87286-91-7Relevant academic research and scientific papers
Compound and coloring composition
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Paragraph 0323-0329; 0339-0343, (2020/11/10)
The invention provides a novel compound and a coloring composition.
COLORED CURABLE RESIN COMPOSITION
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Paragraph 0366-0368, (2016/11/24)
The present invention provides a colored curable resin composition comprising: one or more kinds of colorants (A1) selected from the group of C.I. pigment yellow 138, a green pigment and a yellow pigment, Squarylium dye (A2), resin (B), polymer compounds
COLORED CURABLE RESIN COMPOSITION
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Paragraph 0189; 0190; 0191, (2017/06/09)
The present invention provides a colored curable resin composition comprising: a colorant including a green dye (A); a resin (B); a polymerizable compound (C); a polymerization initiator (D); a solvent (E); and a colorless metal chelating agent (G).C
Aggregation of squaraine dyes: Structure-property relationships and solvent effects
McKerrow, Andrew J.,Buncel, Erwin,Kazmaier, Peter M.
, p. 1605 - 1615 (2007/10/02)
In characterizing the UV-visible absorption properties of a series of seven anilino class squaraine dyes in dimethyl sulfoxide (DMSO)-water mixtures, spectral features characteristic of aggregation were observed.These included hypsochromic and hypochromic
Conformational isomerism in squaraines: saturation transfer NMR studies on hydroxy squaraines
Kazmaier, Peter M.,Hamer, Gordon K.,Burt, Richard A.
, p. 530 - 536 (2007/10/02)
The proton and 13C NMR of azulene and dialkylaminohydroxyphenyl squaraines have been investigated.The four-membered ring carbon resonances occur in the 180-190 ppm range and are attributed to the cyclobutenediylium character of this structure.Some charge delocalization from the central ring to the pendent aromatic substitutents was also observed, indicative of a substituent effect of the squaraine moiety on aminoaromatic systems equivalent to that of a formyl or acetyl group.Hydroxy squaraines 10 and 11 show the presence of two isomeric squaraine species in the proton NMR in deuterochloroform.Saturation transfer experiments confirm that these species are readily interconverted, and cis/trans isomerism (9a 9b) is consistent with these observations.The free energy difference between the two isomers at 318 K is calculated to be 3.0 and 3.2 kJ/mol for hydroxysquaraines 10 and 11 respectively.
