Abstract: The present invention provides: a mononuclear metal complex that has high catalytic activity and can be used as a hydrogenation reduction catalyst that allows efficient hydrogenation reduction of a substance to be reduced; a tautomer or stereoisomer thereof; or a salt thereof. Provided is the mononuclear metal complex represented by the following formula (1), a tautomer or stereoisomer thereof; or a salt thereof. In the formula (1), Ar1 is an aromatic anionic ligand or an aromatic ligand, or is not present, Ar2 is a ligand having aromaticity and may or may not be substituted, and when Ar2 is substituted, the number of substituents may be one or more, M is an atom or ion of a transition metal, A1 and A2 are both carbon atoms, or one of A1 and A2 is a carbon atom and the other is a nitrogen atom, Y is an anionic group or a cationic group, or is not present, L is any ligand or is not present, and m is a positive integer, 0, or a negative integer.

Abstract: The present invention provides a method and a kit for producing hydrogen peroxide, capable of producing hydrogen peroxide at low cost. The present invention further provides a fuel battery capable of utilizing hydrogen peroxide as a low-cost fuel. The method for producing hydrogen peroxide of the present invention includes a hydrogen peroxide generation step of irradiating a reaction system containing water, a water oxidation catalyst, a transition metal complex, and oxygen (O2) with light to generate hydrogen peroxide. The kit of the present invention includes the transition metal complex and the water oxidation catalyst that are used in the method for producing hydrogen peroxide of the present invention. The fuel battery of the present invention includes a fuel container and a fuel battery cell, and the fuel container contains the transition metal complex and the water oxidation catalyst that are used in the method for producing hydrogen peroxide of the present invention.

Abstract: Long-lived charge separation is attained with high efficiency by using a supramolecular complex utilizing pi-pi interaction. A supramolecular complex is formed by pi-pi interaction between extended viologen, the extended viologen having heteroaryls coupled together by a linking group with pi-electron conjugated system, and porphyrin. As a result of study of photoelectron transfer reaction, it has been found that within the supramolecular complex, efficient electron transfer occurs from the singlet excited state of porphyrin to the extended viologen, thereby obtaining a charge separation condition of extremely long lifetime exceeding 1 millisecond.

Abstract: The present invention provides: a mononuclear metal complex that has high catalytic activity and can be used as a hydrogenation reduction catalyst that allows efficient hydrogenation reduction of a substance to be reduced; a tautomer or stereoisomer thereof; or a salt thereof. Provided is the mononuclear metal complex represented by the following formula (1), a tautomer or stereoisomer thereof; or a salt thereof. In the formula (1), Ar1 is an aromatic anionic ligand or an aromatic ligand, or is not present, Ar2 is a ligand having aromaticity and may or may not be substituted, and when Ar2 is substituted, the number of substituents may be one or more, M is an atom or ion of a transition metal, A1 and A2 are both carbon atoms, or one of A1 and A2 is a carbon atom and the other is a nitrogen atom, Y is an anionic group or a cationic group, or is not present, L is any ligand or is not present, and m is a positive integer, 0, or a negative integer.

Abstract: The present invention provides a process for producing an oxidation reaction product of an aromatic compound, having excellent environmental load reduction performance, cost reduction performance, etc. Provided is a process for producing an oxidation reaction product of a raw material aromatic compound by reacting the raw material aromatic compound with an oxidizing agent. The process further uses an electron donor-acceptor linked molecule. The process includes the step of: reacting the electron donor-acceptor linked molecule in an electron-transfer state, the oxidizing agent, and the raw material aromatic compound, thereby generating an oxidation reaction product resulting from oxidation of the raw material aromatic compound.

Abstract: An electron donor-acceptor dyad is provided that can provide a charge-separated state with longevity and not only high oxidizing power but also high reducing power. A compound of the present invention is a quinolinium ion derivative represented by the following formula (I), a stereoisomer or tautomer thereof, or a salt thereof: where R1 is a hydrogen atom or an alkyl group, and Ar1 to Ar3 each are a hydrogen atom or an electron-donating group. The compound of the present invention has the above-mentioned structure and therefore can provide a charge-separated state with longevity and not only high oxidizing power but also high reducing power and can be used for various products such as photocatalysts, photosensitizers, dyes, oxidants, reductants, dye-sensitized solar cells, and organic EL devices.

Abstract: A catalyst for the decomposition of formic acid including a dinuclear metal complex represented by a formula (1) below, a tautomer or stereoisomer thereof, or any of their salts, where M1 and M2 are transition metals; Ar is a ligand having aromaticity and may be unsubstituted or substituted; R1 to R27 are each independently a hydrogen atom, an alkyl group, or the like, or R15 and R16 may together form a —CH?CH—, where Hs in the —CH?CH— may be each independently replaced by an alkyl group or the like, and R23 and R24 may together form a —CH?CH—, where Hs in the —CH?CH— may be each independently replaced by an alkyl group or the like; L is an arbitrary ligand or is absent; and m is a positive integer, 0, or a negative integer.

Abstract: A method of producing of the present invention is a method of producing a cup-shaped nanocarbon formed of graphene sheets. A nanocarbon molecule has a cup shape, a bottom surface and an upper surface thereof being opened. The method of producing of the present invention includes the following processes (A) and (B). (A) a process of preparing a cup-stacked carbon nanotube, in which cup-shaped nanocarbons having openings at the bottom surface and the upper surface are laminated; and (B) a process of separating the cup-shaped nanocarbon from the cup-stacked carbon nanotube by treating the cup-stacked carbon nanotube with a reducing agent.

