A potential naphthyl-thiazole-based organic dye and a ditopic chromogenic probe for CN− and Fe3+ with molecular logic functions. (23rd October 2020)
- Record Type:
- Journal Article
- Title:
- A potential naphthyl-thiazole-based organic dye and a ditopic chromogenic probe for CN− and Fe3+ with molecular logic functions. (23rd October 2020)
- Main Title:
- A potential naphthyl-thiazole-based organic dye and a ditopic chromogenic probe for CN− and Fe3+ with molecular logic functions
- Authors:
- Uahengo, Veikko
Hamukwaya, Eunike N.
Endjala, Paulina T.
Naimhwaka, Johannes H. - Abstract:
- Abstract : Dye sensitizers are entities designed primarily to serve the function of harvesting light photons in the functional wavelength, which is centered on charge transfer mechanisms. Abstract : Dye sensitizers are entities designed primarily to serve the function of harvesting light photons in the functional wavelength, which is centered on charge transfer mechanisms. A metal-free dye sensitizer (J ) based on the naphthyl-thiazole groups was synthesized via a one-step reaction mechanism and characterized using UV-vis, 1 H NMR and fluorescence spectroscopic methods. The applications of J were investigated based on its charge transfer mechanisms of photoinduced electron transfer (PET) and excited-state intermolecular proton transfer (ESIPT) mechanisms. Subsequently, J displayed several charge transfer-based properties complementary to dye sensitizers, chemosensing and molecular logic functions. The properties were investigated and studied primarily in acetonitrile (CH3 CN), as a polar solvent of choice. The optical properties of J were investigated through solvatochromism, aided by theoretical recreation, while chemosensing properties were investigated, thereby in the process establishing that J is a ditopic probe which could selectively discriminate CN −, F − and AcO − as well as Fe 3+ in CH3 CN, among other ions. In addition, the reversibility and reproducibility studies substantiated that J exhibits molecular logic operation properties, based on complementary IMP/INHAbstract : Dye sensitizers are entities designed primarily to serve the function of harvesting light photons in the functional wavelength, which is centered on charge transfer mechanisms. Abstract : Dye sensitizers are entities designed primarily to serve the function of harvesting light photons in the functional wavelength, which is centered on charge transfer mechanisms. A metal-free dye sensitizer (J ) based on the naphthyl-thiazole groups was synthesized via a one-step reaction mechanism and characterized using UV-vis, 1 H NMR and fluorescence spectroscopic methods. The applications of J were investigated based on its charge transfer mechanisms of photoinduced electron transfer (PET) and excited-state intermolecular proton transfer (ESIPT) mechanisms. Subsequently, J displayed several charge transfer-based properties complementary to dye sensitizers, chemosensing and molecular logic functions. The properties were investigated and studied primarily in acetonitrile (CH3 CN), as a polar solvent of choice. The optical properties of J were investigated through solvatochromism, aided by theoretical recreation, while chemosensing properties were investigated, thereby in the process establishing that J is a ditopic probe which could selectively discriminate CN −, F − and AcO − as well as Fe 3+ in CH3 CN, among other ions. In addition, the reversibility and reproducibility studies substantiated that J exhibits molecular logic operation properties, based on complementary IMP/INH logic functions. Thus, J can be utilized as a colorimetric molecular switch modulated by CN − /Hg 2+ . … (more)
- Is Part Of:
- New journal of chemistry. Volume 44:Number 43(2020)
- Journal:
- New journal of chemistry
- Issue:
- Volume 44:Number 43(2020)
- Issue Display:
- Volume 44, Issue 43 (2020)
- Year:
- 2020
- Volume:
- 44
- Issue:
- 43
- Issue Sort Value:
- 2020-0044-0043-0000
- Page Start:
- 18588
- Page End:
- 18600
- Publication Date:
- 2020-10-23
- Subjects:
- Chemistry -- Periodicals
Chimie -- Périodiques
540 - Journal URLs:
- http://www.rsc.org/ ↗
http://www.rsc.org/is/journals/current/newjchem/njc.htm ↗ - DOI:
- 10.1039/d0nj03806g ↗
- Languages:
- English
- ISSNs:
- 1144-0546
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6084.319900
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 14952.xml