to claim 1. The light limiting material containing the compound in any one of Claims 1 thru | or 10. The hardening material of the photocurable resin for optical modeling containing the compound in any one of Claims 1 thru | or 10. A fluorescent dye material for a two-photon fluorescence microscope, comprising the compound according to claim 1. A three-dimensional recording medium comprising at least one type of the compound according to any one of claims 1 to 10 in a recording layer and capable of recording and reproducing in the depth direction with respect to incident light. The optical limiting element containing at least 1 sort (s) of the compound in any one of Claims 1 thru | or 10. An optical modeling system comprising at least one compound according to any one of claims 1 to 10. The two-photon fluorescence microscope apparatus containing at least 1 sort (s) of the compound in any one of Claims 1 thru | or 10.

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