Presenting Porous-Organic-Polymers as Next Generation Invigorating Window for Nanoreactor

2021 ◽  
Author(s):  
John Mondal ◽  
Chitra Sarkar ◽  
Subhash Chandra Shit ◽  
Nitumani Das
Keyword(s):  
Organic Materials ◽  
Building Blocks ◽  
Organic Polymers ◽  
Next Generation ◽  
Porous Organic Polymers ◽  
Covalent Bonds

Porous Organic Polymers (POPs) represent an emerging class of porous organic materials which mainly comprising with organic building blocks, interconnected via strong covalent bonds thereby offering highly cross-linked frameworks with...

Fluorescent porous organic polymers

2019 ◽  
Vol 10 (10) ◽  
pp. 1168-1181 ◽  
Author(s):  
Dongyang Chen ◽  
Cheng Liu ◽  
Juntao Tang ◽  
Linfeng Luo ◽  
Guipeng Yu
Keyword(s):  
Building Blocks ◽  
Organic Polymers ◽  
Porous Organic Polymers ◽  
Covalent Bonds

Porous organic polymers (POPs), which are built from pure organic building blocks through strong covalent bonds, are intriguing platforms with multiple functionalities.

Post-synthetic modifications in porous organic polymers for biomedical and related applications

2022 ◽  
Author(s):  
Ji Hyeon Kim ◽  
Dong Won Kang ◽  
Hongyeol Yun ◽  
Minjung Kang ◽  
Nem Singh ◽  
...  
Keyword(s):  
Building Blocks ◽  
Organic Polymers ◽  
Porous Organic Polymers

Porous organic polymers (POPs) are prepared by crosslinked polymerization of multidimensional rigid aromatic building blocks followed by PSM depending on the application.

scholarly journals Cyclotetrabenzil-Based Porous Organic Polymers with High Carbon Dioxide Affinity

2021 ◽  
Author(s):  
Timur Ashirov ◽  
Maymounah Alrayyani ◽  
Kyung Seob Song ◽  
Ognjen Miljanic ◽  
Ali Coskun
Keyword(s):  
Carbon Dioxide ◽  
Condensation Reaction ◽  
Building Blocks ◽  
Organic Polymer ◽  
Bet Surface Area ◽  
Chloride Salt ◽  
Organic Polymers ◽  
High Carbon ◽  
Porous Organic Polymers ◽  
High Carbon Dioxide

Porous organic polymers (POPs) incorporating macrocyclic units have been investigated in recent years in an effort to transfer macrocycles’ intrinsic host-guest properties onto the porous networks to achieve complex separations. In this regard, highly interesting building blocks are presented by the family of cyclotetrabenzoin macrocycles with rigid, well-defined, electron-deficient cavities. This macrocycle shows high affinity towards linear guest molecules such as carbon dioxide, thus offering an ideal building block for the synthesis of CO2-philic POPs. Herein, we report the synthesis of a porous organic polymer through the condensation reaction between cyclotetrabenzil with 1,2,4,5-tetraaminobenzene under ionothermal conditions using the eutectic zinc chloride/sodium chloride/potassium chloride salt mixture at 250 oC. Notably, following the condensation reaction, the macrocycle favors 3D growth rather than 2D one while retaining the cavity. The resulting polymer, named 3D-mPOP, showed a highly microporous structure with the BET surface area of 1142 m2 g−1 and a high carbon dioxide affinity with a binding enthalpy of 39 kJ mol−1. Moreover, 3D-mPOP showed very high selectivity for carbon dioxide in carbon dioxide/methane and carbon dioxide /nitrogen mixtures.

