The present invention relates generally to the field of organic chemistry and particularly to the organic compound for organic photovoltaic devices. More specifically, the present invention is related to the organic compounds and the organic photovoltaic devices based on these compounds. In one preferred embodiment, this organic compound has the general structural formula

##STR00001##

where Het.sub.1 is a predominantly planar polycyclic molecular system of first type; Het.sub.2 is a predominantly planar polycyclic molecular system of second type; A is a bridging group providing a lateral bond of the molecular system Het.sub.1 with the molecular system Het.sub.2 via strong chemical bonds; n is 1, 2, 3, 4, 5, 6, 7 or 8; B1 and B2 are binding groups; i is 0, 1, 2, 3, 4, 5, 6, 7 or 8; j is 0, 1, 2, 3, 4, 5, 6, 7 or 8; S1 and S2 are groups providing solubility of the organic compound; k is 0, 1, 2, 3, 4, 5, 6, 7 or 8; m is 0, 1, 2, 3, 4, 5, 6, 7 or 8; D1 and D2 are substituents independently selected from a list comprising CH.sub.3, C.sub.2H.sub.5, NO.sub.2, Cl, Br, F, CF.sub.3, CN, OH, OCH.sub.3, OC.sub.2H.sub.5, OCOCH.sub.3, OCN, SCNNH.sub.2, NHCOCH.sub.3, C.sub.2Si(CH.sub.3).sub.3, and CONH.sub.2; y is 0, 1, 2, 3, 4, 5, 6, 7 or 8; and z is 0, 1, 2, 3, 4, 5, 6, 7 or 8. Said organic compound absorbs electromagnetic radiation in at least one predetermined spectral subrange within a wavelength range from 400 to 3000 nm and is capable to form supramolecules. The molecular system Het.sub.1, the bridging group A, and the molecular system Het.sub.2 are capable to form a donor-bridge-acceptor system providing dissociation of excited electron-hole pairs. A solution of the organic compound or its salt is capable of forming a solid photovoltaic layer on a substrate.

The present invention relates generally to the field of organic chemistry and particularly to the organic compound for organic photovoltaic devices. More specifically, the present invention is related to the organic compounds and the organic photovoltaic devices based on these compounds. In one preferred embodiment, this organic compound has the general structural formula

##STR00001##

where Het.sub.1 is a predominantly planar polycyclic molecular system of first type; Het.sub.2 is a predominantly planar polycyclic molecular system of second type; A is a bridging group providing a lateral bond of the molecular system Het.sub.1 with the molecular system Het.sub.2 via strong chemical bonds; n is 1, 2, 3, 4, 5, 6, 7 or 8; B1 and B2 are binding groups; i is 0, 1, 2, 3, 4, 5, 6, 7 or 8; j is 0, 1, 2, 3, 4, 5, 6, 7 or 8; S1 and S2 are groups providing solubility of the organic compound; k is 0, 1, 2, 3, 4, 5, 6, 7 or 8; m is 0, 1, 2, 3, 4, 5, 6, 7 or 8; D1 and D2 are substituents independently selected from a list comprising CH.sub.3, C.sub.2H.sub.5, NO.sub.2, Cl, Br, F, CF.sub.3, CN, OH, OCH.sub.3, OC.sub.2H.sub.5, OCOCH.sub.3, OCN, SCNNH.sub.2, NHCOCH.sub.3, C.sub.2Si(CH.sub.3).sub.3, and CONH.sub.2; y is 0, 1, 2, 3, 4, 5, 6, 7 or 8; and z is 0, 1, 2, 3, 4, 5, 6, 7 or 8. Said organic compound absorbs electromagnetic radiation in at least one predetermined spectral subrange within a wavelength range from 400 to 3000 nm and is capable to form supramolecules. The molecular system Het.sub.1, the bridging group A, and the molecular system Het.sub.2 are capable to form a donor-bridge-acceptor system providing dissociation of excited electron-hole pairs. A solution of the organic compound or its salt is capable of forming a solid photovoltaic layer on a substrate.

