Chemistry Letters
Online ISSN : 1348-0715
Print ISSN : 0366-7022
ISSN-L : 0366-7022
Volume 39, Issue 10
Displaying 1-36 of 36 articles from this issue
Highlight Review
  • Xiaobin Peng, Feng Wang, Ajoy Kumar Bauri, A. F. M. Mustafizur Rahman, ...
    2010 Volume 39 Issue 10 Pages 1022-1027
    Published: October 05, 2010
    Released on J-STAGE: August 21, 2010
    Single-walled carbon nanotubes (SWNTs) have either chiral or achiral form, and synthesized chiral SWNTs include both left- and right-handed structures in equal amounts. Recently, a racemic mixture was found to be resolved through molecular recognition with gable-type chiral diporphyrins, namely, nanotweezers. This novel separation method for SWNTs allowed optical resolution of SWNTs for the first time. The chiral nanotweezers consist of two chiral porphyrins and rigid spacer in between. Therefore, they have potential to discriminate not only the handedness but also the diameters or alignments of the hexagons of SWNTs. We have prepared the following three types of chiral nanotweezers; m-phenylene-, 2,6-pyridylene-, and 3,6-carbazolylene-bridged diporphyrins. In the extraction of SWNTs, different selectivities have been observed among the nanotweezers. This can be attributed to the differences in their structures; namely, the dihedral angles and the distance of the two porphyrins. In this review, we would like to discuss the relationship between the structures of the nanotweezers and the results of the optical and (n,m) enrichments of the extracted SWNTs.
Editor's Choice
Editor's Choice
Editor's Choice