Abstract: The present invention provides a catalyst for the decomposition of formic acid including a dinuclear metal complex represented by a formula (1) below, a tautomer or stereoisomer thereof, or any of their salts, where M1 and M2 are transition metals and may be the same or different; Ar is a ligand having aromaticity and may be unsubstituted or substituted by one or more substituents; R1 to R27 are each independently a hydrogen atom, an alkyl group, or the like, or R15 and R16 may together form a —CH?CH—, where Hs in the —CH?CH— may be each independently replaced by an alkyl group or the like, and R23 and R24 may together form a —CH?CH—, where Hs in the —CH?CH— may be each independently replaced by an alkyl group or the like; L is an arbitrary ligand or is absent; and m is a positive integer, 0, or a negative integer.

Abstract: An electron donor-acceptor dyad is provided that can provide a charge-separated state with longevity and not only high oxidizing power but also high reducing power. A compound of the present invention is a quinolinium ion derivative represented by the following formula (I), a stereoisomer or tautomer thereof, or a salt thereof: where R1 is a hydrogen atom or an alkyl group, and Ar1 to Ar3 each are a hydrogen atom or an electron-donating group. The compound of the present invention has the above-mentioned structure and therefore can provide a charge-separated state with longevity and not only high oxidizing power but also high reducing power and can be used for various products such as photocatalysts, photosensitizers, dyes, oxidants, reductants, dye-sensitized solar cells, and organic EL devices.

Abstract: A photoacid generator comprising a metal hydride complex represented by the formula (I): wherein X represents a metal atom. The iridium hydride complex of the present invention can be used as an acid generator for chemically-amplified photoresists or color filters for liquid crystal, and in addition, can be widely applied in photographic-related or printing-related fields, or the like.

Abstract: Long-lived charge separation is attained with high efficiency by using a supramolecular complex utilizing pi-pi interaction. A supramolecular complex is formed by pi-pi interaction between extended viologen, the extended viologen having heteroaryls coupled together by a linking group with pi-electron conjugated system, and porphyrin. As a result of study of photoelectron transfer reaction, it has been found that within the supramolecular complex, efficient electron transfer occurs from the singlet excited state of porphyrin to the extended viologen, thereby obtaining a charge separation condition of extremely long lifetime exceeding 1 millisecond.

Abstract: An ionization chamber of an analytical apparatus (10) in which high concentration test sample ions are evaporated is provided with an ion introduction control means (8) to control the quantity of the test sample ions introduced to an ion attracting electrode (9). Therefore, an analytical apparatus can be provided that is capable of substantially simultaneous mass spectrometry and absorption, emission, and scattering spectroscopy. The apparatus also includes: a low temperature bath (106) which cools the test sample solution before it is introduced to the sprayer (104); and a cooling gas introduction tube (108), constructed separately from the sprayer, which cools the sprayer and the test sample solution introduced to the sprayer (104). The inclusion enables effective restriction of test sample heating upon high voltage application.

Abstract: A light energy conversion system having a multiplicity of artificial photosynthetic reaction centers and exhibiting a high light-harvesting capability and charge separation capability, constructed by the use of a zinc porphyrin dendrimer supramolecular complex formed by the use of a coordinate bond. Using a zinc porphyrin dendrimer as a spherical zinc porphyrin oligomer, a supramolecule with pyridylnaphthalenediimide was constructed. With respect to the zinc porphyrin dendrimer/pyridylnaphthalenediimide supramolecule, when photoexcitation of the zinc porphyrin was realized, a charge-separated state was generated by photoinduced electron transfer and the lifetime thereof was strikingly long, up to 830 microseconds.

Abstract: Disclosed is a light sensitive planographic printing plate material comprising a support and provided thereon, a light sensitive layer containing a polymerization initiator, a polymerizable ethylenically unsaturated compound, a polymeric binder, and a sensitizing dye, wherein the sensitizing dye is represented by formula (1),

Abstract: A photoacid generator comprising a metal hydride complex represented by the formula (I): wherein X represents a metal atom. The iridium hydride complex of the present invention can be used as an acid generator for chemically-amplified photoresists or color filters for liquid crystal, and in addition, can be widely applied in photographic-related or printing-related fields, or the like.

Abstract: To provide a photocatalyst having a photocatalytic activity far higher than that of flavin, and being excellent in stability as a catalyst. A photocatalyst comprising a flavin-rare earth metal ion complex.

Abstract: To provide a photocatalyst having a photocatalytic activity far higher than that of flavin, and being excellent in stability as a catalyst. A photocatalyst comprising a flavin-rare earth metal ion complex.

Abstract: The present invention relates to a catalyst useful for a photooxidation reaction and also relates to a novel process for producing aldehydes, particularly aromatic aldehydes, which are useful as an intermediate for the production of agrochemical and medical preparations. The catalyst is particularly suitable for the oxidation of a methyl group difficult to oxidize. A photooxidation catalyst according to the invention is a halogenated aromatic nitrile represented by the following formula (1): (wherein X represents a chlorine atom or a fluorine atom, m represents an integer of 1 to 5, n represents an integer of 1 to 5, m+n≦6, and when n is 2 or more, Xs may be the same or different).

Abstract: The present invention relates to a catalyst useful for a photooxidation reaction and also relates to a novel process for producing aldehydes, particularly aromatic aldehydes, which are useful as an intermediate for the production of agrochemical and medical preparations. The catalyst is particularly suitable for the oxidation of a methyl group difficult to oxidize.