HUSCAP logo Hokkaido Univ. logo

Hokkaido University Collection of Scholarly and Academic Papers >
Graduate School of Science / Faculty of Science >
Peer-reviewed Journal Articles, etc >

A Dualistic Arrangement of a Chiral [1]Rotaxane Based on the Assembly of Two Rings and Two Rods

Files in This Item:
revised_manu-jo2023-00069c.docx1.46 MBMicrosoft Word XMLView/Open
Please use this identifier to cite or link to this item:http://hdl.handle.net/2115/91514

Title: A Dualistic Arrangement of a Chiral [1]Rotaxane Based on the Assembly of Two Rings and Two Rods
Authors: Katoono, Ryo Browse this author
Tanioka, Takumi Browse this author
Issue Date: 7-Apr-2023
Publisher: American Chemical Society
Journal Title: Journal of organic chemistry
Volume: 88
Issue: 7
Start Page: 4606
End Page: 4618
Publisher DOI: 10.1021/acs.joc.3c00069
Abstract: We demonstrate the synthesis and chiroptical proper -ties of doubled molecules of a chiral [1]rotaxane, based on the assembly of an achiral ring of a phenylacetylene macrocycle (6PAM) and a p-phenylene ethynylene rod. Two molecules of [1]rotaxane constituted the doubled molecule through the ring fusion of 6PAMs to a 10PAM, which assured stationary occupation relative to each optically active unit. The absorption properties of the 10PAM-based doubled molecule and 6PAM-based original unit were consistently characterized by the independent existence of m-phenylene ethynylene ring(s) and p-phenylene ethynylene rod(s). Thus, molar circular dichroism (CD) was directly compared between the doubled molecule (n = 2) and the original unit (n = 1) to show that molar CD was increased more than expected by an increase in the number of units, or by an increase in absorbance. Due to the invariance of the configuration and the relative occupation of two units arranged adjacent to each other in 10PAM, one more comparison was available with an isomeric molecule of two rings and two rods in a threaded-and-unthreaded form. The additional arrangement of an optically inactive unit in an unthreaded form also led to an increase in molar CD, compared to that of the original chiral unit in a threaded form.
Rights: This document is the Accepted Manuscript version of a Published Work that appeared in final form in Journal of organic chemistry copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://pubs.acs.org/articlesonrequest/AOR-DZC8NNBK2IYNEJHDQJZT
Type: article (author version)
URI: http://hdl.handle.net/2115/91514
Appears in Collections:理学院・理学研究院 (Graduate School of Science / Faculty of Science) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 上遠野 亮

Export metadata:

OAI-PMH ( junii2 , jpcoar_1.0 )

MathJax is now OFF:


 

 - Hokkaido University