Orientation of carbonyl groups in inclusion crystals formed from ketones with aromatic diimide-based macrocycles-Reference-Cited by-同舟云学术

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Orientation of carbonyl groups in inclusion crystals formed from ketones with aromatic diimide-based macrocycles

Published:2023 Issue:8 Volume:25 Page:1295-1300
ISSN:1466-8033
Container-title:CrystEngComm
language:en
Short-container-title:CrystEngComm

Author:

Tominaga Masahide¹^ORCID,Nanbara Sakito¹,Hyodo Tadashi¹,Kawahata Masatoshi²^ORCID,Yamaguchi Kentaro¹^ORCID

Affiliation:

1. Faculty of Pharmaceutical Sciences at Kagawa Campus, Tokushima Bunri University, Sanuki, Kagawa 769-2193, Japan

2. Showa Pharmaceutical University, Machida, Tokyo 194-8543, Japan

Abstract

Inclusion crystals were formed from ketones with aromatic diimide-based macrocycles possessing adamantane units, where the oxygen atoms of guests interacted with the electron-deficient π-surfaces of the aromatic diimides through CO⋯π contacts.

Funder

Japan Society for the Promotion of Science

Publisher

Royal Society of Chemistry (RSC)

Subject

Condensed Matter Physics,General Materials Science,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/CE/D2CE01641A

Reference38 articles.

1. Cyclic aromatic imides as a potential class of molecules for supramolecular interactions

2. Anion−π Interactions with Fluoroarenes

3. Towards design strategies for anion–π interactions in crystal engineering

4. Recent advances of hexaazatriphenylene (HAT) derivatives: Their applications in self-assembly and porous organic materials

5. Exploring Anion−π Interactions and Their Applications in Supramolecular Chemistry

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