Pathways to fluorescence via restriction of intramolecular motion in substituted tetraphenylethylenes-Reference-Cited by-同舟云学术

Pathways to fluorescence via restriction of intramolecular motion in substituted tetraphenylethylenes

Author:

Li Yingchao¹,Aquino Adélia J. A.¹²^ORCID,Siddique Farhan³⁴^ORCID,Niehaus Thomas A.⁵,Lischka Hans¹⁶^ORCID,Nachtigallová Dana⁷⁸

Affiliation:

1. School of Pharmaceutical Science and Technology, Tianjin University, Tianjin 300072, P. R. China

2. Department of Mechanical Engineering, Texas Tech University, Lubbock, TX, 79409, USA

3. Department of Pharmaceutical Chemistry, Bahauddin Zakariya University, 60800 Multan, Pakistan

4. Royal Institute of Medical Sciences, Multan, Pakistan

5. Univ Lyon, Université Claude Bernard Lyon 1, CNRS, Institut Lumière Matière, F-69622, Villeurbanne, France

6. Department of Chemistry and Biochemistry, Texas Tech University Lubbock, TX 79409-1061, USA

7. Institute of Organic Chemistry and Biochemistry v.v.i., The Czech Academy of Sciences, 16610 Prague 6, Czech Republic

8. IT4Innovations, VŠB-Technical University of Ostrava, 70800 Ostrava-Poruba, Czech Republic

Abstract

Functionalization is used to restrict the torsional, excited-state proton transfer and cyclization modes in UV-excited tetraphenylethylenes.

Funder

National Science Foundation

Grantová Agentura České Republiky

Publisher

Royal Society of Chemistry (RSC)

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

Link

Reference72 articles.

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