Facile synthesis of azo-linked porous organic frameworks via reductive homocoupling for selective CO2 capture

DOI: 10.1039/c4ta03015j

Source and publish data:

Journal of Materials Chemistry A p. 13831 - 13834 (2014)

Update date:2022-08-30

Topics:

Authors:

Lu, Jingzhi

Zhang, Jian

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1039/c4ta03015j

A facile Zn-induced reductive homocoupling reaction was used to synthesize azo-linked porous organic frameworks (azo-POFs) from easily accessed nitro monomers. Azo-POF-2 exhibits the highest CO₂/N₂ selectivity of 76 at 273 K among all self-coupled azo-linked porous polymers. This journal is the Partner Organisations 2014.

Full text of DOI:10.1039/c4ta03015j

Products guided by the article

Product name:Tetrakis(p-broMophenyl)Methane

Cas No:105309-59-9

R&D Labs maybe for 105309-59-9

NEM CHEMICAL CO.，LTD

website:http://www.NEM.COM.CN

Contact:+86-393-4411771

Address:The west section of shengli Road,Puyang,Henan Province,China
Yingkou Sanzheng New Technology Chemical Industry Co., Ltd.

Contact:+86-417-2927806

Address:yingkou
xujianqiang

Contact:86-21-57725962

Address:shanghai
Changzhou Sunsheng Chem Co., Ltd

Contact:+1-(989)-854-0648

Address:No. 28 Yinshan Rd., Xixiashu Industrial Park
DU-HOPE INTERNATIONAL GROUP

Contact:+86-25-52346955

Address:199,JIANYE ROAD,NANJING,CHINA

Relevant to this article

Doi:10.1021/ja00476a028
(1978)
Synthesis and bioactivities of Phenazine-1-carboxylic acid derivatives based on the modification of PCA carboxyl group

Doi:10.1016/j.bmcl.2017.03.011
(2017)
Single electron transfer promoted photoaddition reactions of α-trimethylsilyl substituted secondary N-alkylamines with fullerene C₆₀

Doi:10.1039/c6ob02069k
(2016)
Electrocatalytic CO₂ reduction with nickel complexes supported by tunable bipyridyl-N-heterocyclic carbene donors: Understanding redox-active macrocycles

Doi:10.1039/c8cc00266e
(2018)
A Top-Down Strategy to Realize Surface Reconstruction of Small-Sized Platinum-Based Nanoparticles for Selective Hydrogenation

Doi:10.1002/anie.202106459
(2021)
Doi:10.1021/jo01065a635
(1961)

Article Doi