[1] Bruce W H. Silver halide photographic light-sensitive material[P]. US patent,3 214 377. 1965-10-26.
[2] Anthony Loria, Iimaria F Salminen. Two-equivalent thiocyano couplers[P]. US patent,3 253 024. 1966-05-31.
[3] Kobayashi Hidetoshi,Takahashi Toshirou,Hirano Shigeo, et al. Silver halide photographic light-sensitive material[P].US patent,4 390 618. 1983-06-28.
[4] Mihayashi Keiji, Kobayashi Hidetoshe, Takada Shunji. Silver halide photographic light-sensitive material[P]. US patent,4 618 5721984-12-12.
[5] Zhu Z H, Xu Y F, Chen Y. Development-Accelerator-Releasing(DAR) couplers. Part l:The effect of DAR couplers with different normal couplers on the photographic characteristics of color negative material[J]. Dyes and Pigments,1997,34(2):87-92.
[6] Cash D J, Ferguson A N. Complex salts of silver and 1,3, 3a, 7-tetraazaindene derivatives: Coordination and photographic stabilization[J]. J. Photographic Science, 1980,28:121-127.
[7] Zhu Z H, Xu Y F, Chen Y. Development-Accelerator-Releasing(DAR) couplers. Part 2:Effect of the DAR couplers with a different divalent linking group on the photographic characteristics of color negative material[J]. Dyes and Pigments, 1997,34 (4): 267-272.
[8] 马华品,姜子文.DAR成色剂结构和其提高感光度关系的研究[J]影像科学与实践1990,4:9-l0Ma H P,Jiang Z W. Research on the relationship between the structure of DAR coupler and it's increasing sensitivity[J]. Imaging Science and Practice, 1990,4:9-10.
[9] Shinohara K, Bayer E. Mechanism of the “"Hydrazine Effect” caused by N′-acyl-N-phenylhydrazine[J]. J. Photo.Sci., 1987,35(6): 181-190.
[10] James T H. The Theory of the Photographic Process[M]. 4th ed. New York:Macmillan,1977,297-298.
[11] Kitchin J P, Hall K P, et al. An improved process of hydrazine-promoted infectious development[J]. J. Photo. Sci.,1987,35: 162-164.
[12] Kitchin J P,Hall K P,et al. Hydrazine-promoted infectious development of silver halide-An improved process[J].J. Imag. Tech., 1989,15 (6): 282-284.
[13] James T J, Vanselow W. Kinetics of the reaction between silver bromide and an adsorbed layer of allyithiourea[J]. J.Phys. Chem., 1953,57:725.
[14] 王明星,姜子文,宋溪明,等甲酰肼型增强基团成色剂的合成及照相性能研究[J].感光科学与光化学,1999,17(2):184-192.Wang M X, J iang Z W, Song X M, et al. Synthesis and photographic properties of formylhydrzine DAR couplers[J].Photographic Science and Photochemistry. 1999,17(2): 184-192.
[15] Jarris J R,Twist P J. The effect of development accelerator releasing coupler on color negative imaging efficiency[J].J. Imaging Sci., 1989,33:217.
[16] James T H, Vanselow W. Kinetics of the reaction between silver bromide and an adsorbed layer of allylthiourea[J]. J.Phys. Chem., 1953,57:725.
[17] Carroll B H, Hubbard D. Kinetics of reaction between silver bromide and photographic sensitizers[J]. Bur. Standards. J. Research, 1934,12: 329.
[18] Collins R B, Dickinsen H O. High-speed photography: proceedings[C]. In: Proceedings of the 3rd international congress. London: Dept. of Scientific & Industrial Research, 1965.1-15.
[19] Xu Y F, Zhu Z H, Chen J R. Development-accelerator-releasing(DAR) coupler:Part IV. The effect of the DAR couplers with different hydrazines on the photographic characteristics of color negative material[J]. Dyes and Pigments,1998,38(3): 181-184.
[20] Siu-Chung Tsoi, Peter J. Twist. David T. Southby. EP 896 249. 1999-09-28.
[21] Zhu Z H, Chen S L, et al. Color photographic development accelerators. Part I synthesis of novel development-accelerator-releasing colorless couplers[J]. Dyes and Pigments, 1993,22: 255-258. |