Abstract: An indolestyryl compound. The indolestyryl compound has formula (I): wherein Z1 comprises benzene, naphthalene, or heterocyclic ring containing O, S, or N, R2 comprises H, halogen atoms, C1-5 alkyl, nitro, ester, carboxyl, sulfo, sulfonamide, sulfuric ester, amide, C1-3 alkoxy, amino, alkylamino, cyano, C1-6 alkylsulfonyl, or C2-7 alkoxy carbonyl, R3, R4, R5, and R6 comprise H, alkyl, aralkyl, or heterocyclic ring containing O, S, or N, R7 and R8 comprise H or alkyl, R10 comprises H, alkyl, halogen atoms, nitro, hydroxyl, amino, ester, or substituted or non-substituted sulfonyl, W comprises carbon or nitrogen, Y comprises carbon, oxygen, sulfur, selenium, —NR, or —C(CH3)2, m is 1˜3, and X1 comprises an anionic group or an anionic organometallic complex, wherein R3 and R4 are joined to a nitrogen atom or R5 and R6 are joined together to form a ring, and R bonded to nitrogen is C1-5 alkyl.

Abstract: A bis(indolestyryl) compound. The bis(indolestyryl) compound has formula (I): wherein A and B comprise benzene, naphthalene, or heterocyclic ring containing O, S, or N, R1 and R1? are H, halogen, C1-5 alkyl, nitro, ester, carboxyl, sulfo, sulfonamide, amide, sulfo ester, C1-3 alkoxy, amino, alkylamino, cyano, C1-6 alkylsulfonyl, or C2-7 alkoxy carbonyl, R2, R2?, R3, and R3? comprise H, C1-6 alkyl, C6-18 aryl, C2-6 alkenyl, C3-6 cycloalkenyl, or C3-6 cycloalkyl, R4 is H, C1-5 alkyl, hydroxyl, halogen, or alkoxy, R5 and R5? comprise H, halogen, C1-5 alkyl, nitro, C1-3 alkoxy, amino, cyano, C1-6 alkylsulfonyl, or C2-7 alkoxy carbonyl, W comprises oxygen, sulfur, selenium, —NR, or —C(CH3)2, n is 1˜18 and Z1 and Z2 are different and comprise an anion or an anionic organometallic complex with +1 or +2 valence, wherein R bonded to nitrogen is C1-4 alkyl.

Abstract: A bisstyryl compound. The bisstyryl compound has formula (I): wherein Z1 and Z2 are benzene, naphthalene, or heterocyclic ring, R1 is H, C1-5 alkyl, hydroxyl, halogen atoms, or alkoxy, R2 is H, halogen atoms, C1-5 alkyl, nitro, ester, carboxyl, sulfo, sulfonamide, sulfuric ester, amide, C1-3 alkoxy, amino, alkylamino, cyano, C1-6 alkylsulfonyl, or C2-7 alkoxy carbonyl, R3, R4, R5, and R6 are H, halogen atoms, alkyl, aralkyl, or heterocyclic ring containing O, S, or N, or R3 and R4 are joined to a nitrogen atom or R5 and R6 are joined together to form a ring, R7 and R8 are H or alkyl, W is nitrogen with or without Z1 and Z2 or aromatic group without Z1 and Z2, Y is carbon, oxygen, sulfur, selenium, —NR, or —C(CH3)2, m is 1-3, n is 1-18, and X1 and X2 are anionic groups or anionic organometallic complexes.

Abstract: An asymmetric bis(indolestyryl) compound. The asymmetric bis(indolestyryl) compound has formula (I): wherein A and B comprise benzene, naphthalene, or heterocyclic ring containing O, S, or N, R1 and R1? are H, halogen atoms, C1-5 alkyl, nitro, ester, carboxyl, sulfo, C1-3 alkoxy, amine, alkylamine, cyano, C1-6 alkylsulfonyl, or C2-7 alkoxy carbonyl, R2, R2?, R3, and R3? comprise H, C1-6 alkyl, C6-18 aryl, C2-6 alkenyl, C3-6 cycloalkenyl, or C3-6 cycloalkyl, or C3-6 cycloalkyl containing hetero atom, R4 is H, hydroxyl, halogen atoms, or alkoxy, R5 and R5? comprise H, halogen atoms, C1-5 alkyl, nitro, C1-3 alkoxy, amine, cyano, C1-6 alkylsulfonyl, or C2-7 alkoxy carbonyl, n is 1˜18, Y is C(R6R7), C1-3 alkylamino or hetero atom, R6 and R7 are C1-3 alkyl, and Z? is an anion or an anionic organometallic complex. The invention also provides a high density recording medium utilizing the asymmetric bis(indolestyryl) compound.

