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Society of Photographic Scientists

R.M. Schaffert, Electrophotography. Society of Photographic Scientists and Engineers, Eocal Press, London, 1975 (Chapters 1 and 2). [Pg.93]

S. P. Pappas, "Photoinitiated Cationic Polymerization," Proc. Int. Symp. Advances in Photopolymer Systems, 18th Fall Symposium of the Society of Photographic Scientists and Engineers, Washington, D.C., 1978, p. 62. [Pg.481]

Brinkman EM (1971) Proc 3rd Symp. Society of Photographic Scientists and Engineers on Unconventional Photographic Systems, Oct 20-23, 1971, Washington DC, p 13... [Pg.224]

Figure 3.28. SEM of 0.8-[Lm lines and spaces printed in a J- xm CPMS resist. Reproduced with permission from reference 97. Copyright 1982 Society of Photographic Scientists and Engineers.)... Figure 3.28. SEM of 0.8-[Lm lines and spaces printed in a J- xm CPMS resist. Reproduced with permission from reference 97. Copyright 1982 Society of Photographic Scientists and Engineers.)...
Figure 4. Qualitative predictions from the point-dipole expression (Equation 3) for spectral shifting of dimers. Dimer formation splits the excited state into two levels, one which allows transition to the ground state, and one which is silent for the case of parallel molecules in the dimer. The spectral shift depends on the stacking angle of the pair of molecules. The slipped structure is the precursor of the red shifted 1-aggregate, a desirable structure for photographic sensitization. (Reproduced, with permission, from Ref. 9. Copyright 1968, Society of Photographic Scientists and Engineers.)... Figure 4. Qualitative predictions from the point-dipole expression (Equation 3) for spectral shifting of dimers. Dimer formation splits the excited state into two levels, one which allows transition to the ground state, and one which is silent for the case of parallel molecules in the dimer. The spectral shift depends on the stacking angle of the pair of molecules. The slipped structure is the precursor of the red shifted 1-aggregate, a desirable structure for photographic sensitization. (Reproduced, with permission, from Ref. 9. Copyright 1968, Society of Photographic Scientists and Engineers.)...
Figure 5. Slick" molecules in the possible modes of interaction during an optical transition, with transition density represented by vertical displacement from the horizontal sticks. Right, the transition densities cancel each other and are silent, and left, the transition densities add so that the dimer becomes a supermolecule with a single allowed optical transition having the combined dipole strength of the two participating molecules. (Reproduced, with permission, from Ref. 30. Copyright J973, Society of Photographic Scientists and Engineers.)... Figure 5. Slick" molecules in the possible modes of interaction during an optical transition, with transition density represented by vertical displacement from the horizontal sticks. Right, the transition densities cancel each other and are silent, and left, the transition densities add so that the dimer becomes a supermolecule with a single allowed optical transition having the combined dipole strength of the two participating molecules. (Reproduced, with permission, from Ref. 30. Copyright J973, Society of Photographic Scientists and Engineers.)...
Figure 8. Wavelength vs. absorptance for a normal photographic coating of a thiacarbocyanine dye on cubic crystals (a), and on octahedral crystals of AgBr / (2.5% I) (b). The rising absorption to the left of each plot is the intrinsic absorption of the silver halide. (Reproduced, with permission, from Ref. 35. Copyright 1974, Society of Photographic Scientists and Engineers.)... Figure 8. Wavelength vs. absorptance for a normal photographic coating of a thiacarbocyanine dye on cubic crystals (a), and on octahedral crystals of AgBr / (2.5% I) (b). The rising absorption to the left of each plot is the intrinsic absorption of the silver halide. (Reproduced, with permission, from Ref. 35. Copyright 1974, Society of Photographic Scientists and Engineers.)...
Figure 10a. Results of coating matching octahedral AgBr I (1% I) emulsions on clear acetate film base and measuring %R, % T. On incubation at 38°C, the red-shifted aggregates are simply ordered increasingly with time, and a modest red shift occurs. The central ethyl group prevents formation of the 60° structure. (Reproduced, with permission, from Ref. 21. Copyright 1970, Society of Photographic Scientists and Engineers.)... Figure 10a. Results of coating matching octahedral AgBr I (1% I) emulsions on clear acetate film base and measuring %R, % T. On incubation at 38°C, the red-shifted aggregates are simply ordered increasingly with time, and a modest red shift occurs. The central ethyl group prevents formation of the 60° structure. (Reproduced, with permission, from Ref. 21. Copyright 1970, Society of Photographic Scientists and Engineers.)...
The circles represent surface positions tor Ag ions. In the absence of the dye, half of the Ag positions are filled randomly. When an attractive ligand interaction is established between the heterocyclic sulfurs of the dye and two Ag ions, position, A,A are filled, and B,B must be emptied to remove a repulsive interaction between the 7,7 protons of the dye and the Ag ions. Positions C,C will he emptied to maintain local electrical near-neutrality if the dye is a cationic carhocyanine. If a charge-compensated betaine dye (e.g. monosulfopropyl) is added, one of the C.C positions may be filled, or if an anionic dye (Fl.ti -disulfopropyl) is added, both may he filled. (Reproduced, with permission, from Ref. 7. Copyright 1974, Society of Photographic Scientists and Engineers.)... [Pg.31]

M. G. Mason, Abstracts, in Society of Photographic Scientists and Engineers Conf, Rochester, New York, 1987. [Pg.211]

Fox, S. J. Electrofdiotogtiqphy, Second Int. Conf. Society of Photographic Scientists and Engineers Publication, Washington, D. C., 1974, p. 170... [Pg.168]


See other pages where Society of Photographic Scientists is mentioned: [Pg.422]    [Pg.141]    [Pg.5]    [Pg.7]    [Pg.18]    [Pg.26]    [Pg.29]    [Pg.35]    [Pg.35]    [Pg.38]    [Pg.54]    [Pg.141]    [Pg.57]    [Pg.101]   


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