Anthracene–naphthylacetonitrile fluorescent isomers and Cl/H substituent dependent molecular packing, solid-state fluorescence and mechanofluorochromism-Reference-Cited by-同舟云学术

Anthracene–naphthylacetonitrile fluorescent isomers and Cl/H substituent dependent molecular packing, solid-state fluorescence and mechanofluorochromism

Published:2023 Issue:45 Volume:25 Page:6303-6309
ISSN:1466-8033
Container-title:CrystEngComm
language:en
Short-container-title:CrystEngComm

Author:

Ravi Sasikala¹,Priyadharshini Prakash¹,Karthikeyan Subramanian²,Pannipara Mehboobali³⁴,Al-Sehemi Abdullah G.³⁴,Madhu Vedichi⁵^ORCID,Moon Dohyun⁶^ORCID,Anthony Savarimuthu Philip¹^ORCID

Affiliation:

1. School of Chemical & Biotechnology, SASTRA Deemed University, Thanjavur-613401, Tamil Nadu, India

2. PG and Research Department of Chemistry, KhadirMohideen College (affiliated to Bharathidasan University), Adirampattinam, Tamil Nadu, India

3. Research Center for Advanced Materials Science, King Khalid University, Abha 61413, Saudi Arabia

4. Department of Chemistry, King Khalid University, Abha 61413, Saudi Arabia

5. Department of Applied Chemistry, Karunya Institute of Technology and Sciences, Coimbatore-641 114, Tamil Nadu, India

6. Beamline Department, Pohang Accelerator Laboratory, 80 Jigokro-127 beongil, Nam-gu, Pohang, Gyeongbuk, Korea

Abstract

Anthracene aldehyde with naphthylacetonitrile isomers produced unusual and expected fluorophores that showed molecular packing-controlled stimuli-induced reversible fluorescence switching and solid-state fluorescence.

Funder

Science and Engineering Research Board

Department of Science and Technology, Ministry of Science and Technology, India

Deanship of Scientific Research, King Khalid University

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/D3CE00718A

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1. Mechanochromism, thermochromism, protonation effect and discrimination of CHCl3 from organic solvents in a Et2N-substituted Salicylaldehyde Schiff base