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Thiacrown Ethers Engaged C(60) through Charge Transfer: Experimental and Theoretical Study
[Image: see text] UV–Vis spectroscopy is used to study the charge transfer complexes of thiacrown ethers 1–6 with fullerene. The size of TCE1-6 and the nature of the heteroatoms (N, O and S) have been systematically changed to examine the effect of these factors on the HOMO/LUMO energy levels, the o...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7542602/ https://www.ncbi.nlm.nih.gov/pubmed/33043183 http://dx.doi.org/10.1021/acsomega.0c01877 |
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author | Al Khalyfeh, Khaled Afaneh, Akef T. Marashdeh, Ali Almatarneh, Mansour H. Al-Mazaideh, Ghassab M. Mizyed, Shehadeh Ashram, Muhammad |
author_facet | Al Khalyfeh, Khaled Afaneh, Akef T. Marashdeh, Ali Almatarneh, Mansour H. Al-Mazaideh, Ghassab M. Mizyed, Shehadeh Ashram, Muhammad |
author_sort | Al Khalyfeh, Khaled |
collection | PubMed |
description | [Image: see text] UV–Vis spectroscopy is used to study the charge transfer complexes of thiacrown ethers 1–6 with fullerene. The size of TCE1-6 and the nature of the heteroatoms (N, O and S) have been systematically changed to examine the effect of these factors on the HOMO/LUMO energy levels, the optical energy gap and the interactions between TCE’s and C60. The negative and positive values of ΔS designate the structural forming method and the randomness of the free solvent molecules, respectively. Thermodynamics and stability data show that the complexes have a 1:1 ratio that has been emphasized by density functional theory calculations. Additionally, they show a synergetic interplay of donor–acceptor, π–π, and n–π interactions, which are the basis for the affinity of our novel receptors toward C(60). The proposed system of enzyme model suggests a development concept in the future design of enzyme model organic photovoltaic systems. |
format | Online Article Text |
id | pubmed-7542602 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-75426022020-10-09 Thiacrown Ethers Engaged C(60) through Charge Transfer: Experimental and Theoretical Study Al Khalyfeh, Khaled Afaneh, Akef T. Marashdeh, Ali Almatarneh, Mansour H. Al-Mazaideh, Ghassab M. Mizyed, Shehadeh Ashram, Muhammad ACS Omega [Image: see text] UV–Vis spectroscopy is used to study the charge transfer complexes of thiacrown ethers 1–6 with fullerene. The size of TCE1-6 and the nature of the heteroatoms (N, O and S) have been systematically changed to examine the effect of these factors on the HOMO/LUMO energy levels, the optical energy gap and the interactions between TCE’s and C60. The negative and positive values of ΔS designate the structural forming method and the randomness of the free solvent molecules, respectively. Thermodynamics and stability data show that the complexes have a 1:1 ratio that has been emphasized by density functional theory calculations. Additionally, they show a synergetic interplay of donor–acceptor, π–π, and n–π interactions, which are the basis for the affinity of our novel receptors toward C(60). The proposed system of enzyme model suggests a development concept in the future design of enzyme model organic photovoltaic systems. American Chemical Society 2020-09-25 /pmc/articles/PMC7542602/ /pubmed/33043183 http://dx.doi.org/10.1021/acsomega.0c01877 Text en This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Al Khalyfeh, Khaled Afaneh, Akef T. Marashdeh, Ali Almatarneh, Mansour H. Al-Mazaideh, Ghassab M. Mizyed, Shehadeh Ashram, Muhammad Thiacrown Ethers Engaged C(60) through Charge Transfer: Experimental and Theoretical Study |
title | Thiacrown Ethers Engaged C(60) through Charge
Transfer: Experimental and Theoretical Study |
title_full | Thiacrown Ethers Engaged C(60) through Charge
Transfer: Experimental and Theoretical Study |
title_fullStr | Thiacrown Ethers Engaged C(60) through Charge
Transfer: Experimental and Theoretical Study |
title_full_unstemmed | Thiacrown Ethers Engaged C(60) through Charge
Transfer: Experimental and Theoretical Study |
title_short | Thiacrown Ethers Engaged C(60) through Charge
Transfer: Experimental and Theoretical Study |
title_sort | thiacrown ethers engaged c(60) through charge
transfer: experimental and theoretical study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7542602/ https://www.ncbi.nlm.nih.gov/pubmed/33043183 http://dx.doi.org/10.1021/acsomega.0c01877 |
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