Naturally occurring gallic acid derived multifunctional porous polymers for highly efficient CO2 conversion and I2 capture

2018 ◽  
Vol 20 (20) ◽  
pp. 4655-4661 ◽  
Author(s):  
Chao Xie ◽  
Jinliang Song ◽  
Haoran Wu ◽  
Yue Hu ◽  
Huizhen Liu ◽  
...  
Keyword(s):  
Gallic Acid ◽  
Building Blocks ◽  
Porous Polymers ◽  
Co2 Conversion ◽  
Organic Polymers ◽  
Porous Organic Polymers ◽  
Highly Efficient ◽  
Naturally Occurring

Novel porous organic polymers with multifunctional sites using plant-derived polyphenols as the building blocks showed superior applications in CO2 fixation and I2 adsorption.

scholarly journals Novel approach to hydroxy-group-containing porous organic polymers from bisphenol A

2017 ◽  
Vol 13 ◽  
pp. 2131-2137 ◽  
Author(s):  
Tao Wang ◽  
Yan-Chao Zhao ◽  
Li-Min Zhang ◽  
Yi Cui ◽  
Chang-Shan Zhang ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Bisphenol A ◽  
Hydroxy Group ◽  
Phenolic Resin ◽  
Building Blocks ◽  
Organic Polymers ◽  
Porous Organic Polymers ◽  
Carbon Dioxide Uptake ◽  
Novel Approach ◽  
Cp Mas Nmr

We successfully employed bisphenol A and several different formyl-containing monomers as useful building blocks to construct a series of hydroxy-group-containing porous organic polymers in a sealed tube at high temperature. Fourier transform infrared and solid-state 13C CP/MAS NMR spectroscopy are utilized to characterize the possible structure of the obtained polymers. The highest Brunauer–Emmet–Teller specific surface area of the phenolic-resin porous organic polymers (PPOPs) is estimated to be 920 m2 g–1. The PPOPs exhibit a highest carbon dioxide uptake (up to 15.0 wt % (273 K) and 8.8 wt % (298 K) at 1.0 bar), and possess moderate hydrogen storage capacities ranging from 1.28 to 1.04 wt % (77 K) at 1.0 bar. Moreover, the highest uptake of methane for the PPOPs is measured as 4.3 wt % (273 K) at 1.0 bar.

Synthesis of catalytically active porous organic polymers from metalloporphyrin building blocks

2011 ◽  
Vol 2 (4) ◽  
pp. 686 ◽  
Author(s):  
Abraham M. Shultz ◽  
Omar K. Farha ◽  
Joseph T. Hupp ◽  
SonBinh T. Nguyen
Keyword(s):  
Building Blocks ◽  
Organic Polymers ◽  
Porous Organic Polymers ◽  
Catalytically Active

Thienopyrrolocarbazoles: New Building Blocks for Functional Organic Materials

2019 ◽  
Author(s):  
Dorian Bader ◽  
Johannes Fröhlich ◽  
Paul Kautny
Keyword(s):  
Building Block ◽  
Organic Materials ◽  
Building Blocks ◽  
Molecular Properties ◽  
The Family ◽  
Facile Preparation

The facile preparation of three regioisomeric thienopyrrolocarbazoles applying a convenient C-H activation approach is presented. Derived from indolo[3,2,1-<i>jk</i>]carbazole, the incorporation of thiophene into the triarylamine framework significantly impacted the molecular properties of the parent scaffold. The developed thienopyrrolocarbazoles enrich the family of triarylamine donors and constitute a novel building block for functional organic materials.

Thienopyrrolocarbazoles: New Building Blocks for Functional Organic Materials

2019 ◽  
Author(s):  
Dorian Bader ◽  
Johannes Fröhlich ◽  
Paul Kautny
Keyword(s):  
Building Block ◽  
Organic Materials ◽  
Building Blocks ◽  
Molecular Properties ◽  
The Family ◽  
Facile Preparation

The facile preparation of three regioisomeric thienopyrrolocarbazoles applying a convenient C-H activation approach is presented. Derived from indolo[3,2,1-<i>jk</i>]carbazole, the incorporation of thiophene into the triarylamine framework significantly impacted the molecular properties of the parent scaffold. The developed thienopyrrolocarbazoles enrich the family of triarylamine donors and constitute a novel building block for functional organic materials.

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