Abstract: Indolestyryl compounds and use thereof for a high density recording media and method for fabricating the same. The indolestyryl compounds exhibit strong absorbance in the visible light region (400˜700 nm) of the spectrum, resistance to heat and light, high light sensitivity, and excellent solubility, resulting from their special chemical configuration. Furthermore, the indolestyryl compounds can be used as recording layer materials in high density recording media for matching a reading laser wavelength and enhancing the reflective index and carrier-to-noise ratio (CNR) of the high density recording media. Accordingly, the recording sensitivity and the readout characteristics of high density recording media comprising the indolestyryl compound according to the present invention can be improved.

Abstract: An indolestyryl compound. The indolestyryl compound has formula (I): wherein Z1 comprises benzene, naphthalene, or heterocyclic ring containing O, S, or N, R2 comprises H, halogen atoms, C1-5 alkyl, nitro, ester, carboxyl, sulfo, sulfonamide, sulfuric ester, amide, C1-3 alkoxy, amino, alkylamino, cyano, C1-6 alkylsulfonyl, or C2-7 alkoxy carbonyl, R3, R4, R5, and R6 comprise H, alkyl, aralkyl, or heterocyclic ring containing O, S, or N, R7 and R8 comprise H or alkyl, R10 comprises H, alkyl, halogen atoms, nitro, hydroxyl, amino, ester, or substituted or non-substituted sulfonyl, W comprises carbon or nitrogen, Y comprises carbon, oxygen, sulfur, selenium, —NR, or —C(CH3)2, m is 1˜3, and X1 comprises an anionic group or an anionic organometallic complex, wherein R3 and R4 are joined to a nitrogen atom or R5 and R6 are joined together to form a ring, and R bonded to nitrogen is C1-5 alkyl.

Abstract: A bisstyryl compound. The bisstyryl compound has formula (I): wherein Z1 and Z2 are benzene, naphthalene, or heterocyclic ring, R1 is H, C1-5 alkyl, hydroxyl, halogen atoms, or alkoxy, R2 is H, halogen atoms, C1-5 alkyl, nitro, ester, carboxyl, sulfo, sulfonamide, sulfuric ester, amide, C1-3 alkoxy, amino, alkylamino, cyano, C1-6 alkylsulfonyl, or C2-7 alkoxy carbonyl, R3, R4, R5, and R6 are H, halogen atoms, alkyl, aralkyl, or heterocyclic ring containing O, S, or N, or R3 and R4 are joined to a nitrogen atom or R5 and R6 are joined together to form a ring, R7 and R8 are H or alkyl, W is nitrogen with or without Z1 and Z2 or aromatic group without Z1 and Z2, Y is carbon, oxygen, sulfur, selenium, —NR, or —C(CH3)2, m is 1-3, n is 1-18, and X1 and X2 are anionic groups or anionic organometallic complexes.

Abstract: A bis(indolestyryl) compound. The bis(indolestyryl) compound has formula (I): wherein A and B comprise benzene, naphthalene, or heterocyclic ring containing O, S, or N, R1 and R1? are H, halogen atoms, C1-5 alkyl, nitro, ester, carboxyl, sulfo, sulfonamide, amide, sulfo ester, C1-3 alkoxy, amino, alkylamino, cyano, C1-6 alkylsulfonyl, or C2-7 alkoxy carbonyl, R2, R2?, R3, and R3? comprise H, C1-6 alkyl, C6-18 aryl, C2-6 alkenyl, C3-6 cycloalkenyl, or C3-6 cycloalkyl, R4 is H, C1-5 alkyl, hydroxyl, halogen atoms, or alkoxy, R5 and R5? comprise H, halogen atoms, C1-5 alkyl, nitro, C1-3 alkoxy, amino, cyano, C1-6 alkylsulfonyl, or C2-7 alkoxy carbonyl, W comprises oxygen, sulfur, selenium, —NR, or —C(CH3)2, n is 1˜18, and Z1 and Z2 are different and comprise an anion or an anionic organometallic complex with +1 or +2 valence, wherein R bonded to nitrogen is C1-4 alkyl.

Abstract: An asymmetric bis(indolestyryl) compound. The asymmetric bis(indolestyryl) compound has formula (I): wherein A and B comprise benzene, naphthalene, or heterocyclic ring containing O, S, or N, R1 and R1? are H, halogen atoms, C1-5 alkyl, nitro, ester, carboxyl, sulfo, C1-3 alkoxy, amine, alkylamine, cyano, C1-6 alkylsulfonyl, or C2-7 alkoxy carbonyl, R2, R2?, R3, and R3? comprise H, C1-6 alkyl, C6-18 aryl, C2-6 alkenyl, C3-6 cycloalkenyl, or C3-6 cycloalkyl, or C3-6 cycloalkyl containing hetero atom, R4 is H, hydroxyl, halogen atoms, or alkoxy, R5 and R51 comprise H, halogen atoms, C1-5 alkyl, nitro, C1-3 alkoxy, amine, cyano, C1-6 alkylsulfonyl, or C2-7 alkoxy carbonyl, n is 1˜18, Y is C(R6R7), C1-3 alkylamino or hetero atom, R6 and R7 are C1-3 alkyl, and Z? is an anion or an anionic organometallic complex. The invention also provides a high density recording medium utilizing the asymmetric bis(indolestyryl) compound.

