Academic literature on the topic 'Nonlinear optical property'

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Journal articles on the topic "Nonlinear optical property"

1

Nadtoka, Oksana. "Nonlinear Optical Effects in Polymeric Azoesters." Chemistry & Chemical Technology 4, no. 3 (2010): 185–90. http://dx.doi.org/10.23939/chcht04.03.185.

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The new photochromic polymers based on methacrylic azoesters were synthesized. The azobenzene side chains of obtained polymers contain different groups of both acceptor and donor nature as well as flexible alkyl spacer. The third order nonlinear optical susceptibilities (3) of the studied solutions were measured by degenerating four wave mixing (DFWM) method. As a result, the enhancement of the molecular conjugation and the high NLO chromophore concentration in the molecular chain contribute much to heightening the third-order NLO effect. The electronic effect of the substituent on the azobenzol group and the push–pull electronic structure contributes much to enhancing the NLO property
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2

YOKOYAMA, Shiyoshi, and Shinro MASHIKO. "Nonlinear Optical Property of Dipolar Dendrimer." Kobunshi 47, no. 11 (1998): 828. http://dx.doi.org/10.1295/kobunshi.47.828.

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3

Lu, Shunbin, Chujun Zhao, Yanhong Zou, et al. "Third order nonlinear optical property of Bi_2Se_3." Optics Express 21, no. 2 (2013): 2072. http://dx.doi.org/10.1364/oe.21.002072.

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4

Bosshard, Christian, Rolf Spreiter, Peter Günter, Rik R. Trkwinski, Martin Schreiber, and François Diederich. "Structure-property relationships in nonlinear optical tetraethynylethenes." Advanced Materials 8, no. 3 (1996): 231–34. http://dx.doi.org/10.1002/adma.19960080309.

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5

Li, Lin Feng, and Hong Yao Xu. "Preparation and Property of Alkynyl Substituted Azobenzene Optical Limiting Materials." Materials Science Forum 787 (April 2014): 326–31. http://dx.doi.org/10.4028/www.scientific.net/msf.787.326.

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An novel nonlinear optical alkynyl substituted azobenzene 4-(propargyl methyl ester)-4'-[(N,N'-diethyl) amino] azobenzene was synthesized and characterized by FTIR, 1HNMR. The linear optical properties were investigated by UV-Vis spectra. The nonlinear optical properties and optical limiting properties were investigated using 21 ps pulse at 532nm and 4ns pulse at 532nm, respectively. The results show that this novel nonlinear optical alkynyl substituted azobenzene possesses large third nonlinear optical coefficient and good optical limiting properties.
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6

Peng, Baixin, Xiangli Che, Mengjia Luo, et al. "Synthesis, structure, and nonlinear optical property of Bi0.33Sb0.67SI." Journal of Solid State Chemistry 304 (December 2021): 122505. http://dx.doi.org/10.1016/j.jssc.2021.122505.

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7

Ueda, Mitsuru, Yoshimasa Sakai, Tomonari Nakayama, Osamu Haba, Yoshihiko Ishitakat, and Yorihiko Sasakit. "Photosensitive Polyimides with Second-Order Nonlinear Optical Property." Journal of Photopolymer Science and Technology 10, no. 1 (1997): 37–41. http://dx.doi.org/10.2494/photopolymer.10.37.

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8

Xia, Houping, and Qian Ma. "Experimental study on nonlinear−optical property of Ag4P2Se6." Journal of Alloys and Compounds 780 (April 2019): 727–33. http://dx.doi.org/10.1016/j.jallcom.2018.11.403.

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9

Ji, Xiao Li, Shan Yi Guang, Xin Yan Su, and Hong Yao Xu. "Preparation and Nonlinear Optical Property of Triazole-Based Fluorene Functional Polymer." Advanced Materials Research 750-752 (August 2013): 869–72. http://dx.doi.org/10.4028/www.scientific.net/amr.750-752.869.

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The controllable preparation of nonlinear optical polymers is still one of the research hotspots on nonlinear optical field. In this paper, a triazole functional polymer was designed and achieved by high-efficiency click chemistry method. The structure and properties of the polymer was characterized and evaluated with FTIR, NMR, UV, FL, DLLS and nonlinear optical analyses. The results exhibited that the polymer was successfully synthesized and has favorable nonlinear optical property, its third-order nonlinearity up to 3.66×10-10esu.
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10

Li, Yanjun, Yuxun Ding, Yaming Li, et al. "Synthesis, Crystal Structure and Nonlinear Optical Property of RbHgI3." Crystals 7, no. 5 (2017): 148. http://dx.doi.org/10.3390/cryst7050148.

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