Iridium complex immobilized on a high-nitrogen containing covalent triazine framework derived from 2,5-pyrazinedicarbonitrile as a recyclable catalyst for the selective <i>N</i>-alkylation of aminobenzenesulfonamides with alcohols-Reference-Cited by-同舟云学术

Iridium complex immobilized on a high-nitrogen containing covalent triazine framework derived from 2,5-pyrazinedicarbonitrile as a recyclable catalyst for the selective N-alkylation of aminobenzenesulfonamides with alcohols

Published:2022 Issue:20 Volume:6 Page:3006-3015
ISSN:2052-1537
Container-title:Materials Chemistry Frontiers
language:en
Short-container-title:Mater. Chem. Front.

Author:

Yang Chenchen¹,Hao Shushu¹,Shen Lu¹,Liu Peng¹,Yang Jiazhi¹,Li Feng¹^ORCID

Affiliation:

1. School of Chemistry and Chemical Engineering, Nanjing University of Science & Technology, Nanjing 210094, P. R. China

Abstract

A new-type of covalent triazine framework derived from 2,5-pyrazinedicarbonitrile as a monomer with a high N/C ratio was designed and synthesized by trimerization at 400 °C with ZnCl2 as a catalyst and salt melt via the ionothermal technique.

Funder

Natural Science Foundation of Jiangsu Province

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Materials Science

Link

http://pubs.rsc.org/en/content/articlepdf/2022/QM/D2QM00357K

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