A photoelectric conversion element, including: an electron transporting material; and a porphyrin compound represented by General Formula (1) or (2), wherein the electron transporting material is coated with the porphyrin compound: ##STR00001## where R.sub.1 and R.sub.2 each independently denote an aromatic hydrocarbon group which has 6-20 carbon atoms and may have an alkyl or alkoxy group as substituent, R.sub.1 and R.sub.2 may be bonded to form ring structure A1, X denotes a monovalent group expressed by Structural Formula (I), (II) or (III), and Y denotes a phenyl group which may have an alkyl or alkoxy group as a substituent, ##STR00002## where R denotes an aromatic hydrocarbon group which has 6-20 carbon atoms and may have an alkyl or alkoxy group as substituent, X denotes a monovalent group expressed by Structural Formula (I), (II) or (III), and Y denotes a phenyl group which may have an alkyl or alkoxy group as substituent, ##STR00003##

A photoelectric conversion element, including: an electron transporting material; and a porphyrin compound represented by General Formula (1) or (2), wherein the electron transporting material is coated with the porphyrin compound: ##STR00001## where R.sub.1 and R.sub.2 each independently denote an aromatic hydrocarbon group which has 6-20 carbon atoms and may have an alkyl or alkoxy group as substituent, R.sub.1 and R.sub.2 may be bonded to form ring structure A1, X denotes a monovalent group expressed by Structural Formula (I), (II) or (III), and Y denotes a phenyl group which may have an alkyl or alkoxy group as a substituent, ##STR00002## where R denotes an aromatic hydrocarbon group which has 6-20 carbon atoms and may have an alkyl or alkoxy group as substituent, X denotes a monovalent group expressed by Structural Formula (I), (II) or (III), and Y denotes a phenyl group which may have an alkyl or alkoxy group as substituent, ##STR00003##

The invention relates to dyes for dye-sensitized solar cells, and in particular, to perylene functionalized porphyrin dyes for dye-sensitized solar cells. The invention further relates to a dye molecule comprising perylene functionalized porphyrin moiety.

The invention relates to dyes for dye-sensitized solar cells, and in particular, to perylene functionalized porphyrin dyes for dye-sensitized solar cells. The invention further relates to a dye molecule comprising perylene functionalized porphyrin moiety.

A compound that can be used as a donor material in organic photovoltaic devices comprising a non-activated porphyrin fused with one or more non-activated polycyclic aromatic rings or one or more non-activated heterocyclic rings can be obtained by a thermal fusion process. By heating the reaction mixture of non-activated porphyrins with non-activated polycyclic aromatic rings or heterocyclic rings to a fusion temperature and holding for a predetermined time, fusion of one or more polycyclic rings or heterocyclic rings to the non-activated porphyrin core in meso, fashion is achieved resulting in hybrid structures containing a distorted porphyrin ring with annulated aromatic rings. The porphyrin core can be olygoporphyrins.

A compound that can be used as a donor material in organic photovoltaic devices comprising a non-activated porphyrin fused with one or more non-activated polycyclic aromatic rings or one or more non-activated heterocyclic rings can be obtained by a thermal fusion process. By heating the reaction mixture of non-activated porphyrins with non-activated polycyclic aromatic rings or heterocyclic rings to a fusion temperature and holding for a predetermined time, fusion of one or more polycyclic rings or heterocyclic rings to the non-activated porphyrin core in meso, fashion is achieved resulting in hybrid structures containing a distorted porphyrin ring with annulated aromatic rings. The porphyrin core can be olygoporphyrins.

Provided is a pigment multimer whereby a pattern can be appropriately formed during formation of a pattern. Further, provided are a coloring composition using the pigment multimer; and a cured film, a color filter, a method for manufacturing a color filter, a solid-state imaging element, and an image display device, each of which uses the coloring composition. The pigment multimer (A) has a non-nucleophilic counter anion.

Provided is a pigment multimer whereby a pattern can be appropriately formed during formation of a pattern. Further, provided are a coloring composition using the pigment multimer; and a cured film, a color filter, a method for manufacturing a color filter, a solid-state imaging element, and an image display device, each of which uses the coloring composition. The pigment multimer (A) has a non-nucleophilic counter anion.