Abstract: A photographic element having a light sensitive layer and containing a dye of the formula (I): ##STR1## wherein: X.sub.1 and X.sub.2 each independently represents the atoms necessary to complete a 5- or 6-membered heterocyclic nucleus;X.sub.3 represents the atoms necessary to form a 5- or 6-membered ring structure, which may be substituted;R.sub.1 and R.sub.2 each independently represents a substituted or unsubstituted alkyl group or a substituted or unsubstituted aryl group;R.sub.3 represents H, a substituted or unsubstituted alkyl group or a substituted or unsubstituted aryl group;r and s independently are 0 or 1; andW represents one or more counterions as needed to balance the charge of the molecule.

Abstract: A dye of the formula (I) below, and photographic elements having a light sensitive layer and which element contains such a dye: ##STR1## X.sub.1 and X.sub.2 each independently represent the atoms necessary to complete a 5- or 6-membered heterocyclic nucleus;x and y are, independently, integers from 0 to 3 provided x+y is no greater than 4;p and q each independently represents 0 or 1,each L independently represents a methine group;R.sub.1 and R.sub.2 each independently represents an alkyl group or an aryl group, andR.sub.3 represents an alkyl group, aryl group or heteroaryl group;W1 is a counterion as needed to balance the charge of the molecule.

Abstract: A method of synthesizing a compound having a 1,3-thiazolidin-4-one ring appended at the 2-position by a double bond to the active methylene position of a ketomethylene or malononitrile moiety, which comprises reacting the corresponding ketomethylene compound or malononitrile with an isothiocyanate in the presence of a base, reacting the resulting product with a haloacetic acid or haloacetic ester, followed by eliminating water or alcohol to form the 1,3-thiazolidin-4-one ring. A fragment necessary to complete a merocyanine, oxonol, hemicyanine, benzylidene, cinnamylidene or holopolar cyanine dye can be appended to the 1,3-thiazolidin-4-one ring to obtain the desired dye.

Abstract: Novel methyne dyes comprising two auxochromic groups of the type used in a cyanine or merocyanine dye linked by a carbon atom chain wherein each of the carbon atoms have an unsaturated linkage to at least one adjacent carbon atom in the chain and at least one pair of carbon atoms in the chain being joined by a triple bond or, in an alternate resonance form, the chain including three consecutive carbon to carbon double bonds. The dyes are useful as spectral sensitizing dyes for silver halide emulsions and as intermediates for synthesizing chain-substituted methine dyes.

Abstract: Novel methyne dyes comprising two auxochromic groups of the type used in a cyanine or merocyanine dye linked by a carbon atom chain wherein each of the carbon atoms have an unsaturated linkage to at least one adjacent carbon atom in the chain and at least one pair of carbon atoms in the chain being joined by a triple bond or, in an alternate resonance form, the chain including three consecutive carbon to carbon double bonds. The dyes are useful as spectral sensitizing dyes for silver halide emulsions and as intermediates for synthesizing chain-substituted methine dyes.

Abstract: Novel methyne dyes comprising two auxochromic groups of the type used in a cyanine or merocyanine dye linked by a carbon atom chain wherein each of the carbon atoms have an unsaturated linkage to at least one adjacent carbon atom in the chain and at least one pair of carbon atoms in the chain being joined by a triple bond or, in an alternate resonance form, the chain including three consecutive carbon to carbon double bonds. The dyes are useful as spectral sensitizing dyes for silver halide emulsions and as intermediates for synthesizing chain-substituted methine dyes.