Abstract
The dimeric association of α,α′-di(benzylamino)tripyrrin in chloroform was found to be 40 times less effective than that of previously reported α,α′-dianilinotripyrrin, which, however, led us to observe the co-crystal structure of single and double helix forms. Attachment of chiral phenylethylamines on the same tripyrrin platform was also performed to induce helical chirality.
| Original language | English |
|---|---|
| Pages (from-to) | 2617-2620 |
| Number of pages | 4 |
| Journal | Chemical Communications |
| Volume | 57 |
| Issue number | 21 |
| Early online date | 2 Feb 2021 |
| DOIs | |
| Publication status | Published - 14 Mar 2021 |
Bibliographical note
Funding Information:The work at Kyoto was supported by JSPS KAKENHI Grant Number (JP20K05463). K. U. and M. U. acknowledge JSPS Fellowships for Young Scientists. T. T. acknowledges financial support from the TOBEMAKI Scholarship Foundation, Murata Science Foundation and Izumi Science and Technology Foundation. G. D. P. thanks the EPSRC and University of Bath for financial support.
Publisher Copyright:
© The Royal Society of Chemistry 2021.
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
Funding
The work at Kyoto was supported by JSPS KAKENHI Grant Number (JP20K05463). K. U. and M. U. acknowledge JSPS Fellowships for Young Scientists. T. T. acknowledges financial support from the TOBEMAKI Scholarship Foundation, Murata Science Foundation and Izumi Science and Technology Foundation. G. D. P. thanks the EPSRC and University of Bath for financial support.
ASJC Scopus subject areas
- Catalysis
- Electronic, Optical and Magnetic Materials
- Ceramics and Composites
- General Chemistry
- Surfaces, Coatings and Films
- Metals and Alloys
- Materials Chemistry