Preparation and adsorption performance of cross-linked porous polycarbazoles

2014 ◽  
Vol 2 (38) ◽  
pp. 16181-16189 ◽  
Author(s):  
Jian-Hua Zhu ◽  
Qi Chen ◽  
Zhu-Yin Sui ◽  
Long Pan ◽  
Jiaguo Yu ◽  
...  

Hypercrosslinked carbazole-based porous organic polymers were prepared via FeCl3-promoted one-step oxidative coupling reaction and Friedel–Crafts alkylation in one pot.

2015 ◽  
Vol 6 (13) ◽  
pp. 2478-2487 ◽  
Author(s):  
Long Pan ◽  
Qi Chen ◽  
Jian-Hua Zhu ◽  
Jia-Guo Yu ◽  
Yu-Jian He ◽  
...  

Facile preparation of hypercrosslinked carbazole-based porous organic polymers via FeCl3-promoted one-step oxidative coupling reaction and Friedel–Crafts alkylation from the vinyl or hydroxymethyl functionalized carbazole is reported.


2020 ◽  
Vol 85 (18) ◽  
pp. 11934-11941
Author(s):  
Haofeng Wang ◽  
Xin Wu ◽  
Luyu Wang ◽  
Erfei Li ◽  
Xiaoyu Li ◽  
...  

2018 ◽  
Vol 59 (2) ◽  
pp. 94-98 ◽  
Author(s):  
Hoda Yahyavi ◽  
Majid M. Heravi ◽  
Mohammad Mahdavi ◽  
Alireza Foroumadi

2015 ◽  
Vol 13 (34) ◽  
pp. 8958-8977 ◽  
Author(s):  
Vineet Jeena ◽  
Ross S. Robinson

The Ireland one-pot oxidative coupling reaction is reviewed on the occasion of its 30th anniversary.


2019 ◽  
Vol 55 (42) ◽  
pp. 5898-5901 ◽  
Author(s):  
Houbing Zou ◽  
Jinyu Dai ◽  
Runwei Wang

We design and prepare a highly active and stable nanoreactor by encapsulating mesoporous metal nanoparticles for efficient production of α,β-unsaturated ketones via a one-pot oxidative coupling reaction.


ChemInform ◽  
2014 ◽  
Vol 46 (3) ◽  
pp. no-no
Author(s):  
Ling-Jun Li ◽  
Yu-Qin Zhang ◽  
Yang Zhang ◽  
An-Lian Zhu ◽  
Gui-Sheng Zhang

2014 ◽  
Vol 25 (8) ◽  
pp. 1161-1164 ◽  
Author(s):  
Ling-Jun Li ◽  
Yu-Qin Zhang ◽  
Yang Zhang ◽  
An-Lian Zhu ◽  
Gui-Sheng Zhang

Tetrahedron ◽  
2018 ◽  
Vol 74 (19) ◽  
pp. 2383-2390 ◽  
Author(s):  
Guang-Qing Rong ◽  
Jian-Qiang Zhao ◽  
Xiao-Mei Zhang ◽  
Xiao-Ying Xu ◽  
Wei-Cheng Yuan ◽  
...  

2018 ◽  
Vol 15 (7) ◽  
pp. 989-994 ◽  
Author(s):  
Ling Li ◽  
Bo Su ◽  
Yuxiu Liu ◽  
Qingmin Wang

Aim and Objective: During the investigation of sodium nitrite-catalyzed oxidative coupling reaction of aryls, an unprecedented C(sp2)-H and C(sp3)-H coupling of substituted 2-aryl acetonitrile was found. Materials and Methods: The structure of the coupled product was confirmed by 1H and 13C NMR spectroscopy and high-resolution mass spectrometry (HRMS), and comparison of its derivatives with known compounds. The effects of methoxy group in the benzene ring on the reaction were evaluated. Results: The optimized reaction conditions are summarized as follows: CF3SO3H/substrate = 1.5 equiv., NaNO2/substrate = 0.3 equiv., CH3CN as solvent. 2-(4-Methoxyphenyl)acetonitrile and 2-(3,4,5- trimethoxyphenyl)acetonitrile could also generate C(sp2)-H and C(sp3)-H coupling. The coupling reaction occurred as a typical radial mechanism. Conclusion: An unprecedented cyano-induced, NaNO2-catalyzed oxidative C(sp3)-H and C(sp2)-H coupling was reported. The reaction proceeded under very mild conditions, using O2 in the air as terminal oxidant. The unique oxidative manner might provide more inspiration for the development of intriguing oxidative coupling reactions.


Sign in / Sign up

Export Citation Format

Share Document