The effect of substituents and their positions on a series of disubstituted naphthalene bromide salts towards intermolecular interactions and crystal packing-Reference-Cited by-同舟云学术

The effect of substituents and their positions on a series of disubstituted naphthalene bromide salts towards intermolecular interactions and crystal packing

Published:2022 Issue:27 Volume:24 Page:4869-4879
ISSN:1466-8033
Container-title:CrystEngComm
language:en
Short-container-title:CrystEngComm

Author:

Yeoh Wei-Jiun¹,Sobolev Alexandre N.²,Paterson Martin J.³^ORCID,Dalgarno Scott J.³^ORCID,Ling Irene¹^ORCID

Affiliation:

1. School of Science, Monash University Malaysia, Jalan Lagoon Selatan, 47500 Bandar Sunway, Selangor, Malaysia

2. School of Molecular Sciences, M310, The University of Western Australia, 35 Stirling Highway, Perth, WA 6009, Australia

3. School of Engineering and Physical Sciences, Heriot-Watt University, Riccarton, Edinburgh, UK

Abstract

Naphthalene derived dications bearing different N-heterocyclic substituents appended at different positions demonstrated conformational flexibility and interesting self-assembled packing motifs when crystallised in the solid state as bromide salts.

Funder

Monash University

Leverhulme Trust

Engineering and Physical Sciences Research Council

University of Western Australia

Heriot-Watt University

Publisher

Royal Society of Chemistry (RSC)

Subject

Condensed Matter Physics,General Materials Science,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/CE/D2CE00538G

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