- Title
- Optical limiting properties of D-π-A BODIPY dyes in the presence and absence of methyl groups at the 1, 7-positions
- Creator
- May, Aviwe K
- Creator
- Mack, John
- Creator
- Nyokong, Tebello
- Subject
- To be catalogued
- Date Issued
- 2020
- Date
- 2020
- Type
- text
- Type
- article
- Identifier
- http://hdl.handle.net/10962/186146
- Identifier
- vital:44468
- Identifier
- xlink:href="https://doi.org/10.1142/S1088424620500315"
- Description
- The optical limiting properties of three meso-pentafluorophenylstyrylBODIPY dyes are investigated in the presence and absence of methyl groups at the 1,7-positions that hinder free rotation of the meso-aryl group. Pentafluorophenyl groups are introduced at the meso-position, while 4-diethylaminostyryl groups are introduced at the 3- and/or 5-positions to form dyes with strong donor-ππ-acceptor (D-ππ-A) properties to enhance the dipole moment of the molecule. Favorable optical limiting properties are obtained for all three dyes, with the highest second-order hyperpolarizability value obtained for a monostyryl dye with no methyl groups at the 1,7-position. Bromination at the 2,6-positions of a 1,7-methyl substituted dye is found to result in second-order hyperpolarizability that is an order of magnitude lower than that calculated for the analogous non-halogenated dye.
- Format
- computer
- Format
- online resource
- Format
- application/pdf
- Format
- 1 online resource (9 pages)
- Format
- Publisher
- World Scientific Publishing
- Language
- English
- Relation
- Journal of Porphyrins and Phthalocyanines
- Relation
- May, A., Mack, J. and Nyokong, T., 2020. Optical limiting properties of D-π-A BODIPY dyes in the presence and absence of methyl groups at the 1, 7-positions. Journal of Porphyrins and Phthalocyanines, 24(09), pp.1129-1137
- Relation
- Journal of Porphyrins and Phthalocyanines volume 24 number 09 p. 1129 2020 1099-1409
- Rights
- Publisher
- Rights
- Use of this resource is governed by the terms and conditions of the World Scientific Copyright and Permissions Statement (https://0-www.worldscientific.com.wam.seals.ac.za/page/permissions)
- Rights
- Closed Access
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