Abstract: The invention discloses new benzoindole styryl compounds and its use for a high-density optical recording medium. The invention uses the dyes of the new benzoindole styryl compounds to form the recording layer of high-density recording media. The new benzoindole styryl compounds are easy to prepare and purify, so they are cheaper when comparing to the compounds generally used in high-density optical recording media. The benzoindole styryl compounds has a maximum absorption for the light wavelength in the range of 500 nanometers to 700 nanometers. The benzoindole styryl compounds also have high sensitivity and chemical stability for light and heat. Using the new benzoindole styryl compounds to form a high-density optical recording medium can match up with the short-wavelength laser beam for high-density optical recording media and have the advantage of a stable quality.

Abstract: Indolestyryl compounds and use thereof for a high density recording media and method for fabricating the same. The indolestyryl compounds exhibit strong absorbance in the visible light region (400˜700 nm) of the spectrum, resistance to heat and light, high light sensitivity, and excellent solubility, resulting from their special chemical configuration. Furthermore, the indolestyryl compounds can be used as recording layer materials in high density recording media for matching a reading laser wavelength and enhancing the reflective index and carrier-to-noise ratio (CNR) of the high density recording media. Accordingly, the recording sensitivity and the readout characteristics of high density recording media comprising the indolestyryl compound according to the present invention can be improved.

Abstract: The invention discloses new indolestyryl compounds and their uses for a high-density optical recording medium. The invention uses the new indolestyryl compounds to form the recording layer of a high-density recording medium. The new indolestyryl compounds are easy to prepare and purify, so they are cheaper when comparing to the compounds generally used in high-density optical recording media. The indolestyryl compounds have a maximum absorption for light wavelengths in the range of 500 nanometers to 700 nanometers. The indolestyryl compounds also have high sensitivity and chemical stability toward light and heat. Using the new indolestyryl compounds to form high-density optical recording media can match up with the short-wavelength laser beam for high-density optical recording media and have the advantage of a stable quality.

Abstract: This invention provides imin complex dyes for a high-density optical disc recording medium having the following formula (I): wherein Y constitutes oxygen atom, sulfate atom, carbon atom with substitutes (C—R5) or nitrogen atom with substitutes (N—R6); R1 constitutes alkyl group having carbon number one to eighteen with or without substitutes or ether group, p-alkyl benzyl group with or without substitutes; R2, R3, R5, R6, R7 can be same or different groups; and X constitutes halogen atom, ClO4−, BF4−, PF6−, SbF6−, TCNQ−, TCNE−, naphthalenesulfonic acid or organometallic complex.x. The bis-styryl dyes whose spectra maximum absorption in visible light range of wavelength of 300 nm˜800 nm can be used as a high density optical disc recording medium.

Abstract: The invention discloses new benzoindole styryl compounds and its use for a high-density optical recording medium. The invention uses the dyes of the new benzoindole styryl compounds to form the recording layer of high-density recording media. The new benzoindole styryl compounds are easy to prepare and purify, so they are cheaper when comparing to the compounds generally used in high-density optical recording media. The benzoindole styryl compounds has a maximum absorption for the light wavelength in the range of 500 nanometers to 700 nanometers. The benzoindole styryl compounds also have high sensitivity and chemical stability for light and heat. Using the new benzoindole styryl compounds to form a high-density optical recording medium can match up with the short-wavelength laser beam for high-density optical recording media and have the advantage of a stable quality.

Abstract: The invention discloses new indolestyryl compounds and their uses for a high-density optical recording medium. The invention uses the new indolestyryl compounds to form the recording layer of a high-density recording medium. The new indolestyryl compounds are easy to prepare and purify, so they are cheaper when comparing to the compounds generally used in high-density optical recording media. The indolestyryl compounds have a maximum absorption for light wavelengths in the range of 500 nanometers to 700 nanometers. The indolestyryl compounds also have high sensitivity and chemical stability toward light and heat. Using the new indolestyryl compounds to form high-density optical recording media can match up with the short-wavelength laser beam for high-density optical recording media and have the advantage of a stable quality.

Abstract: A process for the purification of water-soluble non-ionic contrast agents from water-soluble non-ionic impurities involves the steps of (a) injecting a raw water-soluble non-ionic contrast agent solution on a chromatographic column containing non-ionic resins; (b) eluting water-soluble impurities contained in the raw water-soluble non-ionic contrast agent solution with deionized water as a first eluent, and (c) eluting a water-soluble non-ionic contrast agent with alcohol as a second eluent.

Abstract: A process for the purification of water-soluble non-ionic contrast agents from water-soluble non-ionic impurities involves the steps of (a) injecting a raw water-soluble non-ionic contrast agent solution on a chromatographic column containing non-ionic resins; (b) eluting water-soluble impurities contained in the raw water-soluble non-ionic contrast agent solution with deionized water as a first eluent, and (c) eluting a water-soluble non-ionic contrast agent with alcohol as a second eluent.