Design and preparation of side chain electro-optic polymeric materials based on novel organic second order nonlinear optical chromophores with double carboxyl groups

2017 ◽  
Vol 29 (3) ◽  
pp. 2577-2584 ◽  
Author(s):  
Li Guo ◽  
Zupeng Guo ◽  
Xiaobing Li
Keyword(s):  
Nonlinear Optical ◽  
Polymeric Materials ◽  
Second Order ◽  
Side Chain ◽  
Carboxyl Groups ◽  
Electro Optic ◽  
Nonlinear Optical Chromophores ◽  
Optical Chromophores

Nonlinear optical chromophores based on Dewar's rules: enhancement of electro-optic activity by introducing heteroatoms into the donor or bridge

2015 ◽  
Vol 17 (44) ◽  
pp. 29679-29688 ◽  
Author(s):  
Huajun Xu ◽  
Dan Yang ◽  
Fenggang Liu ◽  
Mingkai Fu ◽  
Shuhui Bo ◽  
...  
Keyword(s):  
Nonlinear Optical ◽  
Second Order ◽  
Electro Optic ◽  
Nonlinear Optical Chromophore ◽  
Nonlinear Optical Chromophores ◽  
Optical Chromophores

In this work, we investigated the enhancement of the electro-optic response by introducing electron-rich heteroatoms as additional donors to the donor or bridge of a conventional second-order nonlinear optical chromophore.

Synthesis and characterization of two novel second-order nonlinear optical chromophores based on julolidine donors with excellent electro-optic activity

RSC Advances ◽  
2016 ◽  
Vol 6 (102) ◽  
pp. 99743-99751 ◽  
Author(s):  
Hua Zhang ◽  
Fuyang Huo ◽  
Fenggang Liu ◽  
Zhuo Chen ◽  
Jialei Liu ◽  
...  
Keyword(s):  
Nonlinear Optical ◽  
Second Order ◽  
Synthesis And Characterization ◽  
Electro Optic ◽  
Nlo Chromophores ◽  
Nonlinear Optical Chromophores ◽  
Optical Chromophores

Second order NLO chromophores with julolidine donor.

A Synthetic Approach for the Incorporation of Highly Efficient, Thermally Stable Second Order Nonlinear Optical Chromophores Into Side-Chain Polymers

1993 ◽  
Vol 328 ◽  
Author(s):  
Kevin J. Drost ◽  
Alex K-Y. Jen ◽  
V. Pushkara Rao ◽  
R. M. Mininni
Keyword(s):  
Nonlinear Optical ◽  
Second Order ◽  
Side Chain ◽  
Synthetic Approach ◽  
Synthetic Method ◽  
Side Chains ◽  
Thermally Stable ◽  
Highly Efficient ◽  
Nonlinear Optical Chromophores ◽  
Optical Chromophores

ABSTRACTA new synthetic method is developed to incorporate efficient nonlinear optical chromophores containing thiophene conjugating units and tricyanovinyl acceptors into side-chain polymers. This approach emphasizes the incorporation of the tricyanovinyl groups into the pendant side chains after the desired polymer is formed.

Synthesis and electro-optic activities of new side-chain polycarbonates containing nonlinear optical chromophores and isolation groups

RSC Advances ◽  
2014 ◽  
Vol 4 (9) ◽  
pp. 4395-4402 ◽  
Author(s):  
Guowei Deng ◽  
Heyan Huang ◽  
Chengcheng Peng ◽  
Airui Zhang ◽  
Maolin Zhang ◽  
...  
Keyword(s):  
Nonlinear Optical ◽  
Side Chain ◽  
Electro Optic ◽  
Nonlinear Optical Chromophores ◽  
Optical Chromophores

The synthesis of second-order nonlinear optical chromophores with conjugated steric hindrance for electro-optics at 850 nm

2020 ◽  
Vol 8 (16) ◽  
pp. 5494-5500 ◽  
Author(s):  
Jieyun Wu ◽  
Wen Wang ◽  
Kaixin Chen ◽  
Jingdong Luo
Keyword(s):  
Steric Hindrance ◽  
Nonlinear Optical ◽  
Second Order ◽  
Electro Optic ◽  
Nonlinear Optical Chromophore ◽  
Nonlinear Optical Chromophores ◽  
Shortwave Infrared ◽  
Optical Chromophores ◽  
Infrared Window

We show the strategy of introducing a suitable conjugated site-isolator on the bridge of a nonlinear optical chromophore to significantly improve the electro-optic activity at the shortwave infrared window (850 nm) for electro-optic modulation.

Synthesis of nonlinear optical chromophores with isophorone-derived bridges for enhanced thermal stability and electro-optic activity

2020 ◽  
Vol 8 (27) ◽  
pp. 9226-9235 ◽  
Author(s):  
Fenggang Liu ◽  
Songmin Mo ◽  
Zhaofen Zhai ◽  
Meishan Peng ◽  
Shuangke Wu ◽  
...  
Keyword(s):  
Thermal Stability ◽  
Nonlinear Optical ◽  
Electro Optic ◽  
Nonlinear Optical Chromophores ◽  
Optical Chromophores

In this work, we developed a series of nonlinear optical chromophores J1–J4 with the same julolidinyl-based donor and tricyanovinyldihydrofuran acceptor with different modified isophorone-derived bridges.

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