Volume 132, Issue 20 pp. 7774-7779
Zuschrift

Construction of Hydrocarbon Nanobelts

Tan-Hao Shi

Tan-Hao Shi

MOE Key Laboratory of Bioorganic Phosphorous and Chemical Biology, Department of Chemistry, Tsinghua University, Beijing, 100084 China

Search for more papers by this author
Prof. Dr. Shuo Tong

Prof. Dr. Shuo Tong

MOE Key Laboratory of Bioorganic Phosphorous and Chemical Biology, Department of Chemistry, Tsinghua University, Beijing, 100084 China

Search for more papers by this author
Prof. Dr. Mei-Xiang Wang

Corresponding Author

Prof. Dr. Mei-Xiang Wang

MOE Key Laboratory of Bioorganic Phosphorous and Chemical Biology, Department of Chemistry, Tsinghua University, Beijing, 100084 China

Search for more papers by this author
First published: 09 March 2020
Citations: 22

Dedicated to Professor Youqi Tang on the occasion of his 100th birthday

Abstract

Linearly fused hydrocarbon nanobelts are a unique type of double-stranded macrocycles that would serve as not only the powerful hosts in supramolecular science but also the templates to grow zig-zag carbon nanotubes with defined diameters. Fully conjugated hydrocarbon nanobelts such as belt[n]arenes would also possess unique physical and chemical properties. Despite the importance, both fully conjugated and (partially) saturated hydrocarbon nanobelts remain largely unexplored because of the lack of cyclization methods. Reported here is the construction of nanometer sized H12-belt[12]arenes based on the strategy to close up all fjords of resorcin[6]arene by means of six-fold intramolecular alkylation reactions of resorcin[6]arene derivatives. All resulting H12-belt[12]arenes produce a very similar nanobelt core structure with six benzene rings and six boat 1,4-cyclohexadiene rings being alternately linear-fused to give a nearly equilateral hexagonal cylinder. The average long diagonal is around 1 nm and the height of the cylinder is about 0.3 nm. The acquired H12-belt[12]arenes would be the potential precursors to various hydrocarbon nanobelts including fully conjugated belt[12]arenes.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.